Variant report

Variant	nsv1016868
Chromosome Location	chr6:56376165-56417631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1183)
CpG islands
(count:733)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:56375672-56376421	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:56405792-56406934	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:56407528-56407947	K562	blood:	n/a	n/a
4	ARID3A	chr6:56386126-56386671	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:56407505-56408262	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:56375694-56376414	K562	blood:	n/a	n/a
7	ARID3A	chr6:56393076-56393137	K562	blood:	n/a	n/a
8	ATF1	chr6:56406049-56406522	K562	blood:	n/a	n/a
9	ATF1	chr6:56375892-56376849	K562	blood:	n/a	n/a
10	ATF1	chr6:56407166-56408203	K562	blood:	n/a	n/a
11	ATF1	chr6:56387112-56387441	K562	blood:	n/a	n/a
12	ATF2	chr6:56407171-56408263	GM12878	blood:	n/a	n/a
13	ATF2	chr6:56407373-56408031	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:56407255-56408020	GM12878	blood:	n/a	n/a
15	ATF2	chr6:56407196-56408142	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr6:56407572-56407934	K562	blood:	n/a	chr6:56407777-56407790 chr6:56407778-56407791
17	ATF3	chr6:56407635-56407886	K562	blood:	n/a	chr6:56407777-56407790 chr6:56407778-56407791
18	BACH1	chr6:56407432-56407766	K562	blood:	n/a	n/a
19	BACH1	chr6:56407596-56408105	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:56407495-56407907	GM12878	blood:	n/a	chr6:56407777-56407790
21	BCL11A	chr6:56398008-56398320	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:56407145-56407997	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:56407246-56408209	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:56407280-56408103	K562	blood:	n/a	n/a
25	BHLHE40	chr6:56407271-56408106	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:56407388-56408057	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:56376020-56376425	K562	blood:	n/a	n/a
28	BRCA1	chr6:56407311-56407961	HepG2	liver:	n/a	n/a
29	BRCA1	chr6:56407132-56408012	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr6:56407506-56407713	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr6:56407339-56408167	HCT-116	colon:	n/a	n/a
32	CBX3	chr6:56407345-56407867	K562	blood:	n/a	n/a
33	CBX3	chr6:56407120-56407995	K562	blood:	n/a	n/a
34	CCNT2	chr6:56376059-56376370	K562	blood:	n/a	n/a
35	CCNT2	chr6:56407280-56407890	K562	blood:	n/a	n/a
36	CEBPB	chr6:56405742-56406598	HepG2	liver:	n/a	chr6:56406503-56406516 chr6:56405919-56405930 chr6:56406500-56406517
37	CEBPB	chr6:56407216-56407934	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:56382158-56382611	IMR90	lung:	n/a	chr6:56382588-56382600
39	CEBPB	chr6:56376040-56376403	K562	blood:	n/a	n/a
40	CEBPB	chr6:56407135-56407918	K562	blood:	n/a	n/a
41	CEBPB	chr6:56407203-56407944	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:56407310-56407934	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:56386364-56386694	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:56386319-56386693	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:56407616-56407827	K562	blood:	n/a	n/a
46	CEBPB	chr6:56407140-56408011	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:56375754-56376211	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:56407324-56408082	GM12878	blood:	n/a	n/a
49	CEBPB	chr6:56389754-56390604	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:56407624-56407896	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56407956-56408006	AoSMC	blood vessel:	n/a
2	chr6:56407956-56408006	AoSMC	blood vessel:	n/a
3	chr6:56405167-56405217	HEK293	kidney:	embryo
4	chr6:56391215-56391265	BJ	skin:	n/a
5	chr6:56407538-56407588	IMR90	lung:	fetal
6	chr6:56407956-56408006	AG04449	skin:	fetal
7	chr6:56406336-56406386	AG09319	gingival:	n/a
8	chr6:56407725-56407775	HNPCEpiC	eye:	n/a
9	chr6:56406084-56406134	PFSK-1	brain:	n/a
10	chr6:56400181-56400231	AG04449	skin:	fetal
11	chr6:56407956-56408006	Hela-S3	cervix:	n/a
12	chr6:56406336-56406386	NB4	blood:	n/a
13	chr6:56407725-56407775	MCF10A-Er-Src	breast:	n/a
14	chr6:56406084-56406134	MCF-7	breast:	n/a
15	chr6:56407538-56407588	Caco-2	colon:	n/a
16	chr6:56414724-56414774	AoSMC	blood vessel:	n/a
17	chr6:56391215-56391265	ProgFib	skin:	n/a
18	chr6:56407538-56407588	RPTEC	kidney:	n/a
19	chr6:56407725-56407775	HCM	heart:	n/a
20	chr6:56414724-56414774	HCF	heart:	n/a
21	chr6:56389866-56389916	GM06990	blood:	n/a
22	chr6:56414724-56414774	BE2_C	brain:	n/a
23	chr6:56387378-56387428	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:56405167-56405217	HCPEpiC	choroid plexus:	n/a
25	chr6:56387378-56387428	MCF-7	breast:	n/a
26	chr6:56389866-56389916	HEEpiC	esophagus:	n/a
27	chr6:56407725-56407775	AG09309	skin:	n/a
28	chr6:56387378-56387428	SK-N-SH_RA	brain:	n/a
29	chr6:56389866-56389916	A549	lung:	n/a
30	chr6:56407538-56407588	LNCaP	prostate:	n/a
31	chr6:56406084-56406134	SK-N-SH_RA	brain:	n/a
32	chr6:56406336-56406386	BJ	skin:	n/a
33	chr6:56407538-56407588	HMEC	breast:	n/a
34	chr6:56406084-56406134	CMK	blood:	n/a
35	chr6:56406336-56406386	PANC-1	pancreas:	n/a
36	chr6:56406336-56406386	AG04450	lung:	fetal
37	chr6:56405167-56405217	HUVEC	blood vessel:	n/a
38	chr6:56391215-56391265	U87	brain:	n/a
39	chr6:56414724-56414774	NH-A	brain:	n/a
40	chr6:56406084-56406134	NHDF-neo	bronchial:	n/a
41	chr6:56406084-56406134	NH-A	brain:	n/a
42	chr6:56407925-56407975	HMEC	breast:	n/a
43	chr6:56407725-56407775	BJ	skin:	n/a
44	chr6:56407925-56407975	HIPEpiC	eye:	n/a
45	chr6:56387378-56387428	HRE	kidney:	n/a
46	chr6:56407956-56408006	H1-hESC	embryonic stem cell:	embryo
47	chr6:56405167-56405217	SK-N-SH_RA	brain:	n/a
48	chr6:56387378-56387428	HAEpiC	amniotic membrane:	n/a
49	chr6:56391215-56391265	CMK	blood:	n/a
50	chr6:56391215-56391265	NHBE	bronchial:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:56396433..56398982-chr6:56400861..56403143,2	MCF-7	breast:
2	chr6:56234525..56235479-chr6:56413389..56414430,8	MCF-7	breast:
3	chr6:56406220..56410337-chr6:56413126..56418049,5	MCF-7	breast:
4	chr6:56409064..56410806-chr6:56424133..56426193,2	K562	blood:
5	chr1:222517973..222518488-chr6:56394311..56395250,2	MCF-7	breast:
6	chr6:56395761..56397276-chr6:56406032..56407787,2	MCF-7	breast:
7	chr6:56336959..56338872-chr6:56404795..56407459,2	K562	blood:
8	chr6:56386188..56388419-chr6:56391719..56395434,3	MCF-7	breast:
9	chr6:56393226..56394746-chr6:56401973..56403869,2	MCF-7	breast:
10	chr6:56414327..56416748-chr6:56421847..56423517,2	K562	blood:
11	chr6:56383107..56384935-chr6:56387446..56390248,2	K562	blood:
12	chr6:56392217..56393976-chr6:56395740..56397459,2	K562	blood:
13	chr6:56405751..56407545-chr6:56409347..56411136,2	MCF-7	breast:
14	chr6:56406850..56409641-chr6:56410586..56415474,8	K562	blood:
15	chr6:56405751..56407545-chr6:56409347..56411136,2	MCF-7	breast:
16	chr6:56386188..56388419-chr6:56391719..56395434,3	MCF-7	breast:
17	chr6:56330615..56332340-chr6:56407927..56409613,2	K562	blood:
18	chr6:56410167..56412439-chr6:56412999..56414699,2	K562	blood:
19	chr6:56383107..56384935-chr6:56387446..56390248,2	K562	blood:
20	chr6:56370282..56372107-chr6:56378887..56380737,2	K562	blood:
21	chr6:56359297..56362081-chr6:56378593..56380440,2	K562	blood:
22	chr6:56393226..56394746-chr6:56401973..56403869,2	MCF-7	breast:
23	chr6:56386785..56388815-chr6:56390586..56392837,2	MCF-7	breast:
24	chr6:56408981..56412253-chr6:56415239..56417908,3	K562	blood:
25	chr6:56392217..56393976-chr6:56395740..56397459,2	K562	blood:
26	chr6:56403956..56410167-chr6:56410483..56413824,9	K562	blood:
27	chr6:56390066..56391904-chr6:56396984..56399522,2	MCF-7	breast:
28	chr6:56385896..56387722-chr6:56406237..56408892,2	MCF-7	breast:
29	chr6:56413498..56416394-chr6:56417084..56419483,2	K562	blood:
30	chr6:56407110..56407769-chrX:41193124..41193828,2	Hela-S3	cervix:
31	chr6:56390066..56391904-chr6:56396984..56399522,2	MCF-7	breast:
32	chr6:56396433..56398982-chr6:56400861..56403143,2	MCF-7	breast:
33	chr6:56398077..56400962-chr6:56401619..56403800,2	K562	blood:
34	chr6:56402109..56404865-chr6:56433971..56436313,2	K562	blood:
35	chr6:56371302..56373415-chr6:56374644..56377108,2	K562	blood:
36	chr6:56379723..56396922-chr6:56400495..56411638,31	K562	blood:
37	chr6:56333512..56335429-chr6:56408876..56410830,2	K562	blood:
38	chr16:20911628..20912299-chr6:56407760..56408260,2	Hela-S3	cervix:
39	chr6:56383088..56384699-chr6:56407591..56409338,2	K562	blood:
40	chr6:56407223..56407766-chr9:2014757..2015410,2	NB4	blood:
41	chr6:56376106..56377836-chr6:56404859..56408896,4	K562	blood:
42	chr6:56408981..56412253-chr6:56415239..56417908,3	K562	blood:
43	chr6:56319049..56321408-chr6:56387396..56389873,2	K562	blood:
44	chr6:56374485..56377341-chr6:56380470..56384676,4	MCF-7	breast:
45	chr6:56302630..56305077-chr6:56407760..56410392,2	MCF-7	breast:
46	chr6:56410167..56412439-chr6:56412999..56414699,2	K562	blood:
47	chr6:56398077..56400962-chr6:56401619..56403800,2	K562	blood:
48	chr6:56386785..56388815-chr6:56390586..56392837,2	MCF-7	breast:
49	chr6:56406998..56408822-chr6:56409621..56411891,3	MCF-7	breast:
50	chr6:56413498..56416394-chr6:56417084..56419483,2	K562	blood:

No data

Variant related genes	Relation type
DST	TF binding region
DST	CpG island
ENSG00000151914	chromatin interactions
ENSG00000188215	chromatin interactions
ENSG00000080503	chromatin interactions
ENSG00000102897	chromatin interactions
ENSG00000196678	chromatin interactions
ENSG00000215301	chromatin interactions

Extended variants
information (count: 1405 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371649829	chr6:56376174-56376175	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376171977	chr6:56376178-56376179	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369440076	chr6:56376238-56376239	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200585974	chr6:56376246-56376247	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538572177	chr6:56376261-56376262	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs34764862	chr6:56376291-56376292	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376898837	chr6:56376326-56376327	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186145397	chr6:56376397-56376398	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572144918	chr6:56376407-56376408	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543064983	chr6:56376462-56376463	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372425301	chr6:56376471-56376472	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145457176	chr6:56376489-56376490	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576548370	chr6:56376501-56376502	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111602093	chr6:56376514-56376515	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4236139	chr6:56376586-56376587	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188948559	chr6:56376608-56376609	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549370989	chr6:56376625-56376626	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147190506	chr6:56376629-56376630	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552913749	chr6:56376630-56376631	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532853741	chr6:56376652-56376653	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181529593	chr6:56376653-56376654	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9475710	chr6:56376654-56376655	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs112415569	chr6:56376676-56376677	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74509371	chr6:56376766-56376767	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145566792	chr6:56376792-56376793	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186538609	chr6:56376793-56376794	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549686453	chr6:56376849-56376850	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs201155576	chr6:56376851-56376852	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192247111	chr6:56376861-56376862	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182753479	chr6:56376889-56376890	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531833283	chr6:56376910-56376911	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs551612312	chr6:56376985-56376986	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs3924307	chr6:56377026-56377027	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs565686886	chr6:56377050-56377051	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115285613	chr6:56377056-56377057	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533774729	chr6:56377182-56377183	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554984768	chr6:56377222-56377223	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553433947	chr6:56377269-56377270	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4130060	chr6:56377394-56377395	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs114494561	chr6:56377480-56377481	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115417152	chr6:56377485-56377486	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535962681	chr6:56377508-56377509	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557683964	chr6:56377565-56377566	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560111487	chr6:56377628-56377629	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7454479	chr6:56377632-56377633	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375987975	chr6:56377658-56377659	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571972526	chr6:56377668-56377669	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146510238	chr6:56377713-56377714	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141041853	chr6:56377714-56377715	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185903353	chr6:56377752-56377753	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	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
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56341800-56407400	Weak transcription	Spleen	Spleen
2	chr6:56345000-56384200	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:56351800-56386800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:56357000-56382600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:56357000-56383600	Strong transcription	NH-A	brain
6	chr6:56357000-56384000	Strong transcription	HSMM	muscle
7	chr6:56357200-56384200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:56360400-56382200	Strong transcription	Osteobl	bone
9	chr6:56360600-56381800	Strong transcription	Muscle Satellite Cultured Cells	--
10	chr6:56360800-56377200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:56362400-56391200	Weak transcription	Esophagus	oesophagus
12	chr6:56362600-56385800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr6:56362800-56400200	Weak transcription	Colonic Mucosa	Colon
14	chr6:56363000-56402200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:56364800-56378600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:56365600-56379400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr6:56367000-56376600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:56368400-56376800	Strong transcription	GM12878-XiMat	blood
19	chr6:56368400-56382400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:56369400-56378800	Strong transcription	Fetal Muscle Trunk	muscle
21	chr6:56369400-56380600	Strong transcription	HSMMtube	muscle
22	chr6:56370000-56378000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:56370000-56382600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr6:56370600-56380400	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr6:56371000-56378000	Enhancers	Fetal Heart	heart
26	chr6:56371200-56380200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:56371400-56376200	Weak transcription	Small Intestine	intestine
28	chr6:56372200-56378000	Genic enhancers	Liver	Liver
29	chr6:56372200-56384200	Weak transcription	Hela-S3	cervix
30	chr6:56372800-56378600	Strong transcription	Adipose Nuclei	Adipose
31	chr6:56372800-56378800	Strong transcription	Fetal Muscle Leg	muscle
32	chr6:56372800-56380200	Weak transcription	Aorta	Aorta
33	chr6:56373000-56378200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr6:56373000-56378600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:56373000-56382800	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr6:56373000-56390800	Weak transcription	Placenta	Placenta
37	chr6:56373600-56378600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:56373600-56379400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr6:56373800-56380200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr6:56374200-56383400	Weak transcription	Right Ventricle	heart
41	chr6:56374200-56387000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr6:56374200-56390800	Weak transcription	Lung	lung
43	chr6:56374200-56391000	Weak transcription	Right Atrium	heart
44	chr6:56374400-56377000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:56374400-56378400	Weak transcription	NHEK	skin
46	chr6:56374400-56379200	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr6:56374400-56386400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr6:56374400-56392000	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr6:56374400-56396800	Weak transcription	Fetal Brain Female	brain
50	chr6:56374600-56376200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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