Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:125990557-125990575 | Rare:4 | ||||
chr3:139369324-139369525 | Rare:53 | ||||
chr3:142416750-142417010 | Common:1; Rare:54 | ||||
chr3:146104191-146104300 | Common:1; Rare:30 | ||||
chr3:150408843-150409171 | Rare:85 | ||||
chr3:160515232-160515496 | Common:1; Rare:50 | ||||
chr3:169765058-169765274 | Rare:78; Clinvar (pathogenic):1 | ||||
chr3:170726683-170726867 | Rare:32 | ||||
chr3:180948493-180948719 | Common:1; Rare:51 | ||||
chr3:184026453-184026736 | Rare:65 | ||||
chr3:184322392-184322638 | Rare:83; Clinvar:1 | ||||
chr3:184322683-184322852 | Rare:54 | ||||
chr3:184323593-184323950 | Common:3; Rare:73 | ||||
chr3:184710809-184711022 | Common:1; Rare:74 | ||||
chr3:185919449-185919528 | Rare:17 |