Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:99850239-99850662 | Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
chr1:99969907-99970080 | Rare:44 | ||||
chr1:100038001-100038143 | Common:1; Rare:59 | ||||
chr1:100132915-100133196 | Common:2; Rare:98 | ||||
chr1:100266114-100266420 | Common:3; Rare:107 | ||||
chr1:100894801-100894890 | Rare:16 | ||||
chr1:100895948-100896142 | Rare:56 | ||||
chr1:101025763-101025920 | Common:1; Rare:48 | ||||
chr1:101236611-101237052 | Common:5; Rare:88 | ||||
chr1:103525483-103525808 | Rare:83 | ||||
chr1:103525876-103526202 | Common:1; Rare:102 | ||||
chr1:108200131-108200413 | Common:7; Rare:87 | ||||
chr1:108661068-108661329 | Common:1; Rare:92 | ||||
chr1:108692049-108692365 | Common:3; Rare:100 | ||||
chr1:108692533-108692694 | Common:3; Rare:75 |