Variant report

Variant	rs11919075
Chromosome Location	chr3:85898799-85898800
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10511069	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs10511070	1.00[YRI][hapmap]
rs11919633	0.85[YRI][hapmap]
rs11919968	1.00[AMR][1000 genomes]
rs11924201	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13320595	1.00[AMR][1000 genomes]
rs13325188	1.00[AMR][1000 genomes]
rs13353520	1.00[AMR][1000 genomes]
rs17023248	0.94[YRI][hapmap]
rs17023257	0.83[AMR][1000 genomes]
rs17023295	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17023810	1.00[AMR][1000 genomes]
rs28611113	1.00[AMR][1000 genomes]
rs4473548	1.00[AMR][1000 genomes]
rs56787903	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57661808	1.00[AMR][1000 genomes]
rs58770804	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59605482	1.00[AMR][1000 genomes]
rs6549066	1.00[AMR][1000 genomes]
rs6762825	1.00[AMR][1000 genomes]
rs6764756	1.00[AMR][1000 genomes]
rs72906501	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908509	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908511	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908512	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908516	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908517	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908522	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72908582	1.00[AMR][1000 genomes]
rs72908587	1.00[AMR][1000 genomes]
rs72908602	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72910511	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72910559	1.00[AMR][1000 genomes]
rs72912429	1.00[AMR][1000 genomes]
rs72912437	1.00[AMR][1000 genomes]
rs72914830	1.00[AMR][1000 genomes]
rs72914833	1.00[AMR][1000 genomes]
rs72914835	1.00[AMR][1000 genomes]
rs72914844	1.00[AMR][1000 genomes]
rs72914849	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7615008	0.94[YRI][hapmap]
rs7638487	0.87[YRI][hapmap]
rs7640821	0.89[YRI][hapmap]
rs7646697	0.94[YRI][hapmap]
rs7649694	1.00[AMR][1000 genomes]
rs7650035	1.00[AMR][1000 genomes]
rs9856802	1.00[AMR][1000 genomes]
rs9863493	0.88[YRI][hapmap]
rs9872154	1.00[AMR][1000 genomes]
rs9874223	1.00[AMR][1000 genomes]
rs9876097	1.00[AMR][1000 genomes]
rs9880094	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877106	chr3:85814620-86006210	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv877107	chr3:85814620-86037162	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv877108	chr3:85870363-86037162	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv877109	chr3:85892098-86006210	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv877110	chr3:85892098-86037162	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv877111	chr3:85892098-86044224	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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