| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:157837731-157837861 | Rare:27 | ||||
| chr2:157837912-157838884 | Common:9; Rare:479 | ||||
| chr2:157874852-157875538 | Common:3; Rare:168; Clinvar (benign):1 | ||||
| chr2:157875660-157876339 | Common:3; Rare:527 | ||||
| chr2:157876265-157876897 | Common:3; Rare:565 | ||||
| chr2:158456562-158458793 | Common:31; Rare:1884 | ||||
| chr2:158968360-158968740 | Rare:212 | ||||
| chr2:159135374-159135774 | Common:5; Rare:179 | ||||
| chr2:159285898-159286298 | Common:13; Rare:162 | ||||
| chr2:159286600-159287049 | Common:30; Rare:714 | ||||
| chr2:159286980-159287250 | Common:2; Rare:80 | ||||
| chr2:159287281-159287381 | Common:1; Rare:19 | ||||
| chr2:159516142-159516602 | Common:3; Rare:143 | ||||
| chr2:159516547-159516667 | Rare:14 | ||||
| chr2:159614774-159615174 | Common:2; Rare:81 |