Variant report

Variant	rs71423507
Chromosome Location	chr2:178697367-178697368
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12994400	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13004037	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010041	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13012088	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13014074	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13022805	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13026166	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13027484	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13033904	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17329811	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17400931	1.00[ASN][1000 genomes]
rs2360221	1.00[ASN][1000 genomes]
rs34171827	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34356580	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34595897	0.90[EUR][1000 genomes]
rs34648335	0.90[EUR][1000 genomes]
rs34699522	0.90[EUR][1000 genomes]
rs34752624	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34956941	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35305315	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35391362	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35391652	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35586165	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35600620	0.87[ASN][1000 genomes]
rs35678669	0.90[EUR][1000 genomes]
rs35862134	0.90[EUR][1000 genomes]
rs35987785	0.90[EUR][1000 genomes]
rs4243392	1.00[ASN][1000 genomes]
rs4893988	1.00[ASN][1000 genomes]
rs6433695	1.00[ASN][1000 genomes]
rs6756606	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423505	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423508	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71423514	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71423525	0.90[EUR][1000 genomes]
rs7559765	1.00[ASN][1000 genomes]
rs7569826	0.87[EUR][1000 genomes]
rs7588187	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7588301	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7592278	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7596644	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7605249	0.83[AMR][1000 genomes];0.96[EUR][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	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv583690	chr2:178638381-178712283	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv3053	chr2:178690640-178735132	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178696400-178705200	Weak transcription	Psoas Muscle	Psoas
2	chr2:178696800-178698400	Enhancers	Fetal Intestine Large	intestine
3	chr2:178697000-178698000	Enhancers	Gastric	stomach
4	chr2:178697000-178698400	Enhancers	Fetal Intestine Small	intestine

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