Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8176297-8176449 | Rare:55 | ||||
chr17:8248032-8248142 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8249221-8249317 | Common:1; Rare:28 | ||||
chr17:8295334-8295506 | Common:1; Rare:42 | ||||
chr17:8435706-8436034 | Common:4; Rare:125 | ||||
chr17:8965678-8965777 | Common:1; Rare:30 | ||||
chr17:9576602-9576702 | Rare:26 | ||||
chr17:10697417-10697654 | Common:3; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
chr17:10729703-10729816 | Rare:51 | ||||
chr17:10729980-10730105 | Common:3; Rare:30 | ||||
chr17:11997444-11997594 | Rare:50 | ||||
chr17:13017985-13018278 | Common:5; Rare:86 | ||||
chr17:14069384-14069580 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):3 | ||||
chr17:14300806-14301128 | Common:3; Rare:87 | ||||
chr17:15260781-15260961 | Common:1; Rare:58 |