Variant report

Variant	rs10935587
Chromosome Location	chr3:98711455-98711456
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1082403	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1082405	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10935514	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12632798	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12636683	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13071075	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13316760	0.91[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs1371687	0.96[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1383906	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1383907	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2062058	0.82[ASN][1000 genomes]
rs2128052	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2170404	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2340794	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2439237	0.90[JPT][hapmap]
rs2449046	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2470770	0.86[ASN][1000 genomes]
rs2470814	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2470853	0.82[ASN][1000 genomes]
rs2470855	0.82[ASN][1000 genomes]
rs2470870	0.82[ASN][1000 genomes]
rs2470872	0.82[ASN][1000 genomes]
rs2470873	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2470877	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2470878	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2470880	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs278379	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap]
rs278380	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs278381	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs278382	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs278387	0.83[CEU][hapmap];0.95[CHB][hapmap];0.80[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap];0.98[TSI][hapmap]
rs278388	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs35483904	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs35936923	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4546099	0.82[EUR][1000 genomes]
rs4577404	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4857415	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4857416	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6767370	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6774875	0.85[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6791389	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7615628	0.85[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7615856	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap]
rs774535	0.80[AMR][1000 genomes]
rs774537	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs774538	0.83[AMR][1000 genomes]
rs774539	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs774544	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs774547	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs809575	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs828614	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs828616	0.88[CEU][hapmap];0.90[CHB][hapmap];0.80[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.83[MEX][hapmap];0.87[MKK][hapmap];0.95[TSI][hapmap]
rs828617	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap]
rs828621	0.87[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs852701	0.96[CEU][hapmap];0.95[CHB][hapmap];0.81[CHD][hapmap];0.80[GIH][hapmap];0.81[JPT][hapmap];0.88[LWK][hapmap];0.89[MKK][hapmap];0.98[TSI][hapmap]
rs870202	0.82[ASN][1000 genomes]
rs8833	0.91[CEU][hapmap];0.85[CHB][hapmap];0.89[GIH][hapmap];0.90[JPT][hapmap];0.88[LWK][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.95[TSI][hapmap]
rs955351	0.92[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap]
rs964163	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9837206	0.84[AMR][1000 genomes]

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	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv877214	chr3:98445324-98738006	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10935587	DCBLD2	cis	Adipose Subcutaneous	GTEx
rs10935587	ZBTB11	cis	cerebellum	SCAN

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98705000-98713000	Weak transcription	HSMM	muscle
2	chr3:98705200-98712600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:98705600-98716400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:98706200-98712400	Weak transcription	NHDF-Ad	bronchial
5	chr3:98710800-98712400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:98710800-98712400	Weak transcription	A549	lung
7	chr3:98711000-98721200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:98711200-98711600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:98711200-98712400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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