Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:98662073-98662285 | Rare:47 | ||||
chr1:99264193-99264561 | Common:2; Rare:106 | ||||
chr1:99766620-99766695 | Rare:14 | ||||
chr1:99849997-99850142 | Common:1; Rare:55 | ||||
chr1:99969861-99970089 | Rare:49 | ||||
chr1:100037915-100038199 | Common:1; Rare:108 | ||||
chr1:100038347-100038737 | Common:5; Rare:130 | ||||
chr1:100132869-100133249 | Common:3; Rare:147 | ||||
chr1:100249796-100249954 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266089-100266414 | Common:4; Rare:119 | ||||
chr1:100351612-100351733 | Common:1; Rare:39 | ||||
chr1:100352197-100352504 | Rare:72 | ||||
chr1:100719650-100719779 | Common:1; Rare:32 | ||||
chr1:100894778-100894914 | Common:1; Rare:29 | ||||
chr1:100895113-100895454 | Common:2; Rare:64 |