Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116418523-116418719 | Common:3; Rare:112 | ||||
chr1:116433520-116433870 | Common:8; Rare:127 | ||||
chr1:116466072-116466292 | Rare:78 | ||||
chr1:116466320-116466650 | Common:1; Rare:80 | ||||
chr1:116475115-116475630 | Common:3; Rare:153 | ||||
chr1:117366530-117366943 | Common:1; Rare:169 | ||||
chr1:117928877-117929008 | Rare:60 | ||||
chr1:118960610-118960970 | Common:4; Rare:140 | ||||
chr1:119327120-119327620 | Common:2; Rare:191 | ||||
chr1:119341390-119341790 | Rare:136 | ||||
chr1:119712530-119713080 | Common:3; Rare:184 | ||||
chr1:119720901-119721435 | Common:8; Rare:247; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:119736951-119737347 | Common:1; Rare:123; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:121518839-121519247 | Common:5; Rare:140 | ||||
chr1:121519210-121519370 | Rare:90 |