| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17753728-17753913 | Common:2; Rare:68 | ||||
| chr2:19990079-19990203 | Rare:32 | ||||
| chr2:20051541-20051826 | Common:1; Rare:80 | ||||
| chr2:20446860-20447074 | Common:3; Rare:80 | ||||
| chr2:20823064-20823133 | Rare:29 | ||||
| chr2:23940363-23940529 | Common:3; Rare:60 | ||||
| chr2:24076204-24076594 | Rare:106 | ||||
| chr2:24123282-24123480 | Common:1; Rare:49 | ||||
| chr2:24971917-24972153 | Common:1; Rare:75 | ||||
| chr2:26033778-26034159 | Common:3; Rare:138 | ||||
| chr2:26244581-26244965 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345819-26346156 | Common:1; Rare:100 | ||||
| chr2:26764183-26764325 | Common:1; Rare:56 | ||||
| chr2:27032874-27032995 | Rare:46 | ||||
| chr2:27211912-27212065 | Common:3; Rare:62 |