Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:10508237-10508260 | Rare:5 | ||||
chr11:10509985-10510227 | Common:1; Rare:61 | ||||
chr11:10899173-10899205 | Common:1; Rare:3 | ||||
chr11:10899215-10899250 | Rare:2 | ||||
chr11:11965816-11966098 | Rare:86 | ||||
chr11:12086680-12086895 | Common:2; Rare:37 | ||||
chr11:12218365-12218521 | Common:1; Rare:31 | ||||
chr11:12258237-12258549 | Common:4; Rare:64 | ||||
chr11:14479595-14479934 | Common:3; Rare:93 | ||||
chr11:14867227-14867731 | Rare:106 | ||||
chr11:16752547-16752892 | Rare:80 | ||||
chr11:16996368-16996659 | Rare:54 | ||||
chr11:18269573-18269759 | Rare:50; Clinvar (pathogenic):1 | ||||
chr11:19777020-19777209 | Common:3; Rare:62 | ||||
chr11:20049456-20049498 | Rare:5 |