Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:99969908-99970099 | Rare:47 | ||||
chr1:100038006-100038208 | Common:1; Rare:81 | ||||
chr1:100132911-100133202 | Common:2; Rare:104 | ||||
chr1:100249812-100250018 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266089-100266293 | Common:3; Rare:78 | ||||
chr1:100352170-100352544 | Common:1; Rare:88 | ||||
chr1:100894785-100894890 | Rare:20 | ||||
chr1:100895975-100896155 | Rare:49 | ||||
chr1:101025763-101025910 | Common:1; Rare:44 | ||||
chr1:101236611-101237026 | Common:4; Rare:82 | ||||
chr1:103525497-103525762 | Rare:69 | ||||
chr1:103525908-103526063 | Common:1; Rare:44 | ||||
chr1:107056372-107056711 | Common:3; Rare:107 | ||||
chr1:108200131-108200421 | Common:8; Rare:90 | ||||
chr1:108661068-108661319 | Common:1; Rare:87 |