| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237085752-237085976 | Common:2; Rare:83 | ||||
| chr2:237487187-237487287 | Common:1; Rare:28 | ||||
| chr2:237590674-237591252 | Common:12; Rare:126 | ||||
| chr2:237627489-237627653 | Common:2; Rare:62 | ||||
| chr2:237691802-237692213 | Common:6; Rare:87 | ||||
| chr2:237966707-237967078 | Common:5; Rare:117 | ||||
| chr2:238060693-238061141 | Common:7; Rare:144 | ||||
| chr2:238158794-238158973 | Rare:60 | ||||
| chr2:238239834-238239874 | Rare:7 | ||||
| chr2:238239976-238240317 | Common:2; Rare:124 | ||||
| chr2:238240661-238240864 | Common:1; Rare:45 | ||||
| chr2:238288804-238289129 | Rare:111 | ||||
| chr2:238426873-238427076 | Common:1; Rare:76 | ||||
| chr2:239401644-239401720 | Rare:28 | ||||
| chr2:240025226-240025477 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 |