Variant report

Variant	nsv895528
Chromosome Location	chr10:58853784-58991581
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:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:58851859..58854706-chr10:58856434..58858287,2	K562	blood:
2	chr10:58964683..58966262-chr10:58967768..58970622,2	K562	blood:
3	chr10:58975934..58977805-chr10:58980347..58981945,2	K562	blood:
4	chr10:58957814..58958334-chr4:116457976..116458496,2	MCF-7	breast:
5	chr10:58975934..58977805-chr10:58980347..58981945,2	K562	blood:
6	chr10:58981686..58984044-chr10:59073048..59074981,2	MCF-7	breast:
7	chr10:58964683..58966262-chr10:58967768..58970622,2	K562	blood:
8	chr10:58983000..58985770-chr10:58990490..58992498,2	K562	blood:
9	chr10:58887742..58890502-chr10:58913371..58916213,2	MCF-7	breast:
10	chr10:58885374..58887771-chr10:58890005..58892664,2	MCF-7	breast:
11	chr10:58851859..58854706-chr10:58856434..58858287,2	K562	blood:
12	chr10:58885374..58887771-chr10:58890005..58892664,2	MCF-7	breast:
13	chr10:58978500..58980701-chr10:58984657..58986549,2	MCF-7	breast:
14	chr10:58983000..58985770-chr10:58990490..58992498,2	K562	blood:
15	chr10:58887742..58890502-chr10:58913371..58916213,2	MCF-7	breast:
16	chr10:58978500..58980701-chr10:58984657..58986549,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-3	chr10:58872623-58873152	XLOC_008830
2	lnc-ZWINT-2	chr10:58868384-58868602	XLOC_008829
3	lnc-ZWINT-3	chr10:58982372-58982557	XLOC_008830
4	lnc-ZWINT-2	chr10:58867073-58867228	XLOC_008829

No data

Variant related genes	Relation type
C22orf13	miRNA target sites
C2orf29	miRNA target sites

Extended variants
information (count: 5357 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5357 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548598380	chr10:58854020-58854021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544176612	chr10:58854029-58854030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61848446	chr10:58854091-58854092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs578041303	chr10:58854127-58854128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545131188	chr10:58854142-58854143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112961737	chr10:58854170-58854171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183706776	chr10:58854206-58854207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562600169	chr10:58854237-58854238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187936245	chr10:58854274-58854275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543377505	chr10:58854296-58854297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553402842	chr10:58854300-58854301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372347434	chr10:58854307-58854308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531291392	chr10:58854316-58854317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561544040	chr10:58854461-58854462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563132921	chr10:58854509-58854510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11005632	chr10:58854530-58854531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73286532	chr10:58854555-58854556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568721437	chr10:58854570-58854571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191966646	chr10:58854579-58854580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201742468	chr10:58854582-58854583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533053045	chr10:58854587-58854588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551165447	chr10:58854589-58854590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183033100	chr10:58854594-58854595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533721342	chr10:58854641-58854642	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555267995	chr10:58854660-58854661	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7918830	chr10:58854661-58854662	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556529588	chr10:58854687-58854688	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7919772	chr10:58854698-58854699	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545505774	chr10:58854724-58854725	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368471428	chr10:58854750-58854751	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187661987	chr10:58854774-58854775	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113407336	chr10:58854794-58854795	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371911569	chr10:58854798-58854799	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572706378	chr10:58854849-58854850	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369115495	chr10:58854863-58854864	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543241039	chr10:58854883-58854884	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561609892	chr10:58854885-58854886	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376058093	chr10:58854896-58854897	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111824606	chr10:58854952-58854953	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192662653	chr10:58854964-58854965	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11005633	chr10:58854968-58854969	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373430681	chr10:58855008-58855009	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562527313	chr10:58855012-58855013	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370324331	chr10:58855022-58855023	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77555701	chr10:58855025-58855026	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11005634	chr10:58855028-58855029	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185009609	chr10:58855079-58855080	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527527396	chr10:58855107-58855108	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548756582	chr10:58855209-58855210	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11005635	chr10:58855224-58855225	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

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
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
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
Obesity	21956041	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:58854000-58863600	Weak transcription	Right Atrium	heart
2	chr10:58854600-58855000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr10:58854800-58856200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:58854800-58856400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:58855800-58856200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
6	chr10:58856000-58856200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr10:58856200-58856400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr10:58856200-58856600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr10:58856200-58863000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr10:58856400-58861400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr10:58856400-58862600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:58857200-58861400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr10:58857800-58859000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr10:58858400-58858600	Enhancers	Fetal Lung	lung
15	chr10:58858600-58858800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:58858800-58859800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:58859800-58860000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:58860000-58861400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr10:58861000-58863400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr10:58861400-58861600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr10:58861400-58862000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:58861400-58863200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:58861400-58863200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr10:58861400-58863400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr10:58861400-58863400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr10:58861400-58863400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr10:58861400-58863600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr10:58861600-58862600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr10:58861600-58863400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr10:58862000-58862200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr10:58862000-58862200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr10:58862000-58862400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr10:58862200-58862800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr10:58862200-58867400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr10:58862400-58863200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr10:58862600-58863200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr10:58862600-58863200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr10:58862800-58863400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:58863000-58863200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr10:58863200-58865400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr10:58863200-58866200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr10:58863200-58867200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr10:58863200-58870000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr10:58863200-58879400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr10:58863400-58866400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr10:58863400-58866400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr10:58863400-58870200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr10:58863600-58865600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr10:58865400-58867200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:58865600-58867000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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