| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:155978145-155978288 | Rare:32 | ||||
| chr1:155978531-155978697 | Common:1; Rare:49 | ||||
| chr1:155978988-155979289 | Common:1; Rare:45 | ||||
| chr1:156007026-156007204 | Rare:32 | ||||
| chr1:156020869-156021078 | Rare:64 | ||||
| chr1:156052952-156053199 | Common:1; Rare:44 | ||||
| chr1:156053781-156053933 | Rare:33 | ||||
| chr1:156054408-156054890 | Common:4; Rare:123 | ||||
| chr1:156060967-156061212 | Common:1; Rare:63 | ||||
| chr1:156082419-156082707 | Rare:66 | ||||
| chr1:156106441-156106729 | Common:2; Rare:59 | ||||
| chr1:156114484-156114829 | Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:156122946-156123157 | Common:2; Rare:41 | ||||
| chr1:156123324-156123480 | Common:1; Rare:23 | ||||
| chr1:156126332-156126462 | Rare:23 |