Variant report

Variant	rs9895692
Chromosome Location	chr17:67070803-67070804
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs28524118	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28620744	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34498359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34831728	1.00[AMR][1000 genomes]
rs9895065	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9912654	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9915805	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv833526	chr17:66980758-67137034	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1066998	chr17:67060038-67090475	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv908705	chr17:67061898-67112456	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	4 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	chr17:67041400-67072600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr17:67056200-67075200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr17:67057800-67077600	Weak transcription	Fetal Brain Male	brain
4	chr17:67058400-67071600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr17:67062800-67075800	Weak transcription	Left Ventricle	heart
6	chr17:67065600-67076400	Weak transcription	Esophagus	oesophagus
7	chr17:67065600-67088600	Weak transcription	Pancreas	Pancrea
8	chr17:67065800-67076400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr17:67066000-67078800	Weak transcription	NHDF-Ad	bronchial
10	chr17:67067200-67099600	Weak transcription	Gastric	stomach
11	chr17:67067200-67111600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr17:67070000-67071000	ZNF genes & repeats	Ovary	ovary
13	chr17:67070200-67079000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr17:67070400-67076400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr17:67070600-67072800	ZNF genes & repeats	Liver	Liver
16	chr17:67070800-67071000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr17:67070800-67074400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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