| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:160407420-160407790 | Rare:250 | ||||
| chr2:160407783-160408020 | Common:2; Rare:122 | ||||
| chr2:160492490-160492930 | Common:7; Rare:195 | ||||
| chr2:160492920-160493320 | Common:4; Rare:269 | ||||
| chr2:160493367-160493983 | Common:6; Rare:382 | ||||
| chr2:161136806-161136976 | Rare:39 | ||||
| chr2:161160168-161160773 | Common:6; Rare:349 | ||||
| chr2:161160866-161161131 | Common:1; Rare:96 | ||||
| chr2:161308219-161308603 | Common:6; Rare:230 | ||||
| chr2:161415160-161415660 | Common:2; Rare:97 | ||||
| chr2:161623820-161624560 | Common:2; Rare:210 | ||||
| chr2:162073961-162074256 | Common:1; Rare:94 | ||||
| chr2:162317990-162318340 | Rare:212; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:162318556-162318863 | Common:2; Rare:139 | ||||
| chr2:162343854-162344265 | Common:6; Rare:405 |