| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61537039-61537137 | Rare:20 | ||||
| chr2:61538695-61538807 | Rare:31 | ||||
| chr2:61853955-61854105 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888503-61888727 | Common:1; Rare:92 | ||||
| chr2:62506138-62506347 | Common:1; Rare:82 | ||||
| chr2:63588218-63589031 | Common:2; Rare:254; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:63840820-63841154 | Common:2; Rare:92 | ||||
| chr2:63841646-63841935 | Common:2; Rare:102 | ||||
| chr2:64144341-64144652 | Common:4; Rare:89 | ||||
| chr2:64524073-64524520 | Common:3; Rare:144 | ||||
| chr2:64653886-64654071 | Common:1; Rare:62 | ||||
| chr2:64988339-64988501 | Common:1; Rare:30 | ||||
| chr2:65056189-65056467 | Common:2; Rare:97 | ||||
| chr2:65227569-65227856 | Rare:77 | ||||
| chr2:66433248-66433355 | Common:1; Rare:24 |