| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9843659-9843706 | Common:1; Rare:16 | ||||
| chr2:10302719-10302901 | Common:3; Rare:68 | ||||
| chr2:10448381-10448713 | Common:1; Rare:103 | ||||
| chr2:10689901-10690029 | Common:2; Rare:47 | ||||
| chr2:11466084-11466202 | Common:3; Rare:41 | ||||
| chr2:11746369-11746655 | Common:1; Rare:77; Clinvar:2 | ||||
| chr2:12716751-12717048 | Common:1; Rare:87 | ||||
| chr2:14632514-14632795 | Rare:98 | ||||
| chr2:17540393-17540718 | Common:1; Rare:83 | ||||
| chr2:17753064-17753433 | Common:6; Rare:91 | ||||
| chr2:17753645-17754167 | Common:5; Rare:164; Clinvar (benign):1 | ||||
| chr2:18560635-18560808 | Rare:51 | ||||
| chr2:19358612-19358774 | Rare:35 | ||||
| chr2:19901925-19902022 | Common:1; Rare:29 | ||||
| chr2:19990079-19990188 | Rare:26 |