Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226408417-226408669 | Rare:54 | ||||
chr1:226870160-226870677 | Common:10; Rare:345; Clinvar (benign):7 | ||||
chr1:226870690-226871120 | Common:2; Rare:125 | ||||
chr1:226939839-226940369 | Common:5; Rare:1003; Clinvar:20 | ||||
chr1:227316425-227316825 | Common:4; Rare:80 | ||||
chr1:227316857-227318120 | Common:22; Rare:861 | ||||
chr1:227318084-227318221 | Common:8; Rare:68 | ||||
chr1:227318146-227318775 | Common:35; Rare:1098 | ||||
chr1:227318700-227319466 | Common:14; Rare:344 | ||||
chr1:227563340-227563610 | Common:3; Rare:115 | ||||
chr1:227563630-227564380 | Common:9; Rare:400 | ||||
chr1:227734472-227735847 | Common:34; Rare:1798 | ||||
chr1:227748451-227748851 | Common:7; Rare:124 | ||||
chr1:227947830-227948230 | Common:6; Rare:151 | ||||
chr1:228081508-228082270 | Rare:160 |