Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1876142-1876276 | Common:1; Rare:53 | ||||
chr19:2046187-2046438 | Common:3; Rare:103 | ||||
chr19:3120885-3121112 | Rare:74 | ||||
chr19:3977213-3977612 | Common:4; Rare:130; Clinvar (benign):8 | ||||
chr19:3980512-3981003 | Common:1; Rare:181; Clinvar:3; Clinvar (benign):2 | ||||
chr19:4361653-4361969 | Common:2; Rare:124 | ||||
chr19:4363727-4364127 | Common:2; Rare:136 | ||||
chr19:4365516-4365904 | Common:1; Rare:105 | ||||
chr19:4445593-4445734 | Rare:42 | ||||
chr19:4792505-4792701 | Common:1; Rare:79 | ||||
chr19:4793012-4793265 | Rare:86 | ||||
chr19:5035210-5035320 | Rare:26 | ||||
chr19:5148378-5148531 | Common:1; Rare:28 | ||||
chr19:5308884-5309030 | Common:1; Rare:38 | ||||
chr19:6061474-6061688 | Common:2; Rare:37 |