Variant report

Variant	nsv895029
Chromosome Location	chr10:37423197-37497698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:143)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:143 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:37487370-37487673	HepG2	liver:	n/a	n/a
2	CEBPB	chr10:37487363-37487743	A549	lung:	n/a	n/a
3	CEBPB	chr10:37487403-37487685	A549	lung:	n/a	n/a
4	CTCF	chr10:37438290-37438316	GM13976	blood:	n/a	n/a
5	CTCF	chr10:37435400-37435550	HepG2	liver:	n/a	n/a
6	CTCF	chr10:37435480-37435630	A549	lung:	n/a	n/a
7	CTCF	chr10:37435447-37435520	ProgFib	skin:	n/a	n/a
8	CTCF	chr10:37469711-37469782	Lung_OC	lung:	n/a	n/a
9	CTCF	chr10:37442131-37442208	GM20000	blood:	n/a	n/a
10	CTCF	chr10:37477527-37477727	Lung_OC	lung:	n/a	n/a
11	CTCF	chr10:37423479-37423562	Pancreas_OC	pancreas:	n/a	n/a
12	CTCF	chr10:37435386-37435516	MCF-7	breast:	n/a	n/a
13	CTCF	chr10:37435531-37435558	Lung_OC	lung:	n/a	n/a
14	CTCF	chr10:37435382-37435591	MCF-7	breast:	n/a	n/a
15	CTCF	chr10:37435260-37435410	A549	lung:	n/a	n/a
16	CTCF	chr10:37435407-37435587	LNCaP	prostate:	n/a	n/a
17	CTCF	chr10:37481138-37481209	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr10:37435405-37435569	A549	lung:	n/a	n/a
19	CTCF	chr10:37432032-37432118	Pancreas_OC	pancreas:	n/a	n/a
20	CTCF	chr10:37435309-37435701	MCF-7	breast:	n/a	n/a
21	CTCF	chr10:37442159-37442261	K562	blood:	n/a	n/a
22	CTCF	chr10:37424265-37424332	GM10248	blood:	n/a	n/a
23	CTCF	chr10:37452481-37452521	Medullo	brain:	n/a	n/a
24	CTCF	chr10:37435502-37435529	Medullo	brain:	n/a	n/a
25	CTCF	chr10:37486296-37486408	GM13977	blood:	n/a	n/a
26	CTCF	chr10:37486131-37486169	GM20000	blood:	n/a	n/a
27	CTCF	chr10:37435400-37435550	MCF-7	breast:	n/a	n/a
28	CTCF	chr10:37435400-37435550	Caco-2	colon:	n/a	n/a
29	CTCF	chr10:37484346-37484411	GM20000	blood:	n/a	n/a
30	CTCF	chr10:37435360-37435606	MCF-7	breast:	n/a	n/a
31	CTCF	chr10:37430709-37430736	LNCaP	prostate:	n/a	n/a
32	CTCF	chr10:37452696-37452762	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr10:37491863-37491898	Lung_OC	lung:	n/a	n/a
34	CTCF	chr10:37447106-37447182	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr10:37435382-37435557	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:37435360-37435510	HEK293	kidney:	n/a	n/a
37	CTCF	chr10:37435420-37435570	Caco-2	colon:	n/a	n/a
38	CTCF	chr10:37435417-37435570	LNCaP	prostate:	n/a	n/a
39	CTCF	chr10:37491880-37492030	HepG2	liver:	n/a	n/a
40	CTCF	chr10:37446718-37446806	Lung_OC	lung:	n/a	n/a
41	CTCF	chr10:37458752-37458787	Lung_OC	lung:	n/a	n/a
42	CTCF	chr10:37435431-37435556	HepG2	liver:	n/a	n/a
43	CTCF	chr10:37435380-37435587	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:37435400-37435550	NB4	blood:	n/a	n/a
45	CTCF	chr10:37435257-37435682	MCF-7	breast:	n/a	n/a
46	CTCF	chr10:37435440-37435590	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr10:37475018-37475056	Spleen_OC	spleen:	n/a	n/a
48	E2F4	chr10:37446270-37446422	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr10:37497481-37497768	GM12878	blood:	n/a	n/a
50	EP300	chr10:37451298-37451858	A549	lung:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:37188694..37189693-chr10:37435453..37435966,2	MCF-7	breast:

No data

Variant related genes	Relation type
ANKRD30A	TF binding region
RNU6-811P	TF binding region

Extended variants
information (count: 2028 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12765283	chr10:37423197-37423198	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576377354	chr10:37423490-37423491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs545266596	chr10:37423500-37423501	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs377500264	chr10:37423509-37423510	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs183524381	chr10:37423511-37423512	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561853629	chr10:37423517-37423518	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12767106	chr10:37423561-37423562	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs559848008	chr10:37434621-37434622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528617060	chr10:37434656-37434657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376606454	chr10:37434664-37434665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs207470807	chr10:37434680-37434681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548419055	chr10:37434696-37434697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547913764	chr10:37434707-37434708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77293852	chr10:37434717-37434718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79404099	chr10:37434721-37434722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150715575	chr10:37434722-37434723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80218639	chr10:37434740-37434741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74773555	chr10:37434742-37434743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74535533	chr10:37434747-37434748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568625077	chr10:37434751-37434752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78073867	chr10:37434755-37434756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77836096	chr10:37434756-37434757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77890855	chr10:37434800-37434801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78591687	chr10:37434804-37434805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187683305	chr10:37434809-37434810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75055307	chr10:37434813-37434814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370143017	chr10:37434814-37434815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551256045	chr10:37434817-37434818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74392916	chr10:37434823-37434824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77143875	chr10:37434890-37434891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570815556	chr10:37434891-37434892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79570721	chr10:37434898-37434899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79544159	chr10:37434909-37434910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75749506	chr10:37434918-37434919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76920590	chr10:37434921-37434922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539007244	chr10:37434935-37434936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79818095	chr10:37434938-37434939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79265153	chr10:37434945-37434946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77114632	chr10:37434951-37434952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76336998	chr10:37434953-37434954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75873377	chr10:37434958-37434959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72787526	chr10:37434989-37434990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552564777	chr10:37435003-37435004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540412350	chr10:37435005-37435006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72787528	chr10:37435012-37435013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72787529	chr10:37435018-37435019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372748922	chr10:37435043-37435044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562376708	chr10:37435044-37435045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572576473	chr10:37435054-37435055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74794650	chr10:37435065-37435066	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	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
Oral cancer	21386901	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Bethlem myopathy	20302629	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hepatocellular carcinoma	16785998	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:37422800-37423200	Enhancers	Adipose Nuclei	Adipose
2	chr10:37434600-37436000	Enhancers	A549	lung
3	chr10:37435200-37435600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr10:37435200-37435800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr10:37435200-37435800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr10:37435600-37436200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
7	chr10:37436000-37439000	Weak transcription	A549	lung
8	chr10:37439000-37439400	Active TSS	A549	lung
9	chr10:37439400-37441200	Weak transcription	A549	lung
10	chr10:37441200-37441400	Enhancers	A549	lung
11	chr10:37446400-37447200	Weak transcription	A549	lung
12	chr10:37447800-37448400	ZNF genes & repeats	A549	lung
13	chr10:37448400-37454800	Weak transcription	A549	lung
14	chr10:37454800-37455200	Enhancers	A549	lung
15	chr10:37479600-37490800	Weak transcription	A549	lung
16	chr10:37490800-37491200	Strong transcription	A549	lung
17	chr10:37491200-37507600	Weak transcription	A549	lung

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