Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11806694-11806746 | Common:1; Rare:16 | ||||
chr1:11926316-11926655 | Common:6; Rare:92 | ||||
chr1:11934478-11934848 | Common:6; Rare:109; Clinvar:7; Clinvar (benign):1 | ||||
chr1:11934880-11934977 | Rare:25 | ||||
chr1:11979727-11979854 | Rare:15 | ||||
chr1:11979857-11980009 | Rare:28 | ||||
chr1:11980157-11980499 | Common:5; Rare:111; Clinvar:1; Clinvar (benign):5 | ||||
chr1:11980847-11981217 | Common:1; Rare:81 | ||||
chr1:11981677-11981815 | Common:1; Rare:37 | ||||
chr1:11981817-11981851 | Common:1; Rare:8 | ||||
chr1:12019177-12019624 | Common:5; Rare:159 | ||||
chr1:12595944-12596156 | Rare:36 | ||||
chr1:13583681-13583965 | Common:2; Rare:130 | ||||
chr1:13584080-13584337 | Common:2; Rare:91 | ||||
chr1:13584340-13584408 | Rare:11 |