Variant report

Variant	nsv900814
Chromosome Location	chr13:89098616-89189142
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	ATF2	chr13:89124524-89124991	GM12878	blood:	n/a	n/a
2	ATF2	chr13:89113490-89113938	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr13:89123960-89124154	GM12878	blood:	n/a	n/a
4	BATF	chr13:89124780-89124985	GM12878	blood:	n/a	n/a
5	BCL11A	chr13:89113546-89113828	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr13:89113607-89113803	H1-hESC	embryonic stem cell:	n/a	n/a
7	CCNT2	chr13:89100977-89101168	K562	blood:	n/a	n/a
8	CEBPB	chr13:89123031-89123351	IMR90	lung:	n/a	chr13:89123185-89123194 chr13:89123185-89123194 chr13:89123183-89123194 chr13:89123183-89123196 chr13:89123185-89123194 chr13:89123185-89123194 chr13:89123184-89123195
9	CEBPB	chr13:89164725-89164947	HepG2	liver:	n/a	chr13:89164855-89164866
10	CEBPB	chr13:89123038-89123363	HepG2	liver:	n/a	chr13:89123185-89123194 chr13:89123185-89123194 chr13:89123183-89123194 chr13:89123183-89123196 chr13:89123185-89123194 chr13:89123185-89123194 chr13:89123184-89123195
11	CEBPB	chr13:89113568-89114164	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:89109592-89109857	Hela-S3	cervix:	n/a	chr13:89109691-89109702 chr13:89109693-89109704 chr13:89109691-89109704 chr13:89109714-89109725
13	CEBPB	chr13:89178483-89178781	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr13:89116830-89116970	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:89109562-89109844	A549	lung:	n/a	chr13:89109691-89109702 chr13:89109693-89109704 chr13:89109691-89109704 chr13:89109714-89109725
16	CEBPB	chr13:89109545-89109877	HepG2	liver:	n/a	chr13:89109691-89109702 chr13:89109693-89109704 chr13:89109691-89109704 chr13:89109714-89109725
17	CHD2	chr13:89113579-89114208	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr13:89117280-89117318	MCF-7	breast:	n/a	n/a
19	CTCF	chr13:89163095-89163131	Gliobla	brain:	n/a	n/a
20	CTCF	chr13:89117973-89118030	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr13:89117325-89117371	MCF-7	breast:	n/a	n/a
22	CTCF	chr13:89115500-89115650	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr13:89105488-89105509	GM13976	blood:	n/a	n/a
24	CTCF	chr13:89117300-89117450	BE2_C	brain:	n/a	n/a
25	CTCF	chr13:89117276-89117399	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr13:89117296-89117403	Medullo	brain:	n/a	n/a
27	CUX1	chr13:89136507-89136540	GM12878	blood:	n/a	n/a
28	E2F4	chr13:89129783-89129975	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr13:89131384-89131527	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr13:89163598-89163793	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr13:89153644-89153844	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr13:89149686-89149745	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr13:89171437-89171450	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr13:89130706-89130778	GM12878	blood:	n/a	n/a
35	EBF1	chr13:89124765-89124936	GM12878	blood:	n/a	n/a
36	EP300	chr13:89113575-89113949	H1-hESC	embryonic stem cell:	n/a	n/a
37	EP300	chr13:89188967-89189122	GM12878	blood:	n/a	n/a
38	EP300	chr13:89189030-89189045	GM12878	blood:	n/a	n/a
39	EP300	chr13:89124435-89125080	GM12878	blood:	n/a	n/a
40	FOS	chr13:89115713-89115997	MCF10A-Er-Src	breast:	n/a	chr13:89115847-89115854 chr13:89115863-89115875 chr13:89115846-89115855 chr13:89115846-89115854 chr13:89115842-89115853 chr13:89115845-89115854
41	FOS	chr13:89115699-89116012	MCF10A-Er-Src	breast:	n/a	chr13:89115847-89115854 chr13:89115863-89115875 chr13:89115846-89115855 chr13:89115846-89115854 chr13:89115842-89115853 chr13:89115845-89115854
42	FOS	chr13:89109849-89109937	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr13:89115722-89116010	MCF10A-Er-Src	breast:	n/a	chr13:89115847-89115854 chr13:89115863-89115875 chr13:89115846-89115855 chr13:89115846-89115854 chr13:89115842-89115853 chr13:89115845-89115854
44	FOS	chr13:89121511-89121644	MCF10A-Er-Src	breast:	n/a	n/a
45	FOXA2	chr13:89165846-89166147	A549	lung:	n/a	n/a
46	FOXA2	chr13:89116430-89116614	HepG2	liver:	n/a	n/a
47	FOXM1	chr13:89124555-89125001	GM12878	blood:	n/a	n/a
48	GATA3	chr13:89153588-89153714	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr13:89145189-89145588	MCF-7	breast:	n/a	n/a
50	HDAC2	chr13:89113480-89114109	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89179261-89179311	SK-N-SH_RA	brain:	n/a
2	chr13:89179261-89179311	BE2_C	brain:	n/a
3	chr13:89179261-89179311	NHDF-neo	bronchial:	n/a
4	chr13:89179261-89179311	HRE	kidney:	n/a
5	chr13:89179261-89179311	HL-60	blood:	n/a
6	chr13:89179261-89179311	Hepatocyte	liver:	n/a
7	chr13:89179261-89179311	AoSMC	blood vessel:	n/a
8	chr13:89179261-89179311	BJ	skin:	n/a
9	chr13:89179261-89179311	PFSK-1	brain:	n/a
10	chr13:89179261-89179311	AG10803	skin:	n/a
11	chr13:89179261-89179311	AG04449	skin:	fetal
12	chr13:89179261-89179311	U87	brain:	n/a
13	chr13:89179261-89179311	LNCaP	prostate:	n/a
14	chr13:89179261-89179311	MCF-7	breast:	n/a
15	chr13:89179261-89179311	AG04450	lung:	fetal
16	chr13:89179261-89179311	NHBE	bronchial:	n/a
17	chr13:89179261-89179311	HCF	heart:	n/a
18	chr13:89179261-89179311	K562	blood:	n/a
19	chr13:89179261-89179311	AG09319	gingival:	n/a
20	chr13:89179261-89179311	GM12891	blood:	n/a
21	chr13:89179261-89179311	HNPCEpiC	eye:	n/a
22	chr13:89179261-89179311	HRCEpiC	kidney:	n/a
23	chr13:89179261-89179311	SK-N-SH	brain:	n/a
24	chr13:89179261-89179311	ProgFib	skin:	n/a
25	chr13:89179261-89179311	NH-A	brain:	n/a
26	chr13:89179261-89179311	ECC-1	luminal epithelium:	n/a
27	chr13:89179261-89179311	ovcar-3	ovarian:	n/a
28	chr13:89179261-89179311	A549	lung:	n/a
29	chr13:89179261-89179311	GM06990	blood:	n/a
30	chr13:89179261-89179311	GM12878	blood:	n/a
31	chr13:89179261-89179311	HepG2	liver:	n/a
32	chr13:89179261-89179311	CMK	blood:	n/a
33	chr13:89179261-89179311	GM19239	blood:	n/a
34	chr13:89179261-89179311	NB4	blood:	n/a
35	chr13:89179261-89179311	HMEC	breast:	n/a
36	chr13:89179261-89179311	HEK293	kidney:	embryo
37	chr13:89179261-89179311	HAEpiC	amniotic membrane:	n/a
38	chr13:89179261-89179311	Caco-2	colon:	n/a
39	chr13:89179261-89179311	HUVEC	blood vessel:	n/a
40	chr13:89179261-89179311	HCPEpiC	choroid plexus:	n/a
41	chr13:89179261-89179311	MCF10A-Er-Src	breast:	n/a
42	chr13:89179261-89179311	HRPEpiC	eye:	n/a
43	chr13:89179261-89179311	HCM	heart:	n/a
44	chr13:89179261-89179311	Hela-S3	cervix:	n/a
45	chr13:89179261-89179311	Jurkat	blood:	n/a
46	chr13:89179261-89179311	NT2-D1	testis:	n/a
47	chr13:89179261-89179311	SAEC	small airway:	n/a
48	chr13:89179261-89179311	SKMC	muscle:	n/a
49	chr13:89179261-89179311	RPTEC	kidney:	n/a
50	chr13:89179261-89179311	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:89102814..89104712-chr13:89125430..89127283,2	MCF-7	breast:
2	chr13:89102814..89104712-chr13:89125430..89127283,2	MCF-7	breast:

Variant related genes	Relation type
LINC00433	TF binding region
LINC00433	CpG island

Extended variants
information (count: 1564 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1564 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551660460	chr13:89102693-89102694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570360954	chr13:89102700-89102701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372808896	chr13:89102767-89102768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537310547	chr13:89102783-89102784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555362811	chr13:89102857-89102858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562589441	chr13:89102864-89102865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35354119	chr13:89102871-89102872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3928091	chr13:89102881-89102882	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534718819	chr13:89102885-89102886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371005727	chr13:89102891-89102892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371043621	chr13:89104006-89104007	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs474389	chr13:89104017-89104018	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146934187	chr13:89104042-89104043	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs572777219	chr13:89104044-89104045	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs496605	chr13:89104090-89104091	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs542167257	chr13:89104103-89104104	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs533488339	chr13:89104126-89104127	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs7988130	chr13:89104138-89104139	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs34216764	chr13:89104145-89104146	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs11455842	chr13:89104148-89104149	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs375318202	chr13:89104187-89104188	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs186201935	chr13:89104207-89104208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144121089	chr13:89104214-89104215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375219462	chr13:89104215-89104216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138003936	chr13:89104230-89104231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549596595	chr13:89104237-89104238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138200933	chr13:89104273-89104274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144130478	chr13:89104274-89104275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144028653	chr13:89104275-89104276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs386773121	chr13:89104276-89104277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202223529	chr13:89104277-89104278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397939622	chr13:89104280-89104281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369454929	chr13:89104284-89104285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546637863	chr13:89104303-89104304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571130212	chr13:89104307-89104308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190622364	chr13:89104336-89104337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183161807	chr13:89104356-89104357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs499266	chr13:89104357-89104358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568929299	chr13:89104366-89104367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536067068	chr13:89104380-89104381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111796830	chr13:89104399-89104400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375305972	chr13:89104488-89104489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148256037	chr13:89104496-89104497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533807452	chr13:89104525-89104526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188090426	chr13:89104530-89104531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141267505	chr13:89104571-89104572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550766183	chr13:89104573-89104574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545377182	chr13:89104578-89104579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563678117	chr13:89104581-89104582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563113988	chr13:89104582-89104583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-small cell lung cancer	16651412	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89102600-89103000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:89104000-89104200	Enhancers	Fetal Heart	heart
3	chr13:89104000-89104200	ZNF genes & repeats	Gastric	stomach
4	chr13:89104200-89106200	Weak transcription	Gastric	stomach
5	chr13:89104200-89113200	Weak transcription	Fetal Heart	heart
6	chr13:89106200-89106600	Enhancers	Gastric	stomach
7	chr13:89107000-89108800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr13:89107000-89109000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr13:89107000-89112600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr13:89107800-89108400	Active TSS	Monocytes-CD14+_RO01746	blood
11	chr13:89107800-89109400	Enhancers	Primary B cells from cord blood	blood
12	chr13:89107800-89109600	Enhancers	Primary hematopoietic stem cells	blood
13	chr13:89108000-89109000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr13:89108000-89109400	Enhancers	Primary B cells from peripheral blood	blood
15	chr13:89108000-89109800	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr13:89108200-89108800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr13:89108400-89110000	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr13:89111400-89116000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr13:89111600-89111800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr13:89111600-89113200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr13:89111600-89113800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr13:89111600-89115600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:89111800-89115400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr13:89112000-89112800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:89112000-89113400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr13:89112600-89112800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr13:89112600-89113200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr13:89112800-89113400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr13:89112800-89114000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr13:89112800-89114000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr13:89113200-89113600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr13:89113200-89113600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr13:89113200-89113800	Enhancers	Fetal Heart	heart
34	chr13:89113200-89116600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr13:89113400-89114000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr13:89113400-89114200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr13:89113600-89113800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr13:89113600-89114000	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr13:89113800-89114000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr13:89113800-89114200	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr13:89113800-89114400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr13:89113800-89115000	Weak transcription	Fetal Heart	heart
43	chr13:89114000-89114400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr13:89114000-89114400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr13:89114000-89114400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr13:89114000-89114400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr13:89114000-89114600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr13:89114200-89116600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr13:89114400-89114600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr13:89114400-89114800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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