| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203238751-203239133 | Common:3; Rare:133 | ||||
| chr2:203239210-203239320 | Rare:34 | ||||
| chr2:203328157-203328528 | Common:2; Rare:134 | ||||
| chr2:203535155-203535558 | Common:3; Rare:153 | ||||
| chr2:203706447-203706703 | Rare:54 | ||||
| chr2:204545813-204545887 | Rare:14 | ||||
| chr2:204545893-204546112 | Rare:75 | ||||
| chr2:205682351-205682587 | Rare:41 | ||||
| chr2:205683041-205683107 | Rare:7 | ||||
| chr2:206085765-206085981 | Common:1; Rare:62 | ||||
| chr2:206086078-206086210 | Rare:17 | ||||
| chr2:206086229-206086374 | Rare:23 | ||||
| chr2:206159347-206160057 | Common:4; Rare:212; Clinvar (benign):1 | ||||
| chr2:206274916-206275041 | Rare:47 | ||||
| chr2:206765276-206765661 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 |