| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208129823-208130178 | Common:3; Rare:72 | ||||
| chr2:208255032-208255244 | Common:2; Rare:55 | ||||
| chr2:208266053-208266409 | Common:8; Rare:119; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423756-209424132 | Common:1; Rare:111 | ||||
| chr2:209579222-209579365 | Common:8; Rare:24 | ||||
| chr2:209579403-209579496 | Rare:17 | ||||
| chr2:209579557-209579725 | Common:1; Rare:27 | ||||
| chr2:209661396-209661564 | Common:2; Rare:26 | ||||
| chr2:209771920-209772027 | Common:1; Rare:29 | ||||
| chr2:210002467-210002664 | Common:5; Rare:67 | ||||
| chr2:210476622-210476814 | Common:3; Rare:65 | ||||
| chr2:213284232-213284490 | Rare:83 | ||||
| chr2:214809599-214810036 | Common:4; Rare:156; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:215311924-215312139 | Common:7; Rare:93 | ||||
| chr2:215435981-215436261 | Common:2; Rare:87 |