| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:199911083-199911354 | Rare:75 | ||||
| chr2:200509901-200510199 | Common:1; Rare:104 | ||||
| chr2:200608999-200609381 | Common:1; Rare:92 | ||||
| chr2:200811428-200811596 | Common:1; Rare:61 | ||||
| chr2:200864552-200864747 | Common:1; Rare:62 | ||||
| chr2:200889037-200889439 | Common:3; Rare:130 | ||||
| chr2:200963594-200963897 | Common:1; Rare:77 | ||||
| chr2:201071454-201072043 | Rare:133 | ||||
| chr2:201115729-201116068 | Rare:76 | ||||
| chr2:201116411-201116461 | Rare:11 | ||||
| chr2:201117344-201117608 | Rare:32 | ||||
| chr2:201118594-201118877 | Rare:45 | ||||
| chr2:201451389-201451874 | Common:3; Rare:124 | ||||
| chr2:201642660-201642736 | Rare:40 | ||||
| chr2:201643422-201643556 | Rare:43; Clinvar:4; Clinvar (benign):1 |