Variant report

Variant	nsv1020722
Chromosome Location	chr7:14792114-14871907
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	BACH1	chr7:14801803-14801897	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr7:14798788-14799108	HepG2	liver:	n/a	chr7:14798950-14798961
3	CEBPB	chr7:14844768-14845056	H1-hESC	embryonic stem cell:	n/a	chr7:14844888-14844899
4	CEBPB	chr7:14844722-14844997	A549	lung:	n/a	chr7:14844888-14844899
5	CEBPB	chr7:14798805-14799120	A549	lung:	n/a	chr7:14798950-14798961
6	CEBPB	chr7:14844794-14844983	K562	blood:	n/a	chr7:14844888-14844899
7	CEBPB	chr7:14869148-14869168	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:14798864-14799064	K562	blood:	n/a	chr7:14798950-14798961
9	CEBPB	chr7:14832873-14833082	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:14844718-14845080	HepG2	liver:	n/a	chr7:14844888-14844899
11	CEBPB	chr7:14817839-14817999	HepG2	liver:	n/a	chr7:14817887-14817898
12	CEBPB	chr7:14798836-14799033	H1-hESC	embryonic stem cell:	n/a	chr7:14798950-14798961
13	CEBPB	chr7:14869238-14869328	A549	lung:	n/a	n/a
14	CEBPB	chr7:14844731-14845080	IMR90	lung:	n/a	chr7:14844888-14844899
15	CEBPB	chr7:14869095-14869334	Hela-S3	cervix:	n/a	chr7:14869158-14869171
16	CTCF	chr7:14846765-14846809	LNCaP	prostate:	n/a	n/a
17	CTCF	chr7:14829400-14829550	AG09309	skin:	n/a	n/a
18	CTCF	chr7:14829340-14829490	HMF	breast:	n/a	n/a
19	CTCF	chr7:14806140-14806290	AG10803	skin:	n/a	n/a
20	CTCF	chr7:14829420-14829570	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr7:14829480-14829630	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr7:14829554-14829560	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:14829420-14829570	HCPEpiC	choroid plexus:	n/a	n/a
24	E2F4	chr7:14812037-14812156	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr7:14849416-14849566	GM12878	blood:	n/a	n/a
26	EBF1	chr7:14863622-14863819	GM12878	blood:	n/a	n/a
27	EP300	chr7:14800982-14801965	SK-N-SH_RA	brain:	n/a	chr7:14801217-14801227 chr7:14801825-14801835
28	EP300	chr7:14861225-14862178	SK-N-SH	brain:	n/a	n/a
29	EP300	chr7:14800944-14802050	SK-N-SH	brain:	n/a	chr7:14801989-14801998 chr7:14801217-14801227 chr7:14801825-14801835
30	EP300	chr7:14801077-14801971	SK-N-SH_RA	brain:	n/a	chr7:14801217-14801227 chr7:14801825-14801835
31	EP300	chr7:14846339-14846918	SK-N-SH	brain:	n/a	n/a
32	EP300	chr7:14795618-14795819	SK-N-SH_RA	brain:	n/a	n/a
33	FOS	chr7:14799455-14799769	MCF10A-Er-Src	breast:	n/a	chr7:14799625-14799636 chr7:14799610-14799621
34	FOS	chr7:14799413-14799804	HUVEC	blood vessel:	n/a	chr7:14799625-14799636 chr7:14799610-14799621
35	FOS	chr7:14799432-14799769	MCF10A-Er-Src	breast:	n/a	chr7:14799625-14799636 chr7:14799610-14799621
36	FOS	chr7:14794234-14794623	MCF10A-Er-Src	breast:	n/a	chr7:14794421-14794430 chr7:14794421-14794429 chr7:14794419-14794426 chr7:14794419-14794431 chr7:14794422-14794429 chr7:14794419-14794430
37	FOS	chr7:14794055-14794924	HUVEC	blood vessel:	n/a	chr7:14794421-14794430 chr7:14794421-14794429 chr7:14794419-14794426 chr7:14794834-14794843 chr7:14794419-14794431 chr7:14794422-14794429 chr7:14794419-14794430
38	FOS	chr7:14794275-14794558	MCF10A-Er-Src	breast:	n/a	chr7:14794421-14794430 chr7:14794421-14794429 chr7:14794419-14794426 chr7:14794419-14794431 chr7:14794422-14794429 chr7:14794419-14794430
39	FOS	chr7:14842793-14842873	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr7:14799425-14799751	MCF10A-Er-Src	breast:	n/a	chr7:14799625-14799636 chr7:14799610-14799621
41	FOS	chr7:14801220-14801400	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr7:14794275-14794572	MCF10A-Er-Src	breast:	n/a	chr7:14794421-14794430 chr7:14794421-14794429 chr7:14794419-14794426 chr7:14794419-14794431 chr7:14794422-14794429 chr7:14794419-14794430
43	FOS	chr7:14799502-14799651	MCF10A-Er-Src	breast:	n/a	chr7:14799625-14799636 chr7:14799610-14799621
44	FOS	chr7:14794270-14794474	MCF10A-Er-Src	breast:	n/a	chr7:14794421-14794430 chr7:14794421-14794429 chr7:14794419-14794426 chr7:14794419-14794431 chr7:14794422-14794429 chr7:14794419-14794430
45	FOS	chr7:14801237-14801396	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL2	chr7:14801004-14801701	SK-N-SH	brain:	n/a	n/a
47	FOSL2	chr7:14799330-14799896	SK-N-SH	brain:	n/a	n/a
48	FOSL2	chr7:14794130-14794687	SK-N-SH	brain:	n/a	chr7:14794421-14794430 chr7:14794421-14794429 chr7:14794419-14794426 chr7:14794419-14794431 chr7:14794422-14794429
49	FOSL2	chr7:14861279-14862056	SK-N-SH	brain:	n/a	n/a
50	FOSL2	chr7:14861287-14862076	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14809526-14809576	BJ	skin:	n/a
2	chr7:14801527-14801577	RPTEC	kidney:	n/a
3	chr7:14834316-14834366	Hela-S3	cervix:	n/a
4	chr7:14834316-14834366	ProgFib	skin:	n/a
5	chr7:14809526-14809576	T-47D	breast:	n/a
6	chr7:14834316-14834366	SAEC	small airway:	n/a
7	chr7:14809526-14809576	HEEpiC	esophagus:	n/a
8	chr7:14801527-14801577	HRCEpiC	kidney:	n/a
9	chr7:14801527-14801577	Jurkat	blood:	n/a
10	chr7:14801527-14801577	HRE	kidney:	n/a
11	chr7:14801527-14801577	NH-A	brain:	n/a
12	chr7:14809526-14809576	HAEpiC	amniotic membrane:	n/a
13	chr7:14834316-14834366	SK-N-SH_RA	brain:	n/a
14	chr7:14801527-14801577	AG09309	skin:	n/a
15	chr7:14809526-14809576	ProgFib	skin:	n/a
16	chr7:14834316-14834366	AG09309	skin:	n/a
17	chr7:14834316-14834366	MCF10A-Er-Src	breast:	n/a
18	chr7:14809526-14809576	Hela-S3	cervix:	n/a
19	chr7:14834316-14834366	NT2-D1	testis:	n/a
20	chr7:14801527-14801577	AG10803	skin:	n/a
21	chr7:14801527-14801577	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:14801527-14801577	IMR90	lung:	fetal
23	chr7:14801527-14801577	PANC-1	pancreas:	n/a
24	chr7:14834316-14834366	Jurkat	blood:	n/a
25	chr7:14801527-14801577	NHDF-neo	bronchial:	n/a
26	chr7:14809526-14809576	PANC-1	pancreas:	n/a
27	chr7:14809526-14809576	NHDF-neo	bronchial:	n/a
28	chr7:14801527-14801577	PFSK-1	brain:	n/a
29	chr7:14801527-14801577	HCPEpiC	choroid plexus:	n/a
30	chr7:14834316-14834366	SKMC	muscle:	n/a
31	chr7:14801527-14801577	HL-60	blood:	n/a
32	chr7:14809526-14809576	GM19239	blood:	n/a
33	chr7:14801527-14801577	SK-N-SH_RA	brain:	n/a
34	chr7:14834316-14834366	HIPEpiC	eye:	n/a
35	chr7:14809526-14809576	GM12892	blood:	n/a
36	chr7:14834316-14834366	GM06990	blood:	n/a
37	chr7:14809526-14809576	Hepatocyte	liver:	n/a
38	chr7:14801527-14801577	MCF-7	breast:	n/a
39	chr7:14801527-14801577	SKMC	muscle:	n/a
40	chr7:14809526-14809576	Caco-2	colon:	n/a
41	chr7:14834316-14834366	T-47D	breast:	n/a
42	chr7:14834316-14834366	BE2_C	brain:	n/a
43	chr7:14801527-14801577	BE2_C	brain:	n/a
44	chr7:14809526-14809576	HCT-116	colon:	n/a
45	chr7:14834316-14834366	HAEpiC	amniotic membrane:	n/a
46	chr7:14809526-14809576	GM06990	blood:	n/a
47	chr7:14801527-14801577	HRPEpiC	eye:	n/a
48	chr7:14809526-14809576	SKMC	muscle:	n/a
49	chr7:14834316-14834366	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:14801527-14801577	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:14859090..14861878-chr7:14862761..14865091,3	K562	blood:
2	chr19:46171433..46173080-chr7:14824864..14826364,2	K562	blood:
3	chr7:14859090..14861878-chr7:14862761..14865091,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-5	chr7:14856021-14856190	ENSG00000226323.1
2	lnc-AC006035.2-5	chr7:14853756-14853771	ENSG00000226323.1
3	lnc-AC006035.2-5	chr7:14854789-14854865	ENSG00000226323.1

Variant related genes	Relation type
ENSG00000221428	TF binding region
ENSG00000226323	TF binding region
ENSG00000221428	CpG island
ENSG00000226323	CpG island
ENSG00000010310	chromatin interactions

Extended variants
information (count: 2390 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2390 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1614700	chr7:14792114-14792115	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185250864	chr7:14792131-14792132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1525092	chr7:14792208-14792209	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs575808080	chr7:14792212-14792213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190013972	chr7:14792287-14792288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145495086	chr7:14792295-14792296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534798829	chr7:14792349-14792350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540865423	chr7:14792355-14792356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180941018	chr7:14792422-14792423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148438568	chr7:14792426-14792427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577268638	chr7:14792440-14792441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554493998	chr7:14792441-14792442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545835339	chr7:14792489-14792490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369267484	chr7:14792510-14792511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76035456	chr7:14792591-14792592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568535370	chr7:14792595-14792596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144086671	chr7:14792615-14792616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561680145	chr7:14792620-14792621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527475874	chr7:14792648-14792649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1525091	chr7:14792663-14792664	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs570165615	chr7:14792664-14792665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539530027	chr7:14792669-14792670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549479801	chr7:14792681-14792682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182660043	chr7:14792685-14792686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535134154	chr7:14792703-14792704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557502131	chr7:14792704-14792705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555287888	chr7:14792706-14792707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187263202	chr7:14792711-14792712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17168385	chr7:14792725-14792726	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs80306261	chr7:14792726-14792727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577230757	chr7:14792754-14792755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79801581	chr7:14792762-14792763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142823548	chr7:14792769-14792770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182392899	chr7:14792770-14792771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371345385	chr7:14792771-14792772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374218834	chr7:14792773-14792774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540416695	chr7:14792786-14792787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117501391	chr7:14792807-14792808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576367796	chr7:14792851-14792852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1723230	chr7:14792860-14792861	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs561646241	chr7:14792882-14792883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116696901	chr7:14792890-14792891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540787131	chr7:14792986-14792987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564322292	chr7:14793015-14793016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191978990	chr7:14793080-14793081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141106697	chr7:14793106-14793107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569687596	chr7:14793107-14793108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1723229	chr7:14793108-14793109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575608109	chr7:14793126-14793127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367616456	chr7:14793129-14793130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14785800-14792200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:14787400-14792200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:14787400-14801400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:14788200-14793600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:14788400-14794200	Weak transcription	HMEC	breast
6	chr7:14788600-14793800	Weak transcription	Osteobl	bone
7	chr7:14788600-14794400	Weak transcription	NHDF-Ad	bronchial
8	chr7:14788800-14793600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:14790600-14793000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:14791400-14793800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:14791600-14793800	Weak transcription	HUVEC	blood vessel
12	chr7:14792000-14792400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:14792200-14792800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:14792200-14792800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:14792200-14792800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:14792400-14792600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:14792800-14794200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:14792800-14794200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:14793000-14794200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:14793600-14793800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr7:14793600-14793800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr7:14793600-14794000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:14793600-14794600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:14793600-14794600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:14793600-14794800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr7:14793800-14794600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:14793800-14794600	Enhancers	Osteobl	bone
28	chr7:14793800-14794800	Enhancers	HUVEC	blood vessel
29	chr7:14794200-14794400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:14794200-14794600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:14794200-14794600	Enhancers	HMEC	breast
32	chr7:14794200-14794600	Enhancers	HSMMtube	muscle
33	chr7:14794200-14794600	Enhancers	NH-A	brain
34	chr7:14794200-14794800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:14794200-14795200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:14794200-14796000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:14794400-14794600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:14794400-14794600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr7:14794400-14794600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:14794400-14794600	Enhancers	NHDF-Ad	bronchial
41	chr7:14794600-14799400	Weak transcription	Osteobl	bone
42	chr7:14794800-14807000	Weak transcription	HUVEC	blood vessel
43	chr7:14796000-14801800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:14799400-14802400	Enhancers	Osteobl	bone
45	chr7:14799800-14800000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:14800000-14801000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:14800000-14802000	Enhancers	Rectal Smooth Muscle	rectum
48	chr7:14800000-14802600	Enhancers	Colon Smooth Muscle	Colon
49	chr7:14800200-14802800	Enhancers	Fetal Heart	heart
50	chr7:14800200-14804200	Enhancers	Skeletal Muscle Female	skeletal muscle

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