Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68956094-68956203 | Rare:46 | ||||
chr10:68988645-68988830 | Common:1; Rare:58; Clinvar (benign):2 | ||||
chr10:69087974-69088209 | Rare:49 | ||||
chr10:69179932-69180300 | Common:2; Rare:115 | ||||
chr10:69318541-69318944 | Common:5; Rare:108 | ||||
chr10:70052681-70052971 | Rare:61 | ||||
chr10:70170446-70170749 | Common:3; Rare:95 | ||||
chr10:70233348-70233562 | Common:5; Rare:75 | ||||
chr10:70382594-70382816 | Common:4; Rare:86 | ||||
chr10:70403970-70404167 | Rare:73 | ||||
chr10:70815812-70816002 | Rare:72 | ||||
chr10:70888536-70888649 | Common:1; Rare:38; Clinvar:5; Clinvar (benign):1 | ||||
chr10:71773499-71773751 | Common:3; Rare:71 | ||||
chr10:71851229-71851452 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):7 | ||||
chr10:72088669-72088685 | Rare:3 |