Variant report

Variant	esv3362044
Chromosome Location	chr10:45030252-45038251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567751167	chr10:45035638-45035639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554056271	chr10:45035724-45035725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184306600	chr10:45035750-45035751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150569491	chr10:45035774-45035775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571581220	chr10:45035808-45035809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538664844	chr10:45035812-45035813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139302739	chr10:45035840-45035841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542712853	chr10:45035841-45035842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575695337	chr10:45035842-45035843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562481627	chr10:45035850-45035851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536343220	chr10:45035861-45035862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189511318	chr10:45035881-45035882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116663760	chr10:45035882-45035883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541362974	chr10:45035939-45035940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192314178	chr10:45035944-45035945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545327381	chr10:45035945-45035946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200945333	chr10:45035959-45035960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201439378	chr10:45035968-45035969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199801554	chr10:45035969-45035970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74950519	chr10:45035981-45035982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114424136	chr10:45035982-45035983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34223393	chr10:45035996-45035997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577971168	chr10:45036010-45036011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7905279	chr10:45036031-45036032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs371799528	chr10:45036051-45036052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145460745	chr10:45036063-45036064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547607281	chr10:45036078-45036079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183648920	chr10:45036110-45036111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561558434	chr10:45036152-45036153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376496679	chr10:45036212-45036213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528700722	chr10:45036243-45036244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546755902	chr10:45036254-45036255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571616370	chr10:45036264-45036265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2225817	chr10:45036295-45036296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550606285	chr10:45036299-45036300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529368089	chr10:45036328-45036329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147656041	chr10:45036356-45036357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188017446	chr10:45036363-45036364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566926786	chr10:45036403-45036404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10900060	chr10:45036411-45036412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567487560	chr10:45036443-45036444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181350303	chr10:45036446-45036447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72795057	chr10:45036463-45036464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556952845	chr10:45036484-45036485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575109719	chr10:45036491-45036492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10900061	chr10:45036504-45036505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs12773878	chr10:45036518-45036519	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186676982	chr10:45036536-45036537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540429528	chr10:45036548-45036549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189502136	chr10:45036577-45036578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45035600-45037800	Weak transcription	Fetal Brain Male	brain

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