Proximal
GM18507(Human) | 19257 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134359-92134618 | Rare:79 | ||||
| chr7:92134666-92134980 | Common:4; Rare:86 | ||||
| chr7:92245480-92245742 | Rare:69; Clinvar (benign):1 | ||||
| chr7:92245796-92246326 | Common:6; Rare:135; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92246561-92246923 | Common:1; Rare:77 | ||||
| chr7:92447306-92447555 | Common:3; Rare:86 | ||||
| chr7:92447596-92447714 | Rare:39; Clinvar (benign):1 | ||||
| chr7:92447925-92448055 | Common:1; Rare:32; Clinvar (benign):4 | ||||
| chr7:92528395-92528908 | Common:5; Rare:168; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92589792-92590184 | Common:3; Rare:130 | ||||
| chr7:92590278-92590526 | Common:1; Rare:87 | ||||
| chr7:92833453-92833687 | Rare:55 | ||||
| chr7:92833902-92834142 | Rare:58 | ||||
| chr7:92835218-92835622 | Common:3; Rare:105 | ||||
| chr7:92836486-92836626 | Rare:29 |
- 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