Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:52194397-52194510 | Rare:35 | ||||
chr13:52617452-52617547 | Common:1; Rare:19 | ||||
chr13:57629914-57630127 | Common:1; Rare:60 | ||||
chr13:102394502-102394654 | Common:1; Rare:55 | ||||
chr14:23416311-23416361 | Rare:19; Clinvar (benign):1 | ||||
chr14:23417348-23417594 | Common:2; Rare:64; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr14:32203265-32203564 | Common:12; Rare:126 | ||||
chr14:49633902-49634092 | Common:1; Rare:81; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:49862630-49863036 | Common:1; Rare:183 | ||||
chr14:53613935-53614090 | Rare:30 | ||||
chr14:64220279-64220497 | Rare:70; Clinvar:2 | ||||
chr14:65296975-65297097 | Common:1; Rare:19 | ||||
chr14:65302217-65302262 | Rare:6 | ||||
chr14:65302652-65302784 | Common:2; Rare:27 | ||||
chr14:66496541-66496836 | Rare:47 |