| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61891157-61891329 | Common:1; Rare:47 | ||||
| chr11:61891500-61891833 | Common:2; Rare:98 | ||||
| chr11:61917465-61917697 | Common:2; Rare:88 | ||||
| chr11:61949588-61950014 | Common:3; Rare:74; Clinvar (benign):1 | ||||
| chr11:61950043-61950057 | Rare:2 | ||||
| chr11:61955030-61955383 | Common:8; Rare:108; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:61967149-61967298 | Common:1; Rare:46 | ||||
| chr11:61967587-61968007 | Common:6; Rare:137; Clinvar:3 | ||||
| chr11:62123700-62124101 | Common:7; Rare:112 | ||||
| chr11:62124417-62124647 | Common:3; Rare:35 | ||||
| chr11:62337284-62337578 | Common:6; Rare:86 | ||||
| chr11:62337861-62337920 | Common:1; Rare:11 | ||||
| chr11:62545185-62545281 | Rare:16 | ||||
| chr11:62545581-62546217 | Common:1; Rare:156 | ||||
| chr11:62546259-62546401 | Rare:34 |