| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179883892-179884011 | Common:1; Rare:21 | ||||
| chr1:179954468-179954599 | Common:2; Rare:36 | ||||
| chr1:179954679-179955156 | Common:1; Rare:102 | ||||
| chr1:180085394-180085647 | Common:2; Rare:47 | ||||
| chr1:180094797-180094886 | Rare:23 | ||||
| chr1:180094998-180095170 | Common:1; Rare:30 | ||||
| chr1:180154442-180155077 | Common:7; Rare:206 | ||||
| chr1:180502254-180502725 | Common:1; Rare:170 | ||||
| chr1:180502816-180502950 | Rare:54 | ||||
| chr1:180631861-180632187 | Common:5; Rare:118 | ||||
| chr1:181022784-181023195 | Common:25; Rare:190 | ||||
| chr1:181088486-181088731 | Rare:90 | ||||
| chr1:182390886-182391192 | Common:4; Rare:58 | ||||
| chr1:182391303-182391432 | Rare:26 | ||||
| chr1:182391679-182392045 | Common:5; Rare:132; Clinvar:5; Clinvar (benign):5 |