| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159711975-159712289 | Common:2; Rare:86 | ||||
| chr2:159712334-159712621 | Common:2; Rare:102 | ||||
| chr2:160407528-160407679 | Rare:44 | ||||
| chr2:161160209-161160466 | Common:2; Rare:71 | ||||
| chr2:161308351-161308560 | Common:2; Rare:51 | ||||
| chr2:161415557-161415742 | Common:1; Rare:38 | ||||
| chr2:161416006-161416419 | Common:1; Rare:68 | ||||
| chr2:161416522-161416705 | Rare:42 | ||||
| chr2:162343893-162344228 | Common:1; Rare:118 | ||||
| chr2:162838580-162839128 | Common:1; Rare:116 | ||||
| chr2:163735995-163736069 | Rare:14 | ||||
| chr2:165469534-165469722 | Rare:36 | ||||
| chr2:165574110-165574385 | Rare:56 | ||||
| chr2:165953701-165954099 | Common:3; Rare:141; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:166375857-166376322 | Common:5; Rare:119; Clinvar:1; Clinvar (benign):5 |