Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:99141141-99141441 | Common:1; Rare:108 | ||||
chr2:99141671-99141723 | Rare:11 | ||||
chr2:99154863-99155037 | Common:2; Rare:75; Clinvar (benign):1 | ||||
chr2:99180977-99181226 | Common:2; Rare:73 | ||||
chr2:100562732-100563054 | Common:3; Rare:103 | ||||
chr2:101002162-101002313 | Rare:59 | ||||
chr2:101252618-101252917 | Common:5; Rare:104 | ||||
chr2:101308662-101308819 | Rare:68 | ||||
chr2:102736821-102736938 | Common:1; Rare:59 | ||||
chr2:105037884-105038106 | Common:3; Rare:78 | ||||
chr2:105337454-105337578 | Common:1; Rare:59 | ||||
chr2:106194243-106194594 | Common:6; Rare:146 | ||||
chr2:108288610-108288914 | Common:1; Rare:58 | ||||
chr2:108449097-108449260 | Rare:58 | ||||
chr2:108534199-108534483 | Common:7; Rare:117 |