| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24084812-24084938 | Common:2; Rare:19 | ||||
| chr2:24123253-24123522 | Common:1; Rare:71 | ||||
| chr2:24360320-24360677 | Common:4; Rare:107 | ||||
| chr2:24491883-24492031 | Common:1; Rare:29 | ||||
| chr2:24793060-24793171 | Rare:52 | ||||
| chr2:24971603-24971830 | Common:2; Rare:79 | ||||
| chr2:24971900-24972159 | Common:1; Rare:84 | ||||
| chr2:25252232-25252552 | Rare:71 | ||||
| chr2:25342456-25342808 | Common:1; Rare:73 | ||||
| chr2:25878275-25878659 | Common:1; Rare:104 | ||||
| chr2:26033764-26034302 | Common:5; Rare:194 | ||||
| chr2:26034311-26034740 | Common:3; Rare:103 | ||||
| chr2:26194558-26194897 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26195167-26195406 | Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:26244581-26244990 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):9 |