Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659239-99659549 | Common:1; Rare:79 | ||||
chr10:99732032-99732319 | Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
chr10:99913915-99914175 | Rare:73 | ||||
chr10:100009867-100010217 | Common:1; Rare:105 | ||||
chr10:100185908-100186264 | Common:1; Rare:124 | ||||
chr10:100229553-100229757 | Common:2; Rare:60 | ||||
chr10:100267586-100267806 | Common:4; Rare:68 | ||||
chr10:100286098-100286209 | Rare:23 | ||||
chr10:100286315-100286459 | Rare:28 | ||||
chr10:100286642-100286785 | Common:3; Rare:71 | ||||
chr10:100346507-100346696 | Common:3; Rare:40 | ||||
chr10:100346869-100347112 | Rare:50 | ||||
chr10:100519690-100520090 | Common:2; Rare:158 | ||||
chr10:100529803-100530041 | Common:1; Rare:68 | ||||
chr10:100535712-100535988 | Common:6; Rare:105 |