Variant report

Variant	rs17741661
Chromosome Location	chr11:101374276-101374277
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10501979	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10501980	0.91[CHB][hapmap]
rs10501981	0.91[CHB][hapmap]
rs10501986	0.91[CHB][hapmap]
rs10750606	0.82[CHB][hapmap]
rs10791477	0.82[CHB][hapmap]
rs10791478	0.82[CHB][hapmap]
rs10791479	1.00[CHB][hapmap]
rs10791481	1.00[CHB][hapmap]
rs10791485	0.91[CHB][hapmap]
rs10791486	1.00[CHB][hapmap]
rs10791487	1.00[CHB][hapmap]
rs10791490	0.91[CHB][hapmap]
rs10895118	0.82[CHB][hapmap]
rs10895121	0.82[CHB][hapmap]
rs10895122	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10895123	1.00[CHB][hapmap]
rs10895124	0.91[CHB][hapmap]
rs10895125	0.91[CHB][hapmap]
rs10895126	0.83[CHB][hapmap]
rs10895127	0.82[CHB][hapmap]
rs10895128	0.81[CHB][hapmap]
rs10895130	0.84[CHB][hapmap]
rs11224790	1.00[CHB][hapmap]
rs11224791	0.91[CHB][hapmap]
rs11224792	0.91[CHB][hapmap]
rs11224800	1.00[CHB][hapmap]
rs11224801	1.00[CHB][hapmap]
rs11224802	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11224806	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11224807	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11224808	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1218926	1.00[AFR][1000 genomes]
rs1274844	1.00[AFR][1000 genomes]
rs17674687	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17742220	1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4129253	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4129254	0.82[CHB][hapmap]
rs4129255	0.82[CHB][hapmap]
rs4262694	0.91[CHB][hapmap]
rs4272759	0.91[CHB][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes]
rs4275596	0.82[CHB][hapmap]
rs4285844	0.82[CHB][hapmap]
rs4331056	0.83[CHB][hapmap]
rs4403777	0.82[CHB][hapmap]
rs4477408	1.00[CHB][hapmap]
rs4481994	0.82[CHB][hapmap]
rs4492783	0.85[ASN][1000 genomes]
rs4542378	0.89[CHB][hapmap]
rs6590867	0.80[ASN][1000 genomes]
rs6590868	0.80[ASN][1000 genomes]
rs6590870	0.91[CHB][hapmap]
rs6590872	0.91[CHB][hapmap]
rs6590874	0.91[CHB][hapmap]
rs6590877	0.90[CHB][hapmap]
rs7115999	0.82[CHB][hapmap]
rs7116473	0.81[CHB][hapmap]
rs7123199	0.83[CHB][hapmap]
rs7127243	0.82[CHB][hapmap]
rs7925012	0.82[CHB][hapmap]
rs7927661	0.91[CHB][hapmap]
rs7927852	0.83[CHB][hapmap]
rs7927859	0.82[CHB][hapmap]
rs7932871	0.91[CHB][hapmap]
rs7934116	0.81[CHB][hapmap]
rs7934208	0.91[CHB][hapmap]
rs7934219	1.00[CHB][hapmap]
rs7935702	1.00[CHB][hapmap]
rs7937745	0.83[CHB][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	nsv556131	chr11:100985777-101480017	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv530644	chr11:101010088-101486038	Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	esv2830219	chr11:101319531-101382967	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr11:101350000-101384800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:101368400-101374800	Weak transcription	Aorta	Aorta
3	chr11:101371600-101376200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:101372200-101375200	Strong transcription	Ovary	ovary
5	chr11:101372200-101375600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:101372400-101375600	Weak transcription	Fetal Muscle Trunk	muscle
7	chr11:101373400-101375400	Strong transcription	Fetal Lung	lung

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