Proximal
GM18507(Human) | 19257 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154097084-154097294 | Common:1; Rare:31 | ||||
| chrX:154097619-154098098 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):2 | ||||
| chrX:154371153-154371548 | Common:1; Rare:102; Clinvar:7; Clinvar (benign):9 | ||||
| chrX:154371635-154371769 | Rare:22 | ||||
| chrX:154379192-154379452 | Rare:59 | ||||
| chrX:154397502-154397794 | Common:1; Rare:60 | ||||
| chrX:154397923-154398547 | Common:4; Rare:168 | ||||
| chrX:154398786-154399021 | Common:4; Rare:50 | ||||
| chrX:154411206-154411231 | Rare:3 | ||||
| chrX:154411303-154411659 | Rare:66 | ||||
| chrX:154412041-154412212 | Common:2; Rare:25; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:154412663-154412717 | Rare:1 | ||||
| chrX:154428421-154428718 | Common:2; Rare:56 | ||||
| chrX:154436746-154436987 | Common:3; Rare:37 | ||||
| chrX:154437121-154437270 | Rare:59 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box