rs4780476 chr16:12768150 A>C
- Sequence
ccttcaactgaattctatcaacca[A/C]aaggactcttaagacctttctgtt
- ASB in cell types
- K562 (myelogenous leukemia)
- ASB for transcription factors
- RFX1_HUMAN MYNN_HUMAN
View in PheLiGe Color scale
-log10 FDR of Ref (A) ASB
-log10 FDR of Alt (C) 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 | |
|---|---|---|---|---|---|---|---|---|
| RFX1_HUMAN | n/a | 2.79 | 2.00 | n/a | No Hit | |||
| MYNN_HUMAN | n/a | 3.00 | 2.00 | n/a | No Hit |
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Motif analysis
No data available
Genetic associations
GRASP asthma, coronary artery disease (cad), sporadic creutzfeldt-jakob disease, triglycerides change with statins