Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66930067-66930462 | Rare:143 | ||||
chr1:66930604-66930847 | Common:1; Rare:83 | ||||
chr1:67053612-67053845 | Common:4; Rare:105; Clinvar (pathogenic):1 | ||||
chr1:67053920-67054107 | Rare:83 | ||||
chr1:67054303-67054492 | Common:4; Rare:48 | ||||
chr1:67307802-67307873 | Common:1; Rare:25 | ||||
chr1:67429072-67429450 | Rare:91 | ||||
chr1:67429690-67429918 | Common:1; Rare:57 | ||||
chr1:67429967-67429986 | Rare:8 | ||||
chr1:67430306-67430715 | Rare:153 | ||||
chr1:67430804-67431215 | Common:5; Rare:109 | ||||
chr1:67684909-67685512 | Common:3; Rare:179 | ||||
chr1:67686015-67686102 | Rare:37 | ||||
chr1:67832745-67832953 | Common:1; Rare:51 | ||||
chr1:67833069-67833243 | Common:1; Rare:34 |