| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160098481-160098555 | Rare:23 | ||||
| chr1:160098810-160099129 | Common:4; Rare:47 | ||||
| chr1:160151474-160151618 | Common:1; Rare:25 | ||||
| chr1:160205071-160205519 | Common:3; Rare:101 | ||||
| chr1:160211196-160211297 | Rare:21 | ||||
| chr1:160238616-160238919 | Common:2; Rare:62 | ||||
| chr1:160261415-160261731 | Common:1; Rare:55 | ||||
| chr1:160262111-160262652 | Common:1; Rare:155 | ||||
| chr1:160285048-160285198 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:160343181-160343411 | Rare:93 | ||||
| chr1:161020556-161020687 | Common:1; Rare:32 | ||||
| chr1:161021070-161021470 | Common:5; Rare:106 | ||||
| chr1:161038881-161039029 | Common:1; Rare:51 | ||||
| chr1:161045878-161046071 | Common:1; Rare:49 | ||||
| chr1:161098174-161098431 | Common:1; Rare:42 |