Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:97920929-97921110 | Rare:73; Clinvar:3 | ||||
chr1:98661587-98661875 | Common:2; Rare:102 | ||||
chr1:99645900-99646320 | Rare:83 | ||||
chr1:99849975-99850132 | Common:1; Rare:56 | ||||
chr1:99969922-99970069 | Rare:43 | ||||
chr1:100037965-100038165 | Common:1; Rare:81 | ||||
chr1:100132902-100133206 | Common:2; Rare:108 | ||||
chr1:100249809-100249960 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266107-100266275 | Common:3; Rare:66 | ||||
chr1:100894786-100894885 | Rare:18 | ||||
chr1:100895938-100896155 | Rare:61 | ||||
chr1:101025763-101025920 | Common:1; Rare:48 | ||||
chr1:101236611-101236941 | Common:2; Rare:63 | ||||
chr1:103525500-103525749 | Rare:64 | ||||
chr1:103525911-103526013 | Rare:24 |