Variant report

Variant	nsv886150
Chromosome Location	chr6:71888871-71936292
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	chr6:71907040-71907239	A549	lung:	n/a	n/a
4	CEBPB	chr6:71891202-71891646	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr6:71904378-71904750	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:71891162-71891620	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:71891173-71891600	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:71906552-71907457	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:71891195-71891542	A549	lung:	n/a	n/a
10	CEBPB	chr6:71904304-71904811	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr6:71891222-71891569	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr6:71900620-71900770	MCF-7	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
13	CTCF	chr6:71900540-71900850	K562	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
14	CTCF	chr6:71900592-71900746	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
15	CTCF	chr6:71915220-71915370	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr6:71900620-71900770	AoAF	blood vessel:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
17	CTCF	chr6:71900640-71900790	GM12864	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
18	CTCF	chr6:71900620-71900770	AG04449	skin:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
19	CTCF	chr6:71900580-71900730	GM12870	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
20	CTCF	chr6:71900560-71900710	GM12873	blood:	n/a	chr6:71900692-71900710 chr6:71900695-71900708
21	CTCF	chr6:71900619-71900809	HepG2	liver:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
22	CTCF	chr6:71915220-71915370	AG10803	skin:	n/a	n/a
23	CTCF	chr6:71900280-71900430	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr6:71900598-71900818	Medullo	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
25	CTCF	chr6:71900340-71900490	HMEC	breast:	n/a	n/a
26	CTCF	chr6:71900680-71900830	HCT-116	colon:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
27	CTCF	chr6:71900600-71900750	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
28	CTCF	chr6:71900640-71900790	NHDF-neo	bronchial:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
29	CTCF	chr6:71900580-71900730	AG09309	skin:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
30	CTCF	chr6:71900580-71900730	GM12867	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
31	CTCF	chr6:71900640-71900790	MCF-7	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
32	CTCF	chr6:71900641-71900775	K562	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
33	CTCF	chr6:71900568-71900817	A549	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
34	CTCF	chr6:71900620-71900770	NB4	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
35	CTCF	chr6:71900585-71900827	HUVEC	blood vessel:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
36	CTCF	chr6:71900520-71900670	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr6:71900580-71900730	HL-60	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
38	CTCF	chr6:71900660-71900810	AG04450	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
39	CTCF	chr6:71900620-71900770	AG04450	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
40	CTCF	chr6:71900603-71900797	GM12878	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
41	CTCF	chr6:71900700-71900850	HepG2	liver:	n/a	n/a
42	CTCF	chr6:71900620-71900770	Hela-S3	cervix:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
43	CTCF	chr6:71900659-71900778	Hela-S3	cervix:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
44	CTCF	chr6:71900660-71900810	HCPEpiC	choroid plexus:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
45	CTCF	chr6:71900340-71900490	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr6:71900540-71900690	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr6:71900220-71900370	HVMF	connective:	n/a	n/a
48	CTCF	chr6:71900640-71900790	HEK293	kidney:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
49	CTCF	chr6:71900521-71900881	A549	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
50	CTCF	chr6:71900620-71900770	HRPEpiC	eye:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71906754-71906804	NHBE	bronchial:	n/a
2	chr6:71891247-71891297	HRE	kidney:	n/a
3	chr6:71891247-71891297	AG09319	gingival:	n/a
4	chr6:71906754-71906804	HL-60	blood:	n/a
5	chr6:71906754-71906804	HCPEpiC	choroid plexus:	n/a
6	chr6:71891247-71891297	BE2_C	brain:	n/a
7	chr6:71891247-71891297	U87	brain:	n/a
8	chr6:71906754-71906804	NT2-D1	testis:	n/a
9	chr6:71891247-71891297	GM12878	blood:	n/a
10	chr6:71891247-71891297	MCF-7	breast:	n/a
11	chr6:71891247-71891297	PFSK-1	brain:	n/a
12	chr6:71906754-71906804	H1-hESC	embryonic stem cell:	embryo
13	chr6:71891247-71891297	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:71891247-71891297	HAEpiC	amniotic membrane:	n/a
15	chr6:71906754-71906804	SK-N-MC	brain:	n/a
16	chr6:71891247-71891297	GM06990	blood:	n/a
17	chr6:71906754-71906804	SKMC	muscle:	n/a
18	chr6:71891247-71891297	K562	blood:	n/a
19	chr6:71891247-71891297	AG10803	skin:	n/a
20	chr6:71906754-71906804	AG04450	lung:	fetal
21	chr6:71906754-71906804	ovcar-3	ovarian:	n/a
22	chr6:71906754-71906804	ECC-1	luminal epithelium:	n/a
23	chr6:71891247-71891297	ProgFib	skin:	n/a
24	chr6:71906754-71906804	BE2_C	brain:	n/a
25	chr6:71906754-71906804	HMEC	breast:	n/a
26	chr6:71891247-71891297	T-47D	breast:	n/a
27	chr6:71891247-71891297	ovcar-3	ovarian:	n/a
28	chr6:71906754-71906804	Hepatocyte	liver:	n/a
29	chr6:71891247-71891297	NB4	blood:	n/a
30	chr6:71891247-71891297	RPTEC	kidney:	n/a
31	chr6:71891247-71891297	IMR90	lung:	fetal
32	chr6:71906754-71906804	SK-N-SH	brain:	n/a
33	chr6:71906754-71906804	HCT-116	colon:	n/a
34	chr6:71906754-71906804	HCF	heart:	n/a
35	chr6:71906754-71906804	GM12891	blood:	n/a
36	chr6:71891247-71891297	SK-N-SH_RA	brain:	n/a
37	chr6:71906754-71906804	HNPCEpiC	eye:	n/a
38	chr6:71891247-71891297	SK-N-SH	brain:	n/a
39	chr6:71891247-71891297	SK-N-MC	brain:	n/a
40	chr6:71906754-71906804	GM19239	blood:	n/a
41	chr6:71891247-71891297	HMEC	breast:	n/a
42	chr6:71891247-71891297	PrEC	prostate:	n/a
43	chr6:71906754-71906804	HUVEC	blood vessel:	n/a
44	chr6:71891247-71891297	NHBE	bronchial:	n/a
45	chr6:71906754-71906804	MCF10A-Er-Src	breast:	n/a
46	chr6:71906754-71906804	ProgFib	skin:	n/a
47	chr6:71906754-71906804	HRE	kidney:	n/a
48	chr6:71891247-71891297	AG04449	skin:	fetal
49	chr6:71891247-71891297	ECC-1	luminal epithelium:	n/a
50	chr6:71891247-71891297	HIPEpiC	eye:	n/a

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

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

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

Extended variants
information (count: 1574 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1574 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575842696	chr6:71888887-71888888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73501179	chr6:71888889-71888890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559487519	chr6:71888910-71888911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188422954	chr6:71888983-71888984	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs541049104	chr6:71889004-71889005	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559470682	chr6:71889012-71889013	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs533084280	chr6:71889022-71889023	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551277916	chr6:71889042-71889043	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs181268225	chr6:71889054-71889055	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs530623304	chr6:71889081-71889082	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs548827022	chr6:71889110-71889111	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs575266064	chr6:71889133-71889134	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567240871	chr6:71889212-71889213	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs568620885	chr6:71889224-71889225	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs534673318	chr6:71889250-71889251	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185899959	chr6:71889264-71889265	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs571394242	chr6:71889283-71889284	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs539167899	chr6:71889305-71889306	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs547753863	chr6:71889356-71889357	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs140107148	chr6:71889377-71889378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150305565	chr6:71889402-71889403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542867206	chr6:71889407-71889408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555273441	chr6:71889431-71889432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114197837	chr6:71889459-71889460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541012471	chr6:71889471-71889472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559433821	chr6:71889576-71889577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144880476	chr6:71889632-71889633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10080657	chr6:71889634-71889635	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs190820462	chr6:71889792-71889793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530699691	chr6:71889816-71889817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548790370	chr6:71889826-71889827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567205785	chr6:71889866-71889867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528408051	chr6:71889901-71889902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546584492	chr6:71889947-71889948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201921965	chr6:71889992-71889993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571567939	chr6:71890003-71890004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34508795	chr6:71890056-71890057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74871694	chr6:71890067-71890068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs397885407	chr6:71890068-71890069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199632462	chr6:71890164-71890165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547462255	chr6:71890165-71890166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111757263	chr6:71890172-71890173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569275192	chr6:71890189-71890190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372599702	chr6:71890190-71890191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114023070	chr6:71890207-71890208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1418673	chr6:71890237-71890238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78184035	chr6:71890268-71890269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75144035	chr6:71890286-71890287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539638000	chr6:71890355-71890356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12662304	chr6:71890389-71890390	Weak transcription Enhancers	n/a	n/a	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:263 , 50 per page) page: 1 2 3 4 5 6

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	chr6:71887600-71889200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:71888600-71889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:71888800-71889800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:71888800-71889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:71889000-71889600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:71889200-71889600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:71889200-71890000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr6:71889200-71890200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:71889200-71892200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr6:71889400-71889800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr6:71889400-71892200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:71889600-71890600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:71889600-71891200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr6:71889800-71890800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:71889800-71890800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr6:71890000-71890400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr6:71890200-71890600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr6:71890200-71892000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:71890400-71891200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:71890600-71891200	Enhancers	HSMMtube	muscle
23	chr6:71890600-71891800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:71890600-71892000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr6:71890600-71892000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:71890600-71892200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr6:71890600-71892600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:71890800-71891000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:71890800-71891600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr6:71890800-71891600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:71890800-71891600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:71890800-71891800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr6:71890800-71891800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:71890800-71891800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr6:71890800-71891800	Enhancers	A549	lung
36	chr6:71890800-71891800	Enhancers	NHEK	skin
37	chr6:71890800-71891800	Enhancers	Osteobl	bone
38	chr6:71890800-71892000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr6:71890800-71892000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:71890800-71892000	Enhancers	Fetal Heart	heart
41	chr6:71890800-71892000	Enhancers	Hela-S3	cervix
42	chr6:71890800-71892000	Enhancers	HSMM	muscle
43	chr6:71890800-71892000	Enhancers	NHDF-Ad	bronchial
44	chr6:71890800-71892200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr6:71890800-71892200	Enhancers	HMEC	breast
46	chr6:71891000-71891600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:71891000-71891800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:71891000-71891800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr6:71891000-71891800	Enhancers	NH-A	brain
50	chr6:71891000-71891800	Enhancers	NHLF	lung

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