| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189441050-189441495 | Common:3; Rare:136 | ||||
| chr2:189580724-189580938 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189581877-189582157 | Common:2; Rare:38 | ||||
| chr2:189783961-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr2:189784281-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343873-190344031 | Rare:31 | ||||
| chr2:190534640-190534862 | Common:2; Rare:69 | ||||
| chr2:190649462-190649584 | Common:1; Rare:35 | ||||
| chr2:190880619-190880850 | Common:4; Rare:73 | ||||
| chr2:191014069-191014333 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191246162-191246278 | Rare:37 | ||||
| chr2:191263067-191263395 | Common:1; Rare:59 | ||||
| chr2:191677833-191678196 | Common:4; Rare:103 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453195-197453571 | Rare:130 |