Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61333018-61333309 | Common:1; Rare:106 | ||||
chr11:61361850-61362039 | Common:1; Rare:43 | ||||
chr11:61362239-61362433 | Common:2; Rare:54; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61392527-61392652 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429905-61430166 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):5 | ||||
chr11:61791907-61792170 | Common:1; Rare:51 | ||||
chr11:61792564-61792998 | Common:5; Rare:124 | ||||
chr11:61816765-61816961 | Rare:56 | ||||
chr11:61949588-61949876 | Common:3; Rare:51 | ||||
chr11:61950238-61950409 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
chr11:61967125-61967806 | Common:4; Rare:237; Clinvar:4 | ||||
chr11:62123738-62124089 | Common:7; Rare:93 | ||||
chr11:62242097-62242316 | Common:1; Rare:42 | ||||
chr11:62545583-62546170 | Common:1; Rare:134 | ||||
chr11:62591486-62591813 | Rare:108 |