| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9474504-9474632 | Common:6; Rare:62 | ||||
| chr2:9555621-9556018 | Common:2; Rare:132 | ||||
| chr2:9630950-9631338 | Common:3; Rare:124 | ||||
| chr2:9843240-9843544 | Common:6; Rare:92 | ||||
| chr2:10043002-10043070 | Common:1; Rare:21 | ||||
| chr2:10043318-10043752 | Common:4; Rare:186; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:10689910-10690042 | Common:3; Rare:44 | ||||
| chr2:11344981-11345046 | Common:2; Rare:27 | ||||
| chr2:11465848-11466181 | Common:3; Rare:104 | ||||
| chr2:11746401-11746671 | Common:2; Rare:77; Clinvar:4 | ||||
| chr2:12716680-12717062 | Common:1; Rare:117 | ||||
| chr2:12718195-12718238 | Common:1; Rare:4 | ||||
| chr2:17753682-17753874 | Common:2; Rare:67 | ||||
| chr2:18560318-18560605 | Rare:111 | ||||
| chr2:18560684-18560797 | Rare:25 |