| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70248503-70248806 | Common:5; Rare:118 | ||||
| chr2:70257494-70257707 | Common:1; Rare:26 | ||||
| chr2:70257978-70258199 | Common:2; Rare:80 | ||||
| chr2:70293634-70293886 | Common:3; Rare:81 | ||||
| chr2:70978502-70978814 | Common:1; Rare:78 | ||||
| chr2:70978934-70979245 | Common:4; Rare:103 | ||||
| chr2:71068526-71068678 | Rare:73 | ||||
| chr2:71130215-71130698 | Common:7; Rare:141; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:72143107-72143270 | Common:2; Rare:35 | ||||
| chr2:72144373-72144814 | Common:4; Rare:100 | ||||
| chr2:72147761-72148113 | Rare:89 | ||||
| chr2:73233183-73233504 | Common:1; Rare:94 | ||||
| chr2:73234250-73234368 | Common:1; Rare:43 | ||||
| chr2:73234544-73234746 | Rare:69 | ||||
| chr2:73385581-73386076 | Common:4; Rare:221; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 |