| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:170141904-170142204 | Common:2; Rare:60 | ||||
| chr2:171743825-171744145 | Common:2; Rare:71 | ||||
| chr2:172479569-172479720 | Rare:45; Clinvar:1 | ||||
| chr2:172486966-172487077 | Rare:36 | ||||
| chr2:176123281-176123410 | Common:2; Rare:39 | ||||
| chr2:176637517-176637762 | Common:4; Rare:81 | ||||
| chr2:177234162-177234389 | Rare:58; Clinvar:2 | ||||
| chr2:177244174-177244329 | Common:1; Rare:31 | ||||
| chr2:178413880-178413982 | Rare:34 | ||||
| chr2:178433528-178433623 | Rare:18 | ||||
| chr2:178538711-178539068 | Common:3; Rare:101; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr2:178539142-178539466 | Common:1; Rare:79; Clinvar:12; Clinvar (benign):5 | ||||
| chr2:178593297-178593596 | Rare:79; Clinvar:9; Clinvar (benign):5 | ||||
| chr2:181123895-181123957 | Rare:13 | ||||
| chr2:182866355-182866431 | Rare:23 |