Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15684294-15684334 | Common:1; Rare:14 | ||||
chr17:15699514-15699768 | Common:3; Rare:66 | ||||
chr17:15999605-15999956 | Common:3; Rare:167; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
chr17:16215530-16215650 | Common:1; Rare:51 | ||||
chr17:17281182-17281379 | Rare:78 | ||||
chr17:17591567-17591916 | Common:2; Rare:102 | ||||
chr17:18225385-18225649 | Common:3; Rare:81 | ||||
chr17:18314944-18315308 | Rare:104 | ||||
chr17:18363393-18363699 | Common:4; Rare:101 | ||||
chr17:18682211-18682459 | Common:7; Rare:26 | ||||
chr17:18781231-18781318 | Rare:25 | ||||
chr17:19362570-19362804 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
chr17:19977796-19977958 | Common:1; Rare:55 | ||||
chr17:21214148-21214343 | Common:2; Rare:86 | ||||
chr17:27293929-27294122 | Common:1; Rare:79 |