Variant report

Variant	nsv550810
Chromosome Location	chr10:49299274-49360392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:109)
CpG islands
(count:62)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:109 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:49333760-49333984	K562	blood:	n/a	n/a
2	CEBPB	chr10:49333768-49333972	A549	lung:	n/a	n/a
3	CEBPB	chr10:49333765-49333979	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr10:49333765-49333963	IMR90	lung:	n/a	n/a
5	CEBPB	chr10:49334781-49335038	K562	blood:	n/a	n/a
6	CEBPB	chr10:49333603-49334066	K562	blood:	n/a	n/a
7	CEBPB	chr10:49333765-49333977	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr10:49333704-49333958	K562	blood:	n/a	n/a
9	CEBPD	chr10:49333637-49334076	K562	blood:	n/a	n/a
10	CTCF	chr10:49321575-49321626	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr10:49355736-49355777	GM10248	blood:	n/a	n/a
12	CTCF	chr10:49333836-49333926	Lung_OC	lung:	n/a	n/a
13	CTCF	chr10:49333900-49334050	HEK293	kidney:	n/a	n/a
14	CTCF	chr10:49348259-49348321	GM20000	blood:	n/a	n/a
15	CTCF	chr10:49326722-49326782	LNCaP	prostate:	n/a	n/a
16	CTCF	chr10:49341616-49341718	Lung_OC	lung:	n/a	n/a
17	CTCF	chr10:49324167-49324237	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr10:49311815-49311864	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr10:49304272-49304410	Lung_OC	lung:	n/a	n/a
20	CTCF	chr10:49336802-49336879	LNCaP	prostate:	n/a	n/a
21	CTCF	chr10:49333669-49334054	A549	lung:	n/a	n/a
22	CTCF	chr10:49334348-49334444	Medullo	brain:	n/a	n/a
23	CTCF	chr10:49316402-49316423	GM10248	blood:	n/a	n/a
24	CTCF	chr10:49348157-49348273	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr10:49333902-49333943	Gliobla	brain:	n/a	n/a
26	CTCF	chr10:49321280-49321420	GM20000	blood:	n/a	n/a
27	CTCF	chr10:49341639-49341691	LNCaP	prostate:	n/a	n/a
28	CTCF	chr10:49333822-49333971	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr10:49302730-49302762	Lung_OC	lung:	n/a	n/a
30	CTCF	chr10:49333785-49333822	K562	blood:	n/a	n/a
31	CTCF	chr10:49307500-49307547	GM10266	blood:	n/a	n/a
32	CTCF	chr10:49333640-49333790	HPF	lung:	n/a	n/a
33	CTCF	chr10:49333764-49333997	LNCaP	prostate:	n/a	n/a
34	CTCF	chr10:49299734-49299779	GM13976	blood:	n/a	n/a
35	CTCF	chr10:49333960-49334110	AG04450	lung:	n/a	n/a
36	CTCF	chr10:49333771-49333965	LNCaP	prostate:	n/a	n/a
37	CTCF	chr10:49333610-49334097	A549	lung:	n/a	n/a
38	CTCF	chr10:49359722-49359773	LNCaP	prostate:	n/a	n/a
39	CTCF	chr10:49354089-49354143	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr10:49316766-49316812	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr10:49342139-49342208	GM10248	blood:	n/a	n/a
42	CTCF	chr10:49313555-49313613	GM10266	blood:	n/a	n/a
43	CTCF	chr10:49333032-49333082	GM20000	blood:	n/a	n/a
44	CTCF	chr10:49348158-49348251	GM13976	blood:	n/a	n/a
45	CTCF	chr10:49353698-49353773	Lung_OC	lung:	n/a	n/a
46	CTCF	chr10:49310414-49310507	GM13976	blood:	n/a	n/a
47	CTCF	chr10:49316472-49316503	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr10:49333665-49334061	K562	blood:	n/a	n/a
49	CTCF	chr10:49341037-49341100	GM20000	blood:	n/a	n/a
50	CTCF	chr10:49333540-49333690	AG04450	lung:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49348564-49348614	HRPEpiC	eye:	n/a
2	chr10:49348564-49348614	HRPEpiC	eye:	n/a
3	chr10:49348564-49348614	GM12892	blood:	n/a
4	chr10:49348564-49348614	SK-N-MC	brain:	n/a
5	chr10:49348564-49348614	MCF10A-Er-Src	breast:	n/a
6	chr10:49348564-49348614	HCM	heart:	n/a
7	chr10:49348564-49348614	K562	blood:	n/a
8	chr10:49348564-49348614	HMEC	breast:	n/a
9	chr10:49348564-49348614	GM19239	blood:	n/a
10	chr10:49348564-49348614	HepG2	liver:	n/a
11	chr10:49348564-49348614	ECC-1	luminal epithelium:	n/a
12	chr10:49348564-49348614	Caco-2	colon:	n/a
13	chr10:49348564-49348614	NHDF-neo	bronchial:	n/a
14	chr10:49348564-49348614	HAEpiC	amniotic membrane:	n/a
15	chr10:49348564-49348614	HUVEC	blood vessel:	n/a
16	chr10:49348564-49348614	HL-60	blood:	n/a
17	chr10:49348564-49348614	H1-hESC	embryonic stem cell:	embryo
18	chr10:49348564-49348614	HCPEpiC	choroid plexus:	n/a
19	chr10:49348564-49348614	AG09319	gingival:	n/a
20	chr10:49348564-49348614	GM12878	blood:	n/a
21	chr10:49348564-49348614	T-47D	breast:	n/a
22	chr10:49348564-49348614	HIPEpiC	eye:	n/a
23	chr10:49348564-49348614	HEEpiC	esophagus:	n/a
24	chr10:49348564-49348614	NH-A	brain:	n/a
25	chr10:49348564-49348614	U87	brain:	n/a
26	chr10:49348564-49348614	ovcar-3	ovarian:	n/a
27	chr10:49348564-49348614	AG04449	skin:	fetal
28	chr10:49348564-49348614	Jurkat	blood:	n/a
29	chr10:49348564-49348614	RPTEC	kidney:	n/a
30	chr10:49348564-49348614	Hepatocyte	liver:	n/a
31	chr10:49348564-49348614	AG04450	lung:	fetal
32	chr10:49348564-49348614	HEK293	kidney:	embryo
33	chr10:49348564-49348614	SAEC	small airway:	n/a
34	chr10:49348564-49348614	NT2-D1	testis:	n/a
35	chr10:49348564-49348614	GM12891	blood:	n/a
36	chr10:49348564-49348614	HRCEpiC	kidney:	n/a
37	chr10:49348564-49348614	AoSMC	blood vessel:	n/a
38	chr10:49348564-49348614	NHBE	bronchial:	n/a
39	chr10:49348564-49348614	SKMC	muscle:	n/a
40	chr10:49348564-49348614	AG09309	skin:	n/a
41	chr10:49348564-49348614	PANC-1	pancreas:	n/a
42	chr10:49348564-49348614	ProgFib	skin:	n/a
43	chr10:49348564-49348614	HNPCEpiC	eye:	n/a
44	chr10:49348564-49348614	GM06990	blood:	n/a
45	chr10:49348564-49348614	Hela-S3	cervix:	n/a
46	chr10:49348564-49348614	HCT-116	colon:	n/a
47	chr10:49348564-49348614	SK-N-SH_RA	brain:	n/a
48	chr10:49348564-49348614	HRE	kidney:	n/a
49	chr10:49348564-49348614	AG10803	skin:	n/a
50	chr10:49348564-49348614	BJ	skin:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAPK8-5	chr10:49316927-49317254	expReg_chr10_2514_+
2	lnc-MAPK8-6	chr10:49313937-49314716	expReg_chr10_2502_+
3	lnc-PTPN20C-3	chr10:49357092-49357245	ucscGeneNc_uc001jgw_2
4	lnc-PTPN20C-3	chr10:49346057-49347865	ucscGeneNc_uc001jgw_2

No data

Variant related genes	Relation type
PTPN20CP	TF binding region
PTPN20CP	CpG island

Extended variants
information (count: 82 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138195894	chr10:49310509-49310510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185504229	chr10:49310590-49310591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191579497	chr10:49310598-49310599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558449027	chr10:49310648-49310649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143098719	chr10:49310649-49310650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544165530	chr10:49310739-49310740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562733244	chr10:49310782-49310783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529844001	chr10:49311107-49311108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543145062	chr10:49311127-49311128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561324246	chr10:49311144-49311145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565306225	chr10:49314146-49314147	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs182558120	chr10:49314191-49314192	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs551266185	chr10:49314321-49314322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569405478	chr10:49314373-49314374	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs530340159	chr10:49314399-49314400	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs548342006	chr10:49314407-49314408	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs187976247	chr10:49314452-49314453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs536401310	chr10:49314453-49314454	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs533672368	chr10:49314526-49314527	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs558230079	chr10:49314537-49314538	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs570464759	chr10:49314613-49314614	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs199855129	chr10:49318679-49318680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540777286	chr10:49318817-49318818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565338595	chr10:49318856-49318857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577172848	chr10:49318868-49318869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2652370	chr10:49318884-49318885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369804133	chr10:49318978-49318979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150013691	chr10:49319300-49319301	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
29	rs151200482	chr10:49319323-49319324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs556133196	chr10:49319921-49319922	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs983721	chr10:49319933-49319934	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183414315	chr10:49319942-49319943	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs983722	chr10:49319950-49319951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs544679057	chr10:49320027-49320028	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562773805	chr10:49320031-49320032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs374071451	chr10:49320144-49320145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs574775850	chr10:49320146-49320147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572454053	chr10:49320207-49320208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs367989472	chr10:49320287-49320288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199613641	chr10:49320822-49320823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs542161028	chr10:49320960-49320961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560371583	chr10:49321040-49321041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527880328	chr10:49321042-49321043	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552322880	chr10:49321379-49321380	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564220810	chr10:49321530-49321531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs371567115	chr10:49321604-49321605	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368501799	chr10:49321634-49321635	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs371434469	chr10:49321774-49321775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs531339673	chr10:49321782-49321783	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs549824394	chr10:49321818-49321819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49310400-49310800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr10:49310400-49310800	Enhancers	Fetal Thymus	thymus
3	chr10:49310400-49311200	Enhancers	Dnd41	blood
4	chr10:49318600-49319000	Enhancers	Dnd41	blood
5	chr10:49356400-49357000	Enhancers	Dnd41	blood

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