| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:209423828-209424106 | Common:1; Rare:83 | ||||
| chr2:210477568-210477653 | Rare:25 | ||||
| chr2:213284210-213284504 | Rare:97 | ||||
| chr2:214809670-214809995 | Common:1; Rare:120; Clinvar:1 | ||||
| chr2:215311892-215312145 | Common:8; Rare:101 | ||||
| chr2:215409556-215410130 | Rare:151 | ||||
| chr2:215435643-215436166 | Common:3; Rare:130 | ||||
| chr2:216081771-216081926 | Common:1; Rare:56 | ||||
| chr2:216498696-216498906 | Common:7; Rare:92 | ||||
| chr2:216694462-216694833 | Rare:91 | ||||
| chr2:216694840-216695101 | Rare:48 | ||||
| chr2:218002947-218003091 | Common:2; Rare:36 | ||||
| chr2:218216812-218217263 | Common:2; Rare:124 | ||||
| chr2:218270091-218270541 | Common:5; Rare:142; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218292475-218292641 | Common:1; Rare:48 |