Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:64687982-64688198 | Common:1; Rare:60 | ||||
chr3:67654536-67654810 | Common:2; Rare:111 | ||||
chr3:69013590-69013777 | Rare:53 | ||||
chr3:81743134-81743174 | Common:1; Rare:11 | ||||
chr3:81761387-81761685 | Common:7; Rare:116; Clinvar:1; Clinvar (benign):4 | ||||
chr3:81761687-81761873 | Common:1; Rare:53; Clinvar:1 | ||||
chr3:87227244-87227395 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
chr3:88058388-88058742 | Common:2; Rare:112 | ||||
chr3:88058926-88059294 | Common:3; Rare:135 | ||||
chr3:88149655-88150043 | Common:5; Rare:118 | ||||
chr3:94062910-94063011 | Rare:30 | ||||
chr3:97764706-97764802 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
chr3:97821882-97822190 | Common:2; Rare:112 | ||||
chr3:98522601-98522709 | Rare:28 | ||||
chr3:98732434-98732512 | Rare:14 |