| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46942086-46942129 | Rare:9 | ||||
| chr2:47034147-47034658 | Common:4; Rare:132 | ||||
| chr2:47175711-47176062 | Common:6; Rare:127 | ||||
| chr2:47176452-47177078 | Common:8; Rare:271; Clinvar (benign):5 | ||||
| chr2:47344968-47345194 | Common:1; Rare:63 | ||||
| chr2:47345282-47345734 | Common:2; Rare:101 | ||||
| chr2:47368954-47369697 | Common:8; Rare:318; Clinvar:19; Clinvar (benign):7 | ||||
| chr2:47369962-47370078 | Common:1; Rare:44 | ||||
| chr2:47402880-47403225 | Common:1; Rare:161; Clinvar:55; Clinvar (benign):34; Clinvar (pathogenic):1 | ||||
| chr2:47403520-47403700 | Common:2; Rare:57 | ||||
| chr2:47782651-47782706 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr2:47782773-47783214 | Common:4; Rare:183; Clinvar:6; Clinvar (benign):11 | ||||
| chr2:47783338-47783445 | Common:2; Rare:42; Clinvar:20; Clinvar (benign):17 | ||||
| chr2:47783720-47784227 | Common:9; Rare:126; Clinvar (benign):2 | ||||
| chr2:47905335-47905542 | Common:2; Rare:77 |