Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:180830836-180831041 | Common:1; Rare:61 | ||||
chr5:180831559-180831706 | Common:2; Rare:64 | ||||
chr5:181207537-181207751 | Common:4; Rare:61 | ||||
chr5:181246402-181246576 | Common:4; Rare:63 | ||||
chr6:1389074-1389167 | Rare:26 | ||||
chr6:2955587-2955861 | Common:1; Rare:76; Clinvar (benign):2 | ||||
chr6:12957877-12958017 | Rare:24 | ||||
chr6:13710810-13710968 | Rare:59 | ||||
chr6:16760055-16760203 | Rare:52 | ||||
chr6:17600914-17600958 | Rare:22 | ||||
chr6:19838168-19838395 | Common:3; Rare:94 | ||||
chr6:19839091-19839312 | Common:3; Rare:75 | ||||
chr6:26126194-26126355 | Common:2; Rare:37 | ||||
chr6:26195336-26195562 | Rare:44 | ||||
chr6:26521709-26521792 | Rare:20 |