Variant report

Variant	rs73927037
Chromosome Location	chr2:39917706-39917707
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:10)

rs_ID	r²[population]
rs10170450	0.92[ASN][1000 genomes]
rs10193803	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10196294	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10490330	0.92[ASN][1000 genomes]
rs10490331	0.92[ASN][1000 genomes]
rs13422740	0.84[ASN][1000 genomes]
rs13423235	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13427938	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17024139	0.92[ASN][1000 genomes]
rs73927031	0.83[AMR][1000 genomes];0.86[ASN][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	nsv873889	chr2:39830183-39950482	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv833870	chr2:39837022-40026024	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv833881	chr2:39914558-40067256	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39907600-39922200	Weak transcription	HSMM	muscle
2	chr2:39914000-39918800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:39914200-39926800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:39914400-39923400	Weak transcription	Fetal Brain Male	brain
5	chr2:39916800-39917800	Enhancers	HepG2	liver
6	chr2:39917200-39918800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
7	chr2:39917200-39919800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:39917600-39922600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:39917600-39923200	Weak transcription	Aorta	Aorta

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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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