| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208266038-208266306 | Common:9; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:213284238-213284493 | Rare:83 | ||||
| chr2:215138501-215138732 | Common:2; Rare:49 | ||||
| chr2:215435826-215435903 | Rare:12 | ||||
| chr2:215436036-215436253 | Common:2; Rare:71 | ||||
| chr2:216081761-216081879 | Rare:34 | ||||
| chr2:216498754-216498886 | Common:3; Rare:56 | ||||
| chr2:216694488-216694833 | Rare:87 | ||||
| chr2:216695359-216695622 | Rare:47 | ||||
| chr2:218216865-218217246 | Common:2; Rare:112 | ||||
| chr2:218270221-218270538 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218287270-218287411 | Rare:22 | ||||
| chr2:218289981-218290206 | Common:3; Rare:38 | ||||
| chr2:218292475-218292626 | Common:1; Rare:43 | ||||
| chr2:218568290-218568602 | Common:2; Rare:86 |