Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42683255-42683465 | Common:3; Rare:86 | ||||
chr1:42766663-42766722 | Rare:11 | ||||
chr1:42766996-42767309 | Common:4; Rare:105; Clinvar (benign):1 | ||||
chr1:42816943-42817136 | Common:1; Rare:54 | ||||
chr1:42846391-42846638 | Common:1; Rare:69 | ||||
chr1:42958746-42959063 | Common:3; Rare:82; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172228-43172329 | Common:1; Rare:55 | ||||
chr1:43270930-43271098 | Rare:36 | ||||
chr1:43358674-43359005 | Common:7; Rare:102 | ||||
chr1:43367961-43368180 | Rare:56 | ||||
chr1:43389757-43389950 | Common:3; Rare:86 | ||||
chr1:43946585-43947011 | Rare:120 | ||||
chr1:43974861-43975046 | Common:3; Rare:57 | ||||
chr1:44213272-44213549 | Common:2; Rare:58 | ||||
chr1:44355276-44355394 | Common:1; Rare:26 |