Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4143011-4143225 | Rare:71 | ||||
chr17:4807007-4807186 | Common:3; Rare:61 | ||||
chr17:4939916-4940089 | Common:1; Rare:57 | ||||
chr17:5420077-5420202 | Rare:50 | ||||
chr17:5486166-5486386 | Common:4; Rare:98 | ||||
chr17:6640693-6641077 | Common:7; Rare:117 | ||||
chr17:7012317-7012691 | Rare:128 | ||||
chr17:7242305-7242590 | Common:1; Rare:102 | ||||
chr17:7484226-7484370 | Common:1; Rare:59 | ||||
chr17:7583550-7583858 | Common:1; Rare:126; Clinvar:3; Clinvar (benign):3 | ||||
chr17:10697505-10697653 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069481-14069536 | Common:1; Rare:17; Clinvar (benign):2 | ||||
chr17:15699514-15699768 | Common:3; Rare:66 | ||||
chr17:17237133-17237429 | Common:4; Rare:89; Clinvar (benign):2 | ||||
chr17:20868222-20868526 | Common:2; Rare:67 |