Variant report

Variant	rs3852477
Chromosome Location	chr10:19852644-19852645
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10128317	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10430561	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10740909	1.00[JPT][hapmap]
rs10740912	0.87[EUR][1000 genomes]
rs10740913	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10740916	0.88[EUR][1000 genomes]
rs10740921	0.86[EUR][1000 genomes]
rs10764051	0.87[EUR][1000 genomes]
rs10764064	1.00[ASN][1000 genomes]
rs10764080	0.84[EUR][1000 genomes]
rs10827534	0.87[EUR][1000 genomes]
rs10827538	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10827551	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11010274	0.88[EUR][1000 genomes]
rs11010275	0.87[EUR][1000 genomes]
rs11010436	0.86[EUR][1000 genomes]
rs11814784	0.86[ASN][1000 genomes]
rs1332926	1.00[JPT][hapmap]
rs1332927	1.00[JPT][hapmap]
rs1338612	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1537352	0.85[EUR][1000 genomes]
rs16918840	1.00[JPT][hapmap]
rs16919094	0.83[ASN][1000 genomes]
rs1855153	0.93[EUR][1000 genomes]
rs1855154	0.87[EUR][1000 genomes]
rs1855155	0.87[EUR][1000 genomes]
rs2065496	0.83[EUR][1000 genomes]
rs2358417	0.86[EUR][1000 genomes]
rs3843022	0.93[EUR][1000 genomes]
rs3844354	0.93[EUR][1000 genomes]
rs3844355	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3844356	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3844357	0.93[EUR][1000 genomes]
rs3852473	0.87[EUR][1000 genomes]
rs3852474	0.94[EUR][1000 genomes]
rs3852475	0.92[EUR][1000 genomes]
rs3864837	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3864838	1.00[EUR][1000 genomes]
rs3904893	0.94[EUR][1000 genomes]
rs3904894	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3904895	0.87[EUR][1000 genomes]
rs4381258	0.91[EUR][1000 genomes]
rs4747377	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4748591	1.00[JPT][hapmap]
rs4748596	0.88[EUR][1000 genomes]
rs4748598	0.83[ASN][1000 genomes]
rs4748599	0.92[EUR][1000 genomes]
rs4748602	0.85[CHD][hapmap]
rs61841423	0.83[ASN][1000 genomes]
rs61841425	0.83[ASN][1000 genomes]
rs61841437	0.83[ASN][1000 genomes]
rs61841438	0.85[ASN][1000 genomes]
rs61841440	0.90[ASN][1000 genomes]
rs6481966	0.87[EUR][1000 genomes]
rs6481967	0.87[EUR][1000 genomes]
rs6481969	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6481971	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6481972	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6481973	0.94[EUR][1000 genomes]
rs6481982	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7070697	1.00[JPT][hapmap]
rs7071846	0.86[EUR][1000 genomes]
rs7072649	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7074543	0.93[EUR][1000 genomes]
rs7077392	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7078195	0.87[EUR][1000 genomes]
rs7083270	0.87[EUR][1000 genomes]
rs7083715	0.93[EUR][1000 genomes]
rs7084915	0.87[EUR][1000 genomes]
rs7085358	0.81[EUR][1000 genomes]
rs7085701	0.90[EUR][1000 genomes]
rs7092917	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7099094	0.91[EUR][1000 genomes]
rs7100242	0.87[EUR][1000 genomes]
rs7896333	0.87[EUR][1000 genomes]
rs7900285	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7912969	0.87[EUR][1000 genomes]
rs7913304	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv466764	chr10:19400845-19979434	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv550128	chr10:19400845-19979434	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2759737	chr10:19694144-20024994	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2758211	chr10:19714637-20024994	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1049295	chr10:19740296-20509036	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv1042877	chr10:19749314-20067572	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv2757373	chr10:19776910-20004996	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv34306	chr10:19777069-20117944	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	esv3518965	chr10:19786251-20061305	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	esv3518966	chr10:19786310-20061256	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv894931	chr10:19796958-19987644	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv894932	chr10:19804415-19858518	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv825266	chr10:19807019-20037182	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv975766	chr10:19842314-19854108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19839800-19875400	Weak transcription	Fetal Intestine Small	intestine
2	chr10:19840400-19856400	Weak transcription	Fetal Intestine Large	intestine
3	chr10:19851600-19858800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:19852400-19852800	Enhancers	Brain Germinal Matrix	brain
5	chr10:19852400-19853000	Enhancers	Aorta	Aorta
6	chr10:19852600-19853000	Enhancers	Fetal Brain Male	brain

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