Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:183269378-183269611 | Common:1; Rare:40 | ||||
chr3:183273467-183273478 | Rare:3 | ||||
chr3:183447387-183447688 | Common:3; Rare:78 | ||||
chr3:184242642-184242948 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):2 | ||||
chr3:184323472-184323896 | Common:3; Rare:94 | ||||
chr3:184323901-184324247 | Common:2; Rare:80 | ||||
chr3:184513830-184514103 | Common:3; Rare:51 | ||||
chr3:184710393-184710457 | Rare:10 | ||||
chr3:184710517-184710949 | Rare:89 | ||||
chr3:185786390-185786622 | Common:1; Rare:46 | ||||
chr3:185823813-185823877 | Rare:20 | ||||
chr3:185823893-185824081 | Rare:42 | ||||
chr3:185825632-185825679 | Rare:16 | ||||
chr3:186663865-186663996 | Common:2; Rare:22 | ||||
chr3:186827514-186827610 | Common:2; Rare:42 |