Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93345601-93346004 | Common:8; Rare:218 | ||||
chr1:93447977-93448237 | Common:4; Rare:152 | ||||
chr1:93681599-93681910 | Common:4; Rare:158 | ||||
chr1:93845740-93846550 | Common:7; Rare:220 | ||||
chr1:93879122-93879299 | Common:3; Rare:115 | ||||
chr1:93908460-93908970 | Common:4; Rare:82 | ||||
chr1:93909353-93909839 | Common:7; Rare:255 | ||||
chr1:94121290-94121710 | Common:3; Rare:144 | ||||
chr1:94237462-94237744 | Rare:175 | ||||
chr1:94418159-94418525 | Common:4; Rare:228 | ||||
chr1:94541741-94541994 | Rare:145 | ||||
chr1:94820143-94820393 | Common:6; Rare:95 | ||||
chr1:94820440-94820850 | Common:8; Rare:168 | ||||
chr1:94926929-94927481 | Common:5; Rare:316 | ||||
chr1:95072835-95073018 | Common:2; Rare:131; Clinvar (benign):4 |