Variant report

Variant	nsv1016393
Chromosome Location	chr6:71890237-71941786
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	chr6:71891178-71891641	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr6:71891331-71891583	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:71904378-71904750	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:71891195-71891542	A549	lung:	n/a	n/a
5	CEBPB	chr6:71938055-71938858	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:71904304-71904811	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:71891202-71891646	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr6:71907040-71907239	A549	lung:	n/a	n/a
9	CEBPB	chr6:71891162-71891620	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:71891173-71891600	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:71937670-71938910	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:71906552-71907457	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr6:71891222-71891569	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr6:71900595-71900759	LNCaP	prostate:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
15	CTCF	chr6:71900548-71900827	Spleen_OC	spleen:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
16	CTCF	chr6:71900547-71900785	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
17	CTCF	chr6:71900603-71900797	GM12878	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
18	CTCF	chr6:71900660-71900810	GM12874	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
19	CTCF	chr6:71900560-71900710	GM12873	blood:	n/a	chr6:71900692-71900710 chr6:71900695-71900708
20	CTCF	chr6:71900700-71900850	HepG2	liver:	n/a	n/a
21	CTCF	chr6:71900640-71900790	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
22	CTCF	chr6:71900592-71900746	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
23	CTCF	chr6:71900451-71900950	MCF-7	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
24	CTCF	chr6:71900300-71900450	HMEC	breast:	n/a	n/a
25	CTCF	chr6:71900212-71901065	SK-N-SH	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
26	CTCF	chr6:71900480-71900630	WI-38	lung:	n/a	n/a
27	CTCF	chr6:71900620-71900770	BE2_C	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
28	CTCF	chr6:71900580-71900730	BE2_C	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
29	CTCF	chr6:71900620-71900770	HRPEpiC	eye:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
30	CTCF	chr6:71900320-71900470	HFF	foreskin:	n/a	n/a
31	CTCF	chr6:71900641-71900775	K562	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
32	CTCF	chr6:71921580-71921730	GM06990	blood:	n/a	n/a
33	CTCF	chr6:71900580-71900730	AG10803	skin:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
34	CTCF	chr6:71900420-71900570	RPTEC	kidney:	n/a	n/a
35	CTCF	chr6:71900220-71900370	HVMF	connective:	n/a	n/a
36	CTCF	chr6:71900340-71900490	HMEC	breast:	n/a	n/a
37	CTCF	chr6:71900300-71900450	HCM	heart:	n/a	n/a
38	CTCF	chr6:71900740-71900890	NHLF	lung:	n/a	n/a
39	CTCF	chr6:71900628-71900774	Kidney_OC	kidney:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
40	CTCF	chr6:71900620-71900770	HMF	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
41	CTCF	chr6:71900472-71900822	MCF-7	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
42	CTCF	chr6:71900340-71900490	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr6:71900600-71900750	HMEC	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
44	CTCF	chr6:71900660-71900810	AG04450	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
45	CTCF	chr6:71900580-71900730	HPF	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
46	CTCF	chr6:71900640-71900790	HCFaa	heart:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
47	CTCF	chr6:71914880-71915030	HMF	breast:	n/a	n/a
48	CTCF	chr6:71900585-71900869	A549	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
49	CTCF	chr6:71906820-71906970	Caco-2	colon:	n/a	n/a
50	CTCF	chr6:71900500-71900650	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71891247-71891297	IMR90	lung:	fetal
2	chr6:71891247-71891297	IMR90	lung:	fetal
3	chr6:71891247-71891297	U87	brain:	n/a
4	chr6:71906754-71906804	PANC-1	pancreas:	n/a
5	chr6:71906754-71906804	HNPCEpiC	eye:	n/a
6	chr6:71938489-71938539	K562	blood:	n/a
7	chr6:71891247-71891297	HL-60	blood:	n/a
8	chr6:71891247-71891297	CMK	blood:	n/a
9	chr6:71906754-71906804	HepG2	liver:	n/a
10	chr6:71891247-71891297	BJ	skin:	n/a
11	chr6:71938489-71938539	AG10803	skin:	n/a
12	chr6:71891247-71891297	NH-A	brain:	n/a
13	chr6:71938489-71938539	Hela-S3	cervix:	n/a
14	chr6:71906754-71906804	LNCaP	prostate:	n/a
15	chr6:71938489-71938539	SK-N-MC	brain:	n/a
16	chr6:71891247-71891297	HRCEpiC	kidney:	n/a
17	chr6:71891247-71891297	PFSK-1	brain:	n/a
18	chr6:71906754-71906804	SK-N-MC	brain:	n/a
19	chr6:71891247-71891297	HRPEpiC	eye:	n/a
20	chr6:71906754-71906804	GM12891	blood:	n/a
21	chr6:71906754-71906804	ProgFib	skin:	n/a
22	chr6:71938489-71938539	AG04449	skin:	fetal
23	chr6:71906754-71906804	NT2-D1	testis:	n/a
24	chr6:71906754-71906804	AG09309	skin:	n/a
25	chr6:71906754-71906804	NHBE	bronchial:	n/a
26	chr6:71938489-71938539	AG09319	gingival:	n/a
27	chr6:71906754-71906804	Hepatocyte	liver:	n/a
28	chr6:71906754-71906804	MCF10A-Er-Src	breast:	n/a
29	chr6:71906754-71906804	HRPEpiC	eye:	n/a
30	chr6:71938489-71938539	NHBE	bronchial:	n/a
31	chr6:71938489-71938539	SKMC	muscle:	n/a
32	chr6:71938489-71938539	HEK293	kidney:	embryo
33	chr6:71938489-71938539	NH-A	brain:	n/a
34	chr6:71938489-71938539	HL-60	blood:	n/a
35	chr6:71906754-71906804	HCF	heart:	n/a
36	chr6:71906754-71906804	HAEpiC	amniotic membrane:	n/a
37	chr6:71906754-71906804	AoSMC	blood vessel:	n/a
38	chr6:71906754-71906804	NB4	blood:	n/a
39	chr6:71906754-71906804	HEK293	kidney:	embryo
40	chr6:71938489-71938539	SAEC	small airway:	n/a
41	chr6:71906754-71906804	ECC-1	luminal epithelium:	n/a
42	chr6:71938489-71938539	AG04450	lung:	fetal
43	chr6:71938489-71938539	GM12892	blood:	n/a
44	chr6:71938489-71938539	PFSK-1	brain:	n/a
45	chr6:71938489-71938539	Hepatocyte	liver:	n/a
46	chr6:71938489-71938539	BE2_C	brain:	n/a
47	chr6:71891247-71891297	GM06990	blood:	n/a
48	chr6:71906754-71906804	U87	brain:	n/a
49	chr6:71891247-71891297	PrEC	prostate:	n/a
50	chr6:71906754-71906804	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:71900299..71901255-chr6:72058626..72059703,6	MCF-7	breast:
2	chr6:71900253..71901062-chr6:72093080..72093934,3	MCF-7	breast:
3	chr6:71892402..71894327-chr6:71895925..71898197,2	MCF-7	breast:
4	chr6:71892402..71894327-chr6:71895925..71898197,2	MCF-7	breast:
5	chr14:23564639..23565201-chr6:71915696..71916198,2	Hela-S3	cervix:
6	chr6:71900128..71900955-chr6:72058886..72059579,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OGFRL1-10	chr6:71928068-71928651	l_3203_chr6:71873226-71928651_brain
2	lnc-B3GAT2-3	chr6:71932349-71932418	ENSG00000232295.3
3	lnc-B3GAT2-1	chr6:71897277-71897353	XLOC_005760
4	lnc-B3GAT2-3	chr6:71939529-71939630	ENSG00000232295.3
5	lnc-B3GAT2-3	chr6:71931160-71931257	ENSG00000232295.3

Variant related genes	Relation type
RNU6-411P	TF binding region
RNU6-411P	CpG island
ENSG00000100813	chromatin interactions
ENSG00000179933	chromatin interactions

Extended variants
information (count: 1742 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1742 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1418673	chr6:71890237-71890238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78184035	chr6:71890268-71890269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75144035	chr6:71890286-71890287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539638000	chr6:71890355-71890356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12662304	chr6:71890389-71890390	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550170629	chr6:71890473-71890474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529506223	chr6:71890477-71890478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577527157	chr6:71890479-71890480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544696603	chr6:71890543-71890544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563371692	chr6:71890574-71890575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575274171	chr6:71890581-71890582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182362956	chr6:71890593-71890594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112121028	chr6:71890610-71890611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528271376	chr6:71890639-71890640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116683881	chr6:71890679-71890680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565047478	chr6:71890685-71890686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532508269	chr6:71890743-71890744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187318814	chr6:71890757-71890758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1573108	chr6:71890758-71890759	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs76038149	chr6:71890825-71890826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536784856	chr6:71890834-71890835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149071045	chr6:71890841-71890842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567024166	chr6:71890850-71890851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190570166	chr6:71890851-71890852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111555277	chr6:71890862-71890863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559172229	chr6:71890901-71890902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577491439	chr6:71890909-71890910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182909943	chr6:71890981-71890982	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs556720576	chr6:71891052-71891053	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs187590954	chr6:71891054-71891055	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542266896	chr6:71891069-71891070	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs560656903	chr6:71891080-71891081	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs145859824	chr6:71891108-71891109	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs78956243	chr6:71891155-71891156	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs1891524	chr6:71891166-71891167	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190046375	chr6:71891247-71891248	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs550944258	chr6:71891314-71891315	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs370686200	chr6:71891352-71891353	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs562789574	chr6:71891385-71891386	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs530122381	chr6:71891403-71891404	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs548775829	chr6:71891474-71891475	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs183032401	chr6:71891492-71891493	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs78468437	chr6:71891501-71891502	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565809735	chr6:71891509-71891510	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs138834340	chr6:71891552-71891553	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs534364406	chr6:71891576-71891577	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs552527509	chr6:71891589-71891590	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs142792295	chr6:71891593-71891594	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs538200977	chr6:71891594-71891595	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs9364137	chr6:71891609-71891610	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71887200-71891200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:71887400-71892000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:71889200-71892200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr6:71889400-71892200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr6:71889600-71890600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:71889600-71891200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:71889800-71890800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr6:71889800-71890800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr6:71890000-71890400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:71890200-71890600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:71890200-71892000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:71890400-71891200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:71890600-71891200	Enhancers	HSMMtube	muscle
14	chr6:71890600-71891800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:71890600-71892000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:71890600-71892000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:71890600-71892200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:71890600-71892600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:71890800-71891000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:71890800-71891600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr6:71890800-71891600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:71890800-71891600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:71890800-71891800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr6:71890800-71891800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:71890800-71891800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr6:71890800-71891800	Enhancers	A549	lung
27	chr6:71890800-71891800	Enhancers	NHEK	skin
28	chr6:71890800-71891800	Enhancers	Osteobl	bone
29	chr6:71890800-71892000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr6:71890800-71892000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:71890800-71892000	Enhancers	Fetal Heart	heart
32	chr6:71890800-71892000	Enhancers	Hela-S3	cervix
33	chr6:71890800-71892000	Enhancers	HSMM	muscle
34	chr6:71890800-71892000	Enhancers	NHDF-Ad	bronchial
35	chr6:71890800-71892200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr6:71890800-71892200	Enhancers	HMEC	breast
37	chr6:71891000-71891600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:71891000-71891800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:71891000-71891800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr6:71891000-71891800	Enhancers	NH-A	brain
41	chr6:71891000-71891800	Enhancers	NHLF	lung
42	chr6:71891200-71891600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:71891200-71891600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:71891200-71891600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:71891200-71891600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr6:71891200-71891600	Enhancers	Right Atrium	heart
47	chr6:71891200-71891600	Flanking Active TSS	HSMMtube	muscle
48	chr6:71891200-71891800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:71891200-71891800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr6:71891200-71891800	Enhancers	Placenta Amnion	Placenta Amnion

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