Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40342038-40342183 | Common:1; Rare:28 | ||||
chr17:41688592-41688904 | Common:1; Rare:105 | ||||
chr17:41812645-41813021 | Common:2; Rare:86; Clinvar:5 | ||||
chr17:41930527-41930656 | Rare:30 | ||||
chr17:42017388-42017471 | Rare:41 | ||||
chr17:42423071-42423399 | Common:1; Rare:94; Clinvar:2 | ||||
chr17:42458735-42458936 | Common:3; Rare:75 | ||||
chr17:42577706-42577864 | Common:1; Rare:76 | ||||
chr17:42609321-42609705 | Common:8; Rare:158; Clinvar (benign):1 | ||||
chr17:42682382-42682574 | Rare:39 | ||||
chr17:42760974-42761254 | Rare:72 | ||||
chr17:42833333-42833456 | Rare:47 | ||||
chr17:42964428-42964528 | Rare:49 | ||||
chr17:43171003-43171255 | Rare:84 | ||||
chr17:44070612-44070930 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):2 |