| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208254360-208254461 | Rare:26 | ||||
| chr2:208254972-208255238 | Common:2; Rare:67 | ||||
| chr2:208266121-208266302 | Common:6; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002447-210002645 | Common:5; Rare:67 | ||||
| chr2:210477541-210477690 | Rare:43 | ||||
| chr2:215311963-215312164 | Common:7; Rare:91 | ||||
| chr2:215369851-215370127 | Common:4; Rare:44 | ||||
| chr2:215435973-215436241 | Common:2; Rare:86 | ||||
| chr2:216057763-216057907 | Common:1; Rare:18 | ||||
| chr2:216081637-216081932 | Common:1; Rare:101 | ||||
| chr2:216117121-216117186 | Rare:14 | ||||
| chr2:216372117-216372246 | Rare:15 | ||||
| chr2:216372287-216372551 | Rare:64 | ||||
| chr2:216412675-216412791 | Rare:14 | ||||
| chr2:216498732-216498894 | Common:6; Rare:70 |