Variant report

Variant	rs832993
Chromosome Location	chr7:136839586-136839587
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10264746	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10954577	0.81[CEU][hapmap]
rs13244755	0.83[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs1425070	0.80[EUR][1000 genomes]
rs1425077	0.80[EUR][1000 genomes]
rs1425082	0.80[EUR][1000 genomes]
rs1425083	0.80[EUR][1000 genomes]
rs1579354	0.81[CEU][hapmap]
rs1647752	0.81[EUR][1000 genomes]
rs17168993	0.81[CEU][hapmap]
rs67499443	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6971259	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6975389	0.80[EUR][1000 genomes]
rs6975947	0.80[JPT][hapmap]
rs706556	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72611531	0.80[EUR][1000 genomes]
rs7787277	0.81[ASN][1000 genomes]
rs832948	0.80[EUR][1000 genomes]
rs832952	0.80[EUR][1000 genomes]
rs832953	0.80[EUR][1000 genomes]
rs832958	0.83[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs832959	0.82[ASN][1000 genomes]
rs832960	0.83[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs832967	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs832968	0.80[EUR][1000 genomes]
rs832969	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs832971	0.80[EUR][1000 genomes]
rs832997	0.83[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs832998	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs833003	0.96[EUR][1000 genomes]
rs833004	0.96[EUR][1000 genomes]
rs833005	0.94[EUR][1000 genomes]
rs833007	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs833008	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs833009	0.96[EUR][1000 genomes]
rs833010	0.96[EUR][1000 genomes]
rs833013	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs833022	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]

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	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1028902	chr7:136727136-136858804	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv464730	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv608463	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv831149	chr7:136831665-137006468	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1034546	chr7:136832263-136858804	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136839000-136839600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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