Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45750489-45751037 | Common:2; Rare:158 | ||||
chr1:45751043-45751096 | Common:2; Rare:10 | ||||
chr1:45803316-45803712 | Common:2; Rare:117 | ||||
chr1:46132144-46132258 | Rare:20 | ||||
chr1:46132462-46132678 | Common:3; Rare:74 | ||||
chr1:46132839-46133153 | Common:1; Rare:94 | ||||
chr1:46133331-46133441 | Rare:28 | ||||
chr1:46174562-46174699 | Rare:31 | ||||
chr1:46174704-46174863 | Rare:22 | ||||
chr1:46183338-46183544 | Common:1; Rare:37 | ||||
chr1:46183743-46183860 | Common:1; Rare:25 | ||||
chr1:46198215-46198638 | Common:7; Rare:155; Clinvar:1; Clinvar (benign):3 | ||||
chr1:46203174-46203364 | Rare:35 | ||||
chr1:46247236-46247795 | Common:4; Rare:103 | ||||
chr1:46272685-46272802 | Rare:33 |