Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37995870-37996290 | Common:6; Rare:167 | ||||
chr1:38858920-38859230 | Common:8; Rare:108 | ||||
chr1:39799210-39799450 | Common:2; Rare:35 | ||||
chr1:40866350-40866840 | Common:14; Rare:148 | ||||
chr1:40875581-40876040 | Common:5; Rare:140 | ||||
chr1:40877670-40878150 | Common:4; Rare:131 | ||||
chr1:40944330-40944750 | Rare:112 | ||||
chr1:40948810-40949260 | Common:2; Rare:108 | ||||
chr1:41241140-41241590 | Common:2; Rare:138 | ||||
chr1:41496250-41496480 | Common:5; Rare:131 | ||||
chr1:42924260-42924570 | Common:3; Rare:166 | ||||
chr1:43206760-43207380 | Common:2; Rare:245 | ||||
chr1:43348190-43348740 | Common:3; Rare:163 | ||||
chr1:43348910-43349276 | Common:4; Rare:198; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:43523147-43523398 | Rare:43 |