Variant report

Variant	rs60036628
Chromosome Location	chr8:119833213-119833214
allele	A/C
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:18)

rs_ID	r²[population]
rs57859083	1.00[AFR][1000 genomes]
rs58382191	1.00[AFR][1000 genomes]
rs58859156	1.00[AFR][1000 genomes]
rs73709335	1.00[AFR][1000 genomes]
rs73709336	1.00[AFR][1000 genomes]
rs73709337	1.00[AFR][1000 genomes]
rs73709340	1.00[AFR][1000 genomes]
rs73709342	1.00[AFR][1000 genomes]
rs73709357	1.00[AFR][1000 genomes]
rs73709380	1.00[AFR][1000 genomes]
rs73709381	1.00[AFR][1000 genomes]
rs73709383	1.00[AFR][1000 genomes]
rs73709385	1.00[AFR][1000 genomes]
rs73709509	1.00[AFR][1000 genomes]
rs73709522	1.00[AFR][1000 genomes]
rs73711404	1.00[AFR][1000 genomes]
rs73711413	1.00[AFR][1000 genomes]
rs73711414	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891414	chr8:119755490-119881550	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
2	nsv831444	chr8:119757355-119915966	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119825000-119836400	Weak transcription	NHDF-Ad	bronchial
2	chr8:119827800-119839000	Weak transcription	Aorta	Aorta

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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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