Variant report

Variant	rs7308204
Chromosome Location	chr12:62208448-62208449
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10784260	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10784269	0.91[CHB][hapmap];0.91[JPT][hapmap];0.81[YRI][hapmap];0.82[EUR][1000 genomes]
rs10877732	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10877741	0.90[EUR][1000 genomes]
rs10877746	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs10877750	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs10877753	0.95[CHB][hapmap]
rs11174177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12368938	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs1869890	0.96[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap]
rs2198776	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs7137381	0.91[CHB][hapmap];0.83[EUR][1000 genomes]
rs7302585	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7304109	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7961921	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7979443	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7980047	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv899151	chr12:62108648-62227606	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv977138	chr12:62199079-62211306	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv11147	chr12:62199825-62210977	ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3497041	chr12:62200665-62211108	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3497052	chr12:62200665-62211108	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv2421373	chr12:62202570-62210820	ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv442272	chr12:62202570-62210820	ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv514672	chr12:62202621-62210789	ZNF genes & repeats	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
chromosomal regions: chr1:12345-34567

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