Variant report

Variant	rs4896575
Chromosome Location	chr6:142413354-142413355
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11758623	0.91[JPT][hapmap]
rs178783	0.90[JPT][hapmap]
rs225602	0.81[AMR][1000 genomes]
rs225604	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225605	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225606	0.89[CEU][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes]
rs225618	0.90[JPT][hapmap]
rs225620	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225622	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225623	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225624	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225629	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225630	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225631	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225632	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs225633	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225634	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225635	0.90[JPT][hapmap]
rs225639	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225641	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225642	0.89[CEU][hapmap];0.91[JPT][hapmap]
rs225643	0.86[CEU][hapmap];0.91[JPT][hapmap]
rs225652	0.82[CEU][hapmap];0.91[JPT][hapmap]
rs225653	0.81[CEU][hapmap];0.90[JPT][hapmap]
rs225654	0.81[CEU][hapmap];0.90[JPT][hapmap]
rs225656	0.82[CEU][hapmap];0.90[JPT][hapmap]
rs225657	0.82[CEU][hapmap];0.90[JPT][hapmap]
rs225658	0.84[CEU][hapmap];0.91[JPT][hapmap]
rs225659	0.86[CEU][hapmap];0.91[JPT][hapmap]
rs225660	0.81[CEU][hapmap];0.90[JPT][hapmap]
rs225662	0.82[CEU][hapmap];0.91[JPT][hapmap]
rs225663	0.81[CEU][hapmap];0.90[JPT][hapmap]
rs225665	0.81[CEU][hapmap];0.90[JPT][hapmap]
rs225666	0.91[JPT][hapmap]
rs225671	0.90[JPT][hapmap]
rs225673	0.91[JPT][hapmap]
rs225674	0.91[JPT][hapmap]
rs225675	0.91[JPT][hapmap]
rs225676	0.90[JPT][hapmap]
rs225677	0.89[JPT][hapmap]
rs225678	0.90[JPT][hapmap]
rs225679	0.91[JPT][hapmap]
rs225684	0.90[JPT][hapmap]
rs225685	0.90[JPT][hapmap]
rs225687	0.91[JPT][hapmap]
rs225688	0.90[JPT][hapmap]
rs225689	0.91[JPT][hapmap]
rs225695	0.91[JPT][hapmap]
rs225700	0.91[JPT][hapmap]
rs225701	0.89[JPT][hapmap]
rs225702	0.91[JPT][hapmap]
rs225710	0.90[JPT][hapmap]
rs4896574	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs62430456	0.82[ASN][1000 genomes]
rs628311	0.89[CEU][hapmap];0.90[JPT][hapmap]
rs639658	0.88[CEU][hapmap];0.90[JPT][hapmap]
rs6939944	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6939975	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7756012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7774914	0.85[ASN][1000 genomes]
rs7776318	0.81[CHB][hapmap];0.90[JPT][hapmap]

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	nsv886732	chr6:142290338-142536049	Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv886733	chr6:142316672-142514226	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv1027489	chr6:142336722-142429903	Bivalent Enhancer Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv886734	chr6:142347611-142523865	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv830824	chr6:142361107-142544929	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv886735	chr6:142365171-142472294	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv886736	chr6:142365171-142523865	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 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
chromosomal regions: chr1:12345-34567

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