| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915724-46916167 | Common:4; Rare:148; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941677-46941776 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:47176439-47176569 | Rare:93; Clinvar (benign):5 | ||||
| chr2:47402915-47403189 | Common:1; Rare:123; Clinvar:38; Clinvar (benign):26 | ||||
| chr2:47782979-47783180 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:48314400-48314744 | Rare:122 | ||||
| chr2:48314880-48315073 | Common:1; Rare:81 | ||||
| chr2:48440593-48440851 | Common:9; Rare:122 | ||||
| chr2:53767559-53767873 | Common:5; Rare:110 | ||||
| chr2:53786842-53787229 | Common:1; Rare:146 | ||||
| chr2:53970788-53971141 | Common:11; Rare:121 | ||||
| chr2:55050277-55050311 | Rare:17 | ||||
| chr2:55050313-55050763 | Common:5; Rare:139 | ||||
| chr2:55232335-55232726 | Common:2; Rare:113 | ||||
| chr2:55519423-55519853 | Common:2; Rare:140 |