Variant report

Variant	nsv1027073
Chromosome Location	chr6:64723023-64893945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:305)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:64794125-64794597	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:64756462-64757064	HepG2	liver:	n/a	n/a
3	BACH1	chr6:64837165-64837183	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:64791435-64791721	GM12878	blood:	n/a	chr6:64791565-64791576
5	BATF	chr6:64791421-64791660	GM12878	blood:	n/a	chr6:64791565-64791576
6	BHLHE40	chr6:64756591-64756906	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:64755076-64755129	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:64794285-64794421	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:64791352-64791756	GM12878	blood:	n/a	n/a
10	CEBPB	chr6:64745314-64745665	HepG2	liver:	n/a	chr6:64745601-64745614 chr6:64745603-64745614 chr6:64745601-64745614
11	CEBPB	chr6:64728970-64729155	HepG2	liver:	n/a	chr6:64729057-64729068
12	CEBPB	chr6:64748381-64748390	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:64745315-64745575	A549	lung:	n/a	n/a
14	CEBPB	chr6:64835800-64835920	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:64745196-64745567	MCF-7	breast:	n/a	n/a
16	CEBPB	chr6:64745206-64745674	IMR90	lung:	n/a	chr6:64745601-64745614 chr6:64745603-64745614 chr6:64745601-64745614
17	CEBPB	chr6:64793844-64794559	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:64780830-64781201	IMR90	lung:	n/a	chr6:64780946-64780957
19	CEBPB	chr6:64885290-64885438	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:64865494-64865749	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:64780926-64781053	A549	lung:	n/a	chr6:64780946-64780957
22	CEBPB	chr6:64794072-64794495	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:64847863-64848005	IMR90	lung:	n/a	chr6:64847893-64847906
24	CEBPB	chr6:64847855-64848025	A549	lung:	n/a	chr6:64847893-64847906
25	CEBPB	chr6:64732802-64733027	HepG2	liver:	n/a	chr6:64732882-64732893
26	CEBPB	chr6:64748461-64748465	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:64745117-64745693	Hela-S3	cervix:	n/a	chr6:64745601-64745614 chr6:64745603-64745614 chr6:64745601-64745614
28	CEBPB	chr6:64780810-64781227	HepG2	liver:	n/a	chr6:64780946-64780957
29	CEBPB	chr6:64755594-64755685	HepG2	liver:	n/a	chr6:64755666-64755677 chr6:64755667-64755678 chr6:64755666-64755679 chr6:64755666-64755679
30	CEBPB	chr6:64794019-64794233	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr6:64810779-64810850	GM12878	blood:	n/a	n/a
32	CHD2	chr6:64814852-64814857	HepG2	liver:	n/a	n/a
33	CTCF	chr6:64794400-64794550	HepG2	liver:	n/a	n/a
34	CTCF	chr6:64794461-64794514	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:64755340-64755490	GM12874	blood:	n/a	n/a
36	CTCF	chr6:64733594-64733612	GM13977	blood:	n/a	n/a
37	CTCF	chr6:64794460-64794610	HepG2	liver:	n/a	n/a
38	CTCF	chr6:64794376-64794563	HepG2	liver:	n/a	n/a
39	CTCF	chr6:64885601-64885615	Fibrobl	skin:	n/a	n/a
40	CTCF	chr6:64847422-64847468	GM20000	blood:	n/a	n/a
41	CTCF	chr6:64824600-64824750	GM12865	blood:	n/a	n/a
42	CTCF	chr6:64794380-64794530	Caco-2	colon:	n/a	n/a
43	CTCF	chr6:64883162-64883205	GM10248	blood:	n/a	n/a
44	CTCF	chr6:64794380-64794530	HVMF	connective:	n/a	n/a
45	CTCF	chr6:64824460-64824610	BE2_C	brain:	n/a	chr6:64824521-64824537
46	CTCF	chr6:64883283-64883317	Lung_OC	lung:	n/a	n/a
47	CTCF	chr6:64794420-64794570	Caco-2	colon:	n/a	n/a
48	CTCF	chr6:64794400-64794550	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr6:64737433-64737499	GM20000	blood:	n/a	n/a
50	CTCF	chr6:64824961-64825003	GM20000	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:64742105-64742155	GM19239	blood:	n/a
2	chr6:64733737-64733787	U87	brain:	n/a
3	chr6:64733737-64733787	GM12892	blood:	n/a
4	chr6:64729109-64729159	BE2_C	brain:	n/a
5	chr6:64742105-64742155	HepG2	liver:	n/a
6	chr6:64734843-64734893	AG04449	skin:	fetal
7	chr6:64734868-64734918	AG10803	skin:	n/a
8	chr6:64734843-64734893	Jurkat	blood:	n/a
9	chr6:64729109-64729159	GM12891	blood:	n/a
10	chr6:64733737-64733787	HCT-116	colon:	n/a
11	chr6:64742105-64742155	SK-N-SH_RA	brain:	n/a
12	chr6:64742105-64742155	PFSK-1	brain:	n/a
13	chr6:64733737-64733787	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:64733737-64733787	PANC-1	pancreas:	n/a
15	chr6:64734843-64734893	NHDF-neo	bronchial:	n/a
16	chr6:64734868-64734918	HCM	heart:	n/a
17	chr6:64733737-64733787	GM12891	blood:	n/a
18	chr6:64742105-64742155	AG09319	gingival:	n/a
19	chr6:64742105-64742155	T-47D	breast:	n/a
20	chr6:64734868-64734918	HNPCEpiC	eye:	n/a
21	chr6:64742105-64742155	NT2-D1	testis:	n/a
22	chr6:64742105-64742155	Jurkat	blood:	n/a
23	chr6:64734843-64734893	RPTEC	kidney:	n/a
24	chr6:64729109-64729159	HUVEC	blood vessel:	n/a
25	chr6:64729109-64729159	SK-N-SH_RA	brain:	n/a
26	chr6:64734868-64734918	HepG2	liver:	n/a
27	chr6:64729109-64729159	NH-A	brain:	n/a
28	chr6:64742105-64742155	AG10803	skin:	n/a
29	chr6:64729109-64729159	BJ	skin:	n/a
30	chr6:64734843-64734893	GM12892	blood:	n/a
31	chr6:64734843-64734893	AG09319	gingival:	n/a
32	chr6:64733737-64733787	Hela-S3	cervix:	n/a
33	chr6:64742105-64742155	SK-N-MC	brain:	n/a
34	chr6:64734843-64734893	GM06990	blood:	n/a
35	chr6:64734868-64734918	NHDF-neo	bronchial:	n/a
36	chr6:64734843-64734893	NT2-D1	testis:	n/a
37	chr6:64742105-64742155	HL-60	blood:	n/a
38	chr6:64734868-64734918	HL-60	blood:	n/a
39	chr6:64734843-64734893	BJ	skin:	n/a
40	chr6:64742105-64742155	BJ	skin:	n/a
41	chr6:64742105-64742155	NB4	blood:	n/a
42	chr6:64733737-64733787	ProgFib	skin:	n/a
43	chr6:64733737-64733787	AG09319	gingival:	n/a
44	chr6:64734868-64734918	AG04450	lung:	fetal
45	chr6:64734843-64734893	AoSMC	blood vessel:	n/a
46	chr6:64729109-64729159	AG04450	lung:	fetal
47	chr6:64733737-64733787	SK-N-SH	brain:	n/a
48	chr6:64734868-64734918	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:64742105-64742155	Hela-S3	cervix:	n/a
50	chr6:64734843-64734893	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:64822184..64824629-chr6:64828164..64830437,2	K562	blood:
2	chr6:64814684..64816252-chr6:64820717..64823220,2	MCF-7	breast:
3	chr20:46132660..46133356-chr6:64886601..64887388,2	MCF-7	breast:
4	chr6:64825086..64826621-chr6:64878332..64879949,2	K562	blood:
5	chr6:64748612..64751041-chr6:64751525..64753155,2	MCF-7	breast:
6	chr6:64814684..64816252-chr6:64820717..64823220,2	MCF-7	breast:
7	chr6:64822184..64824629-chr6:64828164..64830437,2	K562	blood:
8	chr6:64748612..64751041-chr6:64751525..64753155,2	MCF-7	breast:
9	chr6:64825086..64826621-chr6:64878332..64879949,2	K562	blood:

No data

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

Extended variants
information (count: 2875 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2875 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75414400	chr6:64723026-64723027	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs563665385	chr6:64723082-64723083	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs530796790	chr6:64723083-64723084	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs76485173	chr6:64723101-64723102	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs114370376	chr6:64723104-64723105	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs528438732	chr6:64723110-64723111	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs546778835	chr6:64723136-64723137	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs568168376	chr6:64723184-64723185	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs528951077	chr6:64723196-64723197	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs550416587	chr6:64723222-64723223	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs568966190	chr6:64723244-64723245	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs10944281	chr6:64723265-64723266	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs557377186	chr6:64723268-64723269	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs147161329	chr6:64723277-64723278	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534994627	chr6:64723308-64723309	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553123246	chr6:64723321-64723322	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs574949736	chr6:64723322-64723323	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs377325986	chr6:64723332-64723333	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs542445219	chr6:64723336-64723337	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs139537210	chr6:64723347-64723348	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs116632852	chr6:64723364-64723365	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs536891668	chr6:64723382-64723383	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs546212792	chr6:64723405-64723406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149233892	chr6:64723425-64723426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370706315	chr6:64723430-64723431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528350176	chr6:64723485-64723486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35323031	chr6:64723520-64723521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117363243	chr6:64723524-64723525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561884754	chr6:64723529-64723530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73443012	chr6:64723551-64723552	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532142123	chr6:64723555-64723556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73762530	chr6:64723566-64723567	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs78676795	chr6:64723601-64723602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35777655	chr6:64723605-64723606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531375259	chr6:64723608-64723609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144442089	chr6:64723625-64723626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550920820	chr6:64723635-64723636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377664235	chr6:64723636-64723637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34407346	chr6:64723651-64723652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190437164	chr6:64723684-64723685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550624752	chr6:64723711-64723712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534926024	chr6:64723723-64723724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534951693	chr6:64723769-64723770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183541768	chr6:64723785-64723786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76650194	chr6:64723826-64723827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116201758	chr6:64723841-64723842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143916621	chr6:64723882-64723883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188071418	chr6:64723889-64723890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546325404	chr6:64723912-64723913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558158334	chr6:64723920-64723921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64720400-64725600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:64721600-64723200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr6:64722000-64723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:64722200-64723600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:64722200-64725600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:64722400-64723200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:64722400-64723200	Active TSS	Brain Anterior Caudate	brain
8	chr6:64722400-64723200	Active TSS	Brain Cingulate Gyrus	brain
9	chr6:64722400-64723200	Active TSS	Brain Hippocampus Middle	brain
10	chr6:64722400-64723200	Active TSS	Brain Substantia Nigra	brain
11	chr6:64722400-64723400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr6:64722400-64723400	Flanking Active TSS	Fetal Brain Female	brain
13	chr6:64722400-64723600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:64722600-64723200	Active TSS	Brain Angular Gyrus	brain
15	chr6:64722600-64723200	Flanking Active TSS	Fetal Lung	lung
16	chr6:64722800-64723200	Enhancers	Rectal Smooth Muscle	rectum
17	chr6:64722800-64723200	Active TSS	Right Atrium	heart
18	chr6:64722800-64723400	Active TSS	Brain Germinal Matrix	brain
19	chr6:64722800-64723600	Enhancers	Fetal Kidney	kidney
20	chr6:64722800-64724200	Enhancers	Fetal Brain Male	brain
21	chr6:64722800-64725600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:64723000-64723200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr6:64723000-64723200	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr6:64723000-64723400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
25	chr6:64723000-64724000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:64723000-64724200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:64723000-64725200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:64723200-64723400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:64723200-64723400	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr6:64723200-64723400	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr6:64723200-64723400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr6:64723200-64723600	Enhancers	Fetal Lung	lung
33	chr6:64723400-64723600	Enhancers	Brain Cingulate Gyrus	brain
34	chr6:64723400-64723600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr6:64723400-64723600	Enhancers	Fetal Brain Female	brain
36	chr6:64723400-64725600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr6:64723600-64725600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:64723600-64725600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:64724000-64724600	Enhancers	Primary hematopoietic stem cells	blood
40	chr6:64724000-64724600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:64724000-64725400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:64724200-64725000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:64725200-64731000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:64725600-64725800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:64725600-64725800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:64725600-64725800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:64725600-64726000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr6:64725600-64726000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr6:64725600-64726200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr6:64725600-64726200	Enhancers	HUES64 Cell Line	embryonic stem cell

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