| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:62783544-62783910 | Common:1; Rare:71 | ||||
| chr1:62784029-62784214 | Rare:73 | ||||
| chr1:63367394-63367760 | Rare:112; Clinvar (benign):1 | ||||
| chr1:63367912-63367953 | Rare:5 | ||||
| chr1:63368033-63368109 | Rare:17 | ||||
| chr1:63523144-63523666 | Common:4; Rare:146 | ||||
| chr1:63593157-63593292 | Rare:37 | ||||
| chr1:63594205-63594249 | Rare:7 | ||||
| chr1:63773869-63774213 | Rare:63 | ||||
| chr1:64470542-64470614 | Rare:18 | ||||
| chr1:64505779-64505918 | Common:2; Rare:16 | ||||
| chr1:64744774-64745208 | Common:2; Rare:128 | ||||
| chr1:64745301-64745505 | Common:1; Rare:62 | ||||
| chr1:64966278-64966744 | Common:3; Rare:161 | ||||
| chr1:64966905-64967238 | Common:1; Rare:62 |