Variant report

Variant	rs35332919
Chromosome Location	chr3:133519002-133519003
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12490148	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12595	0.84[AMR][1000 genomes]
rs13079426	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525889	0.83[AMR][1000 genomes]
rs1534165	0.85[ASN][1000 genomes]
rs1830083	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1830084	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4854760	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4854761	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4854762	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6794945	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73217233	0.85[ASN][1000 genomes]
rs7638018	0.84[AMR][1000 genomes]
rs8177260	0.81[EUR][1000 genomes]
rs9813689	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9843728	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9871148	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9882812	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[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	nsv877506	chr3:133423473-133569777	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv933605	chr3:133425907-133680641	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv829729	chr3:133444871-133620387	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv4018	chr3:133485867-133530668	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133518600-133519200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr3:133518600-133519400	Enhancers	Esophagus	oesophagus
3	chr3:133518600-133519400	Enhancers	Fetal Muscle Leg	muscle
4	chr3:133518600-133519400	Enhancers	NHEK	skin
5	chr3:133518600-133519600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:133518600-133519600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:133518600-133519600	Enhancers	Stomach Mucosa	stomach
8	chr3:133518600-133519600	Enhancers	HepG2	liver
9	chr3:133518600-133519600	Enhancers	HMEC	breast
10	chr3:133518600-133519800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:133518800-133519200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr3:133518800-133519200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:133518800-133519200	Enhancers	Hela-S3	cervix
14	chr3:133518800-133519200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr3:133519000-133519200	Enhancers	Brain Substantia Nigra	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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