Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87060164-87060337 | Rare:39 | ||||
chr10:87094404-87094684 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
chr10:87094956-87095235 | Common:1; Rare:68; Clinvar:1 | ||||
chr10:87504835-87504923 | Rare:42 | ||||
chr10:87818135-87818357 | Common:2; Rare:77 | ||||
chr10:88952709-88953046 | Common:2; Rare:60; Clinvar:1 | ||||
chr10:88990312-88990672 | Common:4; Rare:81; Clinvar (benign):3 | ||||
chr10:88990752-88990858 | Common:2; Rare:28; Clinvar (benign):2 | ||||
chr10:88991286-88991451 | Common:2; Rare:34 | ||||
chr10:89327796-89328004 | Common:3; Rare:34 | ||||
chr10:89332198-89332543 | Common:3; Rare:63 | ||||
chr10:89414658-89414798 | Common:3; Rare:69 | ||||
chr10:89701440-89701663 | Common:1; Rare:62 | ||||
chr10:90921079-90921182 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
chr10:91409678-91409710 | Rare:11 |