Variant report

Variant	rs73858577
Chromosome Location	chr3:99242216-99242217
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs58223529	0.83[AFR][1000 genomes]
rs59106684	1.00[AMR][1000 genomes]
rs59832918	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858442	1.00[AMR][1000 genomes]
rs73858445	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858446	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858448	0.92[AFR][1000 genomes]
rs73858453	0.92[AFR][1000 genomes]
rs73858456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858458	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858573	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858576	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858805	1.00[AMR][1000 genomes]
rs73858844	1.00[AMR][1000 genomes]
rs73858850	1.00[AMR][1000 genomes]
rs73861422	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7627465	1.00[AMR][1000 genomes]
rs7641113	1.00[AMR][1000 genomes]
rs7652601	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	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3422853	chr3:99208019-99342748	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99228400-99243000	Weak transcription	Aorta	Aorta
2	chr3:99238200-99242400	Weak transcription	NHDF-Ad	bronchial
3	chr3:99239600-99243000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr3:99241800-99245800	Weak transcription	Fetal Heart	heart
5	chr3:99242000-99243400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr3:99242200-99242600	Enhancers	HSMMtube	muscle
7	chr3:99242200-99242600	Enhancers	HUVEC	blood vessel
8	chr3:99242200-99243400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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