Variant report

Variant	rs7255040
Chromosome Location	chr19:40210439-40210440
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1034867	0.82[ASN][1000 genomes]
rs1034868	0.82[ASN][1000 genomes]
rs10407647	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10409279	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10410864	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10755	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1126158	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17608	0.82[ASN][1000 genomes]
rs2074926	0.82[ASN][1000 genomes]
rs2159169	0.93[ASN][1000 genomes]
rs2159170	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2238678	0.82[ASN][1000 genomes]
rs35837917	0.82[ASN][1000 genomes]
rs364911	0.82[ASN][1000 genomes]
rs367529	0.82[ASN][1000 genomes]
rs367788	0.82[ASN][1000 genomes]
rs372081	0.82[ASN][1000 genomes]
rs372902	0.81[ASN][1000 genomes]
rs373449	0.81[ASN][1000 genomes]
rs375867	0.82[ASN][1000 genomes]
rs378917	0.82[ASN][1000 genomes]
rs383768	0.82[ASN][1000 genomes]
rs384138	0.82[ASN][1000 genomes]
rs385240	0.80[ASN][1000 genomes]
rs385520	0.82[ASN][1000 genomes]
rs388648	0.82[ASN][1000 genomes]
rs391646	0.82[ASN][1000 genomes]
rs391660	0.82[ASN][1000 genomes]
rs395892	0.82[ASN][1000 genomes]
rs396854	0.82[ASN][1000 genomes]
rs399641	0.82[ASN][1000 genomes]
rs4028673	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs412884	0.82[ASN][1000 genomes]
rs4132248	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs414423	0.81[ASN][1000 genomes]
rs416255	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs418664	0.82[ASN][1000 genomes]
rs425218	0.82[ASN][1000 genomes]
rs425265	0.82[ASN][1000 genomes]
rs428007	0.82[ASN][1000 genomes]
rs431329	0.82[ASN][1000 genomes]
rs437780	0.81[ASN][1000 genomes]
rs439881	0.82[ASN][1000 genomes]
rs440191	0.82[ASN][1000 genomes]
rs440334	0.82[ASN][1000 genomes]
rs44048	0.82[ASN][1000 genomes]
rs44049	0.82[ASN][1000 genomes]
rs444817	0.82[ASN][1000 genomes]
rs444963	0.80[ASN][1000 genomes]
rs446425	0.82[ASN][1000 genomes]
rs447034	0.82[ASN][1000 genomes]
rs453827	0.81[ASN][1000 genomes]
rs4802054	0.82[ASN][1000 genomes]
rs4830	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58602176	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6508903	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6508904	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7249575	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7250681	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7253094	0.82[ASN][1000 genomes]
rs7254368	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7254761	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7255025	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7258833	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs8102588	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs8104035	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40201600-40216800	Weak transcription	Placenta	Placenta
2	chr19:40209400-40210600	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr19:40210000-40210600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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