Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77957611-77957623 | Rare:1 | ||||
chr1:84274968-84274999 | Rare:5 | ||||
chr1:85358795-85358979 | Rare:38 | ||||
chr1:85582502-85582854 | Common:1; Rare:112 | ||||
chr1:86915317-86915336 | Rare:4 | ||||
chr1:88804141-88804490 | Common:1; Rare:65 | ||||
chr1:88830000-88830212 | Common:2; Rare:34 | ||||
chr1:89020588-89020871 | Rare:69 | ||||
chr1:90851580-90851762 | Common:2; Rare:49 | ||||
chr1:92840538-92840763 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93324852-93325087 | Rare:32 | ||||
chr1:93524119-93524317 | Rare:35 | ||||
chr1:93571743-93571993 | Common:1; Rare:74 | ||||
chr1:93575779-93575963 | Rare:48 | ||||
chr1:93591954-93592010 | Rare:8 |