Variant report

Variant	nsv606285
Chromosome Location	chr7:15008138-15098004
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	ARID3A	chr7:15055726-15056046	HepG2	liver:	n/a	n/a
2	BACH1	chr7:15035586-15035785	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:15052301-15052317	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:15051037-15051612	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:15055872-15056060	K562	blood:	n/a	n/a
6	BHLHE40	chr7:15055727-15055963	GM12878	blood:	n/a	n/a
7	CEBPB	chr7:15040679-15040860	HepG2	liver:	n/a	chr7:15040775-15040786 chr7:15040775-15040788
8	CEBPB	chr7:15080351-15081311	Hela-S3	cervix:	n/a	chr7:15081129-15081142
9	CEBPB	chr7:15077096-15077349	HepG2	liver:	n/a	chr7:15077196-15077207
10	CEBPB	chr7:15056178-15057050	HCT-116	colon:	n/a	chr7:15056927-15056938
11	CTCF	chr7:15093689-15093709	LNCaP	prostate:	n/a	n/a
12	CTCF	chr7:15055840-15055990	HUVEC	blood vessel:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
13	CTCF	chr7:15047260-15047410	HCM	heart:	n/a	n/a
14	CTCF	chr7:15055880-15056030	HRE	kidney:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
15	CTCF	chr7:15047160-15047310	GM12871	blood:	n/a	n/a
16	CTCF	chr7:15055813-15055952	GM19240	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
17	CTCF	chr7:15055678-15056168	GM12878	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
18	CTCF	chr7:15055821-15055958	Lung_OC	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
19	CTCF	chr7:15055780-15055930	HCT-116	colon:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
20	CTCF	chr7:15047160-15047310	GM12866	blood:	n/a	n/a
21	CTCF	chr7:15055840-15055990	SK-N-SH_RA	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
22	CTCF	chr7:15055840-15055990	NHDF-neo	bronchial:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
23	CTCF	chr7:15047193-15047412	ProgFib	skin:	n/a	n/a
24	CTCF	chr7:15047260-15047410	AG09309	skin:	n/a	n/a
25	CTCF	chr7:15047240-15047390	HPF	lung:	n/a	n/a
26	CTCF	chr7:15047280-15047430	GM12875	blood:	n/a	n/a
27	CTCF	chr7:15047240-15047390	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr7:15047220-15047370	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr7:15055820-15055970	HMF	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
30	CTCF	chr7:15047143-15047375	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr7:15047280-15047430	HVMF	connective:	n/a	n/a
32	CTCF	chr7:15047231-15047341	GM10266	blood:	n/a	n/a
33	CTCF	chr7:15055820-15055970	GM12865	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
34	CTCF	chr7:15055840-15055990	GM12872	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
35	CTCF	chr7:15055540-15055690	GM12865	blood:	n/a	n/a
36	CTCF	chr7:15055820-15055970	AG09309	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
37	CTCF	chr7:15055800-15055950	MCF-7	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
38	CTCF	chr7:15047240-15047390	GM12864	blood:	n/a	n/a
39	CTCF	chr7:15055776-15056017	Gliobla	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
40	CTCF	chr7:15047220-15047370	GM12865	blood:	n/a	n/a
41	CTCF	chr7:15055821-15055936	GM19238	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
42	CTCF	chr7:15047240-15047390	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:15055820-15055970	SAEC	small airway:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
44	CTCF	chr7:15055821-15056001	GM20000	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
45	CTCF	chr7:15047260-15047410	SAEC	small airway:	n/a	n/a
46	CTCF	chr7:15055800-15055950	HCFaa	heart:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
47	CTCF	chr7:15055800-15055950	GM12869	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
48	CTCF	chr7:15046999-15047729	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr7:15047220-15047370	HCT-116	colon:	n/a	n/a
50	CTCF	chr7:15047213-15047380	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15055459-15055509	HUVEC	blood vessel:	n/a
2	chr7:15055459-15055509	SK-N-SH	brain:	n/a
3	chr7:15055459-15055509	Hepatocyte	liver:	n/a
4	chr7:15055459-15055509	HNPCEpiC	eye:	n/a
5	chr7:15055459-15055509	HCPEpiC	choroid plexus:	n/a
6	chr7:15055459-15055509	PFSK-1	brain:	n/a
7	chr7:15055459-15055509	GM06990	blood:	n/a
8	chr7:15055459-15055509	PrEC	prostate:	n/a
9	chr7:15055459-15055509	HMEC	breast:	n/a
10	chr7:15055459-15055509	ProgFib	skin:	n/a
11	chr7:15055459-15055509	HEEpiC	esophagus:	n/a
12	chr7:15055459-15055509	AG10803	skin:	n/a
13	chr7:15055459-15055509	HCM	heart:	n/a
14	chr7:15055459-15055509	LNCaP	prostate:	n/a
15	chr7:15055459-15055509	AG04450	lung:	fetal
16	chr7:15055459-15055509	NH-A	brain:	n/a
17	chr7:15055459-15055509	HEK293	kidney:	embryo
18	chr7:15055459-15055509	AG09309	skin:	n/a
19	chr7:15055459-15055509	GM19239	blood:	n/a
20	chr7:15055459-15055509	SK-N-MC	brain:	n/a
21	chr7:15055459-15055509	U87	brain:	n/a
22	chr7:15055459-15055509	T-47D	breast:	n/a
23	chr7:15055459-15055509	MCF-7	breast:	n/a
24	chr7:15055459-15055509	HRCEpiC	kidney:	n/a
25	chr7:15055459-15055509	H1-hESC	embryonic stem cell:	embryo
26	chr7:15055459-15055509	HRE	kidney:	n/a
27	chr7:15055459-15055509	NHDF-neo	bronchial:	n/a
28	chr7:15055459-15055509	SK-N-SH_RA	brain:	n/a
29	chr7:15055459-15055509	HepG2	liver:	n/a
30	chr7:15055459-15055509	HAEpiC	amniotic membrane:	n/a
31	chr7:15055459-15055509	HCT-116	colon:	n/a
32	chr7:15055459-15055509	AG09319	gingival:	n/a
33	chr7:15055459-15055509	RPTEC	kidney:	n/a
34	chr7:15055459-15055509	GM12891	blood:	n/a
35	chr7:15055459-15055509	CMK	blood:	n/a
36	chr7:15055459-15055509	NT2-D1	testis:	n/a
37	chr7:15055459-15055509	MCF10A-Er-Src	breast:	n/a
38	chr7:15055459-15055509	GM12878	blood:	n/a
39	chr7:15055459-15055509	ECC-1	luminal epithelium:	n/a
40	chr7:15055459-15055509	HRPEpiC	eye:	n/a
41	chr7:15055459-15055509	Caco-2	colon:	n/a
42	chr7:15055459-15055509	PANC-1	pancreas:	n/a
43	chr7:15055459-15055509	HL-60	blood:	n/a
44	chr7:15055459-15055509	HIPEpiC	eye:	n/a
45	chr7:15055459-15055509	Hela-S3	cervix:	n/a
46	chr7:15055459-15055509	AoSMC	blood vessel:	n/a
47	chr7:15055459-15055509	ovcar-3	ovarian:	n/a
48	chr7:15055459-15055509	NB4	blood:	n/a
49	chr7:15055459-15055509	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:15055459-15055509	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:13317591..13319993-chr7:15056107..15057980,2	K562	blood:
2	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
3	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
4	chr7:15002300..15004911-chr7:15009747..15012507,2	MCF-7	breast:
5	chr7:15003480..15005257-chr7:15044429..15047091,2	K562	blood:
6	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
7	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
8	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
9	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:
10	chr7:14995312..14997683-chr7:15009030..15011950,2	K562	blood:
11	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
12	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
13	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
14	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DGKB-1	chr7:15025003-15025699	NONHSAT119271
2	lnc-AC006035.2-9	chr7:15074455-15074801	NONHSAT119273
3	lnc-AC006035.2-9	chr7:15072357-15072662	NONHSAT119273

Variant related genes	Relation type
DGKB	TF binding region
ENSG00000225816	TF binding region
DGKB	CpG island
ENSG00000225816	CpG island

Extended variants
information (count: 3002 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3002 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1990015	chr7:15008138-15008139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533148311	chr7:15008156-15008157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552196939	chr7:15008207-15008208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549932796	chr7:15008220-15008221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569742024	chr7:15008243-15008244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568851366	chr7:15008248-15008249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535111658	chr7:15008290-15008291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555295387	chr7:15008303-15008304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138434481	chr7:15008379-15008380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534547335	chr7:15008413-15008414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369549809	chr7:15008418-15008419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554026920	chr7:15008466-15008467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186603528	chr7:15008476-15008477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34263292	chr7:15008495-15008496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13437681	chr7:15008501-15008502	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556254398	chr7:15008535-15008536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73679600	chr7:15008585-15008586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541862806	chr7:15008602-15008603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191385065	chr7:15008606-15008607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182509219	chr7:15008641-15008642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188130867	chr7:15008687-15008688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs36920	chr7:15008714-15008715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533185602	chr7:15008715-15008716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536739183	chr7:15008745-15008746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193035308	chr7:15008754-15008755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10256582	chr7:15008767-15008768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs10950543	chr7:15008772-15008773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs548792036	chr7:15008773-15008774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148399907	chr7:15008804-15008805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534300987	chr7:15008814-15008815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554065548	chr7:15008845-15008846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570774602	chr7:15008919-15008920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539653413	chr7:15008946-15008947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs217607	chr7:15008959-15008960	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs576560059	chr7:15008962-15008963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554181392	chr7:15008976-15008977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542351096	chr7:15009002-15009003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114203160	chr7:15009016-15009017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141655155	chr7:15009022-15009023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541412110	chr7:15009044-15009045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs66538034	chr7:15009053-15009054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs10227927	chr7:15009082-15009083	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs543734665	chr7:15009106-15009107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563537073	chr7:15009174-15009175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529061151	chr7:15009176-15009177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559244507	chr7:15009197-15009198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60032052	chr7:15009211-15009212	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559155380	chr7:15009227-15009228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs217608	chr7:15009255-15009256	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs150510954	chr7:15009267-15009268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15002800-15010400	Weak transcription	Right Atrium	heart
2	chr7:15005800-15009000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:15008200-15008400	Enhancers	H9 Cell Line	embryonic stem cell
4	chr7:15009000-15009200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr7:15009000-15009400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:15010200-15010400	Enhancers	HUVEC	blood vessel
7	chr7:15010400-15010600	Flanking Active TSS	Right Atrium	heart
8	chr7:15010400-15010600	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr7:15010400-15010800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:15010400-15010800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:15010400-15010800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr7:15010400-15010800	Active TSS	Aorta	Aorta
13	chr7:15010400-15011000	Active TSS	Adipose Nuclei	Adipose
14	chr7:15010400-15011000	Flanking Active TSS	HUVEC	blood vessel
15	chr7:15010400-15011000	Active TSS	Osteobl	bone
16	chr7:15010600-15011000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:15010600-15011000	Active TSS	Right Atrium	heart
18	chr7:15010800-15011600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:15010800-15013600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr7:15011000-15011400	Enhancers	HUVEC	blood vessel
21	chr7:15011400-15017600	Weak transcription	HUVEC	blood vessel
22	chr7:15011600-15011800	Enhancers	Adipose Nuclei	Adipose
23	chr7:15011600-15013600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:15013600-15014000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:15013600-15014000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr7:15013600-15014000	Enhancers	Liver	Liver
27	chr7:15013600-15014200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:15016400-15017200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr7:15017600-15019800	Enhancers	HUVEC	blood vessel
30	chr7:15039000-15040600	Enhancers	Liver	Liver
31	chr7:15039600-15040000	Enhancers	HepG2	liver
32	chr7:15047000-15048200	Enhancers	Liver	Liver
33	chr7:15047400-15047600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:15047600-15055000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:15049400-15049600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr7:15049600-15055000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:15050600-15051000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:15050600-15051600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr7:15050800-15051200	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:15050800-15051200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:15050800-15051800	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:15050800-15052000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr7:15051000-15051400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr7:15051000-15051800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:15051200-15051600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:15051200-15051600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr7:15051200-15052800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:15051200-15054800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr7:15051400-15051600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:15051600-15052200	Enhancers	Skeletal Muscle Male	skeletal muscle

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