Variant report

Variant	rs10781002
Chromosome Location	chr9:71138802-71138803
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:71121474..71124177-chr9:71138175..71140429,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10511958	0.82[GIH][hapmap]
rs10780962	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10780963	1.00[AMR][1000 genomes]
rs10780967	0.90[GIH][hapmap]
rs10780986	0.86[JPT][hapmap];0.84[LWK][hapmap]
rs10780999	0.86[JPT][hapmap]
rs10868851	0.90[GIH][hapmap]
rs10868852	0.90[GIH][hapmap]
rs10868877	0.90[GIH][hapmap];1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs10868961	0.81[AFR][1000 genomes]
rs10868984	0.83[CHB][hapmap];0.95[JPT][hapmap];0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs11142391	0.90[GIH][hapmap]
rs11142449	0.90[GIH][hapmap]
rs11142461	0.90[GIH][hapmap]
rs11142500	0.85[GIH][hapmap]
rs11142549	1.00[AMR][1000 genomes]
rs11142697	0.85[JPT][hapmap];0.81[AFR][1000 genomes]
rs12238439	0.82[GIH][hapmap]
rs12353500	0.82[GIH][hapmap]
rs12375820	0.81[JPT][hapmap]
rs13439981	0.90[GIH][hapmap]
rs1353009	0.82[GIH][hapmap]
rs1887887	0.86[AMR][1000 genomes]
rs265072	0.92[ASN][1000 genomes]
rs265073	0.86[JPT][hapmap];1.00[MEX][hapmap]
rs265083	0.87[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs265087	0.83[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs265089	0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs4745041	0.82[GIH][hapmap]
rs4745048	0.92[AMR][1000 genomes]
rs4745083	0.84[ASN][1000 genomes]
rs7019238	0.86[GIH][hapmap]
rs7034863	0.86[JPT][hapmap]
rs7855134	0.82[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427847	chr9:70318730-71153527	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv893413	chr9:71130848-71196984	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv893411	chr9:71130848-71199545	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv893412	chr9:71130848-71199545	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1024967	chr9:71130848-71210031	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv482506	chr9:71130848-71280888	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers 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	6 gene(s)	inside rSNPs	diseases
7	nsv466392	chr9:71130848-71318817	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv614546	chr9:71130848-71318817	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1026962	chr9:71130848-71357605	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1032210	chr9:71130848-71511987	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71117600-71142800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr9:71130200-71148000	Weak transcription	HSMMtube	muscle
3	chr9:71130600-71144400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:71130600-71144800	Weak transcription	Left Ventricle	heart
5	chr9:71130800-71145400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr9:71131000-71152600	Weak transcription	NHLF	lung
7	chr9:71131600-71145400	Weak transcription	Right Ventricle	heart
8	chr9:71133200-71139200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr9:71133200-71145400	Weak transcription	Fetal Intestine Small	intestine
10	chr9:71133200-71145600	Weak transcription	Aorta	Aorta
11	chr9:71133400-71143400	Weak transcription	Colon Smooth Muscle	Colon
12	chr9:71133600-71139600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:71134000-71144200	Weak transcription	Fetal Lung	lung
14	chr9:71136200-71139400	Enhancers	Placenta	Placenta
15	chr9:71136800-71141400	Strong transcription	Fetal Stomach	stomach
16	chr9:71137000-71144800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr9:71137600-71144200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:71137600-71156000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:71137800-71145400	Weak transcription	Fetal Heart	heart
20	chr9:71138000-71143800	Weak transcription	Fetal Muscle Leg	muscle
21	chr9:71138200-71143200	Weak transcription	Right Atrium	heart
22	chr9:71138200-71145600	Weak transcription	Gastric	stomach
23	chr9:71138200-71146000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr9:71138200-71146600	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr9:71138400-71144800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr9:71138400-71148400	Weak transcription	Esophagus	oesophagus
27	chr9:71138600-71145400	Weak transcription	Fetal Kidney	kidney
28	chr9:71138800-71143600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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