Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8435710-8435996 | Common:4; Rare:116 | ||||
chr17:10697503-10697653 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069436-14069549 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15699521-15699785 | Common:3; Rare:72 | ||||
chr17:16217078-16217249 | Rare:53; Clinvar:1 | ||||
chr17:17591604-17591926 | Common:1; Rare:92 | ||||
chr17:18225352-18225646 | Common:3; Rare:88 | ||||
chr17:18314928-18315319 | Common:1; Rare:112 | ||||
chr17:18721933-18722175 | Common:3; Rare:34 | ||||
chr17:18856195-18856378 | Common:1; Rare:32 | ||||
chr17:19977804-19977917 | Common:1; Rare:37 | ||||
chr17:21214140-21214344 | Common:2; Rare:89 | ||||
chr17:27293997-27294117 | Common:1; Rare:48 | ||||
chr17:28335398-28335841 | Common:1; Rare:104 | ||||
chr17:28357455-28357667 | Common:5; Rare:105 |