Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159924523-159924704 | Rare:49 | ||||
chr1:159925449-159925617 | Common:1; Rare:44 | ||||
chr1:160031817-160032158 | Common:3; Rare:89 | ||||
chr1:160262152-160262292 | Rare:39 | ||||
chr1:160262424-160262617 | Rare:60 | ||||
chr1:160343181-160343409 | Rare:92 | ||||
chr1:161021111-161021499 | Common:2; Rare:99 | ||||
chr1:161045888-161046057 | Common:1; Rare:44 | ||||
chr1:161117971-161118137 | Rare:84 | ||||
chr1:161132426-161132674 | Common:1; Rare:90 | ||||
chr1:161153720-161153803 | Rare:22 | ||||
chr1:161225768-161226063 | Common:10; Rare:43 | ||||
chr1:161314308-161314414 | Common:2; Rare:45; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161721860-161722257 | Common:7; Rare:68 | ||||
chr1:161749638-161749835 | Rare:68 |