Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:93784189-93784376 | Common:3; Rare:55 | ||||
chr11:94128782-94129119 | Common:3; Rare:113 | ||||
chr11:94129415-94129525 | Common:1; Rare:36 | ||||
chr11:94493789-94494049 | Common:4; Rare:77; Clinvar (benign):1 | ||||
chr11:94973524-94973705 | Rare:59 | ||||
chr11:95067452-95067567 | Rare:41 | ||||
chr11:95789484-95790014 | Common:5; Rare:226 | ||||
chr11:95790346-95790580 | Common:1; Rare:97 | ||||
chr11:95923960-95924164 | Rare:85; Clinvar (benign):1 | ||||
chr11:96389854-96390043 | Common:1; Rare:77 | ||||
chr11:101914869-101915025 | Common:1; Rare:40 | ||||
chr11:101915126-101915228 | Rare:20 | ||||
chr11:102110228-102110454 | Rare:89 | ||||
chr11:102347118-102347325 | Common:2; Rare:71 | ||||
chr11:102452619-102452899 | Common:1; Rare:89 |