Variant report

Variant	nsv893751
Chromosome Location	chr9:116846467-116874355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:671)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116872498-116872957	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116870070-116870574	HepG2	liver:	n/a	n/a
3	BACH1	chr9:116870328-116870533	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr9:116870367-116870538	K562	blood:	n/a	n/a
5	BRCA1	chr9:116870252-116870495	HepG2	liver:	n/a	n/a
6	BRCA1	chr9:116870225-116870581	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr9:116864751-116865191	HCT-116	colon:	n/a	n/a
8	CBX3	chr9:116864794-116865133	K562	blood:	n/a	n/a
9	CBX3	chr9:116864807-116865125	K562	blood:	n/a	n/a
10	CEBPB	chr9:116872668-116872869	K562	blood:	n/a	chr9:116872765-116872776
11	CEBPB	chr9:116872399-116872954	HepG2	liver:	n/a	chr9:116872765-116872776
12	CEBPB	chr9:116872346-116873057	A549	lung:	n/a	chr9:116872765-116872776
13	CEBPB	chr9:116872436-116872932	Hela-S3	cervix:	n/a	chr9:116872765-116872776
14	CEBPB	chr9:116872374-116872985	A549	lung:	n/a	chr9:116872765-116872776
15	CEBPB	chr9:116871624-116871881	HepG2	liver:	n/a	chr9:116871746-116871757
16	CEBPB	chr9:116870306-116870552	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:116872272-116872964	IMR90	lung:	n/a	chr9:116872765-116872776
18	CEBPB	chr9:116872397-116872943	A549	lung:	n/a	chr9:116872765-116872776
19	CHD1	chr9:116861095-116861396	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr9:116870219-116870422	HepG2	liver:	n/a	n/a
21	CHD2	chr9:116870235-116870545	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr9:116861454-116861668	HepG2	liver:	n/a	n/a
23	CREB1	chr9:116870162-116870592	A549	lung:	n/a	n/a
24	CTBP2	chr9:116870165-116871289	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr9:116869961-116870716	HCT-116	colon:	n/a	chr9:116870385-116870406
26	CTCF	chr9:116870240-116870390	WI-38	lung:	n/a	n/a
27	CTCF	chr9:116847881-116848156	HCT-116	colon:	n/a	n/a
28	CTCF	chr9:116861498-116861515	MCF-7	breast:	n/a	n/a
29	CTCF	chr9:116870320-116870470	A549	lung:	n/a	chr9:116870385-116870406
30	CTCF	chr9:116858269-116858547	A549	lung:	n/a	n/a
31	CTCF	chr9:116870280-116870430	GM12870	blood:	n/a	chr9:116870385-116870406
32	CTCF	chr9:116858400-116858550	K562	blood:	n/a	n/a
33	CTCF	chr9:116870260-116870504	SK-N-SH_RA	brain:	n/a	chr9:116870385-116870406
34	CTCF	chr9:116870177-116870587	K562	blood:	n/a	chr9:116870385-116870406
35	CTCF	chr9:116870300-116870450	HRE	kidney:	n/a	chr9:116870385-116870406
36	CTCF	chr9:116870249-116870526	Hela-S3	cervix:	n/a	chr9:116870385-116870406
37	CTCF	chr9:116861020-116861170	HRE	kidney:	n/a	n/a
38	CTCF	chr9:116870320-116870470	MCF-7	breast:	n/a	chr9:116870385-116870406
39	CTCF	chr9:116858280-116858430	HRE	kidney:	n/a	n/a
40	CTCF	chr9:116870280-116870430	HL-60	blood:	n/a	chr9:116870385-116870406
41	CTCF	chr9:116870320-116870470	GM12873	blood:	n/a	chr9:116870385-116870406
42	CTCF	chr9:116860980-116861130	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr9:116858360-116858510	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr9:116858348-116858519	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:116847942-116848070	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:116870236-116870491	A549	lung:	n/a	chr9:116870385-116870406
47	CTCF	chr9:116861100-116861250	HRE	kidney:	n/a	n/a
48	CTCF	chr9:116860964-116861150	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr9:116870300-116870450	HPF	lung:	n/a	chr9:116870385-116870406
50	CTCF	chr9:116858380-116858530	HCFaa	heart:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116861532-116861582	LNCaP	prostate:	n/a
2	chr9:116861442-116861492	LNCaP	prostate:	n/a
3	chr9:116861442-116861492	AG04450	lung:	fetal
4	chr9:116861288-116861338	HCM	heart:	n/a
5	chr9:116859631-116859681	SKMC	muscle:	n/a
6	chr9:116870365-116870415	A549	lung:	n/a
7	chr9:116861288-116861338	AG04450	lung:	fetal
8	chr9:116860500-116860550	RPTEC	kidney:	n/a
9	chr9:116861532-116861582	AG04450	lung:	fetal
10	chr9:116860650-116860700	ProgFib	skin:	n/a
11	chr9:116856710-116856760	SAEC	small airway:	n/a
12	chr9:116859631-116859681	GM12892	blood:	n/a
13	chr9:116858634-116858684	HRPEpiC	eye:	n/a
14	chr9:116861288-116861338	IMR90	lung:	fetal
15	chr9:116860500-116860550	GM12892	blood:	n/a
16	chr9:116860437-116860487	GM12891	blood:	n/a
17	chr9:116861442-116861492	ProgFib	skin:	n/a
18	chr9:116861404-116861454	NH-A	brain:	n/a
19	chr9:116861442-116861492	Jurkat	blood:	n/a
20	chr9:116860437-116860487	AG04449	skin:	fetal
21	chr9:116861532-116861582	AoSMC	blood vessel:	n/a
22	chr9:116861404-116861454	HEEpiC	esophagus:	n/a
23	chr9:116861288-116861338	BJ	skin:	n/a
24	chr9:116860500-116860550	U87	brain:	n/a
25	chr9:116861442-116861492	AG09309	skin:	n/a
26	chr9:116860437-116860487	HEEpiC	esophagus:	n/a
27	chr9:116861404-116861454	LNCaP	prostate:	n/a
28	chr9:116870365-116870415	Hela-S3	cervix:	n/a
29	chr9:116870365-116870415	MCF-7	breast:	n/a
30	chr9:116860650-116860700	HEK293	kidney:	embryo
31	chr9:116858634-116858684	LNCaP	prostate:	n/a
32	chr9:116859631-116859681	HCM	heart:	n/a
33	chr9:116861288-116861338	Hepatocyte	liver:	n/a
34	chr9:116861532-116861582	HNPCEpiC	eye:	n/a
35	chr9:116858634-116858684	NH-A	brain:	n/a
36	chr9:116860650-116860700	AG09319	gingival:	n/a
37	chr9:116870365-116870415	HUVEC	blood vessel:	n/a
38	chr9:116856710-116856760	NHDF-neo	bronchial:	n/a
39	chr9:116870365-116870415	ovcar-3	ovarian:	n/a
40	chr9:116860500-116860550	HIPEpiC	eye:	n/a
41	chr9:116860500-116860550	LNCaP	prostate:	n/a
42	chr9:116860437-116860487	MCF-7	breast:	n/a
43	chr9:116860650-116860700	HRCEpiC	kidney:	n/a
44	chr9:116860437-116860487	RPTEC	kidney:	n/a
45	chr9:116859631-116859681	Caco-2	colon:	n/a
46	chr9:116861442-116861492	HEK293	kidney:	embryo
47	chr9:116861442-116861492	SK-N-SH	brain:	n/a
48	chr9:116860650-116860700	GM19239	blood:	n/a
49	chr9:116860650-116860700	Caco-2	colon:	n/a
50	chr9:116856710-116856760	H1-hESC	embryonic stem cell:	embryo

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116845927..116847866-chr9:117052148..117055626,3	MCF-7	breast:
2	chr9:116869961..116870829-chr9:117067901..117068666,2	MCF-7	breast:
3	chr9:116864243..116866474-chr9:116868618..116871598,3	MCF-7	breast:
4	chr9:116637031..116639708-chr9:116859646..116861440,2	MCF-7	breast:
5	chr9:116869916..116870857-chr9:117067860..117068426,2	K562	blood:
6	chr9:116869923..116871115-chr9:117053002..117053726,3	K562	blood:
7	chr9:116841868..116844591-chr9:116846288..116849534,3	MCF-7	breast:
8	chr9:116869941..116870862-chr9:117026162..117027038,2	K562	blood:
9	chr9:116870953..116873166-chr9:117066845..117069372,2	MCF-7	breast:
10	chr9:116848752..116850800-chr9:116852040..116854106,2	MCF-7	breast:
11	chr9:116869902..116871221-chr9:117033694..117034751,11	MCF-7	breast:
12	chr9:116846559..116847181-chr9:117043604..117044541,2	MCF-7	breast:
13	chr9:116870044..116870759-chr9:117033677..117034476,3	MCF-7	breast:
14	chr9:116847982..116849837-chr9:116858325..116860933,2	MCF-7	breast:
15	chr9:116856264..116859004-chr9:116870407..116871935,2	MCF-7	breast:
16	chr9:116870116..116870941-chr9:116916806..116918287,4	MCF-7	breast:
17	chr9:116869949..116870838-chr9:116915614..116916621,9	MCF-7	breast:
18	chr9:116846785..116849126-chr9:116861196..116862830,2	MCF-7	breast:
19	chr9:116869934..116871127-chr9:117052704..117054035,13	MCF-7	breast:
20	chr9:116845277..116847223-chr9:116852930..116854750,2	K562	blood:
21	chr9:116870237..116871907-chr9:116924776..116927376,2	MCF-7	breast:
22	chr9:116869905..116870808-chr9:117026020..117026989,3	MCF-7	breast:
23	chr9:116870168..116870856-chr9:116901035..116901659,2	MCF-7	breast:
24	chr9:116848752..116850800-chr9:116852040..116854106,2	MCF-7	breast:
25	chr9:116869891..116870803-chr9:116915238..116916605,3	MCF-7	breast:
26	chr9:116849164..116851925-chr9:116855946..116857898,2	MCF-7	breast:
27	chr9:116845277..116847223-chr9:116852930..116854750,2	K562	blood:
28	chr9:116846273..116847216-chr9:116922173..116922681,2	MCF-7	breast:
29	chr9:116869935..116870873-chr9:117052125..117052932,3	K562	blood:
30	chr9:116844518..116845085-chr9:116869930..116870489,2	MCF-7	breast:
31	chr9:116856264..116859004-chr9:116870407..116871935,2	MCF-7	breast:
32	chr9:116869078..116871087-chr9:117033811..117035957,3	MCF-7	breast:
33	chr9:116843708..116846188-chr9:116846451..116849353,3	MCF-7	breast:
34	chr9:116844821..116845361-chr9:116869981..116870487,2	MCF-7	breast:
35	chr9:116867191..116869854-chr9:116876924..116878733,2	K562	blood:
36	chr9:116850338..116853324-chr9:116855246..116858808,3	K562	blood:
37	chr9:116871367..116873297-chr9:116878606..116880633,2	K562	blood:
38	chr9:116842742..116844725-chr9:116847223..116849817,2	K562	blood:
39	chr9:116867846..116870014-chr9:116881182..116883188,2	MCF-7	breast:
40	chr9:116864243..116866474-chr9:116868618..116871598,3	MCF-7	breast:
41	chr9:116869952..116870601-chr9:117067846..117068685,2	MCF-7	breast:
42	chr9:116870303..116871233-chr9:117051501..117052146,3	MCF-7	breast:
43	chr9:116859675..116862094-chr9:116864175..116866038,2	MCF-7	breast:
44	chr9:116870773..116871584-chr9:117033510..117034155,2	K562	blood:
45	chr9:116869895..116870973-chr9:117052879..117053661,10	MCF-7	breast:
46	chr9:116837426..116839732-chr9:116847214..116849059,3	MCF-7	breast:
47	chr9:116850338..116853034-chr9:116856193..116858808,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF12-1	chr9:116856166-116856197	NONHSAT134365
2	lnc-KIF12-1	chr9:116848406-116848504	NONHSAT134365
3	lnc-KIF12-1	chr9:116855509-116855777	NONHSAT134365

No data

Variant related genes	Relation type
KIF12	TF binding region
KIF12	CpG island
ENSG00000196739	chromatin interactions
ENSG00000136883	chromatin interactions
ENSG00000157657	chromatin interactions

Extended variants
information (count: 1239 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10121775	chr9:116846467-116846468	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547223836	chr9:116846532-116846533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71503585	chr9:116846580-116846581	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs563280616	chr9:116846583-116846584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71503586	chr9:116846597-116846598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184106416	chr9:116846685-116846686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566401641	chr9:116846690-116846691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528764664	chr9:116846699-116846700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368839218	chr9:116846732-116846733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117230277	chr9:116846783-116846784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571807235	chr9:116846845-116846846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142709856	chr9:116846859-116846860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557003208	chr9:116846870-116846871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73658329	chr9:116846902-116846903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs536277192	chr9:116846964-116846965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs193158877	chr9:116846970-116846971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs117874314	chr9:116847018-116847019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183837027	chr9:116847062-116847063	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187166503	chr9:116847063-116847064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143426778	chr9:116847094-116847095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543167772	chr9:116847153-116847154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563343919	chr9:116847183-116847184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs891725	chr9:116847201-116847202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs542676041	chr9:116847205-116847206	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78679765	chr9:116847283-116847284	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148009840	chr9:116847299-116847300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552002115	chr9:116847312-116847313	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs891724	chr9:116847365-116847366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs535939712	chr9:116847394-116847395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191269795	chr9:116847420-116847421	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs550743113	chr9:116847479-116847480	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553976475	chr9:116847501-116847502	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs183732895	chr9:116847503-116847504	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546637373	chr9:116847545-116847546	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566812507	chr9:116847569-116847570	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534623883	chr9:116847591-116847592	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs113914668	chr9:116847601-116847602	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs10982060	chr9:116847621-116847622	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577782861	chr9:116847638-116847639	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537271036	chr9:116847681-116847682	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78007457	chr9:116847684-116847685	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190584070	chr9:116847688-116847689	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141658083	chr9:116847745-116847746	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150890798	chr9:116847748-116847749	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572765960	chr9:116847749-116847750	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545401784	chr9:116847755-116847756	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368325939	chr9:116847788-116847789	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558055910	chr9:116847803-116847804	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576389569	chr9:116847804-116847805	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114471592	chr9:116847832-116847833	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116840000-116847000	Enhancers	Fetal Intestine Large	intestine
2	chr9:116843000-116858800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:116844800-116851800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:116844800-116855400	Weak transcription	Gastric	stomach
5	chr9:116845000-116847200	Enhancers	Fetal Stomach	stomach
6	chr9:116845000-116847400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:116845200-116846800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr9:116845200-116849000	Enhancers	HepG2	liver
9	chr9:116845200-116850000	Weak transcription	Fetal Lung	lung
10	chr9:116845200-116854200	Weak transcription	Pancreas	Pancrea
11	chr9:116845200-116854600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:116845200-116855000	Weak transcription	Duodenum Mucosa	Duodenum
13	chr9:116845400-116847400	Enhancers	A549	lung
14	chr9:116846000-116847200	Enhancers	Stomach Smooth Muscle	stomach
15	chr9:116846200-116847600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:116846200-116848000	Weak transcription	Fetal Intestine Small	intestine
17	chr9:116846200-116854400	Weak transcription	Liver	Liver
18	chr9:116846400-116847400	Enhancers	Fetal Kidney	kidney
19	chr9:116846800-116847000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:116846800-116847600	Enhancers	Fetal Muscle Trunk	muscle
21	chr9:116847000-116853200	Weak transcription	Fetal Intestine Large	intestine
22	chr9:116847400-116847600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:116847400-116848400	Weak transcription	A549	lung
24	chr9:116847400-116856400	Weak transcription	Fetal Kidney	kidney
25	chr9:116847600-116848200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr9:116848000-116849200	Strong transcription	Fetal Intestine Small	intestine
27	chr9:116848400-116848800	Enhancers	A549	lung
28	chr9:116848400-116849000	Enhancers	HMEC	breast
29	chr9:116848600-116848800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr9:116849000-116858800	Weak transcription	HepG2	liver
31	chr9:116849200-116851200	Weak transcription	Fetal Intestine Small	intestine
32	chr9:116850000-116850600	Enhancers	Fetal Lung	lung
33	chr9:116850200-116850400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr9:116850600-116850800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr9:116850600-116851400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:116850600-116856800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr9:116851200-116857400	Strong transcription	Fetal Intestine Small	intestine
38	chr9:116851800-116852200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr9:116852200-116853000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr9:116853000-116854000	Weak transcription	Fetal Stomach	stomach
41	chr9:116853000-116858600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:116853200-116858400	Strong transcription	Fetal Intestine Large	intestine
43	chr9:116854000-116854400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr9:116854000-116857200	Strong transcription	Fetal Stomach	stomach
45	chr9:116854000-116858600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr9:116854200-116854400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr9:116854200-116858600	Strong transcription	Pancreas	Pancrea
48	chr9:116854400-116857000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr9:116854400-116858200	Strong transcription	Liver	Liver
50	chr9:116854600-116857000	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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