| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237798728-237798810 | Rare:26 | ||||
| chr2:237966776-237967089 | Common:4; Rare:99 | ||||
| chr2:238060734-238061029 | Common:4; Rare:89 | ||||
| chr2:238203583-238203826 | Common:3; Rare:106 | ||||
| chr2:238288678-238288981 | Rare:112 | ||||
| chr2:238320412-238320607 | Common:1; Rare:70 | ||||
| chr2:238426648-238427067 | Common:6; Rare:123 | ||||
| chr2:238435014-238435177 | Common:1; Rare:37 | ||||
| chr2:239140962-239141117 | Common:1; Rare:38 | ||||
| chr2:239154968-239155096 | Common:1; Rare:31 | ||||
| chr2:239400998-239401438 | Common:3; Rare:136 | ||||
| chr2:239401632-239401825 | Common:1; Rare:102 | ||||
| chr2:240025225-240025435 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240136252-240136389 | Rare:53 | ||||
| chr2:240557931-240558178 | Common:2; Rare:85 |