Variant report

Variant	nsv604664
Chromosome Location	chr6:131004998-131115817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:983)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:131097575-131098146	GM12878	blood:	n/a	n/a
2	BACH1	chr6:131006798-131006819	K562	blood:	n/a	n/a
3	BACH1	chr6:131081053-131081073	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr6:131109214-131109610	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:131019004-131019389	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:131081251-131081485	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr6:131081106-131081619	HCT-116	colon:	n/a	n/a
8	CBX3	chr6:131081055-131081656	HCT-116	colon:	n/a	n/a
9	CEBPB	chr6:131100094-131100744	IMR90	lung:	n/a	chr6:131100568-131100579
10	CEBPB	chr6:131014429-131014694	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:131100533-131100627	HepG2	liver:	n/a	chr6:131100568-131100579
12	CEBPB	chr6:131081264-131081459	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr6:131104424-131104563	A549	lung:	n/a	chr6:131104528-131104539 chr6:131104499-131104510
14	CEBPB	chr6:131061365-131061605	HepG2	liver:	n/a	chr6:131061518-131061529
15	CEBPB	chr6:131061473-131061640	A549	lung:	n/a	chr6:131061518-131061529
16	CEBPB	chr6:131073432-131073804	IMR90	lung:	n/a	chr6:131073611-131073620 chr6:131073611-131073620 chr6:131073610-131073621 chr6:131073611-131073620 chr6:131073611-131073620 chr6:131073609-131073622 chr6:131073609-131073620
17	CEBPB	chr6:131091042-131091276	HepG2	liver:	n/a	chr6:131091192-131091203
18	CEBPB	chr6:131018579-131018891	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:131104378-131104597	HepG2	liver:	n/a	chr6:131104528-131104539 chr6:131104499-131104510
20	CEBPB	chr6:131061352-131061627	IMR90	lung:	n/a	chr6:131061518-131061529
21	CEBPB	chr6:131058406-131058712	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:131073443-131073783	HepG2	liver:	n/a	chr6:131073611-131073620 chr6:131073611-131073620 chr6:131073610-131073621 chr6:131073611-131073620 chr6:131073611-131073620 chr6:131073609-131073622 chr6:131073609-131073620
23	CHD1	chr6:131081253-131081384	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr6:131064380-131064515	HepG2	liver:	n/a	n/a
25	CHD2	chr6:131081158-131081446	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr6:131034242-131034648	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr6:131070683-131070733	GM19238	blood:	n/a	n/a
28	CTCF	chr6:131081300-131081450	HPF	lung:	n/a	n/a
29	CTCF	chr6:131019190-131019374	GM20000	blood:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276
30	CTCF	chr6:131019200-131019350	HVMF	connective:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276
31	CTCF	chr6:131019200-131019350	GM12864	blood:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276
32	CTCF	chr6:131081255-131081426	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:131106380-131106530	HepG2	liver:	n/a	n/a
34	CTCF	chr6:131019180-131019330	HMEC	breast:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276
35	CTCF	chr6:131081280-131081430	HepG2	liver:	n/a	n/a
36	CTCF	chr6:131081170-131081540	GM12878	blood:	n/a	n/a
37	CTCF	chr6:131081320-131081470	HMEC	breast:	n/a	n/a
38	CTCF	chr6:131070620-131070770	GM06990	blood:	n/a	n/a
39	CTCF	chr6:131019192-131019349	GM12891	blood:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276
40	CTCF	chr6:131081320-131081470	NHLF	lung:	n/a	n/a
41	CTCF	chr6:131081320-131081470	GM12873	blood:	n/a	n/a
42	CTCF	chr6:131070620-131070770	Caco-2	colon:	n/a	n/a
43	CTCF	chr6:131021706-131021725	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr6:131064600-131064750	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:131019200-131019350	HEEpiC	esophagus:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276
46	CTCF	chr6:131081300-131081450	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr6:131064478-131064601	IMR90	lung:	n/a	n/a
48	CTCF	chr6:131064440-131064590	HCT-116	colon:	n/a	n/a
49	CTCF	chr6:131070560-131070710	HCT-116	colon:	n/a	n/a
50	CTCF	chr6:131019092-131019374	H1-hESC	embryonic stem cell:	n/a	chr6:131019260-131019278 chr6:131019261-131019277 chr6:131019255-131019276

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131101115-131101165	PrEC	prostate:	n/a
2	chr6:131101115-131101165	GM12891	blood:	n/a
3	chr6:131101115-131101165	SAEC	small airway:	n/a
4	chr6:131101115-131101165	NB4	blood:	n/a
5	chr6:131101115-131101165	NHBE	bronchial:	n/a
6	chr6:131101115-131101165	Hela-S3	cervix:	n/a
7	chr6:131101115-131101165	AG09309	skin:	n/a
8	chr6:131101115-131101165	Jurkat	blood:	n/a
9	chr6:131101115-131101165	SK-N-SH_RA	brain:	n/a
10	chr6:131101115-131101165	Caco-2	colon:	n/a
11	chr6:131101115-131101165	HEEpiC	esophagus:	n/a
12	chr6:131101115-131101165	SK-N-MC	brain:	n/a
13	chr6:131101115-131101165	HEK293	kidney:	embryo
14	chr6:131101115-131101165	NT2-D1	testis:	n/a
15	chr6:131101115-131101165	U87	brain:	n/a
16	chr6:131101115-131101165	BJ	skin:	n/a
17	chr6:131101115-131101165	HCF	heart:	n/a
18	chr6:131101115-131101165	HIPEpiC	eye:	n/a
19	chr6:131101115-131101165	HCM	heart:	n/a
20	chr6:131101115-131101165	AG10803	skin:	n/a
21	chr6:131101115-131101165	BE2_C	brain:	n/a
22	chr6:131101115-131101165	HCPEpiC	choroid plexus:	n/a
23	chr6:131101115-131101165	GM12878	blood:	n/a
24	chr6:131101115-131101165	CMK	blood:	n/a
25	chr6:131101115-131101165	GM19239	blood:	n/a
26	chr6:131101115-131101165	HCT-116	colon:	n/a
27	chr6:131101115-131101165	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:131101115-131101165	NHDF-neo	bronchial:	n/a
29	chr6:131101115-131101165	MCF-7	breast:	n/a
30	chr6:131101115-131101165	SK-N-SH	brain:	n/a
31	chr6:131101115-131101165	HNPCEpiC	eye:	n/a
32	chr6:131101115-131101165	AG09319	gingival:	n/a
33	chr6:131101115-131101165	ECC-1	luminal epithelium:	n/a
34	chr6:131101115-131101165	HUVEC	blood vessel:	n/a
35	chr6:131101115-131101165	RPTEC	kidney:	n/a
36	chr6:131101115-131101165	A549	lung:	n/a
37	chr6:131101115-131101165	HMEC	breast:	n/a
38	chr6:131101115-131101165	GM12892	blood:	n/a
39	chr6:131101115-131101165	SKMC	muscle:	n/a
40	chr6:131101115-131101165	HRE	kidney:	n/a
41	chr6:131101115-131101165	Hepatocyte	liver:	n/a
42	chr6:131101115-131101165	AG04449	skin:	fetal
43	chr6:131101115-131101165	AoSMC	blood vessel:	n/a
44	chr6:131101115-131101165	ProgFib	skin:	n/a
45	chr6:131101115-131101165	NH-A	brain:	n/a
46	chr6:131101115-131101165	AG04450	lung:	fetal
47	chr6:131101115-131101165	H1-hESC	embryonic stem cell:	embryo
48	chr6:131101115-131101165	HepG2	liver:	n/a
49	chr6:131101115-131101165	PANC-1	pancreas:	n/a
50	chr6:131101115-131101165	T-47D	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:131062388..131064947-chr6:131067740..131069514,2	K562	blood:
2	chr6:130643796..130644450-chr6:131018869..131019419,2	MCF-7	breast:
3	chr6:130643524..130644551-chr6:131018759..131019797,15	MCF-7	breast:
4	chr6:131019021..131019768-chr6:131080914..131081754,2	MCF-7	breast:
5	chr6:131088960..131091588-chr6:131094520..131097000,2	K562	blood:
6	chr6:131062388..131064947-chr6:131067740..131069514,2	K562	blood:
7	chr6:130994751..130996672-chr6:131006100..131008606,2	K562	blood:
8	chr6:131068465..131070607-chr6:131098057..131100480,2	K562	blood:
9	chr6:131088960..131091588-chr6:131094520..131097000,2	K562	blood:
10	chr6:131019021..131019768-chr6:131080914..131081754,2	MCF-7	breast:
11	chr6:131085476..131087927-chr6:131091434..131093029,2	MCF-7	breast:
12	chr6:131085476..131087927-chr6:131091434..131093029,2	MCF-7	breast:
13	chr6:130614261..130615556-chr6:131018820..131019730,3	MCF-7	breast:
14	chr6:130643591..130644896-chr6:131080866..131081825,5	MCF-7	breast:
15	chr6:130614632..130615507-chr6:131081118..131081796,2	MCF-7	breast:
16	chr6:131068465..131070607-chr6:131098057..131100480,2	K562	blood:
17	chr6:131109093..131109911-chr6:131164434..131164971,2	MCF-7	breast:
18	chr6:130614691..130615581-chr6:131080850..131081759,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-324N14.2.1-2	chr6:131018663-131018923	ENSG00000229923.2
2	lnc-RP3-324N14.2.1-2	chr6:131018457-131018529	ENSG00000229923.2
3	lnc-RP3-324N14.2.1-3	chr6:131060355-131060616	NONHSAT114907
4	lnc-RP3-324N14.2.1-2	chr6:131018457-131018529	XLOC_005462
5	lnc-RP3-324N14.2.1-3	chr6:131060150-131060222	NONHSAT114907
6	lnc-RP3-324N14.2.1-2	chr6:131018662-131018923	XLOC_005462

No data

Variant related genes	Relation type
ENSG00000229923	TF binding region
ENSG00000229923	CpG island
EP300	miRNA target sites
ENTPD1	miRNA target sites

Extended variants
information (count: 3699 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3699 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9388831	chr6:131004998-131004999	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547488726	chr6:131005072-131005073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35720631	chr6:131005225-131005226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145920217	chr6:131005250-131005251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539288820	chr6:131005269-131005270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138579222	chr6:131005273-131005274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149304552	chr6:131005296-131005297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536624641	chr6:131005311-131005312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555307600	chr6:131005362-131005363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528672581	chr6:131005388-131005389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79446429	chr6:131005397-131005398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375227096	chr6:131005404-131005405	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs62431619	chr6:131005406-131005407	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs143600193	chr6:131005418-131005419	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs76190766	chr6:131005419-131005420	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs564535240	chr6:131005429-131005430	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs367710387	chr6:131005432-131005433	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs559531993	chr6:131005444-131005445	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs374977613	chr6:131005445-131005446	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs572673638	chr6:131005447-131005448	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs563044615	chr6:131005464-131005465	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs192457721	chr6:131005476-131005477	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs148070333	chr6:131005477-131005478	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs116802099	chr6:131005486-131005487	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs183350639	chr6:131005487-131005488	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs562066625	chr6:131005491-131005492	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs529257735	chr6:131005503-131005504	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs370132252	chr6:131005504-131005505	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs186896008	chr6:131005517-131005518	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs114956536	chr6:131005533-131005534	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs551586141	chr6:131005539-131005540	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs569766777	chr6:131005549-131005550	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs141915098	chr6:131005554-131005555	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs573670627	chr6:131005555-131005556	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs368132072	chr6:131005557-131005558	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs545632900	chr6:131005577-131005578	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs534652504	chr6:131005585-131005586	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs569300785	chr6:131005589-131005590	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs551941975	chr6:131005598-131005599	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs562809620	chr6:131005610-131005611	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs374355936	chr6:131005677-131005678	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs566629131	chr6:131005678-131005679	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs146302348	chr6:131005685-131005686	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs139591013	chr6:131005704-131005705	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs564675607	chr6:131005713-131005714	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs376615426	chr6:131005817-131005818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72992285	chr6:131005842-131005843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs562282599	chr6:131005892-131005893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529244225	chr6:131005893-131005894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142868353	chr6:131005943-131005944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Autism	21448237	CNVD
Autism	22495311	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
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Brain cancer	19584924	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:130993800-131005400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:130997600-131005400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:131003000-131005200	Weak transcription	NHDF-Ad	bronchial
4	chr6:131003200-131005000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:131004400-131006000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:131004600-131005600	Enhancers	Ovary	ovary
7	chr6:131004600-131006000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:131005000-131005600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:131005200-131005600	Enhancers	Primary hematopoietic stem cells	blood
10	chr6:131005200-131005600	Enhancers	Brain Hippocampus Middle	brain
11	chr6:131005400-131005600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:131005400-131005600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:131005400-131005600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:131005400-131005600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr6:131005400-131005600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:131005400-131005600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:131005400-131005600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:131005400-131005600	Active TSS	Fetal Kidney	kidney
19	chr6:131005400-131005600	Flanking Bivalent TSS/Enh	Fetal Lung	lung
20	chr6:131005400-131005600	Enhancers	Gastric	stomach
21	chr6:131005400-131005600	ZNF genes & repeats	Lung	lung
22	chr6:131005400-131005600	Enhancers	NHDF-Ad	bronchial
23	chr6:131005400-131005800	Bivalent Enhancer	Aorta	Aorta
24	chr6:131005600-131017800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:131014200-131016400	Enhancers	Ovary	ovary
26	chr6:131014600-131016200	Enhancers	Primary T cells from cord blood	blood
27	chr6:131014800-131015600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr6:131014800-131015800	Enhancers	Dnd41	blood
29	chr6:131014800-131016200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr6:131014800-131018400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:131015000-131015400	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr6:131015200-131015400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:131015200-131015800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr6:131015400-131016200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:131015400-131017600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr6:131015400-131018400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr6:131015600-131016400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:131015600-131017600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr6:131015800-131016000	Enhancers	Osteobl	bone
40	chr6:131015800-131016800	Enhancers	NHDF-Ad	bronchial
41	chr6:131015800-131018000	Weak transcription	Dnd41	blood
42	chr6:131015800-131019000	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:131016000-131016200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr6:131016000-131016200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:131016200-131017600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:131016200-131017600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:131016200-131017600	Weak transcription	Osteobl	bone
48	chr6:131016200-131017800	Weak transcription	Primary T cells from cord blood	blood
49	chr6:131016200-131018200	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr6:131016400-131017600	Weak transcription	Muscle Satellite Cultured Cells	--

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