Variant report

Variant	rs497144
Chromosome Location	chr19:37377159-37377160
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10401212	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10404981	0.82[JPT][hapmap]
rs10408951	0.87[CEU][hapmap];0.93[JPT][hapmap]
rs10410594	0.82[JPT][hapmap]
rs10416732	0.85[ASN][1000 genomes]
rs10416960	0.93[JPT][hapmap]
rs10418176	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs11084868	0.83[EUR][1000 genomes]
rs12981965	1.00[JPT][hapmap]
rs1624293	0.82[JPT][hapmap]
rs16971771	0.87[CEU][hapmap];0.93[JPT][hapmap]
rs16971772	0.87[CEU][hapmap];0.93[JPT][hapmap]
rs16971850	0.92[JPT][hapmap]
rs17707101	0.93[JPT][hapmap]
rs2385470	0.87[ASN][1000 genomes]
rs34201634	0.86[ASN][1000 genomes]
rs3816391	0.86[JPT][hapmap]
rs3955478	0.88[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs477725	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs477942	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs478272	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4805189	1.00[CEU][hapmap];0.93[JPT][hapmap]
rs4805190	0.92[JPT][hapmap]
rs486466	0.94[CHB][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs491898	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs493482	0.94[CHB][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs502110	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs503956	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs503959	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs505896	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs506463	0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs546693	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs553981	0.82[CHB][hapmap];0.85[EUR][1000 genomes]
rs555023	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs559008	0.83[CHB][hapmap];0.85[EUR][1000 genomes]
rs560085	0.81[EUR][1000 genomes]
rs566432	0.94[CHB][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs571074	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs577093	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs578699	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs579445	0.85[EUR][1000 genomes]
rs580168	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs581194	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62115611	0.85[ASN][1000 genomes]
rs9304878	0.87[CEU][hapmap];0.93[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064851	chr19:36910259-37689721	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv1065698	chr19:36916796-37690124	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv543999	chr19:36916796-37690124	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv529817	chr19:36930549-37654062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv918028	chr19:37020645-38014526	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
6	nsv521605	chr19:37261810-37483444	ZNF genes & repeats Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv1060155	chr19:37274915-37458788	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv544000	chr19:37274915-37458788	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	esv3507199	chr19:37284708-37805639	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	esv3507200	chr19:37284708-37805639	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	esv3497360	chr19:37290273-37745365	ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers 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 target site	25 gene(s)	inside rSNPs	diseases
12	esv3497361	chr19:37290273-37745365	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
13	nsv911651	chr19:37300554-37428465	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv458568	chr19:37325826-37747108	Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS 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	22 gene(s)	inside rSNPs	diseases
15	nsv579461	chr19:37325826-37747108	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
16	nsv458569	chr19:37331614-37412887	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	nsv579462	chr19:37331614-37412887	Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers 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
18	nsv523848	chr19:37357289-37487632	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37344400-37406400	ZNF genes & repeats	Liver	Liver
2	chr19:37346400-37404600	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr19:37353400-37405000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:37369400-37380800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr19:37373800-37378600	ZNF genes & repeats	Fetal Lung	lung
6	chr19:37373800-37403400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
7	chr19:37374000-37377600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
8	chr19:37374000-37400400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr19:37374000-37405400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr19:37374200-37377400	ZNF genes & repeats	Brain Anterior Caudate	brain
11	chr19:37374200-37377400	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
12	chr19:37374200-37390400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
13	chr19:37374200-37404200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
14	chr19:37374400-37377400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
15	chr19:37374400-37378800	ZNF genes & repeats	Ovary	ovary
16	chr19:37374400-37395000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr19:37374400-37395800	ZNF genes & repeats	Brain Germinal Matrix	brain
18	chr19:37374400-37400400	ZNF genes & repeats	Fetal Brain Female	brain
19	chr19:37374400-37406400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:37374600-37377400	ZNF genes & repeats	Primary T cells from cord blood	blood
21	chr19:37374600-37400400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr19:37375000-37377400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
23	chr19:37375000-37377400	ZNF genes & repeats	Fetal Brain Male	brain
24	chr19:37375000-37378200	ZNF genes & repeats	Aorta	Aorta
25	chr19:37375000-37378800	ZNF genes & repeats	Left Ventricle	heart
26	chr19:37375000-37386600	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
27	chr19:37375000-37397200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr19:37375200-37377200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr19:37375200-37377200	ZNF genes & repeats	Stomach Smooth Muscle	stomach
30	chr19:37375200-37377400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
31	chr19:37375200-37377400	ZNF genes & repeats	Brain Substantia Nigra	brain
32	chr19:37375200-37377400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
33	chr19:37375200-37377400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
34	chr19:37375200-37390200	ZNF genes & repeats	Brain Hippocampus Middle	brain
35	chr19:37375200-37390600	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
36	chr19:37375200-37393400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr19:37375400-37377200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
38	chr19:37375400-37377200	ZNF genes & repeats	Small Intestine	intestine
39	chr19:37375400-37377400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
40	chr19:37375400-37377400	ZNF genes & repeats	Colon Smooth Muscle	Colon
41	chr19:37375400-37377400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
42	chr19:37375400-37378600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr19:37375800-37377200	Weak transcription	Lung	lung
44	chr19:37375800-37379600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr19:37375800-37379600	Weak transcription	Pancreas	Pancrea
46	chr19:37375800-37380600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:37376600-37377400	ZNF genes & repeats	Fetal Kidney	kidney
48	chr19:37376600-37377400	Strong transcription	Placenta	Placenta
49	chr19:37377000-37377400	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
50	chr19:37377000-37377400	ZNF genes & repeats	NH-A	brain

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