Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7561786-7562134 | Common:3; Rare:92 | ||||
chr17:7583491-7583868 | Common:1; Rare:148; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7857453-7857714 | Common:2; Rare:85 | ||||
chr17:7931906-7932223 | Common:5; Rare:88 | ||||
chr17:10697503-10697616 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
chr17:15651857-15652127 | Rare:44 | ||||
chr17:15999586-15999851 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:16215522-16215649 | Common:1; Rare:52 | ||||
chr17:18039162-18039420 | Common:3; Rare:68 | ||||
chr17:18314913-18315348 | Common:1; Rare:125 | ||||
chr17:19377911-19378029 | Common:1; Rare:26 | ||||
chr17:19378191-19378560 | Common:2; Rare:87 | ||||
chr17:19977820-19977881 | Rare:11 | ||||
chr17:21214138-21214341 | Common:2; Rare:88 | ||||
chr17:27293953-27294122 | Common:1; Rare:73 |