Variant report

Variant	rs57766637
Chromosome Location	chr8:104286337-104286338
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	chr8:104285760..104288656-chr8:104356267..104358351,3	K562	blood:
2	chr8:104285055..104288416-chr8:104382209..104384778,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164932	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10089245	0.82[ASN][1000 genomes]
rs10097018	0.82[ASN][1000 genomes]
rs10103573	0.84[ASN][1000 genomes]
rs10955313	0.84[ASN][1000 genomes]
rs11782632	0.82[ASN][1000 genomes]
rs12678419	0.91[ASN][1000 genomes]
rs16870240	0.93[EUR][1000 genomes]
rs17799574	0.82[ASN][1000 genomes]
rs2201369	0.82[ASN][1000 genomes]
rs2201370	0.82[ASN][1000 genomes]
rs34602800	0.82[ASN][1000 genomes]
rs35710705	0.82[ASN][1000 genomes]
rs3736045	0.88[ASN][1000 genomes]
rs60751214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62525471	0.91[ASN][1000 genomes]
rs6985929	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6997475	0.93[EUR][1000 genomes]
rs7002454	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7005789	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73283939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73283943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73283949	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7817074	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7818987	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7822939	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7835655	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7844873	0.84[ASN][1000 genomes]
rs996200	0.85[ASN][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	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv1015965	chr8:104192086-104361108	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1017326	chr8:104236193-104313235	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104284000-104289600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:104284400-104287000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:104284800-104289600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:104284800-104295400	Weak transcription	Aorta	Aorta
5	chr8:104286000-104289400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:104286200-104286400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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