Variant report

Variant	rs16925083
Chromosome Location	chr9:108734485-108734486
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:108733704..108736486-chr9:108737620..108740615,3	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12001396	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12004099	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13302213	1.00[EUR][1000 genomes]
rs16925055	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16925065	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17285222	1.00[EUR][1000 genomes]
rs34235964	0.97[EUR][1000 genomes]
rs34773238	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34778810	0.83[EUR][1000 genomes]
rs35115335	0.82[EUR][1000 genomes]
rs56105641	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58788162	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs60607803	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61312776	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7031020	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs71494570	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs71494574	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7847775	0.92[AMR][1000 genomes]
rs7850106	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7861494	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893694	chr9:108486533-108854018	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv831679	chr9:108603112-108785347	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1047166	chr9:108693810-108921872	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108726800-108736800	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:108729000-108736800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:108731800-108734800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:108732200-108741000	Weak transcription	Brain Germinal Matrix	brain
5	chr9:108732400-108738400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:108732600-108735600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr9:108732600-108736200	Weak transcription	Fetal Brain Male	brain
8	chr9:108732600-108738000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr9:108732600-108738400	Weak transcription	Fetal Brain Female	brain
10	chr9:108732800-108734800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr9:108733000-108734600	Weak transcription	Brain Anterior Caudate	brain
12	chr9:108733400-108734800	Weak transcription	Brain Angular Gyrus	brain
13	chr9:108733400-108737000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:108733600-108734600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr9:108733600-108743000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:108733800-108735000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr9:108734000-108734600	Enhancers	Adipose Nuclei	Adipose
18	chr9:108734000-108735400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr9:108734200-108735200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr9:108734200-108735200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:108734200-108738400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:108734200-108738400	Enhancers	Brain Cingulate Gyrus	brain
23	chr9:108734400-108736200	Weak transcription	Fetal Kidney	kidney
24	chr9:108734400-108736800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:108734400-108738400	Enhancers	Brain Hippocampus Middle	brain
26	chr9:108734400-108740600	Enhancers	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links