Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:88149654-88150044 | Common:5; Rare:120 | ||||
chr3:94062904-94063040 | Rare:39 | ||||
chr3:97764706-97764795 | Common:1; Rare:17; Clinvar (benign):1 | ||||
chr3:97821868-97822068 | Rare:76 | ||||
chr3:98522623-98522715 | Rare:25 | ||||
chr3:99876129-99876323 | Common:1; Rare:53 | ||||
chr3:100401393-100401580 | Common:1; Rare:38 | ||||
chr3:100492422-100492664 | Common:2; Rare:79 | ||||
chr3:100709181-100709690 | Common:9; Rare:152; Clinvar (benign):1 | ||||
chr3:101513122-101513306 | Common:8; Rare:37 | ||||
chr3:101574064-101574230 | Rare:56 | ||||
chr3:101677092-101677178 | Rare:37 | ||||
chr3:101686672-101686870 | Common:2; Rare:83 | ||||
chr3:101724562-101724638 | Rare:23 | ||||
chr3:101779070-101779222 | Common:2; Rare:41 |