| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178644011-178644110 | Rare:19 | ||||
| chr2:178670076-178670218 | Rare:21 | ||||
| chr2:178673607-178673748 | Rare:35; Clinvar:5; Clinvar (benign):3 | ||||
| chr2:178689513-178689899 | Common:2; Rare:96; Clinvar:9; Clinvar (benign):11 | ||||
| chr2:178701526-178701827 | Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:178710633-178711351 | Common:3; Rare:198; Clinvar:26; Clinvar (benign):21 | ||||
| chr2:178719963-178720665 | Common:2; Rare:186; Clinvar:18; Clinvar (benign):14 | ||||
| chr2:178764175-178764812 | Common:3; Rare:158; Clinvar:24; Clinvar (benign):17 | ||||
| chr2:178769677-178770321 | Common:3; Rare:148; Clinvar:16; Clinvar (benign):13 | ||||
| chr2:178773461-178774111 | Common:2; Rare:182; Clinvar:23; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
| chr2:182056116-182056214 | Rare:14 | ||||
| chr2:191846502-191846542 | Common:1; Rare:17 | ||||
| chr2:202376111-202376209 | Rare:55 | ||||
| chr2:216692154-216692393 | Common:5; Rare:58 | ||||
| chr2:219220872-219221147 | Common:1; Rare:90 |