Variant report

Variant	rs16954239
Chromosome Location	chr13:98293004-98293005
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16954214	1.00[EUR][1000 genomes]
rs16954221	1.00[EUR][1000 genomes]
rs16954230	1.00[EUR][1000 genomes]
rs16954245	1.00[EUR][1000 genomes]
rs16954252	1.00[EUR][1000 genomes]
rs28667337	1.00[AMR][1000 genomes]
rs73550064	1.00[EUR][1000 genomes]
rs73552096	1.00[EUR][1000 genomes]
rs7998899	1.00[EUR][1000 genomes]
rs9556737	1.00[AMR][1000 genomes]
rs9556738	1.00[AMR][1000 genomes]
rs9556739	1.00[AMR][1000 genomes]
rs9556741	1.00[AMR][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	nsv1043113	chr13:98136208-98485012	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv541884	chr13:98136208-98485012	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:98289000-98293800	Weak transcription	Fetal Brain Male	brain
2	chr13:98292600-98293200	Enhancers	Fetal Heart	heart
3	chr13:98292800-98293600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr13:98293000-98293400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr13:98293000-98293600	Active TSS	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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