Variant report

Variant	rs2367293
Chromosome Location	chr4:74739267-74739268
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	chr4:74717554..74719920-chr4:74738464..74740646,2	K562	blood:

Variant related genes	Relation type
ENSG00000109272	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10007826	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10021230	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10028419	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1366946	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1366949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16850137	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2115691	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2145615	0.92[ASN][1000 genomes]
rs24772	0.92[ASN][1000 genomes]
rs28404022	0.89[AMR][1000 genomes]
rs2886969	0.86[AMR][1000 genomes]
rs2886970	0.86[AMR][1000 genomes]
rs2968710	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3097409	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3097412	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3111697	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3111698	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4074	0.94[ASN][1000 genomes]
rs482239	0.92[ASN][1000 genomes]
rs492155	0.92[ASN][1000 genomes]
rs493091	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs508977	0.92[ASN][1000 genomes]
rs512606	0.92[ASN][1000 genomes]
rs516224	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs518632	0.92[ASN][1000 genomes]
rs519565	0.92[ASN][1000 genomes]
rs537373	0.92[ASN][1000 genomes]
rs541923	0.92[ASN][1000 genomes]
rs548068	0.92[ASN][1000 genomes]
rs551744	0.92[ASN][1000 genomes]
rs561454	0.82[ASN][1000 genomes]
rs562213	0.82[ASN][1000 genomes]
rs569390	0.92[ASN][1000 genomes]
rs573878	0.92[ASN][1000 genomes]
rs593641	0.92[ASN][1000 genomes]
rs596352	0.92[ASN][1000 genomes]
rs623659	0.92[ASN][1000 genomes]
rs634304	0.81[AMR][1000 genomes]
rs638767	0.92[ASN][1000 genomes]
rs654871	0.92[ASN][1000 genomes]
rs655328	0.92[ASN][1000 genomes]
rs680044	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs680452	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs683671	0.92[ASN][1000 genomes]
rs684080	0.92[ASN][1000 genomes]
rs6858086	0.94[ASN][1000 genomes]
rs7674809	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7692638	0.86[AMR][1000 genomes]
rs9991272	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv432612	chr4:74723372-74774372	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74736000-74741600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:74736400-74739800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:74736800-74740600	Weak transcription	NHDF-Ad	bronchial
4	chr4:74736800-74749000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:74737000-74740600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:74737000-74740800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr4:74737000-74741600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:74737200-74739600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:74737400-74739800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:74737800-74741000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr4:74738000-74741600	Weak transcription	Fetal Stomach	stomach
12	chr4:74738400-74740800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr4:74739200-74739600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr4:74739200-74740200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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