| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219598021-219598333 | Common:1; Rare:97 | ||||
| chr2:221572293-221572548 | Common:6; Rare:90 | ||||
| chr2:222298951-222299182 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr2:222424137-222424234 | Rare:24 | ||||
| chr2:222424320-222424606 | Rare:83 | ||||
| chr2:222425001-222425360 | Rare:85 | ||||
| chr2:222655918-222656508 | Common:4; Rare:192 | ||||
| chr2:222860822-222861091 | Common:2; Rare:98 | ||||
| chr2:222861469-222861651 | Common:1; Rare:44 | ||||
| chr2:223837493-223838111 | Common:3; Rare:141 | ||||
| chr2:223945217-223945524 | Common:1; Rare:107 | ||||
| chr2:223957192-223957550 | Common:4; Rare:139; Clinvar (benign):2 | ||||
| chr2:223957645-223957661 | Rare:5; Clinvar (benign):1 | ||||
| chr2:224039271-224039400 | Rare:49 | ||||
| chr2:224584911-224585021 | Rare:35 |