Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:29942516-29942801 | Common:42; Rare:130 | ||||
chr6:30061154-30061384 | Common:1; Rare:42 | ||||
chr6:30067007-30067313 | Common:3; Rare:56 | ||||
chr6:30326375-30326525 | Common:1; Rare:26 | ||||
chr6:30326819-30326943 | Rare:36 | ||||
chr6:30489270-30489547 | Common:2; Rare:51 | ||||
chr6:30556218-30556372 | Rare:52 | ||||
chr6:30556452-30556705 | Common:1; Rare:63 | ||||
chr6:30557218-30557338 | Common:1; Rare:46 | ||||
chr6:30571207-30571517 | Common:1; Rare:100 | ||||
chr6:30617808-30617878 | Rare:32 | ||||
chr6:30686636-30686763 | Common:1; Rare:25 | ||||
chr6:30717259-30717574 | Common:1; Rare:72 | ||||
chr6:30742638-30742985 | Common:2; Rare:83 | ||||
chr6:30914190-30914363 | Rare:68; Clinvar (benign):2 |