Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7931906-7932258 | Common:5; Rare:98 | ||||
chr17:8151221-8151491 | Common:3; Rare:63 | ||||
chr17:8152378-8152696 | Common:4; Rare:77 | ||||
chr17:8162890-8163103 | Rare:76 | ||||
chr17:8176333-8176518 | Rare:52 | ||||
chr17:8248042-8248119 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8376672-8376769 | Common:1; Rare:36 | ||||
chr17:8435705-8436014 | Common:4; Rare:121 | ||||
chr17:10697505-10697644 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
chr17:13017968-13018272 | Common:6; Rare:89; Clinvar (benign):1 | ||||
chr17:14069440-14069580 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
chr17:15684246-15684325 | Common:3; Rare:32 | ||||
chr17:15699497-15699785 | Common:3; Rare:76 | ||||
chr17:15999620-15999989 | Common:3; Rare:168; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:16215522-16215651 | Common:1; Rare:52 |