Variant report

Variant	rs2837043
Chromosome Location	chr21:40851556-40851557
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:40845066..40847673-chr21:40849022..40851771,3	MCF-7	breast:

Extended variants
information (count: 66 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11088478	0.96[ASN][1000 genomes]
rs11701190	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11701232	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11702769	0.97[ASN][1000 genomes]
rs12482418	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs13046275	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13050145	0.96[ASN][1000 genomes]
rs13051411	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1474384	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1475593	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1524929	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2009713	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2026268	0.97[ASN][1000 genomes]
rs2037668	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2178881	1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2246616	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2837045	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2837046	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2837047	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2837048	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2837049	0.97[ASN][1000 genomes]
rs2837050	0.97[ASN][1000 genomes]
rs2837051	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2837052	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2837053	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2837054	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2837055	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs28634277	0.98[ASN][1000 genomes]
rs3787927	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs4118060	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4816629	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4818038	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4818039	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4818040	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4818041	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4818042	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4818044	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4818045	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4818046	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6517553	0.97[ASN][1000 genomes]
rs7277107	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7278885	0.95[ASN][1000 genomes]
rs7280971	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7281076	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8126715	0.94[ASN][1000 genomes]
rs8126729	0.89[CEU][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8126860	0.97[ASN][1000 genomes]
rs8127748	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs8128567	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8128795	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8131355	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8132867	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8132996	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8133292	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8133862	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9974333	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9976202	0.97[ASN][1000 genomes]
rs9976208	0.97[ASN][1000 genomes]
rs9983297	0.98[ASN][1000 genomes]
rs9983428	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9984540	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059868	chr21:40711535-41043291	Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1061454	chr21:40757973-41265404	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1062088	chr21:40838027-40919253	Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1067330	chr21:40841948-40879552	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2755103	chr21:40847196-40877805	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2837043	LCA5L	cis	Thyroid	GTEx
rs2837043	LCA5L	cis	lung	GTEx
rs2837043	LCA5L	cis	Muscle Skeletal	GTEx
rs2837043	LCA5L	cis	Nerve Tibial	GTEx

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40824000-40852400	Weak transcription	Pancreas	Pancrea
2	chr21:40827400-40879800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr21:40829800-40856200	Weak transcription	Aorta	Aorta
4	chr21:40836200-40852200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr21:40836400-40894800	Weak transcription	Right Ventricle	heart
6	chr21:40844800-40855800	Weak transcription	Adipose Nuclei	Adipose
7	chr21:40845000-40856600	Weak transcription	Colon Smooth Muscle	Colon
8	chr21:40846800-40854600	Weak transcription	Psoas Muscle	Psoas
9	chr21:40846800-40862800	Weak transcription	Gastric	stomach
10	chr21:40848200-40851600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr21:40848200-40852200	Weak transcription	Brain Angular Gyrus	brain
12	chr21:40848200-40852400	Weak transcription	Brain Anterior Caudate	brain
13	chr21:40848200-40895600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr21:40848400-40853800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr21:40848400-40863600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr21:40848400-40872400	Weak transcription	Left Ventricle	heart
17	chr21:40850400-40859200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr21:40850800-40852600	Enhancers	Fetal Heart	heart
19	chr21:40851000-40852600	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr21:40851000-40853000	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr21:40851400-40852200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr21:40851400-40852400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr21:40851400-40852600	Enhancers	Brain Substantia Nigra	brain
24	chr21:40851400-40852800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr21:40851400-40853000	Enhancers	Brain Hippocampus Middle	brain

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