Variant report

Variant	rs7850003
Chromosome Location	chr9:116108231-116108232
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:116106104..116109704-chr9:116111339..116114258,3	K562	blood:

Variant related genes	Relation type
ENSG00000119411	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10114352	0.84[AFR][1000 genomes]
rs10120336	0.84[AFR][1000 genomes]
rs10122035	0.84[AFR][1000 genomes]
rs10124515	0.85[ASN][1000 genomes]
rs10481672	0.84[AFR][1000 genomes]
rs10481675	0.92[AFR][1000 genomes]
rs10817477	0.96[EUR][1000 genomes]
rs10981711	0.84[EUR][1000 genomes]
rs10981714	0.94[EUR][1000 genomes]
rs10981718	0.94[EUR][1000 genomes]
rs10981719	0.94[EUR][1000 genomes]
rs10981721	0.91[EUR][1000 genomes]
rs10981725	0.94[EUR][1000 genomes]
rs10981734	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10981736	0.96[EUR][1000 genomes]
rs10981753	0.92[AFR][1000 genomes]
rs10981754	0.94[EUR][1000 genomes]
rs11787602	0.83[ASN][1000 genomes]
rs12347798	0.84[AFR][1000 genomes]
rs12350332	0.84[AFR][1000 genomes]
rs12350377	0.84[AFR][1000 genomes]
rs12352852	0.84[AFR][1000 genomes]
rs12352895	0.84[AFR][1000 genomes]
rs12684385	0.96[EUR][1000 genomes]
rs13289574	1.00[EUR][1000 genomes]
rs16932083	0.94[EUR][1000 genomes]
rs16932730	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16932806	0.98[EUR][1000 genomes]
rs2296075	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2296076	0.96[EUR][1000 genomes]
rs2418249	0.92[EUR][1000 genomes]
rs28480972	0.86[EUR][1000 genomes]
rs28488898	0.84[AFR][1000 genomes]
rs28597401	0.92[AFR][1000 genomes]
rs28725394	0.92[AFR][1000 genomes]
rs34289746	0.86[EUR][1000 genomes]
rs34294772	0.96[EUR][1000 genomes]
rs34429100	1.00[EUR][1000 genomes]
rs34749539	0.86[EUR][1000 genomes]
rs35275471	1.00[EUR][1000 genomes]
rs35772163	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35860025	1.00[EUR][1000 genomes]
rs35915957	0.85[EUR][1000 genomes]
rs3810920	0.94[EUR][1000 genomes]
rs59841233	0.94[EUR][1000 genomes]
rs61161242	0.86[EUR][1000 genomes]
rs6478004	0.83[ASN][1000 genomes]
rs6478005	0.83[ASN][1000 genomes]
rs71503561	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7873862	0.88[ASN][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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1042663	chr9:115920158-116167140	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv893744	chr9:115934852-116170227	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7850003	CDC26	cis	lung	GTEx

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116103000-116111800	Weak transcription	Lung	lung
2	chr9:116103200-116108600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:116103200-116108800	Weak transcription	Placenta	Placenta
4	chr9:116103200-116110000	Weak transcription	Right Atrium	heart
5	chr9:116103200-116111400	Weak transcription	Stomach Mucosa	stomach
6	chr9:116103200-116111400	Weak transcription	GM12878-XiMat	blood
7	chr9:116104000-116108400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr9:116105400-116108800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:116105800-116110200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr9:116105800-116111400	Enhancers	Fetal Intestine Small	intestine
11	chr9:116105800-116111400	Weak transcription	Right Ventricle	heart
12	chr9:116106200-116111400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr9:116106400-116108800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:116106400-116109200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr9:116106400-116110400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr9:116106600-116109400	Weak transcription	Colonic Mucosa	Colon
17	chr9:116106600-116110000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:116106600-116111400	Weak transcription	Liver	Liver
19	chr9:116106600-116111400	Weak transcription	Esophagus	oesophagus
20	chr9:116106600-116111400	Weak transcription	Pancreas	Pancrea
21	chr9:116106600-116111800	Weak transcription	K562	blood
22	chr9:116107200-116108800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr9:116107600-116111600	Weak transcription	Colon Smooth Muscle	Colon
24	chr9:116107800-116110000	Weak transcription	Primary hematopoietic stem cells	blood
25	chr9:116107800-116110000	Weak transcription	Small Intestine	intestine
26	chr9:116107800-116111200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr9:116108000-116108400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr9:116108000-116110000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr9:116108000-116110000	Weak transcription	Fetal Heart	heart
30	chr9:116108000-116111400	Weak transcription	Brain Anterior Caudate	brain
31	chr9:116108000-116111600	Weak transcription	Brain Angular Gyrus	brain
32	chr9:116108000-116112000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr9:116108200-116109600	Weak transcription	Fetal Intestine Large	intestine
34	chr9:116108200-116109600	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr9:116108200-116111200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr9:116108200-116112000	Weak transcription	Brain Substantia Nigra	brain

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