| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210170590-210171010 | Common:3; Rare:249 | ||||
| chr2:210171140-210171630 | Common:8; Rare:245 | ||||
| chr2:210476597-210476867 | Common:3; Rare:135 | ||||
| chr2:210477540-210477734 | Rare:107; Clinvar (benign):1 | ||||
| chr2:210556080-210556447 | Common:6; Rare:84 | ||||
| chr2:210556459-210556855 | Common:8; Rare:134; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:210577117-210577543 | Common:2; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:212539131-212539367 | Common:7; Rare:46 | ||||
| chr2:213151590-213151990 | Common:2; Rare:247 | ||||
| chr2:213284214-213284499 | Rare:160 | ||||
| chr2:214808870-214809550 | Common:14; Rare:281; Clinvar:28; Clinvar (benign):21 | ||||
| chr2:214809536-214810253 | Common:15; Rare:293; Clinvar:7; Clinvar (benign):10 | ||||
| chr2:215311852-215312220 | Common:15; Rare:241 | ||||
| chr2:216013492-216013735 | Common:1; Rare:51 | ||||
| chr2:216081728-216081882 | Rare:44 |