Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47848325-47848406 | Rare:40 | ||||
chr11:57514852-57515146 | Common:3; Rare:51 | ||||
chr11:57567612-57567753 | Rare:46 | ||||
chr11:57712175-57712618 | Common:9; Rare:148 | ||||
chr11:58578065-58578138 | Rare:18 | ||||
chr11:58578199-58578498 | Common:4; Rare:96 | ||||
chr11:59142681-59142884 | Rare:31 | ||||
chr11:59668993-59669312 | Rare:107 | ||||
chr11:60906414-60906664 | Rare:64 | ||||
chr11:61333038-61333266 | Rare:80 | ||||
chr11:61361818-61361985 | Common:1; Rare:42 | ||||
chr11:61362255-61362400 | Common:1; Rare:41; Clinvar:6 | ||||
chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429896-61430149 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):3 | ||||
chr11:61792564-61792944 | Common:5; Rare:103 |