Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8210555-8210712 | Common:2; Rare:30 | ||||
chr17:8248042-8248169 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8249207-8249319 | Common:1; Rare:32 | ||||
chr17:8867661-8867774 | Common:1; Rare:19 | ||||
chr17:10697505-10697654 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:10729592-10729784 | Common:3; Rare:70 | ||||
chr17:11997444-11997594 | Rare:50 | ||||
chr17:12665960-12666080 | Common:1; Rare:27 | ||||
chr17:14069436-14069580 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):3 | ||||
chr17:15262460-15262738 | Rare:61 | ||||
chr17:15265293-15265483 | Rare:35; Clinvar:1 | ||||
chr17:15699500-15699773 | Common:3; Rare:71 | ||||
chr17:15999598-16000028 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16380728-16381042 | Common:2; Rare:78 | ||||
chr17:17496392-17496575 | Common:2; Rare:51 |