| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177263782-177264051 | Common:2; Rare:65 | ||||
| chr2:177264293-177264441 | Rare:45 | ||||
| chr2:177264613-177265366 | Common:7; Rare:188 | ||||
| chr2:177265444-177265547 | Rare:23 | ||||
| chr2:177392413-177392837 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:177392891-177393018 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:177552646-177553164 | Common:5; Rare:181 | ||||
| chr2:177618615-177618798 | Common:1; Rare:89 | ||||
| chr2:177618879-177619069 | Common:3; Rare:59 | ||||
| chr2:178072705-178072973 | Common:1; Rare:65 | ||||
| chr2:178112272-178112568 | Common:1; Rare:92 | ||||
| chr2:178194349-178194599 | Common:2; Rare:74 | ||||
| chr2:178450223-178450532 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr2:178450636-178450988 | Common:1; Rare:135; Clinvar:1 | ||||
| chr2:178451036-178451688 | Common:8; Rare:184; Clinvar:12; Clinvar (benign):4 |