Variant report

Variant	rs11208924
Chromosome Location	chr1:67083647-67083648
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10493411	0.88[CEU][hapmap];0.80[CHB][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10789211	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10889629	0.85[ASN][1000 genomes]
rs10889638	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11208908	0.86[ASN][1000 genomes]
rs11208910	1.00[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11208916	1.00[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11208929	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11208930	1.00[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11208937	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes]
rs1156618	0.85[ASN][1000 genomes]
rs12021913	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12023176	0.90[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs12034344	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12039282	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12041930	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12046520	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12402181	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12565798	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12567556	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1373909	0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs17129039	0.82[CEU][hapmap]
rs17129041	0.82[CEU][hapmap]
rs1925342	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2312153	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3795531	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4655498	0.86[ASN][1000 genomes]
rs4655620	0.86[ASN][1000 genomes]
rs587125	0.80[CEU][hapmap]
rs6588209	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6588214	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6680968	0.86[ASN][1000 genomes]
rs6686606	1.00[CEU][hapmap];0.95[CHB][hapmap];0.88[JPT][hapmap]
rs6687137	0.86[ASN][1000 genomes]
rs6699123	0.82[CEU][hapmap]
rs6701907	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6701988	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72918447	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7512692	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7519639	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7525509	0.80[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs7526812	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs7535076	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7537440	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7547794	0.80[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7547857	0.80[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7547866	0.85[ASN][1000 genomes]
rs7551301	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs963140	0.84[CHB][hapmap];0.94[JPT][hapmap];0.86[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	nsv1221	chr1:67047908-67092696	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv869413	chr1:67082512-67414286	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11208924	SGIP1	cis	Whole Blood	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67058000-67092200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:67066200-67083800	Weak transcription	NHLF	lung
3	chr1:67066400-67089600	Weak transcription	Brain Angular Gyrus	brain
4	chr1:67071600-67094800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:67078000-67088400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:67079400-67083800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:67081400-67084000	Weak transcription	Brain Anterior Caudate	brain
8	chr1:67081400-67084800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr1:67081600-67084200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:67082000-67089400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr1:67082600-67085000	Enhancers	NHDF-Ad	bronchial
12	chr1:67082800-67084800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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