Variant report

Variant	rs73523126
Chromosome Location	chr6:109851737-109851738
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs56801512	1.00[AFR][1000 genomes]
rs60971740	1.00[AFR][1000 genomes]
rs73520943	1.00[AFR][1000 genomes]
rs73520966	1.00[AFR][1000 genomes]
rs73520974	1.00[AFR][1000 genomes]
rs73520984	0.83[AFR][1000 genomes]
rs73523117	0.91[AFR][1000 genomes]
rs73523125	1.00[AFR][1000 genomes]
rs73523129	1.00[AFR][1000 genomes]
rs73523136	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	nsv1026012	chr6:109851638-109999379	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109838600-109861400	Weak transcription	Thymus	Thymus
2	chr6:109848400-109865600	Weak transcription	Aorta	Aorta
3	chr6:109848400-109870400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:109850800-109870000	Weak transcription	Left Ventricle	heart
5	chr6:109851000-109853000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:109851400-109854400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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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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