Variant report

Variant	rs67807514
Chromosome Location	chr9:8727206-8727207
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10977264	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10977265	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10977266	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12002364	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12003700	0.83[AFR][1000 genomes]
rs12004150	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12005542	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55840753	1.00[ASN][1000 genomes]
rs56189765	1.00[ASN][1000 genomes]
rs56227950	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58302765	1.00[ASN][1000 genomes]
rs58997119	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61070023	1.00[ASN][1000 genomes]
rs61188633	1.00[ASN][1000 genomes]
rs66523670	1.00[ASN][1000 genomes]
rs67646591	1.00[ASN][1000 genomes]
rs7042240	1.00[ASN][1000 genomes]
rs72700400	1.00[ASN][1000 genomes]
rs73427580	1.00[ASN][1000 genomes]
rs73429608	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv892235	chr9:8700396-8865925	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv6474	chr9:8706602-8751414	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1025800	chr9:8712487-9030627	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv539980	chr9:8712487-9030627	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3404858	chr9:8725852-8727850	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8704400-8731800	Weak transcription	Fetal Lung	lung
2	chr9:8710600-8733600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:8716200-8732600	Weak transcription	Fetal Brain Female	brain
4	chr9:8718400-8733600	Weak transcription	Psoas Muscle	Psoas
5	chr9:8718800-8730800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:8718800-8732800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:8719000-8730800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:8719000-8733200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:8719000-8733200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:8720600-8731800	Weak transcription	Brain Anterior Caudate	brain
11	chr9:8720600-8732600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:8721000-8728800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:8721000-8732200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr9:8722000-8744600	Weak transcription	Dnd41	blood
15	chr9:8723400-8730400	Weak transcription	Primary hematopoietic stem cells	blood
16	chr9:8723400-8732800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr9:8723600-8730800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:8724600-8727400	Weak transcription	Fetal Kidney	kidney
19	chr9:8724600-8730800	Weak transcription	Brain Angular Gyrus	brain
20	chr9:8724800-8732400	Weak transcription	Brain Substantia Nigra	brain
21	chr9:8724800-8733400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:8725000-8732200	Weak transcription	Fetal Muscle Leg	muscle
23	chr9:8725000-8733200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr9:8725000-8733600	Weak transcription	Ovary	ovary
25	chr9:8725800-8733200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr9:8727000-8733600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:8727200-8727400	Enhancers	Brain Germinal Matrix	brain
28	chr9:8727200-8727600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:8727200-8727600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr9:8727200-8727800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links