Variant report

Variant	rs739693
Chromosome Location	chr7:116889414-116889415
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:116696376..116698519-chr7:116888439..116890411,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10226864	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10235236	1.00[CEU][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10245615	0.85[JPT][hapmap]
rs10254103	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10255896	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10256129	1.00[CEU][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10271623	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10280067	1.00[CEU][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10953839	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11760825	0.83[ASN][1000 genomes]
rs11981089	0.83[CHD][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs13224335	0.85[ASN][1000 genomes]
rs1468655	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1860698	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2402176	0.80[AMR][1000 genomes]
rs38902	0.85[ASN][1000 genomes]
rs38909	0.85[ASN][1000 genomes]
rs38916	0.84[ASN][1000 genomes]
rs4612282	0.80[YRI][hapmap]
rs6466605	0.90[CHD][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];0.80[MEX][hapmap];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6466606	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6466607	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6942558	0.85[JPT][hapmap];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6946781	0.89[GIH][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6947786	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6958283	0.95[CEU][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];0.85[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6965467	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6968768	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6974937	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6975501	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6979800	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs718738	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7457422	0.86[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap]
rs7776963	1.00[CEU][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7802930	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831108	chr7:116749534-116952011	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv516761	chr7:116888161-116892846	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs739693	GPR85	cis	cerebellum	SCAN

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116888000-116890200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:116888000-116892400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:116888600-116889600	Enhancers	Brain Cingulate Gyrus	brain
4	chr7:116888600-116889800	Enhancers	NHLF	lung
5	chr7:116888800-116889600	Enhancers	Placenta	Placenta
6	chr7:116888800-116890200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr7:116888800-116891200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:116888800-116892600	Enhancers	NHDF-Ad	bronchial
9	chr7:116888800-116892600	Enhancers	Osteobl	bone
10	chr7:116889000-116889600	Enhancers	Fetal Stomach	stomach
11	chr7:116889200-116889600	Enhancers	Brain Anterior Caudate	brain
12	chr7:116889200-116890800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:116889400-116889600	Enhancers	Brain Hippocampus Middle	brain
14	chr7:116889400-116890600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:116889400-116892600	Enhancers	GM12878-XiMat	blood

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