Variant report

Variant	rs2618960
Chromosome Location	chr4:22677149-22677150
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12501294	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478964	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1843485	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2127177	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2219802	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2581964	0.88[EUR][1000 genomes]
rs2581968	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2581980	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2581991	0.87[ASN][1000 genomes]
rs2581992	0.87[ASN][1000 genomes]
rs2618951	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2618953	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2629975	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3101799	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4697333	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57301753	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349061	chr4:22379581-22887563	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv821634	chr4:22427074-22865948	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv829883	chr4:22666326-22842517	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22670400-22678600	Enhancers	Primary T helper naive cells from peripheral blood	blood
2	chr4:22670600-22681800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:22674000-22678800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr4:22674600-22679000	Enhancers	Primary T cells from cord blood	blood
5	chr4:22675000-22677400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr4:22675000-22677800	Weak transcription	Primary B cells from cord blood	blood
7	chr4:22675200-22679400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:22675800-22677800	Weak transcription	Thymus	Thymus
9	chr4:22675800-22678800	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr4:22676000-22677400	Weak transcription	Fetal Thymus	thymus
11	chr4:22676000-22678600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr4:22676200-22678600	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr4:22676400-22677200	Weak transcription	Colon Smooth Muscle	Colon
14	chr4:22676400-22678400	Enhancers	Primary B cells from peripheral blood	blood
15	chr4:22676800-22677200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr4:22677000-22677200	Enhancers	Fetal Lung	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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