Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8248050-8248119 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
chr17:10697505-10697653 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069430-14069565 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
chr17:18087833-18087979 | Rare:32 | ||||
chr17:18314944-18315297 | Rare:103 | ||||
chr17:19377638-19377788 | Common:2; Rare:41 | ||||
chr17:19377882-19378033 | Common:1; Rare:38 | ||||
chr17:19378180-19378539 | Common:2; Rare:91 | ||||
chr17:19977804-19977974 | Common:1; Rare:58 | ||||
chr17:21214140-21214316 | Common:2; Rare:70 | ||||
chr17:27293933-27294132 | Common:1; Rare:82 | ||||
chr17:28318939-28319216 | Common:3; Rare:94 | ||||
chr17:28335381-28335850 | Common:1; Rare:112 | ||||
chr17:28357455-28357667 | Common:5; Rare:105 | ||||
chr17:28598994-28599150 | Common:2; Rare:43 |