| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40040389-40040897 | Common:4; Rare:159 | ||||
| chr1:40097179-40097367 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr1:40097674-40097825 | Rare:29 | ||||
| chr1:40161236-40161454 | Common:1; Rare:74 | ||||
| chr1:40257683-40258290 | Common:5; Rare:158; Clinvar:9; Clinvar (benign):1 | ||||
| chr1:40305026-40305249 | Common:7; Rare:37 | ||||
| chr1:40315359-40315584 | Common:4; Rare:53; Clinvar (benign):1 | ||||
| chr1:40315890-40316380 | Common:4; Rare:185 | ||||
| chr1:40316611-40316840 | Common:2; Rare:54 | ||||
| chr1:40373492-40373774 | Common:1; Rare:70 | ||||
| chr1:40374538-40374667 | Common:12; Rare:29 | ||||
| chr1:40531470-40531765 | Common:1; Rare:78 | ||||
| chr1:40665652-40665824 | Common:1; Rare:47 | ||||
| chr1:40691436-40691850 | Common:3; Rare:180 | ||||
| chr1:40692036-40692249 | Common:1; Rare:67 |