Variant report

Variant	nsv527265
Chromosome Location	chr6:71867477-71902656
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	chr6:71891173-71891600	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:71891195-71891542	A549	lung:	n/a	n/a
5	CEBPB	chr6:71891202-71891646	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:71891162-71891620	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr6:71891222-71891569	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr6:71900640-71900790	AoAF	blood vessel:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
9	CTCF	chr6:71900540-71900690	GM12874	blood:	n/a	n/a
10	CTCF	chr6:71900460-71900610	HAc	cerebellar:	n/a	n/a
11	CTCF	chr6:71900740-71900890	NHLF	lung:	n/a	n/a
12	CTCF	chr6:71900600-71900750	BJ	skin:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
13	CTCF	chr6:71900580-71900730	HL-60	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
14	CTCF	chr6:71900659-71900778	Hela-S3	cervix:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
15	CTCF	chr6:71900318-71900932	A549	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
16	CTCF	chr6:71900628-71900774	Kidney_OC	kidney:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
17	CTCF	chr6:71900400-71900550	HVMF	connective:	n/a	n/a
18	CTCF	chr6:71900631-71900839	A549	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
19	CTCF	chr6:71900600-71900750	GM12865	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
20	CTCF	chr6:71900620-71900770	Hela-S3	cervix:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
21	CTCF	chr6:71869440-71869590	GM12871	blood:	n/a	n/a
22	CTCF	chr6:71900664-71900763	GM10248	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
23	CTCF	chr6:71900560-71900710	HFF-Myc	foreskin:	n/a	chr6:71900692-71900710 chr6:71900695-71900708
24	CTCF	chr6:71900640-71900790	HVMF	connective:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
25	CTCF	chr6:71900540-71900690	HFF	foreskin:	n/a	n/a
26	CTCF	chr6:71900610-71900835	LNCaP	prostate:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
27	CTCF	chr6:71900680-71900830	HRE	kidney:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
28	CTCF	chr6:71900600-71900750	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
29	CTCF	chr6:71900220-71900370	HVMF	connective:	n/a	n/a
30	CTCF	chr6:71900280-71900430	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr6:71900670-71900766	Pancreas_OC	pancreas:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
32	CTCF	chr6:71900598-71900818	Medullo	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
33	CTCF	chr6:71900360-71900510	HRE	kidney:	n/a	n/a
34	CTCF	chr6:71900620-71900770	HRE	kidney:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
35	CTCF	chr6:71900300-71900450	HCM	heart:	n/a	n/a
36	CTCF	chr6:71900620-71900770	HBMEC	blood vessel:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
37	CTCF	chr6:71900600-71900750	HPF	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
38	CTCF	chr6:71900212-71901065	SK-N-SH	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
39	CTCF	chr6:71900720-71900870	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr6:71900383-71900977	HCT-116	colon:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
41	CTCF	chr6:71900280-71900430	HPF	lung:	n/a	n/a
42	CTCF	chr6:71900640-71900790	MCF-7	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
43	CTCF	chr6:71900580-71900730	BE2_C	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
44	CTCF	chr6:71900620-71900770	AoAF	blood vessel:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
45	CTCF	chr6:71900580-71900730	GM12867	blood:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
46	CTCF	chr6:71900568-71900817	A549	lung:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
47	CTCF	chr6:71900360-71900510	HMF	breast:	n/a	n/a
48	CTCF	chr6:71900620-71900770	MCF-7	breast:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
49	CTCF	chr6:71900547-71900785	SK-N-SH_RA	brain:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708
50	CTCF	chr6:71900600-71900750	HA-sp	spinal cord:	n/a	chr6:71900692-71900710 chr6:71900694-71900715 chr6:71900695-71900708

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71874784-71874834	HL-60	blood:	n/a
2	chr6:71874830-71874880	BE2_C	brain:	n/a
3	chr6:71868519-71868569	HCT-116	colon:	n/a
4	chr6:71868519-71868569	CMK	blood:	n/a
5	chr6:71868519-71868569	MCF-7	breast:	n/a
6	chr6:71874711-71874761	Caco-2	colon:	n/a
7	chr6:71874784-71874834	AG09319	gingival:	n/a
8	chr6:71868519-71868569	Hela-S3	cervix:	n/a
9	chr6:71874784-71874834	RPTEC	kidney:	n/a
10	chr6:71874830-71874880	AoSMC	blood vessel:	n/a
11	chr6:71874711-71874761	SAEC	small airway:	n/a
12	chr6:71891247-71891297	HEK293	kidney:	embryo
13	chr6:71891247-71891297	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:71868519-71868569	HAEpiC	amniotic membrane:	n/a
15	chr6:71874711-71874761	RPTEC	kidney:	n/a
16	chr6:71868519-71868569	GM19239	blood:	n/a
17	chr6:71874711-71874761	ProgFib	skin:	n/a
18	chr6:71891247-71891297	PrEC	prostate:	n/a
19	chr6:71874711-71874761	SKMC	muscle:	n/a
20	chr6:71874784-71874834	HMEC	breast:	n/a
21	chr6:71874830-71874880	GM06990	blood:	n/a
22	chr6:71874711-71874761	PrEC	prostate:	n/a
23	chr6:71874784-71874834	SAEC	small airway:	n/a
24	chr6:71874711-71874761	IMR90	lung:	fetal
25	chr6:71868519-71868569	RPTEC	kidney:	n/a
26	chr6:71891247-71891297	ovcar-3	ovarian:	n/a
27	chr6:71891247-71891297	BJ	skin:	n/a
28	chr6:71868519-71868569	GM12892	blood:	n/a
29	chr6:71868519-71868569	K562	blood:	n/a
30	chr6:71874830-71874880	HCT-116	colon:	n/a
31	chr6:71891247-71891297	Jurkat	blood:	n/a
32	chr6:71891247-71891297	SAEC	small airway:	n/a
33	chr6:71874784-71874834	HEK293	kidney:	embryo
34	chr6:71874830-71874880	NHDF-neo	bronchial:	n/a
35	chr6:71868519-71868569	Hepatocyte	liver:	n/a
36	chr6:71874784-71874834	Caco-2	colon:	n/a
37	chr6:71874830-71874880	K562	blood:	n/a
38	chr6:71874830-71874880	ProgFib	skin:	n/a
39	chr6:71891247-71891297	BE2_C	brain:	n/a
40	chr6:71891247-71891297	SKMC	muscle:	n/a
41	chr6:71874784-71874834	A549	lung:	n/a
42	chr6:71891247-71891297	GM12892	blood:	n/a
43	chr6:71874711-71874761	PFSK-1	brain:	n/a
44	chr6:71874711-71874761	SK-N-SH	brain:	n/a
45	chr6:71868519-71868569	BJ	skin:	n/a
46	chr6:71868519-71868569	ProgFib	skin:	n/a
47	chr6:71874784-71874834	Hela-S3	cervix:	n/a
48	chr6:71868519-71868569	HEK293	kidney:	embryo
49	chr6:71874784-71874834	U87	brain:	n/a
50	chr6:71874711-71874761	HEK293	kidney:	embryo

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B3GAT2-1	chr6:71897277-71897353	XLOC_005760
2	lnc-OGFRL1-10	chr6:71873227-71873515	l_3203_chr6:71873226-71928651_brain
3	lnc-OGFRL1-9	chr6:71874779-71875473	NONHSAT113463

Variant related genes	Relation type
RNU6-411P	TF binding region
LYPLA1P3	TF binding region
RNU6-411P	CpG island
LYPLA1P3	CpG island

Extended variants
information (count: 983 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1418684	chr6:71867477-71867478	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566326322	chr6:71867492-71867493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570621091	chr6:71867499-71867500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539665366	chr6:71867510-71867511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35915602	chr6:71867511-71867512	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549887078	chr6:71867568-71867569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370957851	chr6:71867613-71867614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182676617	chr6:71867638-71867639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576468091	chr6:71867715-71867716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535947251	chr6:71867798-71867799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374364895	chr6:71867818-71867819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368224160	chr6:71867848-71867849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187281608	chr6:71867859-71867860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563407989	chr6:71867870-71867871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527691384	chr6:71867941-71867942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539603572	chr6:71867945-71867946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537580870	chr6:71867948-71867949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141165407	chr6:71868002-71868003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9455364	chr6:71868026-71868027	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs144874907	chr6:71868036-71868037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562127273	chr6:71868073-71868074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191365235	chr6:71868079-71868080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541427194	chr6:71868082-71868083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116107405	chr6:71868109-71868110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371765620	chr6:71868180-71868181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76706691	chr6:71868187-71868188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184171365	chr6:71868190-71868191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138818640	chr6:71868199-71868200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140422011	chr6:71868200-71868201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112784064	chr6:71868217-71868218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529256246	chr6:71868223-71868224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547820015	chr6:71868247-71868248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566142613	chr6:71868275-71868276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569524360	chr6:71868276-71868277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73749821	chr6:71868280-71868281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34462498	chr6:71868281-71868282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372456514	chr6:71868286-71868287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115464300	chr6:71868287-71868288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72151546	chr6:71868288-71868289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78017010	chr6:71868303-71868304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9455365	chr6:71868304-71868305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9446347	chr6:71868311-71868312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570264653	chr6:71868319-71868320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537335293	chr6:71868327-71868328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555594337	chr6:71868366-71868367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574003925	chr6:71868368-71868369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541392102	chr6:71868381-71868382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35116244	chr6:71868490-71868491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77034903	chr6:71868514-71868515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150435368	chr6:71868520-71868521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	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:134 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71862000-71868000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:71866400-71869800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:71866600-71868400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:71866600-71869800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:71866800-71867600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:71866800-71868400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:71866800-71868400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:71866800-71870000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr6:71867000-71867600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:71867000-71867600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:71867000-71867800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr6:71867000-71868600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:71867200-71869800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:71867400-71868600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr6:71867400-71868800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr6:71867600-71868600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:71868000-71869400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:71868400-71868800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:71868400-71869400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr6:71868400-71869400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr6:71868600-71868800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr6:71868600-71869400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr6:71868800-71869200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr6:71868800-71869200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:71868800-71869600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr6:71869200-71869600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr6:71869400-71869600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr6:71869400-71869600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:71869400-71870000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:71877600-71878000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:71877600-71878200	Enhancers	Fetal Lung	lung
32	chr6:71877800-71880000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr6:71878000-71878400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:71879400-71880000	Enhancers	Fetal Stomach	stomach
35	chr6:71880400-71881400	Enhancers	Fetal Intestine Small	intestine
36	chr6:71880600-71881800	Enhancers	Fetal Intestine Large	intestine
37	chr6:71887000-71887200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:71887000-71887200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr6:71887000-71887600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr6:71887200-71887400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr6:71887200-71887400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:71887200-71891200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:71887400-71887600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr6:71887400-71892000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:71887600-71889200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr6:71888600-71888800	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:71888600-71889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:71888800-71889800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:71888800-71889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:71889000-71889600	Enhancers	HUES64 Cell Line	embryonic stem cell

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