| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:26318629-26319044 | Rare:140 | ||||
| chr1:26336249-26337031 | Common:34; Rare:1953 | ||||
| chr1:26431963-26432496 | Common:35; Rare:706; Clinvar:14; Clinvar (benign):7 | ||||
| chr1:26432576-26432997 | Common:2; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26471227-26471978 | Common:3; Rare:197; Clinvar:1 | ||||
| chr1:26471912-26472638 | Common:29; Rare:829 | ||||
| chr1:26472805-26473251 | Common:5; Rare:850 | ||||
| chr1:26529245-26530220 | Common:22; Rare:748 | ||||
| chr1:26531181-26531581 | Common:5; Rare:130 | ||||
| chr1:26542432-26542832 | Common:2; Rare:69 | ||||
| chr1:26555645-26556045 | Rare:73 | ||||
| chr1:26695393-26696479 | Common:9; Rare:1382; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26696382-26697407 | Common:3; Rare:598; Clinvar:12; Clinvar (benign):16 | ||||
| chr1:26771390-26772036 | Common:3; Rare:257 | ||||
| chr1:26786701-26788436 | Common:26; Rare:1798; Clinvar:12; Clinvar (benign):13 |