Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7584084-7584113 | Rare:6 | ||||
chr17:7686397-7686677 | Rare:69 | ||||
chr17:7688117-7688371 | Common:4; Rare:58; Clinvar:1 | ||||
chr17:7857460-7857679 | Common:2; Rare:72 | ||||
chr17:7857875-7858069 | Rare:64 | ||||
chr17:7885196-7885346 | Rare:43 | ||||
chr17:7931821-7932248 | Common:5; Rare:119 | ||||
chr17:8162911-8163072 | Rare:50 | ||||
chr17:8176331-8176455 | Rare:41 | ||||
chr17:8435728-8436003 | Common:4; Rare:111 | ||||
chr17:10697504-10697654 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
chr17:13017960-13018324 | Common:6; Rare:116; Clinvar (benign):2 | ||||
chr17:13601885-13602063 | Common:3; Rare:54 | ||||
chr17:14069440-14069545 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15699500-15699773 | Common:3; Rare:71 |