Variant report

Variant	rs8036472
Chromosome Location	chr15:58496750-58496751
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs16939897	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs16939914	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4306445	1.00[CHB][hapmap]
rs4775022	0.90[AFR][1000 genomes]
rs7173859	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs7174552	1.00[EUR][1000 genomes]
rs7179233	1.00[ASN][1000 genomes]
rs8023365	1.00[EUR][1000 genomes]
rs8024186	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs8025123	1.00[EUR][1000 genomes]
rs8025133	1.00[EUR][1000 genomes]
rs8027422	1.00[EUR][1000 genomes]
rs8036167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8037075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8043218	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs935211	1.00[CHB][hapmap]
rs9652471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv1047246	chr15:58375607-58707158	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833024	chr15:58447459-58621963	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv2752813	chr15:58461006-58507064	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1050473	chr15:58479888-58562270	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58492800-58497800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr15:58492800-58498400	Enhancers	NHDF-Ad	bronchial
3	chr15:58493400-58497000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr15:58493400-58497400	Enhancers	NHLF	lung
5	chr15:58493600-58496800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr15:58494000-58500800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:58495400-58497000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:58495400-58498400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:58495600-58497200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr15:58496200-58501000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr15:58496400-58498200	Weak transcription	K562	blood
12	chr15:58496400-58500600	Weak transcription	Right Atrium	heart
13	chr15:58496400-58501000	Weak transcription	NH-A	brain
14	chr15:58496600-58500800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr15:58496600-58501000	Weak transcription	Osteobl	bone
16	chr15:58496600-58501400	Weak transcription	HUVEC	blood vessel
17	chr15:58496600-58502000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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

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