| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208025503-208025610 | Rare:25 | ||||
| chr2:208255032-208255228 | Common:2; Rare:51 | ||||
| chr2:208266074-208266315 | Common:7; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002439-210002664 | Common:6; Rare:81 | ||||
| chr2:213284210-213284499 | Rare:94 | ||||
| chr2:215435627-215436181 | Common:3; Rare:142 | ||||
| chr2:216081782-216081925 | Common:1; Rare:50 | ||||
| chr2:216498779-216498907 | Common:4; Rare:67 | ||||
| chr2:218270062-218270541 | Common:5; Rare:151; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218568283-218568659 | Common:3; Rare:100 | ||||
| chr2:218659339-218659743 | Common:4; Rare:95 | ||||
| chr2:218671954-218672327 | Common:2; Rare:99 | ||||
| chr2:219176926-219177068 | Common:4; Rare:44 | ||||
| chr2:219178142-219178442 | Common:6; Rare:129 | ||||
| chr2:219206683-219206916 | Rare:86 |