Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:85580176-85580250 | Common:1; Rare:9 | ||||
chr1:89198135-89198330 | Common:2; Rare:39 | ||||
chr1:92833386-92833660 | Common:1; Rare:66; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:92840614-92840719 | Rare:32; Clinvar:1 | ||||
chr1:94863995-94864223 | Rare:37 | ||||
chr1:94866510-94866711 | Rare:31 | ||||
chr1:101235955-101236219 | Common:2; Rare:56 | ||||
chr1:108747386-108747505 | Rare:17 | ||||
chr1:111364669-111365012 | Rare:69 | ||||
chr1:111749581-111749626 | Rare:4 | ||||
chr1:112849813-112849897 | Common:1; Rare:13 | ||||
chr1:112955351-112955450 | Common:2; Rare:15 | ||||
chr1:112997897-112998149 | Common:1; Rare:37 | ||||
chr1:113093234-113093545 | Common:2; Rare:77 | ||||
chr1:115073907-115074067 | Common:2; Rare:35 |