Variant report

Variant	rs1528910
Chromosome Location	chr4:74547731-74547732
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	chr4:74546704..74548843-chr4:74564571..74566434,2	K562	blood:
2	chr4:74543508..74545459-chr4:74546568..74548588,2	MCF-7	breast:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10025373	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10029200	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10938089	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10938091	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11722921	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11938646	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1247605	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247607	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247608	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247611	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247620	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247633	1.00[ASN][1000 genomes]
rs1247634	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247635	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1247639	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1247687	0.98[ASN][1000 genomes]
rs1247689	0.99[ASN][1000 genomes]
rs12508451	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1261935	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12642878	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12643076	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12643148	0.98[ASN][1000 genomes]
rs12646031	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12649614	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1269764	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1269766	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1358594	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1406498	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528912	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1528913	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1729722	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1745246	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1951702	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1951703	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.85[TSI][hapmap];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1951704	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1951705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2091587	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2141467	0.98[ASN][1000 genomes]
rs2141468	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2178291	0.98[ASN][1000 genomes]
rs2367273	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2886918	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3796679	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4127802	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4259030	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4568212	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4637366	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4694633	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs56785010	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61101665	0.98[ASN][1000 genomes]
rs6446950	0.91[ASN][1000 genomes]
rs6446951	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.83[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6446953	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6446954	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6818711	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6836038	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6857472	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs720702	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72865497	0.98[ASN][1000 genomes]
rs72865502	0.98[ASN][1000 genomes]
rs7655660	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7656501	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7656608	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7657356	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7657358	0.98[ASN][1000 genomes]
rs7660448	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7660923	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7665606	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7678280	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7678307	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7681924	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7681932	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7682745	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7683759	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7689702	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs942051	0.98[ASN][1000 genomes]
rs9991585	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[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	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1008104	chr4:74468434-74621952	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1012198	chr4:74487793-74621952	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv537139	chr4:74487793-74621952	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74536000-74548400	Weak transcription	Stomach Mucosa	stomach
2	chr4:74540600-74548400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:74543000-74549800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:74543400-74548400	Weak transcription	Hela-S3	cervix
5	chr4:74543800-74548000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr4:74546000-74547800	Weak transcription	A549	lung
7	chr4:74546000-74548200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:74546000-74548400	Weak transcription	NHEK	skin
9	chr4:74546000-74549800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:74546000-74555600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:74546200-74549600	Weak transcription	NHDF-Ad	bronchial
12	chr4:74546200-74550600	Weak transcription	Osteobl	bone
13	chr4:74546400-74548000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:74547600-74547800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr4:74547600-74547800	Enhancers	HMEC	breast
16	chr4:74547600-74549400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:74547600-74550000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:74547600-74551000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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