ADASTRA v5.1.3
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rs289818
chr15:63503638
A
>
G
Sequence
agaggtcagagggtcagggatcca[A/G]tctccatacagatcaacaagttac
ASB in cell types
K562 (myelogenous leukemia)
HCASMC (Human coronary artery smooth muscle cells)
ASB for transcription factors
CTCF_HUMAN
TCF21_HUMAN
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View in PheLiGe
0.05
FDR threshold
0
ES threshold
Color scale
-log10 FDR of Ref (
A
) ASB
-log10 FDR of Alt (
G
) ASB
Details
Transcription factors
Cell types
Effect size Ref
(+6 others)
Selected columns
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Uniprot ID
Effect size Ref
Effect size Alt
FDR Ref
FDR Alt
Mean BAD
Motif fold change
Motif concordance
CTCF_HUMAN
0.45
1.12
0.68
5.8·10
-3
1.02
n/a
No Hit
TCF21_HUMAN
2.07
n/a
0.02
1.00
2.50
n/a
n/a
Items per page:
5
1 – 2 of 2
Motif analysis
No data available
Genetic associations
GRASP
celiac disease
,
fasting blood glucose
,
primary rhegmatogenous retinal detachment
,
rheumatoid arthritis
GTEx eQTL
Adipose_Subcutaneous
,
Brain_Cerebellum
,
Esophagus_Mucosa
,
Heart_Left_Ventricle
,
Whole_Blood
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Generated by ADASTRA database
2022.05.19 v5.1.3 Bill Cipher
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SNP set annotation with ANANASTRA
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+/-100bp
log2-scale
log2(Alt/Ref motif p-value)