Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43545630-43545822 | Common:1; Rare:47 | ||||
chr17:43545882-43546108 | Common:2; Rare:33 | ||||
chr17:43661289-43661484 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr17:43778868-43779073 | Rare:48 | ||||
chr17:44005436-44005725 | Rare:64; Clinvar:1 | ||||
chr17:44005912-44006057 | Rare:54 | ||||
chr17:44070619-44070947 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123580-44123863 | Common:3; Rare:83 | ||||
chr17:44170549-44170714 | Rare:27 | ||||
chr17:44186658-44187026 | Common:1; Rare:132 | ||||
chr17:44187161-44187290 | Rare:33 | ||||
chr17:44210790-44211202 | Common:1; Rare:122 | ||||
chr17:44218988-44219188 | Rare:64 | ||||
chr17:44219194-44219244 | Rare:15 | ||||
chr17:44220797-44220986 | Rare:57 |