| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47176401-47176569 | Rare:116; Clinvar (benign):5 | ||||
| chr2:47176922-47176957 | Common:3; Rare:15 | ||||
| chr2:47402951-47403194 | Common:1; Rare:111; Clinvar:36; Clinvar (benign):26 | ||||
| chr2:47782946-47783215 | Common:2; Rare:119; Clinvar:6; Clinvar (benign):10 | ||||
| chr2:48314186-48314468 | Common:1; Rare:91 | ||||
| chr2:48314593-48314744 | Rare:59 | ||||
| chr2:48440612-48440850 | Common:8; Rare:112 | ||||
| chr2:53767559-53767889 | Common:5; Rare:119 | ||||
| chr2:53786856-53787203 | Common:1; Rare:132 | ||||
| chr2:53970755-53971126 | Common:10; Rare:128 | ||||
| chr2:54115774-54116039 | Common:5; Rare:100 | ||||
| chr2:55050434-55050763 | Common:4; Rare:100 | ||||
| chr2:55231920-55231945 | Rare:9 | ||||
| chr2:55232133-55232744 | Common:5; Rare:171 | ||||
| chr2:55519411-55519757 | Common:1; Rare:98 |