Variant report

Variant	rs59795312
Chromosome Location	chr19:19978169-19978170
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:19975991..19979508-chr19:19981059..19984923,4	K562	blood:
2	chr19:19976218..19978192-chr19:20011161..20013662,4	K562	blood:
3	chr19:19857732..19859328-chr19:19976906..19978604,2	MCF-7	breast:
4	chr19:19966687..19968532-chr19:19975349..19978266,2	MCF-7	breast:
5	chr19:19977897..19980887-chr19:19981343..19982993,2	K562	blood:
6	chr19:19779650..19782100-chr19:19976513..19978467,2	MCF-7	breast:
7	chr19:19976692..19979119-chr19:20011140..20013486,2	K562	blood:

Variant related genes	Relation type
ENSG00000270325	Chromatin interaction
ENSG00000184635	Chromatin interaction
ENSG00000270270	Chromatin interaction
ENSG00000267268	Chromatin interaction
ENSG00000181896	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10406883	0.93[EUR][1000 genomes]
rs11786	0.93[EUR][1000 genomes]
rs11881376	0.93[EUR][1000 genomes]
rs16994693	1.00[EUR][1000 genomes]
rs2060238	0.93[EUR][1000 genomes]
rs2335372	0.82[EUR][1000 genomes]
rs55696844	0.82[EUR][1000 genomes]
rs55849911	0.82[EUR][1000 genomes]
rs55984158	0.93[EUR][1000 genomes]
rs57088108	0.82[EUR][1000 genomes]
rs57575150	0.82[EUR][1000 genomes]
rs57920747	0.82[EUR][1000 genomes]
rs58948242	0.93[EUR][1000 genomes]
rs59511604	0.82[EUR][1000 genomes]
rs60409469	0.82[EUR][1000 genomes]
rs60588790	1.00[EUR][1000 genomes]
rs7249318	0.93[EUR][1000 genomes]
rs7251285	0.93[EUR][1000 genomes]
rs7253023	0.82[EUR][1000 genomes]
rs7254824	0.82[EUR][1000 genomes]
rs73530903	0.93[EUR][1000 genomes]
rs73530906	0.93[EUR][1000 genomes]
rs73530911	0.93[EUR][1000 genomes]
rs73530918	0.85[AFR][1000 genomes]
rs73530927	1.00[EUR][1000 genomes]
rs73530932	0.93[EUR][1000 genomes]
rs73530989	1.00[EUR][1000 genomes]
rs73925530	1.00[EUR][1000 genomes]
rs73925536	1.00[EUR][1000 genomes]
rs73925537	0.93[EUR][1000 genomes]
rs8104442	1.00[EUR][1000 genomes]
rs8104555	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv911314	chr19:19866371-20021046	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS 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	27 gene(s)	inside rSNPs	diseases
3	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
4	nsv911315	chr19:19872093-20021046	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv911316	chr19:19890450-20021046	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription 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	20 gene(s)	inside rSNPs	diseases
6	nsv961192	chr19:19906394-20083740	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer 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	56 gene(s)	inside rSNPs	diseases
9	esv3413756	chr19:19936066-20072059	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	esv3380276	chr19:19936583-20073601	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv1066792	chr19:19940585-20000701	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	esv3429980	chr19:19943721-20102072	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1061846	chr19:19946927-20595412	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
14	esv3390957	chr19:19965887-20819154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
15	nsv869122	chr19:19969851-20595412	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription 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	47 gene(s)	inside rSNPs	diseases
16	nsv1057569	chr19:19973268-20193556	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS 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	23 gene(s)	inside rSNPs	diseases
17	nsv1059158	chr19:19973489-20576161	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19975800-19978400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr19:19975800-19978400	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr19:19975800-19978800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr19:19976000-19978200	Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr19:19976000-19978200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr19:19976000-19978200	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr19:19976000-19978400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr19:19976000-19978400	Active TSS	Rectal Smooth Muscle	rectum
9	chr19:19976000-19978400	Active TSS	HMEC	breast
10	chr19:19976000-19978600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr19:19976000-19978600	Active TSS	Muscle Satellite Cultured Cells	--
12	chr19:19976000-19978600	Active TSS	Colon Smooth Muscle	Colon
13	chr19:19976000-19978800	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr19:19976000-19978800	Active TSS	Duodenum Mucosa	Duodenum
15	chr19:19976000-19979000	Active TSS	Brain Angular Gyrus	brain
16	chr19:19976000-19979200	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr19:19976000-19979200	Active TSS	Right Atrium	heart
18	chr19:19976200-19978200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
19	chr19:19976200-19978200	Active TSS	Brain Hippocampus Middle	brain
20	chr19:19976200-19978200	Active TSS	Brain Substantia Nigra	brain
21	chr19:19976200-19978200	Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr19:19976200-19978600	Active TSS	H9 Cell Line	embryonic stem cell
23	chr19:19976200-19978600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr19:19976200-19978600	Active TSS	Fetal Stomach	stomach
25	chr19:19976200-19978600	Active TSS	Right Ventricle	heart
26	chr19:19976200-19979200	Active TSS	Brain Germinal Matrix	brain
27	chr19:19976200-19979200	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr19:19976200-19979200	Active TSS	Stomach Smooth Muscle	stomach
29	chr19:19976400-19978200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr19:19976400-19978200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr19:19976400-19978200	Active TSS	Liver	Liver
32	chr19:19976400-19978200	Active TSS	HUVEC	blood vessel
33	chr19:19976400-19978400	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr19:19976400-19978400	Active TSS	NH-A	brain
35	chr19:19976400-19978600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr19:19976400-19978600	Active TSS	Fetal Kidney	kidney
37	chr19:19976400-19979200	Active TSS	K562	blood
38	chr19:19976400-19979600	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr19:19976600-19978200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:19976600-19978200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:19976600-19978200	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr19:19976600-19978200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:19976600-19978200	Active TSS	Esophagus	oesophagus
44	chr19:19976600-19978200	Active TSS	Left Ventricle	heart
45	chr19:19976600-19978200	Active TSS	Pancreas	Pancrea
46	chr19:19976600-19978200	Active TSS	Psoas Muscle	Psoas
47	chr19:19976600-19978200	Active TSS	Small Intestine	intestine
48	chr19:19976600-19978200	Active TSS	GM12878-XiMat	blood
49	chr19:19976600-19978400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr19:19976600-19978400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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