Variant report

Variant	rs1603288
Chromosome Location	chr8:90713264-90713265
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:90707734..90710584-chr8:90712902..90714410,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10447970	0.82[AMR][1000 genomes]
rs10956226	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs160408	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs160409	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs160410	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs160418	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs160445	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs160447	0.80[EUR][1000 genomes]
rs183363	0.81[EUR][1000 genomes]
rs2088198	0.80[EUR][1000 genomes]
rs2132348	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs216986	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs216990	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs218892	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs218896	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs218898	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs218904	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs218915	0.82[EUR][1000 genomes]
rs218918	0.82[EUR][1000 genomes]
rs218920	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs218943	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs218945	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs218949	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs218950	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs218951	0.93[EUR][1000 genomes]
rs218952	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2735886	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28819479	0.83[EUR][1000 genomes]
rs419004	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4961159	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6999425	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7828553	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv870380	chr8:90546585-90720182	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1026523	chr8:90558935-90722580	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv831389	chr8:90575517-90753120	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv1017263	chr8:90605445-90722580	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1031578	chr8:90670102-90757821	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	esv3340425	chr8:90686312-90722629	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv891180	chr8:90697810-90802491	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
10	nsv933502	chr8:90702392-91049100	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
11	nsv6294	chr8:90705780-90750101	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90693200-90715600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90709000-90720200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:90710000-90716200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:90710000-90730000	Weak transcription	HSMMtube	muscle
5	chr8:90710200-90715800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:90710200-90716400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:90710200-90729600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:90710200-90730400	Weak transcription	A549	lung
9	chr8:90710200-90731200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr8:90710200-90736200	Weak transcription	Adipose Nuclei	Adipose
11	chr8:90710600-90715800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:90711200-90715400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:90711200-90733800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr8:90711400-90720200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr8:90712200-90715600	Weak transcription	Aorta	Aorta
16	chr8:90712800-90713400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:90713200-90713400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:90713200-90714200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:90713200-90715400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:90713200-90716400	Weak transcription	Spleen	Spleen
21	chr8:90713200-90717600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr8:90713200-90741200	Weak transcription	Left Ventricle	heart

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