Variant report

Variant	nsv1037787
Chromosome Location	chr9:71635338-71807648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4372)
CpG islands
(count:2320)
Chromatin interactive
region (count:184)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4372 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71788981-71788988	K562	blood:	n/a	n/a
2	ARID3A	chr9:71719221-71720293	HepG2	liver:	n/a	chr9:71719768-71719784 chr9:71719315-71719331
3	ARID3A	chr9:71787032-71787270	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:71800451-71800521	K562	blood:	n/a	n/a
5	ARID3A	chr9:71795418-71795995	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:71642563-71642873	K562	blood:	n/a	n/a
8	ARID3A	chr9:71650526-71650743	K562	blood:	n/a	n/a
9	ARID3A	chr9:71701730-71702036	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:71650444-71651128	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:71801110-71801635	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:71783969-71784100	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:71795383-71796025	K562	blood:	n/a	n/a
14	ARID3A	chr9:71785862-71786328	K562	blood:	n/a	n/a
15	ARID3A	chr9:71802085-71802622	K562	blood:	n/a	n/a
16	ARID3A	chr9:71785228-71785657	K562	blood:	n/a	n/a
17	ARID3A	chr9:71793431-71794296	HepG2	liver:	n/a	n/a
18	ARID3A	chr9:71805069-71805695	HepG2	liver:	n/a	chr9:71805429-71805445 chr9:71805430-71805446
19	ARID3A	chr9:71801237-71801527	K562	blood:	n/a	n/a
20	ARID3A	chr9:71803674-71804222	K562	blood:	n/a	n/a
21	ARID3A	chr9:71768528-71769284	HepG2	liver:	n/a	n/a
22	ARID3A	chr9:71746529-71747015	HepG2	liver:	n/a	n/a
23	ARID3A	chr9:71635426-71635919	K562	blood:	n/a	n/a
24	ARID3A	chr9:71651502-71651839	K562	blood:	n/a	n/a
25	ATF1	chr9:71642591-71642873	K562	blood:	n/a	n/a
26	ATF1	chr9:71795567-71795986	K562	blood:	n/a	n/a
27	ATF1	chr9:71802159-71802633	K562	blood:	n/a	n/a
28	ATF1	chr9:71785927-71786382	K562	blood:	n/a	n/a
29	ATF1	chr9:71635543-71635967	K562	blood:	n/a	n/a
30	ATF1	chr9:71803941-71804270	K562	blood:	n/a	n/a
31	ATF2	chr9:71789602-71790821	GM12878	blood:	n/a	n/a
32	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr9:71783777-71784242	GM12878	blood:	n/a	n/a
34	ATF2	chr9:71783919-71784211	GM12878	blood:	n/a	n/a
35	ATF2	chr9:71735153-71736138	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr9:71650325-71650801	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr9:71735106-71735934	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr9:71737566-71738148	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr9:71650422-71650822	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr9:71789577-71790776	GM12878	blood:	n/a	n/a
41	ATF3	chr9:71795739-71795903	K562	blood:	n/a	n/a
42	ATF3	chr9:71795571-71796013	K562	blood:	n/a	n/a
43	ATF3	chr9:71650292-71651027	A549	lung:	n/a	n/a
44	BACH1	chr9:71788674-71789685	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr9:71650535-71650996	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr9:71785970-71786100	K562	blood:	n/a	n/a
47	BACH1	chr9:71735251-71735859	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr9:71737585-71738101	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr9:71789894-71790492	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr9:71783680-71784242	GM12878	blood:	n/a	n/a

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71652532-71652582	HEEpiC	esophagus:	n/a
2	chr9:71661107-71661157	AG09319	gingival:	n/a
3	chr9:71652532-71652582	HEEpiC	esophagus:	n/a
4	chr9:71661107-71661157	AG09319	gingival:	n/a
5	chr9:71787160-71787210	HCF	heart:	n/a
6	chr9:71792936-71792986	Caco-2	colon:	n/a
7	chr9:71713728-71713778	AG09319	gingival:	n/a
8	chr9:71713728-71713778	ovcar-3	ovarian:	n/a
9	chr9:71736999-71737049	HRPEpiC	eye:	n/a
10	chr9:71650719-71650769	GM06990	blood:	n/a
11	chr9:71650237-71650287	Caco-2	colon:	n/a
12	chr9:71654823-71654873	K562	blood:	n/a
13	chr9:71683936-71683986	GM06990	blood:	n/a
14	chr9:71736409-71736459	LNCaP	prostate:	n/a
15	chr9:71736999-71737049	H1-hESC	embryonic stem cell:	embryo
16	chr9:71650331-71650381	ProgFib	skin:	n/a
17	chr9:71691305-71691355	HUVEC	blood vessel:	n/a
18	chr9:71788759-71788809	NT2-D1	testis:	n/a
19	chr9:71713728-71713778	AG09309	skin:	n/a
20	chr9:71669714-71669764	Hepatocyte	liver:	n/a
21	chr9:71651175-71651225	PANC-1	pancreas:	n/a
22	chr9:71787160-71787210	U87	brain:	n/a
23	chr9:71713728-71713778	NB4	blood:	n/a
24	chr9:71651175-71651225	SAEC	small airway:	n/a
25	chr9:71736409-71736459	AG04449	skin:	fetal
26	chr9:71736854-71736904	BE2_C	brain:	n/a
27	chr9:71785587-71785637	GM19239	blood:	n/a
28	chr9:71735648-71735698	HPAEpiC	pulmonary alveolar:	n/a
29	chr9:71654823-71654873	GM12891	blood:	n/a
30	chr9:71691305-71691355	HCT-116	colon:	n/a
31	chr9:71652532-71652582	HepG2	liver:	n/a
32	chr9:71802071-71802121	LNCaP	prostate:	n/a
33	chr9:71736854-71736904	SAEC	small airway:	n/a
34	chr9:71683936-71683986	HRCEpiC	kidney:	n/a
35	chr9:71732345-71732395	RPTEC	kidney:	n/a
36	chr9:71785587-71785637	NT2-D1	testis:	n/a
37	chr9:71682105-71682155	NB4	blood:	n/a
38	chr9:71685390-71685440	GM19239	blood:	n/a
39	chr9:71787778-71787828	NHDF-neo	bronchial:	n/a
40	chr9:71732345-71732395	ovcar-3	ovarian:	n/a
41	chr9:71652532-71652582	HCT-116	colon:	n/a
42	chr9:71795999-71796049	PrEC	prostate:	n/a
43	chr9:71654823-71654873	Hepatocyte	liver:	n/a
44	chr9:71682302-71682352	HEEpiC	esophagus:	n/a
45	chr9:71789653-71789703	MCF-7	breast:	n/a
46	chr9:71651331-71651381	AG04449	skin:	fetal
47	chr9:71682105-71682155	HIPEpiC	eye:	n/a
48	chr9:71713728-71713778	NHBE	bronchial:	n/a
49	chr9:71682105-71682155	PrEC	prostate:	n/a
50	chr9:71787160-71787210	NB4	blood:	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
2	chr9:71704381..71705131-chr9:71714234..71715231,2	MCF-7	breast:
3	chr9:71726688..71731938-chr9:71734130..71739301,8	MCF-7	breast:
4	chr9:71732215..71735155-chr9:71735593..71737924,2	MCF-7	breast:
5	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
6	chr9:71671960..71674521-chr9:71677007..71679466,3	K562	blood:
7	chr9:71655862..71658846-chr9:71661896..71664645,2	MCF-7	breast:
8	chr9:71720466..71722349-chr9:71729146..71730891,2	MCF-7	breast:
9	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
10	chr9:71745166..71747792-chr9:71751582..71754371,2	K562	blood:
11	chr9:71800754..71805797-chr9:71805912..71810495,5	K562	blood:
12	chr9:71779588..71781228-chr9:71781515..71783848,2	MCF-7	breast:
13	chr9:71392487..71395427-chr9:71649569..71651600,2	K562	blood:
14	chr6:41040678..41041408-chr9:71735768..71736686,2	Hela-S3	cervix:
15	chr9:71779511..71782336-chr9:71782342..71784212,2	MCF-7	breast:
16	chr1:146555490..146556430-chr9:71736325..71736974,2	Hela-S3	cervix:
17	chr9:71735162..71738367-chr9:71767115..71770867,6	MCF-7	breast:
18	chr9:71700139..71702820-chr9:71819428..71821529,2	MCF-7	breast:
19	chr9:71686014..71689293-chr9:71805643..71807349,3	K562	blood:
20	chr9:71704008..71706268-chr9:71714594..71717470,2	MCF-7	breast:
21	chr9:71649461..71652506-chr9:71658685..71662535,4	MCF-7	breast:
22	chr9:71779588..71781228-chr9:71781515..71783848,2	MCF-7	breast:
23	chr9:71794571..71798394-chr9:71798897..71802534,4	K562	blood:
24	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
25	chr9:71790152..71792261-chr9:71797735..71799818,2	MCF-7	breast:
26	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
27	chr9:71793727..71795446-chr9:71807376..71809123,2	MCF-7	breast:
28	chr9:71806704..71808402-chr9:71829211..71831372,2	K562	blood:
29	chr9:71666774..71669833-chr9:71734752..71737934,3	MCF-7	breast:
30	chr9:71671307..71672957-chr9:71675793..71678189,2	MCF-7	breast:
31	chr9:71735247..71737414-chr9:71784064..71786040,3	MCF-7	breast:
32	chr9:71790152..71792261-chr9:71797735..71799818,2	MCF-7	breast:
33	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
34	chr9:71745818..71747384-chr9:71762840..71764725,2	K562	blood:
35	chr9:71668686..71669450-chr9:71838137..71838734,2	MCF-7	breast:
36	chr9:71699941..71701534-chr9:71703830..71705802,2	MCF-7	breast:
37	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
38	chr9:71733940..71739343-chr9:71741877..71748941,25	MCF-7	breast:
39	chr9:71793542..71796888-chr9:71798932..71802737,4	MCF-7	breast:
40	chr9:71735548..71738179-chr9:71802464..71805527,4	MCF-7	breast:
41	chr9:71761121..71762822-chr9:71762920..71764542,2	K562	blood:
42	chr9:71758408..71761844-chr9:71769245..71771910,3	MCF-7	breast:
43	chr9:71650420..71652084-chr9:71654261..71655791,2	MCF-7	breast:
44	chr9:71651712..71654573-chr9:71656499..71659593,3	K562	blood:
45	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
46	chr9:71199108..71199619-chr9:71642191..71643182,2	K562	blood:
47	chr9:71751405..71753557-chr9:71754610..71757893,3	MCF-7	breast:
48	chr9:71671307..71672957-chr9:71675793..71678189,2	MCF-7	breast:
49	chr9:71668853..71671288-chr9:71790657..71793201,2	MCF-7	breast:
50	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TJP2-1	chr9:71736209-71736281	ENSG00000227410.1
2	lnc-TJP2-1	chr9:71736400-71737148	ENSG00000227410.1
3	lnc-PRKACG-2	chr9:71780235-71782388	ENSG00000250944
4	lnc-PRKACG-2	chr9:71785572-71785971	ENSG00000250944

No data

Variant related genes	Relation type
TJP2	TF binding region
FXN	TF binding region
ENSG00000270236	TF binding region
TJP2	CpG island
FXN	CpG island
ENSG00000270236	CpG island
ENSG00000136143	chromatin interactions
ENSG00000272434	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000163812	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000126216	chromatin interactions
ENSG00000270236	chromatin interactions
ENSG00000165060	chromatin interactions
ENSG00000187866	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000075914	chromatin interactions
ENSG00000165059	chromatin interactions
ENSG00000001167	chromatin interactions
APITD1	miRNA target sites
FLOT1	miRNA target sites

Extended variants
information (count: 6588 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6588 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539250011	chr9:71635354-71635355	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs558849822	chr9:71635443-71635444	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565807854	chr9:71635445-71635446	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536236192	chr9:71635592-71635593	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs554587296	chr9:71635612-71635613	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs191673091	chr9:71635620-71635621	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376195689	chr9:71635638-71635639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543652936	chr9:71635662-71635663	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141352739	chr9:71635774-71635775	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576596651	chr9:71635775-71635776	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540850749	chr9:71635824-71635825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560193275	chr9:71635843-71635844	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs367899857	chr9:71635880-71635881	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547720140	chr9:71635948-71635949	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150365986	chr9:71635994-71635995	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs561381643	chr9:71636007-71636008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531616859	chr9:71636052-71636053	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs138083099	chr9:71636065-71636066	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs565460885	chr9:71636066-71636067	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532731133	chr9:71636082-71636083	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548042173	chr9:71636087-71636088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143678184	chr9:71636094-71636095	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535482342	chr9:71636115-71636116	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs547981966	chr9:71636118-71636119	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569594981	chr9:71636157-71636158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs35095641	chr9:71636220-71636221	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570619035	chr9:71636222-71636223	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs536666246	chr9:71636234-71636235	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371398990	chr9:71636239-71636240	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576757657	chr9:71636288-71636289	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566359258	chr9:71636339-71636340	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371674720	chr9:71636386-71636387	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572205878	chr9:71636424-71636425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs55885080	chr9:71636431-71636432	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543062958	chr9:71636475-71636476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147187774	chr9:71636480-71636481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183442530	chr9:71636499-71636500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188152732	chr9:71636504-71636505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs548692932	chr9:71636541-71636542	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs78487669	chr9:71636549-71636550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547128157	chr9:71636552-71636553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373352290	chr9:71636571-71636572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191724255	chr9:71636572-71636573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532893415	chr9:71636588-71636589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140018587	chr9:71636622-71636623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182775517	chr9:71636634-71636635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1590944	chr9:71636650-71636651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186779934	chr9:71636670-71636671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569675380	chr9:71636681-71636682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537031411	chr9:71636694-71636695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Melanoma	22183965	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:5483 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71598800-71644600	Weak transcription	Right Atrium	heart
2	chr9:71631800-71638400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr9:71631800-71638400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr9:71631800-71638400	Weak transcription	Ovary	ovary
5	chr9:71632000-71636400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr9:71633200-71635800	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr9:71633200-71637000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr9:71633400-71636000	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr9:71633400-71639800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr9:71633600-71635800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr9:71633600-71636000	Enhancers	Primary hematopoietic stem cells	blood
12	chr9:71633600-71636000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr9:71633600-71636000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr9:71633600-71636000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr9:71633800-71635800	Enhancers	Primary T cells from cord blood	blood
16	chr9:71633800-71635800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr9:71633800-71636000	Enhancers	Primary T cells fromperipheralblood	blood
18	chr9:71633800-71636000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr9:71633800-71636600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr9:71634200-71637400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr9:71634600-71635400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:71634600-71635600	Enhancers	Dnd41	blood
23	chr9:71634600-71635800	Enhancers	Fetal Heart	heart
24	chr9:71634600-71635800	Flanking Active TSS	K562	blood
25	chr9:71635000-71635400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr9:71635000-71635600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:71635000-71635800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr9:71635000-71642400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr9:71635200-71635400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr9:71635200-71635600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr9:71635200-71638000	Weak transcription	Fetal Intestine Small	intestine
32	chr9:71635400-71635800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr9:71635400-71639800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:71635600-71638600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr9:71635600-71639000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:71635800-71636200	Enhancers	K562	blood
37	chr9:71635800-71639000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr9:71635800-71642200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr9:71635800-71642200	Weak transcription	Fetal Heart	heart
40	chr9:71635800-71642400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:71636000-71636600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr9:71636000-71636600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr9:71636000-71641600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr9:71636200-71636400	Flanking Active TSS	K562	blood
45	chr9:71636400-71636800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr9:71636400-71640000	Enhancers	K562	blood
47	chr9:71636600-71636800	Enhancers	Primary hematopoietic stem cells	blood
48	chr9:71636600-71636800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr9:71636600-71642000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr9:71636800-71638400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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