Variant report

Variant	nsv481959
Chromosome Location	chr6:163019491-163202495
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	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
4	ATF1	chr6:163183429-163183540	K562	blood:	n/a	n/a
5	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
6	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
7	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
8	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
9	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
10	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
11	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
12	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
13	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
14	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
15	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
16	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
17	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
18	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
20	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
21	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
22	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
23	BHLHE40	chr6:163148697-163149088	GM12878	blood:	n/a	chr6:163148747-163148763
24	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
26	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
27	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
30	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
31	CCNT2	chr6:163148390-163149101	K562	blood:	n/a	chr6:163148913-163148922 chr6:163148970-163148979 chr6:163149075-163149084
32	CEBPB	chr6:163192112-163192351	A549	lung:	n/a	chr6:163192194-163192205
33	CEBPB	chr6:163148738-163149145	K562	blood:	n/a	n/a
34	CEBPB	chr6:163122194-163122394	HepG2	liver:	n/a	chr6:163122352-163122363
35	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:163148750-163149181	K562	blood:	n/a	n/a
37	CEBPB	chr6:163095532-163095810	A549	lung:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
38	CEBPB	chr6:163106060-163106305	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:163185436-163185658	HepG2	liver:	n/a	chr6:163185502-163185513 chr6:163185502-163185515 chr6:163185504-163185515 chr6:163185525-163185536
40	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
41	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
42	CEBPB	chr6:163102535-163102869	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
44	CEBPB	chr6:163148771-163149153	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
46	CEBPB	chr6:163148643-163149149	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:163148788-163149168	A549	lung:	n/a	n/a
48	CEBPB	chr6:163148800-163149065	K562	blood:	n/a	n/a
49	CEBPB	chr6:163095503-163095821	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
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	chr6:163110854-163110904	SK-N-SH_RA	brain:	n/a
2	chr6:163149167-163149217	Hepatocyte	liver:	n/a
3	chr6:163110854-163110904	HCPEpiC	choroid plexus:	n/a
4	chr6:163110854-163110904	PANC-1	pancreas:	n/a
5	chr6:163148777-163148827	MCF-7	breast:	n/a
6	chr6:163200038-163200088	CMK	blood:	n/a
7	chr6:163149453-163149503	PrEC	prostate:	n/a
8	chr6:163148903-163148953	SK-N-SH_RA	brain:	n/a
9	chr6:163148018-163148068	K562	blood:	n/a
10	chr6:163149320-163149370	HUVEC	blood vessel:	n/a
11	chr6:163148903-163148953	U87	brain:	n/a
12	chr6:163147737-163147787	PANC-1	pancreas:	n/a
13	chr6:163148018-163148068	SK-N-MC	brain:	n/a
14	chr6:163149169-163149219	HNPCEpiC	eye:	n/a
15	chr6:163110854-163110904	Jurkat	blood:	n/a
16	chr6:163147733-163147783	GM12892	blood:	n/a
17	chr6:163147999-163148049	ProgFib	skin:	n/a
18	chr6:163146217-163146267	ProgFib	skin:	n/a
19	chr6:163199983-163200033	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:163148853-163148903	HEEpiC	esophagus:	n/a
21	chr6:163135177-163135227	T-47D	breast:	n/a
22	chr6:163147737-163147787	HRPEpiC	eye:	n/a
23	chr6:163200038-163200088	H1-hESC	embryonic stem cell:	embryo
24	chr6:163110854-163110904	Hepatocyte	liver:	n/a
25	chr6:163149169-163149219	HCF	heart:	n/a
26	chr6:163148022-163148072	HCM	heart:	n/a
27	chr6:163024624-163024674	HRE	kidney:	n/a
28	chr6:163148777-163148827	RPTEC	kidney:	n/a
29	chr6:163148718-163148768	HEK293	kidney:	embryo
30	chr6:163024624-163024674	NB4	blood:	n/a
31	chr6:163148777-163148827	BE2_C	brain:	n/a
32	chr6:163148777-163148827	A549	lung:	n/a
33	chr6:163148501-163148551	HUVEC	blood vessel:	n/a
34	chr6:163149169-163149219	HepG2	liver:	n/a
35	chr6:163148853-163148903	HRPEpiC	eye:	n/a
36	chr6:163146217-163146267	RPTEC	kidney:	n/a
37	chr6:163146217-163146267	ovcar-3	ovarian:	n/a
38	chr6:163147999-163148049	H1-hESC	embryonic stem cell:	embryo
39	chr6:163147737-163147787	GM06990	blood:	n/a
40	chr6:163146217-163146267	GM12891	blood:	n/a
41	chr6:163146217-163146267	HUVEC	blood vessel:	n/a
42	chr6:163147737-163147787	HCPEpiC	choroid plexus:	n/a
43	chr6:163148853-163148903	AoSMC	blood vessel:	n/a
44	chr6:163149320-163149370	K562	blood:	n/a
45	chr6:163149169-163149219	Hepatocyte	liver:	n/a
46	chr6:163110854-163110904	SAEC	small airway:	n/a
47	chr6:163147999-163148049	HCF	heart:	n/a
48	chr6:163148903-163148953	AG09319	gingival:	n/a
49	chr6:163110854-163110904	Hela-S3	cervix:	n/a
50	chr6:163146217-163146267	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
2	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
3	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
4	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
5	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
6	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
7	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
8	chr6:163139294..163141851-chr6:163147296..163150092,3	MCF-7	breast:
9	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
10	chr6:163146966..163150271-chr6:163157232..163160053,3	K562	blood:
11	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
12	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
13	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
14	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
15	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
16	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
17	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
18	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
19	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:
20	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
21	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
22	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
23	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
24	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
25	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
26	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
27	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:

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

Extended variants
information (count: 5550 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5550 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185343185	chr6:163019494-163019495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574845232	chr6:163019512-163019513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112195572	chr6:163019521-163019522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553875323	chr6:163019545-163019546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577192998	chr6:163019579-163019580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189919505	chr6:163019585-163019586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs59503315	chr6:163019612-163019613	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540407076	chr6:163019613-163019614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576205382	chr6:163019617-163019618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542024667	chr6:163019627-163019628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561406626	chr6:163019651-163019652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527388087	chr6:163019656-163019657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558764414	chr6:163019663-163019664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547516217	chr6:163019688-163019689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551904526	chr6:163019690-163019691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563905227	chr6:163019734-163019735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532957696	chr6:163019777-163019778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555084130	chr6:163019793-163019794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2846544	chr6:163019799-163019800	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569968203	chr6:163019808-163019809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113024642	chr6:163019841-163019842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35219327	chr6:163019886-163019887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200676711	chr6:163019891-163019892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182496386	chr6:163019923-163019924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375761055	chr6:163019999-163020000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565912034	chr6:163020013-163020014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573752940	chr6:163020065-163020066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571414685	chr6:163020090-163020091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534011986	chr6:163020184-163020185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554272697	chr6:163020187-163020188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570725189	chr6:163020248-163020249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539472895	chr6:163020260-163020261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544475623	chr6:163020279-163020280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576339573	chr6:163020324-163020325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542157364	chr6:163020325-163020326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145420621	chr6:163020339-163020340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369065643	chr6:163020353-163020354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572629089	chr6:163020427-163020428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150635333	chr6:163020434-163020435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78556811	chr6:163020490-163020491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373786720	chr6:163020512-163020513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71927433	chr6:163020532-163020533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74879857	chr6:163020534-163020535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564228284	chr6:163020545-163020546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375581059	chr6:163020552-163020553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375822259	chr6:163020598-163020599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9355400	chr6:163020623-163020624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543450782	chr6:163020635-163020636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35760705	chr6:163020637-163020638	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs529196850	chr6:163020645-163020646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163018000-163019600	Weak transcription	Left Ventricle	heart
2	chr6:163018000-163022000	Weak transcription	Right Atrium	heart
3	chr6:163018000-163036400	Weak transcription	Pancreas	Pancrea
4	chr6:163018400-163019800	Enhancers	Fetal Brain Male	brain
5	chr6:163019600-163020400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:163019600-163020800	Enhancers	Left Ventricle	heart
7	chr6:163019800-163020400	Weak transcription	Fetal Brain Male	brain
8	chr6:163020000-163020400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:163020000-163020400	Enhancers	Adipose Nuclei	Adipose
10	chr6:163020400-163020600	Enhancers	Fetal Brain Male	brain
11	chr6:163020600-163024400	Weak transcription	Fetal Brain Male	brain
12	chr6:163020800-163024400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:163020800-163024800	Weak transcription	Left Ventricle	heart
14	chr6:163023200-163023400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:163023600-163024400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:163023800-163024000	Enhancers	Brain Anterior Caudate	brain
17	chr6:163023800-163024600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr6:163024000-163027400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:163024200-163025600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:163024200-163025800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:163024200-163026000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:163024400-163024600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:163024400-163025000	Enhancers	Fetal Brain Male	brain
24	chr6:163024400-163025200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr6:163024400-163025200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:163024400-163025200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:163024400-163025200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:163024400-163025400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:163024400-163025600	Enhancers	Fetal Brain Female	brain
30	chr6:163024400-163027400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:163024600-163025000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:163024600-163025200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr6:163024600-163025400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:163024600-163025400	Enhancers	Fetal Heart	heart
35	chr6:163024800-163025200	Enhancers	Left Ventricle	heart
36	chr6:163025000-163025400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:163025000-163025400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:163025200-163025400	Enhancers	Psoas Muscle	Psoas
39	chr6:163025200-163025600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:163025200-163029800	Weak transcription	Left Ventricle	heart
41	chr6:163025400-163043400	Weak transcription	Psoas Muscle	Psoas
42	chr6:163026400-163031200	Weak transcription	Aorta	Aorta
43	chr6:163027200-163036400	Weak transcription	Ovary	ovary
44	chr6:163027400-163036000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:163029800-163030200	Enhancers	Right Ventricle	heart
46	chr6:163029800-163030400	Enhancers	Left Ventricle	heart
47	chr6:163031200-163031400	ZNF genes & repeats	Aorta	Aorta
48	chr6:163031400-163032000	Weak transcription	Aorta	Aorta
49	chr6:163035200-163036600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:163035800-163037000	Enhancers	Adipose Nuclei	Adipose

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