| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19933413-19933721 | Common:4; Rare:65; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:19954586-19954591 | |||||
| chr2:19985333-19985572 | Common:5; Rare:19 | ||||
| chr2:20037313-20037747 | Rare:114 | ||||
| chr2:20246494-20246559 | Rare:13 | ||||
| chr2:20258234-20258528 | Common:1; Rare:68 | ||||
| chr2:20271344-20271582 | Rare:43 | ||||
| chr2:20282084-20282114 | Rare:3 | ||||
| chr2:20290439-20290661 | Rare:42 | ||||
| chr2:20291739-20291942 | Common:3; Rare:38 | ||||
| chr2:20291978-20292287 | Rare:67 | ||||
| chr2:20300682-20300779 | Rare:14 | ||||
| chr2:20303233-20303429 | Rare:30 | ||||
| chr2:20317518-20317729 | Rare:49 | ||||
| chr2:20444461-20444730 | Common:7; Rare:56 |