Variant report

Variant	rs6448042
Chromosome Location	chr4:21282541-21282542
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10006105	0.80[CEU][hapmap]
rs10018523	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10516376	0.89[CEU][hapmap]
rs10516377	0.80[CEU][hapmap]
rs11936275	1.00[CEU][hapmap]
rs11943249	1.00[CEU][hapmap]
rs12640602	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12642021	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12648055	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1364834	0.90[CEU][hapmap]
rs1425333	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs16867638	0.80[CEU][hapmap]
rs16870654	1.00[CEU][hapmap]
rs16870658	0.92[YRI][hapmap]
rs16870672	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs16870719	0.83[YRI][hapmap]
rs17458108	0.89[CEU][hapmap]
rs1967398	0.89[CEU][hapmap]
rs2322881	1.00[CEU][hapmap]
rs60195094	0.95[EUR][1000 genomes]
rs6448043	1.00[CEU][hapmap];0.93[CHB][hapmap]
rs6821700	0.90[CEU][hapmap]
rs6832734	0.80[CEU][hapmap]
rs6839686	1.00[CEU][hapmap]
rs6839994	1.00[CEU][hapmap]
rs6850985	0.92[YRI][hapmap]
rs6858044	0.92[YRI][hapmap]
rs73249526	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73249540	0.98[EUR][1000 genomes]
rs7669586	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs993610	0.85[YRI][hapmap]
rs9998813	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1014062	chr4:21270358-21479027	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 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
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