Variant report

Variant	rs13432334
Chromosome Location	chr2:11851023-11851024
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:11837517..11840283-chr2:11849750..11852700,2	MCF-7	breast:
2	chr2:11850587..11853159-chr2:11857216..11858736,3	K562	blood:
3	chr2:11850587..11853159-chr2:11857216..11858736,2	K562	blood:
4	chr2:11850515..11852161-chr2:11877592..11880491,2	MCF-7	breast:
5	chr2:11850883..11854568-chr2:11860179..11862646,3	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10164822	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10179409	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10182021	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10206665	0.94[YRI][hapmap];0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10209047	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11683832	0.89[AFR][1000 genomes]
rs13386239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13387137	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13390584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13398067	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13407243	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13407481	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13420573	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13426765	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13428600	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13431864	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4622687	0.83[EUR][1000 genomes]
rs55773509	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57281558	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58196703	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs59844400	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66763856	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6708244	1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716051	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6716192	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6725991	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6736015	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6748533	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7560325	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7570592	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7573725	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7574891	0.92[AFR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7580112	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7588803	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7591517	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9287737	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9287738	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS 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 miRNA	26 gene(s)	inside rSNPs	diseases
4	nsv469449	chr2:11808654-11854012	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv580972	chr2:11808654-11854012	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11844200-11854200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr2:11844600-11856400	Weak transcription	Psoas Muscle	Psoas
3	chr2:11848600-11852200	Weak transcription	Placenta	Placenta
4	chr2:11848800-11854600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:11848800-11855400	Weak transcription	Pancreas	Pancrea
6	chr2:11849000-11854400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:11849400-11852800	Enhancers	Brain Cingulate Gyrus	brain
8	chr2:11849800-11851200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:11849800-11851400	Enhancers	HMEC	breast
10	chr2:11849800-11851400	Enhancers	NH-A	brain
11	chr2:11849800-11852000	Enhancers	Colon Smooth Muscle	Colon
12	chr2:11849800-11852800	Enhancers	NHLF	lung
13	chr2:11849800-11853200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:11849800-11853200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr2:11849800-11853400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:11850000-11851400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:11850000-11851400	Enhancers	Rectal Smooth Muscle	rectum
18	chr2:11850000-11851400	Enhancers	NHEK	skin
19	chr2:11850000-11851600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:11850000-11851600	Enhancers	NHDF-Ad	bronchial
21	chr2:11850000-11851600	Enhancers	Osteobl	bone
22	chr2:11850000-11852000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:11850000-11852000	Enhancers	Stomach Smooth Muscle	stomach
24	chr2:11850000-11852600	Enhancers	Brain Substantia Nigra	brain
25	chr2:11850000-11852600	Enhancers	Ovary	ovary
26	chr2:11850200-11851400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:11850200-11851400	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr2:11850200-11851400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr2:11850200-11851800	Enhancers	Fetal Lung	lung
30	chr2:11850200-11851800	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr2:11850200-11852000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:11850200-11852000	Enhancers	Fetal Stomach	stomach
33	chr2:11850200-11852600	Enhancers	Brain Hippocampus Middle	brain
34	chr2:11850200-11852800	Enhancers	Brain Angular Gyrus	brain
35	chr2:11850400-11851800	Enhancers	Fetal Heart	heart
36	chr2:11850400-11852200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:11850400-11853000	Enhancers	Brain Anterior Caudate	brain
38	chr2:11850600-11851400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr2:11850600-11851400	Enhancers	HSMMtube	muscle
40	chr2:11850600-11852000	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr2:11850600-11856400	Weak transcription	Hela-S3	cervix
42	chr2:11850800-11851800	Weak transcription	Aorta	Aorta
43	chr2:11850800-11852600	Active TSS	Esophagus	oesophagus
44	chr2:11850800-11852600	Enhancers	Fetal Muscle Leg	muscle
45	chr2:11850800-11853200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:11850800-11856200	Weak transcription	Right Atrium	heart
47	chr2:11851000-11851400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:11851000-11851600	Enhancers	Liver	Liver
49	chr2:11851000-11851800	Enhancers	Fetal Brain Male	brain
50	chr2:11851000-11852600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links