Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100351590-100351827 | Common:2; Rare:81 | ||||
chr1:100352145-100352519 | Common:1; Rare:84 | ||||
chr1:100352700-100353391 | Common:8; Rare:229; Clinvar (benign):2 | ||||
chr1:100894807-100894916 | Rare:21 | ||||
chr1:100895127-100895261 | Common:1; Rare:23 | ||||
chr1:100895849-100896170 | Rare:83 | ||||
chr1:101025729-101025951 | Common:1; Rare:64 | ||||
chr1:101236602-101237052 | Common:5; Rare:90 | ||||
chr1:103108447-103108832 | Rare:89 | ||||
chr1:103525435-103525723 | Rare:81 | ||||
chr1:103525780-103526070 | Common:1; Rare:75 | ||||
chr1:107056544-107056849 | Common:2; Rare:132 | ||||
chr1:107056937-107057087 | Rare:53 | ||||
chr1:107677715-107678115 | Common:2; Rare:88 | ||||
chr1:108200275-108200438 | Common:6; Rare:47 |