Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10535071-10535366 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:16438672-16439057 | Common:1; Rare:95 | ||||
chr17:17567227-17567401 | Common:4; Rare:24 | ||||
chr17:17752283-17752485 | Common:1; Rare:71 | ||||
chr17:29133147-29133323 | Common:2; Rare:35 | ||||
chr17:29639301-29639584 | Common:1; Rare:49 | ||||
chr17:29676968-29677284 | Common:1; Rare:26 | ||||
chr17:32496076-32496138 | Rare:15 | ||||
chr17:35313403-35313643 | Rare:55 | ||||
chr17:39209846-39209947 | Rare:20 | ||||
chr17:40019007-40019022 | Rare:3 | ||||
chr17:40108215-40108447 | Rare:51 | ||||
chr17:42333696-42334015 | Rare:67; Clinvar:1 | ||||
chr17:43315640-43315920 | Common:7; Rare:118 | ||||
chr17:46266813-46267108 | Common:16; Rare:67 |