Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:102736844-102736932 | Common:1; Rare:38 | ||||
chr2:105337457-105337602 | Common:1; Rare:73 | ||||
chr2:108449108-108449257 | Rare:51 | ||||
chr2:108534204-108534483 | Common:7; Rare:116 | ||||
chr2:108719383-108719586 | Common:3; Rare:85; Clinvar (benign):2 | ||||
chr2:109613813-109614003 | Common:2; Rare:67 | ||||
chr2:111884147-111884249 | Rare:28 | ||||
chr2:111898304-111898630 | Common:2; Rare:71 | ||||
chr2:112055459-112055608 | Common:2; Rare:42 | ||||
chr2:112275394-112275637 | Common:1; Rare:82 | ||||
chr2:112584410-112584633 | Common:1; Rare:61 | ||||
chr2:112645701-112645940 | Common:1; Rare:87 | ||||
chr2:113117852-113118021 | Common:4; Rare:44; Clinvar:2; Clinvar (benign):3 | ||||
chr2:113627058-113627325 | Common:4; Rare:78 | ||||
chr2:113756483-113756753 | Common:3; Rare:81 |