| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85047451-85047590 | Common:2; Rare:27 | ||||
| chr2:85047603-85047820 | Common:1; Rare:33 | ||||
| chr2:85049131-85049557 | Common:1; Rare:103 | ||||
| chr2:85135661-85135749 | Common:1; Rare:19 | ||||
| chr2:85340652-85340904 | Common:1; Rare:44 | ||||
| chr2:85386710-85386933 | Common:3; Rare:41 | ||||
| chr2:85542423-85543148 | Common:4; Rare:184; Clinvar:1; Clinvar (benign):12 | ||||
| chr2:85551996-85552295 | Common:1; Rare:50 | ||||
| chr2:85742560-85742808 | Common:4; Rare:46 | ||||
| chr2:85772324-85772634 | Rare:78 | ||||
| chr2:86135575-86135920 | Rare:79 | ||||
| chr2:86136812-86137141 | Common:1; Rare:70 | ||||
| chr2:86153525-86153576 | Rare:13 | ||||
| chr2:86159632-86159863 | Rare:44 | ||||
| chr2:86172805-86172993 | Common:5; Rare:27 |