| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218403012-218403278 | Common:4; Rare:96 | ||||
| chr2:218429280-218429673 | Common:4; Rare:132; Clinvar (benign):1 | ||||
| chr2:219001977-219002212 | Common:2; Rare:49 | ||||
| chr2:226798863-226799028 | Rare:37 | ||||
| chr2:227372847-227372881 | Common:1; Rare:6 | ||||
| chr2:231412421-231412593 | Common:2; Rare:28 | ||||
| chr2:232457002-232457320 | Common:3; Rare:120 | ||||
| chr2:232458009-232458330 | Common:4; Rare:132 | ||||
| chr2:232760354-232760582 | Rare:48 | ||||
| chr2:232773691-232773987 | Rare:48 | ||||
| chr2:233012509-233012663 | Common:2; Rare:26 | ||||
| chr2:233462546-233462700 | Rare:56 | ||||
| chr2:237576926-237577082 | Common:3; Rare:39 | ||||
| chr2:240620824-240620884 | Rare:11 | ||||
| chr2:240622611-240622807 | Common:2; Rare:55 |