Variant report

Variant	nsv607657
Chromosome Location	chr7:78329795-78483211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:427)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:78350699-78350703	K562	blood:	n/a	n/a
2	ARID3A	chr7:78338872-78339618	HepG2	liver:	n/a	n/a
3	BATF	chr7:78399104-78399340	GM12878	blood:	n/a	n/a
4	BATF	chr7:78399034-78399449	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:78399136-78399379	GM12878	blood:	n/a	n/a
6	BRCA1	chr7:78399076-78399125	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr7:78364149-78364157	GM12878	blood:	n/a	n/a
8	CCNT2	chr7:78356655-78356873	K562	blood:	n/a	n/a
9	CEBPB	chr7:78339190-78339624	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:78355056-78355097	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr7:78399659-78399974	A549	lung:	n/a	chr7:78399817-78399828 chr7:78399817-78399830
12	CEBPB	chr7:78399667-78400010	IMR90	lung:	n/a	chr7:78399817-78399828 chr7:78399817-78399830 chr7:78399991-78400002
13	CEBPB	chr7:78332077-78332646	IMR90	lung:	n/a	chr7:78332556-78332569
14	CEBPB	chr7:78479464-78479733	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:78362296-78362788	HepG2	liver:	n/a	chr7:78362622-78362633
16	CEBPB	chr7:78361530-78361735	HepG2	liver:	n/a	chr7:78361574-78361585 chr7:78361574-78361587
17	CEBPB	chr7:78366796-78366971	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:78352655-78352846	HepG2	liver:	n/a	chr7:78352766-78352777
19	CEBPB	chr7:78339315-78339573	A549	lung:	n/a	n/a
20	CEBPB	chr7:78386055-78386101	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:78399670-78399988	HepG2	liver:	n/a	chr7:78399817-78399828 chr7:78399817-78399830
22	CHD1	chr7:78399345-78399548	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr7:78400306-78400793	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr7:78399928-78400725	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:78409261-78409346	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:78398240-78398390	HFF	foreskin:	n/a	chr7:78398313-78398326
27	CTCF	chr7:78398300-78398450	GM12875	blood:	n/a	chr7:78398313-78398326
28	CTCF	chr7:78398240-78398390	GM12873	blood:	n/a	chr7:78398313-78398326
29	CTCF	chr7:78425529-78425585	GM13976	blood:	n/a	n/a
30	CTCF	chr7:78398280-78398430	GM12873	blood:	n/a	chr7:78398313-78398326
31	CTCF	chr7:78375880-78376030	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:78398280-78398430	AG04449	skin:	n/a	chr7:78398313-78398326
33	CTCF	chr7:78398160-78398310	HPF	lung:	n/a	n/a
34	CTCF	chr7:78409298-78409349	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr7:78409114-78409404	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:78398200-78398350	SK-N-SH_RA	brain:	n/a	chr7:78398313-78398326
37	CTCF	chr7:78398314-78398339	ProgFib	skin:	n/a	n/a
38	CTCF	chr7:78398220-78398370	HBMEC	blood vessel:	n/a	chr7:78398313-78398326
39	CTCF	chr7:78400436-78400507	Fibrobl	skin:	n/a	n/a
40	CTCF	chr7:78409260-78409410	RPTEC	kidney:	n/a	n/a
41	CTCF	chr7:78454098-78454215	GM13976	blood:	n/a	n/a
42	CTCF	chr7:78409231-78409378	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:78409114-78409475	GM12878	blood:	n/a	n/a
44	CTCF	chr7:78409200-78409350	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr7:78398260-78398410	GM12866	blood:	n/a	chr7:78398313-78398326
46	CTCF	chr7:78375760-78375910	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr7:78375906-78375965	NHEK	skin:	n/a	n/a
48	CTCF	chr7:78398300-78398450	HAc	cerebellar:	n/a	chr7:78398313-78398326
49	CTCF	chr7:78375800-78375950	NHEK	skin:	n/a	n/a
50	CTCF	chr7:78398280-78398430	AG04450	lung:	n/a	chr7:78398313-78398326

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:78376399-78376449	HCT-116	colon:	n/a
2	chr7:78422673-78422723	K562	blood:	n/a
3	chr7:78386131-78386181	BE2_C	brain:	n/a
4	chr7:78376399-78376449	Jurkat	blood:	n/a
5	chr7:78386131-78386181	NH-A	brain:	n/a
6	chr7:78368660-78368710	NT2-D1	testis:	n/a
7	chr7:78376399-78376449	SK-N-SH	brain:	n/a
8	chr7:78376399-78376449	HIPEpiC	eye:	n/a
9	chr7:78386131-78386181	HCT-116	colon:	n/a
10	chr7:78422673-78422723	Jurkat	blood:	n/a
11	chr7:78376399-78376449	H1-hESC	embryonic stem cell:	embryo
12	chr7:78422673-78422723	HL-60	blood:	n/a
13	chr7:78346166-78346216	GM19239	blood:	n/a
14	chr7:78422673-78422723	GM19239	blood:	n/a
15	chr7:78368660-78368710	K562	blood:	n/a
16	chr7:78368756-78368806	CMK	blood:	n/a
17	chr7:78376399-78376449	SAEC	small airway:	n/a
18	chr7:78346166-78346216	AG09309	skin:	n/a
19	chr7:78376399-78376449	CMK	blood:	n/a
20	chr7:78346166-78346216	HCF	heart:	n/a
21	chr7:78386131-78386181	U87	brain:	n/a
22	chr7:78376399-78376449	IMR90	lung:	fetal
23	chr7:78368660-78368710	Hela-S3	cervix:	n/a
24	chr7:78386131-78386181	AG09319	gingival:	n/a
25	chr7:78368756-78368806	HCM	heart:	n/a
26	chr7:78368660-78368710	HepG2	liver:	n/a
27	chr7:78368660-78368710	HRE	kidney:	n/a
28	chr7:78346166-78346216	NHBE	bronchial:	n/a
29	chr7:78386131-78386181	PANC-1	pancreas:	n/a
30	chr7:78422673-78422723	HUVEC	blood vessel:	n/a
31	chr7:78415591-78415641	H1-hESC	embryonic stem cell:	embryo
32	chr7:78346166-78346216	AG10803	skin:	n/a
33	chr7:78368660-78368710	HCF	heart:	n/a
34	chr7:78415591-78415641	SK-N-SH_RA	brain:	n/a
35	chr7:78415591-78415641	GM12892	blood:	n/a
36	chr7:78368756-78368806	SKMC	muscle:	n/a
37	chr7:78415591-78415641	HEEpiC	esophagus:	n/a
38	chr7:78422673-78422723	IMR90	lung:	fetal
39	chr7:78368756-78368806	HIPEpiC	eye:	n/a
40	chr7:78415591-78415641	HCT-116	colon:	n/a
41	chr7:78368756-78368806	NHBE	bronchial:	n/a
42	chr7:78386131-78386181	LNCaP	prostate:	n/a
43	chr7:78415591-78415641	BE2_C	brain:	n/a
44	chr7:78368660-78368710	BJ	skin:	n/a
45	chr7:78368660-78368710	HEEpiC	esophagus:	n/a
46	chr7:78386131-78386181	Hela-S3	cervix:	n/a
47	chr7:78368660-78368710	SKMC	muscle:	n/a
48	chr7:78422673-78422723	AG10803	skin:	n/a
49	chr7:78422673-78422723	PrEC	prostate:	n/a
50	chr7:78386131-78386181	MCF10A-Er-Src	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:78354533..78356785-chr7:78357118..78359771,2	K562	blood:
2	chr2:57140755..57141275-chr7:78397919..78398439,2	MCF-7	breast:
3	chr7:78405474..78407016-chr7:78415742..78418693,2	K562	blood:
4	chr7:78354533..78356785-chr7:78357118..78359771,2	K562	blood:
5	chr7:78405474..78407016-chr7:78415742..78418693,2	K562	blood:
6	chr7:78291912..78294336-chr7:78364604..78366410,2	K562	blood:

No data

Variant related genes	Relation type
MAGI2	TF binding region
MAGI2	CpG island

Extended variants
information (count: 4546 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4546 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10245825	chr7:78329795-78329796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10245860	chr7:78329854-78329855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541587324	chr7:78329923-78329924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540510412	chr7:78329956-78329957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553730308	chr7:78329975-78329976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573756090	chr7:78329986-78329987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144913947	chr7:78330010-78330011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561818218	chr7:78330075-78330076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562984024	chr7:78330107-78330108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531808578	chr7:78330111-78330112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189313560	chr7:78330171-78330172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182013114	chr7:78330181-78330182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184924504	chr7:78330197-78330198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111926388	chr7:78330234-78330235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556908664	chr7:78330251-78330252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12669245	chr7:78330256-78330257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs67685698	chr7:78330274-78330275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71085556	chr7:78330277-78330278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376113400	chr7:78330279-78330280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs398005222	chr7:78330281-78330282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530300417	chr7:78330295-78330296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549929444	chr7:78330403-78330404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114435396	chr7:78330430-78330431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537501103	chr7:78330434-78330435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149110459	chr7:78330454-78330455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546860696	chr7:78330465-78330466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73382106	chr7:78330494-78330495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115526268	chr7:78330497-78330498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10953668	chr7:78330515-78330516	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs12667769	chr7:78330567-78330568	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs322002	chr7:78330595-78330596	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs10246852	chr7:78330616-78330617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs567097813	chr7:78330720-78330721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34075097	chr7:78330731-78330732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534390109	chr7:78330735-78330736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78743125	chr7:78330752-78330753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs118053557	chr7:78330784-78330785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77634772	chr7:78330789-78330790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537495525	chr7:78330841-78330842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541397347	chr7:78330845-78330846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369850858	chr7:78330846-78330847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80219641	chr7:78330847-78330848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530302930	chr7:78330857-78330858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10239807	chr7:78330863-78330864	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563501031	chr7:78330871-78330872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188175536	chr7:78330886-78330887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551039489	chr7:78331043-78331044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181185952	chr7:78331051-78331052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13246026	chr7:78331066-78331067	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs75485382	chr7:78331097-78331098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Williams-beuren syndrome	16826523	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD

Chromatin state (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78313800-78334200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:78327800-78341200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:78328200-78336600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:78328800-78329800	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr7:78329600-78331000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:78330800-78331000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:78330800-78333200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:78331000-78333200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:78331000-78333400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:78331000-78333400	Enhancers	NHLF	lung
11	chr7:78331400-78332200	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr7:78331400-78333000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:78331400-78333200	Enhancers	NH-A	brain
14	chr7:78331400-78333200	Enhancers	Osteobl	bone
15	chr7:78331400-78333600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr7:78331600-78332800	Enhancers	NHEK	skin
17	chr7:78331800-78332800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:78331800-78332800	Enhancers	HSMM	muscle
19	chr7:78331800-78333000	Enhancers	NHDF-Ad	bronchial
20	chr7:78332000-78333000	Enhancers	HSMMtube	muscle
21	chr7:78332200-78332600	Enhancers	Colon Smooth Muscle	Colon
22	chr7:78333200-78336000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:78334200-78336400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:78336000-78336400	Enhancers	Brain Substantia Nigra	brain
25	chr7:78336000-78336600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:78336200-78338800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:78336400-78336800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:78336400-78343800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:78336600-78338000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:78336800-78338600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:78338000-78338200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr7:78338000-78341400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:78338200-78339200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr7:78338600-78338800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:78338600-78339800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:78338600-78339800	Enhancers	HepG2	liver
37	chr7:78338600-78340000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:78338800-78339000	Enhancers	Brain Hippocampus Middle	brain
39	chr7:78338800-78339400	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr7:78338800-78342000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:78339000-78341400	Weak transcription	Brain Hippocampus Middle	brain
42	chr7:78339200-78339800	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:78339400-78339600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:78339600-78341400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr7:78339800-78340000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:78339800-78340600	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr7:78339800-78341800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr7:78339800-78342600	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr7:78340000-78341200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:78340200-78341400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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