Variant report

Variant	rs17197252
Chromosome Location	chr4:91842917-91842918
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs17017809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17197161	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28643477	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs28718569	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6532261	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6838874	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72665409	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72665427	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661724	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7662254	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7676047	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7688258	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7690597	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9307092	0.83[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs9994918	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879553	chr4:91691313-91868576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv879555	chr4:91743538-91967602	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv491945	chr4:91753638-92240582	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2755332	chr4:91782522-91869222	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv10533	chr4:91842776-91935992	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	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
chromosomal regions: chr1:12345-34567

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