Variant report

Variant	rs2608501
Chromosome Location	chr19:52943263-52943264
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:52941897..52944459-chr19:52948865..52951747,2	K562	blood:

Extended variants
information (count: 133 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:127)

rs_ID	r²[population]
rs10408608	0.88[ASN][1000 genomes]
rs10410134	0.84[ASN][1000 genomes]
rs10853848	0.83[ASN][1000 genomes]
rs10853849	0.83[ASN][1000 genomes]
rs11084159	0.83[ASN][1000 genomes]
rs11084160	0.83[ASN][1000 genomes]
rs11084161	0.83[ASN][1000 genomes]
rs11084162	0.83[ASN][1000 genomes]
rs11084163	0.83[ASN][1000 genomes]
rs1112889	0.81[ASN][1000 genomes]
rs1115659	0.81[ASN][1000 genomes]
rs1115660	0.81[ASN][1000 genomes]
rs12459176	0.87[ASN][1000 genomes]
rs12460429	0.87[ASN][1000 genomes]
rs1366257	0.86[ASN][1000 genomes]
rs1366258	0.86[ASN][1000 genomes]
rs1366259	0.86[ASN][1000 genomes]
rs1428177	0.87[ASN][1000 genomes]
rs1428178	0.85[ASN][1000 genomes]
rs1428179	0.85[ASN][1000 genomes]
rs1428180	0.85[ASN][1000 genomes]
rs1457854	0.87[ASN][1000 genomes]
rs1457855	0.87[ASN][1000 genomes]
rs1457856	0.87[ASN][1000 genomes]
rs1457857	0.81[ASN][1000 genomes]
rs1465558	0.86[ASN][1000 genomes]
rs1465559	0.87[ASN][1000 genomes]
rs1582914	0.81[ASN][1000 genomes]
rs1651527	0.81[ASN][1000 genomes]
rs1673893	0.81[ASN][1000 genomes]
rs1817266	0.84[ASN][1000 genomes]
rs1840997	0.81[ASN][1000 genomes]
rs1840998	0.81[ASN][1000 genomes]
rs1896644	0.88[ASN][1000 genomes]
rs2042912	0.86[ASN][1000 genomes]
rs2099053	0.88[ASN][1000 genomes]
rs2115101	0.87[ASN][1000 genomes]
rs2115103	0.88[ASN][1000 genomes]
rs2168792	0.87[ASN][1000 genomes]
rs2434459	0.83[ASN][1000 genomes]
rs2434461	0.88[ASN][1000 genomes]
rs2446078	0.85[ASN][1000 genomes]
rs2446079	0.95[ASN][1000 genomes]
rs2560997	0.82[ASN][1000 genomes]
rs2560998	0.84[ASN][1000 genomes]
rs2560999	0.83[ASN][1000 genomes]
rs2561000	0.85[ASN][1000 genomes]
rs2561001	0.84[ASN][1000 genomes]
rs2561002	0.88[ASN][1000 genomes]
rs2561003	0.85[ASN][1000 genomes]
rs2561004	0.82[ASN][1000 genomes]
rs2561005	0.88[ASN][1000 genomes]
rs2561006	0.88[ASN][1000 genomes]
rs2561007	0.88[ASN][1000 genomes]
rs2561008	0.88[ASN][1000 genomes]
rs2561009	0.88[ASN][1000 genomes]
rs2561010	0.92[ASN][1000 genomes]
rs2561011	0.88[ASN][1000 genomes]
rs2561012	0.88[ASN][1000 genomes]
rs2561013	0.88[ASN][1000 genomes]
rs2561014	0.88[ASN][1000 genomes]
rs2561023	0.86[ASN][1000 genomes]
rs2561024	0.86[ASN][1000 genomes]
rs2561025	0.88[ASN][1000 genomes]
rs2561026	0.88[ASN][1000 genomes]
rs2561027	0.88[ASN][1000 genomes]
rs2561028	0.88[ASN][1000 genomes]
rs2608487	0.83[ASN][1000 genomes]
rs2608488	0.83[ASN][1000 genomes]
rs2608489	0.82[ASN][1000 genomes]
rs2608491	0.85[ASN][1000 genomes]
rs2608492	0.85[ASN][1000 genomes]
rs2608493	0.85[ASN][1000 genomes]
rs2608494	0.85[ASN][1000 genomes]
rs2608495	0.85[ASN][1000 genomes]
rs2608496	0.85[ASN][1000 genomes]
rs2608497	0.86[ASN][1000 genomes]
rs2608498	0.86[ASN][1000 genomes]
rs2608499	0.87[ASN][1000 genomes]
rs2608500	0.98[ASN][1000 genomes]
rs2608502	0.88[ASN][1000 genomes]
rs2608503	0.83[ASN][1000 genomes]
rs2608504	0.86[ASN][1000 genomes]
rs2608505	0.88[ASN][1000 genomes]
rs2608506	0.88[ASN][1000 genomes]
rs2608536	0.88[ASN][1000 genomes]
rs2608537	0.88[ASN][1000 genomes]
rs2608541	0.88[ASN][1000 genomes]
rs28451504	0.88[ASN][1000 genomes]
rs2903895	0.84[ASN][1000 genomes]
rs324092	0.87[ASN][1000 genomes]
rs324096	0.87[ASN][1000 genomes]
rs324103	0.85[ASN][1000 genomes]
rs324104	0.88[ASN][1000 genomes]
rs324106	0.88[ASN][1000 genomes]
rs324107	0.88[ASN][1000 genomes]
rs324113	0.84[ASN][1000 genomes]
rs324114	0.84[ASN][1000 genomes]
rs324115	0.81[ASN][1000 genomes]
rs324116	0.81[ASN][1000 genomes]
rs324117	0.81[ASN][1000 genomes]
rs324118	0.81[ASN][1000 genomes]
rs35170850	0.81[ASN][1000 genomes]
rs4404182	0.88[ASN][1000 genomes]
rs4553728	0.88[ASN][1000 genomes]
rs4801916	0.86[ASN][1000 genomes]
rs4802939	0.88[ASN][1000 genomes]
rs4802944	0.88[ASN][1000 genomes]
rs4802945	0.88[ASN][1000 genomes]
rs4802949	0.86[ASN][1000 genomes]
rs4802950	0.84[ASN][1000 genomes]
rs4802951	0.83[ASN][1000 genomes]
rs4802952	0.84[ASN][1000 genomes]
rs4802953	0.84[ASN][1000 genomes]
rs6509636	0.83[ASN][1000 genomes]
rs6509637	0.82[ASN][1000 genomes]
rs6509638	0.82[ASN][1000 genomes]
rs6509641	0.84[ASN][1000 genomes]
rs6509643	0.81[ASN][1000 genomes]
rs7246597	0.81[ASN][1000 genomes]
rs7247031	0.81[ASN][1000 genomes]
rs7247289	0.81[ASN][1000 genomes]
rs7252655	0.81[ASN][1000 genomes]
rs8102815	0.88[ASN][1000 genomes]
rs8110808	0.86[ASN][1000 genomes]
rs8110920	0.84[ASN][1000 genomes]
rs970555	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066537	chr19:52794424-53044977	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv544060	chr19:52794424-53044977	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	esv2762048	chr19:52895166-52997571	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv580026	chr19:52937100-53059872	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1063648	chr19:52938131-53041119	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv3415774	chr19:52938189-52970794	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr19:52940200-52943400	Weak transcription	Brain Germinal Matrix	brain
2	chr19:52940800-52946200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr19:52941200-52946200	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr19:52942200-52944000	Weak transcription	Ovary	ovary
5	chr19:52942600-52943400	Weak transcription	Brain Anterior Caudate	brain

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