Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94926844-94926926 | Rare:21 | ||||
chr1:94926930-94927439 | Common:4; Rare:161 | ||||
chr1:95072866-95072995 | Common:1; Rare:51; Clinvar (benign):1 | ||||
chr1:95117289-95117461 | Rare:55 | ||||
chr1:95233933-95234236 | Common:5; Rare:89 | ||||
chr1:98661590-98661869 | Common:2; Rare:99 | ||||
chr1:99850319-99850407 | Rare:27; Clinvar:1 | ||||
chr1:99969902-99970106 | Rare:54 | ||||
chr1:100038001-100038178 | Common:1; Rare:70 | ||||
chr1:100132895-100133230 | Common:2; Rare:130 | ||||
chr1:100266096-100266418 | Common:4; Rare:114 | ||||
chr1:100352350-100352526 | Rare:44 | ||||
chr1:100894810-100894914 | Rare:20 | ||||
chr1:100895975-100896147 | Rare:47 | ||||
chr1:101025763-101025910 | Common:1; Rare:44 |