Variant report

Variant	rs73226560
Chromosome Location	chr4:15795981-15795982
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11574921	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12644506	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12651439	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2302229	0.89[EUR][1000 genomes]
rs3796867	1.00[ASN][1000 genomes]
rs4634217	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73224697	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73226564	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73226572	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73226574	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7436920	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv10460	chr4:15757611-15818206	ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1013204	chr4:15762970-15836237	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1010597	chr4:15776181-15836237	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15786200-15796000	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr4:15786400-15807400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr4:15794000-15812200	Genic enhancers	Dnd41	blood
4	chr4:15794200-15796000	Enhancers	Fetal Brain Male	brain
5	chr4:15794600-15796000	Strong transcription	Thymus	Thymus
6	chr4:15794600-15796200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:15794600-15796200	Strong transcription	Fetal Thymus	thymus
8	chr4:15795200-15796000	Strong transcription	Primary B cells from cord blood	blood
9	chr4:15795200-15796000	Enhancers	Psoas Muscle	Psoas
10	chr4:15795200-15796000	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr4:15795200-15797400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr4:15795200-15797600	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr4:15795400-15796000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:15795400-15796000	Weak transcription	Small Intestine	intestine
15	chr4:15795400-15797600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr4:15795600-15796000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:15795600-15796000	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr4:15795600-15796000	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr4:15795600-15796800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr4:15795800-15796000	Enhancers	Spleen	Spleen
21	chr4:15795800-15797000	Enhancers	GM12878-XiMat	blood
22	chr4:15795800-15797400	Enhancers	Primary T cells from cord blood	blood

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