Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107929163-107929338 | Common:1; Rare:48 | ||||
chr7:112205578-112205893 | Common:4; Rare:61 | ||||
chr7:114419870-114420000 | Rare:17 | ||||
chr7:116211462-116211599 | Rare:27 | ||||
chr7:128530471-128530590 | Rare:28 | ||||
chr7:128531608-128531780 | Common:2; Rare:55 | ||||
chr7:128842623-128842942 | Common:4; Rare:115; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
chr7:131106332-131106553 | Common:1; Rare:45 | ||||
chr7:131107025-131107329 | Common:2; Rare:49 | ||||
chr7:131107878-131108223 | Common:2; Rare:65 | ||||
chr7:134783239-134783332 | Common:1; Rare:16 | ||||
chr7:134787621-134787894 | Common:3; Rare:46 | ||||
chr7:134865675-134865743 | Rare:14 | ||||
chr7:134932796-134932941 | Common:1; Rare:30 | ||||
chr7:143836678-143836925 | Common:1; Rare:10 |