Variant report

Variant	rs4526430
Chromosome Location	chr9:118015032-118015033
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10817738	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10982625	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10982643	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1100324	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs11496558	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11790089	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1335329	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1335337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1557602	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs1557604	0.89[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2027156	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2225749	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs62578010	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr9:118013400-118016600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:118013800-118015200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr9:118013800-118015600	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:118013800-118016200	Weak transcription	Fetal Stomach	stomach
5	chr9:118014000-118015400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:118014000-118016600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:118014000-118017000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:118014000-118017000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr9:118014000-118023400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:118014200-118015600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr9:118014200-118016600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:118014200-118023000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr9:118014400-118023800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr9:118014600-118015200	Enhancers	Fetal Muscle Leg	muscle
15	chr9:118014800-118015600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
16	chr9:118015000-118015800	Strong transcription	ES-I3 Cell Line	embryonic stem cell

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

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