Variant report

Variant	rs9481788
Chromosome Location	chr6:118731124-118731125
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10080340	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10155773	0.80[AFR][1000 genomes]
rs10214801	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10457339	0.80[AFR][1000 genomes]
rs10457340	0.80[AFR][1000 genomes]
rs11153749	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11153751	1.00[EUR][1000 genomes]
rs11153762	0.80[AFR][1000 genomes]
rs12191529	0.80[AFR][1000 genomes]
rs12191962	0.86[EUR][1000 genomes]
rs12198458	0.85[EUR][1000 genomes]
rs12199189	1.00[EUR][1000 genomes]
rs12199190	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12199786	1.00[EUR][1000 genomes]
rs12202832	1.00[EUR][1000 genomes]
rs12202932	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12203556	1.00[EUR][1000 genomes]
rs12206369	0.80[AFR][1000 genomes]
rs12206459	0.80[AFR][1000 genomes]
rs12207121	1.00[EUR][1000 genomes]
rs12207554	0.80[AFR][1000 genomes]
rs12209500	0.80[AFR][1000 genomes]
rs12212089	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12215706	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13328242	0.80[AFR][1000 genomes]
rs13437148	0.80[AFR][1000 genomes]
rs13437314	0.80[AFR][1000 genomes]
rs6903291	0.80[AFR][1000 genomes]
rs6903632	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6904070	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6904344	0.80[AFR][1000 genomes]
rs6934770	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6939873	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7743702	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7755203	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7759420	1.00[EUR][1000 genomes]
rs7764014	0.80[AFR][1000 genomes]
rs9320657	0.80[AFR][1000 genomes]
rs9387573	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9387582	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9398488	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9401069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481786	0.82[EUR][1000 genomes]
rs9481793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481796	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481809	0.87[EUR][1000 genomes]
rs9481812	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9481818	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9481822	0.80[AFR][1000 genomes]
rs9481823	0.80[AFR][1000 genomes]
rs9481824	0.80[AFR][1000 genomes]
rs9481829	0.80[AFR][1000 genomes]
rs9481830	0.80[AFR][1000 genomes]
rs9481835	0.80[AFR][1000 genomes]
rs9489363	1.00[EUR][1000 genomes]
rs9489364	0.82[EUR][1000 genomes]
rs9489365	0.88[AFR][1000 genomes]
rs9489370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489374	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489382	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489398	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9489402	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9489408	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9489410	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9489415	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9489422	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9489430	0.80[AFR][1000 genomes]
rs9489434	0.80[AFR][1000 genomes]
rs9489435	0.80[AFR][1000 genomes]
rs9489451	0.80[AFR][1000 genomes]
rs9489464	0.80[AFR][1000 genomes]
rs9489468	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv830787	chr6:118631902-118805106	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription 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	9 gene(s)	inside rSNPs	diseases
10	nsv604555	chr6:118695049-118856822	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
11	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
12	nsv1025097	chr6:118699752-119058789	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
13	nsv1020586	chr6:118711098-118900012	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
14	nsv532052	chr6:118711850-119057295	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv432959	chr6:118716318-119010307	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
16	nsv604556	chr6:118722589-119065365	Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
17	nsv432960	chr6:118723307-118826307	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
18	nsv525179	chr6:118726243-118876092	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118715800-118731800	Weak transcription	Pancreas	Pancrea
2	chr6:118721400-118731200	Weak transcription	Gastric	stomach
3	chr6:118730400-118745000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links