Variant report

Variant	rs7981934
Chromosome Location	chr13:63058321-63058322
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1336140	0.82[AFR][1000 genomes]
rs13378225	0.97[EUR][1000 genomes]
rs13378226	0.94[EUR][1000 genomes]
rs1591527	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs727918	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7319919	0.89[EUR][1000 genomes]
rs73503726	0.97[EUR][1000 genomes]
rs73503768	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7989348	0.86[AFR][1000 genomes]
rs9598450	0.95[EUR][1000 genomes]
rs9598464	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9598466	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9598467	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9598470	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9805472	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038992	chr13:62827929-63369497	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv541795	chr13:62827929-63369497	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1038215	chr13:62836702-63405446	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:63057400-63058600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:63057600-63058400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr13:63057600-63058400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr13:63057600-63059000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr13:63057800-63058400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:63057800-63058400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:63057800-63058400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr13:63057800-63058400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr13:63057800-63062200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr13:63058000-63062200	Weak transcription	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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