Variant report

Variant	rs72704374
Chromosome Location	chr9:8895843-8895844
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:7844225..7844973-chr9:8895548..8896327,4	MCF-7	breast:
2	chr9:7569797..7570734-chr9:8895690..8896630,4	MCF-7	breast:
3	chr9:8485590..8486306-chr9:8895648..8896453,2	MCF-7	breast:
4	chr9:7569880..7570683-chr9:8895710..8896327,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000153707	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1019955	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10511511	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10977342	0.87[ASN][1000 genomes]
rs12551425	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12551480	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12551769	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12552171	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12552175	0.86[EUR][1000 genomes]
rs12552247	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12552617	0.90[EUR][1000 genomes]
rs12554855	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1433541	0.89[ASN][1000 genomes]
rs1433542	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1897671	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2016766	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34657422	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34958914	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35114587	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57781824	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59834115	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7027460	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72704370	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72704378	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72704379	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72704381	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72706221	0.82[EUR][1000 genomes]
rs976385	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	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
3	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
4	nsv1015898	chr9:8753534-9011443	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv892242	chr9:8879472-8941668	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv892243	chr9:8885476-8898464	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv892244	chr9:8889419-8898464	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8891600-8896400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:8892400-8899400	Weak transcription	Brain Angular Gyrus	brain
3	chr9:8894600-8896200	Enhancers	Fetal Lung	lung
4	chr9:8894800-8896000	Enhancers	Brain Substantia Nigra	brain
5	chr9:8895000-8897600	Enhancers	Fetal Heart	heart
6	chr9:8895400-8896200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:8895600-8896000	Enhancers	Adipose Nuclei	Adipose
8	chr9:8895600-8896000	Active TSS	Brain Hippocampus Middle	brain
9	chr9:8895600-8896000	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr9:8895600-8896000	Active TSS	Psoas Muscle	Psoas
11	chr9:8895600-8896000	Active TSS	Stomach Smooth Muscle	stomach
12	chr9:8895600-8896200	Enhancers	Fetal Muscle Leg	muscle
13	chr9:8895600-8896200	Enhancers	Ovary	ovary
14	chr9:8895600-8896400	Active TSS	Brain Anterior Caudate	brain
15	chr9:8895800-8896600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:8895800-8899400	Weak transcription	Brain Cingulate Gyrus	brain

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