Variant report

Variant	rs8190493
Chromosome Location	chr9:99062025-99062026
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs28932191	1.00[AFR][1000 genomes]
rs7023428	1.00[AMR][1000 genomes]
rs73654853	1.00[AMR][1000 genomes]
rs73654881	1.00[AFR][1000 genomes]
rs8190481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8190482	1.00[AMR][1000 genomes]
rs8190488	1.00[AMR][1000 genomes]
rs8190497	1.00[AMR][1000 genomes]
rs8190506	1.00[AMR][1000 genomes]
rs9785250	1.00[AMR][1000 genomes]
rs9785268	1.00[AMR][1000 genomes]
rs9942940	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532433	chr9:98857250-99382944	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99049600-99064400	Weak transcription	Right Ventricle	heart
2	chr9:99052400-99067200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:99056400-99064400	Weak transcription	NH-A	brain
4	chr9:99056800-99075600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr9:99058800-99067600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:99059200-99063200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:99061400-99062600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:99061400-99062600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:99061400-99063200	Enhancers	Hela-S3	cervix
10	chr9:99061400-99063600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:99061600-99062400	Enhancers	Placenta Amnion	Placenta Amnion
12	chr9:99061600-99062600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:99061600-99062600	Enhancers	HSMM	muscle
14	chr9:99061600-99062800	Enhancers	HMEC	breast
15	chr9:99061800-99062600	Enhancers	HSMMtube	muscle
16	chr9:99062000-99063200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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