Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:60924391-60924548 | Common:2; Rare:47 | ||||
chr11:60952299-60952570 | Rare:52 | ||||
chr11:61333034-61333302 | Common:1; Rare:97 | ||||
chr11:61361842-61361972 | Common:1; Rare:32 | ||||
chr11:61362239-61362410 | Common:2; Rare:51; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429890-61430166 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):5 | ||||
chr11:61792564-61792955 | Common:5; Rare:108 | ||||
chr11:61816128-61816407 | Rare:81 | ||||
chr11:61816541-61816585 | Rare:7 | ||||
chr11:61816781-61816964 | Rare:52 | ||||
chr11:61967311-61967552 | Rare:89; Clinvar:1 | ||||
chr11:61967584-61967748 | Common:2; Rare:63; Clinvar:3 | ||||
chr11:62545565-62545987 | Common:1; Rare:95 | ||||
chr11:62556234-62556421 | Common:1; Rare:31 |