Variant report

Variant	rs57331149
Chromosome Location	chr8:69885012-69885013
allele	C/T
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:11)

rs_ID	r²[population]
rs55914427	1.00[AFR][1000 genomes]
rs56350065	1.00[AFR][1000 genomes]
rs58281208	1.00[AFR][1000 genomes]
rs60314331	1.00[AFR][1000 genomes]
rs73683739	1.00[AFR][1000 genomes]
rs73683741	1.00[AFR][1000 genomes]
rs73683750	1.00[AFR][1000 genomes]
rs73683754	1.00[AFR][1000 genomes]
rs73683755	1.00[AFR][1000 genomes]
rs73683792	1.00[AFR][1000 genomes]
rs73683794	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	nsv1031633	chr8:69766575-70322790	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv33049	chr8:69836813-69943360	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69879600-69917200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:69880200-69885600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:69885000-69885200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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