| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46617019-46617262 | Common:7; Rare:106 | ||||
| chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916032-46916167 | Common:2; Rare:46 | ||||
| chr2:47402916-47403197 | Common:1; Rare:129; Clinvar:43; Clinvar (benign):27 | ||||
| chr2:47782946-47783214 | Common:2; Rare:119; Clinvar:6; Clinvar (benign):10 | ||||
| chr2:48440609-48440861 | Common:8; Rare:119 | ||||
| chr2:53767773-53767867 | Common:2; Rare:37 | ||||
| chr2:53786842-53787179 | Common:1; Rare:127 | ||||
| chr2:53970775-53971152 | Common:11; Rare:137 | ||||
| chr2:54115518-54115672 | Rare:52 | ||||
| chr2:55050414-55050818 | Common:4; Rare:123 | ||||
| chr2:55232256-55232726 | Common:3; Rare:131 | ||||
| chr2:55269176-55269393 | Common:2; Rare:61 | ||||
| chr2:55519414-55519858 | Common:2; Rare:145 | ||||
| chr2:55923700-55924013 | Common:5; Rare:105; Clinvar:2; Clinvar (benign):9 |