Variant report

Variant	nsv893591
Chromosome Location	chr9:96849137-96883271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:122)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:96862904-96863149	K562	blood:	n/a	n/a
2	ARID3A	chr9:96873101-96873841	K562	blood:	n/a	n/a
3	ARID3A	chr9:96875134-96875677	K562	blood:	n/a	n/a
4	ATF1	chr9:96875013-96875701	K562	blood:	n/a	n/a
5	ATF1	chr9:96872973-96873553	K562	blood:	n/a	n/a
6	ATF3	chr9:96873201-96873498	K562	blood:	n/a	n/a
7	CBX3	chr9:96875090-96875847	K562	blood:	n/a	n/a
8	CBX3	chr9:96879616-96879882	K562	blood:	n/a	n/a
9	CCNT2	chr9:96859774-96860136	K562	blood:	n/a	n/a
10	CCNT2	chr9:96873159-96873548	K562	blood:	n/a	n/a
11	CEBPB	chr9:96875227-96875657	K562	blood:	n/a	n/a
12	CEBPB	chr9:96882400-96882776	K562	blood:	n/a	chr9:96882582-96882593
13	CEBPB	chr9:96882574-96882590	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:96882457-96882789	K562	blood:	n/a	chr9:96882582-96882593
15	CEBPB	chr9:96865368-96865451	HepG2	liver:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
16	CEBPB	chr9:96873097-96873603	K562	blood:	n/a	n/a
17	CEBPB	chr9:96865300-96865580	K562	blood:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
18	CEBPB	chr9:96882428-96882761	HepG2	liver:	n/a	chr9:96882582-96882593
19	CEBPB	chr9:96882474-96882755	IMR90	lung:	n/a	chr9:96882582-96882593
20	CEBPB	chr9:96882513-96882801	MCF-7	breast:	n/a	chr9:96882582-96882593
21	CEBPB	chr9:96873130-96873720	K562	blood:	n/a	n/a
22	CEBPB	chr9:96873172-96873508	K562	blood:	n/a	n/a
23	CEBPB	chr9:96859969-96860484	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:96865307-96865507	A549	lung:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
25	CEBPB	chr9:96882496-96882734	K562	blood:	n/a	chr9:96882582-96882593
26	CEBPB	chr9:96873059-96873855	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:96865262-96865552	IMR90	lung:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
28	CEBPB	chr9:96858936-96858963	K562	blood:	n/a	chr9:96858939-96858950 chr9:96858937-96858950 chr9:96858937-96858950 chr9:96858937-96858950
29	CEBPB	chr9:96882443-96882690	A549	lung:	n/a	chr9:96882582-96882593
30	CEBPD	chr9:96873123-96873594	K562	blood:	n/a	n/a
31	CEBPD	chr9:96873058-96873637	K562	blood:	n/a	n/a
32	CHD2	chr9:96850202-96850205	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr9:96870880-96871030	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr9:96856640-96856790	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:96873403-96873537	K562	blood:	n/a	n/a
36	CTCF	chr9:96873880-96874030	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr9:96856700-96856850	SAEC	small airway:	n/a	n/a
38	CTCF	chr9:96860020-96860170	GM12869	blood:	n/a	n/a
39	CTCF	chr9:96856640-96856790	HEK293	kidney:	n/a	n/a
40	CUX1	chr9:96873242-96873637	K562	blood:	n/a	n/a
41	CUX1	chr9:96861502-96861644	K562	blood:	n/a	n/a
42	E2F4	chr9:96860004-96860283	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr9:96859188-96859600	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr9:96849377-96849443	MCF10A-Er-Src	breast:	n/a	n/a
45	EP300	chr9:96848606-96849444	SK-N-SH	brain:	n/a	n/a
46	EP300	chr9:96875497-96875520	GM12878	blood:	n/a	n/a
47	EP300	chr9:96875229-96875717	K562	blood:	n/a	n/a
48	EP300	chr9:96859983-96860510	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr9:96848730-96849395	SK-N-SH	brain:	n/a	n/a
50	EP300	chr9:96848563-96849631	SK-N-SH	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96872879-96872929	IMR90	lung:	fetal
2	chr9:96872879-96872929	HepG2	liver:	n/a
3	chr9:96858147-96858197	SKMC	muscle:	n/a
4	chr9:96872879-96872929	AoSMC	blood vessel:	n/a
5	chr9:96858147-96858197	ProgFib	skin:	n/a
6	chr9:96872879-96872929	HRPEpiC	eye:	n/a
7	chr9:96858147-96858197	HIPEpiC	eye:	n/a
8	chr9:96858147-96858197	AG04450	lung:	fetal
9	chr9:96872879-96872929	HEK293	kidney:	embryo
10	chr9:96872879-96872929	ECC-1	luminal epithelium:	n/a
11	chr9:96872879-96872929	AG09309	skin:	n/a
12	chr9:96872879-96872929	HCPEpiC	choroid plexus:	n/a
13	chr9:96858147-96858197	NB4	blood:	n/a
14	chr9:96872879-96872929	HL-60	blood:	n/a
15	chr9:96858147-96858197	MCF-7	breast:	n/a
16	chr9:96872879-96872929	BJ	skin:	n/a
17	chr9:96872879-96872929	A549	lung:	n/a
18	chr9:96872879-96872929	Hepatocyte	liver:	n/a
19	chr9:96872879-96872929	Caco-2	colon:	n/a
20	chr9:96858147-96858197	IMR90	lung:	fetal
21	chr9:96872879-96872929	HMEC	breast:	n/a
22	chr9:96872879-96872929	LNCaP	prostate:	n/a
23	chr9:96858147-96858197	BE2_C	brain:	n/a
24	chr9:96858147-96858197	HUVEC	blood vessel:	n/a
25	chr9:96858147-96858197	H1-hESC	embryonic stem cell:	embryo
26	chr9:96858147-96858197	HCM	heart:	n/a
27	chr9:96872879-96872929	HEEpiC	esophagus:	n/a
28	chr9:96872879-96872929	GM12892	blood:	n/a
29	chr9:96858147-96858197	PrEC	prostate:	n/a
30	chr9:96872879-96872929	Hela-S3	cervix:	n/a
31	chr9:96872879-96872929	HNPCEpiC	eye:	n/a
32	chr9:96872879-96872929	SK-N-SH_RA	brain:	n/a
33	chr9:96858147-96858197	RPTEC	kidney:	n/a
34	chr9:96872879-96872929	AG10803	skin:	n/a
35	chr9:96872879-96872929	HRE	kidney:	n/a
36	chr9:96858147-96858197	Hepatocyte	liver:	n/a
37	chr9:96858147-96858197	AG09319	gingival:	n/a
38	chr9:96858147-96858197	MCF10A-Er-Src	breast:	n/a
39	chr9:96872879-96872929	HRCEpiC	kidney:	n/a
40	chr9:96858147-96858197	Jurkat	blood:	n/a
41	chr9:96858147-96858197	K562	blood:	n/a
42	chr9:96858147-96858197	HepG2	liver:	n/a
43	chr9:96858147-96858197	AG09309	skin:	n/a
44	chr9:96858147-96858197	CMK	blood:	n/a
45	chr9:96858147-96858197	ovcar-3	ovarian:	n/a
46	chr9:96872879-96872929	HCT-116	colon:	n/a
47	chr9:96872879-96872929	MCF-7	breast:	n/a
48	chr9:96858147-96858197	NT2-D1	testis:	n/a
49	chr9:96858147-96858197	SK-N-SH	brain:	n/a
50	chr9:96872879-96872929	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:96847188..96849533-chr9:96856467..96859477,3	K562	blood:
2	chr9:96793114..96795953-chr9:96849084..96851331,2	K562	blood:
3	chr9:96871682..96874612-chr9:96882240..96883990,2	MCF-7	breast:
4	chr9:96866936..96868703-chr9:96870555..96872203,2	K562	blood:
5	chr9:96856390..96858828-chr9:96926161..96928705,2	K562	blood:
6	chr9:96871070..96874023-chr9:96892477..96895183,2	MCF-7	breast:
7	chr9:96864692..96867836-chr9:96868310..96870488,3	K562	blood:
8	chr9:96864659..96867120-chr9:96928060..96930580,2	K562	blood:
9	chr9:96858833..96861735-chr9:96944084..96946628,2	K562	blood:
10	chr9:96873250..96875198-chr9:96927135..96929620,4	K562	blood:
11	chr9:96847188..96849533-chr9:96856467..96859477,3	K562	blood:
12	chr9:96864692..96867836-chr9:96868310..96870488,3	K562	blood:
13	chr9:96845151..96850974-chr9:96927067..96931575,8	K562	blood:
14	chr9:96860361..96862564-chr9:96873614..96875631,2	K562	blood:
15	chr9:96848883..96850819-chr9:96911987..96913565,2	MCF-7	breast:
16	chr9:96859686..96862226-chr9:96927604..96929691,2	K562	blood:
17	chr9:96861323..96864485-chr9:96867388..96870622,3	K562	blood:
18	chr9:96856357..96859423-chr9:96862063..96865399,3	MCF-7	breast:
19	chr9:96825007..96827841-chr9:96858083..96859846,2	K562	blood:
20	chr9:96863435..96865449-chr9:96927688..96930142,2	MCF-7	breast:
21	chr9:96846694..96848203-chr9:96862701..96864601,2	MCF-7	breast:
22	chr9:96857107..96860210-chr9:96870662..96873792,3	MCF-7	breast:
23	chr9:96847639..96850039-chr9:96863471..96865147,2	MCF-7	breast:
24	chr9:96860355..96862707-chr9:96868776..96872890,3	K562	blood:
25	chr9:96872510..96875198-chr9:96927204..96929620,4	K562	blood:
26	chr9:96855903..96857740-chr9:96900937..96903523,2	MCF-7	breast:
27	chr9:96847639..96850039-chr9:96863471..96865147,2	MCF-7	breast:
28	chr9:96873193..96875324-chr9:96934781..96937611,2	K562	blood:
29	chr9:96866436..96868575-chr9:96873729..96876347,3	K562	blood:
30	chr9:96791853..96794356-chr9:96860367..96862558,2	MCF-7	breast:
31	chr9:96845151..96851769-chr9:96927067..96931565,10	K562	blood:
32	chr9:96848027..96849533-chr9:96856014..96858976,2	K562	blood:
33	chr9:96866436..96868575-chr9:96873729..96876347,3	K562	blood:
34	chr9:96849522..96851731-chr9:96920134..96921738,2	MCF-7	breast:
35	chr9:96861428..96863422-chr9:96927160..96928732,2	MCF-7	breast:
36	chr9:96866936..96868703-chr9:96870555..96872203,2	K562	blood:
37	chr9:96855901..96860991-chr9:96926600..96930762,9	MCF-7	breast:
38	chr9:96857107..96860210-chr9:96870662..96873792,3	MCF-7	breast:
39	chr9:96871682..96874612-chr9:96882240..96883990,2	MCF-7	breast:
40	chr9:96848027..96849533-chr9:96856014..96858976,2	K562	blood:
41	chr9:96856270..96858806-chr9:96864043..96866239,3	MCF-7	breast:
42	chr9:96791026..96792800-chr9:96856915..96858416,2	MCF-7	breast:
43	chr9:96873433..96875351-chr9:96903210..96905278,2	MCF-7	breast:
44	chr9:96856270..96858806-chr9:96864043..96866239,3	MCF-7	breast:
45	chr9:96858917..96860519-chr9:133389418..133391095,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTPDC1	hsa-miR-21-5p	chr9:96870389-96870410
2	PTPDC1	hsa-miR-340-5p	chr9:96871285-96871306

Variant related genes	Relation type
PTPDC1	TF binding region
PTPDC1	CpG island
ENSG00000158079	chromatin interactions
ENSG00000269946	chromatin interactions

Extended variants
information (count: 1117 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10739968	chr9:96849137-96849138	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537922955	chr9:96849179-96849180	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs73653406	chr9:96849281-96849282	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs577682646	chr9:96849289-96849290	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545715949	chr9:96849387-96849388	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554462880	chr9:96849391-96849392	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577304508	chr9:96849399-96849400	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373727571	chr9:96849441-96849442	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185275031	chr9:96849486-96849487	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572698625	chr9:96849572-96849573	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542883636	chr9:96849605-96849606	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544687011	chr9:96849632-96849633	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs71496467	chr9:96849656-96849657	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs367801965	chr9:96849680-96849681	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150356787	chr9:96849708-96849709	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543485083	chr9:96849747-96849748	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564940701	chr9:96849760-96849761	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188594344	chr9:96849826-96849827	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547377250	chr9:96849861-96849862	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566700029	chr9:96849884-96849885	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527560113	chr9:96849889-96849890	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374692468	chr9:96849908-96849909	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112431737	chr9:96849927-96849928	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548939229	chr9:96850003-96850004	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577758008	chr9:96850022-96850023	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371926853	chr9:96850028-96850029	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs567418185	chr9:96850030-96850031	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562987111	chr9:96850033-96850034	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530267741	chr9:96850035-96850036	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs80063943	chr9:96850040-96850041	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs537959729	chr9:96850073-96850074	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144991491	chr9:96850091-96850092	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375938955	chr9:96850192-96850193	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200036336	chr9:96850196-96850197	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372238421	chr9:96850216-96850217	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375301116	chr9:96850217-96850218	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369816434	chr9:96850218-96850219	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113036431	chr9:96850233-96850234	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538675297	chr9:96850244-96850245	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558917157	chr9:96850295-96850296	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370959581	chr9:96850306-96850307	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200790224	chr9:96850374-96850375	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572687251	chr9:96850380-96850381	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs373766809	chr9:96850387-96850388	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200410457	chr9:96850391-96850392	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554888301	chr9:96850433-96850434	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141059694	chr9:96850460-96850461	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369568736	chr9:96850469-96850470	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs372776249	chr9:96850488-96850489	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs377427630	chr9:96850533-96850534	Genic enhancers Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 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
Mental retardation	21693067	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
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96822400-96859800	Weak transcription	Psoas Muscle	Psoas
2	chr9:96824200-96860000	Weak transcription	Aorta	Aorta
3	chr9:96824200-96869600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr9:96824400-96850000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:96828200-96859600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr9:96828200-96860800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr9:96828200-96862000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr9:96828200-96868200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr9:96829600-96872400	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr9:96832000-96859800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:96834400-96859800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr9:96835400-96861800	Weak transcription	Primary B cells from cord blood	blood
13	chr9:96837000-96857400	Weak transcription	HSMM	muscle
14	chr9:96837200-96857400	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr9:96837200-96858600	Weak transcription	Dnd41	blood
16	chr9:96837200-96859800	Weak transcription	Fetal Intestine Small	intestine
17	chr9:96837400-96850600	Weak transcription	Adipose Nuclei	Adipose
18	chr9:96837400-96860200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:96837600-96859200	Weak transcription	Primary T cells from cord blood	blood
20	chr9:96840200-96863600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:96840400-96850000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:96842600-96858200	Weak transcription	HSMMtube	muscle
23	chr9:96843600-96857000	Weak transcription	Colonic Mucosa	Colon
24	chr9:96845000-96853400	Weak transcription	GM12878-XiMat	blood
25	chr9:96845200-96857600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr9:96845600-96858200	Weak transcription	Right Ventricle	heart
27	chr9:96845600-96858400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr9:96845600-96885400	Weak transcription	Gastric	stomach
29	chr9:96846000-96870600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr9:96846200-96859800	Weak transcription	Ovary	ovary
31	chr9:96846800-96849400	Enhancers	NH-A	brain
32	chr9:96847000-96850400	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:96847000-96857000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:96847000-96859000	Weak transcription	Lung	lung
35	chr9:96847000-96859800	Weak transcription	Pancreas	Pancrea
36	chr9:96847000-96860200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr9:96847200-96859000	Weak transcription	Fetal Brain Male	brain
38	chr9:96847200-96859000	Weak transcription	Fetal Brain Female	brain
39	chr9:96847400-96849400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr9:96847400-96849400	Enhancers	Osteobl	bone
41	chr9:96847400-96850200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:96847600-96849600	Enhancers	NHEK	skin
43	chr9:96847600-96850000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:96847600-96856800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr9:96847600-96859200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr9:96847800-96849200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr9:96847800-96849400	Enhancers	Brain Angular Gyrus	brain
48	chr9:96847800-96849800	Enhancers	Brain Hippocampus Middle	brain
49	chr9:96847800-96850000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:96847800-96850200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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