Variant report

Variant	rs73815168
Chromosome Location	chr4:31047885-31047886
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12499716	0.89[AFR][1000 genomes]
rs55971541	0.89[AFR][1000 genomes]
rs56009522	0.89[AFR][1000 genomes]
rs56344969	0.89[AFR][1000 genomes]
rs56372203	0.89[AFR][1000 genomes]
rs56674207	0.89[AFR][1000 genomes]
rs57615189	0.89[AFR][1000 genomes]
rs58844173	0.89[AFR][1000 genomes]
rs73812503	0.89[AFR][1000 genomes]
rs73812505	0.89[AFR][1000 genomes]
rs73812510	0.89[AFR][1000 genomes]
rs73812702	0.89[AFR][1000 genomes]
rs73815113	1.00[AFR][1000 genomes]
rs73815149	0.89[AFR][1000 genomes]
rs73815155	0.89[AFR][1000 genomes]
rs73815161	0.89[AFR][1000 genomes]
rs73815164	0.89[AFR][1000 genomes]
rs73815169	0.89[AFR][1000 genomes]
rs73815170	0.89[AFR][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	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr4:31043200-31050600	Weak transcription	Psoas Muscle	Psoas
2	chr4:31043800-31050000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:31043800-31052800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:31046000-31049800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:31046000-31052800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:31047600-31048800	Weak transcription	Fetal Heart	heart
7	chr4:31047800-31048800	Weak transcription	hESC Derived CD184+ Endoderm 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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