Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42154967-42155295 | Common:4; Rare:86 | ||||
chr17:42577660-42577824 | Rare:73 | ||||
chr17:42609354-42609711 | Common:6; Rare:144; Clinvar (benign):1 | ||||
chr17:42798685-42798767 | Rare:21 | ||||
chr17:42833378-42833479 | Rare:41 | ||||
chr17:42998211-42998486 | Common:3; Rare:79 | ||||
chr17:43125354-43125642 | Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171043-43171227 | Rare:54 | ||||
chr17:44324780-44324966 | Common:2; Rare:65 | ||||
chr17:44503385-44503711 | Rare:130 | ||||
chr17:44899424-44899735 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060984-45061341 | Common:2; Rare:97 | ||||
chr17:47941368-47941610 | Rare:49; Clinvar:1 | ||||
chr17:48048039-48048379 | Common:1; Rare:91 | ||||
chr17:48101375-48101632 | Common:2; Rare:81 |