Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8965667-8965982 | Common:2; Rare:75 | ||||
chr17:8966057-8966157 | Rare:19 | ||||
chr17:9021466-9021552 | Rare:42 | ||||
chr17:9575661-9575993 | Common:8; Rare:88 | ||||
chr17:9644549-9644784 | Common:2; Rare:38 | ||||
chr17:10059636-10059945 | Common:2; Rare:58 | ||||
chr17:10198858-10198935 | Common:1; Rare:29 | ||||
chr17:10697415-10697845 | Common:7; Rare:158; Clinvar:5; Clinvar (benign):5 | ||||
chr17:10697874-10698023 | Common:2; Rare:27 | ||||
chr17:10729995-10730082 | Common:3; Rare:19 | ||||
chr17:11997284-11997862 | Common:4; Rare:177 | ||||
chr17:12020687-12020995 | Common:2; Rare:123 | ||||
chr17:13017614-13018375 | Common:9; Rare:289; Clinvar:3; Clinvar (benign):6 | ||||
chr17:14069278-14069654 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:14069874-14069929 | Rare:14 |