Variant report

Variant	nsv830857
Chromosome Location	chr6:163064811-163245813
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	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
3	ARID3A	chr6:163148619-163149118	HepG2	liver:	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	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
7	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
8	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
9	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
10	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
11	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
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	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
15	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
16	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:163209996-163210055	K562	blood:	n/a	n/a
18	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
19	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
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	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
23	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
24	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
26	CCNT2	chr6:163148390-163149101	K562	blood:	n/a	chr6:163148913-163148922 chr6:163148970-163148979 chr6:163149075-163149084
27	CEBPB	chr6:163106060-163106305	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:163148769-163149119	MCF-7	breast:	n/a	n/a
29	CEBPB	chr6:163206936-163207086	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:163148788-163149168	A549	lung:	n/a	n/a
31	CEBPB	chr6:163148713-163149149	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:163206905-163207198	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:163206844-163207228	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:163121033-163121335	HepG2	liver:	n/a	chr6:163121209-163121220
35	CEBPB	chr6:163148686-163149168	A549	lung:	n/a	n/a
36	CEBPB	chr6:163206961-163207175	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr6:163192112-163192351	A549	lung:	n/a	chr6:163192194-163192205
38	CEBPB	chr6:163148771-163149153	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	chr6:163148563-163149157	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:163171040-163171207	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:163206848-163207222	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:163196390-163196524	A549	lung:	n/a	chr6:163196436-163196445 chr6:163196436-163196445 chr6:163196434-163196447 chr6:163196436-163196445
44	CEBPB	chr6:163095583-163095738	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
45	CEBPB	chr6:163218870-163218983	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:163148769-163149149	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:163206824-163207160	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr6:163121018-163121310	A549	lung:	n/a	chr6:163121209-163121220
49	CEBPB	chr6:163148738-163149145	K562	blood:	n/a	n/a
50	CEBPB	chr6:163206891-163207206	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163148018-163148068	SAEC	small airway:	n/a
2	chr6:163148018-163148068	SAEC	small airway:	n/a
3	chr6:163199983-163200033	MCF-7	breast:	n/a
4	chr6:163110854-163110904	MCF10A-Er-Src	breast:	n/a
5	chr6:163147737-163147787	PANC-1	pancreas:	n/a
6	chr6:163147733-163147783	BJ	skin:	n/a
7	chr6:163149674-163149724	K562	blood:	n/a
8	chr6:163149320-163149370	BE2_C	brain:	n/a
9	chr6:163149169-163149219	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:163147737-163147787	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:163148903-163148953	Jurkat	blood:	n/a
12	chr6:163149674-163149724	SK-N-SH	brain:	n/a
13	chr6:163149167-163149217	MCF-7	breast:	n/a
14	chr6:163147733-163147783	U87	brain:	n/a
15	chr6:163148762-163148812	ProgFib	skin:	n/a
16	chr6:163148718-163148768	PFSK-1	brain:	n/a
17	chr6:163149674-163149724	HEK293	kidney:	embryo
18	chr6:163148762-163148812	AG09319	gingival:	n/a
19	chr6:163199983-163200033	H1-hESC	embryonic stem cell:	embryo
20	chr6:163149453-163149503	H1-hESC	embryonic stem cell:	embryo
21	chr6:163148018-163148068	SK-N-SH	brain:	n/a
22	chr6:163148290-163148340	NT2-D1	testis:	n/a
23	chr6:163148718-163148768	GM12878	blood:	n/a
24	chr6:163147999-163148049	PANC-1	pancreas:	n/a
25	chr6:163148018-163148068	ovcar-3	ovarian:	n/a
26	chr6:163149453-163149503	HRPEpiC	eye:	n/a
27	chr6:163200038-163200088	HepG2	liver:	n/a
28	chr6:163148718-163148768	K562	blood:	n/a
29	chr6:163110854-163110904	Jurkat	blood:	n/a
30	chr6:163148777-163148827	GM12891	blood:	n/a
31	chr6:163147999-163148049	HEEpiC	esophagus:	n/a
32	chr6:163135177-163135227	HRE	kidney:	n/a
33	chr6:163147737-163147787	T-47D	breast:	n/a
34	chr6:163149167-163149217	SK-N-SH	brain:	n/a
35	chr6:163148762-163148812	NHDF-neo	bronchial:	n/a
36	chr6:163148501-163148551	HEEpiC	esophagus:	n/a
37	chr6:163148022-163148072	ProgFib	skin:	n/a
38	chr6:163148501-163148551	SK-N-SH	brain:	n/a
39	chr6:163148022-163148072	ECC-1	luminal epithelium:	n/a
40	chr6:163110854-163110904	HCPEpiC	choroid plexus:	n/a
41	chr6:163148290-163148340	GM12892	blood:	n/a
42	chr6:163110854-163110904	ECC-1	luminal epithelium:	n/a
43	chr6:163149167-163149217	PFSK-1	brain:	n/a
44	chr6:163200038-163200088	HNPCEpiC	eye:	n/a
45	chr6:163148022-163148072	GM19239	blood:	n/a
46	chr6:163149167-163149217	MCF10A-Er-Src	breast:	n/a
47	chr6:163148501-163148551	HCF	heart:	n/a
48	chr6:163149167-163149217	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:163199983-163200033	HMEC	breast:	n/a
50	chr6:163200038-163200088	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
2	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
3	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
4	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
5	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
6	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
7	chr6:163146966..163150271-chr6:163157232..163160053,3	K562	blood:
8	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
9	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
10	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
11	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
12	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
13	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
14	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
15	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
16	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
17	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
18	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:
19	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
20	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
21	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
22	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
23	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
24	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
25	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
26	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
27	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
28	chr6:163139294..163141851-chr6:163147296..163150092,3	MCF-7	breast:
29	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
30	chr6:163100762..163102270-chr6:163108804..163111519,2	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: 4254 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4254 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538280348	chr6:163064830-163064831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73597944	chr6:163064840-163064841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575653203	chr6:163064853-163064854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559338631	chr6:163064870-163064871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532271298	chr6:163064899-163064900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544383074	chr6:163064985-163064986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2803108	chr6:163065019-163065020	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs77999446	chr6:163065078-163065079	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs139590525	chr6:163065133-163065134	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs559625382	chr6:163065164-163065165	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs189358993	chr6:163065189-163065190	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs554475055	chr6:163065202-163065203	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs200320700	chr6:163065250-163065251	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs367983508	chr6:163065252-163065253	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs201676980	chr6:163065266-163065267	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs149718492	chr6:163065273-163065274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs545112805	chr6:163065274-163065275	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs371736280	chr6:163065308-163065309	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs565197133	chr6:163065319-163065320	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs145627960	chr6:163065387-163065388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs367798496	chr6:163065435-163065436	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs191928990	chr6:163065469-163065470	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs57387338	chr6:163065496-163065497	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs530262752	chr6:163065515-163065516	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546651221	chr6:163065539-163065540	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs80180366	chr6:163065559-163065560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs538622844	chr6:163065576-163065577	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369928789	chr6:163065583-163065584	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs184147733	chr6:163065588-163065589	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs569129102	chr6:163065645-163065646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538165185	chr6:163065679-163065680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554772177	chr6:163065707-163065708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2803106	chr6:163065752-163065753	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs540083370	chr6:163065753-163065754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571065252	chr6:163065812-163065813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146415061	chr6:163065814-163065815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371853720	chr6:163065832-163065833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374688791	chr6:163065834-163065835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571042660	chr6:163065839-163065840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534863233	chr6:163065871-163065872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538131410	chr6:163065923-163065924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375495311	chr6:163065933-163065934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2846533	chr6:163065934-163065935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs568857965	chr6:163065937-163065938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79919182	chr6:163065954-163065955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558811030	chr6:163065999-163066000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2849549	chr6:163066003-163066004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs531074200	chr6:163066078-163066079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544485938	chr6:163066091-163066092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188527494	chr6:163066093-163066094	Weak transcription	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:891 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163052800-163065000	Weak transcription	Psoas Muscle	Psoas
2	chr6:163057000-163071200	Weak transcription	Right Atrium	heart
3	chr6:163058000-163065200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:163058600-163065000	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:163058600-163065000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:163065000-163065200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:163065000-163065400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:163065000-163065600	Enhancers	Left Ventricle	heart
9	chr6:163065000-163065600	Enhancers	Psoas Muscle	Psoas
10	chr6:163065000-163065600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr6:163065000-163065600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr6:163065200-163065400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:163065200-163065400	Enhancers	Esophagus	oesophagus
14	chr6:163065600-163065800	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr6:163065600-163066000	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr6:163071000-163071400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:163072000-163072600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:163082600-163100600	Weak transcription	Ovary	ovary
19	chr6:163083600-163092800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:163084000-163091400	Weak transcription	Psoas Muscle	Psoas
21	chr6:163085400-163094800	Weak transcription	Fetal Intestine Small	intestine
22	chr6:163087000-163087600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:163088200-163091600	Weak transcription	Pancreas	Pancrea
24	chr6:163089400-163089600	Enhancers	Left Ventricle	heart
25	chr6:163089400-163089600	Enhancers	Lung	lung
26	chr6:163089400-163089600	Enhancers	Right Atrium	heart
27	chr6:163089400-163089800	Enhancers	Right Ventricle	heart
28	chr6:163089400-163090000	Enhancers	Spleen	Spleen
29	chr6:163089600-163091200	Weak transcription	Right Atrium	heart
30	chr6:163089600-163091400	Weak transcription	Left Ventricle	heart
31	chr6:163090600-163091600	Enhancers	Fetal Heart	heart
32	chr6:163090600-163092200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:163090600-163093200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:163091200-163091600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:163091200-163091600	Enhancers	Right Atrium	heart
36	chr6:163091200-163091800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:163091400-163091600	Enhancers	Left Ventricle	heart
38	chr6:163091400-163091800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:163091400-163091800	Enhancers	Liver	Liver
40	chr6:163091400-163091800	Enhancers	Psoas Muscle	Psoas
41	chr6:163091600-163092400	Enhancers	Pancreas	Pancrea
42	chr6:163091600-163094200	Weak transcription	Right Atrium	heart
43	chr6:163091800-163094200	Weak transcription	Psoas Muscle	Psoas
44	chr6:163092400-163102600	Weak transcription	Pancreas	Pancrea
45	chr6:163092800-163093000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:163094200-163094400	Enhancers	Psoas Muscle	Psoas
47	chr6:163094200-163094400	Enhancers	Right Atrium	heart
48	chr6:163094200-163095000	Enhancers	NHEK	skin
49	chr6:163094400-163094600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr6:163094400-163094600	Weak transcription	Right Atrium	heart

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