Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:101914869-101915022 | Common:1; Rare:40 | ||||
chr11:102317333-102317526 | Rare:45 | ||||
chr11:102347111-102347283 | Common:2; Rare:52 | ||||
chr11:102452619-102452949 | Common:2; Rare:102 | ||||
chr11:103092083-103092286 | Common:2; Rare:75 | ||||
chr11:106077306-106077723 | Common:2; Rare:126 | ||||
chr11:107457806-107457951 | Common:2; Rare:43 | ||||
chr11:108008888-108008989 | Rare:37 | ||||
chr11:108009287-108009351 | Rare:34 | ||||
chr11:108121375-108121620 | Common:5; Rare:79; Clinvar:1; Clinvar (benign):5 | ||||
chr11:108222556-108222964 | Rare:140; Clinvar:3 | ||||
chr11:108223004-108223128 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr11:111379179-111379438 | Common:1; Rare:49 | ||||
chr11:111379604-111379889 | Common:1; Rare:47 | ||||
chr11:111380010-111380113 | Common:3; Rare:21 |