Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7479526-7479709 | Common:1; Rare:30 | ||||
chr17:7484207-7484370 | Common:1; Rare:66 | ||||
chr17:7583524-7583858 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7686413-7686692 | Rare:69 | ||||
chr17:7687476-7687611 | Rare:29 | ||||
chr17:7857383-7857778 | Common:3; Rare:127 | ||||
chr17:7931869-7932243 | Common:5; Rare:98 | ||||
chr17:8176313-8176449 | Rare:47 | ||||
chr17:8248042-8248136 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
chr17:10697505-10697653 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:11997444-11997594 | Rare:50 | ||||
chr17:13017978-13018275 | Common:6; Rare:87 | ||||
chr17:14069440-14069546 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15260734-15260998 | Common:2; Rare:91; Clinvar (benign):4 | ||||
chr17:15262493-15262649 | Rare:41 |