| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113077861-113078003 | Common:3; Rare:27 | ||||
| chr2:113584012-113584116 | Rare:27 | ||||
| chr2:127084193-127084325 | Rare:30 | ||||
| chr2:127103611-127103924 | Common:2; Rare:67 | ||||
| chr2:127147162-127147373 | Common:1; Rare:41 | ||||
| chr2:131682413-131682531 | Common:2; Rare:38 | ||||
| chr2:160270311-160270623 | Common:2; Rare:75 | ||||
| chr2:168644138-168644266 | Common:2; Rare:19 | ||||
| chr2:178539185-178539432 | Common:1; Rare:62; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:178598504-178598826 | Common:3; Rare:88; Clinvar:11; Clinvar (benign):7 | ||||
| chr2:178614930-178615024 | Common:1; Rare:20 | ||||
| chr2:178617124-178617437 | Common:1; Rare:87; Clinvar:16; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr2:178629573-178629621 | Rare:9 | ||||
| chr2:178649613-178649867 | Common:3; Rare:62; Clinvar:7; Clinvar (benign):4 | ||||
| chr2:188997170-188997390 | Common:5; Rare:56; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):4 |