Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:89250833-89251048 | Common:1; Rare:45 | ||||
chr10:91807525-91807691 | Rare:30 | ||||
chr10:94729585-94729683 | Rare:19 | ||||
chr10:95278228-95278441 | Common:1; Rare:33 | ||||
chr10:95289645-95289889 | Common:1; Rare:39 | ||||
chr10:95655903-95656093 | Common:2; Rare:33 | ||||
chr10:96272388-96272731 | Common:1; Rare:72 | ||||
chr10:97664430-97664730 | Common:2; Rare:44 | ||||
chr10:97772476-97772860 | Common:1; Rare:61 | ||||
chr10:97789025-97789292 | Rare:50 | ||||
chr10:98435478-98435733 | Common:2; Rare:54; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr10:99926908-99927215 | Common:2; Rare:47 | ||||
chr10:99929630-99929959 | Common:1; Rare:94 | ||||
chr10:99930525-99930547 | Rare:7 | ||||
chr10:99930774-99930822 | Rare:14 |