Variant report

Variant	nsv886914
Chromosome Location	chr6:163142272-163282067
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	ARID3A	chr6:163148619-163149118	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
3	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
4	ATF1	chr6:163183429-163183540	K562	blood:	n/a	n/a
5	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
6	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
7	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
8	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
9	ATF3	chr6:163148498-163149119	HepG2	liver:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
10	ATF3	chr6:163148729-163149180	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
11	ATF3	chr6:163148710-163149085	K562	blood:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
12	ATF3	chr6:163148738-163149179	K562	blood:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
13	ATF3	chr6:163148789-163149068	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
14	BACH1	chr6:163209996-163210055	K562	blood:	n/a	n/a
15	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:163277893-163278240	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
18	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
19	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
20	BHLHE40	chr6:163148697-163149088	GM12878	blood:	n/a	chr6:163148747-163148763
21	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
22	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
24	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
25	CCNT2	chr6:163148390-163149101	K562	blood:	n/a	chr6:163148913-163148922 chr6:163148970-163148979 chr6:163149075-163149084
26	CEBPB	chr6:163274043-163274199	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:163206834-163207227	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:163185436-163185658	HepG2	liver:	n/a	chr6:163185502-163185513 chr6:163185502-163185515 chr6:163185504-163185515 chr6:163185525-163185536
29	CEBPB	chr6:163218815-163219032	A549	lung:	n/a	n/a
30	CEBPB	chr6:163148800-163149065	K562	blood:	n/a	n/a
31	CEBPB	chr6:163254840-163255091	HepG2	liver:	n/a	chr6:163254848-163254861 chr6:163254971-163254982
32	CEBPB	chr6:163206936-163207086	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:163148769-163149119	MCF-7	breast:	n/a	n/a
34	CEBPB	chr6:163265469-163265817	HepG2	liver:	n/a	chr6:163265628-163265639
35	CEBPB	chr6:163265498-163265698	K562	blood:	n/a	chr6:163265628-163265639
36	CEBPB	chr6:163206901-163207158	K562	blood:	n/a	n/a
37	CEBPB	chr6:163206848-163207222	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:163196390-163196524	A549	lung:	n/a	chr6:163196436-163196445 chr6:163196436-163196445 chr6:163196434-163196447 chr6:163196436-163196445
39	CEBPB	chr6:163218870-163218983	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:163206896-163207154	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:163206961-163207175	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr6:163148686-163149168	A549	lung:	n/a	n/a
43	CEBPB	chr6:163206844-163207228	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr6:163206896-163207232	A549	lung:	n/a	n/a
45	CEBPB	chr6:163148750-163149181	K562	blood:	n/a	n/a
46	CEBPB	chr6:163270461-163270490	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:163171040-163171207	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:163206905-163207198	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:163148769-163149149	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:163196280-163196606	HepG2	liver:	n/a	chr6:163196436-163196445 chr6:163196436-163196445 chr6:163196569-163196580 chr6:163196434-163196447 chr6:163196436-163196445

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163276038-163276088	GM12891	blood:	n/a
2	chr6:163278126-163278176	HRCEpiC	kidney:	n/a
3	chr6:163148853-163148903	GM19239	blood:	n/a
4	chr6:163149320-163149370	GM12878	blood:	n/a
5	chr6:163278126-163278176	CMK	blood:	n/a
6	chr6:163146217-163146267	AG09309	skin:	n/a
7	chr6:163148903-163148953	HEK293	kidney:	embryo
8	chr6:163148777-163148827	NB4	blood:	n/a
9	chr6:163148762-163148812	PFSK-1	brain:	n/a
10	chr6:163148853-163148903	PrEC	prostate:	n/a
11	chr6:163200038-163200088	PANC-1	pancreas:	n/a
12	chr6:163148290-163148340	HRCEpiC	kidney:	n/a
13	chr6:163148290-163148340	Hepatocyte	liver:	n/a
14	chr6:163147733-163147783	HRE	kidney:	n/a
15	chr6:163149167-163149217	NHBE	bronchial:	n/a
16	chr6:163278126-163278176	SKMC	muscle:	n/a
17	chr6:163275980-163276030	PrEC	prostate:	n/a
18	chr6:163148903-163148953	NT2-D1	testis:	n/a
19	chr6:163147733-163147783	Hela-S3	cervix:	n/a
20	chr6:163149169-163149219	HRCEpiC	kidney:	n/a
21	chr6:163146217-163146267	U87	brain:	n/a
22	chr6:163148022-163148072	HNPCEpiC	eye:	n/a
23	chr6:163149674-163149724	AoSMC	blood vessel:	n/a
24	chr6:163149674-163149724	HNPCEpiC	eye:	n/a
25	chr6:163275952-163276002	AoSMC	blood vessel:	n/a
26	chr6:163149674-163149724	AG09319	gingival:	n/a
27	chr6:163148022-163148072	T-47D	breast:	n/a
28	chr6:163149320-163149370	BJ	skin:	n/a
29	chr6:163149453-163149503	Hela-S3	cervix:	n/a
30	chr6:163278126-163278176	HCT-116	colon:	n/a
31	chr6:163149320-163149370	HAEpiC	amniotic membrane:	n/a
32	chr6:163149453-163149503	SK-N-MC	brain:	n/a
33	chr6:163148022-163148072	RPTEC	kidney:	n/a
34	chr6:163148853-163148903	HCF	heart:	n/a
35	chr6:163149674-163149724	K562	blood:	n/a
36	chr6:163199983-163200033	NHDF-neo	bronchial:	n/a
37	chr6:163148853-163148903	Jurkat	blood:	n/a
38	chr6:163148018-163148068	HNPCEpiC	eye:	n/a
39	chr6:163149167-163149217	AG10803	skin:	n/a
40	chr6:163149169-163149219	PrEC	prostate:	n/a
41	chr6:163147737-163147787	HCF	heart:	n/a
42	chr6:163148501-163148551	HIPEpiC	eye:	n/a
43	chr6:163149453-163149503	HCF	heart:	n/a
44	chr6:163148018-163148068	HAEpiC	amniotic membrane:	n/a
45	chr6:163147733-163147783	AoSMC	blood vessel:	n/a
46	chr6:163148718-163148768	HCT-116	colon:	n/a
47	chr6:163149674-163149724	BE2_C	brain:	n/a
48	chr6:163273217-163273267	HNPCEpiC	eye:	n/a
49	chr6:163149169-163149219	NB4	blood:	n/a
50	chr6:163146217-163146267	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163146966..163150271-chr6:163157232..163160053,3	K562	blood:
2	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
3	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
4	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
5	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
6	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
7	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
8	chr4:72393798..72394589-chr6:163273105..163273631,2	MCF-7	breast:
9	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
10	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
11	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
12	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
13	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
14	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:

Variant related genes	Relation type
PACRG	TF binding region
PARK2	TF binding region
PACRG	CpG island
PARK2	CpG island
ENSG00000112530	chromatin interactions
ENSG00000185345	chromatin interactions

Extended variants
information (count: 2535 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2535 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2156259	chr6:163142272-163142273	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557068112	chr6:163142290-163142291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75605642	chr6:163142299-163142300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374516996	chr6:163142313-163142314	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146382582	chr6:163142368-163142369	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532916146	chr6:163142430-163142431	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112479241	chr6:163142456-163142457	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139255430	chr6:163142464-163142465	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575089561	chr6:163142466-163142467	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs377752920	chr6:163142471-163142472	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76190375	chr6:163142581-163142582	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs565763186	chr6:163142582-163142583	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs201872791	chr6:163142584-163142585	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs10945859	chr6:163142602-163142603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2803085	chr6:163142618-163142619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs149982731	chr6:163142629-163142630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144306872	chr6:163142658-163142659	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556181138	chr6:163142690-163142691	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs186768777	chr6:163142717-163142718	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542188270	chr6:163142724-163142725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191914640	chr6:163142775-163142776	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182709541	chr6:163142781-163142782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs376472079	chr6:163142874-163142875	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs186989840	chr6:163142881-163142882	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148739600	chr6:163142884-163142885	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs75076725	chr6:163142939-163142940	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs193175014	chr6:163142959-163142960	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146205584	chr6:163142985-163142986	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185042261	chr6:163143026-163143027	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569701169	chr6:163143112-163143113	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529178328	chr6:163143134-163143135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs548975952	chr6:163143152-163143153	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs190775957	chr6:163143160-163143161	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10945860	chr6:163143199-163143200	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147620484	chr6:163143207-163143208	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570605010	chr6:163143292-163143293	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs193059659	chr6:163143369-163143370	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs538317455	chr6:163143381-163143382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs576002007	chr6:163143425-163143426	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs535858610	chr6:163143461-163143462	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs555743695	chr6:163143506-163143507	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs572702553	chr6:163143513-163143514	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556427818	chr6:163143568-163143569	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs541262180	chr6:163143582-163143583	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs375469641	chr6:163143614-163143615	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs564709564	chr6:163143623-163143624	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs76030170	chr6:163143627-163143628	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs2187196	chr6:163143702-163143703	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs542399158	chr6:163143703-163143704	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs142131376	chr6:163143714-163143715	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 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
Renal cell carcinoma	18592004	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
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163132800-163142400	Weak transcription	Psoas Muscle	Psoas
2	chr6:163135600-163148200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:163137000-163148000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:163138200-163145800	Weak transcription	Pancreas	Pancrea
5	chr6:163138400-163146000	Weak transcription	Left Ventricle	heart
6	chr6:163138400-163148000	Weak transcription	Aorta	Aorta
7	chr6:163140600-163144400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:163140800-163142400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:163140800-163144200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:163140800-163144200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr6:163140800-163144800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:163140800-163147600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:163141800-163142400	Enhancers	Fetal Heart	heart
14	chr6:163142200-163142400	Weak transcription	Right Ventricle	heart
15	chr6:163142200-163142600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr6:163142400-163142600	Flanking Active TSS	Fetal Heart	heart
17	chr6:163142400-163142600	Enhancers	Right Ventricle	heart
18	chr6:163142400-163143000	Enhancers	Psoas Muscle	Psoas
19	chr6:163142400-163143200	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr6:163142400-163146000	Weak transcription	Stomach Mucosa	stomach
21	chr6:163142600-163142800	Enhancers	Fetal Heart	heart
22	chr6:163142600-163142800	Enhancers	Right Atrium	heart
23	chr6:163142600-163147600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr6:163142600-163147800	Weak transcription	Right Ventricle	heart
25	chr6:163142800-163143000	Flanking Active TSS	Fetal Heart	heart
26	chr6:163142800-163143200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:163142800-163145800	Weak transcription	Right Atrium	heart
28	chr6:163143000-163145200	Weak transcription	Fetal Heart	heart
29	chr6:163143000-163146000	Weak transcription	Psoas Muscle	Psoas
30	chr6:163143200-163144400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr6:163143200-163147400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:163143400-163144600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr6:163143600-163144600	Enhancers	Liver	Liver
34	chr6:163144000-163144200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:163144000-163144600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:163144200-163144400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:163144200-163144600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr6:163144200-163147600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:163144400-163144600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:163144400-163144600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr6:163144400-163144600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr6:163144400-163145200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr6:163144600-163146400	Weak transcription	Liver	Liver
44	chr6:163144600-163146800	Enhancers	Fetal Intestine Small	intestine
45	chr6:163144600-163147400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr6:163144600-163147600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr6:163144600-163147600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:163144600-163147600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:163144600-163147600	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr6:163144800-163145400	Enhancers	HUES48 Cell Line	embryonic stem cell

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