| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160647009-160647286 | Common:3; Rare:52 | ||||
| chr1:161021112-161021520 | Common:2; Rare:104 | ||||
| chr1:161045091-161045470 | Common:1; Rare:71 | ||||
| chr1:161045819-161046140 | Common:1; Rare:88 | ||||
| chr1:161046244-161046303 | Rare:15 | ||||
| chr1:161098251-161098471 | Common:2; Rare:48 | ||||
| chr1:161117443-161117650 | Rare:39 | ||||
| chr1:161117900-161118265 | Common:1; Rare:162 | ||||
| chr1:161131642-161131948 | Common:1; Rare:62 | ||||
| chr1:161132421-161132647 | Common:1; Rare:78 | ||||
| chr1:161132651-161133073 | Common:2; Rare:96 | ||||
| chr1:161133121-161133275 | Rare:30 | ||||
| chr1:161153427-161153470 | Rare:9 | ||||
| chr1:161153745-161153836 | Rare:24 | ||||
| chr1:161153841-161154142 | Common:1; Rare:97; Clinvar (pathogenic):1 |