Variant report

Variant	rs73812503
Chromosome Location	chr4:31055332-31055333
allele	A/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:24)

rs_ID	r²[population]
rs55971541	1.00[AFR][1000 genomes]
rs56009522	1.00[AFR][1000 genomes]
rs56344969	1.00[AFR][1000 genomes]
rs56372203	1.00[AFR][1000 genomes]
rs56674207	1.00[AFR][1000 genomes]
rs57182771	0.90[AFR][1000 genomes]
rs58844173	1.00[AFR][1000 genomes]
rs60946225	0.81[AFR][1000 genomes]
rs73812505	1.00[AFR][1000 genomes]
rs73815113	0.89[AFR][1000 genomes]
rs73815123	0.90[AFR][1000 genomes]
rs73815124	0.90[AFR][1000 genomes]
rs73815125	0.90[AFR][1000 genomes]
rs73815131	0.90[AFR][1000 genomes]
rs73815132	0.90[AFR][1000 genomes]
rs73815137	0.90[AFR][1000 genomes]
rs73815142	0.90[AFR][1000 genomes]
rs73815149	1.00[AFR][1000 genomes]
rs73815155	1.00[AFR][1000 genomes]
rs73815161	1.00[AFR][1000 genomes]
rs73815164	1.00[AFR][1000 genomes]
rs73815168	0.89[AFR][1000 genomes]
rs73815169	1.00[AFR][1000 genomes]
rs73815170	1.00[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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:31050200-31057600	Weak transcription	Aorta	Aorta
2	chr4:31054200-31056000	Weak transcription	Fetal Lung	lung
3	chr4:31054400-31056000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:31055000-31056800	Enhancers	Fetal Heart	heart

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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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