Variant report

Variant	rs7837892
Chromosome Location	chr8:124931666-124931667
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:124927561..124929328-chr8:124931006..124932558,2	MCF-7	breast:
2	chr8:124835624..124840070-chr8:124931025..124937507,8	MCF-7	breast:
3	chr8:124779448..124782514-chr8:124930705..124935453,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000176853	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1007106	0.86[JPT][hapmap]
rs11987138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13250190	0.87[JPT][hapmap]
rs13260693	0.84[ASN][1000 genomes]
rs13268486	0.87[JPT][hapmap]
rs13268977	0.87[JPT][hapmap]
rs13277597	0.91[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs13280610	0.82[JPT][hapmap]
rs16893054	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16899008	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs16899027	0.96[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs16899029	0.91[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs16899037	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16899040	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16899044	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16899047	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34895349	0.87[ASN][1000 genomes]
rs34943415	0.92[ASN][1000 genomes]
rs35444607	0.90[ASN][1000 genomes]
rs4242351	0.87[JPT][hapmap]
rs4285468	0.81[CEU][hapmap]
rs4299983	0.87[JPT][hapmap]
rs4355755	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4413758	0.87[JPT][hapmap]
rs4478556	0.81[CEU][hapmap]
rs4492357	0.87[JPT][hapmap]
rs4509302	0.87[JPT][hapmap]
rs4537289	0.81[CEU][hapmap]
rs4587311	0.81[CEU][hapmap]
rs4596635	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4870873	0.88[ASN][1000 genomes]
rs4870874	0.87[ASN][1000 genomes]
rs4870875	0.95[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs4870876	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871417	0.86[JPT][hapmap]
rs4871421	0.92[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs4871422	0.96[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4871423	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871424	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871425	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871426	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871428	0.87[JPT][hapmap]
rs4871429	0.86[JPT][hapmap]
rs4871430	0.87[JPT][hapmap]
rs4871431	0.87[JPT][hapmap]
rs4871432	0.90[JPT][hapmap]
rs4871433	0.91[JPT][hapmap]
rs4871434	0.87[JPT][hapmap]
rs4871435	0.86[JPT][hapmap]
rs4871436	0.86[JPT][hapmap]
rs4871437	0.86[JPT][hapmap]
rs4871439	0.87[JPT][hapmap]
rs55834043	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66846856	0.82[ASN][1000 genomes]
rs6984557	0.86[JPT][hapmap]
rs7005131	0.88[ASN][1000 genomes]
rs7464664	0.87[JPT][hapmap]
rs746745	0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs746746	0.85[ASN][1000 genomes]
rs746747	0.81[CEU][hapmap];0.85[ASN][1000 genomes]
rs7821233	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7822699	0.89[ASN][1000 genomes]
rs7838453	0.86[JPT][hapmap]
rs7838473	0.87[JPT][hapmap]
rs7839327	0.87[JPT][hapmap]
rs7839570	0.89[ASN][1000 genomes]
rs7842762	0.86[JPT][hapmap]

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	nsv1033617	chr8:124895516-125012783	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1035035	chr8:124895516-125020472	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv612141	chr8:124895809-125006490	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv612142	chr8:124896389-125006490	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv612143	chr8:124927711-124988267	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124927000-124932600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:124927600-124932800	Weak transcription	Stomach Mucosa	stomach
3	chr8:124927600-124934000	Weak transcription	HSMMtube	muscle
4	chr8:124927600-124934000	Weak transcription	K562	blood
5	chr8:124928600-124932400	Weak transcription	Fetal Intestine Small	intestine
6	chr8:124928800-124934000	Weak transcription	Primary B cells from peripheral blood	blood
7	chr8:124929200-124932200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr8:124929200-124933600	Weak transcription	Fetal Muscle Leg	muscle
9	chr8:124930200-124932200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:124931000-124934600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:124931400-124936000	Enhancers	Fetal Intestine Large	intestine

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