Variant report

Variant	rs73449037
Chromosome Location	chr7:126327124-126327125
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10229382	0.94[AFR][1000 genomes]
rs10244102	0.87[AFR][1000 genomes]
rs10244659	0.94[AFR][1000 genomes]
rs10247812	1.00[AFR][1000 genomes]
rs10253111	1.00[AFR][1000 genomes]
rs10254454	0.94[AFR][1000 genomes]
rs10258741	0.97[AFR][1000 genomes]
rs10267217	0.89[AFR][1000 genomes]
rs10272830	0.97[AFR][1000 genomes]
rs10273625	1.00[AFR][1000 genomes]
rs28452678	0.94[AFR][1000 genomes]
rs28654948	0.97[AFR][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	nsv529300	chr7:125669493-126587858	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1032938	chr7:126067684-126587859	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv539119	chr7:126067684-126587859	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv889187	chr7:126219766-126478190	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1032108	chr7:126278349-126362592	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126321800-126328800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr7:126323600-126328600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:126326000-126331200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:126326600-126327200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:126326600-126330200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:126326800-126327200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:126326800-126330200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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