Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111766359-111766427 | Rare:34 | ||||
chr11:111879158-111879539 | Rare:112 | ||||
chr11:111912724-111912774 | Rare:4 | ||||
chr11:111913131-111913303 | Rare:45 | ||||
chr11:111977097-111977364 | Common:4; Rare:57 | ||||
chr11:112025369-112025467 | Rare:22; Clinvar:1; Clinvar (benign):1 | ||||
chr11:112074018-112074349 | Common:1; Rare:67 | ||||
chr11:112086722-112086905 | Rare:76; Clinvar:1 | ||||
chr11:112164087-112164102 | Rare:2 | ||||
chr11:112226271-112226446 | Rare:75 | ||||
chr11:113875493-113875804 | Common:4; Rare:118 | ||||
chr11:114059385-114059793 | Rare:86 | ||||
chr11:114257497-114257818 | Rare:63 | ||||
chr11:114296235-114296722 | Rare:109 | ||||
chr11:114298335-114298386 | Common:1; Rare:10 |