Variant report

Variant	esv3323019
Chromosome Location	chr19:53598040-53599038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:53596128..53598162-chr19:53599456..53601173,2	MCF-7	breast:
2	chr19:53598253..53601018-chr19:53604672..53606722,3	MCF-7	breast:
3	chr19:53588688..53591621-chr19:53593968..53598410,4	K562	blood:
4	chr19:53592779..53599104-chr19:53601029..53609520,13	K562	blood:
5	chr19:53586275..53589046-chr19:53598456..53600578,2	K562	blood:
6	chr19:53592480..53599104-chr19:53600939..53607737,12	K562	blood:

Variant related genes	Relation type
ENSG00000170949	chromatin interactions

Extended variants
information (count: 63 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2162787	chr19:53598080-53598081	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559262275	chr19:53598099-53598100	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs137973344	chr19:53598125-53598126	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531322745	chr19:53598145-53598146	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543400009	chr19:53598152-53598153	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78091722	chr19:53598160-53598161	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs74489508	chr19:53598162-53598163	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561724394	chr19:53598179-53598180	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs113243803	chr19:53598198-53598199	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528956167	chr19:53598205-53598206	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2059813	chr19:53598228-53598229	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528695236	chr19:53598233-53598234	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10409828	chr19:53598265-53598266	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527910921	chr19:53598280-53598281	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12981019	chr19:53598284-53598285	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552450119	chr19:53598295-53598296	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570852198	chr19:53598317-53598318	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs12981470	chr19:53598350-53598351	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12981472	chr19:53598352-53598353	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2560952	chr19:53598357-53598358	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs12981480	chr19:53598361-53598362	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12981481	chr19:53598364-53598365	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12981258	chr19:53598374-53598375	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10410437	chr19:53598386-53598387	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs12981505	chr19:53598389-53598390	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12983331	chr19:53598403-53598404	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs12981521	chr19:53598404-53598405	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12981695	chr19:53598410-53598411	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12983514	chr19:53598412-53598413	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12982135	chr19:53598419-53598420	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12981707	chr19:53598424-53598425	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13343938	chr19:53598436-53598437	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs13343940	chr19:53598458-53598459	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568457586	chr19:53598495-53598496	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs535562616	chr19:53598514-53598515	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113807355	chr19:53598526-53598527	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs56944972	chr19:53598533-53598534	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs397802567	chr19:53598535-53598536	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554268347	chr19:53598571-53598572	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572266134	chr19:53598614-53598615	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546058732	chr19:53598620-53598621	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557991930	chr19:53598640-53598641	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576354922	chr19:53598665-53598666	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569288671	chr19:53598667-53598668	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536221564	chr19:53598684-53598685	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs111381591	chr19:53598687-53598688	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144337584	chr19:53598689-53598690	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528920248	chr19:53598706-53598707	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192960519	chr19:53598725-53598726	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs13344020	chr19:53598777-53598778	Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53573600-53604800	Weak transcription	Hela-S3	cervix
2	chr19:53574800-53599600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr19:53575600-53598600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:53575600-53601000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr19:53576800-53605200	Weak transcription	Stomach Mucosa	stomach
6	chr19:53584000-53599000	Strong transcription	Muscle Satellite Cultured Cells	--
7	chr19:53584600-53599400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr19:53584600-53599800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr19:53585200-53599400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:53585200-53599600	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr19:53585400-53604800	Weak transcription	Psoas Muscle	Psoas
12	chr19:53585600-53598800	Strong transcription	HSMMtube	muscle
13	chr19:53585600-53599000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:53585600-53599200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr19:53586000-53599000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr19:53586000-53599200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr19:53586000-53599600	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr19:53586200-53598800	Strong transcription	Fetal Stomach	stomach
19	chr19:53586400-53599400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:53586400-53599800	Strong transcription	Duodenum Mucosa	Duodenum
21	chr19:53586400-53603400	Strong transcription	Primary T cells from cord blood	blood
22	chr19:53586600-53599200	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr19:53586600-53599600	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr19:53586600-53600000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr19:53586800-53599600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr19:53588200-53601200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr19:53588400-53603400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr19:53588600-53599800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:53589200-53604800	Weak transcription	Fetal Brain Male	brain
30	chr19:53589600-53604800	Weak transcription	Small Intestine	intestine
31	chr19:53590200-53599600	Strong transcription	Fetal Muscle Trunk	muscle
32	chr19:53590400-53605000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr19:53590600-53599000	Strong transcription	Fetal Muscle Leg	muscle
34	chr19:53591200-53599600	Genic enhancers	Fetal Intestine Large	intestine
35	chr19:53591600-53598600	Genic enhancers	Fetal Intestine Small	intestine
36	chr19:53591800-53599200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr19:53592800-53604800	Weak transcription	HUVEC	blood vessel
38	chr19:53593400-53599600	ZNF genes & repeats	A549	lung
39	chr19:53594000-53599000	Strong transcription	K562	blood
40	chr19:53594400-53600600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr19:53594400-53601000	Weak transcription	Primary B cells from cord blood	blood
42	chr19:53594400-53603400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr19:53594400-53605200	Weak transcription	Fetal Lung	lung
44	chr19:53594600-53600800	Weak transcription	Stomach Smooth Muscle	stomach
45	chr19:53594600-53604800	Weak transcription	Fetal Kidney	kidney
46	chr19:53594600-53604800	Weak transcription	NHEK	skin
47	chr19:53595000-53598400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr19:53595000-53600000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr19:53595000-53600800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr19:53595000-53600800	Weak transcription	Colon Smooth Muscle	Colon

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