Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:97920899-97921198 | Common:2; Rare:114; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:97921324-97921574 | Common:3; Rare:43 | ||||
chr1:98661492-98661886 | Common:4; Rare:135 | ||||
chr1:99004710-99005160 | Common:4; Rare:131 | ||||
chr1:99264260-99264630 | Common:2; Rare:118 | ||||
chr1:99646305-99646572 | Common:1; Rare:56 | ||||
chr1:99766602-99766943 | Common:1; Rare:54 | ||||
chr1:99849992-99850127 | Common:1; Rare:51 | ||||
chr1:99850140-99850480 | Rare:87; Clinvar:3; Clinvar (benign):2 | ||||
chr1:99969892-99970075 | Rare:46 | ||||
chr1:100037948-100038253 | Common:1; Rare:115 | ||||
chr1:100132908-100133247 | Common:2; Rare:132 | ||||
chr1:100249761-100249991 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:100266086-100266296 | Common:3; Rare:82 | ||||
chr1:100351296-100351436 | Rare:31 |