Proximal
H1(Human) | 12287 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35829071-35829285 | Common:1; Rare:55 | ||||
| chr9:36037014-36037077 | Common:2; Rare:12 | ||||
| chr9:36190715-36191019 | Common:2; Rare:101 | ||||
| chr9:36191240-36191277 | Rare:7 | ||||
| chr9:36258404-36258625 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400239-36400395 | Common:3; Rare:53 | ||||
| chr9:36487662-36487961 | Common:2; Rare:112 | ||||
| chr9:37120183-37120511 | Common:2; Rare:91 | ||||
| chr9:37422580-37422810 | Common:2; Rare:110; Clinvar:1 | ||||
| chr9:37431809-37432041 | Common:1; Rare:64; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr9:37465117-37465537 | Common:3; Rare:138 | ||||
| chr9:37485737-37486068 | Common:3; Rare:118 | ||||
| chr9:37576202-37576387 | Rare:45 | ||||
| chr9:37592461-37592643 | Common:2; Rare:71 | ||||
| chr9:37784720-37785149 | Common:1; Rare:189; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):4 |
- 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