Variant report

Variant	rs11120516
Chromosome Location	chr1:215349506-215349507
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10127521	0.82[ASN][1000 genomes]
rs10127656	0.96[ASN][1000 genomes]
rs10779639	0.95[ASN][1000 genomes]
rs10779640	0.96[ASN][1000 genomes]
rs10779642	0.83[ASN][1000 genomes]
rs10779643	0.83[ASN][1000 genomes]
rs10779644	0.98[ASN][1000 genomes]
rs10779645	0.98[ASN][1000 genomes]
rs10779646	0.98[ASN][1000 genomes]
rs10779647	0.98[ASN][1000 genomes]
rs10779648	0.91[ASN][1000 genomes]
rs10779649	0.84[ASN][1000 genomes]
rs10779650	0.84[ASN][1000 genomes]
rs10779651	0.84[ASN][1000 genomes]
rs10864153	0.94[ASN][1000 genomes]
rs10864154	0.96[ASN][1000 genomes]
rs11120495	0.80[ASN][1000 genomes]
rs11120496	0.96[ASN][1000 genomes]
rs11120498	0.97[ASN][1000 genomes]
rs11120499	0.95[ASN][1000 genomes]
rs11120500	0.82[ASN][1000 genomes]
rs11120506	0.98[ASN][1000 genomes]
rs11120508	0.98[ASN][1000 genomes]
rs11120511	0.98[ASN][1000 genomes]
rs11120513	0.98[ASN][1000 genomes]
rs11120517	0.96[ASN][1000 genomes]
rs1112101	0.82[ASN][1000 genomes]
rs12031308	0.98[ASN][1000 genomes]
rs12061916	0.97[ASN][1000 genomes]
rs12062098	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12068734	0.98[ASN][1000 genomes]
rs12120091	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12121761	0.95[ASN][1000 genomes]
rs12135076	0.84[ASN][1000 genomes]
rs12138497	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12141874	0.85[ASN][1000 genomes]
rs12143339	0.98[ASN][1000 genomes]
rs12410041	0.82[ASN][1000 genomes]
rs12411068	0.80[ASN][1000 genomes]
rs12567520	0.84[ASN][1000 genomes]
rs12742137	0.96[ASN][1000 genomes]
rs1339405	0.96[ASN][1000 genomes]
rs1339406	0.96[ASN][1000 genomes]
rs1361340	0.85[ASN][1000 genomes]
rs1416647	0.82[ASN][1000 genomes]
rs1578137	0.82[ASN][1000 genomes]
rs2363554	0.98[ASN][1000 genomes]
rs2363556	0.84[ASN][1000 genomes]
rs2363557	0.83[ASN][1000 genomes]
rs2363564	0.94[ASN][1000 genomes]
rs2363565	0.98[ASN][1000 genomes]
rs2363566	0.85[ASN][1000 genomes]
rs2363567	0.85[ASN][1000 genomes]
rs2885812	0.98[ASN][1000 genomes]
rs2885813	0.83[ASN][1000 genomes]
rs2885815	0.95[ASN][1000 genomes]
rs3931584	0.99[ASN][1000 genomes]
rs4269745	0.83[ASN][1000 genomes]
rs4300189	0.82[ASN][1000 genomes]
rs4303048	0.83[ASN][1000 genomes]
rs4394614	0.96[ASN][1000 genomes]
rs4411107	0.97[ASN][1000 genomes]
rs4428856	0.97[ASN][1000 genomes]
rs4440833	0.96[ASN][1000 genomes]
rs4497183	0.98[ASN][1000 genomes]
rs4509552	0.98[ASN][1000 genomes]
rs4509553	0.98[ASN][1000 genomes]
rs4531266	0.96[ASN][1000 genomes]
rs4571941	0.93[ASN][1000 genomes]
rs4573492	0.97[ASN][1000 genomes]
rs4607848	0.82[ASN][1000 genomes]
rs4655276	0.98[ASN][1000 genomes]
rs4655277	0.84[ASN][1000 genomes]
rs4655278	0.85[ASN][1000 genomes]
rs4655391	0.98[ASN][1000 genomes]
rs4655392	0.98[ASN][1000 genomes]
rs4655393	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4655394	0.85[ASN][1000 genomes]
rs4655395	0.85[ASN][1000 genomes]
rs61818320	0.82[ASN][1000 genomes]
rs61818328	0.83[ASN][1000 genomes]
rs6657313	0.85[ASN][1000 genomes]
rs6662353	0.82[ASN][1000 genomes]
rs6666828	0.96[ASN][1000 genomes]
rs6667764	0.94[ASN][1000 genomes]
rs6672978	0.99[ASN][1000 genomes]
rs6673739	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6675926	0.83[ASN][1000 genomes]
rs6678758	0.83[ASN][1000 genomes]
rs6683041	0.97[ASN][1000 genomes]
rs6684084	0.84[ASN][1000 genomes]
rs6695967	0.83[ASN][1000 genomes]
rs6696333	0.82[ASN][1000 genomes]
rs72735359	0.83[ASN][1000 genomes]
rs7417100	0.98[ASN][1000 genomes]
rs7513709	0.96[ASN][1000 genomes]
rs7541543	0.96[ASN][1000 genomes]
rs7547572	0.85[ASN][1000 genomes]
rs7549136	0.97[ASN][1000 genomes]
rs7551415	0.95[ASN][1000 genomes]
rs9793695	0.91[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	nsv873169	chr1:215264486-215453286	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215340800-215355000	Weak transcription	Osteobl	bone
2	chr1:215342200-215351800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:215343800-215349600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr1:215346000-215352000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:215348000-215355000	Weak transcription	Brain Germinal Matrix	brain
6	chr1:215349000-215350000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:215349200-215350000	ZNF genes & repeats	NHDF-Ad	bronchial

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