| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44361484-44362018 | Common:4; Rare:170 | ||||
| chr2:46297249-46297446 | Common:4; Rare:67; Clinvar (benign):1 | ||||
| chr2:46616984-46617262 | Common:7; Rare:121 | ||||
| chr2:46698989-46699350 | Common:1; Rare:110 | ||||
| chr2:46915722-46915950 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916135 | Common:2; Rare:38 | ||||
| chr2:46941715-46941810 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr2:47176444-47176864 | Common:4; Rare:186; Clinvar (benign):5 | ||||
| chr2:47369178-47369526 | Common:3; Rare:143; Clinvar:11; Clinvar (benign):4 | ||||
| chr2:47905496-47905766 | Common:3; Rare:126 | ||||
| chr2:48440631-48440858 | Common:7; Rare:111 | ||||
| chr2:53767559-53767849 | Common:4; Rare:101 | ||||
| chr2:53786831-53787170 | Common:1; Rare:126 | ||||
| chr2:53859930-53860102 | Rare:57 | ||||
| chr2:53970748-53971157 | Common:11; Rare:152 |