Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:81937246-81937455 | Rare:86 | ||||
chr17:81977443-81977640 | Rare:70 | ||||
chr18:812254-812437 | Common:3; Rare:68 | ||||
chr18:2571474-2571608 | Rare:36 | ||||
chr18:3247359-3247514 | Common:1; Rare:44 | ||||
chr18:3247747-3247877 | Rare:43 | ||||
chr18:3261830-3262211 | Common:6; Rare:124 | ||||
chr18:9102489-9102758 | Common:2; Rare:104; Clinvar:5; Clinvar (benign):2 | ||||
chr18:12702665-12703083 | Common:3; Rare:167 | ||||
chr18:21612197-21612428 | Common:1; Rare:70 | ||||
chr18:35290234-35290377 | Common:1; Rare:49 | ||||
chr18:36828736-36829132 | Common:3; Rare:152 | ||||
chr18:46098253-46098569 | Common:11; Rare:84; Clinvar (benign):5 | ||||
chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
chr18:49561890-49562071 | Rare:44 |