| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206765284-206765652 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166088 | Rare:29 | ||||
| chr2:207529754-207530041 | Common:3; Rare:91 | ||||
| chr2:208255025-208255238 | Common:2; Rare:56 | ||||
| chr2:208266040-208266272 | Common:9; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002467-210002659 | Common:5; Rare:62 | ||||
| chr2:215311879-215312119 | Common:6; Rare:92 | ||||
| chr2:215435779-215435903 | Rare:26 | ||||
| chr2:215435993-215436382 | Common:2; Rare:114 | ||||
| chr2:216081788-216081904 | Common:1; Rare:35 | ||||
| chr2:216412709-216412786 | Rare:11 | ||||
| chr2:216498721-216498894 | Common:7; Rare:72 | ||||
| chr2:218216985-218217246 | Common:2; Rare:90 | ||||
| chr2:218270095-218270557 | Common:5; Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:218568301-218568688 | Common:4; Rare:96 |