Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44503366-44503713 | Rare:134 | ||||
chr17:44899367-44899729 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060964-45061354 | Common:2; Rare:110 | ||||
chr17:45136028-45136216 | Rare:35 | ||||
chr17:45148159-45148631 | Common:1; Rare:162 | ||||
chr17:45148947-45149144 | Common:4; Rare:50 | ||||
chr17:45490708-45490888 | Rare:61 | ||||
chr17:45894317-45894570 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):1 | ||||
chr17:46833056-46833255 | Common:2; Rare:35 | ||||
chr17:46922876-46923216 | Common:4; Rare:105; Clinvar:4; Clinvar (benign):9 | ||||
chr17:47189241-47189587 | Rare:87 | ||||
chr17:47323856-47323987 | Common:2; Rare:45 | ||||
chr17:47649636-47649980 | Common:1; Rare:130 | ||||
chr17:47650005-47650284 | Rare:86 | ||||
chr17:47941350-47941813 | Rare:122; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 |