Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4143597-4143750 | Common:4; Rare:90 | ||||
chr17:4263934-4264042 | Rare:47 | ||||
chr17:4555312-4555503 | Common:3; Rare:88 | ||||
chr17:4704097-4704231 | Rare:72 | ||||
chr17:4806989-4807203 | Common:4; Rare:66 | ||||
chr17:4939912-4940285 | Common:2; Rare:114 | ||||
chr17:4948914-4949184 | Common:2; Rare:92 | ||||
chr17:4967772-4967976 | Rare:81 | ||||
chr17:4987426-4987753 | Common:3; Rare:107 | ||||
chr17:5007032-5007315 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr17:5191838-5192081 | Common:1; Rare:79 | ||||
chr17:5419618-5419811 | Common:3; Rare:79 | ||||
chr17:5420080-5420213 | Rare:55 | ||||
chr17:5486157-5486602 | Common:5; Rare:152 | ||||
chr17:5584460-5584605 | Common:1; Rare:32 |