Variant report

Variant	nsv972779
Chromosome Location	chr9:94910607-94920083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:166)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:166 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr9:94916779-94916993	K562	blood:	n/a	n/a
2	CEBPB	chr9:94914008-94914678	MCF-7	breast:	n/a	chr9:94914193-94914210
3	CEBPB	chr9:94914022-94914600	IMR90	lung:	n/a	chr9:94914193-94914210
4	CTCF	chr9:94916886-94916923	GM19239	blood:	n/a	n/a
5	CTCF	chr9:94914020-94914170	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr9:94919114-94919166	GM20000	blood:	n/a	n/a
7	ELF1	chr9:94914020-94914771	MCF-7	breast:	n/a	n/a
8	ELF1	chr9:94913984-94914709	MCF-7	breast:	n/a	n/a
9	EP300	chr9:94914309-94914751	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr9:94914000-94914870	MCF-7	breast:	n/a	chr9:94914197-94914205
11	EP300	chr9:94914225-94914717	T-47D	breast:	n/a	n/a
12	EP300	chr9:94914117-94914788	MCF-7	breast:	n/a	chr9:94914197-94914205
13	EP300	chr9:94913989-94914898	SK-N-SH	brain:	n/a	chr9:94914197-94914205
14	EP300	chr9:94914122-94915162	SK-N-SH	brain:	n/a	chr9:94914197-94914205
15	EP300	chr9:94914193-94914691	T-47D	breast:	n/a	chr9:94914197-94914205
16	EP300	chr9:94914315-94914785	SK-N-SH_RA	brain:	n/a	n/a
17	ESR1	chr9:94914089-94914742	ECC-1	luminal epithelium:	n/a	n/a
18	ESR1	chr9:94914235-94914651	T-47D	breast:	n/a	n/a
19	ESR1	chr9:94914261-94914598	T-47D	breast:	n/a	n/a
20	ESR1	chr9:94914119-94914700	ECC-1	luminal epithelium:	n/a	n/a
21	ESR1	chr9:94914095-94914639	ECC-1	luminal epithelium:	n/a	n/a
22	ESR1	chr9:94914262-94914602	ECC-1	luminal epithelium:	n/a	n/a
23	ESR1	chr9:94914320-94914637	T-47D	breast:	n/a	n/a
24	ESR1	chr9:94914262-94914707	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr9:94914166-94914672	T-47D	breast:	n/a	n/a
26	ESR1	chr9:94914112-94914668	T-47D	breast:	n/a	n/a
27	ESR1	chr9:94914277-94914632	ECC-1	luminal epithelium:	n/a	n/a
28	FOS	chr9:94914185-94914246	MCF10A-Er-Src	breast:	n/a	chr9:94914196-94914205
29	FOS	chr9:94914159-94914243	MCF10A-Er-Src	breast:	n/a	chr9:94914196-94914205
30	FOS	chr9:94915890-94915977	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr9:94914087-94914273	MCF10A-Er-Src	breast:	n/a	chr9:94914196-94914205
32	FOSL2	chr9:94913916-94914781	SK-N-SH	brain:	n/a	chr9:94914196-94914205
33	FOXA1	chr9:94914657-94914878	T-47D	breast:	n/a	n/a
34	FOXA1	chr9:94914729-94914905	T-47D	breast:	n/a	n/a
35	FOXA1	chr9:94914323-94914601	T-47D	breast:	n/a	n/a
36	FOXM1	chr9:94914109-94914766	MCF-7	breast:	n/a	n/a
37	FOXM1	chr9:94914093-94914910	MCF-7	breast:	n/a	n/a
38	GATA1	chr9:94914244-94915048	PBDE	blood:	n/a	n/a
39	GATA2	chr9:94914082-94914842	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr9:94913949-94914979	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr9:94913860-94915025	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr9:94914145-94914732	MCF-7	breast:	n/a	n/a
43	GATA3	chr9:94914383-94914786	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr9:94914285-94914796	T-47D	breast:	n/a	n/a
45	GATA3	chr9:94914033-94914991	MCF-7	breast:	n/a	n/a
46	GATA3	chr9:94913935-94914867	MCF-7	breast:	n/a	n/a
47	GATA3	chr9:94914010-94914877	MCF-7	breast:	n/a	n/a
48	GATA3	chr9:94914284-94914793	T-47D	breast:	n/a	n/a
49	HA-E2F1	chr9:94913925-94914743	MCF-7	breast:	n/a	n/a
50	HDAC2	chr9:94915869-94916021	K562	blood:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:94907081..94909170-chr9:94913018..94916076,3	MCF-7	breast:
2	chr9:94896533..94899071-chr9:94912382..94914127,2	MCF-7	breast:
3	chr9:94906006..94908675-chr9:94917827..94919493,2	MCF-7	breast:
4	chr9:94909662..94911780-chr9:94913646..94915674,2	K562	blood:
5	chr9:94900325..94903739-chr9:94909399..94912070,4	MCF-7	breast:
6	chr9:94916927..94919162-chr9:95004838..95007173,2	MCF-7	breast:
7	chr9:94909662..94911780-chr9:94913646..94915674,2	K562	blood:
8	chr9:94903732..94905881-chr9:94913415..94915626,3	MCF-7	breast:
9	chr10:132897127..132897964-chr9:94913983..94914829,2	MCF-7	breast:
10	chr9:94909350..94911414-chr9:94915017..94917948,2	K562	blood:
11	chr9:94903265..94904181-chr9:94913861..94914694,3	MCF-7	breast:
12	chr9:94912447..94914532-chr9:94951103..94952987,2	MCF-7	breast:
13	chr9:94907222..94909546-chr9:94910880..94913844,2	K562	blood:
14	chr9:94909200..94911052-chr9:95430848..95432803,2	K562	blood:
15	chr9:94920054..94922956-chr9:94923750..94925745,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CENPP-3	chr9:94918392-94918571	ENSG00000225511
2	lnc-CENPP-3	chr9:94919969-94920155	ENSG00000225511
3	lnc-CENPP-3	chr9:94915019-94915146	ENSG00000225511
4	lnc-CENPP-3	chr9:94914876-94914911	ENSG00000225511

No data

Variant related genes	Relation type
ENSG00000238996	TF binding region
ENSG00000236717	TF binding region
LINC00475	TF binding region
ENSG00000225511	chromatin interactions
ENSG00000238996	chromatin interactions
ENSG00000196305	chromatin interactions
ENSG00000127080	chromatin interactions

Extended variants
information (count: 349 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7046734	chr9:94910630-94910631	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185411910	chr9:94910651-94910652	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs190210478	chr9:94910660-94910661	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs573079226	chr9:94910690-94910691	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs58444264	chr9:94910698-94910699	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs546416222	chr9:94910710-94910711	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs555267644	chr9:94910713-94910714	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs182189198	chr9:94910726-94910727	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs544008099	chr9:94910740-94910741	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs377635040	chr9:94910787-94910788	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs533310192	chr9:94910808-94910809	Enhancers Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs7049168	chr9:94910815-94910816	Enhancers Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs573425639	chr9:94910824-94910825	Enhancers Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs186796494	chr9:94910836-94910837	Enhancers Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs531443617	chr9:94910838-94910839	Enhancers Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs527967041	chr9:94910843-94910844	Enhancers Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs549670314	chr9:94910859-94910860	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs567975368	chr9:94910870-94910871	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540934914	chr9:94910883-94910884	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs531894435	chr9:94910888-94910889	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs369885634	chr9:94910895-94910896	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs550155177	chr9:94910940-94910941	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs192359719	chr9:94910957-94910958	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs145457747	chr9:94910958-94910959	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs183859318	chr9:94910987-94910988	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs199723252	chr9:94910999-94911000	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs151192896	chr9:94911000-94911001	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs139170216	chr9:94911010-94911011	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs57413357	chr9:94911035-94911036	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573599351	chr9:94911051-94911052	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs188853420	chr9:94911114-94911115	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs535673579	chr9:94911136-94911137	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs75995081	chr9:94911224-94911225	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561023819	chr9:94911268-94911269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116123269	chr9:94911274-94911275	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs140072595	chr9:94911298-94911299	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539399655	chr9:94911307-94911308	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs117594971	chr9:94911362-94911363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560657345	chr9:94911436-94911437	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs576071368	chr9:94911442-94911443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs111834786	chr9:94911449-94911450	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs193037395	chr9:94911452-94911453	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543047661	chr9:94911481-94911482	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs184659782	chr9:94911497-94911498	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs532086262	chr9:94911520-94911521	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188671876	chr9:94911531-94911532	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs145126546	chr9:94911572-94911573	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532766278	chr9:94911573-94911574	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs191923128	chr9:94911682-94911683	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs184218326	chr9:94911701-94911702	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94906800-94911200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:94908400-94911000	Enhancers	Fetal Muscle Trunk	muscle
3	chr9:94908800-94911000	Enhancers	Placenta	Placenta
4	chr9:94909800-94914400	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:94910000-94911000	Enhancers	Esophagus	oesophagus
6	chr9:94910000-94911200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:94910000-94913000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:94910000-94914000	Weak transcription	Brain Hippocampus Middle	brain
9	chr9:94910000-94914000	Weak transcription	Colon Smooth Muscle	Colon
10	chr9:94910200-94910800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr9:94910200-94913000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:94910200-94913800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr9:94910200-94914000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:94910200-94914200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:94910200-94914200	Weak transcription	Pancreas	Pancrea
16	chr9:94910200-94914600	Weak transcription	Fetal Lung	lung
17	chr9:94910200-94923800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr9:94910400-94911000	Enhancers	HSMMtube	muscle
19	chr9:94910400-94911200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:94910400-94912400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr9:94910400-94912400	Weak transcription	HSMM	muscle
22	chr9:94910400-94913400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:94910400-94913400	Weak transcription	NH-A	brain
24	chr9:94910400-94913400	Weak transcription	NHDF-Ad	bronchial
25	chr9:94910400-94913400	Weak transcription	Osteobl	bone
26	chr9:94910400-94913800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:94910400-94913800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr9:94910400-94913800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:94910400-94913800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:94910400-94913800	Weak transcription	Fetal Muscle Leg	muscle
31	chr9:94910400-94913800	Weak transcription	Ovary	ovary
32	chr9:94910400-94913800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr9:94910400-94913800	Weak transcription	HMEC	breast
34	chr9:94910400-94913800	Weak transcription	NHLF	lung
35	chr9:94910400-94914000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr9:94910400-94914000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:94910400-94914000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:94910400-94914000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr9:94910400-94914000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr9:94910400-94914000	Weak transcription	Stomach Smooth Muscle	stomach
41	chr9:94910400-94914000	Weak transcription	A549	lung
42	chr9:94910400-94914000	Weak transcription	HUVEC	blood vessel
43	chr9:94910400-94914000	Weak transcription	NHEK	skin
44	chr9:94910400-94914200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr9:94910400-94914200	Weak transcription	K562	blood
46	chr9:94910400-94914400	Weak transcription	Left Ventricle	heart
47	chr9:94910600-94910800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:94910600-94911000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:94910800-94911000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:94911000-94911200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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