Variant report

Variant	esv3371347
Chromosome Location	chr19:40717612-40722010
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40719578..40724896-chr19:40726262..40733162,10	MCF-7	breast:
2	chr19:40722002..40724261-chr19:40789079..40792675,3	MCF-7	breast:
3	chr19:40721100..40722836-chr19:40775767..40777934,2	MCF-7	breast:
4	chr19:40721117..40723953-chr19:40725760..40727528,2	K562	blood:
5	chr19:40677692..40680136-chr19:40719454..40721512,2	K562	blood:
6	chr19:40718966..40720557-chr19:40970045..40972641,2	MCF-7	breast:
7	chr19:40697182..40698721-chr19:40720965..40722825,2	MCF-7	breast:
8	chr19:40714420..40716705-chr19:40721840..40724225,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MAP3K10	hsa-miR-155-5p	chr19:40721456-40721463
2	MAP3K10	hsa-miR-155-5p	chr19:40721440-40721463
3	MAP3K10	hsa-miR-181b-5p	chr19:40721232-40721239

Variant related genes	Relation type
ENSG00000105221	chromatin interactions
ENSG00000130758	chromatin interactions
ENSG00000090013	chromatin interactions
ENSG00000105219	chromatin interactions
ENSG00000160460	chromatin interactions

Extended variants
information (count: 210 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:210 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528832530	chr19:40717616-40717617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550314127	chr19:40717658-40717659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569139733	chr19:40717662-40717663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182210415	chr19:40717683-40717684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186835831	chr19:40717693-40717694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191723412	chr19:40717694-40717695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533790934	chr19:40717709-40717710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112708552	chr19:40717741-40717742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181213860	chr19:40717756-40717757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368225088	chr19:40717779-40717780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574841394	chr19:40717795-40717796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542168314	chr19:40717854-40717855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542038042	chr19:40717855-40717856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7259191	chr19:40717899-40717900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372351196	chr19:40717909-40717910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546069949	chr19:40717922-40717923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557538464	chr19:40717955-40717956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564477335	chr19:40717981-40717982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555306967	chr19:40718010-40718011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143856151	chr19:40718029-40718030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540473690	chr19:40718081-40718082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569401550	chr19:40718129-40718130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373605410	chr19:40718134-40718135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115806385	chr19:40718150-40718151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113888448	chr19:40718191-40718192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550568293	chr19:40718239-40718240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568849723	chr19:40718296-40718297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111496656	chr19:40718360-40718361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147252553	chr19:40718361-40718362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551691594	chr19:40718376-40718377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566822166	chr19:40718385-40718386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533944181	chr19:40718468-40718469	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs139613036	chr19:40718471-40718472	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs73933217	chr19:40718494-40718495	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs377342288	chr19:40718524-40718525	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs573223829	chr19:40718565-40718566	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs540306525	chr19:40718585-40718586	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs535554378	chr19:40718597-40718598	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs144544839	chr19:40718619-40718620	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs575221154	chr19:40718636-40718637	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs376108994	chr19:40718689-40718690	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs561487474	chr19:40718703-40718704	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs371610120	chr19:40718713-40718714	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs374566110	chr19:40718720-40718721	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs150700695	chr19:40718750-40718751	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs138936945	chr19:40718768-40718769	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs577404853	chr19:40718778-40718779	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs150843563	chr19:40718779-40718780	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs199739175	chr19:40718786-40718787	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs376246139	chr19:40718810-40718811	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40698600-40721200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr19:40698800-40719600	Weak transcription	HSMM	muscle
3	chr19:40698800-40720200	Weak transcription	NHEK	skin
4	chr19:40698800-40721400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:40698800-40722000	Weak transcription	Fetal Thymus	thymus
6	chr19:40699000-40720400	Weak transcription	Psoas Muscle	Psoas
7	chr19:40699000-40722200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr19:40699000-40722200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr19:40699000-40722400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr19:40699200-40720200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr19:40699200-40720400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr19:40699200-40721200	Weak transcription	NH-A	brain
13	chr19:40699200-40721400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr19:40699400-40721200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr19:40699600-40722000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:40699600-40722200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr19:40699800-40720000	Weak transcription	NHDF-Ad	bronchial
18	chr19:40699800-40720600	Weak transcription	HepG2	liver
19	chr19:40707000-40722400	Weak transcription	HMEC	breast
20	chr19:40709000-40718200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr19:40709800-40722000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr19:40710600-40721200	Weak transcription	Primary B cells from peripheral blood	blood
23	chr19:40710600-40722200	Weak transcription	Primary B cells from cord blood	blood
24	chr19:40711200-40721800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr19:40711200-40731800	Weak transcription	Right Atrium	heart
26	chr19:40711400-40718800	Weak transcription	Brain Substantia Nigra	brain
27	chr19:40711600-40719800	Weak transcription	Colonic Mucosa	Colon
28	chr19:40711600-40720400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr19:40711600-40721000	Weak transcription	HSMMtube	muscle
30	chr19:40711600-40721800	Weak transcription	Fetal Brain Male	brain
31	chr19:40711600-40722600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr19:40711800-40720600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr19:40712000-40719000	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr19:40712200-40720400	Strong transcription	Fetal Stomach	stomach
35	chr19:40712200-40722400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr19:40712200-40722600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr19:40712200-40722600	Weak transcription	Esophagus	oesophagus
38	chr19:40712400-40718600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr19:40712600-40718200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr19:40713200-40719200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr19:40713200-40725200	Weak transcription	Hela-S3	cervix
42	chr19:40714000-40720800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr19:40714200-40722000	Strong transcription	Brain Germinal Matrix	brain
44	chr19:40714400-40720800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr19:40714600-40718400	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr19:40714600-40718600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr19:40714600-40718600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr19:40714600-40718800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr19:40714600-40719000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr19:40714600-40719000	Strong transcription	Adipose Nuclei	Adipose

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