Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110308516-110308632 | Common:1; Rare:24 | ||||
chr13:110340884-110341191 | Common:3; Rare:67 | ||||
chr13:110388286-110388306 | Rare:4 | ||||
chr13:110424731-110424996 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110449486-110449786 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr13:110503870-110504261 | Common:4; Rare:128; Clinvar:1; Clinvar (benign):3 | ||||
chr14:21082735-21082876 | Common:2; Rare:43 | ||||
chr14:21088643-21088840 | Common:1; Rare:48 | ||||
chr14:32203245-32203616 | Common:13; Rare:163 | ||||
chr14:34873895-34874231 | Common:2; Rare:70 | ||||
chr14:49633956-49634070 | Common:1; Rare:45; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49778360-49778429 | Rare:17 | ||||
chr14:49789497-49789726 | Rare:51 | ||||
chr14:49862264-49862568 | Common:1; Rare:71 | ||||
chr14:49862635-49862874 | Common:1; Rare:122 |