Proximal
H1(Human) | 12287 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153794025-153794260 | Common:2; Rare:47 | ||||
| chrX:153794324-153794699 | Common:1; Rare:118; Clinvar (benign):2 | ||||
| chrX:153830861-153831132 | Common:1; Rare:32 | ||||
| chrX:153886117-153886296 | Common:1; Rare:31 | ||||
| chrX:153944604-153944853 | Common:2; Rare:48 | ||||
| chrX:153971157-153971294 | Rare:29 | ||||
| chrX:153971792-153971944 | Rare:42 | ||||
| chrX:153972694-153972810 | Common:1; Rare:35 | ||||
| chrX:154019846-154019997 | Rare:26 | ||||
| chrX:154097609-154098029 | Common:2; Rare:87; Clinvar:6; Clinvar (benign):2 | ||||
| chrX:154351842-154352318 | Common:3; Rare:94; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chrX:154352326-154352553 | Rare:49; Clinvar:1; Clinvar (benign):8 | ||||
| chrX:154353161-154353368 | Common:3; Rare:46; Clinvar:3; Clinvar (benign):8 | ||||
| chrX:154371328-154371609 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:154374598-154374610 | Rare:1 |
- 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