Variant report

Variant	rs73582234
Chromosome Location	chr11:120262468-120262469
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120256139..120258853-chr11:120261413..120263735,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17123835	1.00[AMR][1000 genomes]
rs55816695	1.00[AMR][1000 genomes]
rs7110919	1.00[AMR][1000 genomes]
rs73578290	1.00[AMR][1000 genomes]
rs73582257	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73582276	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73582290	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73584104	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7927594	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7945341	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv529003	chr11:120209386-120355230	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1050935	chr11:120224544-120276373	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1036694	chr11:120230243-120285603	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1037573	chr11:120230243-120286918	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1047982	chr11:120238962-120276373	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1050789	chr11:120238962-120286918	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1046430	chr11:120238962-120294026	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1043248	chr11:120238962-120299598	Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv1051672	chr11:120238962-120314178	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv1050709	chr11:120246224-120276373	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1051783	chr11:120246224-120314178	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120232000-120274800	Weak transcription	Ovary	ovary
2	chr11:120254600-120265000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:120254600-120266400	Weak transcription	Gastric	stomach
4	chr11:120254600-120271000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:120257800-120263200	Weak transcription	NHLF	lung
6	chr11:120258000-120263000	Weak transcription	Osteobl	bone
7	chr11:120258000-120263400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:120258200-120262800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr11:120258200-120262800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:120260600-120262800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:120260600-120262800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:120260600-120262800	Enhancers	HUVEC	blood vessel
13	chr11:120260600-120263200	Enhancers	Liver	Liver
14	chr11:120260800-120262600	Enhancers	A549	lung
15	chr11:120260800-120263000	Enhancers	Stomach Mucosa	stomach
16	chr11:120260800-120263600	Enhancers	Fetal Intestine Large	intestine
17	chr11:120260800-120263600	Enhancers	HMEC	breast
18	chr11:120260800-120263800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:120260800-120263800	Enhancers	Fetal Intestine Small	intestine
20	chr11:120261000-120263200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr11:120261000-120263600	Enhancers	Adipose Nuclei	Adipose
22	chr11:120261000-120263600	Enhancers	Brain Hippocampus Middle	brain
23	chr11:120261000-120263600	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr11:120261000-120263800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr11:120261000-120263800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:120261000-120263800	Enhancers	Brain Cingulate Gyrus	brain
27	chr11:120261000-120264000	Enhancers	Brain Anterior Caudate	brain
28	chr11:120261200-120263600	Enhancers	Brain Angular Gyrus	brain
29	chr11:120261200-120263600	Enhancers	Colon Smooth Muscle	Colon
30	chr11:120261200-120263800	Enhancers	Brain Substantia Nigra	brain
31	chr11:120261200-120263800	Enhancers	NHEK	skin
32	chr11:120261200-120264000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:120261200-120271400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:120261400-120262600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr11:120261400-120263200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:120261600-120262800	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr11:120261600-120263400	Enhancers	Fetal Heart	heart
38	chr11:120261600-120263800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr11:120261800-120262600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr11:120261800-120262600	Enhancers	Small Intestine	intestine
41	chr11:120261800-120262800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr11:120261800-120263000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:120261800-120263200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr11:120262000-120262800	Enhancers	Psoas Muscle	Psoas
45	chr11:120262000-120262800	Weak transcription	Rectal Smooth Muscle	rectum
46	chr11:120262000-120263000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:120262000-120263000	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr11:120262000-120263000	Enhancers	Fetal Kidney	kidney
49	chr11:120262000-120263400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr11:120262000-120263400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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