Variant report

Variant	rs10982413
Chromosome Location	chr9:117572030-117572031
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1075074	0.80[EUR][1000 genomes]
rs10982412	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10982416	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10982424	0.80[EUR][1000 genomes]
rs10982425	0.80[EUR][1000 genomes]
rs10982439	0.86[EUR][1000 genomes]
rs11560576	0.80[EUR][1000 genomes]
rs12237626	0.84[EUR][1000 genomes]
rs1590256	0.81[EUR][1000 genomes]
rs17292046	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2145930	0.81[EUR][1000 genomes]
rs56235203	0.80[EUR][1000 genomes]
rs6478111	0.81[EUR][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	nsv831695	chr9:117567626-117726247	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr9:117568800-117572800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:117568800-117576200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:117569000-117573000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr9:117569000-117573800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:117569200-117573600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr9:117569600-117573600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:117569800-117573400	Weak transcription	HMEC	breast
8	chr9:117569800-117573600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:117569800-117582600	Weak transcription	Pancreas	Pancrea
10	chr9:117571600-117572800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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