Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3965168-3965215 | Rare:13 | ||||
chr17:4007864-4007956 | Rare:22 | ||||
chr17:4134454-4134614 | Rare:30 | ||||
chr17:4138908-4139277 | Common:9; Rare:50 | ||||
chr17:4144286-4144578 | Common:6; Rare:71 | ||||
chr17:4970447-4970646 | Rare:63 | ||||
chr17:4989010-4989068 | Rare:7 | ||||
chr17:5003563-5003916 | Common:1; Rare:118; Clinvar (benign):1 | ||||
chr17:5004431-5004634 | Rare:66; Clinvar (benign):2 | ||||
chr17:5362819-5363007 | Rare:43 | ||||
chr17:5379270-5379386 | Rare:28 | ||||
chr17:7308873-7308971 | Rare:22 | ||||
chr17:7836331-7836479 | Common:1; Rare:43 | ||||
chr17:7840948-7841220 | Rare:54 | ||||
chr17:7841430-7841496 | Rare:14 |