| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189784233-189784565 | Common:23; Rare:548; Clinvar:44; Clinvar (benign):12 | ||||
| chr2:189784470-189784870 | Common:9; Rare:149; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:190180101-190180564 | Common:11; Rare:277 | ||||
| chr2:190180604-190181374 | Common:2; Rare:342 | ||||
| chr2:190319034-190319434 | Common:1; Rare:78 | ||||
| chr2:190319488-190320160 | Common:35; Rare:830; Clinvar (benign):38 | ||||
| chr2:190356128-190356788 | Common:6; Rare:131 | ||||
| chr2:190407698-190408098 | Common:2; Rare:132 | ||||
| chr2:190408144-190408389 | Common:6; Rare:162 | ||||
| chr2:190408580-190408950 | Common:7; Rare:119 | ||||
| chr2:190469250-190469560 | Common:5; Rare:88 | ||||
| chr2:190534180-190535007 | Common:34; Rare:872 | ||||
| chr2:190534950-190535529 | Common:2; Rare:151 | ||||
| chr2:190648070-190648470 | Common:1; Rare:98 | ||||
| chr2:190648650-190649277 | Common:12; Rare:832 |