Variant report

Variant	nsv900371
Chromosome Location	chr13:65434926-65568081
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	BATF	chr13:65503121-65503331	GM12878	blood:	n/a	n/a
2	BCL11A	chr13:65512859-65513178	GM12878	blood:	n/a	n/a
3	BCL11A	chr13:65512818-65513084	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:65512810-65513130	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:65449866-65450161	HepG2	liver:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
6	CEBPB	chr13:65503090-65503733	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr13:65499086-65499312	A549	lung:	n/a	chr13:65499202-65499213
8	CEBPB	chr13:65549486-65549834	IMR90	lung:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
9	CEBPB	chr13:65449858-65450171	IMR90	lung:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
10	CEBPB	chr13:65449988-65450076	H1-hESC	embryonic stem cell:	n/a	chr13:65450034-65450043 chr13:65450033-65450044 chr13:65450032-65450045 chr13:65450032-65450045 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450034-65450043 chr13:65450032-65450043 chr13:65450032-65450045 chr13:65450032-65450043
11	CEBPB	chr13:65499086-65499360	HepG2	liver:	n/a	chr13:65499202-65499213
12	CEBPB	chr13:65530999-65531037	HepG2	liver:	n/a	chr13:65531013-65531026 chr13:65531015-65531026 chr13:65531010-65531027 chr13:65531013-65531024 chr13:65531013-65531026
13	CEBPB	chr13:65549489-65549824	HepG2	liver:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
14	CEBPB	chr13:65503142-65503716	IMR90	lung:	n/a	n/a
15	CEBPB	chr13:65486134-65486601	A549	lung:	n/a	n/a
16	CEBPB	chr13:65463368-65463605	IMR90	lung:	n/a	n/a
17	CHD2	chr13:65499635-65499713	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr13:65567966-65568470	GM12878	blood:	n/a	n/a
19	CTCF	chr13:65566920-65567070	AG04449	skin:	n/a	n/a
20	CTCF	chr13:65551897-65551982	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr13:65559841-65559911	Lung_OC	lung:	n/a	n/a
22	CTCF	chr13:65460240-65460390	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr13:65532360-65532510	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr13:65530122-65530177	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr13:65519389-65519419	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr13:65502073-65502093	Fibrobl	skin:	n/a	n/a
27	CTCF	chr13:65532436-65532505	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr13:65446280-65446290	ProgFib	skin:	n/a	n/a
29	CTCF	chr13:65480102-65480131	GM13976	blood:	n/a	n/a
30	CTCF	chr13:65519280-65519430	HPAF	blood vessel:	n/a	chr13:65519402-65519423
31	CTCF	chr13:65519390-65519427	Gliobla	brain:	n/a	chr13:65519402-65519423
32	CTCF	chr13:65519380-65519530	HMEC	breast:	n/a	chr13:65519402-65519423
33	CTCF	chr13:65475340-65475433	NHEK	skin:	n/a	n/a
34	CTCF	chr13:65515436-65515516	GM10248	blood:	n/a	n/a
35	CTCF	chr13:65519300-65519450	HMEC	breast:	n/a	chr13:65519402-65519423
36	CTCF	chr13:65552346-65552377	GM13976	blood:	n/a	n/a
37	CTCF	chr13:65519300-65519450	AG10803	skin:	n/a	chr13:65519402-65519423
38	CTCF	chr13:65503954-65504015	GM10248	blood:	n/a	n/a
39	CTCF	chr13:65434969-65435038	Lung_OC	lung:	n/a	n/a
40	CTCF	chr13:65445940-65446090	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr13:65502048-65502064	Fibrobl	skin:	n/a	n/a
42	CTCF	chr13:65519389-65519432	ProgFib	skin:	n/a	chr13:65519402-65519423
43	CTCF	chr13:65499005-65499076	GM19238	blood:	n/a	n/a
44	CTCF	chr13:65446120-65446270	GM12871	blood:	n/a	n/a
45	E2F4	chr13:65503219-65503293	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr13:65455856-65456086	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr13:65547649-65547844	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr13:65438147-65438460	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr13:65461254-65461267	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr13:65517477-65517669	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65500141-65500191	PFSK-1	brain:	n/a
2	chr13:65533139-65533189	K562	blood:	n/a
3	chr13:65532820-65532870	GM06990	blood:	n/a
4	chr13:65533139-65533189	ovcar-3	ovarian:	n/a
5	chr13:65532408-65532458	SK-N-MC	brain:	n/a
6	chr13:65532273-65532323	CMK	blood:	n/a
7	chr13:65532581-65532631	AG09319	gingival:	n/a
8	chr13:65533500-65533550	Jurkat	blood:	n/a
9	chr13:65532408-65532458	AG09319	gingival:	n/a
10	chr13:65500072-65500122	PrEC	prostate:	n/a
11	chr13:65532796-65532846	SK-N-SH	brain:	n/a
12	chr13:65532820-65532870	GM19239	blood:	n/a
13	chr13:65532878-65532928	Jurkat	blood:	n/a
14	chr13:65532820-65532870	NH-A	brain:	n/a
15	chr13:65532796-65532846	HIPEpiC	eye:	n/a
16	chr13:65532820-65532870	HMEC	breast:	n/a
17	chr13:65532273-65532323	A549	lung:	n/a
18	chr13:65533500-65533550	A549	lung:	n/a
19	chr13:65532273-65532323	RPTEC	kidney:	n/a
20	chr13:65533500-65533550	AoSMC	blood vessel:	n/a
21	chr13:65532796-65532846	SK-N-SH_RA	brain:	n/a
22	chr13:65532581-65532631	Caco-2	colon:	n/a
23	chr13:65500124-65500174	HRCEpiC	kidney:	n/a
24	chr13:65533500-65533550	HEEpiC	esophagus:	n/a
25	chr13:65532581-65532631	Jurkat	blood:	n/a
26	chr13:65533500-65533550	SK-N-MC	brain:	n/a
27	chr13:65533139-65533189	GM19239	blood:	n/a
28	chr13:65532878-65532928	U87	brain:	n/a
29	chr13:65500072-65500122	AG10803	skin:	n/a
30	chr13:65532408-65532458	PFSK-1	brain:	n/a
31	chr13:65500124-65500174	AoSMC	blood vessel:	n/a
32	chr13:65532273-65532323	U87	brain:	n/a
33	chr13:65532820-65532870	SK-N-SH	brain:	n/a
34	chr13:65532408-65532458	HCM	heart:	n/a
35	chr13:65532820-65532870	BJ	skin:	n/a
36	chr13:65532878-65532928	AoSMC	blood vessel:	n/a
37	chr13:65532796-65532846	HRPEpiC	eye:	n/a
38	chr13:65532878-65532928	GM12892	blood:	n/a
39	chr13:65533500-65533550	BJ	skin:	n/a
40	chr13:65532408-65532458	NB4	blood:	n/a
41	chr13:65532820-65532870	ECC-1	luminal epithelium:	n/a
42	chr13:65532408-65532458	BJ	skin:	n/a
43	chr13:65532796-65532846	AG04449	skin:	fetal
44	chr13:65533139-65533189	Hepatocyte	liver:	n/a
45	chr13:65500124-65500174	AG04449	skin:	fetal
46	chr13:65500124-65500174	T-47D	breast:	n/a
47	chr13:65532820-65532870	HIPEpiC	eye:	n/a
48	chr13:65532878-65532928	AG09309	skin:	n/a
49	chr13:65533139-65533189	BE2_C	brain:	n/a
50	chr13:65532581-65532631	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:65501223..65502743-chr17:41399641..41401888,2	K562	blood:
2	chr13:65502724..65504224-chr17:41400395..41402648,2	MCF-7	breast:
3	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
4	chr13:65501243..65504224-chr17:41399641..41402005,2	K562	blood:
5	chr13:65490694..65491214-chr8:101576105..101576870,2	K562	blood:
6	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
7	chr13:65452228..65453752-chr13:65456863..65459026,2	MCF-7	breast:
8	chr13:65452228..65453752-chr13:65456863..65459026,2	MCF-7	breast:

Variant related genes	Relation type
LGMNP1	TF binding region
LGMNP1	CpG island

Extended variants
information (count: 1518 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1518 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550532183	chr13:65435013-65435014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185344052	chr13:65435014-65435015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542362984	chr13:65435062-65435063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559078190	chr13:65435065-65435066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116195404	chr13:65435068-65435069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114853056	chr13:65435089-65435090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189709339	chr13:65435098-65435099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529710604	chr13:65435099-65435100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550978456	chr13:65435103-65435104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144271385	chr13:65435154-65435155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536739243	chr13:65435189-65435190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6562376	chr13:65435190-65435191	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183091874	chr13:65435206-65435207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150721647	chr13:65435257-65435258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79655105	chr13:65435262-65435263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559174387	chr13:65435273-65435274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575834683	chr13:65435287-65435288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544547070	chr13:65435298-65435299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35349751	chr13:65435361-65435362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556538411	chr13:65435411-65435412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112697418	chr13:65435434-65435435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188175851	chr13:65435490-65435491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191715591	chr13:65435493-65435494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528263465	chr13:65435504-65435505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544855263	chr13:65435534-65435535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183611315	chr13:65435567-65435568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373402133	chr13:65435569-65435570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565121920	chr13:65435613-65435614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377412792	chr13:65435650-65435651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530704631	chr13:65435659-65435660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375285047	chr13:65435674-65435675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567616827	chr13:65435695-65435696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530124513	chr13:65435728-65435729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547078965	chr13:65435750-65435751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187931314	chr13:65435768-65435769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77977296	chr13:65435780-65435781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192497796	chr13:65435781-65435782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78346985	chr13:65435807-65435808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9540245	chr13:65435818-65435819	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544013254	chr13:65435840-65435841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538105485	chr13:65435872-65435873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78864372	chr13:65435893-65435894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573267756	chr13:65435938-65435939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182386266	chr13:65435947-65435948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373511545	chr13:65435978-65435979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572362774	chr13:65435983-65435984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542238221	chr13:65435985-65435986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546080684	chr13:65436051-65436052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558086782	chr13:65436106-65436107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552963128	chr13:65436125-65436126	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65435000-65436400	Enhancers	Liver	Liver
2	chr13:65440600-65441000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:65440600-65441000	Enhancers	Fetal Stomach	stomach
4	chr13:65443400-65443800	Enhancers	HUVEC	blood vessel
5	chr13:65443800-65445800	Weak transcription	HUVEC	blood vessel
6	chr13:65445800-65446200	Enhancers	HUVEC	blood vessel
7	chr13:65446200-65446400	ZNF genes & repeats	Pancreas	Pancrea
8	chr13:65446200-65446600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:65446600-65451400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:65451400-65451600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:65470000-65470400	Active TSS	Gastric	stomach
12	chr13:65474200-65474400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr13:65482800-65483800	Enhancers	HUVEC	blood vessel
14	chr13:65483000-65483400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr13:65483000-65483400	Enhancers	HMEC	breast
16	chr13:65483000-65483600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr13:65483400-65484400	Weak transcription	HMEC	breast
18	chr13:65483400-65485600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr13:65483600-65485600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr13:65483800-65485600	Weak transcription	HUVEC	blood vessel
21	chr13:65484400-65485000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr13:65484400-65487000	Enhancers	HMEC	breast
23	chr13:65485000-65485400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr13:65485400-65486200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr13:65485600-65485800	Enhancers	A549	lung
26	chr13:65485600-65486200	Enhancers	NHEK	skin
27	chr13:65485600-65487000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr13:65485600-65487000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr13:65485600-65487000	Enhancers	HUVEC	blood vessel
30	chr13:65485600-65487200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:65485600-65487200	Enhancers	NH-A	brain
32	chr13:65485800-65486000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr13:65485800-65486000	Flanking Active TSS	A549	lung
34	chr13:65486000-65486400	Active TSS	A549	lung
35	chr13:65486200-65489000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr13:65486400-65486800	Enhancers	A549	lung
37	chr13:65486600-65486800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr13:65486800-65487000	Active TSS	A549	lung
39	chr13:65487000-65487600	Weak transcription	HUVEC	blood vessel
40	chr13:65487600-65487800	ZNF genes & repeats	HUVEC	blood vessel
41	chr13:65487800-65488000	Weak transcription	HUVEC	blood vessel
42	chr13:65498600-65499000	Active TSS	Gastric	stomach
43	chr13:65499400-65499600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:65499400-65499800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr13:65499600-65502800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr13:65499800-65500000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr13:65500000-65500200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr13:65502400-65503400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:65502400-65503800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr13:65502400-65504400	Enhancers	Placenta Amnion	Placenta Amnion

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