rs2366773 chr5:90642770 C>T
- Sequence
gaccctatgttataaaagtaagta[C/T]gaaaaaaacttccatttattctgt
- ASB in cell types
- K562 (myelogenous leukemia)
- ASB for transcription factors
- ENL_HUMAN NFRKB_HUMAN AFF1_HUMAN
View in PheLiGe Color scale
-log10 FDR of Ref (C) ASB
-log10 FDR of Alt (T) ASB
Details
Transcription factors
Cell types
Uniprot ID | Effect size Ref | Effect size Alt | FDR Ref | FDR Alt | Mean BAD | Motif fold change | Motif concordance | |
|---|---|---|---|---|---|---|---|---|
| ENL_HUMAN | 0.75 | 2.73 | 1.78 | n/a | n/a | |||
| NFRKB_HUMAN | n/a | 2.54 | 2.00 | n/a | n/a | |||
| AFF1_HUMAN | -1.49 | 1.94 | 2.00 | n/a | n/a |
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Motif analysis
No data available
Genetic associations
GRASP autism, diabetic retinopathy in type 2 diabetes mellitus, neuroblastoma (brain cancer), paternal transmission distortion, transmission distortion
GTEx eQTL Adipose_Visceral_Omentum, Adrenal_Gland, Artery_Aorta, Artery_Tibial, Brain_Cerebellar_Hemisphere, Brain_Cerebellum, Colon_Transverse, Heart_Atrial_Appendage, Heart_Left_Ventricle, Lung, Muscle_Skeletal, Nerve_Tibial, Skin_Not_Sun_Exposed_Suprapubic, Spleen, Stomach, Thyroid, Whole_Blood