Variant report

Variant	rs2389506
Chromosome Location	chr4:118983949-118983950
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10020473	0.82[ASN][1000 genomes]
rs10021128	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10024910	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10027893	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11098421	1.00[ASN][1000 genomes]
rs11098422	0.82[ASN][1000 genomes]
rs11722962	0.82[ASN][1000 genomes]
rs11730611	1.00[ASN][1000 genomes]
rs11733562	0.82[ASN][1000 genomes]
rs12499751	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12505642	1.00[ASN][1000 genomes]
rs13135646	0.81[ASN][1000 genomes]
rs13137083	1.00[ASN][1000 genomes]
rs13139875	0.82[ASN][1000 genomes]
rs1872771	0.96[ASN][1000 genomes]
rs1994384	0.82[ASN][1000 genomes]
rs2389500	1.00[ASN][1000 genomes]
rs2389501	1.00[ASN][1000 genomes]
rs2389503	1.00[ASN][1000 genomes]
rs2389505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2389508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2389509	1.00[ASN][1000 genomes]
rs2389510	0.82[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2389511	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2389512	0.82[ASN][1000 genomes]
rs2389513	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs2389514	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs2892785	0.92[ASN][1000 genomes]
rs2892786	1.00[ASN][1000 genomes]
rs2892787	0.82[ASN][1000 genomes]
rs4240313	1.00[ASN][1000 genomes]
rs4240314	1.00[ASN][1000 genomes]
rs4437319	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4558930	0.81[ASN][1000 genomes]
rs4833566	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs4834656	0.82[ASN][1000 genomes]
rs582448	0.93[JPT][hapmap]
rs586073	0.91[CHB][hapmap];0.93[JPT][hapmap]
rs586224	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs613083	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6816778	1.00[ASN][1000 genomes]
rs6818042	1.00[ASN][1000 genomes]
rs7677274	0.82[ASN][1000 genomes]
rs7687849	0.99[ASN][1000 genomes]
rs7688063	1.00[ASN][1000 genomes]
rs7688443	1.00[ASN][1000 genomes]
rs788662	0.93[CHB][hapmap];0.93[JPT][hapmap]

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	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS 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	39 gene(s)	inside rSNPs	diseases
2	nsv1009076	chr4:118949490-119269424	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1001236	chr4:118949490-119271243	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv879839	chr4:118967196-119010126	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118979200-118987000	Strong transcription	Dnd41	blood

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