Proximal
GM18507(Human) | 19257 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95316874-95317062 | Common:1; Rare:49 | ||||
| chr9:95317207-95317535 | Common:6; Rare:110; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:95317669-95317901 | Common:1; Rare:75; Clinvar:2 | ||||
| chr9:95505876-95506252 | Common:2; Rare:132 | ||||
| chr9:95506515-95506786 | Common:1; Rare:91; Clinvar:7; Clinvar (benign):7 | ||||
| chr9:95507601-95507730 | Rare:48 | ||||
| chr9:95875387-95875751 | Common:1; Rare:123 | ||||
| chr9:95875759-95876206 | Common:8; Rare:150; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383681-96383824 | Rare:47 | ||||
| chr9:96418270-96418946 | Common:6; Rare:211 | ||||
| chr9:96449942-96450249 | Common:4; Rare:110 | ||||
| chr9:96566630-96566861 | Common:2; Rare:79 | ||||
| chr9:96566935-96567110 | Rare:41 | ||||
| chr9:96654662-96654895 | Common:2; Rare:81 | ||||
| chr9:96655271-96655488 | Rare:63 |
- 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