Proximal
GM19238(Human) | 21581 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322694-128322947 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr9:128340137-128340237 | Common:2; Rare:46 | ||||
| chr9:128340372-128340740 | Common:2; Rare:118 | ||||
| chr9:128371081-128371484 | Common:1; Rare:134 | ||||
| chr9:128371598-128371660 | Common:2; Rare:14 | ||||
| chr9:128420745-128420887 | Common:1; Rare:52 | ||||
| chr9:128455929-128456252 | Common:2; Rare:102 | ||||
| chr9:128456353-128456519 | Common:1; Rare:44 | ||||
| chr9:128456822-128456999 | Common:1; Rare:45 | ||||
| chr9:128504456-128504815 | Common:2; Rare:131; Clinvar:6 | ||||
| chr9:128551995-128552175 | Common:1; Rare:46 | ||||
| chr9:128552185-128552675 | Common:2; Rare:171; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:128552834-128552849 | Rare:2 | ||||
| chr9:128552977-128553176 | Rare:53 | ||||
| chr9:128656349-128656835 | Common:4; Rare:170; Clinvar (benign):1; Clinvar (pathogenic):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