Variant report

Variant	nsv886679
Chromosome Location	chr6:133578733-133635272
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	ATF3	chr6:133594012-133594132	K562	blood:	n/a	n/a
2	ATF3	chr6:133593811-133594231	A549	lung:	n/a	n/a
3	ATF3	chr6:133593875-133594187	A549	lung:	n/a	n/a
4	BACH1	chr6:133593897-133594281	K562	blood:	n/a	n/a
5	BCL3	chr6:133593947-133594201	K562	blood:	n/a	n/a
6	BCLAF1	chr6:133593903-133594192	K562	blood:	n/a	n/a
7	BRCA1	chr6:133593847-133594280	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr6:133593847-133594281	GM12878	blood:	n/a	n/a
9	CCNT2	chr6:133593901-133594281	K562	blood:	n/a	n/a
10	CEBPB	chr6:133627113-133627388	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:133630758-133631086	IMR90	lung:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
12	CEBPB	chr6:133630694-133631192	ECC-1	luminal epithelium:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
13	CEBPB	chr6:133611199-133611388	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:133608065-133608276	A549	lung:	n/a	n/a
15	CEBPB	chr6:133630769-133631097	HepG2	liver:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
16	CEBPB	chr6:133607961-133608263	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:133612150-133612485	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:133630813-133631078	A549	lung:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
19	CEBPB	chr6:133630750-133631095	Hela-S3	cervix:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
20	CEBPB	chr6:133630707-133631115	ECC-1	luminal epithelium:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
21	CHD1	chr6:133634686-133634749	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:133593795-133594279	K562	blood:	n/a	n/a
23	CHD2	chr6:133593795-133594281	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr6:133593948-133594145	A549	lung:	n/a	n/a
25	CTCF	chr6:133593980-133594130	GM12872	blood:	n/a	n/a
26	CTCF	chr6:133608020-133608170	AG09309	skin:	n/a	n/a
27	CTCF	chr6:133593940-133594090	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr6:133634380-133634530	HMEC	breast:	n/a	n/a
29	CTCF	chr6:133608084-133608148	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr6:133608000-133608150	GM12872	blood:	n/a	n/a
31	CTCF	chr6:133634320-133634470	AG09319	gingival:	n/a	n/a
32	CTCF	chr6:133608060-133608210	GM12867	blood:	n/a	n/a
33	CTCF	chr6:133608000-133608150	HRE	kidney:	n/a	n/a
34	CTCF	chr6:133593960-133594110	GM12874	blood:	n/a	n/a
35	CTCF	chr6:133594020-133594170	GM12865	blood:	n/a	n/a
36	CTCF	chr6:133593898-133594281	GM12878	blood:	n/a	n/a
37	CTCF	chr6:133607960-133608110	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr6:133607980-133608130	NB4	blood:	n/a	n/a
39	CTCF	chr6:133607980-133608130	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr6:133607998-133608201	HepG2	liver:	n/a	n/a
41	CTCF	chr6:133608020-133608170	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr6:133593980-133594130	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr6:133608000-133608150	GM12878	blood:	n/a	n/a
44	CTCF	chr6:133593980-133594130	GM12868	blood:	n/a	n/a
45	CTCF	chr6:133608060-133608210	GM12864	blood:	n/a	n/a
46	CTCF	chr6:133608091-133608133	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr6:133608002-133608164	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr6:133608000-133608150	HCFaa	heart:	n/a	n/a
49	CTCF	chr6:133594000-133594150	AG10803	skin:	n/a	n/a
50	CTCF	chr6:133593940-133594090	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:133584189-133584239	BJ	skin:	n/a
2	chr6:133584189-133584239	HIPEpiC	eye:	n/a
3	chr6:133584189-133584239	NT2-D1	testis:	n/a
4	chr6:133584189-133584239	HepG2	liver:	n/a
5	chr6:133584189-133584239	HCM	heart:	n/a
6	chr6:133584189-133584239	IMR90	lung:	fetal
7	chr6:133584189-133584239	Jurkat	blood:	n/a
8	chr6:133584189-133584239	SKMC	muscle:	n/a
9	chr6:133584189-133584239	LNCaP	prostate:	n/a
10	chr6:133584189-133584239	Caco-2	colon:	n/a
11	chr6:133584189-133584239	NB4	blood:	n/a
12	chr6:133584189-133584239	GM12891	blood:	n/a
13	chr6:133584189-133584239	ECC-1	luminal epithelium:	n/a
14	chr6:133584189-133584239	HMEC	breast:	n/a
15	chr6:133584189-133584239	HCF	heart:	n/a
16	chr6:133584189-133584239	AG10803	skin:	n/a
17	chr6:133584189-133584239	HAEpiC	amniotic membrane:	n/a
18	chr6:133584189-133584239	ovcar-3	ovarian:	n/a
19	chr6:133584189-133584239	T-47D	breast:	n/a
20	chr6:133584189-133584239	NHBE	bronchial:	n/a
21	chr6:133584189-133584239	K562	blood:	n/a
22	chr6:133584189-133584239	AoSMC	blood vessel:	n/a
23	chr6:133584189-133584239	Hela-S3	cervix:	n/a
24	chr6:133584189-133584239	GM19239	blood:	n/a
25	chr6:133584189-133584239	SK-N-SH	brain:	n/a
26	chr6:133584189-133584239	HL-60	blood:	n/a
27	chr6:133584189-133584239	BE2_C	brain:	n/a
28	chr6:133584189-133584239	ProgFib	skin:	n/a
29	chr6:133584189-133584239	GM12878	blood:	n/a
30	chr6:133584189-133584239	HUVEC	blood vessel:	n/a
31	chr6:133584189-133584239	NH-A	brain:	n/a
32	chr6:133584189-133584239	HEK293	kidney:	embryo
33	chr6:133584189-133584239	HCT-116	colon:	n/a
34	chr6:133584189-133584239	H1-hESC	embryonic stem cell:	embryo
35	chr6:133584189-133584239	PrEC	prostate:	n/a
36	chr6:133584189-133584239	GM12892	blood:	n/a
37	chr6:133584189-133584239	HEEpiC	esophagus:	n/a
38	chr6:133584189-133584239	AG04449	skin:	fetal
39	chr6:133584189-133584239	MCF10A-Er-Src	breast:	n/a
40	chr6:133584189-133584239	A549	lung:	n/a
41	chr6:133584189-133584239	PFSK-1	brain:	n/a
42	chr6:133584189-133584239	Hepatocyte	liver:	n/a
43	chr6:133584189-133584239	AG09319	gingival:	n/a
44	chr6:133584189-133584239	HNPCEpiC	eye:	n/a
45	chr6:133584189-133584239	HCPEpiC	choroid plexus:	n/a
46	chr6:133584189-133584239	CMK	blood:	n/a
47	chr6:133584189-133584239	SAEC	small airway:	n/a
48	chr6:133584189-133584239	AG04450	lung:	fetal
49	chr6:133584189-133584239	NHDF-neo	bronchial:	n/a
50	chr6:133584189-133584239	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:133585301..133587177-chr6:133589198..133590844,2	K562	blood:
2	chr6:133608130..133609733-chr6:133662657..133665396,2	K562	blood:
3	chr6:133607788..133608605-chr6:133833232..133834126,4	MCF-7	breast:
4	chr6:133607841..133608895-chr6:133689474..133690346,4	MCF-7	breast:
5	chr6:133585301..133587177-chr6:133589198..133590844,2	K562	blood:
6	chr6:133608197..133610275-chr6:133661303..133663477,2	MCF-7	breast:
7	chr19:24184476..24185016-chr6:133593470..133593971,2	MCF-7	breast:
8	chr19:24184300..24184982-chr6:133593600..133594102,2	MCF-7	breast:
9	chr4:70296625..70297182-chr6:133594074..133594625,3	MCF-7	breast:

Variant related genes	Relation type
EYA4	TF binding region
EYA4	CpG island

Extended variants
information (count: 2237 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2237 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs973714	chr6:133578733-133578734	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533619354	chr6:133578786-133578787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553856013	chr6:133578898-133578899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576744533	chr6:133578924-133578925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539457410	chr6:133578936-133578937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538648593	chr6:133578961-133578962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557665551	chr6:133579001-133579002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556028045	chr6:133579007-133579008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189457988	chr6:133579016-133579017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71735749	chr6:133579028-133579029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs3836961	chr6:133579031-133579032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181910292	chr6:133579032-133579033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185049654	chr6:133579054-133579055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113094067	chr6:133579102-133579103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561503901	chr6:133579169-133579170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1022695	chr6:133579170-133579171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541137988	chr6:133579178-133579179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114763092	chr6:133579200-133579201	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376980410	chr6:133579221-133579222	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145586486	chr6:133579237-133579238	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550195372	chr6:133579246-133579247	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148875692	chr6:133579294-133579295	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529572731	chr6:133579340-133579341	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549715406	chr6:133579350-133579351	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566250466	chr6:133579351-133579352	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567275057	chr6:133579381-133579382	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535252292	chr6:133579382-133579383	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547163750	chr6:133579425-133579426	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77120830	chr6:133579439-133579440	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570569912	chr6:133579474-133579475	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190242980	chr6:133579493-133579494	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181121251	chr6:133579500-133579501	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115654699	chr6:133579532-133579533	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3777790	chr6:133579535-133579536	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575639887	chr6:133579557-133579558	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186758610	chr6:133579558-133579559	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555265680	chr6:133579642-133579643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572126031	chr6:133579700-133579701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77466381	chr6:133579701-133579702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537929510	chr6:133579706-133579707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189768182	chr6:133579724-133579725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181001860	chr6:133579730-133579731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371432549	chr6:133579732-133579733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142694607	chr6:133579745-133579746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34845106	chr6:133579770-133579771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370048402	chr6:133579774-133579775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563638167	chr6:133579789-133579790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529325557	chr6:133579822-133579823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185385951	chr6:133579833-133579834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556702865	chr6:133579846-133579847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133567400-133583600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:133575200-133585200	Weak transcription	Psoas Muscle	Psoas
3	chr6:133576200-133580400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:133576600-133585200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:133577800-133579200	Enhancers	Hela-S3	cervix
6	chr6:133578000-133579000	Enhancers	A549	lung
7	chr6:133579000-133580400	Weak transcription	A549	lung
8	chr6:133579200-133579600	Genic enhancers	Hela-S3	cervix
9	chr6:133579200-133585200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr6:133579600-133581400	Enhancers	Hela-S3	cervix
11	chr6:133580400-133580600	Bivalent Enhancer	Fetal Heart	heart
12	chr6:133580400-133581000	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr6:133580400-133581000	Enhancers	A549	lung
14	chr6:133581000-133582200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:133581000-133599000	Weak transcription	A549	lung
16	chr6:133581400-133593800	Weak transcription	Hela-S3	cervix
17	chr6:133582200-133582400	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr6:133582200-133585800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr6:133582400-133582800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr6:133582800-133585400	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr6:133583600-133584200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr6:133583800-133584000	Weak transcription	Pancreas	Pancrea
23	chr6:133584000-133584200	Enhancers	Pancreas	Pancrea
24	chr6:133584000-133584200	Enhancers	Right Atrium	heart
25	chr6:133584000-133584400	Enhancers	Fetal Muscle Trunk	muscle
26	chr6:133584000-133585400	Enhancers	Fetal Muscle Leg	muscle
27	chr6:133584200-133584800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr6:133584200-133590000	Weak transcription	Pancreas	Pancrea
29	chr6:133584400-133585200	Weak transcription	Right Atrium	heart
30	chr6:133584400-133594000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr6:133584800-133586000	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr6:133585200-133586000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:133585200-133586000	Enhancers	Left Ventricle	heart
34	chr6:133585200-133586200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr6:133585200-133586200	Enhancers	Psoas Muscle	Psoas
36	chr6:133585400-133587400	Weak transcription	Right Atrium	heart
37	chr6:133585400-133593400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:133585400-133593800	Weak transcription	Fetal Muscle Leg	muscle
39	chr6:133585800-133589400	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr6:133586000-133589600	Weak transcription	Left Ventricle	heart
41	chr6:133586000-133590000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr6:133586000-133593400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr6:133586200-133589600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:133586200-133589600	Weak transcription	Psoas Muscle	Psoas
45	chr6:133587400-133587600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:133587400-133587600	Enhancers	Right Atrium	heart
47	chr6:133587400-133587600	Enhancers	Right Ventricle	heart
48	chr6:133587600-133589600	Weak transcription	Right Atrium	heart
49	chr6:133587600-133594000	Weak transcription	Right Ventricle	heart
50	chr6:133589000-133593800	Weak transcription	H9 Cell Line	embryonic stem cell

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