Variant report

Variant	nsv945404
Chromosome Location	chr1:241336290-241376563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:62)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:241344490-241344539	K562	blood:	n/a	n/a
2	BACH1	chr1:241376435-241376489	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr1:241375778-241375925	K562	blood:	n/a	n/a
4	CEBPB	chr1:241348934-241349093	HepG2	liver:	n/a	chr1:241349004-241349015
5	CHD2	chr1:241365768-241365913	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr1:241375960-241376110	A549	lung:	n/a	n/a
7	E2F4	chr1:241376547-241376677	MCF10A-Er-Src	breast:	n/a	n/a
8	E2F4	chr1:241345774-241345778	MCF10A-Er-Src	breast:	n/a	n/a
9	EP300	chr1:241371947-241372973	SK-N-SH	brain:	n/a	n/a
10	EP300	chr1:241372251-241372675	SK-N-SH_RA	brain:	n/a	n/a
11	EP300	chr1:241372214-241372659	SK-N-SH_RA	brain:	n/a	n/a
12	FOS	chr1:241349352-241349673	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr1:241376355-241376788	MCF10A-Er-Src	breast:	n/a	chr1:241376644-241376654 chr1:241376646-241376657
14	FOS	chr1:241349360-241349664	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:241350238-241350267	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr1:241344910-241345170	HUVEC	blood vessel:	n/a	n/a
17	FOS	chr1:241347409-241347822	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr1:241376265-241376886	MCF10A-Er-Src	breast:	n/a	chr1:241376644-241376654 chr1:241376646-241376657
19	FOS	chr1:241347376-241347850	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:241376348-241376842	MCF10A-Er-Src	breast:	n/a	chr1:241376644-241376654 chr1:241376646-241376657
21	FOS	chr1:241347457-241347751	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:241376322-241376886	MCF10A-Er-Src	breast:	n/a	chr1:241376644-241376654 chr1:241376646-241376657
23	FOS	chr1:241349374-241349674	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr1:241347510-241347681	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:241349352-241349675	MCF10A-Er-Src	breast:	n/a	n/a
26	GATA2	chr1:241372121-241372973	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr1:241372181-241372788	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr1:241372235-241372790	SK-N-SH	brain:	n/a	n/a
29	GATA3	chr1:241372303-241372708	SK-N-SH	brain:	n/a	n/a
30	HNF4A	chr1:241355084-241355388	HepG2	liver:	n/a	chr1:241355298-241355313
31	HNF4A	chr1:241355100-241355465	HepG2	liver:	n/a	chr1:241355298-241355313
32	HNF4G	chr1:241355178-241355447	HepG2	liver:	n/a	chr1:241355297-241355312
33	HNF4G	chr1:241355041-241355570	HepG2	liver:	n/a	chr1:241355297-241355312
34	JUND	chr1:241365628-241365887	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAFF	chr1:241340978-241341341	HepG2	liver:	n/a	chr1:241341150-241341168
36	MAFF	chr1:241340996-241341321	K562	blood:	n/a	chr1:241341150-241341168
37	MAFK	chr1:241340979-241341346	IMR90	lung:	n/a	chr1:241341152-241341167
38	MAFK	chr1:241340988-241341326	K562	blood:	n/a	chr1:241341152-241341167
39	MAFK	chr1:241340978-241341344	HepG2	liver:	n/a	chr1:241341152-241341167
40	MAFK	chr1:241340976-241341348	HepG2	liver:	n/a	chr1:241341152-241341167
41	MAFK	chr1:241340987-241341310	Hela-S3	cervix:	n/a	chr1:241341152-241341167
42	MAFK	chr1:241340977-241341312	H1-hESC	embryonic stem cell:	n/a	chr1:241341152-241341167
43	MAFK	chr1:241340952-241341318	GM12878	blood:	n/a	chr1:241341152-241341167
44	MAFK	chr1:241349233-241349245	H1-hESC	embryonic stem cell:	n/a	n/a
45	MYC	chr1:241365262-241365462	H1-hESC	embryonic stem cell:	n/a	n/a
46	MYC	chr1:241347055-241347075	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr1:241376408-241376703	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr1:241352625-241352675	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr1:241366483-241366602	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr1:241352716-241353084	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:241371615-241371665	H1-hESC	embryonic stem cell:	embryo
2	chr1:241371615-241371665	H1-hESC	embryonic stem cell:	embryo
3	chr1:241371615-241371665	A549	lung:	n/a
4	chr1:241371615-241371665	AG09309	skin:	n/a
5	chr1:241371615-241371665	PFSK-1	brain:	n/a
6	chr1:241371615-241371665	ovcar-3	ovarian:	n/a
7	chr1:241371615-241371665	GM19239	blood:	n/a
8	chr1:241371615-241371665	SK-N-MC	brain:	n/a
9	chr1:241371615-241371665	BJ	skin:	n/a
10	chr1:241371615-241371665	MCF10A-Er-Src	breast:	n/a
11	chr1:241371615-241371665	MCF-7	breast:	n/a
12	chr1:241371615-241371665	Hela-S3	cervix:	n/a
13	chr1:241371615-241371665	HCT-116	colon:	n/a
14	chr1:241371615-241371665	PrEC	prostate:	n/a
15	chr1:241371615-241371665	BE2_C	brain:	n/a
16	chr1:241371615-241371665	Jurkat	blood:	n/a
17	chr1:241371615-241371665	HEK293	kidney:	embryo
18	chr1:241371615-241371665	LNCaP	prostate:	n/a
19	chr1:241371615-241371665	AG09319	gingival:	n/a
20	chr1:241371615-241371665	U87	brain:	n/a
21	chr1:241371615-241371665	HRCEpiC	kidney:	n/a
22	chr1:241371615-241371665	AG10803	skin:	n/a
23	chr1:241371615-241371665	GM12891	blood:	n/a
24	chr1:241371615-241371665	T-47D	breast:	n/a
25	chr1:241371615-241371665	GM12878	blood:	n/a
26	chr1:241371615-241371665	HMEC	breast:	n/a
27	chr1:241371615-241371665	Caco-2	colon:	n/a
28	chr1:241371615-241371665	HEEpiC	esophagus:	n/a
29	chr1:241371615-241371665	RPTEC	kidney:	n/a
30	chr1:241371615-241371665	SKMC	muscle:	n/a
31	chr1:241371615-241371665	NB4	blood:	n/a
32	chr1:241371615-241371665	IMR90	lung:	fetal
33	chr1:241371615-241371665	NT2-D1	testis:	n/a
34	chr1:241371615-241371665	K562	blood:	n/a
35	chr1:241371615-241371665	NHBE	bronchial:	n/a
36	chr1:241371615-241371665	GM12892	blood:	n/a
37	chr1:241371615-241371665	HepG2	liver:	n/a
38	chr1:241371615-241371665	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:241371615-241371665	SAEC	small airway:	n/a
40	chr1:241371615-241371665	HUVEC	blood vessel:	n/a
41	chr1:241371615-241371665	HNPCEpiC	eye:	n/a
42	chr1:241371615-241371665	AG04450	lung:	fetal
43	chr1:241371615-241371665	HRE	kidney:	n/a
44	chr1:241371615-241371665	Hepatocyte	liver:	n/a
45	chr1:241371615-241371665	HIPEpiC	eye:	n/a
46	chr1:241371615-241371665	SK-N-SH	brain:	n/a
47	chr1:241371615-241371665	HL-60	blood:	n/a
48	chr1:241371615-241371665	AoSMC	blood vessel:	n/a
49	chr1:241371615-241371665	HAEpiC	amniotic membrane:	n/a
50	chr1:241371615-241371665	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:241373926..241376648-chr1:241377366..241379773,2	MCF-7	breast:
2	chr1:241328987..241330488-chr1:241335172..241337428,2	MCF-7	breast:

No data

Variant related genes	Relation type
RGS7	TF binding region
RGS7	CpG island

Extended variants
information (count: 1353 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1353 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540562587	chr1:241336307-241336308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565091936	chr1:241336363-241336364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565705881	chr1:241336373-241336374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192983228	chr1:241336387-241336388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565219555	chr1:241336443-241336444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6658400	chr1:241336456-241336457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs7535928	chr1:241336481-241336482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs185673936	chr1:241336544-241336545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556917042	chr1:241336591-241336592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61833782	chr1:241336615-241336616	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs542542830	chr1:241336620-241336621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114156381	chr1:241336650-241336651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566867602	chr1:241336679-241336680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114622058	chr1:241336704-241336705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199803311	chr1:241336791-241336792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545024993	chr1:241336813-241336814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564993437	chr1:241336827-241336828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534087123	chr1:241336891-241336892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530920868	chr1:241336934-241336935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544779641	chr1:241336955-241336956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139048683	chr1:241337057-241337058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558730087	chr1:241337062-241337063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530396294	chr1:241337095-241337096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201147056	chr1:241337097-241337098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547349967	chr1:241337136-241337137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116698001	chr1:241337182-241337183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377306218	chr1:241337236-241337237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370732590	chr1:241337241-241337242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570760642	chr1:241337357-241337358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188783127	chr1:241337370-241337371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373212246	chr1:241337375-241337376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538142133	chr1:241337378-241337379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530213293	chr1:241337398-241337399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149897519	chr1:241337426-241337427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7545275	chr1:241337427-241337428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs377415292	chr1:241337431-241337432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535117776	chr1:241337454-241337455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs36032687	chr1:241337459-241337460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4660037	chr1:241337461-241337462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs144963600	chr1:241337478-241337479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142155915	chr1:241337486-241337487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4660038	chr1:241337545-241337546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7514324	chr1:241337695-241337696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147849933	chr1:241337802-241337803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368816268	chr1:241337811-241337812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575687152	chr1:241337868-241337869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371456117	chr1:241337877-241337878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544405883	chr1:241337937-241337938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191149113	chr1:241337946-241337947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183702053	chr1:241337976-241337977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	19759907	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241323200-241338800	Weak transcription	Fetal Kidney	kidney
2	chr1:241335400-241336400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr1:241338800-241339400	Enhancers	Fetal Kidney	kidney
4	chr1:241339400-241341000	Weak transcription	Fetal Kidney	kidney
5	chr1:241341200-241341400	Enhancers	Fetal Kidney	kidney
6	chr1:241342600-241343000	Enhancers	Fetal Intestine Large	intestine
7	chr1:241342800-241343200	Enhancers	Fetal Intestine Small	intestine
8	chr1:241345400-241345600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr1:241345800-241348000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr1:241346400-241347400	Enhancers	Stomach Mucosa	stomach
11	chr1:241347000-241347400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr1:241347000-241347600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:241347400-241349200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr1:241347400-241355600	Weak transcription	Stomach Mucosa	stomach
15	chr1:241347600-241348800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:241348800-241349800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:241349200-241349800	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr1:241349800-241350200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr1:241350200-241351200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr1:241351200-241355800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr1:241354600-241356200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr1:241354600-241356800	Enhancers	Fetal Intestine Large	intestine
23	chr1:241354800-241355600	Enhancers	HepG2	liver
24	chr1:241354800-241356000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr1:241355000-241355600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:241355000-241356000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:241355000-241356000	Enhancers	Liver	Liver
28	chr1:241355000-241356200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:241355000-241356200	Enhancers	Fetal Intestine Small	intestine
30	chr1:241355400-241355800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr1:241355600-241356400	Enhancers	Stomach Mucosa	stomach
32	chr1:241355800-241356800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr1:241356000-241360800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr1:241356400-241358000	Weak transcription	Stomach Mucosa	stomach
35	chr1:241358000-241358200	Enhancers	Stomach Mucosa	stomach
36	chr1:241360200-241360400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr1:241362400-241362600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr1:241365000-241367800	Enhancers	Fetal Intestine Large	intestine
39	chr1:241365200-241365400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:241365200-241365400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr1:241365200-241365600	Enhancers	Fetal Lung	lung
42	chr1:241365200-241366400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr1:241365200-241366400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:241365200-241366400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:241365200-241366600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr1:241365200-241366800	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:241365400-241366000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr1:241365400-241366200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr1:241365400-241366400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:241365400-241366400	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links