Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100249812-100250006 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266114-100266326 | Common:2; Rare:75 | ||||
chr1:100894802-100894914 | Rare:22 | ||||
chr1:100895987-100896142 | Rare:42 | ||||
chr1:101025763-101025920 | Common:1; Rare:48 | ||||
chr1:103525519-103525730 | Rare:46 | ||||
chr1:103525911-103526005 | Rare:23 | ||||
chr1:108200129-108200450 | Common:9; Rare:99 | ||||
chr1:108661031-108661140 | Rare:41 | ||||
chr1:108661247-108661554 | Common:7; Rare:92 | ||||
chr1:108692189-108692368 | Common:1; Rare:72 | ||||
chr1:109090602-109090811 | Common:4; Rare:39 | ||||
chr1:109283113-109283313 | Common:2; Rare:47 | ||||
chr1:109548471-109548686 | Common:4; Rare:82 | ||||
chr1:109619769-109619858 | Rare:20 |