Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:9869807-9870528 | Common:15; Rare:206 | ||||
chr18:9899070-9899330 | Rare:75 | ||||
chr18:11947090-11947570 | Common:7; Rare:122 | ||||
chr18:12730210-12730510 | Rare:55 | ||||
chr18:13137950-13138410 | Common:8; Rare:170 | ||||
chr18:13338458-13338654 | Rare:56 | ||||
chr18:22002050-22002480 | Rare:88 | ||||
chr18:22020051-22020547 | Common:3; Rare:116 | ||||
chr18:23141520-23142160 | Common:2; Rare:199 | ||||
chr18:23356970-23357590 | Common:1; Rare:142 | ||||
chr18:23385050-23385460 | Common:1; Rare:178 | ||||
chr18:23556002-23556856 | Common:10; Rare:377; Clinvar:20; Clinvar (benign):15; Clinvar (pathogenic):11 | ||||
chr18:26548537-26548673 | Common:1; Rare:30 | ||||
chr18:31101090-31101410 | Common:6; Rare:99 | ||||
chr18:32769475-32769691 | Common:4; Rare:46 |