Variant report

Variant	rs7709455
Chromosome Location	chr5:36713033-36713034
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	chr5:36712965..36715129-chr5:36719061..36721012,2	K562	blood:
2	chr5:36708211..36710665-chr5:36712049..36713673,3	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10056070	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10061940	0.80[CHD][hapmap];0.88[GIH][hapmap];0.81[MEX][hapmap]
rs10067333	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1025052	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10461973	0.87[ASN][1000 genomes]
rs10491377	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10941314	0.93[ASN][1000 genomes]
rs12658012	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12697368	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13160879	0.88[ASN][1000 genomes]
rs13178390	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1566444	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16903296	0.95[ASN][1000 genomes]
rs1976377	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2161609	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6451305	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6867429	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6878201	0.95[ASN][1000 genomes]
rs6890097	0.86[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.87[MEX][hapmap];0.96[MKK][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7734294	0.81[ASW][hapmap];0.81[CEU][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.87[MEX][hapmap];0.99[MKK][hapmap];0.88[YRI][hapmap];0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs919300	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs919301	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs986341	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[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	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv830263	chr5:36576504-36755093	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr5:36700200-36724200	Weak transcription	Primary T cells from cord blood	blood
2	chr5:36705800-36724600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr5:36709200-36721800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:36709600-36713800	Weak transcription	GM12878-XiMat	blood
5	chr5:36710000-36714200	Strong transcription	Primary B cells from cord blood	blood
6	chr5:36710000-36721200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:36711000-36713200	Strong transcription	Primary B cells from peripheral blood	blood
8	chr5:36711400-36714000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr5:36711800-36721000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:36712200-36713200	Weak transcription	Esophagus	oesophagus
11	chr5:36712200-36721800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr5:36712400-36713200	Enhancers	Fetal Heart	heart
13	chr5:36712600-36713400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:36712600-36713600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr5:36712600-36713600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:36712600-36713800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr5:36712800-36713400	Enhancers	NHEK	skin
18	chr5:36712800-36713600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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