| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19990034-19990195 | Rare:45 | ||||
| chr2:20446854-20447091 | Common:3; Rare:100 | ||||
| chr2:20447279-20447479 | Common:1; Rare:74 | ||||
| chr2:20651047-20651276 | Rare:74 | ||||
| chr2:20823064-20823140 | Rare:30 | ||||
| chr2:21123835-21124006 | Common:1; Rare:56 | ||||
| chr2:23927057-23927325 | Common:3; Rare:92 | ||||
| chr2:24076284-24076590 | Rare:78 | ||||
| chr2:24123262-24123526 | Common:1; Rare:71 | ||||
| chr2:24360315-24360658 | Common:4; Rare:104 | ||||
| chr2:24971705-24972157 | Common:3; Rare:158 | ||||
| chr2:25878304-25878387 | Rare:18 | ||||
| chr2:26033751-26034159 | Common:4; Rare:154 | ||||
| chr2:26034390-26034623 | Common:2; Rare:61 | ||||
| chr2:26244528-26245118 | Common:2; Rare:196; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 |