Variant report

Variant	rs10131798
Chromosome Location	chr14:65652051-65652052
allele	A/C
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:17)

rs_ID	r²[population]
rs55650089	0.93[EUR][1000 genomes]
rs57176753	0.89[EUR][1000 genomes]
rs57341434	0.89[EUR][1000 genomes]
rs57901560	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58501174	0.89[EUR][1000 genomes]
rs61244338	0.93[EUR][1000 genomes]
rs61607569	0.93[EUR][1000 genomes]
rs7154885	0.90[EUR][1000 genomes]
rs7155272	0.93[EUR][1000 genomes]
rs7160899	0.97[EUR][1000 genomes]
rs74056693	0.93[EUR][1000 genomes]
rs74056696	0.92[EUR][1000 genomes]
rs74056698	0.92[EUR][1000 genomes]
rs74056699	0.93[EUR][1000 genomes]
rs74056700	0.93[EUR][1000 genomes]
rs8020793	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8022029	0.93[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	nsv832817	chr14:65637069-65810406	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65641600-65653400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:65641600-65653600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:65641600-65658200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:65641800-65653600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:65647800-65659800	Weak transcription	Fetal Intestine Large	intestine
6	chr14:65648200-65652400	Weak transcription	Pancreas	Pancrea
7	chr14:65650000-65653200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:65651000-65653800	Enhancers	Fetal Heart	heart
9	chr14:65651200-65653200	Weak transcription	GM12878-XiMat	blood
10	chr14:65651200-65654400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr14:65651400-65652400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:65651400-65652400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:65651400-65654400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr14:65651400-65658200	Weak transcription	H1 BMP4 Derived Mesendoderm 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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