Variant report

Variant	rs2309752
Chromosome Location	chr2:100762169-100762170
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:100761253..100763849-chr2:100766044..100767965,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10185059	0.93[ASN][1000 genomes]
rs10185510	0.93[ASN][1000 genomes]
rs10197987	0.94[ASN][1000 genomes]
rs10496344	0.90[ASN][1000 genomes]
rs11123809	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11123810	0.96[ASN][1000 genomes]
rs11123811	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11123812	0.96[ASN][1000 genomes]
rs11123813	0.94[ASN][1000 genomes]
rs11679078	0.81[ASN][1000 genomes]
rs11681227	0.93[ASN][1000 genomes]
rs11681966	0.96[ASN][1000 genomes]
rs11690905	0.96[ASN][1000 genomes]
rs11694875	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11885529	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11891046	0.94[ASN][1000 genomes]
rs11899489	0.93[ASN][1000 genomes]
rs11900482	0.96[ASN][1000 genomes]
rs11902705	0.91[ASN][1000 genomes]
rs12712064	0.94[ASN][1000 genomes]
rs12712065	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12712067	0.94[ASN][1000 genomes]
rs12712068	0.94[ASN][1000 genomes]
rs12712071	0.93[ASN][1000 genomes]
rs12987209	0.96[ASN][1000 genomes]
rs12987212	0.96[ASN][1000 genomes]
rs13003982	0.96[ASN][1000 genomes]
rs13005282	0.88[ASN][1000 genomes]
rs13019618	0.81[ASN][1000 genomes]
rs13032454	0.94[ASN][1000 genomes]
rs13415465	0.94[ASN][1000 genomes]
rs13415583	0.94[ASN][1000 genomes]
rs1370353	0.94[ASN][1000 genomes]
rs1561230	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1821826	0.94[ASN][1000 genomes]
rs1821827	0.94[ASN][1000 genomes]
rs2009094	0.94[ASN][1000 genomes]
rs2009095	0.94[ASN][1000 genomes]
rs4490209	0.92[ASN][1000 genomes]
rs4850920	0.81[ASN][1000 genomes]
rs4850921	0.94[ASN][1000 genomes]
rs4851252	0.94[ASN][1000 genomes]
rs4851253	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4851256	0.94[ASN][1000 genomes]
rs4851257	0.93[ASN][1000 genomes]
rs56054309	0.91[ASN][1000 genomes]
rs7565967	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7575877	0.82[EUR][1000 genomes]
rs7590378	0.94[ASN][1000 genomes]
rs7593261	0.94[ASN][1000 genomes]
rs7608424	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003343	chr2:100241560-100848900	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv535843	chr2:100241560-100848900	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv582530	chr2:100739970-100774287	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv527481	chr2:100753490-100763006	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	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	chr2:100746200-100764800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:100758800-100765600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:100759000-100763000	Weak transcription	Adipose Nuclei	Adipose
4	chr2:100759200-100763400	Enhancers	Primary B cells from peripheral blood	blood
5	chr2:100760000-100765400	Weak transcription	Thymus	Thymus

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