Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:35699292-35699497 | Rare:71; Clinvar (benign):3 | ||||
chr20:35740837-35741167 | Common:3; Rare:84 | ||||
chr20:35741624-35741693 | Rare:23 | ||||
chr20:35742161-35742651 | Common:5; Rare:154 | ||||
chr20:35771796-35772044 | Common:2; Rare:77 | ||||
chr20:36573406-36573504 | Rare:41 | ||||
chr20:36746065-36746291 | Common:2; Rare:82 | ||||
chr20:36773744-36773978 | Common:2; Rare:77 | ||||
chr20:37289577-37289669 | Common:1; Rare:28 | ||||
chr20:37527863-37528191 | Common:5; Rare:116 | ||||
chr20:38033416-38033779 | Common:2; Rare:104 | ||||
chr20:38165254-38165396 | Rare:42 | ||||
chr20:38962152-38962382 | Common:1; Rare:96 | ||||
chr20:41028562-41028861 | Rare:108 | ||||
chr20:43457802-43457907 | Rare:47 |