Variant report

Variant	rs10116513
Chromosome Location	chr9:2686871-2686872
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10114279	0.88[AFR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10116375	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10117473	0.93[EUR][1000 genomes]
rs10124200	0.84[EUR][1000 genomes]
rs10125245	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10757628	0.94[EUR][1000 genomes]
rs10812468	0.80[EUR][1000 genomes]
rs10812469	0.80[EUR][1000 genomes]
rs10812470	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10812471	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10812472	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10812473	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10812474	0.88[EUR][1000 genomes]
rs10812475	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10812481	0.81[EUR][1000 genomes]
rs10967492	0.92[EUR][1000 genomes]
rs10967512	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10967526	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10967529	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10967570	0.80[EUR][1000 genomes]
rs28473277	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530929	chr9:1998911-2925112	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv916750	chr9:2430846-2826706	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv531564	chr9:2452325-2700375	Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1017581	chr9:2494815-3172020	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv539934	chr9:2494815-3172020	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv892077	chr9:2663639-2690980	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv892078	chr9:2668085-2705874	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv466084	chr9:2681397-2710537	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv613138	chr9:2681397-2710537	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv892079	chr9:2681430-2931341	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv531565	chr9:2682523-2784028	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr9:2679400-2692400	Weak transcription	Psoas Muscle	Psoas
2	chr9:2680400-2687600	Weak transcription	Aorta	Aorta
3	chr9:2686600-2687000	Enhancers	Esophagus	oesophagus
4	chr9:2686800-2687000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:2686800-2687000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:2686800-2687200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr9:2686800-2687200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:2686800-2687200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:2686800-2687200	Enhancers	Placenta	Placenta
10	chr9:2686800-2687200	Enhancers	Right Atrium	heart
11	chr9:2686800-2687400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr9:2686800-2687400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr9:2686800-2687400	Enhancers	Ovary	ovary
14	chr9:2686800-2688600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links