| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv886011 |
chr6:65873577-66237309 |
Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv886012 |
chr6:65905998-66354809 |
Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv933487 |
chr6:65947165-66134134 |
Flanking Active TSS Enhancers Weak transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv516417 |
chr6:65952526-66083780 |
Enhancers Flanking Active TSS Weak transcription
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv886016 |
chr6:66002389-66103595 |
Enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv886018 |
chr6:66009103-66091351 |
Enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 7 |
nsv886019 |
chr6:66009103-66103595 |
Enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 8 |
esv3447152 |
chr6:66027938-66253181 |
Enhancers Weak transcription Active TSS
|
TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 9 |
nsv886020 |
chr6:66030650-66091351 |
Enhancers
|
Chromatin interactive regionmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv886021 |
chr6:66030650-66192399 |
Enhancers Weak transcription Active TSS
|
TF binding regionChromatin interactive regionlncRNAmiRNA target site
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 11 |
nsv462980 |
chr6:66039601-66083780 |
Enhancers
|
Chromatin interactive regionmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
nsv603434 |
chr6:66039601-66083780 |
Enhancers
|
Chromatin interactive regionmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
nsv886022 |
chr6:66039601-66091351 |
Enhancers
|
Chromatin interactive regionmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
nsv886023 |
chr6:66039601-66103595 |
Enhancers
|
Chromatin interactive regionmiRNA target site
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
nsv886024 |
chr6:66039601-66201364 |
Enhancers Weak transcription Active TSS
|
TF binding regionChromatin interactive regionlncRNAmiRNA target site
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 16 |
nsv886025 |
chr6:66050797-66192399 |
Enhancers Weak transcription Active TSS
|
TF binding regionChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 17 |
nsv603435 |
chr6:66052294-66091351 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
nsv462981 |
chr6:66052294-66115654 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
nsv603436 |
chr6:66052294-66115654 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
nsv462982 |
chr6:66052294-66122359 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
nsv603437 |
chr6:66052294-66122359 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
nsv1015632 |
chr6:66056747-66114121 |
Enhancers Weak transcription
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
nsv520449 |
chr6:66072542-66091351 |
Enhancers
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page:
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