Variant report

Variant	rs7021176
Chromosome Location	chr9:73497518-73497519
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11142636	0.81[ASN][1000 genomes]
rs2039643	0.87[ASN][1000 genomes]
rs4143737	0.85[ASN][1000 genomes]
rs7021289	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7851915	0.98[ASN][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	nsv893441	chr9:73486034-73594114	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 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	chr9:73493800-73498000	Enhancers	Fetal Heart	heart
2	chr9:73496800-73498600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr9:73496800-73499200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:73496800-73499400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr9:73496800-73499800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:73497400-73499200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr9:73497400-73500400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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