| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084269-37084561 | Common:4; Rare:110 | ||||
| chr2:37231519-37231703 | Common:5; Rare:102; Clinvar (benign):3 | ||||
| chr2:37324743-37324918 | Common:1; Rare:74 | ||||
| chr2:38875886-38876047 | Common:1; Rare:58 | ||||
| chr2:39437078-39437453 | Common:4; Rare:134 | ||||
| chr2:42169185-42169444 | Common:1; Rare:132 | ||||
| chr2:42792525-42792749 | Common:2; Rare:67 | ||||
| chr2:43226602-43226811 | Common:1; Rare:75 | ||||
| chr2:43595931-43596146 | Common:1; Rare:70 | ||||
| chr2:44361479-44362007 | Common:3; Rare:165 | ||||
| chr2:46616984-46617270 | Common:7; Rare:127 | ||||
| chr2:46915724-46916175 | Common:4; Rare:150; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176439-47176760 | Common:4; Rare:157; Clinvar (benign):5 | ||||
| chr2:47345052-47345148 | Rare:26 | ||||
| chr2:47369178-47369508 | Common:3; Rare:132; Clinvar:8; Clinvar (benign):2 |