Variant report

Variant	esv1801890
Chromosome Location	chr9:98660433-98701801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:98670150-98670415	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:98686091-98686500	HepG2	liver:	n/a	n/a
3	CEBPB	chr9:98676617-98676711	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr9:98675089-98675403	IMR90	lung:	n/a	chr9:98675237-98675248
5	CEBPB	chr9:98686160-98686330	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:98682388-98682498	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:98675122-98675322	H1-hESC	embryonic stem cell:	n/a	chr9:98675237-98675248
8	CEBPB	chr9:98675090-98675411	A549	lung:	n/a	chr9:98675237-98675248
9	CEBPB	chr9:98675075-98675407	HepG2	liver:	n/a	chr9:98675237-98675248
10	CEBPB	chr9:98675071-98675416	Hela-S3	cervix:	n/a	chr9:98675237-98675248
11	CEBPB	chr9:98682416-98682553	A549	lung:	n/a	n/a
12	CEBPB	chr9:98686086-98686471	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:98666788-98666918	HepG2	liver:	n/a	chr9:98666840-98666851
14	CEBPB	chr9:98675106-98675353	K562	blood:	n/a	chr9:98675237-98675248
15	CTCF	chr9:98670320-98670470	HFF-Myc	foreskin:	n/a	n/a
16	CTCF	chr9:98670240-98670390	GM12864	blood:	n/a	n/a
17	CTCF	chr9:98701160-98701310	HPF	lung:	n/a	n/a
18	CTCF	chr9:98670200-98670350	GM12865	blood:	n/a	n/a
19	CTCF	chr9:98670320-98670470	GM12866	blood:	n/a	n/a
20	CTCF	chr9:98670240-98670390	GM06990	blood:	n/a	n/a
21	CTCF	chr9:98701160-98701310	HEK293	kidney:	n/a	n/a
22	CTCF	chr9:98670180-98670330	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr9:98701180-98701330	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr9:98670205-98670402	MCF-7	breast:	n/a	n/a
25	CTCF	chr9:98701169-98701342	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr9:98670177-98670411	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr9:98701220-98701370	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr9:98701080-98701230	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr9:98701240-98701390	WI-38	lung:	n/a	n/a
30	CTCF	chr9:98701220-98701370	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr9:98670179-98670397	Medullo	brain:	n/a	n/a
32	CTCF	chr9:98670200-98670350	AG10803	skin:	n/a	n/a
33	CTCF	chr9:98670160-98670310	GM12873	blood:	n/a	n/a
34	CTCF	chr9:98670220-98670370	AG04450	lung:	n/a	n/a
35	CTCF	chr9:98701160-98701310	AG09319	gingival:	n/a	n/a
36	CTCF	chr9:98670200-98670350	BJ	skin:	n/a	n/a
37	CTCF	chr9:98670180-98670330	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr9:98670220-98670370	MCF-7	breast:	n/a	n/a
39	CTCF	chr9:98670139-98670475	IMR90	lung:	n/a	n/a
40	CTCF	chr9:98670220-98670370	HMEC	breast:	n/a	n/a
41	CTCF	chr9:98670240-98670390	HRE	kidney:	n/a	n/a
42	CTCF	chr9:98670200-98670350	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr9:98670220-98670370	HVMF	connective:	n/a	n/a
44	CTCF	chr9:98670260-98670410	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr9:98670160-98670310	HCFaa	heart:	n/a	n/a
46	CTCF	chr9:98687260-98687410	MCF-7	breast:	n/a	chr9:98687396-98687404
47	CTCF	chr9:98670280-98670430	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr9:98700700-98700970	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr9:98670200-98670350	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr9:98670280-98670430	GM12872	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98699195-98699245	T-47D	breast:	n/a
2	chr9:98699195-98699245	K562	blood:	n/a
3	chr9:98699195-98699245	HEEpiC	esophagus:	n/a
4	chr9:98699195-98699245	GM12878	blood:	n/a
5	chr9:98699195-98699245	NT2-D1	testis:	n/a
6	chr9:98699195-98699245	AG09309	skin:	n/a
7	chr9:98699195-98699245	H1-hESC	embryonic stem cell:	embryo
8	chr9:98699195-98699245	MCF10A-Er-Src	breast:	n/a
9	chr9:98699195-98699245	HEK293	kidney:	embryo
10	chr9:98699195-98699245	SKMC	muscle:	n/a
11	chr9:98699195-98699245	Hepatocyte	liver:	n/a
12	chr9:98699195-98699245	HMEC	breast:	n/a
13	chr9:98699195-98699245	HUVEC	blood vessel:	n/a
14	chr9:98699195-98699245	RPTEC	kidney:	n/a
15	chr9:98699195-98699245	MCF-7	breast:	n/a
16	chr9:98699195-98699245	Caco-2	colon:	n/a
17	chr9:98699195-98699245	SK-N-MC	brain:	n/a
18	chr9:98699195-98699245	HRPEpiC	eye:	n/a
19	chr9:98699195-98699245	HL-60	blood:	n/a
20	chr9:98699195-98699245	Jurkat	blood:	n/a
21	chr9:98699195-98699245	NHDF-neo	bronchial:	n/a
22	chr9:98699195-98699245	GM19239	blood:	n/a
23	chr9:98699195-98699245	PFSK-1	brain:	n/a
24	chr9:98699195-98699245	ECC-1	luminal epithelium:	n/a
25	chr9:98699195-98699245	PANC-1	pancreas:	n/a
26	chr9:98699195-98699245	SK-N-SH_RA	brain:	n/a
27	chr9:98699195-98699245	HCT-116	colon:	n/a
28	chr9:98699195-98699245	AG10803	skin:	n/a
29	chr9:98699195-98699245	GM12892	blood:	n/a
30	chr9:98699195-98699245	AG04449	skin:	fetal
31	chr9:98699195-98699245	SK-N-SH	brain:	n/a
32	chr9:98699195-98699245	CMK	blood:	n/a
33	chr9:98699195-98699245	NB4	blood:	n/a
34	chr9:98699195-98699245	ovcar-3	ovarian:	n/a
35	chr9:98699195-98699245	AoSMC	blood vessel:	n/a
36	chr9:98699195-98699245	HRCEpiC	kidney:	n/a
37	chr9:98699195-98699245	BE2_C	brain:	n/a
38	chr9:98699195-98699245	BJ	skin:	n/a
39	chr9:98699195-98699245	HIPEpiC	eye:	n/a
40	chr9:98699195-98699245	U87	brain:	n/a
41	chr9:98699195-98699245	SAEC	small airway:	n/a
42	chr9:98699195-98699245	HCF	heart:	n/a
43	chr9:98699195-98699245	HRE	kidney:	n/a
44	chr9:98699195-98699245	A549	lung:	n/a
45	chr9:98699195-98699245	PrEC	prostate:	n/a
46	chr9:98699195-98699245	HNPCEpiC	eye:	n/a
47	chr9:98699195-98699245	LNCaP	prostate:	n/a
48	chr9:98699195-98699245	NH-A	brain:	n/a
49	chr9:98699195-98699245	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:98699195-98699245	GM12891	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:98637509..98639412-chr9:98700188..98702295,2	MCF-7	breast:
2	chr16:55447777..55449277-chr9:98661264..98663174,2	MCF-7	breast:
3	chr9:98659421..98661282-chr9:98663215..98665400,2	MCF-7	breast:
4	chr9:98637758..98639329-chr9:98663637..98666308,2	K562	blood:
5	chr9:98657722..98660032-chr9:98669881..98671421,2	K562	blood:
6	chr9:98636561..98638222-chr9:98688892..98691285,2	K562	blood:
7	chr9:98692437..98694773-chr9:98695538..98697868,2	K562	blood:
8	chr9:98644374..98646998-chr9:98660119..98662324,2	MCF-7	breast:
9	chr9:98666802..98669304-chr9:98670282..98671938,2	K562	blood:
10	chr9:98692437..98694595-chr9:98695109..98697038,2	K562	blood:
11	chr9:98684128..98686659-chr9:98692175..98694024,2	K562	blood:
12	chr9:98692437..98694773-chr9:98695538..98697868,2	K562	blood:
13	chr9:98637084..98640693-chr9:98667295..98670393,4	K562	blood:
14	chr9:98636376..98639087-chr9:98667887..98670748,3	MCF-7	breast:
15	chr9:98654370..98657235-chr9:98658443..98661205,2	K562	blood:
16	chr9:98681098..98682813-chr9:98750330..98752671,2	K562	blood:
17	chr9:98686171..98688902-chr9:98698379..98700318,2	K562	blood:
18	chr9:98686572..98689249-chr9:98695203..98698057,2	MCF-7	breast:
19	chr9:98663269..98664821-chr9:98672386..98673903,2	K562	blood:
20	chr9:98682356..98686313-chr9:98688317..98691201,4	K562	blood:
21	chr9:98636642..98638699-chr9:98681632..98683270,2	K562	blood:
22	chr9:98686171..98688902-chr9:98698379..98700318,2	K562	blood:
23	chr9:98665770..98668209-chr9:98683792..98686437,2	K562	blood:
24	chr9:98692437..98694595-chr9:98695109..98697038,2	K562	blood:
25	chr9:98636642..98639611-chr9:98680367..98683270,2	K562	blood:
26	chr9:98636799..98639182-chr9:98659870..98662837,3	MCF-7	breast:
27	chr9:98666764..98669288-chr9:98669709..98671840,2	MCF-7	breast:
28	chr9:98636162..98639165-chr9:98683503..98686735,3	MCF-7	breast:
29	chr9:98637191..98639517-chr9:98666345..98668961,2	MCF-7	breast:
30	chr9:98557263..98558873-chr9:98672395..98674331,2	K562	blood:
31	chr9:98636151..98639083-chr9:98689561..98691084,2	MCF-7	breast:
32	chr9:98663269..98664821-chr9:98672386..98673903,2	K562	blood:
33	chr9:98657048..98659286-chr9:98663988..98665978,2	MCF-7	breast:
34	chr9:98637758..98639724-chr9:98662859..98665137,2	K562	blood:
35	chr9:98659421..98661282-chr9:98663215..98665400,2	MCF-7	breast:
36	chr9:98670435..98672345-chr9:98679876..98682025,2	MCF-7	breast:
37	chr9:98636168..98638789-chr9:98670448..98673046,3	MCF-7	breast:
38	chr9:98631788..98634188-chr9:98659492..98662197,2	K562	blood:
39	chr9:98637024..98638791-chr9:98682127..98684213,2	MCF-7	breast:
40	chr9:98665770..98668209-chr9:98683792..98686437,2	K562	blood:
41	chr9:98636306..98639029-chr9:98675119..98677767,3	MCF-7	breast:
42	chr9:98638841..98641088-chr9:98696754..98699064,2	K562	blood:
43	chr9:98635837..98638885-chr9:98657790..98660488,3	K562	blood:
44	chr9:98686572..98689249-chr9:98695203..98698057,2	MCF-7	breast:
45	chr9:98637678..98640109-chr9:98685155..98688009,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000237631	TF binding region
ERCC6L2	TF binding region
RNA5SP289	TF binding region
ENSG00000237631	CpG island
ERCC6L2	CpG island
RNA5SP289	CpG island
ENSG00000199202	chromatin interactions
ENSG00000182150	chromatin interactions
ENSG00000175611	chromatin interactions
ENSG00000237631	chromatin interactions

Extended variants
information (count: 1435 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1435 , 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	rs77062260	chr9:98660593-98660594	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs561641337	chr9:98660655-98660656	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs370600907	chr9:98660667-98660668	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531945235	chr9:98660754-98660755	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567636177	chr9:98660755-98660756	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550427111	chr9:98660804-98660805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs536933667	chr9:98660829-98660830	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189560381	chr9:98660834-98660835	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545211304	chr9:98660846-98660847	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555326666	chr9:98660873-98660874	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs532712808	chr9:98660883-98660884	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547518652	chr9:98660891-98660892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs531771152	chr9:98661012-98661013	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565754380	chr9:98661041-98661042	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs146871304	chr9:98661052-98661053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573598622	chr9:98661063-98661064	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75514263	chr9:98661156-98661157	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
18	rs140734636	chr9:98661213-98661214	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs115749178	chr9:98661266-98661267	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs370381312	chr9:98661330-98661331	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558807711	chr9:98661348-98661349	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576634213	chr9:98661349-98661350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs71499917	chr9:98661376-98661377	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534461672	chr9:98661381-98661382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553867968	chr9:98661387-98661388	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564963952	chr9:98661393-98661394	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575178486	chr9:98661417-98661418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs150446001	chr9:98661458-98661459	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138285544	chr9:98661484-98661485	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs116592960	chr9:98661496-98661497	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs559200537	chr9:98661506-98661507	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs115111113	chr9:98661627-98661628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532775419	chr9:98661669-98661670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571911039	chr9:98661674-98661675	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs149153118	chr9:98661685-98661686	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs150595611	chr9:98661872-98661873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559973010	chr9:98661882-98661883	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs2063783	chr9:98661884-98661885	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12351955	chr9:98661886-98661887	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs113318013	chr9:98661888-98661889	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537012910	chr9:98661890-98661891	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147472512	chr9:98661912-98661913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs56991965	chr9:98661913-98661914	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143578081	chr9:98661914-98661915	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2770838	chr9:98661915-98661916	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
46	rs10987772	chr9:98661916-98661917	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570387725	chr9:98662098-98662099	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577666027	chr9:98662126-98662127	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs77209725	chr9:98662146-98662147	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
50	rs142998148	chr9:98662173-98662174	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	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
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Neurodevelopmental disorder	22521361	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1203 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98638800-98702200	Weak transcription	Pancreas	Pancrea
2	chr9:98639400-98677800	Weak transcription	Placenta	Placenta
3	chr9:98639400-98678000	Weak transcription	Ovary	ovary
4	chr9:98639600-98678000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr9:98639800-98664200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr9:98639800-98677800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:98640000-98661600	Weak transcription	Right Atrium	heart
8	chr9:98640000-98663600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:98640000-98678200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr9:98640000-98680600	Weak transcription	Colonic Mucosa	Colon
11	chr9:98640000-98685600	Weak transcription	Right Ventricle	heart
12	chr9:98640000-98718600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr9:98640200-98678200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr9:98640400-98664800	Weak transcription	Brain Substantia Nigra	brain
15	chr9:98640400-98677800	Weak transcription	Psoas Muscle	Psoas
16	chr9:98640600-98678000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr9:98642200-98663600	Weak transcription	Hela-S3	cervix
18	chr9:98642600-98678000	Weak transcription	Colon Smooth Muscle	Colon
19	chr9:98642600-98680600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr9:98642800-98668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr9:98642800-98681800	Weak transcription	Fetal Kidney	kidney
22	chr9:98644200-98670600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr9:98644400-98678400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr9:98644400-98685600	Weak transcription	Gastric	stomach
25	chr9:98644600-98670200	Weak transcription	Left Ventricle	heart
26	chr9:98644600-98678000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr9:98644600-98690800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:98644800-98677400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr9:98645000-98662400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:98645600-98684200	Weak transcription	Brain Hippocampus Middle	brain
31	chr9:98645800-98670400	Weak transcription	Brain Germinal Matrix	brain
32	chr9:98645800-98672600	Weak transcription	HUVEC	blood vessel
33	chr9:98645800-98678400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr9:98645800-98702200	Weak transcription	Aorta	Aorta
35	chr9:98646000-98680200	Weak transcription	K562	blood
36	chr9:98646400-98663800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:98646600-98667800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr9:98646600-98670000	Weak transcription	Adipose Nuclei	Adipose
39	chr9:98646600-98681800	Weak transcription	HSMMtube	muscle
40	chr9:98646800-98672400	Weak transcription	NHDF-Ad	bronchial
41	chr9:98647400-98672800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr9:98647600-98661600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:98647600-98678000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr9:98647800-98677400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr9:98648200-98660800	Weak transcription	HepG2	liver
46	chr9:98648200-98662000	Weak transcription	Duodenum Mucosa	Duodenum
47	chr9:98648200-98666200	Weak transcription	HSMM	muscle
48	chr9:98648200-98677800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr9:98648200-98678600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr9:98649000-98667800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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