| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3575089-3575447 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9003957-9004095 | Rare:57 | ||||
| chr2:9423427-9423801 | Rare:115 | ||||
| chr2:9555630-9555916 | Common:2; Rare:90 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:9843250-9843553 | Common:6; Rare:90 | ||||
| chr2:10689934-10690098 | Common:5; Rare:53 | ||||
| chr2:11466118-11466213 | Common:3; Rare:28 | ||||
| chr2:11482662-11482924 | Common:2; Rare:78 | ||||
| chr2:12716614-12716961 | Common:3; Rare:109 | ||||
| chr2:15561294-15561421 | Rare:49 | ||||
| chr2:17540443-17540806 | Common:2; Rare:78 | ||||
| chr2:17753695-17754181 | Common:4; Rare:151; Clinvar (benign):1 | ||||
| chr2:18560647-18560800 | Rare:44 | ||||
| chr2:19901646-19901798 | Common:1; Rare:83 |