Variant report

Variant	rs16929473
Chromosome Location	chr9:12767086-12767087
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10960766	0.86[EUR][1000 genomes]
rs10960767	0.86[EUR][1000 genomes]
rs10960768	0.86[EUR][1000 genomes]
rs11787674	0.81[EUR][1000 genomes]
rs11787999	0.85[CEU][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs11788192	0.86[EUR][1000 genomes]
rs11789339	0.93[EUR][1000 genomes]
rs11789481	0.98[EUR][1000 genomes]
rs11789805	0.93[EUR][1000 genomes]
rs11791137	0.88[EUR][1000 genomes]
rs11791392	0.83[EUR][1000 genomes]
rs11791954	0.81[EUR][1000 genomes]
rs11793178	0.93[EUR][1000 genomes]
rs11793280	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs11793312	0.82[YRI][hapmap]
rs11794050	0.86[EUR][1000 genomes]
rs11794202	0.86[EUR][1000 genomes]
rs11795082	0.88[EUR][1000 genomes]
rs12001299	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs12001737	0.86[EUR][1000 genomes]
rs12001745	0.86[EUR][1000 genomes]
rs12001885	0.86[EUR][1000 genomes]
rs12001964	0.86[EUR][1000 genomes]
rs12005881	0.86[EUR][1000 genomes]
rs16929383	0.83[EUR][1000 genomes]
rs16929385	0.83[EUR][1000 genomes]
rs16929391	0.83[EUR][1000 genomes]
rs16929400	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs17280279	0.85[CEU][hapmap]
rs17280629	0.83[EUR][1000 genomes]
rs17346748	0.83[EUR][1000 genomes]
rs2209278	0.85[CEU][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs34509359	0.83[EUR][1000 genomes]
rs35238630	0.93[EUR][1000 genomes]
rs35852762	0.86[EUR][1000 genomes]
rs35866166	0.83[EUR][1000 genomes]
rs3891858	0.81[EUR][1000 genomes]
rs41306290	0.83[EUR][1000 genomes]
rs61758391	0.81[EUR][1000 genomes]
rs61758394	0.81[EUR][1000 genomes]
rs62638049	0.81[EUR][1000 genomes]
rs7025241	0.86[EUR][1000 genomes]
rs7025758	0.86[EUR][1000 genomes]
rs7026121	0.86[EUR][1000 genomes]
rs7026199	0.86[EUR][1000 genomes]
rs7030751	0.90[EUR][1000 genomes]
rs7033962	0.90[EUR][1000 genomes]
rs7040346	0.83[EUR][1000 genomes]
rs7041590	0.86[EUR][1000 genomes]
rs7041735	0.86[EUR][1000 genomes]
rs71507329	0.85[EUR][1000 genomes]
rs73402088	1.00[EUR][1000 genomes]
rs73402092	1.00[EUR][1000 genomes]
rs768617	0.83[EUR][1000 genomes]
rs7875424	0.83[EUR][1000 genomes]
rs7876041	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759671	chr9:12235048-12784092	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1034393	chr9:12278703-12798236	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv869288	chr9:12286919-12816766	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv498136	chr9:12387840-12984158	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv1029415	chr9:12424340-12794623	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv540064	chr9:12424340-12794623	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	esv2422212	chr9:12448789-13127738	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	esv2758182	chr9:12621991-12784092	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv613613	chr9:12641987-12773263	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1030835	chr9:12717405-12840928	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats 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
11	nsv892573	chr9:12730636-12874703	Enhancers Weak transcription Active TSS ZNF genes & repeats 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	10 gene(s)	inside rSNPs	diseases
12	nsv892574	chr9:12754969-12918226	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12761200-12771800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:12761600-12774800	Weak transcription	NHLF	lung
3	chr9:12765400-12770000	Weak transcription	Fetal Intestine Large	intestine
4	chr9:12765400-12772000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr9:12766000-12767200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:12766800-12770000	Weak transcription	Fetal Intestine Small	intestine
7	chr9:12766800-12770200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:12766800-12771400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr9:12766800-12774800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr9:12766800-12774800	Weak transcription	HSMMtube	muscle
11	chr9:12767000-12767400	Weak transcription	Fetal Lung	lung
12	chr9:12767000-12771800	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links