Variant report

Variant	rs60982740
Chromosome Location	chr9:14912663-14912664
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:9)

rs_ID	r²[population]
rs10961790	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12002382	0.92[ASN][1000 genomes]
rs59947970	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60446733	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73419715	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73642461	0.95[ASN][1000 genomes]
rs73642463	0.92[ASN][1000 genomes]
rs73642464	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7870510	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029491	chr9:14033607-14942373	Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831518	chr9:14760638-14953501	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1018416	chr9:14846753-14921247	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14907400-14915000	Weak transcription	Small Intestine	intestine
2	chr9:14910400-14921000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:14910800-14913000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:14910800-14915800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr9:14911000-14912800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr9:14911000-14913400	Enhancers	Fetal Lung	lung
7	chr9:14911200-14912800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:14911200-14913200	Enhancers	Fetal Kidney	kidney
9	chr9:14911400-14912800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:14911400-14912800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr9:14912400-14913800	Enhancers	HepG2	liver
12	chr9:14912600-14912800	Enhancers	Fetal Heart	heart
13	chr9:14912600-14913400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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