Variant report

Variant	rs1335349
Chromosome Location	chr9:117964874-117964875
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10759761	0.82[YRI][hapmap];0.81[AFR][1000 genomes]
rs10817723	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1335343	0.85[YRI][hapmap]
rs1335350	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1414145	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1414146	0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs4978627	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62577989	0.84[ASN][1000 genomes]
rs7024589	0.92[JPT][hapmap];0.82[EUR][1000 genomes]
rs7032660	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7040243	0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs7849266	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7851185	0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7866695	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831697	chr9:117860416-118023927	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893769	chr9:117936903-117985886	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117955600-117969000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:117959400-117968600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:117960600-117967400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:117960600-117969000	Weak transcription	Spleen	Spleen
5	chr9:117960800-117965000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:117960800-117968800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:117960800-117969400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:117960800-117975800	Weak transcription	Fetal Kidney	kidney
9	chr9:117961600-117965600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:117962200-117972600	Enhancers	NHDF-Ad	bronchial
11	chr9:117962400-117966400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:117962400-117972400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:117963000-117965600	Enhancers	Adipose Nuclei	Adipose
14	chr9:117963000-117972600	Enhancers	NHEK	skin
15	chr9:117963000-117972600	Enhancers	Osteobl	bone
16	chr9:117963000-117977200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr9:117963200-117969800	Enhancers	NHLF	lung
18	chr9:117963600-117965200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr9:117963600-117967000	Weak transcription	HSMM	muscle
20	chr9:117963600-117969000	Weak transcription	Esophagus	oesophagus
21	chr9:117963800-117965000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr9:117963800-117965400	Weak transcription	Psoas Muscle	Psoas
23	chr9:117963800-117966000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:117963800-117967000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:117963800-117967800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:117964000-117965200	Weak transcription	HMEC	breast
27	chr9:117964200-117966200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:117964400-117966000	Enhancers	Colon Smooth Muscle	Colon
29	chr9:117964400-117966000	Enhancers	Fetal Muscle Leg	muscle
30	chr9:117964600-117966000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:117964600-117966000	Enhancers	Fetal Lung	lung
32	chr9:117964600-117966200	Enhancers	Fetal Stomach	stomach
33	chr9:117964600-117970000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:117964600-117972800	Enhancers	NH-A	brain

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