| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:213284210-213284481 | Rare:86 | ||||
| chr2:215311879-215312145 | Common:8; Rare:104 | ||||
| chr2:215435648-215436166 | Common:3; Rare:129 | ||||
| chr2:216081761-216081906 | Common:1; Rare:47 | ||||
| chr2:216412667-216412775 | Rare:13 | ||||
| chr2:216498719-216498911 | Common:7; Rare:87 | ||||
| chr2:216694463-216694671 | Rare:48 | ||||
| chr2:216694674-216694803 | Rare:37 | ||||
| chr2:218002846-218003106 | Common:2; Rare:68 | ||||
| chr2:218217057-218217226 | Common:1; Rare:62 | ||||
| chr2:218270062-218270587 | Common:5; Rare:167; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218287258-218287361 | Rare:18 | ||||
| chr2:218322986-218323275 | Common:6; Rare:95 | ||||
| chr2:218399538-218399723 | Common:1; Rare:82 | ||||
| chr2:218568293-218568679 | Common:4; Rare:98 |