Variant report

Variant	rs1523211
Chromosome Location	chr9:14937012-14937013
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10756628	0.89[ASN][1000 genomes]
rs10810293	0.81[ASN][1000 genomes]
rs10961796	0.92[ASN][1000 genomes]
rs12348103	0.86[ASN][1000 genomes]
rs12352935	0.94[EUR][1000 genomes]
rs1855141	0.97[ASN][1000 genomes]
rs4295763	0.87[ASN][1000 genomes]
rs7030532	0.83[ASN][1000 genomes]
rs7851561	0.86[ASN][1000 genomes]
rs7862132	0.86[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	nsv1029491	chr9:14033607-14942373	Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831518	chr9:14760638-14953501	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv892620	chr9:14922877-15086021	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv892621	chr9:14928013-15043692	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14925200-14945400	Weak transcription	Aorta	Aorta
2	chr9:14933000-14941800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:14933200-14957200	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:14934600-14937400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr9:14934600-14938200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:14935000-14937600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr9:14935200-14937200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr9:14935200-14937200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr9:14935200-14937200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:14935200-14937400	Enhancers	Colon Smooth Muscle	Colon
11	chr9:14935200-14937600	Enhancers	Fetal Stomach	stomach
12	chr9:14935200-14939200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:14935400-14937400	Enhancers	Fetal Brain Female	brain
14	chr9:14935800-14938800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:14936000-14937200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:14936200-14937200	Enhancers	Fetal Brain Male	brain
17	chr9:14936600-14937200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr9:14936600-14942000	Weak transcription	Fetal Kidney	kidney
19	chr9:14936800-14947200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:14937000-14937200	Enhancers	Fetal Lung	lung
21	chr9:14937000-14937600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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