| No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
| 1 |
nsv1045954 |
chr13:65495013-65842827 |
Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 2 |
nsv1046706 |
chr13:65495013-66210226 |
Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 3 |
nsv541809 |
chr13:65495013-66210226 |
Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers
|
TF binding regionCpG islandChromatin interactive regionlncRNA
|
4 gene(s)
|
inside rSNPs
|
diseases
|
| 4 |
nsv900373 |
chr13:65495897-65775294 |
Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers
|
TF binding regionCpG islandChromatin interactive region
|
1 gene(s)
|
inside rSNPs
|
diseases
|
| 5 |
nsv915632 |
chr13:65531495-65834877 |
Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats
|
TF binding regionCpG islandChromatin interactive region
|
3 gene(s)
|
inside rSNPs
|
diseases
|
| 6 |
nsv1037329 |
chr13:65583733-65673656 |
Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 7 |
esv2761796 |
chr13:65617000-65688686 |
Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 8 |
nsv900377 |
chr13:65620889-65746182 |
Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats
|
Chromatin interactive region
|
n/a
|
inside rSNPs
|
diseases
|
| 9 |
esv3421218 |
chr13:65635851-65640149 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 10 |
nsv512324 |
chr13:65635965-65639115 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 11 |
esv3323306 |
chr13:65636776-65639524 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 12 |
esv3337947 |
chr13:65637101-65639199 |
Enhancers Weak transcription
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 13 |
esv995936 |
chr13:65637419-65638230 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 14 |
esv7260 |
chr13:65637563-65638463 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 15 |
esv3420830 |
chr13:65637601-65638749 |
Weak transcription Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 16 |
esv3339045 |
chr13:65637692-65638305 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 17 |
esv3499067 |
chr13:65637706-65638323 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 18 |
esv3409967 |
chr13:65637716-65638297 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 19 |
esv3499071 |
chr13:65637720-65638251 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 20 |
esv3499068 |
chr13:65637722-65638247 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 21 |
esv3511896 |
chr13:65637729-65638283 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 22 |
esv3511918 |
chr13:65637734-65638281 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 23 |
esv3511885 |
chr13:65637748-65638238 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 24 |
esv3499070 |
chr13:65637750-65638260 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 25 |
esv3499069 |
chr13:65637751-65638260 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 26 |
esv4726 |
chr13:65637762-65638274 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 27 |
esv3430202 |
chr13:65637770-65638230 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 28 |
esv3511907 |
chr13:65637795-65638215 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 29 |
esv3499072 |
chr13:65637805-65638213 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 30 |
esv3499073 |
chr13:65637809-65638211 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
| 31 |
esv3511929 |
chr13:65637809-65638211 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page:
1
