Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44503369-44503727 | Rare:137 | ||||
chr17:44899393-44899748 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
chr17:44915476-44915672 | Rare:45; Clinvar (benign):1 | ||||
chr17:45051420-45051692 | Common:1; Rare:88 | ||||
chr17:45060987-45061338 | Common:2; Rare:93 | ||||
chr17:45161530-45161906 | Common:1; Rare:90 | ||||
chr17:45490713-45490888 | Rare:59 | ||||
chr17:45620232-45620362 | Rare:29 | ||||
chr17:45894247-45894685 | Common:4; Rare:126; Clinvar:5; Clinvar (benign):3 | ||||
chr17:46225347-46225480 | Common:1; Rare:33 | ||||
chr17:46922844-46923179 | Common:3; Rare:89; Clinvar (benign):6 | ||||
chr17:47189242-47189545 | Rare:76 | ||||
chr17:47831516-47831738 | Rare:62 | ||||
chr17:47941348-47941607 | Rare:51; Clinvar:1 | ||||
chr17:47970759-47971146 | Common:4; Rare:88 |