Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15758427-15758866 | Common:1; Rare:85 | ||||
chr1:16156038-16156169 | Rare:30; Clinvar:1 | ||||
chr1:16352419-16352557 | Common:1; Rare:71 | ||||
chr1:16980586-16980789 | Common:4; Rare:74 | ||||
chr1:17439656-17439853 | Rare:61 | ||||
chr1:19210243-19210420 | Rare:67 | ||||
chr1:19251486-19251870 | Common:6; Rare:132 | ||||
chr1:19312035-19312350 | Common:8; Rare:152 | ||||
chr1:19485438-19485797 | Common:1; Rare:136 | ||||
chr1:20485645-20485946 | Common:1; Rare:51 | ||||
chr1:20485963-20486063 | Rare:17 | ||||
chr1:20486140-20486275 | Rare:32 | ||||
chr1:20660966-20661285 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr1:20786595-20786965 | Rare:143 | ||||
chr1:21176818-21177109 | Rare:84 |