Variant report

Variant	esv3461302
Chromosome Location	chr3:195773080-195775928
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195775087..195781112-chr3:195806132..195810328,7	K562	blood:
2	chr3:195773121..195775698-chr3:195778391..195781329,2	MCF-7	breast:
3	chr3:195774978..195780765-chr3:195803293..195810200,8	K562	blood:
4	chr3:195774337..195776699-chr3:195790526..195792198,2	K562	blood:
5	chr3:195772434..195774325-chr3:195781653..195784506,3	K562	blood:
6	chr3:195751254..195754207-chr3:195773192..195776278,3	K562	blood:
7	chr3:195774592..195777044-chr3:195910665..195912937,2	K562	blood:
8	chr3:195774699..195776571-chr3:195794634..195796757,3	K562	blood:
9	chr3:195774337..195780265-chr3:195790698..195793878,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000072274	chromatin interactions

Extended variants
information (count: 185 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:185 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562130015	chr3:195773085-195773086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs62284010	chr3:195773092-195773093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547690878	chr3:195773107-195773108	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs139718738	chr3:195773182-195773183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150185669	chr3:195773212-195773213	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112503157	chr3:195773222-195773223	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150324749	chr3:195773226-195773227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183034345	chr3:195773230-195773231	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570358115	chr3:195773232-195773233	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370012192	chr3:195773233-195773234	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555692091	chr3:195773317-195773318	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs9637534	chr3:195773339-195773340	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs376635625	chr3:195773377-195773378	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535088195	chr3:195773381-195773382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs9325431	chr3:195773399-195773400	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs138819616	chr3:195773434-195773435	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs74854275	chr3:195773448-195773449	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557677778	chr3:195773457-195773458	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs73079255	chr3:195773459-195773460	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76218546	chr3:195773461-195773462	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561693575	chr3:195773468-195773469	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs10452050	chr3:195773476-195773477	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76110095	chr3:195773485-195773486	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567532038	chr3:195773499-195773500	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559172116	chr3:195773547-195773548	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs74852239	chr3:195773550-195773551	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573933064	chr3:195773560-195773561	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535180298	chr3:195773575-195773576	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144064956	chr3:195773613-195773614	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557066227	chr3:195773614-195773615	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370218147	chr3:195773670-195773671	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs80033945	chr3:195773687-195773688	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140501542	chr3:195773739-195773740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77341611	chr3:195773752-195773753	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs13092821	chr3:195773775-195773776	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113955389	chr3:195773786-195773787	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186353410	chr3:195773797-195773798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191664820	chr3:195773802-195773803	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs377484893	chr3:195773816-195773817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571404297	chr3:195773833-195773834	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539255214	chr3:195773839-195773840	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557492185	chr3:195773842-195773843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564343905	chr3:195773851-195773852	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs578223253	chr3:195773884-195773885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537326484	chr3:195773911-195773912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201435988	chr3:195773916-195773917	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147434248	chr3:195773934-195773935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139719844	chr3:195773943-195773944	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559399738	chr3:195773970-195773971	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577771833	chr3:195773971-195773972	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195762800-195780200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:195763000-195774600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:195765000-195775200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr3:195767200-195775400	Weak transcription	Fetal Brain Female	brain
5	chr3:195768400-195775200	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr3:195768400-195781600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:195768600-195775400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr3:195768600-195778800	Weak transcription	Fetal Stomach	stomach
9	chr3:195769000-195773600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr3:195769000-195774600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr3:195769200-195776000	Weak transcription	K562	blood
12	chr3:195769400-195774400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr3:195769400-195775400	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr3:195769600-195774400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr3:195769600-195775400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr3:195769600-195775400	Weak transcription	Small Intestine	intestine
17	chr3:195769800-195775000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:195769800-195775000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr3:195769800-195775400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr3:195769800-195775800	Weak transcription	Aorta	Aorta
21	chr3:195769800-195776400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr3:195770000-195774200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:195770000-195774200	Weak transcription	A549	lung
24	chr3:195770000-195774800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr3:195770000-195775800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr3:195770000-195778800	Weak transcription	Gastric	stomach
27	chr3:195770200-195773200	Weak transcription	Left Ventricle	heart
28	chr3:195770200-195774600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr3:195770200-195775200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:195770200-195775400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr3:195770200-195775400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr3:195770200-195778000	Weak transcription	Ovary	ovary
33	chr3:195770200-195778800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:195770400-195773400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:195770400-195776800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr3:195770400-195778200	Weak transcription	Fetal Kidney	kidney
37	chr3:195770600-195775800	Weak transcription	GM12878-XiMat	blood
38	chr3:195770800-195774400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr3:195770800-195774600	Weak transcription	HMEC	breast
40	chr3:195770800-195776000	Weak transcription	Brain Germinal Matrix	brain
41	chr3:195771000-195774400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr3:195771000-195774600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr3:195771000-195775600	Weak transcription	NH-A	brain
44	chr3:195771000-195776600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr3:195771200-195775600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:195771400-195804000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:195771600-195776400	Weak transcription	Stomach Smooth Muscle	stomach
48	chr3:195771800-195773200	Weak transcription	Fetal Thymus	thymus
49	chr3:195771800-195774200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:195771800-195775400	Weak transcription	Esophagus	oesophagus

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