Variant report

Variant	rs2501871
Chromosome Location	chr1:161239979-161239980
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10908829	0.80[ASN][1000 genomes]
rs11265583	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12088460	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12409590	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12750393	0.81[ASN][1000 genomes]
rs2501867	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2501875	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2502812	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2502813	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34740003	0.90[EUR][1000 genomes]
rs4255401	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4582821	0.80[AMR][1000 genomes]
rs4636483	0.82[EUR][1000 genomes]
rs4636484	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4657002	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4657004	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4657005	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4657006	0.92[EUR][1000 genomes]
rs4657007	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4657008	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4657009	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4657013	0.81[AMR][1000 genomes]
rs55748379	0.90[ASN][1000 genomes]
rs61802084	0.83[EUR][1000 genomes]
rs6427580	0.85[ASN][1000 genomes]
rs6427581	0.99[ASN][1000 genomes]
rs6427583	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6427584	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6657761	1.00[ASN][1000 genomes]
rs6681182	0.90[EUR][1000 genomes]
rs6682220	0.99[ASN][1000 genomes]
rs6690484	0.89[EUR][1000 genomes]
rs7532915	0.81[EUR][1000 genomes]
rs9427370	0.85[EUR][1000 genomes]
rs9651035	0.90[ASN][1000 genomes]
rs9651049	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530077	chr1:160836448-161284904	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv432986	chr1:161221133-161673682	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161237400-161242800	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr1:161237400-161242800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:161237400-161250600	Weak transcription	Pancreas	Pancrea
4	chr1:161238000-161242600	Weak transcription	Fetal Stomach	stomach
5	chr1:161238200-161257600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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