| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200963630-200963816 | Common:1; Rare:43 | ||||
| chr2:201071620-201072031 | Rare:87 | ||||
| chr2:201115941-201116261 | Common:2; Rare:56 | ||||
| chr2:201451450-201451767 | Common:1; Rare:73 | ||||
| chr2:203238779-203239030 | Common:1; Rare:89 | ||||
| chr2:206159342-206159900 | Common:4; Rare:149; Clinvar (benign):1 | ||||
| chr2:206765290-206765670 | Common:3; Rare:103; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:207165906-207166094 | Rare:37 | ||||
| chr2:207529771-207530118 | Common:3; Rare:95 | ||||
| chr2:208255047-208255234 | Common:2; Rare:49 | ||||
| chr2:208266121-208266302 | Common:6; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477535-210477690 | Rare:46 | ||||
| chr2:215311970-215312139 | Common:7; Rare:72 | ||||
| chr2:216081753-216081916 | Common:1; Rare:58 | ||||
| chr2:216498689-216498877 | Common:6; Rare:74 |