Variant report

Variant	rs10123011
Chromosome Location	chr9:16470462-16470463
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10118670	0.89[ASN][1000 genomes]
rs10810567	0.88[ASN][1000 genomes]
rs10962446	0.80[ASN][1000 genomes]
rs11788735	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11793518	0.96[ASN][1000 genomes]
rs2274557	0.90[ASN][1000 genomes]
rs755180	0.90[ASN][1000 genomes]
rs7874842	0.86[EUR][1000 genomes]
rs997693	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16457800-16493400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:16459600-16470800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:16459600-16482400	Weak transcription	A549	lung
4	chr9:16459600-16499800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:16459600-16500000	Weak transcription	NHLF	lung
6	chr9:16460800-16485400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr9:16462000-16470600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr9:16462000-16476400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr9:16462200-16474000	Weak transcription	Fetal Lung	lung
10	chr9:16463200-16470600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr9:16463200-16478000	Weak transcription	Ovary	ovary
12	chr9:16463200-16483800	Weak transcription	Fetal Stomach	stomach
13	chr9:16468400-16473400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr9:16469200-16476000	Weak transcription	Osteobl	bone
15	chr9:16469800-16475600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:16470400-16471000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:16470400-16471000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:16470400-16471200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:16470400-16471200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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