| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086268-70086292 | Common:1; Rare:6 | ||||
| chr2:74377431-74377727 | Common:1; Rare:75 | ||||
| chr2:86158601-86158989 | Common:5; Rare:79 | ||||
| chr2:94587033-94587240 | Rare:54 | ||||
| chr2:95526718-95526815 | Common:1; Rare:35 | ||||
| chr2:99404819-99404896 | Rare:15 | ||||
| chr2:101010933-101011094 | Rare:36 | ||||
| chr2:131682352-131682519 | Common:3; Rare:44 | ||||
| chr2:160270293-160270493 | Common:1; Rare:55 | ||||
| chr2:168643982-168644275 | Common:3; Rare:41 | ||||
| chr2:170770764-170771048 | Common:1; Rare:48 | ||||
| chr2:178543833-178544507 | Common:1; Rare:190; Clinvar:32; Clinvar (benign):20; Clinvar (pathogenic):2 | ||||
| chr2:178546214-178546906 | Common:2; Rare:202; Clinvar:28; Clinvar (benign):18; Clinvar (pathogenic):2 | ||||
| chr2:178547001-178547698 | Rare:205; Clinvar:24; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr2:178576527-178577509 | Common:3; Rare:268; Clinvar:34; Clinvar (benign):20; Clinvar (pathogenic):2 |