Variant report

Variant	nsv1023649
Chromosome Location	chr6:167026469-167060732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:2135)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:167047252-167047515	K562	blood:	n/a	n/a
2	ATF1	chr6:167043173-167043565	K562	blood:	n/a	n/a
3	ATF2	chr6:167041056-167041381	GM12878	blood:	n/a	n/a
4	ATF2	chr6:167041025-167041424	GM12878	blood:	n/a	n/a
5	ATF3	chr6:167047221-167047476	K562	blood:	n/a	n/a
6	BACH1	chr6:167051743-167051753	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:167039835-167042182	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr6:167056191-167056497	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:167041029-167041717	GM12878	blood:	n/a	chr6:167041543-167041556 chr6:167041144-167041152 chr6:167041389-167041402 chr6:167041101-167041114 chr6:167041582-167041589 chr6:167041047-167041060
10	BHLHE40	chr6:167040650-167041533	K562	blood:	n/a	chr6:167040795-167040811 chr6:167041145-167041161 chr6:167041505-167041521
11	BHLHE40	chr6:167047239-167047538	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:167047156-167047572	K562	blood:	n/a	n/a
13	BHLHE40	chr6:167047279-167047479	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:167040617-167041306	GM12878	blood:	n/a	chr6:167040795-167040811 chr6:167041145-167041161
15	BRCA1	chr6:167041185-167042165	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr6:167040157-167040300	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr6:167041101-167041127	HepG2	liver:	n/a	n/a
18	CBX3	chr6:167040659-167041117	K562	blood:	n/a	n/a
19	CCNT2	chr6:167040540-167041740	K562	blood:	n/a	chr6:167041047-167041056
20	CEBPB	chr6:167033466-167033841	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr6:167039705-167039968	A549	lung:	n/a	chr6:167039824-167039835
22	CEBPB	chr6:167036824-167037243	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:167041786-167042442	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:167039650-167039996	H1-hESC	embryonic stem cell:	n/a	chr6:167039824-167039835
25	CEBPB	chr6:167043274-167043509	K562	blood:	n/a	n/a
26	CEBPB	chr6:167033277-167033955	HCT-116	colon:	n/a	n/a
27	CEBPB	chr6:167043041-167043592	IMR90	lung:	n/a	chr6:167043131-167043143 chr6:167043048-167043059
28	CEBPB	chr6:167043147-167043546	K562	blood:	n/a	n/a
29	CEBPB	chr6:167033357-167034366	IMR90	lung:	n/a	n/a
30	CEBPB	chr6:167047306-167047655	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:167033531-167033672	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:167039647-167040018	IMR90	lung:	n/a	chr6:167039824-167039835
33	CEBPB	chr6:167043242-167043464	K562	blood:	n/a	n/a
34	CEBPB	chr6:167033444-167033834	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr6:167033401-167033925	HCT-116	colon:	n/a	n/a
36	CEBPB	chr6:167047396-167047570	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:167039761-167039967	HepG2	liver:	n/a	chr6:167039824-167039835
38	CEBPB	chr6:167036819-167037220	IMR90	lung:	n/a	n/a
39	CEBPB	chr6:167033404-167033893	ECC-1	luminal epithelium:	n/a	n/a
40	CHD1	chr6:167040136-167040322	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr6:167040345-167041473	H1-hESC	embryonic stem cell:	n/a	chr6:167040841-167040851 chr6:167041461-167041468 chr6:167040630-167040640 chr6:167040644-167040654 chr6:167040807-167040817 chr6:167040508-167040518
42	CHD2	chr6:167040730-167041245	K562	blood:	n/a	chr6:167040841-167040851 chr6:167040807-167040817
43	CHD2	chr6:167040943-167041123	HepG2	liver:	n/a	n/a
44	CHD2	chr6:167040642-167041295	GM12878	blood:	n/a	chr6:167040841-167040851 chr6:167040644-167040654 chr6:167040807-167040817
45	CHD2	chr6:167040105-167040122	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr6:167040888-167041366	Hela-S3	cervix:	n/a	n/a
47	CREB1	chr6:167040560-167041313	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr6:167040540-167041258	K562	blood:	n/a	n/a
49	CREB1	chr6:167040563-167041277	A549	lung:	n/a	n/a
50	CREB1	chr6:167040558-167041671	GM12878	blood:	n/a	n/a

(count:2135 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167040925-167040975	HCM	heart:	n/a
2	chr6:167032403-167032453	NHBE	bronchial:	n/a
3	chr6:167040925-167040975	HCPEpiC	choroid plexus:	n/a
4	chr6:167032502-167032552	HEK293	kidney:	embryo
5	chr6:167051518-167051568	CMK	blood:	n/a
6	chr6:167051518-167051568	HCT-116	colon:	n/a
7	chr6:167051744-167051794	LNCaP	prostate:	n/a
8	chr6:167047842-167047892	MCF10A-Er-Src	breast:	n/a
9	chr6:167032443-167032493	NT2-D1	testis:	n/a
10	chr6:167051781-167051831	AoSMC	blood vessel:	n/a
11	chr6:167042108-167042158	GM12892	blood:	n/a
12	chr6:167032443-167032493	HCPEpiC	choroid plexus:	n/a
13	chr6:167047877-167047927	AG09309	skin:	n/a
14	chr6:167042108-167042158	SK-N-SH	brain:	n/a
15	chr6:167031282-167031332	HepG2	liver:	n/a
16	chr6:167051744-167051794	ECC-1	luminal epithelium:	n/a
17	chr6:167031297-167031347	AG04450	lung:	fetal
18	chr6:167038658-167038708	H1-hESC	embryonic stem cell:	embryo
19	chr6:167031282-167031332	HCM	heart:	n/a
20	chr6:167031411-167031461	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:167032443-167032493	K562	blood:	n/a
22	chr6:167033966-167034016	AoSMC	blood vessel:	n/a
23	chr6:167041530-167041580	HEEpiC	esophagus:	n/a
24	chr6:167033966-167034016	PrEC	prostate:	n/a
25	chr6:167031273-167031323	NB4	blood:	n/a
26	chr6:167042108-167042158	AoSMC	blood vessel:	n/a
27	chr6:167040675-167040725	AG04450	lung:	fetal
28	chr6:167051518-167051568	NH-A	brain:	n/a
29	chr6:167039963-167040013	NHDF-neo	bronchial:	n/a
30	chr6:167051536-167051586	GM06990	blood:	n/a
31	chr6:167042138-167042188	HUVEC	blood vessel:	n/a
32	chr6:167033966-167034016	Jurkat	blood:	n/a
33	chr6:167032403-167032453	MCF-7	breast:	n/a
34	chr6:167041649-167041699	HepG2	liver:	n/a
35	chr6:167051518-167051568	SAEC	small airway:	n/a
36	chr6:167040925-167040975	SAEC	small airway:	n/a
37	chr6:167040925-167040975	HRE	kidney:	n/a
38	chr6:167042108-167042158	Hela-S3	cervix:	n/a
39	chr6:167051536-167051586	Hela-S3	cervix:	n/a
40	chr6:167040954-167041004	AG09309	skin:	n/a
41	chr6:167041530-167041580	U87	brain:	n/a
42	chr6:167040925-167040975	AG04450	lung:	fetal
43	chr6:167040440-167040490	K562	blood:	n/a
44	chr6:167051781-167051831	HMEC	breast:	n/a
45	chr6:167040925-167040975	MCF-7	breast:	n/a
46	chr6:167040440-167040490	NT2-D1	testis:	n/a
47	chr6:167054318-167054368	Caco-2	colon:	n/a
48	chr6:167032331-167032381	HL-60	blood:	n/a
49	chr6:167033966-167034016	BE2_C	brain:	n/a
50	chr6:167032443-167032493	SK-N-MC	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167035604..167038235-chr6:167040017..167042758,3	K562	blood:
2	chr6:166999043..167001912-chr6:167027558..167029377,2	K562	blood:
3	chr6:167027450..167030161-chr6:167032275..167034525,2	MCF-7	breast:
4	chr6:167042473..167044859-chr6:167051026..167053525,2	MCF-7	breast:
5	chr6:167042665..167045576-chr6:167045886..167047673,3	K562	blood:
6	chr6:167042665..167045576-chr6:167045886..167047673,3	K562	blood:
7	chr6:167050618..167053160-chr6:167077513..167080245,2	K562	blood:
8	chr6:167059027..167061692-chr6:167062613..167064872,3	K562	blood:
9	chr6:167045626..167049988-chr6:167051387..167056754,6	K562	blood:
10	chr6:167028450..167030849-chr6:167031302..167033259,3	K562	blood:
11	chr6:167042473..167044859-chr6:167051026..167053525,2	MCF-7	breast:
12	chr6:167027136..167029744-chr6:167037956..167040696,2	K562	blood:
13	chr6:167044666..167049346-chr6:167050228..167055763,8	K562	blood:
14	chr6:166928192..166929030-chr6:167027760..167028686,4	MCF-7	breast:
15	chr6:167044666..167049346-chr6:167050228..167055763,8	K562	blood:
16	chr6:167027450..167030161-chr6:167032275..167034525,2	MCF-7	breast:
17	chr6:167021736..167024085-chr6:167052097..167054804,2	K562	blood:
18	chr6:167059230..167061692-chr6:167062688..167064872,2	K562	blood:
19	chr6:167040000..167042307-chr6:167045871..167048705,3	MCF-7	breast:
20	chr6:167027136..167029744-chr6:167037956..167040696,2	K562	blood:
21	chr6:167045626..167049988-chr6:167051387..167056754,6	K562	blood:
22	chr6:167019640..167022664-chr6:167027634..167030471,3	K562	blood:
23	chr6:167040717..167042560-chr6:167055383..167058084,2	MCF-7	breast:
24	chr6:167028450..167030849-chr6:167031302..167033259,3	K562	blood:

No data

Variant related genes	Relation type
RPS6KA2	TF binding region
RPS6KA2	CpG island
ENSG00000071242	chromatin interactions
ENSG00000235272	chromatin interactions

Extended variants
information (count: 1372 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188735413	chr6:167026477-167026478	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539125300	chr6:167026505-167026506	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191888848	chr6:167026599-167026600	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569629478	chr6:167026720-167026721	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561858046	chr6:167026750-167026751	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528832390	chr6:167026766-167026767	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184802177	chr6:167026770-167026771	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367992720	chr6:167026774-167026775	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562234018	chr6:167026794-167026795	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532909002	chr6:167026826-167026827	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370684137	chr6:167026841-167026842	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189365674	chr6:167026858-167026859	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566756011	chr6:167026898-167026899	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534142659	chr6:167026899-167026900	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549622066	chr6:167026910-167026911	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548910318	chr6:167026980-167026981	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112606204	chr6:167026996-167026997	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74595132	chr6:167027048-167027049	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556331926	chr6:167027060-167027061	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578130746	chr6:167027070-167027071	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539170340	chr6:167027104-167027105	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565888472	chr6:167027113-167027114	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554324049	chr6:167027116-167027117	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573047646	chr6:167027117-167027118	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540058498	chr6:167027163-167027164	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139564974	chr6:167027167-167027168	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368512404	chr6:167027168-167027169	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544191551	chr6:167027231-167027232	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562172592	chr6:167027239-167027240	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149704968	chr6:167027242-167027243	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551025123	chr6:167027268-167027269	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11753144	chr6:167027289-167027290	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9355588	chr6:167027297-167027298	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527837425	chr6:167027301-167027302	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375527444	chr6:167027326-167027327	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549353724	chr6:167027347-167027348	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12195830	chr6:167027355-167027356	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9348154	chr6:167027358-167027359	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146640984	chr6:167027386-167027387	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12204247	chr6:167027387-167027388	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550183479	chr6:167027394-167027395	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571635103	chr6:167027460-167027461	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555339571	chr6:167027505-167027506	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180860377	chr6:167027541-167027542	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113599292	chr6:167027544-167027545	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539059875	chr6:167027548-167027549	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566185620	chr6:167027550-167027551	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149205083	chr6:167027578-167027579	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs77234156	chr6:167027593-167027594	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142407922	chr6:167027603-167027604	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1686 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167012400-167034400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:167012600-167027600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:167012800-167027800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:167013200-167031000	Weak transcription	Fetal Intestine Small	intestine
5	chr6:167013400-167028800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:167013600-167027800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:167013600-167028200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:167013800-167027000	Weak transcription	Esophagus	oesophagus
9	chr6:167013800-167027400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr6:167014000-167028000	Weak transcription	Brain Anterior Caudate	brain
11	chr6:167014200-167028400	Weak transcription	Stomach Mucosa	stomach
12	chr6:167014400-167027600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr6:167015000-167028400	Weak transcription	Osteobl	bone
14	chr6:167016000-167027400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:167016000-167027800	Weak transcription	Brain Angular Gyrus	brain
16	chr6:167016000-167028200	Weak transcription	Gastric	stomach
17	chr6:167016000-167034400	Weak transcription	Aorta	Aorta
18	chr6:167016200-167028400	Weak transcription	NH-A	brain
19	chr6:167016600-167032800	Weak transcription	Colon Smooth Muscle	Colon
20	chr6:167016800-167030200	Weak transcription	Brain Germinal Matrix	brain
21	chr6:167017200-167028600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:167017200-167032200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr6:167017400-167030400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:167017600-167028400	Weak transcription	HSMM	muscle
25	chr6:167019800-167028200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:167021200-167028400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr6:167021200-167028400	Weak transcription	NHDF-Ad	bronchial
28	chr6:167021800-167028200	Weak transcription	HSMMtube	muscle
29	chr6:167022400-167026600	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr6:167022400-167028400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:167022400-167029000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:167022600-167028400	Weak transcription	Brain Hippocampus Middle	brain
33	chr6:167022800-167027600	Weak transcription	HUVEC	blood vessel
34	chr6:167022800-167027800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr6:167022800-167028000	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:167022800-167028400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:167022800-167028800	Weak transcription	Brain Substantia Nigra	brain
38	chr6:167022800-167031200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr6:167023400-167030400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr6:167023600-167033200	Weak transcription	Primary B cells from cord blood	blood
41	chr6:167023800-167031600	Weak transcription	Fetal Brain Female	brain
42	chr6:167024000-167028000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr6:167024000-167028400	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr6:167024000-167028400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:167024000-167032400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr6:167024000-167033600	Weak transcription	Fetal Brain Male	brain
47	chr6:167024200-167028200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr6:167024200-167029000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr6:167024200-167032800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr6:167024800-167026600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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