| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:15592240-15592825 | Common:4; Rare:202 | ||||
| chr2:16665770-16666100 | Common:4; Rare:66 | ||||
| chr2:17517780-17518180 | Common:1; Rare:129 | ||||
| chr2:17518220-17518800 | Common:27; Rare:741 | ||||
| chr2:17538790-17539160 | Common:3; Rare:107 | ||||
| chr2:17752860-17753410 | Common:9; Rare:327 | ||||
| chr2:17753630-17754511 | Common:40; Rare:1098; Clinvar (benign):7 | ||||
| chr2:17878410-17878770 | Common:18; Rare:242 | ||||
| chr2:18559617-18561266 | Common:10; Rare:1426 | ||||
| chr2:19900754-19901154 | Common:2; Rare:102 | ||||
| chr2:19901470-19902610 | Common:46; Rare:1468 | ||||
| chr2:19989694-19990094 | Rare:108; Clinvar:1 | ||||
| chr2:19990025-19990272 | Rare:184 | ||||
| chr2:20051520-20051969 | Common:7; Rare:504 | ||||
| chr2:20051950-20052260 | Common:7; Rare:163 |