| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190880614-190880887 | Common:4; Rare:92 | ||||
| chr2:191014080-191014353 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245541 | Common:3; Rare:98 | ||||
| chr2:191246162-191246351 | Common:1; Rare:49 | ||||
| chr2:191677846-191678161 | Common:4; Rare:89 | ||||
| chr2:196068770-196068928 | Common:1; Rare:48 | ||||
| chr2:196799597-196799777 | Common:1; Rare:57 | ||||
| chr2:196926728-196926793 | Common:1; Rare:21 | ||||
| chr2:197407996-197408394 | Common:1; Rare:75 | ||||
| chr2:197434970-197435198 | Rare:76 | ||||
| chr2:197453103-197453561 | Rare:155 | ||||
| chr2:197515835-197516107 | Common:2; Rare:98 | ||||
| chr2:197705156-197705424 | Common:3; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:199911112-199911457 | Rare:121 | ||||
| chr2:200509907-200510155 | Common:1; Rare:87 |