Variant report

Variant	rs7140973
Chromosome Location	chr14:72847555-72847556
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:72845757..72848710-chr14:72852431..72853988,2	MCF-7	breast:

Extended variants
information (count: 69 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10129799	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10137579	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10138152	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1072166	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1099968	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1356841	0.81[EUR][1000 genomes]
rs1356843	0.88[EUR][1000 genomes]
rs1812041	0.88[EUR][1000 genomes]
rs1915132	0.86[EUR][1000 genomes]
rs2079504	0.86[EUR][1000 genomes]
rs2079505	0.86[EUR][1000 genomes]
rs2079506	0.85[EUR][1000 genomes]
rs2176841	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2190508	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2214965	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2239229	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2239230	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2239232	0.88[EUR][1000 genomes]
rs2239234	0.88[EUR][1000 genomes]
rs2239235	0.86[EUR][1000 genomes]
rs2239238	0.86[EUR][1000 genomes]
rs2239239	0.86[EUR][1000 genomes]
rs2239241	0.86[EUR][1000 genomes]
rs2239243	0.86[EUR][1000 genomes]
rs2247090	0.88[EUR][1000 genomes]
rs2283385	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2283388	0.84[EUR][1000 genomes]
rs2332832	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2529457	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2529467	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2529468	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2529470	0.88[EUR][1000 genomes]
rs2529471	0.88[EUR][1000 genomes]
rs2681727	0.88[EUR][1000 genomes]
rs2681730	0.92[EUR][1000 genomes]
rs2681731	0.88[EUR][1000 genomes]
rs2681733	0.92[EUR][1000 genomes]
rs2681734	0.88[EUR][1000 genomes]
rs2681735	0.91[EUR][1000 genomes]
rs2681736	0.92[EUR][1000 genomes]
rs2681737	0.82[EUR][1000 genomes]
rs2681741	0.88[EUR][1000 genomes]
rs2681743	0.88[EUR][1000 genomes]
rs2681744	0.88[EUR][1000 genomes]
rs2681745	0.87[EUR][1000 genomes]
rs2681747	0.90[ASN][1000 genomes]
rs2681749	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2681751	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2681752	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2681753	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2681757	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2681767	0.86[EUR][1000 genomes]
rs2681768	0.86[EUR][1000 genomes]
rs2681769	0.86[EUR][1000 genomes]
rs2681771	0.86[EUR][1000 genomes]
rs34582179	0.81[EUR][1000 genomes]
rs7150465	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7151325	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8003559	0.86[EUR][1000 genomes]
rs8003591	0.86[EUR][1000 genomes]
rs8015917	0.92[EUR][1000 genomes]
rs8016720	0.82[EUR][1000 genomes]
rs8019358	0.86[EUR][1000 genomes]
rs8022859	0.86[EUR][1000 genomes]
rs8022956	0.86[EUR][1000 genomes]
rs886826	0.88[EUR][1000 genomes]
rs929413	0.88[EUR][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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72836000-72851400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:72846800-72848000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr14:72847000-72847600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:72847200-72847600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links