| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208255019-208255235 | Common:2; Rare:56 | ||||
| chr2:208266032-208266298 | Common:9; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002433-210002659 | Common:6; Rare:77 | ||||
| chr2:210477560-210477690 | Rare:40 | ||||
| chr2:213284238-213284483 | Rare:79 | ||||
| chr2:215138520-215138736 | Common:2; Rare:47 | ||||
| chr2:215311883-215312139 | Common:8; Rare:99 | ||||
| chr2:215435996-215436248 | Common:2; Rare:80 | ||||
| chr2:216081777-216081889 | Rare:36 | ||||
| chr2:216412726-216412786 | Rare:8 | ||||
| chr2:216498721-216498894 | Common:7; Rare:72 | ||||
| chr2:218217057-218217246 | Common:1; Rare:67 | ||||
| chr2:218270075-218270573 | Common:5; Rare:161; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218568270-218568659 | Common:4; Rare:104 | ||||
| chr2:218568753-218568961 | Common:1; Rare:62 |