Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:3855547-3855766 | Common:2; Rare:45 | ||||
chr11:3856063-3856249 | Rare:64 | ||||
chr11:5624893-5625025 | Rare:19 | ||||
chr11:6390221-6390502 | Common:2; Rare:82 | ||||
chr11:6481304-6481545 | Common:4; Rare:107 | ||||
chr11:6603532-6603822 | Common:4; Rare:90; Clinvar (benign):3 | ||||
chr11:7513634-7513979 | Common:5; Rare:105 | ||||
chr11:8682630-8682852 | Common:2; Rare:101 | ||||
chr11:8683115-8683265 | Common:1; Rare:48 | ||||
chr11:8910928-8911251 | Common:6; Rare:91 | ||||
chr11:8964360-8964518 | Common:4; Rare:57 | ||||
chr11:8964916-8964982 | Common:1; Rare:14 | ||||
chr11:9384774-9384846 | Common:1; Rare:24 | ||||
chr11:9460627-9461048 | Common:4; Rare:109 | ||||
chr11:9664000-9664182 | Common:4; Rare:67 |