Variant report

Variant	rs2189315
Chromosome Location	chr7:11542674-11542675
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10486133	0.84[ASW][hapmap];1.00[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10486134	0.82[CEU][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10486136	0.82[CEU][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12216656	1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12531326	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12531791	1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12536466	0.82[CEU][hapmap];0.80[TSI][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12536515	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12536556	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12537175	0.82[CEU][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17149861	0.87[CEU][hapmap];0.80[TSI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17556469	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17556497	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17557036	0.82[CEU][hapmap];0.80[TSI][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17557433	0.87[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17632003	0.82[CEU][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17632075	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17632105	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17632187	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17632560	0.82[CEU][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4141318	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6967171	1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6967452	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73068764	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73068765	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73068778	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73068781	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73068790	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73068794	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73070814	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024171	chr7:10810444-11559156	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv817291	chr7:10875417-11562683	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv1028326	chr7:11221209-11754436	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv538733	chr7:11221209-11754436	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv830903	chr7:11384957-11586376	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1023665	chr7:11457493-11773517	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv887606	chr7:11473561-11771288	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv1028614	chr7:11511684-11596934	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1020765	chr7:11522119-11573756	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv464366	chr7:11522525-11602899	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv606200	chr7:11522525-11602899	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv967452	chr7:11535987-11571414	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	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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