Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44899379-44899735 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060969-45061339 | Common:2; Rare:97 | ||||
chr17:45132313-45132629 | Common:2; Rare:91 | ||||
chr17:45148152-45148489 | Common:1; Rare:101 | ||||
chr17:45490701-45490867 | Common:1; Rare:58 | ||||
chr17:45894273-45894570 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
chr17:46923077-46923187 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47188838-47189039 | Common:1; Rare:40 | ||||
chr17:47189187-47189321 | Common:1; Rare:43 | ||||
chr17:47253690-47253931 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
chr17:47323894-47324005 | Common:1; Rare:34 | ||||
chr17:47650091-47650284 | Rare:55 | ||||
chr17:47941348-47941712 | Rare:98; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048069-48048405 | Rare:86 | ||||
chr17:48048606-48048857 | Common:4; Rare:39 |