| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206765273-206765654 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165937-207166138 | Rare:38 | ||||
| chr2:207529684-207530113 | Common:3; Rare:122 | ||||
| chr2:207625176-207625417 | Common:1; Rare:70 | ||||
| chr2:208254391-208254511 | Rare:30 | ||||
| chr2:208255047-208255238 | Common:2; Rare:51 | ||||
| chr2:208266032-208266306 | Common:9; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477573-210477685 | Rare:36 | ||||
| chr2:215311993-215312133 | Common:7; Rare:63 | ||||
| chr2:215375212-215375721 | Common:2; Rare:138 | ||||
| chr2:215435656-215435902 | Common:2; Rare:59 | ||||
| chr2:215435906-215436079 | Common:1; Rare:39 | ||||
| chr2:216081756-216081889 | Rare:44 | ||||
| chr2:216498743-216498876 | Common:4; Rare:54 | ||||
| chr2:216694570-216694719 | Rare:38 |