Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:10803033-10803296 | Common:1; Rare:63 | ||||
chr11:12961633-12961696 | Rare:8 | ||||
chr11:13405784-13406135 | Rare:56 | ||||
chr11:16996509-16996655 | Rare:31 | ||||
chr11:18269574-18269737 | Rare:40 | ||||
chr11:27555711-27555823 | Rare:22 | ||||
chr11:35141706-35141837 | Common:1; Rare:29 | ||||
chr11:35145919-35146154 | Common:3; Rare:45 | ||||
chr11:35663496-35663713 | Rare:67; Clinvar (pathogenic):1 | ||||
chr11:46428870-46428950 | Common:1; Rare:18 | ||||
chr11:46916847-46916958 | Rare:27 | ||||
chr11:47165445-47165666 | Common:8; Rare:72 | ||||
chr11:57332382-57332689 | Rare:71 | ||||
chr11:57792334-57792395 | Rare:8 | ||||
chr11:61353790-61354199 | Rare:94 |