Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:117263756-117263981 | Rare:29 | ||||
chr7:120013445-120013723 | Common:1; Rare:49 | ||||
chr7:121491581-121491613 | Common:1; Rare:7 | ||||
chr7:121511100-121511371 | Common:5; Rare:54 | ||||
chr7:122078310-122078565 | Common:4; Rare:64 | ||||
chr7:122098437-122098816 | Common:1; Rare:91 | ||||
chr7:122099500-122099685 | Rare:26 | ||||
chr7:122099804-122099939 | Rare:26 | ||||
chr7:122099969-122100222 | Rare:51 | ||||
chr7:122100373-122100446 | Rare:7 | ||||
chr7:122101365-122101673 | Common:1; Rare:79; Clinvar (benign):1 | ||||
chr7:122116630-122116984 | Common:1; Rare:103; Clinvar (pathogenic):1 | ||||
chr7:122118305-122118628 | Rare:85 | ||||
chr7:122123950-122124242 | Rare:45 | ||||
chr7:122126285-122126452 | Rare:41 |