Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:98661484-98661974 | Common:4; Rare:150 | ||||
chr1:98661989-98662208 | Rare:52 | ||||
chr1:99264382-99264512 | Common:1; Rare:52 | ||||
chr1:99766511-99766945 | Common:2; Rare:68 | ||||
chr1:99849992-99850191 | Common:1; Rare:71 | ||||
chr1:99969678-99970087 | Common:1; Rare:87 | ||||
chr1:99970379-99970544 | Rare:39 | ||||
chr1:100037941-100038179 | Common:1; Rare:91 | ||||
chr1:100132865-100133249 | Common:3; Rare:148 | ||||
chr1:100249765-100250018 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:100266058-100266317 | Common:3; Rare:94 | ||||
chr1:100351310-100351436 | Rare:28 | ||||
chr1:100351599-100351733 | Common:2; Rare:46 | ||||
chr1:100352156-100352572 | Common:1; Rare:94 | ||||
chr1:100894786-100894989 | Rare:41 |