Variant report

Variant	rs73215583
Chromosome Location	chr7:118386987-118386988
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:17)

rs_ID	r²[population]
rs10953874	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10953875	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11768006	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11769440	0.95[EUR][1000 genomes]
rs12532831	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2590585	0.94[EUR][1000 genomes]
rs2699732	0.94[EUR][1000 genomes]
rs2699734	0.94[EUR][1000 genomes]
rs2699736	0.94[EUR][1000 genomes]
rs6971646	0.90[EUR][1000 genomes]
rs73215585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73215597	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73215598	0.97[EUR][1000 genomes]
rs73217505	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73217506	0.95[EUR][1000 genomes]
rs73217508	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7809424	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv831109	chr7:118300593-118501778	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv436538	chr7:118382039-118391253	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3477479	chr7:118382577-118391377	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3477477	chr7:118382615-118391363	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3477478	chr7:118382696-118391233	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3477480	chr7:118382696-118391233	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv20211	chr7:118382903-118391350	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118385600-118387000	Enhancers	Fetal Lung	lung
2	chr7:118386400-118387000	Enhancers	Fetal Stomach	stomach
3	chr7:118386800-118387000	Enhancers	hESC Derived CD56+ Mesoderm 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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