Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367761-169368008 | Common:2; Rare:44 | ||||
chr1:169485694-169486202 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794878-169795103 | Common:3; Rare:63 | ||||
chr1:170531904-170532147 | Common:2; Rare:58 | ||||
chr1:171485314-171485622 | Rare:108 | ||||
chr1:171742014-171742191 | Common:1; Rare:58 | ||||
chr1:173477040-173477488 | Common:5; Rare:154 | ||||
chr1:173824133-173824237 | Rare:26 | ||||
chr1:173824384-173824725 | Rare:61; Clinvar:2 | ||||
chr1:173824877-173824982 | Rare:22 | ||||
chr1:174159332-174159581 | Common:2; Rare:95 | ||||
chr1:174999655-175000008 | Common:1; Rare:94 | ||||
chr1:179081894-179082114 | Common:1; Rare:69 | ||||
chr1:179142983-179143238 | Common:1; Rare:49 | ||||
chr1:179882159-179882316 | Common:1; Rare:31 |