Variant report

Variant	rs7997362
Chromosome Location	chr13:38771058-38771059
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1011484	1.00[CHB][hapmap]
rs10507469	1.00[CHB][hapmap]
rs10507470	1.00[CHB][hapmap]
rs1330972	1.00[ASN][1000 genomes]
rs1330973	1.00[ASN][1000 genomes]
rs17057355	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17057380	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001430	1.00[ASN][1000 genomes]
rs2019516	1.00[CHB][hapmap]
rs2134209	1.00[ASN][1000 genomes]
rs2173952	1.00[ASN][1000 genomes]
rs2202121	1.00[ASN][1000 genomes]
rs2460319	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2460324	1.00[ASN][1000 genomes]
rs2485779	1.00[CHB][hapmap]
rs3903006	1.00[ASN][1000 genomes]
rs4054427	1.00[ASN][1000 genomes]
rs4054430	1.00[ASN][1000 genomes]
rs4383021	1.00[ASN][1000 genomes]
rs4418934	1.00[ASN][1000 genomes]
rs4436666	1.00[ASN][1000 genomes]
rs4453349	1.00[ASN][1000 genomes]
rs4466961	1.00[ASN][1000 genomes]
rs4473056	1.00[ASN][1000 genomes]
rs4520716	1.00[ASN][1000 genomes]
rs4534702	1.00[ASN][1000 genomes]
rs4547225	1.00[ASN][1000 genomes]
rs4592525	1.00[ASN][1000 genomes]
rs4594119	1.00[ASN][1000 genomes]
rs4614591	1.00[ASN][1000 genomes]
rs486259	1.00[ASN][1000 genomes]
rs528967	1.00[ASN][1000 genomes]
rs604312	1.00[ASN][1000 genomes]
rs605680	1.00[ASN][1000 genomes]
rs619090	1.00[ASN][1000 genomes]
rs660187	1.00[ASN][1000 genomes]
rs7325481	1.00[ASN][1000 genomes]
rs73456013	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73456059	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73456084	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7997942	1.00[ASN][1000 genomes]
rs7999258	1.00[ASN][1000 genomes]
rs9315559	1.00[ASN][1000 genomes]
rs9315560	1.00[ASN][1000 genomes]
rs9315563	1.00[ASN][1000 genomes]
rs9315566	1.00[ASN][1000 genomes]
rs9315567	1.00[ASN][1000 genomes]
rs9532186	1.00[ASN][1000 genomes]
rs9548242	1.00[ASN][1000 genomes]
rs9548253	1.00[ASN][1000 genomes]
rs9566318	1.00[ASN][1000 genomes]
rs9576478	1.00[ASN][1000 genomes]
rs9576484	1.00[ASN][1000 genomes]
rs9576485	1.00[ASN][1000 genomes]
rs9576495	1.00[ASN][1000 genomes]
rs971225	1.00[ASN][1000 genomes]
rs9888482	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv869125	chr13:38550449-39132813	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949406	chr13:38561474-39033484	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38771000-38771200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:38771000-38771800	Enhancers	H9 Cell Line	embryonic stem cell
3	chr13:38771000-38774800	Weak transcription	Pancreas	Pancrea

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