| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv894916 |
chr10:19095467-19429415 |
Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv427857 |
chr10:19253828-19599493 |
Enhancers Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv894917 |
chr10:19259024-19463367 |
Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv550126 |
chr10:19270068-19572729 |
Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
2 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv894918 |
chr10:19390046-19466344 |
Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 6 |
esv2465653 |
chr10:19396815-19398443 |
Strong transcription Weak transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv9019 |
chr10:19397056-19397891 |
ZNF genes & repeats Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
esv2030521 |
chr10:19397114-19397846 |
Weak transcription ZNF genes & repeats
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3420560 |
chr10:19397210-19397733 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
esv3322227 |
chr10:19397214-19397757 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3486974 |
chr10:19397218-19397743 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3486973 |
chr10:19397236-19397684 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv3478174 |
chr10:19397245-19397719 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv3486977 |
chr10:19397250-19397695 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3478063 |
chr10:19397265-19397673 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3486976 |
chr10:19397265-19397694 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3626 |
chr10:19397267-19397701 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3437081 |
chr10:19397269-19397717 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3477952 |
chr10:19397295-19397650 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3478285 |
chr10:19397309-19397655 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3486978 |
chr10:19397318-19397656 |
Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page:
1
