Variant report

Variant	rs1806738
Chromosome Location	chr4:78307215-78307216
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78307066..78309627-chr4:78338398..78341247,3	MCF-7	breast:
2	chr4:78306484..78307565-chr4:78351707..78352604,5	MCF-7	breast:
3	chr4:78306285..78307276-chr4:78351745..78352760,5	MCF-7	breast:
4	chr4:78306279..78307489-chr4:78353325..78355121,9	MCF-7	breast:
5	chr4:78306138..78307360-chr4:78339239..78340037,9	MCF-7	breast:
6	chr4:78306262..78307241-chr4:78353866..78354908,3	MCF-7	breast:
7	chr4:78306456..78307324-chr4:78354247..78354761,2	K562	blood:
8	chr4:78306562..78308497-chr4:78334856..78338257,3	MCF-7	breast:

No data

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10016230	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11930470	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11936421	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12500776	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12501577	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12502346	0.92[EUR][1000 genomes]
rs12503990	0.92[EUR][1000 genomes]
rs12505837	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12506515	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12506585	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12511631	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17002580	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1806786	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1962168	0.83[EUR][1000 genomes]
rs1962351	0.83[EUR][1000 genomes]
rs28413838	0.92[EUR][1000 genomes]
rs28437320	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28454139	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28522639	0.92[EUR][1000 genomes]
rs2866287	0.92[EUR][1000 genomes]
rs2866288	0.92[EUR][1000 genomes]
rs2866289	0.85[EUR][1000 genomes]
rs2866290	0.83[EUR][1000 genomes]
rs28711853	0.92[EUR][1000 genomes]
rs4282207	0.92[EUR][1000 genomes]
rs4579145	0.92[EUR][1000 genomes]
rs55905288	0.83[EUR][1000 genomes]
rs57104380	0.83[EUR][1000 genomes]
rs59732128	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6650924	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67084501	0.92[EUR][1000 genomes]
rs67295944	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67714872	0.92[EUR][1000 genomes]
rs67955395	0.92[EUR][1000 genomes]
rs72648554	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72648556	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72648557	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72648559	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72648560	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72648563	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs72648565	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72648566	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72648573	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72648575	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72648578	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72648580	0.97[ASN][1000 genomes]
rs72648581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72648583	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72648584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72648585	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72648586	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72650413	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72864744	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7674431	0.83[EUR][1000 genomes]
rs7695467	0.83[EUR][1000 genomes]
rs9990691	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006017	chr4:78139780-78312974	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1010450	chr4:78182037-78317840	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1004824	chr4:78188691-78312974	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv1845782	chr4:78237955-78321598	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv829974	chr4:78240718-78415642	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv3442840	chr4:78277532-78309591	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv594698	chr4:78291876-78334483	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv967998	chr4:78301212-78311035	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78306200-78308200	Enhancers	Fetal Intestine Small	intestine
2	chr4:78306800-78308200	Enhancers	Fetal Intestine Large	intestine
3	chr4:78307000-78308800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:78307000-78308800	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:78307200-78308800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links