Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100132895-100133210 | Common:2; Rare:114 | ||||
chr1:100178163-100178465 | Common:6; Rare:43 | ||||
chr1:100249803-100249966 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266089-100266419 | Common:4; Rare:120 | ||||
chr1:100352344-100352533 | Rare:46 | ||||
chr1:100719423-100719756 | Common:1; Rare:78 | ||||
chr1:100894637-100894945 | Common:2; Rare:73 | ||||
chr1:100895124-100895291 | Common:2; Rare:28 | ||||
chr1:100895975-100896155 | Rare:49 | ||||
chr1:101025754-101025937 | Common:1; Rare:54 | ||||
chr1:101026101-101026309 | Rare:35 | ||||
chr1:101236600-101237068 | Common:5; Rare:97 | ||||
chr1:103525477-103525774 | Rare:82 | ||||
chr1:103525891-103526221 | Common:1; Rare:103 | ||||
chr1:107056587-107056788 | Common:1; Rare:88 |