Variant report

Variant	rs67609961
Chromosome Location	chr7:16465283-16465284
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10277754	0.81[EUR][1000 genomes]
rs10464288	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17674339	0.81[EUR][1000 genomes]
rs1921843	0.86[EUR][1000 genomes]
rs1921845	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2389633	0.81[EUR][1000 genomes]
rs2389638	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55746209	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55944246	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56061198	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56176134	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56199980	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs59379368	0.81[EUR][1000 genomes]
rs6461247	0.81[EUR][1000 genomes]
rs67088819	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7791775	0.83[AMR][1000 genomes];0.87[EUR][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	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1034151	chr7:16415497-16578081	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 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	chr7:16461400-16469000	Weak transcription	Aorta	Aorta
2	chr7:16461600-16469600	Weak transcription	Gastric	stomach
3	chr7:16461600-16478600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:16462000-16468000	Weak transcription	NH-A	brain
5	chr7:16462200-16468000	Weak transcription	NHDF-Ad	bronchial
6	chr7:16462200-16468600	Weak transcription	NHLF	lung
7	chr7:16462200-16473200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:16462600-16467800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:16462600-16468200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:16462600-16473400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:16462800-16468000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:16462800-16468000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:16462800-16468000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:16464000-16468000	Weak transcription	K562	blood
15	chr7:16464200-16468000	Weak transcription	Stomach Mucosa	stomach

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

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