Variant report

Variant	rs11625798
Chromosome Location	chr14:31630918-31630919
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11620816	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11622403	0.88[CEU][hapmap];0.96[EUR][1000 genomes]
rs11624437	0.86[CEU][hapmap]
rs11625570	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs11626343	0.97[EUR][1000 genomes]
rs11845860	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11848094	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11848563	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17097688	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs17097735	1.00[CEU][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17097741	0.86[CEU][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17097743	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34039100	0.87[EUR][1000 genomes]
rs34684806	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34745649	0.97[EUR][1000 genomes]
rs3954287	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs45610935	0.88[EUR][1000 genomes]
rs55907561	0.83[EUR][1000 genomes]
rs56168081	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56346233	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs57000706	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57893693	0.97[EUR][1000 genomes]
rs58071351	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58204331	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58771204	0.88[EUR][1000 genomes]
rs59458716	0.97[EUR][1000 genomes]
rs59933112	0.96[EUR][1000 genomes]
rs60350855	0.96[EUR][1000 genomes]
rs60928004	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61592116	0.96[EUR][1000 genomes]
rs66528205	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs67960414	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72670334	0.86[EUR][1000 genomes]
rs72670351	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72670364	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72670371	0.97[EUR][1000 genomes]
rs72670374	0.97[EUR][1000 genomes]
rs72670375	0.97[EUR][1000 genomes]
rs72670377	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72670385	0.97[EUR][1000 genomes]
rs72670390	0.97[EUR][1000 genomes]
rs72670391	0.97[EUR][1000 genomes]
rs72670396	0.97[EUR][1000 genomes]
rs72670398	0.94[EUR][1000 genomes]
rs72670399	0.97[EUR][1000 genomes]
rs9888564	1.00[CEU][hapmap];0.97[EUR][1000 genomes];0.83[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	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv832763	chr14:31501597-31680021	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1050054	chr14:31501703-31733642	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv1043033	chr14:31538984-31686696	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv901588	chr14:31595666-31639111	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31563800-31650000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:31564800-31648600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr14:31565600-31648000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:31566200-31635200	Strong transcription	Placenta	Placenta
5	chr14:31566200-31648200	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:31567000-31647600	Strong transcription	Duodenum Mucosa	Duodenum
7	chr14:31567000-31651200	Strong transcription	Dnd41	blood
8	chr14:31573000-31650200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr14:31573800-31648200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:31591800-31656400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:31593800-31648200	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr14:31595000-31649000	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:31597600-31648400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr14:31598000-31648200	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr14:31598200-31633200	Strong transcription	HepG2	liver
16	chr14:31598200-31648000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:31598200-31651200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr14:31598400-31633200	Strong transcription	Liver	Liver
19	chr14:31598400-31648000	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr14:31598600-31631000	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr14:31598600-31632000	Weak transcription	Fetal Brain Male	brain
22	chr14:31598600-31633000	Weak transcription	Stomach Mucosa	stomach
23	chr14:31598600-31635400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr14:31598600-31648400	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr14:31598600-31648400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr14:31598600-31648600	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr14:31598600-31649000	Strong transcription	Primary B cells from peripheral blood	blood
28	chr14:31598600-31649400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:31598800-31633200	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr14:31600600-31634400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:31600600-31649800	Strong transcription	Fetal Muscle Trunk	muscle
32	chr14:31603800-31653400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:31605400-31633000	Strong transcription	Fetal Intestine Large	intestine
34	chr14:31605400-31635200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr14:31608600-31632000	Weak transcription	Brain Angular Gyrus	brain
36	chr14:31608600-31633200	Weak transcription	Fetal Heart	heart
37	chr14:31608800-31634200	Weak transcription	Aorta	Aorta
38	chr14:31609200-31648400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:31610600-31647800	Strong transcription	Fetal Thymus	thymus
40	chr14:31613800-31646800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr14:31614200-31631800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:31614200-31631800	Weak transcription	Gastric	stomach
43	chr14:31614200-31632000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr14:31616000-31634400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr14:31616600-31632000	Weak transcription	Brain Germinal Matrix	brain
46	chr14:31618200-31633800	Strong transcription	Fetal Intestine Small	intestine
47	chr14:31618400-31634000	Strong transcription	Fetal Stomach	stomach
48	chr14:31620200-31632600	Weak transcription	Small Intestine	intestine
49	chr14:31620400-31635400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr14:31621000-31647800	Strong transcription	Sigmoid Colon	Sigmoid Colon

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