Variant report

Variant	rs2238678
Chromosome Location	chr19:40226710-40226711
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1034867	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1034868	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10407647	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs10409279	0.82[ASN][1000 genomes]
rs10410864	0.82[ASN][1000 genomes]
rs10755	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs1126158	0.95[JPT][hapmap]
rs17608	1.00[ASN][1000 genomes]
rs2074926	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35837917	1.00[ASN][1000 genomes]
rs364911	1.00[ASN][1000 genomes]
rs367529	1.00[ASN][1000 genomes]
rs367788	1.00[ASN][1000 genomes]
rs372081	1.00[ASN][1000 genomes]
rs372902	0.99[ASN][1000 genomes]
rs373449	0.99[ASN][1000 genomes]
rs375867	1.00[ASN][1000 genomes]
rs378917	1.00[ASN][1000 genomes]
rs383768	1.00[ASN][1000 genomes]
rs384138	1.00[ASN][1000 genomes]
rs385240	0.98[ASN][1000 genomes]
rs385288	0.96[ASN][1000 genomes]
rs385520	1.00[ASN][1000 genomes]
rs388648	1.00[ASN][1000 genomes]
rs391646	1.00[ASN][1000 genomes]
rs391660	1.00[ASN][1000 genomes]
rs395892	1.00[ASN][1000 genomes]
rs396854	1.00[ASN][1000 genomes]
rs399641	1.00[ASN][1000 genomes]
rs412884	1.00[ASN][1000 genomes]
rs414423	0.99[ASN][1000 genomes]
rs416255	0.81[ASN][1000 genomes]
rs418664	1.00[ASN][1000 genomes]
rs425218	1.00[ASN][1000 genomes]
rs425265	1.00[ASN][1000 genomes]
rs428007	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs431329	1.00[ASN][1000 genomes]
rs437780	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs439881	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs440191	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs440334	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs44048	1.00[ASN][1000 genomes]
rs44049	1.00[ASN][1000 genomes]
rs444817	1.00[ASN][1000 genomes]
rs444963	0.98[ASN][1000 genomes]
rs446425	1.00[ASN][1000 genomes]
rs447034	1.00[ASN][1000 genomes]
rs453827	0.99[ASN][1000 genomes]
rs4802054	1.00[ASN][1000 genomes]
rs4830	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs6508903	0.95[JPT][hapmap]
rs7248018	0.90[ASN][1000 genomes]
rs7248344	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7249415	0.89[ASN][1000 genomes]
rs7253094	1.00[ASN][1000 genomes]
rs7254368	0.95[JPT][hapmap]
rs7254761	0.95[JPT][hapmap]
rs7255040	0.82[ASN][1000 genomes]
rs7258833	0.90[JPT][hapmap]
rs8104035	0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057361	chr19:40123868-40310996	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1061361	chr19:40131820-40310996	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv579511	chr19:40132825-40310497	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1062394	chr19:40133229-40310186	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv544004	chr19:40133229-40310186	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1059691	chr19:40168862-40306373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv544005	chr19:40168862-40306373	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	esv3332670	chr19:40181720-40297955	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv3329492	chr19:40198535-40437035	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv911695	chr19:40217794-40235008	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv962985	chr19:40220376-40228783	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv9723	chr19:40221468-40227714	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40225600-40229400	Enhancers	GM12878-XiMat	blood
2	chr19:40226000-40228600	Weak transcription	Placenta	Placenta
3	chr19:40226000-40228800	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr19:40226200-40229200	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr19:40226400-40227000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr19:40226400-40228200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr19:40226600-40227800	Weak transcription	Rectal Mucosa Donor 29	rectum

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