Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:657495-657801 | Common:9; Rare:95 | ||||
chr18:657812-657867 | Rare:14 | ||||
chr18:2571472-2571616 | Rare:40 | ||||
chr18:3247374-3247530 | Common:1; Rare:42 | ||||
chr18:3261743-3262235 | Common:7; Rare:153 | ||||
chr18:3450029-3450206 | Rare:53 | ||||
chr18:7117787-7117941 | Common:3; Rare:46 | ||||
chr18:9102484-9102789 | Common:2; Rare:122; Clinvar:6; Clinvar (benign):2 | ||||
chr18:9334467-9334906 | Common:1; Rare:109 | ||||
chr18:11751528-11751643 | Rare:33 | ||||
chr18:11752656-11752861 | Common:2; Rare:56 | ||||
chr18:11851243-11851490 | Common:3; Rare:92 | ||||
chr18:12307980-12308278 | Common:5; Rare:116 | ||||
chr18:12376970-12377069 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chr18:12658084-12658181 | Common:2; Rare:40 |