Variant report

Variant	rs7853025
Chromosome Location	chr9:17006093-17006094
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1023121	1.00[AMR][1000 genomes]
rs1041391	1.00[AMR][1000 genomes]
rs7024714	1.00[AMR][1000 genomes]
rs7029144	1.00[AMR][1000 genomes]
rs7036367	1.00[AMR][1000 genomes]
rs7856179	1.00[AMR][1000 genomes]
rs7856550	1.00[AMR][1000 genomes]
rs7864861	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv2764141	chr9:16903446-17351711	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv613692	chr9:16963863-17070633	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17004000-17006200	Enhancers	Fetal Lung	lung
2	chr9:17004600-17006200	Enhancers	HepG2	liver
3	chr9:17005200-17006400	Enhancers	Stomach Mucosa	stomach
4	chr9:17005600-17006200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:17005600-17006200	Enhancers	Fetal Kidney	kidney
6	chr9:17005600-17006400	Enhancers	Duodenum Mucosa	Duodenum
7	chr9:17005600-17006800	Enhancers	Fetal Intestine Small	intestine
8	chr9:17005800-17006400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr9:17005800-17008200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:17006000-17006400	Weak transcription	Fetal Intestine Large	intestine

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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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