Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:44680703-44681015 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
chr18:45967231-45967466 | Rare:85; Clinvar (pathogenic):1 | ||||
chr18:46098224-46098639 | Common:11; Rare:118; Clinvar (benign):6 | ||||
chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
chr18:46104783-46104814 | Rare:8 | ||||
chr18:46173909-46174114 | Common:1; Rare:53 | ||||
chr18:46333534-46333600 | Common:1; Rare:12 | ||||
chr18:46333620-46333651 | Rare:12 | ||||
chr18:46333744-46333971 | Common:2; Rare:55 | ||||
chr18:46917341-46917649 | Common:3; Rare:134 | ||||
chr18:47150429-47150575 | Common:4; Rare:58 | ||||
chr18:47930787-47931203 | Rare:145 | ||||
chr18:48538980-48539312 | Common:2; Rare:71 | ||||
chr18:48539674-48539819 | Rare:34 | ||||
chr18:48539926-48540012 | Rare:10 |