Variant report

Variant	rs16905671
Chromosome Location	chr10:55945231-55945232
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1020198	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1020199	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1020200	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10825267	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10825269	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10825270	1.00[JPT][hapmap]
rs11004129	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11593951	1.00[JPT][hapmap]
rs11816146	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11816562	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12242300	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12253569	1.00[CHB][hapmap]
rs16905674	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16905760	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs16905780	1.00[CEU][hapmap]
rs2044000	1.00[JPT][hapmap]
rs4295959	1.00[JPT][hapmap]
rs4313480	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7084434	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7087966	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7095082	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7893192	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7893350	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7900069	1.00[CHB][hapmap]
rs7901520	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7916480	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7921598	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8667	chr10:55803106-56022647	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv428557	chr10:55815334-55988225	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv870252	chr10:55823123-56029435	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv948730	chr10:55845301-56093271	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1035173	chr10:55847066-56005288	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv467214	chr10:55881720-55948714	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv430232	chr10:55883194-56027294	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv895431	chr10:55898144-55955444	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv2829924	chr10:55906112-56038831	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv895432	chr10:55922706-55959660	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1054364	chr10:55925471-56196447	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv540633	chr10:55925471-56196447	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv20105	chr10:55939729-56047721	ZNF genes & repeats Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv467215	chr10:55943184-56019194	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv550951	chr10:55943184-56019194	Active TSS ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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