Variant report

Variant	rs290703
Chromosome Location	chr1:72876286-72876287
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10789338	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1084439	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1084440	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1084441	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10889955	0.82[EUR][1000 genomes]
rs11209961	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11209968	0.80[EUR][1000 genomes]
rs11209969	0.80[EUR][1000 genomes]
rs11209972	0.80[EUR][1000 genomes]
rs12026130	0.82[EUR][1000 genomes]
rs12033462	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12035943	0.83[EUR][1000 genomes]
rs12759396	0.80[EUR][1000 genomes]
rs1373913	0.83[EUR][1000 genomes]
rs1445581	0.82[EUR][1000 genomes]
rs1445582	0.83[EUR][1000 genomes]
rs1596762	0.83[EUR][1000 genomes]
rs1599334	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1822977	0.83[EUR][1000 genomes]
rs1822979	0.80[EUR][1000 genomes]
rs1824530	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1838662	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1903372	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2121055	0.80[EUR][1000 genomes]
rs2121056	0.83[EUR][1000 genomes]
rs2568955	0.85[JPT][hapmap]
rs2568958	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs2613473	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2815767	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs290702	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3101336	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs3101338	0.85[JPT][hapmap]
rs4649956	0.83[EUR][1000 genomes]
rs4649957	0.80[EUR][1000 genomes]
rs4650133	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4650138	0.80[EUR][1000 genomes]
rs4650139	0.80[EUR][1000 genomes]
rs6424471	0.83[EUR][1000 genomes]
rs7523080	0.80[EUR][1000 genomes]
rs7531797	0.83[EUR][1000 genomes]
rs7534013	0.83[EUR][1000 genomes]
rs7535539	0.80[EUR][1000 genomes]
rs7536869	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7550173	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs782207	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs782208	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs782210	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs782212	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs782219	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs782239	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs782243	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs782244	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs782246	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs782252	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs813004	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428454	chr1:72504469-72926256	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	esv2757734	chr1:72742396-72886813	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv2758939	chr1:72742396-72886813	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv830204	chr1:72749851-72938571	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv947113	chr1:72810737-72948614	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	esv2422432	chr1:72821856-73148651	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv871873	chr1:72861847-72975877	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv870463	chr1:72861847-72995398	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv871758	chr1:72861847-72995398	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv830215	chr1:72869049-73029787	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72873800-72877600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:72876000-72878000	Weak transcription	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links