| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26244530-26245170 | Common:14; Rare:1117; Clinvar:41; Clinvar (benign):59; Clinvar (pathogenic):1 | ||||
| chr2:26245088-26245514 | Common:13; Rare:226 | ||||
| chr2:26345051-26345505 | Common:2; Rare:134 | ||||
| chr2:26345688-26346220 | Common:10; Rare:872 | ||||
| chr2:26346458-26347669 | Common:7; Rare:420 | ||||
| chr2:26764110-26764406 | Common:11; Rare:421 | ||||
| chr2:26785297-26786136 | Common:9; Rare:790 | ||||
| chr2:26786414-26787048 | Common:5; Rare:185 | ||||
| chr2:26938400-26938740 | Common:2; Rare:59 | ||||
| chr2:26970271-26970683 | Rare:233 | ||||
| chr2:26970710-26971100 | Rare:83 | ||||
| chr2:27015129-27015536 | Rare:144 | ||||
| chr2:27032077-27032477 | Common:3; Rare:58 | ||||
| chr2:27032718-27033143 | Rare:626 | ||||
| chr2:27050449-27051228 | Common:12; Rare:459 |