rs394625 chr14:58899646 T>C
- Sequence
gttccattctatgcatccacaact[T/C]atgcaatctttatgattttctttt
- ASB in cell types
- HCASMC (Human coronary artery smooth muscle cells)
- ASB for transcription factors
- TCF21_HUMAN
View in PheLiGe Color scale
-log10 FDR of Ref (T) 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 | |
|---|---|---|---|---|---|---|---|---|
| TCF21_HUMAN | 0.47 | 2.05 | 1.25 | n/a | No Hit |
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Motif analysis
No data available
Genetic associations
GRASP autism, partial epilepsy, paternal transmission distortion, sporadic creutzfeldt-jakob disease, transmission distortion