Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43860960-43861173 | Common:1; Rare:42 | ||||
chr17:43861542-43861869 | Common:2; Rare:81 | ||||
chr17:44091382-44091655 | Rare:74 | ||||
chr17:44325379-44325471 | Common:1; Rare:16 | ||||
chr17:45149902-45150023 | Rare:27 | ||||
chr17:45585173-45585202 | Rare:2 | ||||
chr17:47100248-47100399 | Rare:39 | ||||
chr17:47492458-47492710 | Common:2; Rare:82 | ||||
chr17:47532147-47532233 | Common:1; Rare:23 | ||||
chr17:48050546-48050662 | Rare:22 | ||||
chr17:50189892-50190038 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):3 | ||||
chr17:51121810-51122028 | Rare:48 | ||||
chr17:55420728-55420851 | Rare:24 | ||||
chr17:58332475-58332677 | Common:2; Rare:52 | ||||
chr17:58631832-58632150 | Common:3; Rare:137 |