Variant report

Variant	rs10837872
Chromosome Location	chr11:5368373-5368374
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5337010..5339667-chr11:5367362..5370323,2	K562	blood:

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs10768828	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768830	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10768831	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837867	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837868	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837870	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837871	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837873	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837874	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10837878	0.98[ASN][1000 genomes]
rs10837950	1.00[JPT][hapmap]
rs10837953	0.89[JPT][hapmap]
rs10837965	1.00[JPT][hapmap]
rs10837995	1.00[JPT][hapmap]
rs11036912	0.81[JPT][hapmap]
rs11036923	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11036924	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11036925	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11036927	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11036930	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11036936	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11037129	1.00[JPT][hapmap]
rs11037137	1.00[JPT][hapmap]
rs11037143	1.00[JPT][hapmap]
rs11037144	1.00[JPT][hapmap]
rs11037145	1.00[JPT][hapmap]
rs11037150	1.00[JPT][hapmap]
rs11037152	1.00[JPT][hapmap]
rs11037153	1.00[JPT][hapmap]
rs11037178	1.00[JPT][hapmap]
rs11037215	1.00[JPT][hapmap]
rs11601176	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11601662	0.89[JPT][hapmap];0.81[ASN][1000 genomes]
rs11603059	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11604159	1.00[JPT][hapmap]
rs11604201	1.00[JPT][hapmap]
rs11604520	1.00[JPT][hapmap]
rs11604556	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11604883	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11607365	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12275713	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12360697	1.00[JPT][hapmap]
rs12364011	1.00[JPT][hapmap]
rs12365474	1.00[JPT][hapmap]
rs12796030	1.00[JPT][hapmap]
rs12801179	1.00[JPT][hapmap]
rs16913820	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17270517	1.00[JPT][hapmap]
rs17270776	1.00[JPT][hapmap]
rs17270818	1.00[JPT][hapmap]
rs17270832	1.00[JPT][hapmap]
rs17270894	1.00[JPT][hapmap]
rs17271552	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17271573	0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs17355605	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17356328	0.81[ASN][1000 genomes]
rs17356445	1.00[JPT][hapmap]
rs17356507	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17356535	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1846319	1.00[JPT][hapmap]
rs1846320	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1909257	1.00[JPT][hapmap]
rs2340323	0.86[JPT][hapmap]
rs2467229	0.90[JPT][hapmap]
rs2467232	1.00[JPT][hapmap]
rs2647598	1.00[JPT][hapmap]
rs2647599	1.00[JPT][hapmap]
rs2647600	1.00[JPT][hapmap]
rs2647601	1.00[JPT][hapmap]
rs2647606	1.00[JPT][hapmap]
rs2723380	1.00[JPT][hapmap]
rs2723387	1.00[JPT][hapmap]
rs2736553	1.00[JPT][hapmap]
rs2736555	1.00[JPT][hapmap]
rs2736557	1.00[JPT][hapmap]
rs2736560	1.00[JPT][hapmap]
rs2736561	1.00[JPT][hapmap]
rs2736565	1.00[JPT][hapmap]
rs28819138	0.81[ASN][1000 genomes]
rs4078480	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4255565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4269953	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4271412	0.87[ASN][1000 genomes]
rs4304811	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4312094	0.81[JPT][hapmap]
rs4326830	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4345997	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4463873	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4492850	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4495917	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4623930	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4910551	0.81[JPT][hapmap]
rs4910552	1.00[JPT][hapmap]
rs4910757	1.00[JPT][hapmap]
rs4910760	1.00[JPT][hapmap]
rs4910762	1.00[JPT][hapmap]
rs4910764	0.81[ASN][1000 genomes]
rs4910765	1.00[JPT][hapmap]
rs4910770	1.00[JPT][hapmap]
rs4910771	1.00[JPT][hapmap]
rs5019249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5024037	1.00[JPT][hapmap]
rs6578611	0.81[JPT][hapmap]
rs7106330	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7109909	1.00[JPT][hapmap]
rs7113291	1.00[JPT][hapmap]
rs7116471	1.00[JPT][hapmap]
rs728925	1.00[JPT][hapmap]
rs7483786	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7929631	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7930818	1.00[JPT][hapmap]
rs7942877	1.00[JPT][hapmap]
rs7943181	0.81[ASN][1000 genomes]
rs884222	1.00[JPT][hapmap]

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	nsv524400	chr11:5328361-5416622	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv1048608	chr11:5328516-5645179	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
3	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
4	nsv896931	chr11:5357881-5505149	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 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	chr11:5365400-5369600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:5365400-5369600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr11:5365600-5369600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr11:5365600-5382600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:5367600-5369000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:5367600-5371000	Weak transcription	Osteobl	bone
7	chr11:5368200-5369800	Weak transcription	K562	blood

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