Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100132891-100133202 | Common:2; Rare:112 | ||||
chr1:100249809-100250018 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266112-100266301 | Common:2; Rare:69 | ||||
chr1:100894644-100894914 | Common:2; Rare:65 | ||||
chr1:100895975-100896139 | Rare:43 | ||||
chr1:101025763-101025930 | Common:1; Rare:50 | ||||
chr1:101236611-101236954 | Common:2; Rare:68 | ||||
chr1:103525534-103525754 | Rare:46 | ||||
chr1:103525900-103526073 | Common:1; Rare:48 | ||||
chr1:107056651-107056709 | Rare:27 | ||||
chr1:108200100-108200429 | Common:8; Rare:108 | ||||
chr1:108661032-108661343 | Common:1; Rare:109 | ||||
chr1:108692218-108692365 | Common:1; Rare:51 | ||||
chr1:108692557-108692594 | Common:1; Rare:25 | ||||
chr1:108963405-108963563 | Common:1; Rare:60 |