Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95923785-95923863 | Common:1; Rare:22; Clinvar (benign):1 | ||||
chr11:95923950-95924157 | Rare:91; Clinvar (benign):1 | ||||
chr11:96389846-96390044 | Common:1; Rare:83 | ||||
chr11:101914929-101915317 | Common:8; Rare:109 | ||||
chr11:102317296-102317499 | Rare:42 | ||||
chr11:102347105-102347279 | Common:2; Rare:50 | ||||
chr11:102452526-102452943 | Common:2; Rare:137 | ||||
chr11:103109306-103109577 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr11:106077317-106077706 | Common:2; Rare:117 | ||||
chr11:107859172-107859336 | Rare:39 | ||||
chr11:108009117-108009168 | Rare:10 | ||||
chr11:108009273-108009359 | Rare:41 | ||||
chr11:108222609-108223128 | Common:1; Rare:161; Clinvar:8; Clinvar (benign):1 | ||||
chr11:111299673-111299894 | Common:5; Rare:57 | ||||
chr11:111602226-111602566 | Common:1; Rare:114 |