| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9630944-9631316 | Common:3; Rare:119 | ||||
| chr2:9843284-9843541 | Common:6; Rare:78 | ||||
| chr2:10689934-10690012 | Common:2; Rare:25 | ||||
| chr2:11746556-11746648 | Common:1; Rare:34; Clinvar:2 | ||||
| chr2:15561302-15561423 | Rare:49 | ||||
| chr2:15940351-15940602 | Rare:65 | ||||
| chr2:15940683-15940715 | Rare:3 | ||||
| chr2:16665789-16665962 | Common:4; Rare:36 | ||||
| chr2:17540459-17540802 | Common:2; Rare:73 | ||||
| chr2:17753731-17754159 | Common:3; Rare:138; Clinvar (benign):1 | ||||
| chr2:19358583-19358819 | Rare:54 | ||||
| chr2:19901628-19901746 | Common:1; Rare:62 | ||||
| chr2:19901937-19902037 | Common:1; Rare:31 | ||||
| chr2:19990039-19990211 | Rare:47 | ||||
| chr2:20350831-20351050 | Common:1; Rare:90 |