Variant report

Variant	rs11051985
Chromosome Location	chr12:32555090-32555091
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1055876	0.83[ASN][1000 genomes]
rs11051969	0.83[ASN][1000 genomes]
rs11051973	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11051975	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11051976	0.89[ASN][1000 genomes]
rs11051986	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11051987	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11051988	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11051989	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11051991	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11051992	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11052002	0.83[EUR][1000 genomes]
rs12227991	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12228004	0.84[ASN][1000 genomes]
rs12229856	0.83[ASN][1000 genomes]
rs2728709	0.85[EUR][1000 genomes]
rs4931013	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4931623	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56670459	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6488050	0.83[ASN][1000 genomes]
rs7132235	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7297381	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73084099	0.84[ASN][1000 genomes]
rs73084101	0.91[ASN][1000 genomes]
rs73086036	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73086040	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73088096	0.83[EUR][1000 genomes]
rs7309706	0.84[ASN][1000 genomes]
rs7313432	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv469346	chr12:32531220-32587465	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv558188	chr12:32531220-32587465	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1054191	chr12:32534619-32733066	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv541455	chr12:32534619-32733066	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	esv3342938	chr12:32551041-32716745	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32551800-32555200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:32552000-32555200	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr12:32552000-32555400	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr12:32553200-32555600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:32553400-32555200	Active TSS	Duodenum Mucosa	Duodenum
6	chr12:32553400-32555200	Weak transcription	Lung	lung
7	chr12:32553400-32572200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:32553400-32572200	Weak transcription	HSMMtube	muscle
9	chr12:32553400-32572400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr12:32553600-32555200	Weak transcription	Gastric	stomach
11	chr12:32553600-32555200	Weak transcription	Pancreas	Pancrea
12	chr12:32553600-32556000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr12:32553600-32572600	Weak transcription	Esophagus	oesophagus
14	chr12:32553800-32556000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr12:32553800-32571600	Weak transcription	Left Ventricle	heart
16	chr12:32554000-32555200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr12:32554000-32555200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr12:32554000-32572200	Weak transcription	Right Ventricle	heart
19	chr12:32554200-32555200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr12:32554200-32555600	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr12:32554200-32556000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr12:32554200-32556000	Enhancers	NHEK	skin
23	chr12:32554200-32559600	Weak transcription	A549	lung
24	chr12:32554200-32561200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr12:32554200-32566400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr12:32554200-32571800	Weak transcription	Ovary	ovary
27	chr12:32554200-32573800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:32554400-32555200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr12:32554400-32555200	Enhancers	Placenta	Placenta
30	chr12:32554400-32555800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:32554400-32556800	Weak transcription	Colonic Mucosa	Colon
32	chr12:32554400-32559800	Weak transcription	Psoas Muscle	Psoas
33	chr12:32554600-32555200	Weak transcription	Adipose Nuclei	Adipose
34	chr12:32554600-32555200	Weak transcription	Stomach Mucosa	stomach
35	chr12:32554600-32555200	Weak transcription	HMEC	breast
36	chr12:32554600-32555600	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr12:32554600-32556000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:32554600-32556200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr12:32554600-32557000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr12:32554600-32572400	Weak transcription	Fetal Intestine Large	intestine
41	chr12:32554600-32593200	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr12:32554800-32555200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr12:32554800-32555200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:32554800-32555200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:32554800-32555200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr12:32554800-32555800	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr12:32554800-32556000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr12:32554800-32556200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:32554800-32556800	Weak transcription	Liver	Liver
50	chr12:32555000-32555400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links