Variant report

Variant	rs9291692
Chromosome Location	chr5:59835549-59835550
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	chr5:59831215..59833995-chr5:59834537..59838360,3	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10036678	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10044835	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10056275	0.98[AFR][1000 genomes]
rs10065640	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10074908	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10075757	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10078847	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs1379112	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16878206	0.92[ASN][1000 genomes]
rs16878207	0.92[ASN][1000 genomes]
rs28531078	0.99[AFR][1000 genomes]
rs3857235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4081739	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4133470	1.00[JPT][hapmap]
rs6449475	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6891919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6898521	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73093136	0.82[ASN][1000 genomes]
rs7707672	0.89[AFR][1000 genomes]
rs7712091	0.92[ASN][1000 genomes]
rs7712117	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7723306	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7724442	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7727343	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7729652	0.82[ASN][1000 genomes]
rs7729781	0.82[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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv598288	chr5:59627555-60003460	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1018614	chr5:59708223-59910308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv881711	chr5:59724947-59890278	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv598297	chr5:59734004-59862453	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59828000-59837000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:59833400-59838200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:59833400-59838800	Enhancers	Primary T cells from cord blood	blood
4	chr5:59834000-59839200	Enhancers	Primary B cells from peripheral blood	blood
5	chr5:59834200-59838200	Enhancers	Brain Angular Gyrus	brain
6	chr5:59834400-59835600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:59834600-59835800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:59834600-59836200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr5:59834600-59838200	Enhancers	Brain Substantia Nigra	brain
10	chr5:59834800-59836600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:59835000-59837000	Enhancers	GM12878-XiMat	blood
12	chr5:59835200-59835600	Enhancers	Stomach Mucosa	stomach
13	chr5:59835200-59835600	Enhancers	A549	lung
14	chr5:59835200-59835800	Enhancers	Colon Smooth Muscle	Colon
15	chr5:59835200-59839000	Enhancers	HepG2	liver
16	chr5:59835400-59835600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr5:59835400-59835800	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr5:59835400-59835800	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr5:59835400-59835800	Enhancers	Fetal Thymus	thymus
20	chr5:59835400-59835800	Enhancers	Spleen	Spleen
21	chr5:59835400-59836000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr5:59835400-59836000	Enhancers	Rectal Smooth Muscle	rectum
23	chr5:59835400-59836000	Enhancers	Right Atrium	heart
24	chr5:59835400-59836200	Enhancers	Brain Hippocampus Middle	brain
25	chr5:59835400-59836400	Enhancers	Gastric	stomach
26	chr5:59835400-59837600	Enhancers	Ovary	ovary

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