Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:105037884-105038095 | Common:3; Rare:72 | ||||
chr2:105337435-105337620 | Common:3; Rare:88 | ||||
chr2:105396876-105397190 | Common:6; Rare:83 | ||||
chr2:105398951-105399197 | Common:1; Rare:89 | ||||
chr2:105399361-105399642 | Rare:84 | ||||
chr2:105438433-105438774 | Common:3; Rare:74 | ||||
chr2:106194206-106194547 | Common:6; Rare:145 | ||||
chr2:108449098-108449277 | Rare:73 | ||||
chr2:108534157-108534477 | Common:7; Rare:129 | ||||
chr2:108654748-108655056 | Rare:64 | ||||
chr2:108719404-108719625 | Common:2; Rare:90; Clinvar (benign):2 | ||||
chr2:109613835-109614002 | Common:2; Rare:61 | ||||
chr2:110115815-110115931 | Common:2; Rare:27 | ||||
chr2:111122425-111122744 | Common:3; Rare:134 | ||||
chr2:111884081-111884240 | Common:1; Rare:47 |