Variant report

Variant	rs2337383
Chromosome Location	chr2:21320516-21320517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11693545	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11693760	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11693775	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11693870	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12052779	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1367113	0.83[EUR][1000 genomes]
rs1367115	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1367117	0.81[CEU][hapmap];0.82[JPT][hapmap]
rs1713223	1.00[JPT][hapmap]
rs17395333	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17395512	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17399144	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1897083	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2115838	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2163203	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2195597	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2878956	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4665176	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4665178	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4665179	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4665492	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56079819	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56090741	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56201838	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56306424	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588245	0.91[JPT][hapmap]
rs61539677	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62122514	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62122515	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62122516	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62122520	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62133263	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs62133264	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62135035	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6548010	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6548011	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6726115	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs754523	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs754524	0.92[ASN][1000 genomes]
rs7566030	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7575840	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7590135	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs934198	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription 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	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21312800-21321000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:21315800-21326400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:21318200-21322800	Enhancers	Fetal Intestine Large	intestine
4	chr2:21318200-21323600	Enhancers	Fetal Intestine Small	intestine
5	chr2:21318400-21322400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:21320000-21320600	Flanking Active TSS	HepG2	liver
7	chr2:21320000-21321000	Flanking Active TSS	Liver	Liver
8	chr2:21320400-21320800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr2:21320400-21320800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr2:21320400-21321200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:21320400-21321600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:21320400-21321800	Enhancers	Duodenum Mucosa	Duodenum
13	chr2:21320400-21322400	Enhancers	Adipose Nuclei	Adipose

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