Variant report

Variant	nsv608471
Chromosome Location	chr7:137808839-137847598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:635)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:137843324-137844196	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:137836674-137837544	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:137832489-137832563	K562	blood:	n/a	n/a
4	ARID3A	chr7:137846294-137846901	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:137822296-137822442	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:137828569-137829154	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:137810323-137810515	K562	blood:	n/a	n/a
8	ATF1	chr7:137810396-137810695	K562	blood:	n/a	n/a
9	ATF1	chr7:137832201-137832540	K562	blood:	n/a	n/a
10	ATF2	chr7:137810335-137810890	GM12878	blood:	n/a	n/a
11	ATF3	chr7:137846218-137846596	K562	blood:	n/a	n/a
12	BATF	chr7:137822566-137822769	GM12878	blood:	n/a	n/a
13	BATF	chr7:137846324-137846588	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:137810391-137810691	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:137836759-137837178	HepG2	liver:	n/a	n/a
16	BHLHE40	chr7:137822602-137822802	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:137846306-137846621	K562	blood:	n/a	n/a
18	BHLHE40	chr7:137810334-137810739	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:137836881-137837118	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:137846298-137846597	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:137836827-137837143	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:137816216-137816352	HepG2	liver:	n/a	chr7:137816265-137816276
23	CEBPB	chr7:137834876-137835023	IMR90	lung:	n/a	chr7:137834958-137834969
24	CEBPB	chr7:137825300-137825500	HepG2	liver:	n/a	chr7:137825416-137825425
25	CEBPB	chr7:137834820-137835112	K562	blood:	n/a	chr7:137834958-137834969
26	CEBPB	chr7:137828769-137829156	HepG2	liver:	n/a	chr7:137828802-137828810
27	CEBPB	chr7:137834848-137835068	HepG2	liver:	n/a	chr7:137834958-137834969
28	CEBPB	chr7:137834816-137835035	A549	lung:	n/a	chr7:137834958-137834969
29	CEBPB	chr7:137811305-137811348	K562	blood:	n/a	n/a
30	CEBPB	chr7:137809987-137810847	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:137811257-137811357	A549	lung:	n/a	n/a
32	CEBPB	chr7:137828852-137829058	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:137836555-137836915	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:137832481-137832525	K562	blood:	n/a	n/a
35	CEBPB	chr7:137828730-137829147	HepG2	liver:	n/a	chr7:137828802-137828810
36	CEBPB	chr7:137825317-137825517	K562	blood:	n/a	chr7:137825416-137825425
37	CHD1	chr7:137810542-137810770	GM12878	blood:	n/a	n/a
38	CHD2	chr7:137846812-137846876	HepG2	liver:	n/a	n/a
39	CHD2	chr7:137811831-137811992	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr7:137810411-137810753	GM12878	blood:	n/a	n/a
41	CTCF	chr7:137846360-137846510	SK-N-SH_RA	brain:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
42	CTCF	chr7:137846300-137846450	HCM	heart:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
43	CTCF	chr7:137846380-137846530	AG09319	gingival:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
44	CTCF	chr7:137846380-137846530	GM12875	blood:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
45	CTCF	chr7:137846320-137846470	HCT-116	colon:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
46	CTCF	chr7:137846320-137846470	HA-sp	spinal cord:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
47	CTCF	chr7:137846360-137846510	HUVEC	blood vessel:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
48	CTCF	chr7:137846380-137846530	SAEC	small airway:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
49	CTCF	chr7:137846380-137846530	Hela-S3	cervix:	n/a	chr7:137846435-137846445 chr7:137846431-137846447
50	CTCF	chr7:137830657-137830736	Pancreas_OC	pancreas:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137830988-137831038	NHDF-neo	bronchial:	n/a
2	chr7:137830988-137831038	PANC-1	pancreas:	n/a
3	chr7:137830988-137831038	ovcar-3	ovarian:	n/a
4	chr7:137830988-137831038	AG09309	skin:	n/a
5	chr7:137830988-137831038	CMK	blood:	n/a
6	chr7:137830988-137831038	MCF10A-Er-Src	breast:	n/a
7	chr7:137830988-137831038	Hepatocyte	liver:	n/a
8	chr7:137830988-137831038	AoSMC	blood vessel:	n/a
9	chr7:137830988-137831038	NT2-D1	testis:	n/a
10	chr7:137830988-137831038	HAEpiC	amniotic membrane:	n/a
11	chr7:137830988-137831038	ECC-1	luminal epithelium:	n/a
12	chr7:137830988-137831038	HCF	heart:	n/a
13	chr7:137830988-137831038	T-47D	breast:	n/a
14	chr7:137830988-137831038	HCPEpiC	choroid plexus:	n/a
15	chr7:137830988-137831038	HL-60	blood:	n/a
16	chr7:137830988-137831038	MCF-7	breast:	n/a
17	chr7:137830988-137831038	GM06990	blood:	n/a
18	chr7:137830988-137831038	SAEC	small airway:	n/a
19	chr7:137830988-137831038	A549	lung:	n/a
20	chr7:137830988-137831038	ProgFib	skin:	n/a
21	chr7:137830988-137831038	SK-N-MC	brain:	n/a
22	chr7:137830988-137831038	Hela-S3	cervix:	n/a
23	chr7:137830988-137831038	GM19239	blood:	n/a
24	chr7:137830988-137831038	BJ	skin:	n/a
25	chr7:137830988-137831038	Jurkat	blood:	n/a
26	chr7:137830988-137831038	U87	brain:	n/a
27	chr7:137830988-137831038	HNPCEpiC	eye:	n/a
28	chr7:137830988-137831038	AG10803	skin:	n/a
29	chr7:137830988-137831038	NHBE	bronchial:	n/a
30	chr7:137830988-137831038	Caco-2	colon:	n/a
31	chr7:137830988-137831038	GM12892	blood:	n/a
32	chr7:137830988-137831038	HMEC	breast:	n/a
33	chr7:137830988-137831038	NH-A	brain:	n/a
34	chr7:137830988-137831038	HEK293	kidney:	embryo
35	chr7:137830988-137831038	GM12891	blood:	n/a
36	chr7:137830988-137831038	GM12878	blood:	n/a
37	chr7:137830988-137831038	IMR90	lung:	fetal
38	chr7:137830988-137831038	SKMC	muscle:	n/a
39	chr7:137830988-137831038	HUVEC	blood vessel:	n/a
40	chr7:137830988-137831038	HepG2	liver:	n/a
41	chr7:137830988-137831038	HEEpiC	esophagus:	n/a
42	chr7:137830988-137831038	HIPEpiC	eye:	n/a
43	chr7:137830988-137831038	HCT-116	colon:	n/a
44	chr7:137830988-137831038	HCM	heart:	n/a
45	chr7:137830988-137831038	PrEC	prostate:	n/a
46	chr7:137830988-137831038	HRE	kidney:	n/a
47	chr7:137830988-137831038	SK-N-SH_RA	brain:	n/a
48	chr7:137830988-137831038	K562	blood:	n/a
49	chr7:137830988-137831038	H1-hESC	embryonic stem cell:	embryo
50	chr7:137830988-137831038	HRCEpiC	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:137816714..137818662-chr7:137822102..137823677,2	K562	blood:
2	chr7:137845735..137846635-chr7:138201766..138202517,3	MCF-7	breast:
3	chr7:137846378..137846934-chr7:138144707..138145358,2	MCF-7	breast:
4	chr7:137808206..137811036-chr7:137813988..137816221,2	K562	blood:
5	chr7:137588282..137589029-chr7:137845978..137846860,2	K562	blood:
6	chr7:137845962..137846888-chr7:138422836..138424129,6	K562	blood:
7	chr7:137845964..137846544-chr7:138410692..138411250,3	K562	blood:
8	chr7:137843474..137846683-chr7:138143795..138145728,3	K562	blood:
9	chr7:137816714..137818662-chr7:137822102..137823677,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000225559	TF binding region
ENSG00000225559	CpG island
ENSG00000122779	chromatin interactions
ENSG00000266193	chromatin interactions

Extended variants
information (count: 1416 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1416 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17169524	chr7:137808839-137808840	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554681040	chr7:137808843-137808844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534889420	chr7:137808927-137808928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554269492	chr7:137808929-137808930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73155764	chr7:137808956-137808957	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536638388	chr7:137808957-137808958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184969069	chr7:137808980-137808981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576505833	chr7:137809005-137809006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545304826	chr7:137809006-137809007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559082024	chr7:137809014-137809015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138903496	chr7:137809038-137809039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559915273	chr7:137809048-137809049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190958282	chr7:137809056-137809057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183682846	chr7:137809080-137809081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186991135	chr7:137809095-137809096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576383071	chr7:137809103-137809104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532618251	chr7:137809108-137809109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149391685	chr7:137809110-137809111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552108061	chr7:137809111-137809112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565821072	chr7:137809153-137809154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528383382	chr7:137809175-137809176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190686	chr7:137809294-137809295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11976842	chr7:137809314-137809315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568009192	chr7:137809335-137809336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138308643	chr7:137809370-137809371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533663407	chr7:137809371-137809372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570237526	chr7:137809447-137809448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539474092	chr7:137809453-137809454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17169525	chr7:137809469-137809470	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs113941502	chr7:137809477-137809478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572642036	chr7:137809505-137809506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534903232	chr7:137809523-137809524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142812607	chr7:137809606-137809607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191574386	chr7:137809655-137809656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377646671	chr7:137809659-137809660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543854997	chr7:137809669-137809670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6942538	chr7:137809761-137809762	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs550873228	chr7:137809767-137809768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183434948	chr7:137809779-137809780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6960318	chr7:137809824-137809825	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs77074099	chr7:137809860-137809861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112158419	chr7:137809910-137809911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548055335	chr7:137809951-137809952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561679943	chr7:137809956-137809957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146054518	chr7:137810053-137810054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530150003	chr7:137810057-137810058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370277395	chr7:137810085-137810086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186899182	chr7:137810087-137810088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577546254	chr7:137810095-137810096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550166090	chr7:137810153-137810154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	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
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute promyelocytic leukemia	20824076	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137802200-137809800	Weak transcription	Fetal Intestine Small	intestine
2	chr7:137805000-137810000	Weak transcription	Liver	Liver
3	chr7:137806400-137809400	Weak transcription	HepG2	liver
4	chr7:137807000-137810200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:137808600-137809600	Weak transcription	GM12878-XiMat	blood
6	chr7:137808800-137809000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr7:137809000-137809800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:137809200-137809600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:137809200-137810800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:137809200-137810800	Enhancers	NH-A	brain
11	chr7:137809200-137811000	Enhancers	HMEC	breast
12	chr7:137809200-137811200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:137809200-137811200	Enhancers	Hela-S3	cervix
14	chr7:137809400-137809800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:137809400-137809800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:137809400-137811000	Enhancers	HepG2	liver
17	chr7:137809400-137812600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:137809600-137810200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:137809600-137810400	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr7:137809600-137810600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:137809600-137811000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:137809600-137811000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr7:137809600-137811000	Enhancers	GM12878-XiMat	blood
24	chr7:137809800-137810200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr7:137809800-137810200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:137809800-137810200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:137809800-137810200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr7:137809800-137810200	Enhancers	Fetal Muscle Leg	muscle
29	chr7:137809800-137810200	Enhancers	Ovary	ovary
30	chr7:137809800-137810200	Enhancers	NHEK	skin
31	chr7:137809800-137810400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:137809800-137810400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr7:137809800-137810600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:137809800-137810800	Enhancers	Fetal Intestine Large	intestine
35	chr7:137809800-137810800	Enhancers	Fetal Intestine Small	intestine
36	chr7:137809800-137811000	Enhancers	Osteobl	bone
37	chr7:137810000-137810200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:137810000-137810800	Enhancers	Primary B cells from peripheral blood	blood
39	chr7:137810000-137810800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:137810000-137810800	Enhancers	A549	lung
41	chr7:137810000-137811000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:137810000-137811000	Enhancers	Liver	Liver
43	chr7:137810200-137810400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr7:137810200-137810800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr7:137810200-137813800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:137810400-137813200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:137810800-137811800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr7:137811000-137812400	Weak transcription	HMEC	breast
49	chr7:137811000-137814400	Weak transcription	HepG2	liver
50	chr7:137811200-137811600	Weak transcription	Hela-S3	cervix

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