Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:101126819-101127106 | Common:1; Rare:64 | ||||
chr7:101217850-101218192 | Common:3; Rare:106 | ||||
chr7:101245060-101245173 | Common:1; Rare:40 | ||||
chr7:101321733-101321866 | Common:3; Rare:47 | ||||
chr7:105532066-105532201 | Rare:35 | ||||
chr7:106661152-106661411 | Common:1; Rare:42 | ||||
chr7:107563894-107563988 | Common:1; Rare:57; Clinvar (benign):1 | ||||
chr7:107580144-107580294 | Common:2; Rare:61 | ||||
chr7:107744086-107744159 | Rare:27 | ||||
chr7:108569584-108569931 | Common:1; Rare:120 | ||||
chr7:116499514-116499784 | Common:3; Rare:91 | ||||
chr7:116526143-116526392 | Common:2; Rare:77 | ||||
chr7:123748968-123749223 | Common:2; Rare:91 | ||||
chr7:129055113-129055234 | Common:1; Rare:22 | ||||
chr7:131327785-131327894 | Rare:41 |