| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208254066-208254224 | Common:1; Rare:27 | ||||
| chr2:208255068-208255244 | Common:2; Rare:48 | ||||
| chr2:208266116-208266315 | Common:6; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477582-210477641 | Rare:20 | ||||
| chr2:215311867-215312145 | Common:8; Rare:107 | ||||
| chr2:216081756-216081906 | Common:1; Rare:50 | ||||
| chr2:216412715-216412775 | Rare:9 | ||||
| chr2:216498753-216498876 | Common:3; Rare:50 | ||||
| chr2:216694576-216694833 | Rare:68 | ||||
| chr2:217809822-217810318 | Common:2; Rare:129 | ||||
| chr2:217905306-217905628 | Rare:71 | ||||
| chr2:217978616-217978724 | Rare:29 | ||||
| chr2:217978769-217978951 | Common:1; Rare:57 | ||||
| chr2:218217049-218217246 | Common:1; Rare:70 | ||||
| chr2:218270099-218270573 | Common:5; Rare:150; Clinvar:5; Clinvar (benign):2 |