Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11980175-11980473 | Common:5; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12230001-12230108 | Common:1; Rare:39 | ||||
chr1:12616696-12617018 | Rare:53 | ||||
chr1:12617196-12617331 | Rare:40 | ||||
chr1:12617344-12617507 | Rare:39 | ||||
chr1:12617580-12617881 | Common:5; Rare:30 | ||||
chr1:12618117-12618449 | Common:2; Rare:71 | ||||
chr1:13584154-13584341 | Common:2; Rare:60 | ||||
chr1:13700166-13700277 | Rare:45 | ||||
chr1:13749171-13749479 | Common:2; Rare:116 | ||||
chr1:15152303-15152569 | Rare:42 | ||||
chr1:15153009-15153165 | Common:2; Rare:34 | ||||
chr1:15410186-15410279 | Rare:26 | ||||
chr1:15524172-15524574 | Common:2; Rare:110 | ||||
chr1:15526550-15526924 | Common:2; Rare:122 |