Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12617202-12617604 | Rare:96 | ||||
chr1:12617677-12618047 | Common:5; Rare:48 | ||||
chr1:12618207-12618482 | Common:1; Rare:56 | ||||
chr1:13749120-13749451 | Common:2; Rare:114 | ||||
chr1:15524187-15524601 | Common:3; Rare:106 | ||||
chr1:15526600-15526940 | Common:2; Rare:107 | ||||
chr1:15736101-15736350 | Common:3; Rare:51 | ||||
chr1:16017763-16018253 | Common:9; Rare:176 | ||||
chr1:16019592-16019725 | Common:2; Rare:36 | ||||
chr1:16020454-16020598 | Common:1; Rare:27 | ||||
chr1:16352411-16352569 | Common:2; Rare:89 | ||||
chr1:16980586-16980944 | Common:5; Rare:100 | ||||
chr1:17053949-17054285 | Common:3; Rare:112; Clinvar:16; Clinvar (benign):12 | ||||
chr1:19210211-19210515 | Rare:104 | ||||
chr1:19251510-19251848 | Common:6; Rare:110 |