Variant report

Variant	nsv608943
Chromosome Location	chr7:147001077-147086045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:147046880-147047030	HRE	kidney:	n/a	chr7:147046987-147047008
2	CTCF	chr7:147064300-147064450	K562	blood:	n/a	n/a
3	CTCF	chr7:147070297-147070319	Spleen_OC	spleen:	n/a	n/a
4	E2F4	chr7:147073871-147074078	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F4	chr7:147072817-147072968	MCF10A-Er-Src	breast:	n/a	n/a
6	E2F4	chr7:147035845-147036045	MCF10A-Er-Src	breast:	n/a	n/a
7	E2F4	chr7:147012918-147013118	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr7:147072276-147072558	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr7:147072241-147072532	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr7:147072276-147072481	MCF10A-Er-Src	breast:	n/a	n/a
11	GATA1	chr7:147073175-147073938	PBDE	blood:	n/a	n/a
12	GATA3	chr7:147064988-147065828	SK-N-SH	brain:	n/a	n/a
13	GATA3	chr7:147064965-147065926	SK-N-SH	brain:	n/a	n/a
14	GATA3	chr7:147027321-147027437	SH-SY5Y	brain:	n/a	n/a
15	GATA3	chr7:147006227-147006306	SH-SY5Y	brain:	n/a	n/a
16	GATA3	chr7:147023776-147023781	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr7:147031572-147031772	SH-SY5Y	brain:	n/a	chr7:147031725-147031735
18	GATA3	chr7:147049047-147049198	SH-SY5Y	brain:	n/a	chr7:147049123-147049132
19	JUN	chr7:147016914-147017078	K562	blood:	n/a	n/a
20	JUND	chr7:147064663-147064725	HepG2	liver:	n/a	chr7:147064687-147064696 chr7:147064686-147064695 chr7:147064685-147064696
21	JUND	chr7:147047036-147047258	HepG2	liver:	n/a	n/a
22	KAP1	chr7:147074689-147074906	K562	blood:	n/a	n/a
23	MAFF	chr7:147076661-147076914	HepG2	liver:	n/a	n/a
24	MAFF	chr7:147058795-147059113	K562	blood:	n/a	chr7:147058922-147058940
25	MAFF	chr7:147058778-147059117	HepG2	liver:	n/a	chr7:147058922-147058940
26	MAFK	chr7:147013091-147013271	HepG2	liver:	n/a	n/a
27	MAFK	chr7:147076737-147076845	K562	blood:	n/a	chr7:147076772-147076787
28	MAFK	chr7:147058756-147059114	HepG2	liver:	n/a	chr7:147058924-147058939
29	MAFK	chr7:147076622-147076946	HepG2	liver:	n/a	chr7:147076772-147076787
30	MAFK	chr7:147058752-147059111	IMR90	lung:	n/a	chr7:147058924-147058939
31	MAFK	chr7:147058802-147059072	K562	blood:	n/a	chr7:147058924-147058939
32	MAFK	chr7:147076631-147076877	HepG2	liver:	n/a	chr7:147076772-147076787
33	MAFK	chr7:147071386-147071623	IMR90	lung:	n/a	n/a
34	MAFK	chr7:147058774-147059112	HepG2	liver:	n/a	chr7:147058924-147058939
35	MAFK	chr7:147058875-147059072	Hela-S3	cervix:	n/a	chr7:147058924-147058939
36	MAFK	chr7:147071397-147071597	HepG2	liver:	n/a	n/a
37	MAFK	chr7:147055738-147055768	HepG2	liver:	n/a	n/a
38	MXI1	chr7:147068675-147068723	GM12878	blood:	n/a	n/a
39	MYC	chr7:147072539-147072906	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr7:147072380-147072441	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr7:147070905-147070930	GM12878	blood:	n/a	n/a
42	POLR2A	chr7:147028590-147028673	Gliobla	brain:	n/a	n/a
43	POLR2A	chr7:147057546-147057733	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr7:147006176-147006369	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr7:147079663-147079797	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr7:147070904-147071071	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr7:147066412-147066430	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr7:147018364-147018491	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr7:147045903-147045991	ProgFib	skin:	n/a	n/a
50	POLR2A	chr7:147007867-147007958	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:147065665-147065715	HL-60	blood:	n/a
2	chr7:147065665-147065715	AG04450	lung:	fetal
3	chr7:147065665-147065715	NHDF-neo	bronchial:	n/a
4	chr7:147065665-147065715	PANC-1	pancreas:	n/a
5	chr7:147065665-147065715	H1-hESC	embryonic stem cell:	embryo
6	chr7:147065665-147065715	ProgFib	skin:	n/a
7	chr7:147065665-147065715	NH-A	brain:	n/a
8	chr7:147065665-147065715	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:147065665-147065715	A549	lung:	n/a
10	chr7:147065665-147065715	HRPEpiC	eye:	n/a
11	chr7:147065665-147065715	HRE	kidney:	n/a
12	chr7:147065665-147065715	GM12892	blood:	n/a
13	chr7:147065665-147065715	ovcar-3	ovarian:	n/a
14	chr7:147065665-147065715	BJ	skin:	n/a
15	chr7:147065665-147065715	HCPEpiC	choroid plexus:	n/a
16	chr7:147065665-147065715	AG10803	skin:	n/a
17	chr7:147065665-147065715	NT2-D1	testis:	n/a
18	chr7:147065665-147065715	Hepatocyte	liver:	n/a
19	chr7:147065665-147065715	SKMC	muscle:	n/a
20	chr7:147065665-147065715	HIPEpiC	eye:	n/a
21	chr7:147065665-147065715	IMR90	lung:	fetal
22	chr7:147065665-147065715	AG04449	skin:	fetal
23	chr7:147065665-147065715	Hela-S3	cervix:	n/a
24	chr7:147065665-147065715	HEEpiC	esophagus:	n/a
25	chr7:147065665-147065715	GM12891	blood:	n/a
26	chr7:147065665-147065715	BE2_C	brain:	n/a
27	chr7:147065665-147065715	HepG2	liver:	n/a
28	chr7:147065665-147065715	CMK	blood:	n/a
29	chr7:147065665-147065715	K562	blood:	n/a
30	chr7:147065665-147065715	SAEC	small airway:	n/a
31	chr7:147065665-147065715	MCF-7	breast:	n/a
32	chr7:147065665-147065715	LNCaP	prostate:	n/a
33	chr7:147065665-147065715	NB4	blood:	n/a
34	chr7:147065665-147065715	HAEpiC	amniotic membrane:	n/a
35	chr7:147065665-147065715	HCF	heart:	n/a
36	chr7:147065665-147065715	Jurkat	blood:	n/a
37	chr7:147065665-147065715	PrEC	prostate:	n/a
38	chr7:147065665-147065715	HMEC	breast:	n/a
39	chr7:147065665-147065715	RPTEC	kidney:	n/a
40	chr7:147065665-147065715	U87	brain:	n/a
41	chr7:147065665-147065715	MCF10A-Er-Src	breast:	n/a
42	chr7:147065665-147065715	HNPCEpiC	eye:	n/a
43	chr7:147065665-147065715	HEK293	kidney:	embryo
44	chr7:147065665-147065715	GM06990	blood:	n/a
45	chr7:147065665-147065715	T-47D	breast:	n/a
46	chr7:147065665-147065715	AG09319	gingival:	n/a
47	chr7:147065665-147065715	SK-N-SH_RA	brain:	n/a
48	chr7:147065665-147065715	HCT-116	colon:	n/a
49	chr7:147065665-147065715	HUVEC	blood vessel:	n/a
50	chr7:147065665-147065715	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:147063148..147065759-chr7:147077085..147079029,2	K562	blood:
2	chr7:146993664..146995748-chr7:147006294..147008294,2	MCF-7	breast:
3	chr7:147065836..147067829-chr7:147068950..147071013,2	MCF-7	breast:
4	chr7:147045457..147047946-chr7:147059907..147061995,2	K562	blood:
5	chr7:147018041..147019987-chr7:147042337..147044392,2	K562	blood:
6	chr7:147045457..147047946-chr7:147059907..147061995,2	K562	blood:
7	chr7:147018041..147019987-chr7:147042337..147044392,2	K562	blood:
8	chr1:83035755..83036717-chr7:147026373..147027195,2	MCF-7	breast:
9	chr7:147063148..147065759-chr7:147077085..147079029,2	K562	blood:
10	chr7:147065836..147067829-chr7:147068950..147071013,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chr7:147075133-147075151	MIMAT0005895_3

No data

Variant related genes	Relation type
MIR548F4	TF binding region
MIR548F4	CpG island

Extended variants
information (count: 940 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1467330	chr7:147001077-147001078	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191330136	chr7:147001078-147001079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182638502	chr7:147001080-147001081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528750930	chr7:147001111-147001112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185211361	chr7:147001114-147001115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76109948	chr7:147001115-147001116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573627963	chr7:147001147-147001148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544065913	chr7:147001155-147001156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578100850	chr7:147001183-147001184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569640520	chr7:147001197-147001198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545628229	chr7:147001214-147001215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191056637	chr7:147001232-147001233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565344032	chr7:147001235-147001236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371920820	chr7:147001247-147001248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557650944	chr7:147001249-147001250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183256004	chr7:147001257-147001258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs36074712	chr7:147001264-147001265	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs557164080	chr7:147001304-147001305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532745638	chr7:147001305-147001306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187858381	chr7:147001340-147001341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545097023	chr7:147001362-147001363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191775342	chr7:147001389-147001390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183581032	chr7:147001467-147001468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529799913	chr7:147001522-147001523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs17170407	chr7:147001523-147001524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565418761	chr7:147001556-147001557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575928104	chr7:147001568-147001569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147659374	chr7:147001577-147001578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142335359	chr7:147001618-147001619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528939861	chr7:147001682-147001683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548683487	chr7:147001694-147001695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117518985	chr7:147001723-147001724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528053986	chr7:147001751-147001752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111568789	chr7:147001781-147001782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146915993	chr7:147001816-147001817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114687851	chr7:147001836-147001837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537403106	chr7:147001851-147001852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73742533	chr7:147001919-147001920	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567464574	chr7:147001922-147001923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188120846	chr7:147001928-147001929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553528202	chr7:147001931-147001932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573403235	chr7:147001940-147001941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2620441	chr7:147001975-147001976	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs192842299	chr7:147001988-147001989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575801677	chr7:147001999-147002000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544897176	chr7:147002007-147002008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139349137	chr7:147002016-147002017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35954878	chr7:147002042-147002043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574711643	chr7:147002077-147002078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549625185	chr7:147002124-147002125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146996400-147008000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:147000600-147002600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:147000800-147001400	Enhancers	Primary hematopoietic stem cells	blood
4	chr7:147000800-147002200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:147001000-147002200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:147001400-147001800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:147001800-147002200	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:147002600-147008000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:147008000-147008800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:147008000-147009000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr7:147008000-147009000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:147008400-147008800	Enhancers	Brain Hippocampus Middle	brain
13	chr7:147008400-147008800	Enhancers	Fetal Muscle Trunk	muscle
14	chr7:147029800-147030200	Enhancers	Fetal Lung	lung
15	chr7:147030000-147030200	Enhancers	Fetal Brain Male	brain
16	chr7:147030000-147030400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:147030800-147031000	Enhancers	Fetal Brain Male	brain
18	chr7:147034800-147035400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:147052200-147055800	Weak transcription	Brain Hippocampus Middle	brain
20	chr7:147055800-147056200	Enhancers	Brain Hippocampus Middle	brain
21	chr7:147059000-147059600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:147059600-147062200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:147062200-147062400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:147064400-147064600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr7:147064600-147065800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr7:147064800-147065600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr7:147064800-147065800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr7:147065200-147065800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:147065200-147065800	Enhancers	HSMMtube	muscle
30	chr7:147065400-147066400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:147065400-147066600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr7:147065600-147066600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr7:147065800-147066200	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr7:147065800-147066400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:147065800-147066800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr7:147066200-147066600	Enhancers	H9 Cell Line	embryonic stem cell
37	chr7:147076600-147077000	Enhancers	Fetal Brain Male	brain
38	chr7:147077000-147077400	Weak transcription	Fetal Brain Male	brain
39	chr7:147077400-147078400	Enhancers	Fetal Brain Male	brain
40	chr7:147078200-147078800	Enhancers	HSMM	muscle

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