Variant report

Variant	rs56151073
Chromosome Location	chr12:50512200-50512201
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:50510457..50512619-chr12:50512712..50515354,2	MCF-7	breast:
2	chr12:50506379..50508104-chr12:50510403..50512251,3	K562	blood:
3	chr12:50512025..50513776-chr12:50559393..50561969,2	MCF-7	breast:
4	chr12:50504789..50507930-chr12:50509010..50512332,8	MCF-7	breast:
5	chr12:50510353..50512301-chr12:50513057..50515415,2	K562	blood:

Variant related genes	Relation type
ENSG00000139624	Chromatin interaction
ENSG00000178449	Chromatin interaction
ENSG00000272368	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10735822	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10735823	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10747571	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10783334	0.87[EUR][1000 genomes]
rs10783336	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10783337	0.81[EUR][1000 genomes]
rs10783339	0.84[EUR][1000 genomes]
rs10875999	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10876001	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10876002	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10876006	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10876007	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11169275	0.86[EUR][1000 genomes]
rs11169283	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11169284	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11169285	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12229758	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12314572	0.81[ASN][1000 genomes]
rs17124448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2008537	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2242507	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2277355	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55639096	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7131794	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7297864	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7306213	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7314598	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7316344	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7486874	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7953174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[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	nsv1045327	chr12:49975040-50551375	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
2	nsv541490	chr12:49975040-50551375	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
3	nsv530671	chr12:50233858-50708991	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
4	esv3392138	chr12:50394642-50645326	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
5	nsv558840	chr12:50449976-50523964	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50506800-50521000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:50506800-50523600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:50507000-50513000	Weak transcription	Esophagus	oesophagus
4	chr12:50507000-50513200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr12:50507000-50513200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:50507000-50513600	Weak transcription	Fetal Kidney	kidney
7	chr12:50507000-50513800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:50507000-50520800	Weak transcription	Fetal Lung	lung
9	chr12:50507000-50520800	Weak transcription	NH-A	brain
10	chr12:50507000-50522400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr12:50507000-50522800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr12:50507000-50522800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr12:50507000-50523600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr12:50507000-50537400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr12:50507000-50539600	Weak transcription	Stomach Mucosa	stomach
16	chr12:50507200-50512600	Weak transcription	HMEC	breast
17	chr12:50507200-50512800	Weak transcription	Brain Germinal Matrix	brain
18	chr12:50507200-50513000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr12:50507200-50513000	Weak transcription	Osteobl	bone
20	chr12:50507200-50513200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr12:50507200-50513200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:50507200-50513800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr12:50507200-50515400	Weak transcription	Fetal Brain Male	brain
24	chr12:50507200-50519000	Weak transcription	HUVEC	blood vessel
25	chr12:50507200-50520800	Weak transcription	NHDF-Ad	bronchial
26	chr12:50507200-50520800	Weak transcription	NHLF	lung
27	chr12:50507200-50521400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr12:50507200-50522600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr12:50507200-50523600	Weak transcription	Right Atrium	heart
30	chr12:50507200-50532000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr12:50507400-50513200	Weak transcription	Brain Anterior Caudate	brain
32	chr12:50507400-50514600	Genic enhancers	Primary T cells fromperipheralblood	blood
33	chr12:50508000-50512800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr12:50508000-50513200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr12:50508000-50513200	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr12:50508000-50513200	Weak transcription	Aorta	Aorta
37	chr12:50508400-50512600	Weak transcription	K562	blood
38	chr12:50508400-50513000	Weak transcription	HepG2	liver
39	chr12:50508400-50513400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr12:50508400-50513800	Weak transcription	Colonic Mucosa	Colon
41	chr12:50508400-50518200	Strong transcription	Fetal Stomach	stomach
42	chr12:50508600-50513400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr12:50508600-50518200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr12:50508600-50518200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr12:50508800-50518000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:50509200-50512400	Strong transcription	Thymus	Thymus
47	chr12:50509200-50518200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr12:50509200-50518400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr12:50509400-50512400	Strong transcription	Primary T cells from cord blood	blood
50	chr12:50509400-50518000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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