Variant report

Variant	nsv524727
Chromosome Location	chr1:120023971-120056401
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	CTCF	chr1:120055810-120055860	GM13976	blood:	n/a	n/a
2	CTCF	chr1:120025899-120025945	H1-hESC	embryonic stem cell:	n/a	chr1:120025929-120025938
3	CTCF	chr1:120055520-120055670	HCT-116	colon:	n/a	chr1:120055660-120055668
4	CTCF	chr1:120050077-120050097	GM13976	blood:	n/a	n/a
5	CTCF	chr1:120048463-120048507	GM13976	blood:	n/a	n/a
6	CTCF	chr1:120038780-120038930	GM12868	blood:	n/a	n/a
7	CTCF	chr1:120024349-120024355	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr1:120052618-120052676	LNCaP	prostate:	n/a	n/a
9	CTCF	chr1:120037160-120037310	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr1:120055641-120055703	MCF-7	breast:	n/a	chr1:120055670-120055688 chr1:120055660-120055668 chr1:120055672-120055693
11	CTCF	chr1:120024243-120024348	Kidney_OC	kidney:	n/a	n/a
12	E2F4	chr1:120037824-120038063	MCF10A-Er-Src	breast:	n/a	n/a
13	ELF1	chr1:120046878-120047131	K562	blood:	n/a	chr1:120047004-120047017
14	ELK1	chr1:120036196-120036215	K562	blood:	n/a	n/a
15	EP300	chr1:120046568-120046616	K562	blood:	n/a	n/a
16	FOS	chr1:120052872-120052896	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr1:120052729-120053060	MCF10A-Er-Src	breast:	n/a	n/a
18	FOXA2	chr1:120040426-120041060	A549	lung:	n/a	n/a
19	GATA2	chr1:120049594-120049929	SH-SY5Y	brain:	n/a	chr1:120049718-120049732 chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
20	GATA2	chr1:120049582-120049879	HUVEC	blood vessel:	n/a	chr1:120049718-120049732 chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
21	GATA3	chr1:120049654-120049865	SH-SY5Y	brain:	n/a	chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
22	GATA3	chr1:120049600-120049965	MCF-7	breast:	n/a	chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
23	GATA3	chr1:120049598-120049925	MCF-7	breast:	n/a	chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
24	GATA3	chr1:120049584-120049980	SK-N-SH	brain:	n/a	chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
25	GATA3	chr1:120049466-120049943	MCF-7	breast:	n/a	chr1:120049719-120049729 chr1:120049664-120049674 chr1:120049824-120049834 chr1:120049721-120049728 chr1:120049770-120049786 chr1:120049770-120049786
26	GATA3	chr1:120051619-120051805	SH-SY5Y	brain:	n/a	n/a
27	HNF4A	chr1:120035475-120035744	HepG2	liver:	n/a	chr1:120035625-120035640 chr1:120035627-120035639 chr1:120035625-120035640 chr1:120035626-120035634 chr1:120035625-120035640 chr1:120035625-120035640 chr1:120035627-120035639 chr1:120035625-120035640
28	JUN	chr1:120052579-120052693	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAFF	chr1:120056045-120056208	HepG2	liver:	n/a	n/a
30	MAFK	chr1:120055993-120056287	HepG2	liver:	n/a	n/a
31	MAX	chr1:120027057-120027257	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAZ	chr1:120029229-120029277	HepG2	liver:	n/a	n/a
33	MAZ	chr1:120032665-120032719	HepG2	liver:	n/a	n/a
34	MYC	chr1:120043859-120043975	HepG2	liver:	n/a	n/a
35	NR2F2	chr1:120049526-120049874	MCF-7	breast:	n/a	chr1:120049698-120049713
36	POLR2A	chr1:120055476-120055544	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr1:120048954-120048993	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr1:120036219-120036280	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr1:120027726-120027785	MCF10A-Er-Src	breast:	n/a	n/a
40	RCOR1	chr1:120038327-120038358	HepG2	liver:	n/a	n/a
41	REST	chr1:120047521-120047684	H1-hESC	embryonic stem cell:	n/a	chr1:120047597-120047605
42	RFX5	chr1:120038798-120039069	HepG2	liver:	n/a	chr1:120038947-120038962
43	SETDB1	chr1:120035547-120035913	U2OS	brain:	n/a	n/a
44	STAT3	chr1:120052716-120052887	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr1:120055275-120055429	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr1:120052804-120052971	MCF10A-Er-Src	breast:	n/a	n/a
47	TCF7L2	chr1:120035551-120036241	HEK293	kidney:	n/a	chr1:120036035-120036051 chr1:120036036-120036050 chr1:120036035-120036051

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120049183-120049233	GM12891	blood:	n/a
2	chr1:120049183-120049233	GM12891	blood:	n/a
3	chr1:120048352-120048402	T-47D	breast:	n/a
4	chr1:120050104-120050154	PFSK-1	brain:	n/a
5	chr1:120050104-120050154	Hela-S3	cervix:	n/a
6	chr1:120050104-120050154	HRE	kidney:	n/a
7	chr1:120050104-120050154	SK-N-MC	brain:	n/a
8	chr1:120049183-120049233	HRPEpiC	eye:	n/a
9	chr1:120048352-120048402	Hepatocyte	liver:	n/a
10	chr1:120048352-120048402	HCF	heart:	n/a
11	chr1:120049183-120049233	SKMC	muscle:	n/a
12	chr1:120049183-120049233	MCF10A-Er-Src	breast:	n/a
13	chr1:120049183-120049233	ECC-1	luminal epithelium:	n/a
14	chr1:120048352-120048402	ovcar-3	ovarian:	n/a
15	chr1:120048352-120048402	NT2-D1	testis:	n/a
16	chr1:120050104-120050154	GM12892	blood:	n/a
17	chr1:120048352-120048402	SK-N-MC	brain:	n/a
18	chr1:120050104-120050154	MCF10A-Er-Src	breast:	n/a
19	chr1:120049183-120049233	BJ	skin:	n/a
20	chr1:120049183-120049233	SK-N-MC	brain:	n/a
21	chr1:120050104-120050154	AoSMC	blood vessel:	n/a
22	chr1:120049183-120049233	BE2_C	brain:	n/a
23	chr1:120050104-120050154	GM06990	blood:	n/a
24	chr1:120049183-120049233	PANC-1	pancreas:	n/a
25	chr1:120050104-120050154	HL-60	blood:	n/a
26	chr1:120049183-120049233	HepG2	liver:	n/a
27	chr1:120048352-120048402	Caco-2	colon:	n/a
28	chr1:120050104-120050154	Hepatocyte	liver:	n/a
29	chr1:120049183-120049233	HCF	heart:	n/a
30	chr1:120050104-120050154	HepG2	liver:	n/a
31	chr1:120050104-120050154	NHBE	bronchial:	n/a
32	chr1:120049183-120049233	HCM	heart:	n/a
33	chr1:120050104-120050154	HCF	heart:	n/a
34	chr1:120048352-120048402	NB4	blood:	n/a
35	chr1:120049183-120049233	Jurkat	blood:	n/a
36	chr1:120050104-120050154	AG04450	lung:	fetal
37	chr1:120048352-120048402	IMR90	lung:	fetal
38	chr1:120049183-120049233	K562	blood:	n/a
39	chr1:120048352-120048402	HCPEpiC	choroid plexus:	n/a
40	chr1:120049183-120049233	HCPEpiC	choroid plexus:	n/a
41	chr1:120049183-120049233	GM19239	blood:	n/a
42	chr1:120048352-120048402	ProgFib	skin:	n/a
43	chr1:120048352-120048402	PrEC	prostate:	n/a
44	chr1:120049183-120049233	HRE	kidney:	n/a
45	chr1:120048352-120048402	RPTEC	kidney:	n/a
46	chr1:120050104-120050154	HEK293	kidney:	embryo
47	chr1:120048352-120048402	GM12891	blood:	n/a
48	chr1:120049183-120049233	U87	brain:	n/a
49	chr1:120049183-120049233	AG04450	lung:	fetal
50	chr1:120048352-120048402	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:120018999..120023274-chr1:120024082..120027954,3	K562	blood:
2	chr1:120046437..120049249-chr1:120049394..120051111,2	MCF-7	breast:
3	chr1:120033409..120034120-chr21:39626869..39627676,2	MCF-7	breast:

Variant related genes	Relation type
HSD3B1	TF binding region
GAPDHP58	TF binding region
HSD3B1	CpG island
GAPDHP58	CpG island
ENSG00000203857	chromatin interactions

Extended variants
information (count: 1148 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1148 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs911244	chr1:120023971-120023972	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587665438	chr1:120024006-120024007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10754397	chr1:120024021-120024022	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs587618449	chr1:120024027-120024028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17023805	chr1:120024078-120024079	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs587752944	chr1:120024093-120024094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587620754	chr1:120024114-120024115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587682340	chr1:120024118-120024119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17023809	chr1:120024127-120024128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs188949145	chr1:120024137-120024138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112169915	chr1:120024183-120024184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587735963	chr1:120024193-120024194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587776302	chr1:120024199-120024200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192573832	chr1:120024217-120024218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373258120	chr1:120024229-120024230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587718077	chr1:120024239-120024240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140297826	chr1:120024265-120024266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184363608	chr1:120024291-120024292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs3862257	chr1:120024321-120024322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587603917	chr1:120024330-120024331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113546671	chr1:120024354-120024355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114087927	chr1:120024362-120024363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188440737	chr1:120024364-120024365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587673466	chr1:120024388-120024389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587723937	chr1:120024426-120024427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587625983	chr1:120024492-120024493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587676354	chr1:120024496-120024497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4077147	chr1:120024504-120024505	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs115108852	chr1:120024564-120024565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373136325	chr1:120024595-120024596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141628688	chr1:120024602-120024603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151125746	chr1:120024687-120024688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs876574	chr1:120024691-120024692	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184109404	chr1:120024713-120024714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587700365	chr1:120024776-120024777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112369829	chr1:120024802-120024803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587652648	chr1:120024911-120024912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587705479	chr1:120024939-120024940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs911245	chr1:120024974-120024975	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs587640893	chr1:120024976-120024977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201555264	chr1:120024985-120024986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150600292	chr1:120024992-120024993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367633303	chr1:120025018-120025019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371532990	chr1:120025052-120025053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587740350	chr1:120025081-120025082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138637153	chr1:120025091-120025092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587663937	chr1:120025112-120025113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149304436	chr1:120025180-120025181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10923841	chr1:120025190-120025191	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79396019	chr1:120025217-120025218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21760589	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120019000-120026400	Weak transcription	Fetal Intestine Small	intestine
2	chr1:120021000-120025800	Weak transcription	Liver	Liver
3	chr1:120022200-120028200	Enhancers	Placenta	Placenta
4	chr1:120024200-120027200	Enhancers	HSMMtube	muscle
5	chr1:120024400-120026000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:120024400-120027000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:120024400-120027400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:120024600-120028400	Enhancers	Fetal Intestine Large	intestine
9	chr1:120024800-120026800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:120024800-120026800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr1:120024800-120028200	Enhancers	Fetal Heart	heart
12	chr1:120025000-120026800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr1:120025200-120026400	Enhancers	Pancreas	Pancrea
14	chr1:120025400-120026000	Enhancers	Adipose Nuclei	Adipose
15	chr1:120025400-120026400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:120025400-120026800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:120025600-120026400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:120025600-120027000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr1:120025800-120026000	Enhancers	Fetal Muscle Leg	muscle
20	chr1:120025800-120026800	Enhancers	Liver	Liver
21	chr1:120026000-120026200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:120026000-120026400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr1:120026000-120026800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:120026000-120030600	Weak transcription	Adipose Nuclei	Adipose
25	chr1:120026000-120034200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:120026200-120026400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:120026200-120027000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:120026200-120027400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:120026400-120028400	Enhancers	Fetal Intestine Small	intestine
30	chr1:120026400-120030400	Weak transcription	Pancreas	Pancrea
31	chr1:120026800-120030400	Weak transcription	Liver	Liver
32	chr1:120027000-120027200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:120028200-120030400	Weak transcription	Placenta	Placenta
34	chr1:120028200-120031000	Weak transcription	Fetal Heart	heart
35	chr1:120030400-120030800	Enhancers	Pancreas	Pancrea
36	chr1:120030400-120031600	Enhancers	Liver	Liver
37	chr1:120030600-120030800	Enhancers	Placenta	Placenta
38	chr1:120030600-120031000	Enhancers	Adipose Nuclei	Adipose
39	chr1:120031000-120032400	Enhancers	Fetal Heart	heart
40	chr1:120031600-120032800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr1:120031600-120035800	Weak transcription	Liver	Liver
42	chr1:120031800-120032600	Bivalent Enhancer	HSMMtube	muscle
43	chr1:120032800-120038400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:120033600-120033800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:120034200-120036000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:120035800-120036200	Enhancers	Liver	Liver
47	chr1:120036200-120036600	Weak transcription	Liver	Liver
48	chr1:120036600-120037400	ZNF genes & repeats	Liver	Liver
49	chr1:120038000-120040200	Weak transcription	Brain Angular Gyrus	brain
50	chr1:120038400-120039200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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