| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37231542-37231703 | Common:4; Rare:92; Clinvar (benign):3 | ||||
| chr2:38076149-38076265 | Rare:28 | ||||
| chr2:38751348-38751636 | Common:4; Rare:131 | ||||
| chr2:38875892-38876059 | Common:1; Rare:60 | ||||
| chr2:39437077-39437453 | Common:4; Rare:135 | ||||
| chr2:42792543-42792849 | Common:3; Rare:89 | ||||
| chr2:43595978-43596146 | Common:1; Rare:51 | ||||
| chr2:43637086-43637342 | Common:2; Rare:83 | ||||
| chr2:44361479-44362022 | Common:4; Rare:171 | ||||
| chr2:46617016-46617275 | Common:7; Rare:114 | ||||
| chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176444-47176582 | Rare:101; Clinvar (benign):5 | ||||
| chr2:47345052-47345148 | Rare:26 | ||||
| chr2:48440631-48440824 | Common:5; Rare:87 | ||||
| chr2:53786851-53787191 | Common:1; Rare:130 |