Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:3797488-3797829 | Rare:123 | ||||
chr11:3840914-3841079 | Rare:70 | ||||
chr11:3855579-3855683 | Common:2; Rare:22 | ||||
chr11:4094571-4094897 | Common:2; Rare:90 | ||||
chr11:4393651-4393814 | Rare:41 | ||||
chr11:4608171-4608405 | Common:1; Rare:64 | ||||
chr11:5624893-5625029 | Rare:22 | ||||
chr11:6390237-6390499 | Common:2; Rare:74 | ||||
chr11:6473879-6474124 | Rare:74 | ||||
chr11:6481283-6481558 | Common:5; Rare:125 | ||||
chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr11:6683241-6683660 | Common:6; Rare:159 | ||||
chr11:8594145-8594309 | Rare:58 | ||||
chr11:8682628-8683054 | Common:2; Rare:177 | ||||
chr11:8717868-8718188 | Common:7; Rare:81 |