Variant report

Variant	rs4869076
Chromosome Location	chr5:167259301-167259302
allele	C/G/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]
rs1035374	0.89[ASN][1000 genomes]
rs12153261	0.80[ASN][1000 genomes]
rs12519816	0.88[ASN][1000 genomes]
rs12521018	0.85[ASN][1000 genomes]
rs1421989	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1421990	0.82[ASN][1000 genomes]
rs1549151	0.89[ASN][1000 genomes]
rs1549152	0.88[ASN][1000 genomes]
rs2052466	0.81[ASN][1000 genomes]
rs4869075	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs55698578	0.88[ASN][1000 genomes]
rs73388370	0.81[ASN][1000 genomes]
rs7714210	0.84[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	nsv932627	chr5:166744408-167290959	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1027805	chr5:167082800-167285008	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167248600-167270000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:167251400-167262200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:167251800-167299000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:167252600-167276000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:167255200-167262400	Weak transcription	HSMM	muscle
6	chr5:167255400-167264800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:167255600-167262200	Weak transcription	HMEC	breast
8	chr5:167256200-167261000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:167258000-167259400	Enhancers	Fetal Kidney	kidney
10	chr5:167258000-167259600	Enhancers	Fetal Lung	lung
11	chr5:167258600-167260400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:167258800-167259600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:167258800-167262000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:167259200-167261000	Strong transcription	NHEK	skin

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

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