Variant report

Variant	nsv1038798
Chromosome Location	chr13:98008467-98068130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:98011710-98012033	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:98047795-98048028	K562	blood:	n/a	n/a
3	ARID3A	chr13:98011687-98012161	K562	blood:	n/a	chr13:98012132-98012148
4	ATF1	chr13:98065959-98066262	K562	blood:	n/a	n/a
5	BACH1	chr13:98064664-98064715	K562	blood:	n/a	n/a
6	BACH1	chr13:98019491-98020073	H1-hESC	embryonic stem cell:	n/a	chr13:98019811-98019825
7	BCLAF1	chr13:98011725-98012052	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:98019431-98019631	K562	blood:	n/a	n/a
9	BHLHE40	chr13:98048953-98049153	K562	blood:	n/a	n/a
10	BRCA1	chr13:98011753-98012024	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr13:98021780-98021969	K562	blood:	n/a	n/a
12	CEBPB	chr13:98047568-98048051	A549	lung:	n/a	chr13:98047832-98047843 chr13:98047832-98047845
13	CEBPB	chr13:98019424-98020083	IMR90	lung:	n/a	n/a
14	CEBPB	chr13:98011631-98012051	K562	blood:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
15	CEBPB	chr13:98039955-98039972	K562	blood:	n/a	n/a
16	CEBPB	chr13:98011624-98012039	IMR90	lung:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
17	CEBPB	chr13:98047671-98048001	A549	lung:	n/a	chr13:98047832-98047843 chr13:98047832-98047845
18	CEBPB	chr13:98011626-98012035	H1-hESC	embryonic stem cell:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
19	CEBPB	chr13:98011611-98012061	MCF-7	breast:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
20	CEBPB	chr13:98011654-98012003	ECC-1	luminal epithelium:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
21	CEBPB	chr13:98047686-98048020	Hela-S3	cervix:	n/a	chr13:98047832-98047843 chr13:98047832-98047845
22	CEBPB	chr13:98018912-98019169	HepG2	liver:	n/a	chr13:98019040-98019053 chr13:98019040-98019051 chr13:98019042-98019051
23	CEBPB	chr13:98011479-98012154	A549	lung:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
24	CEBPB	chr13:98019875-98020040	A549	lung:	n/a	n/a
25	CEBPB	chr13:98058473-98058780	Hela-S3	cervix:	n/a	chr13:98058641-98058652 chr13:98058611-98058622
26	CEBPB	chr13:98011695-98011897	HepG2	liver:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
27	CEBPB	chr13:98056745-98056790	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:98041900-98042011	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr13:98053757-98054017	HepG2	liver:	n/a	n/a
30	CEBPB	chr13:98058463-98058784	HepG2	liver:	n/a	chr13:98058641-98058652 chr13:98058611-98058622
31	CEBPB	chr13:98011514-98012186	HCT-116	colon:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
32	CEBPB	chr13:98047727-98047927	K562	blood:	n/a	chr13:98047832-98047843 chr13:98047832-98047845
33	CEBPB	chr13:98053766-98054015	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:98047648-98048033	IMR90	lung:	n/a	chr13:98047832-98047843 chr13:98047832-98047845
35	CEBPB	chr13:98039871-98040008	IMR90	lung:	n/a	chr13:98039968-98039979
36	CEBPB	chr13:98053771-98054019	A549	lung:	n/a	n/a
37	CEBPB	chr13:98058485-98058790	K562	blood:	n/a	chr13:98058641-98058652 chr13:98058611-98058622
38	CEBPB	chr13:98029417-98029595	HepG2	liver:	n/a	n/a
39	CEBPB	chr13:98011662-98012131	HCT-116	colon:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
40	CEBPB	chr13:98060665-98060772	HepG2	liver:	n/a	chr13:98060727-98060738 chr13:98060726-98060739 chr13:98060726-98060739 chr13:98060726-98060737
41	CEBPB	chr13:98011569-98012080	ECC-1	luminal epithelium:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
42	CEBPB	chr13:98058455-98058763	A549	lung:	n/a	chr13:98058641-98058652 chr13:98058611-98058622
43	CEBPB	chr13:98011645-98012020	A549	lung:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
44	CEBPB	chr13:98011615-98012018	K562	blood:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
45	CEBPB	chr13:98011612-98012026	A549	lung:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
46	CEBPB	chr13:98011655-98011966	K562	blood:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
47	CEBPB	chr13:98011579-98012097	MCF-7	breast:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
48	CEBPB	chr13:98047681-98048010	A549	lung:	n/a	chr13:98047832-98047843 chr13:98047832-98047845
49	CEBPB	chr13:98011600-98012072	Hela-S3	cervix:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824
50	CEBPB	chr13:98011628-98012019	HepG2	liver:	n/a	chr13:98011815-98011824 chr13:98011815-98011824 chr13:98011815-98011824

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:98019621-98019671	Hepatocyte	liver:	n/a
2	chr13:98044144-98044194	Hela-S3	cervix:	n/a
3	chr13:98019621-98019671	ECC-1	luminal epithelium:	n/a
4	chr13:98044144-98044194	HNPCEpiC	eye:	n/a
5	chr13:98010450-98010500	PANC-1	pancreas:	n/a
6	chr13:98019621-98019671	SK-N-MC	brain:	n/a
7	chr13:98044144-98044194	GM19239	blood:	n/a
8	chr13:98044144-98044194	AoSMC	blood vessel:	n/a
9	chr13:98010450-98010500	HCPEpiC	choroid plexus:	n/a
10	chr13:98048838-98048888	AG09309	skin:	n/a
11	chr13:98010450-98010500	AG09319	gingival:	n/a
12	chr13:98010450-98010500	T-47D	breast:	n/a
13	chr13:98048838-98048888	HEK293	kidney:	embryo
14	chr13:98010450-98010500	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:98019621-98019671	NHBE	bronchial:	n/a
16	chr13:98048838-98048888	HPAEpiC	pulmonary alveolar:	n/a
17	chr13:98019621-98019671	NB4	blood:	n/a
18	chr13:98019621-98019671	HCT-116	colon:	n/a
19	chr13:98010450-98010500	GM19239	blood:	n/a
20	chr13:98010450-98010500	Jurkat	blood:	n/a
21	chr13:98044144-98044194	HCM	heart:	n/a
22	chr13:98010450-98010500	U87	brain:	n/a
23	chr13:98010450-98010500	BJ	skin:	n/a
24	chr13:98048838-98048888	ECC-1	luminal epithelium:	n/a
25	chr13:98048838-98048888	AG04449	skin:	fetal
26	chr13:98048838-98048888	BE2_C	brain:	n/a
27	chr13:98044144-98044194	NT2-D1	testis:	n/a
28	chr13:98048838-98048888	HepG2	liver:	n/a
29	chr13:98044144-98044194	U87	brain:	n/a
30	chr13:98048838-98048888	U87	brain:	n/a
31	chr13:98010450-98010500	HIPEpiC	eye:	n/a
32	chr13:98019621-98019671	PANC-1	pancreas:	n/a
33	chr13:98010450-98010500	AG04450	lung:	fetal
34	chr13:98044144-98044194	HPAEpiC	pulmonary alveolar:	n/a
35	chr13:98048838-98048888	Hepatocyte	liver:	n/a
36	chr13:98044144-98044194	ProgFib	skin:	n/a
37	chr13:98019621-98019671	LNCaP	prostate:	n/a
38	chr13:98019621-98019671	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:98010450-98010500	NH-A	brain:	n/a
40	chr13:98019621-98019671	HAEpiC	amniotic membrane:	n/a
41	chr13:98044144-98044194	SAEC	small airway:	n/a
42	chr13:98019621-98019671	GM12891	blood:	n/a
43	chr13:98010450-98010500	HRPEpiC	eye:	n/a
44	chr13:98010450-98010500	ovcar-3	ovarian:	n/a
45	chr13:98010450-98010500	HNPCEpiC	eye:	n/a
46	chr13:98019621-98019671	GM12892	blood:	n/a
47	chr13:98010450-98010500	MCF-7	breast:	n/a
48	chr13:98044144-98044194	T-47D	breast:	n/a
49	chr13:98048838-98048888	BJ	skin:	n/a
50	chr13:98019621-98019671	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:97895427..97898016-chr13:98009372..98010999,2	MCF-7	breast:
2	chr13:98047283..98049852-chr13:98064242..98066608,2	K562	blood:
3	chr13:97874376..97874930-chr13:98011461..98012391,2	K562	blood:
4	chr13:97683065..97683655-chr13:98011459..98012220,3	MCF-7	breast:
5	chr13:98031666..98034483-chr13:98038323..98040718,2	K562	blood:
6	chr13:98064161..98066633-chr13:98085870..98087529,2	K562	blood:
7	chr13:98047283..98049852-chr13:98064242..98066608,2	K562	blood:
8	chr13:97992267..97994078-chr13:98009808..98011602,2	K562	blood:
9	chr13:97761876..97762424-chr13:98011415..98011920,2	K562	blood:
10	chr13:98031666..98034483-chr13:98038323..98040718,2	K562	blood:
11	chr13:98011835..98013519-chr13:98027401..98029954,2	K562	blood:
12	chr13:98011835..98013519-chr13:98027401..98029954,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	MBNL2	hsa-miR-218-5p	chr13:98044948-98044968
2	MBNL2	hsa-miR-302d-3p	chr13:98046157-98046180
3	MBNL2	hsa-miR-372-3p	chr13:98009763-98009784
4	MBNL2	hsa-miR-302d-3p	chr13:98046173-98046179
5	MBNL2	hsa-miR-372-3p	chr13:98046173-98046179
6	MBNL2	hsa-miR-218-5p	chr13:98044172-98044191
7	MBNL2	hsa-miR-218-5p	chr13:98044184-98044191
8	MBNL2	hsa-miR-372-3p	chr13:98046157-98046180
9	MBNL2	hsa-miR-302d-3p	chr13:98009763-98009784

Variant related genes	Relation type
MBNL2	TF binding region
RNA5SP37	TF binding region
MBNL2	CpG island
RNA5SP37	CpG island
ENSG00000139793	chromatin interactions
ENSG00000125249	chromatin interactions

Extended variants
information (count: 1847 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1847 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11069259	chr13:98008467-98008468	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566657709	chr13:98008485-98008486	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs11349751	chr13:98008492-98008493	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs562628475	chr13:98008522-98008523	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs538809340	chr13:98008549-98008550	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139574635	chr13:98008576-98008577	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577380452	chr13:98008593-98008594	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs575396074	chr13:98008676-98008677	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs11349752	chr13:98008677-98008678	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs75590612	chr13:98008685-98008686	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544351298	chr13:98008735-98008736	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs564910711	chr13:98008878-98008879	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs77878546	chr13:98009092-98009093	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554265156	chr13:98009125-98009126	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189741755	chr13:98009154-98009155	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539855321	chr13:98009180-98009181	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183196624	chr13:98009208-98009209	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530866698	chr13:98009253-98009254	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9556709	chr13:98009321-98009322	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs187935194	chr13:98009346-98009347	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531533769	chr13:98009355-98009356	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551737637	chr13:98009363-98009364	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560593660	chr13:98009429-98009430	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551097595	chr13:98009430-98009431	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548446794	chr13:98009481-98009482	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530058813	chr13:98009616-98009617	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191995368	chr13:98009629-98009630	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566738484	chr13:98009651-98009652	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7317666	chr13:98009661-98009662	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538970043	chr13:98009681-98009682	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs202237961	chr13:98009722-98009723	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370743900	chr13:98009754-98009755	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537929130	chr13:98009803-98009804	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs140597546	chr13:98009807-98009808	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs374402320	chr13:98009810-98009811	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567748263	chr13:98009819-98009820	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs147103026	chr13:98009859-98009860	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs199878294	chr13:98009879-98009880	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs150652145	chr13:98009909-98009910	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs372237643	chr13:98009911-98009912	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs201007433	chr13:98009912-98009913	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs533752239	chr13:98010012-98010013	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546147960	chr13:98010023-98010024	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111556064	chr13:98010035-98010036	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566244995	chr13:98010065-98010066	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537745095	chr13:98010143-98010144	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35163826	chr13:98010153-98010154	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553500557	chr13:98010230-98010231	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568809118	chr13:98010269-98010270	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573182173	chr13:98010355-98010356	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21785460	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Colorectal cancer	21645411	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1921 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:97982000-98009000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:97982600-98020800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr13:97991600-98020800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr13:97992800-98020800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr13:97994200-98016200	Weak transcription	NHDF-Ad	bronchial
6	chr13:97995200-98011000	Strong transcription	Placenta	Placenta
7	chr13:97995400-98050200	Weak transcription	Small Intestine	intestine
8	chr13:97996200-98019400	Weak transcription	GM12878-XiMat	blood
9	chr13:97997400-98011600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr13:97997400-98019000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr13:97998400-98015800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr13:97999600-98019200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr13:98000000-98009600	Weak transcription	Gastric	stomach
14	chr13:98000200-98008800	Weak transcription	Right Ventricle	heart
15	chr13:98002200-98009600	Weak transcription	Esophagus	oesophagus
16	chr13:98002400-98009000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr13:98002400-98027200	Weak transcription	Lung	lung
18	chr13:98002400-98039600	Weak transcription	Spleen	Spleen
19	chr13:98002600-98013600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr13:98002600-98021600	Weak transcription	Colonic Mucosa	Colon
21	chr13:98002800-98009800	Weak transcription	Fetal Thymus	thymus
22	chr13:98003200-98021200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr13:98003600-98009800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:98003800-98009600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr13:98003800-98009800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr13:98003800-98011600	Weak transcription	Brain Germinal Matrix	brain
27	chr13:98003800-98011600	Weak transcription	Colon Smooth Muscle	Colon
28	chr13:98003800-98012800	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr13:98003800-98013000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr13:98003800-98018000	Weak transcription	Fetal Brain Male	brain
31	chr13:98003800-98019000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr13:98004000-98009000	Weak transcription	A549	lung
33	chr13:98004000-98009400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr13:98004000-98009600	Weak transcription	Pancreas	Pancrea
35	chr13:98004000-98013000	Weak transcription	Ovary	ovary
36	chr13:98004000-98013200	Weak transcription	Fetal Kidney	kidney
37	chr13:98004000-98018600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr13:98004000-98019200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr13:98004000-98021000	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr13:98004200-98008800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr13:98004200-98009400	Weak transcription	Aorta	Aorta
42	chr13:98004200-98009600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr13:98004200-98010200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:98004200-98012800	Weak transcription	Fetal Stomach	stomach
45	chr13:98004200-98014200	Weak transcription	Fetal Intestine Small	intestine
46	chr13:98004400-98011000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr13:98004400-98011600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr13:98004400-98019400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr13:98005400-98012800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr13:98005400-98021600	Weak transcription	Thymus	Thymus

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