Variant report

Variant	esv1818340
Chromosome Location	chr1:56359741-56408597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:56363900-56364158	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:56385231-56385412	A549	lung:	n/a	n/a
3	CEBPB	chr1:56363833-56364209	A549	lung:	n/a	n/a
4	CEBPB	chr1:56363895-56364260	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:56363937-56364197	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:56382264-56382622	MCF-7	breast:	n/a	n/a
7	CEBPB	chr1:56363850-56364274	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:56393772-56393875	IMR90	lung:	n/a	n/a
9	CEBPB	chr1:56363954-56364224	A549	lung:	n/a	n/a
10	CEBPB	chr1:56382219-56382613	MCF-7	breast:	n/a	n/a
11	CEBPB	chr1:56363929-56364222	A549	lung:	n/a	n/a
12	CEBPB	chr1:56382227-56382613	IMR90	lung:	n/a	n/a
13	CTCF	chr1:56379315-56379392	Fibrobl	skin:	n/a	n/a
14	CTCF	chr1:56360340-56360490	AG10803	skin:	n/a	n/a
15	CTCF	chr1:56360380-56360530	HCFaa	heart:	n/a	n/a
16	CTCF	chr1:56360340-56360490	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr1:56360400-56360550	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr1:56379322-56379327	GM10248	blood:	n/a	n/a
19	CTCF	chr1:56382220-56382370	AG10803	skin:	n/a	n/a
20	CTCF	chr1:56360360-56360510	HMF	breast:	n/a	n/a
21	CTCF	chr1:56401005-56401029	GM13977	blood:	n/a	n/a
22	CTCF	chr1:56360340-56360490	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr1:56360380-56360530	AG10803	skin:	n/a	n/a
24	CTCF	chr1:56379440-56379590	GM12867	blood:	n/a	n/a
25	CTCF	chr1:56360400-56360550	AG09309	skin:	n/a	n/a
26	CTCF	chr1:56404240-56404390	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr1:56382320-56382470	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr1:56360420-56360570	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr1:56360420-56360570	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr1:56360380-56360530	HCM	heart:	n/a	n/a
31	CTCF	chr1:56360370-56360632	IMR90	lung:	n/a	n/a
32	CTCF	chr1:56400326-56400374	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:56360360-56360510	AG04449	skin:	n/a	n/a
34	CTCF	chr1:56404540-56404690	HepG2	liver:	n/a	n/a
35	CTCF	chr1:56360380-56360530	HMF	breast:	n/a	n/a
36	CTCF	chr1:56381714-56381753	GM13976	blood:	n/a	n/a
37	CTCF	chr1:56360380-56360530	HFF	foreskin:	n/a	n/a
38	E2F4	chr1:56382631-56382841	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr1:56392160-56392274	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr1:56388066-56388266	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr1:56363872-56364181	MCF10A-Er-Src	breast:	n/a	n/a
42	EP300	chr1:56382098-56382330	SK-N-SH_RA	brain:	n/a	chr1:56382304-56382313
43	EP300	chr1:56396868-56397086	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr1:56396442-56398054	SK-N-SH	brain:	n/a	chr1:56397996-56398010
45	EP300	chr1:56396699-56397435	SK-N-SH	brain:	n/a	n/a
46	EP300	chr1:56396864-56397158	SK-N-SH_RA	brain:	n/a	n/a
47	FAM48A	chr1:56377185-56377244	GM12878	blood:	n/a	n/a
48	FAM48A	chr1:56382683-56382716	GM12878	blood:	n/a	n/a
49	FOS	chr1:56363869-56364272	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:56397396-56397681	MCF10A-Er-Src	breast:	n/a	chr1:56397452-56397464

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:56397400-56397450	ovcar-3	ovarian:	n/a
2	chr1:56397447-56397497	HEEpiC	esophagus:	n/a
3	chr1:56394286-56394336	GM12878	blood:	n/a
4	chr1:56397447-56397497	HRPEpiC	eye:	n/a
5	chr1:56397400-56397450	ECC-1	luminal epithelium:	n/a
6	chr1:56397447-56397497	MCF10A-Er-Src	breast:	n/a
7	chr1:56397400-56397450	MCF10A-Er-Src	breast:	n/a
8	chr1:56397400-56397450	IMR90	lung:	fetal
9	chr1:56397400-56397450	ProgFib	skin:	n/a
10	chr1:56394286-56394336	H1-hESC	embryonic stem cell:	embryo
11	chr1:56397447-56397497	ProgFib	skin:	n/a
12	chr1:56394286-56394336	AG04450	lung:	fetal
13	chr1:56394286-56394336	PFSK-1	brain:	n/a
14	chr1:56397400-56397450	AG09309	skin:	n/a
15	chr1:56394286-56394336	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:56394286-56394336	PANC-1	pancreas:	n/a
17	chr1:56394286-56394336	HCT-116	colon:	n/a
18	chr1:56397447-56397497	AG04450	lung:	fetal
19	chr1:56397400-56397450	AG04450	lung:	fetal
20	chr1:56397400-56397450	HCT-116	colon:	n/a
21	chr1:56397400-56397450	HEEpiC	esophagus:	n/a
22	chr1:56394286-56394336	MCF10A-Er-Src	breast:	n/a
23	chr1:56397400-56397450	HRE	kidney:	n/a
24	chr1:56397400-56397450	HMEC	breast:	n/a
25	chr1:56397447-56397497	SK-N-MC	brain:	n/a
26	chr1:56397447-56397497	GM12892	blood:	n/a
27	chr1:56397400-56397450	BE2_C	brain:	n/a
28	chr1:56397400-56397450	MCF-7	breast:	n/a
29	chr1:56397447-56397497	IMR90	lung:	fetal
30	chr1:56397447-56397497	HNPCEpiC	eye:	n/a
31	chr1:56397447-56397497	GM12878	blood:	n/a
32	chr1:56394286-56394336	BE2_C	brain:	n/a
33	chr1:56397400-56397450	HRCEpiC	kidney:	n/a
34	chr1:56394286-56394336	AG09319	gingival:	n/a
35	chr1:56397400-56397450	SAEC	small airway:	n/a
36	chr1:56397447-56397497	NB4	blood:	n/a
37	chr1:56394286-56394336	HRE	kidney:	n/a
38	chr1:56397400-56397450	BJ	skin:	n/a
39	chr1:56397447-56397497	AG09319	gingival:	n/a
40	chr1:56397447-56397497	AG10803	skin:	n/a
41	chr1:56394286-56394336	HCPEpiC	choroid plexus:	n/a
42	chr1:56397400-56397450	NHDF-neo	bronchial:	n/a
43	chr1:56394286-56394336	NHBE	bronchial:	n/a
44	chr1:56397447-56397497	PrEC	prostate:	n/a
45	chr1:56397400-56397450	LNCaP	prostate:	n/a
46	chr1:56397447-56397497	HCM	heart:	n/a
47	chr1:56397400-56397450	HAEpiC	amniotic membrane:	n/a
48	chr1:56397400-56397450	GM12878	blood:	n/a
49	chr1:56394286-56394336	A549	lung:	n/a
50	chr1:56394286-56394336	HRPEpiC	eye:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:56385562..56386307-chr1:56396787..56397745,2	MCF-7	breast:
2	chr1:56381262..56382928-chr1:56386333..56388137,2	MCF-7	breast:
3	chr1:56381262..56382928-chr1:56386333..56388137,2	MCF-7	breast:
4	chr1:56385562..56386307-chr1:56396787..56397745,2	MCF-7	breast:
5	chr1:56403818..56405745-chr1:56407271..56408987,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKAA2-11	chr1:56393186-56393484	NONHSAT003427
2	lnc-PPAP2B-8	chr1:56404387-56404650	NONHSAT003428
3	lnc-PPAP2B-8	chr1:56404788-56404953	NONHSAT003428
4	lnc-PRKAA2-11	chr1:56383981-56384141	NONHSAT003427
5	lnc-PPAP2B-5	chr1:56387038-56387084	ENSG00000230250.1
6	lnc-PRKAA2-11	chr1:56389261-56389531	NONHSAT003427
7	lnc-PPAP2B-5	chr1:56381282-56381817	ENSG00000230250.1

No data

Variant related genes	Relation type
PIGQP1	TF binding region
ENSG00000233079	TF binding region
PIGQP1	CpG island
ENSG00000233079	CpG island
ENSG00000227104	chromatin interactions

Extended variants
information (count: 2004 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2004 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9803781	chr1:56359741-56359742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs17113092	chr1:56359754-56359755	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547023685	chr1:56359787-56359788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557341433	chr1:56359803-56359804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6684428	chr1:56359813-56359814	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
6	rs145248387	chr1:56359870-56359871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571542974	chr1:56359906-56359907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537313459	chr1:56359914-56359915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75213753	chr1:56359952-56359953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545921952	chr1:56359956-56359957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573733461	chr1:56360010-56360011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536008475	chr1:56360023-56360024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149115500	chr1:56360046-56360047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60320048	chr1:56360047-56360048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553024696	chr1:56360110-56360111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190655633	chr1:56360114-56360115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs59647629	chr1:56360121-56360122	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs564513659	chr1:56360124-56360125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575551870	chr1:56360125-56360126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145047056	chr1:56360173-56360174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183475598	chr1:56360287-56360288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530310959	chr1:56360290-56360291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187813518	chr1:56360331-56360332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560618463	chr1:56360332-56360333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532428644	chr1:56360348-56360349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4926702	chr1:56360382-56360383	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs569240370	chr1:56360436-56360437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148691035	chr1:56360446-56360447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562010827	chr1:56360465-56360466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550890598	chr1:56360481-56360482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567388713	chr1:56360486-56360487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549128530	chr1:56360487-56360488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192298921	chr1:56360488-56360489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142246022	chr1:56360532-56360533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs151141221	chr1:56360565-56360566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140254521	chr1:56360572-56360573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540834374	chr1:56360592-56360593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574849856	chr1:56360608-56360609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144031852	chr1:56360640-56360641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111789557	chr1:56360669-56360670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574969904	chr1:56360680-56360681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12750698	chr1:56360685-56360686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12079927	chr1:56360693-56360694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183004836	chr1:56360708-56360709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532668628	chr1:56360711-56360712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546272426	chr1:56360790-56360791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562916636	chr1:56360854-56360855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531727562	chr1:56360864-56360865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188162677	chr1:56360893-56360894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192918221	chr1:56360955-56360956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	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
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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:188 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56359400-56361600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:56359600-56359800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:56359800-56360000	Enhancers	A549	lung
4	chr1:56359800-56360800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:56360000-56360400	Enhancers	NHDF-Ad	bronchial
6	chr1:56360000-56360800	Enhancers	Osteobl	bone
7	chr1:56360000-56364000	Weak transcription	A549	lung
8	chr1:56360200-56360600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr1:56360200-56360800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:56360400-56363600	Weak transcription	NHDF-Ad	bronchial
11	chr1:56360600-56363600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:56360800-56363600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:56360800-56363600	Weak transcription	Osteobl	bone
14	chr1:56361000-56361600	Enhancers	Fetal Intestine Small	intestine
15	chr1:56361600-56363400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:56363400-56365200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:56363600-56364000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr1:56363600-56364000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr1:56363600-56364000	Enhancers	Fetal Intestine Large	intestine
20	chr1:56363600-56364000	Enhancers	Osteobl	bone
21	chr1:56363600-56364600	Enhancers	NHDF-Ad	bronchial
22	chr1:56363600-56364800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:56364000-56364200	Enhancers	A549	lung
24	chr1:56365200-56382200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:56370000-56370400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:56370000-56370800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:56370000-56370800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr1:56370200-56370800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:56373400-56373800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:56373400-56373800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr1:56373800-56376600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:56373800-56378000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:56376400-56376800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr1:56376400-56376800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:56376600-56377000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr1:56377000-56378000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr1:56378000-56378200	Enhancers	Spleen	Spleen
38	chr1:56378000-56379600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:56378000-56383200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr1:56378200-56379400	ZNF genes & repeats	Spleen	Spleen
41	chr1:56379200-56379400	Enhancers	Gastric	stomach
42	chr1:56379400-56380200	Weak transcription	Spleen	Spleen
43	chr1:56379600-56381200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:56380800-56381600	Enhancers	Placenta	Placenta
45	chr1:56381200-56381600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:56381400-56382600	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:56381600-56383400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:56381600-56386400	Weak transcription	Placenta	Placenta
49	chr1:56381800-56382800	Enhancers	Fetal Lung	lung
50	chr1:56382000-56383000	Enhancers	Rectal Smooth Muscle	rectum

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