Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26787859-26787994 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26863082-26863728 | Common:1; Rare:186 | ||||
chr1:26890241-26890323 | Common:1; Rare:37 | ||||
chr1:26900067-26900198 | Rare:51 | ||||
chr1:26900441-26900559 | Rare:38 | ||||
chr1:26921577-26921837 | Common:3; Rare:79 | ||||
chr1:26960361-26960527 | Common:1; Rare:34 | ||||
chr1:27322063-27322299 | Common:1; Rare:82 | ||||
chr1:27341880-27342100 | Rare:53 | ||||
chr1:27490033-27490330 | Rare:100 | ||||
chr1:27725762-27725991 | Common:2; Rare:57 | ||||
chr1:28088565-28088793 | Common:3; Rare:76 | ||||
chr1:28328910-28329087 | Common:1; Rare:53 | ||||
chr1:28369516-28369816 | Common:3; Rare:116 | ||||
chr1:28505806-28506050 | Common:2; Rare:92 |