| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71466579-71466749 | Common:3; Rare:38 | ||||
| chr2:72825840-72826121 | Rare:89 | ||||
| chr2:72887307-72887433 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr2:72887867-72888093 | Common:1; Rare:53 | ||||
| chr2:73069986-73070821 | Common:9; Rare:394 | ||||
| chr2:73071225-73071526 | Common:2; Rare:105 | ||||
| chr2:73071685-73071891 | Common:2; Rare:84 | ||||
| chr2:73113098-73113498 | Common:9; Rare:139 | ||||
| chr2:73214134-73214280 | Common:1; Rare:47 | ||||
| chr2:73233234-73233577 | Common:1; Rare:101 | ||||
| chr2:73234137-73234347 | Common:1; Rare:50 | ||||
| chr2:73284259-73284679 | Common:2; Rare:202 | ||||
| chr2:73385537-73385879 | Common:2; Rare:119; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:73385901-73386090 | Common:2; Rare:112; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr2:73737237-73737610 | Common:3; Rare:121 |