Variant report

Variant	rs6773448
Chromosome Location	chr3:136785847-136785848
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	chr3:136785565..136787654-chr3:136790492..136792454,2	MCF-7	breast:
2	chr3:136774568..136777097-chr3:136784828..136786633,2	MCF-7	breast:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1023765	0.85[AMR][1000 genomes]
rs10935221	0.84[AMR][1000 genomes]
rs13098923	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1351892	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1470143	0.85[AMR][1000 genomes]
rs1484787	0.85[AMR][1000 genomes]
rs1484794	0.83[AMR][1000 genomes]
rs3899122	0.83[AMR][1000 genomes]
rs4678286	0.83[AMR][1000 genomes]
rs6439683	0.84[AMR][1000 genomes]
rs6439685	0.84[AMR][1000 genomes]
rs6439686	0.84[AMR][1000 genomes]
rs6763000	0.80[EUR][1000 genomes]
rs6781928	0.85[AMR][1000 genomes]
rs6795587	0.84[ASN][1000 genomes]
rs6806914	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6807138	0.84[AMR][1000 genomes]
rs6808049	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6808051	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7627723	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7646139	0.85[AMR][1000 genomes]
rs9289525	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969329	0.83[AMR][1000 genomes]
rs9810065	0.85[ASN][1000 genomes]
rs9818478	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9818918	0.85[AMR][1000 genomes]
rs9819250	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9822931	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9826507	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9838513	0.85[AMR][1000 genomes]
rs9843104	0.87[AMR][1000 genomes]
rs9843219	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9856620	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9870582	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9874836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9882135	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv524856	chr3:136693459-137190765	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1012111	chr3:136695367-137343430	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:136757000-136794000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr3:136769400-136796200	Weak transcription	NHEK	skin
3	chr3:136782000-136804600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:136783400-136786200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:136784800-136786000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:136785400-136786000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr3:136785400-136786000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:136785400-136786400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr3:136785400-136790000	Weak transcription	Esophagus	oesophagus
10	chr3:136785400-136790000	Weak transcription	GM12878-XiMat	blood
11	chr3:136785800-136786200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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