Variant report

Variant	nsv831672
Chromosome Location	chr9:104300755-104480849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1451)
CpG islands
(count:367)
Chromatin interactive
region (count:41)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1451 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104333522-104333644	K562	blood:	n/a	n/a
2	ATF1	chr9:104397420-104397568	K562	blood:	n/a	n/a
3	ATF2	chr9:104364431-104364849	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr9:104344911-104345228	K562	blood:	n/a	n/a
5	ATF3	chr9:104390446-104390788	K562	blood:	n/a	n/a
6	BACH1	chr9:104388336-104388499	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:104365147-104365162	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr9:104329547-104329786	GM12878	blood:	n/a	n/a
9	BATF	chr9:104381008-104381267	GM12878	blood:	n/a	n/a
10	BATF	chr9:104348957-104349325	GM12878	blood:	n/a	chr9:104349134-104349144 chr9:104349138-104349148 chr9:104349137-104349148
11	BATF	chr9:104348916-104349355	GM12878	blood:	n/a	chr9:104349134-104349144 chr9:104349138-104349148 chr9:104349137-104349148
12	BATF	chr9:104311800-104312003	GM12878	blood:	n/a	n/a
13	BATF	chr9:104329511-104329874	GM12878	blood:	n/a	n/a
14	BATF	chr9:104380995-104381316	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:104349027-104349291	GM12878	blood:	n/a	chr9:104349137-104349146 chr9:104349136-104349145
16	BCL3	chr9:104385443-104385668	GM12878	blood:	n/a	chr9:104385479-104385488
17	BRCA1	chr9:104364506-104364922	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr9:104331744-104331753	HepG2	liver:	n/a	n/a
19	CCNT2	chr9:104369821-104369931	K562	blood:	n/a	n/a
20	CCNT2	chr9:104397371-104397571	K562	blood:	n/a	n/a
21	CEBPB	chr9:104455904-104456204	A549	lung:	n/a	chr9:104456091-104456102
22	CEBPB	chr9:104390525-104390845	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr9:104353213-104353473	K562	blood:	n/a	chr9:104353309-104353326
24	CEBPB	chr9:104389471-104389557	HepG2	liver:	n/a	chr9:104389544-104389555 chr9:104389498-104389509 chr9:104389496-104389507 chr9:104389516-104389529 chr9:104389496-104389509 chr9:104389516-104389527 chr9:104389544-104389555 chr9:104389498-104389509
25	CEBPB	chr9:104364515-104364796	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:104332069-104332437	K562	blood:	n/a	n/a
27	CEBPB	chr9:104445437-104445760	A549	lung:	n/a	n/a
28	CEBPB	chr9:104469329-104469476	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:104364439-104364786	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr9:104392202-104392446	HepG2	liver:	n/a	chr9:104392339-104392356
31	CEBPB	chr9:104353162-104353447	IMR90	lung:	n/a	chr9:104353309-104353326
32	CEBPB	chr9:104445412-104445727	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:104445414-104445684	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:104468726-104469015	IMR90	lung:	n/a	chr9:104468821-104468834 chr9:104468822-104468833 chr9:104468821-104468832
35	CEBPB	chr9:104468653-104469005	HepG2	liver:	n/a	chr9:104468821-104468834 chr9:104468822-104468833 chr9:104468821-104468832
36	CEBPB	chr9:104332087-104332442	K562	blood:	n/a	n/a
37	CEBPB	chr9:104445442-104445711	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr9:104389009-104389081	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:104364482-104364733	K562	blood:	n/a	n/a
40	CEBPB	chr9:104390520-104390820	K562	blood:	n/a	n/a
41	CEBPB	chr9:104376605-104376731	HepG2	liver:	n/a	chr9:104376697-104376708
42	CEBPB	chr9:104364521-104364681	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:104445388-104445676	MCF-7	breast:	n/a	n/a
44	CEBPB	chr9:104445480-104445653	K562	blood:	n/a	n/a
45	CEBPB	chr9:104390491-104390824	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:104468723-104469002	A549	lung:	n/a	chr9:104468821-104468834 chr9:104468822-104468833 chr9:104468821-104468832
47	CEBPB	chr9:104390485-104390888	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr9:104394668-104394781	HepG2	liver:	n/a	chr9:104394708-104394719
49	CEBPB	chr9:104390479-104390762	MCF-7	breast:	n/a	n/a
50	CEBPB	chr9:104390565-104390829	ECC-1	luminal epithelium:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104334427-104334477	SK-N-SH	brain:	n/a
2	chr9:104334427-104334477	SK-N-SH	brain:	n/a
3	chr9:104357177-104357227	T-47D	breast:	n/a
4	chr9:104356619-104356669	U87	brain:	n/a
5	chr9:104357967-104358017	SKMC	muscle:	n/a
6	chr9:104357967-104358017	HCF	heart:	n/a
7	chr9:104305608-104305658	SKMC	muscle:	n/a
8	chr9:104305608-104305658	ovcar-3	ovarian:	n/a
9	chr9:104334427-104334477	HEK293	kidney:	embryo
10	chr9:104357967-104358017	NHDF-neo	bronchial:	n/a
11	chr9:104305608-104305658	GM12892	blood:	n/a
12	chr9:104305608-104305658	AG04449	skin:	fetal
13	chr9:104357967-104358017	AoSMC	blood vessel:	n/a
14	chr9:104358101-104358151	CMK	blood:	n/a
15	chr9:104358101-104358151	GM12892	blood:	n/a
16	chr9:104357967-104358017	PANC-1	pancreas:	n/a
17	chr9:104358101-104358151	U87	brain:	n/a
18	chr9:104356619-104356669	RPTEC	kidney:	n/a
19	chr9:104305608-104305658	AG04450	lung:	fetal
20	chr9:104305608-104305658	AoSMC	blood vessel:	n/a
21	chr9:104358101-104358151	HRCEpiC	kidney:	n/a
22	chr9:104356619-104356669	H1-hESC	embryonic stem cell:	embryo
23	chr9:104358101-104358151	Hela-S3	cervix:	n/a
24	chr9:104357177-104357227	NT2-D1	testis:	n/a
25	chr9:104357967-104358017	T-47D	breast:	n/a
26	chr9:104356619-104356669	GM12891	blood:	n/a
27	chr9:104356619-104356669	Hepatocyte	liver:	n/a
28	chr9:104334427-104334477	Hepatocyte	liver:	n/a
29	chr9:104357177-104357227	AG10803	skin:	n/a
30	chr9:104334427-104334477	AoSMC	blood vessel:	n/a
31	chr9:104357967-104358017	NH-A	brain:	n/a
32	chr9:104334427-104334477	MCF-7	breast:	n/a
33	chr9:104334427-104334477	K562	blood:	n/a
34	chr9:104357967-104358017	HL-60	blood:	n/a
35	chr9:104334427-104334477	HUVEC	blood vessel:	n/a
36	chr9:104305608-104305658	HRPEpiC	eye:	n/a
37	chr9:104305608-104305658	SK-N-MC	brain:	n/a
38	chr9:104334427-104334477	AG04450	lung:	fetal
39	chr9:104356619-104356669	CMK	blood:	n/a
40	chr9:104305608-104305658	BE2_C	brain:	n/a
41	chr9:104358101-104358151	AoSMC	blood vessel:	n/a
42	chr9:104358101-104358151	NHBE	bronchial:	n/a
43	chr9:104358101-104358151	HEEpiC	esophagus:	n/a
44	chr9:104357967-104358017	BJ	skin:	n/a
45	chr9:104358101-104358151	IMR90	lung:	fetal
46	chr9:104358101-104358151	HCF	heart:	n/a
47	chr9:104357967-104358017	HEK293	kidney:	embryo
48	chr9:104334427-104334477	Jurkat	blood:	n/a
49	chr9:104358101-104358151	Hepatocyte	liver:	n/a
50	chr9:104358101-104358151	HepG2	liver:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:104411321..104412861-chr9:104413323..104416226,2	K562	blood:
2	chr9:104358419..104360916-chr9:104365030..104366580,2	MCF-7	breast:
3	chr9:104311857..104314554-chr9:104326998..104328848,2	K562	blood:
4	chr9:104304678..104307406-chr9:104312351..104313863,2	MCF-7	breast:
5	chr9:104463930..104467725-chr9:104467754..104469771,4	MCF-7	breast:
6	chr9:104437852..104440174-chr9:104442279..104444495,2	K562	blood:
7	chr9:104369041..104371983-chr9:104372682..104374513,2	MCF-7	breast:
8	chr9:104387846..104390209-chr9:107506903..107509823,2	K562	blood:
9	chr9:104411321..104412861-chr9:104413323..104416226,2	K562	blood:
10	chr9:104325829..104329191-chr9:104331276..104334207,4	K562	blood:
11	chr9:104332562..104334673-chr9:104335549..104338409,2	MCF-7	breast:
12	chr9:104355931..104357895-chr9:104361066..104363280,2	K562	blood:
13	chr9:104329440..104331713-chr9:104334657..104336622,3	K562	blood:
14	chr9:104303266..104305565-chr9:104316225..104317922,2	K562	blood:
15	chr9:104441179..104443367-chr9:104448568..104451134,2	K562	blood:
16	chr9:104211304..104212259-chr9:104329523..104330518,2	K562	blood:
17	chr9:104221444..104221955-chr9:104329285..104330133,2	K562	blood:
18	chr9:104325829..104329191-chr9:104331276..104334207,4	K562	blood:
19	chr9:104211411..104211984-chr9:104329284..104330026,2	MCF-7	breast:
20	chr9:104332562..104334673-chr9:104335549..104338409,2	MCF-7	breast:
21	chr9:104332352..104334996-chr9:104342895..104344528,3	MCF-7	breast:
22	chr9:104295436..104297637-chr9:104304728..104307313,2	K562	blood:
23	chr9:104441179..104443367-chr9:104448568..104451134,2	K562	blood:
24	chr9:104472870..104474526-chr9:104475820..104477413,2	K562	blood:
25	chr9:104302143..104304850-chr9:104306401..104308642,2	K562	blood:
26	chr9:104369041..104371983-chr9:104372682..104374513,2	MCF-7	breast:
27	chr9:104332352..104334996-chr9:104342895..104344528,3	MCF-7	breast:
28	chr9:104303266..104305565-chr9:104316225..104317922,2	K562	blood:
29	chr9:104221036..104221738-chr9:104355766..104356658,2	MCF-7	breast:
30	chr9:104417427..104419641-chr9:104422911..104425722,2	K562	blood:
31	chr9:104417427..104419641-chr9:104422911..104425722,2	K562	blood:
32	chr9:104358419..104360916-chr9:104365030..104366580,2	MCF-7	breast:
33	chr9:104463930..104467725-chr9:104467754..104469771,4	MCF-7	breast:
34	chr9:104329440..104331713-chr9:104334657..104336622,3	K562	blood:
35	chr9:104364128..104365110-chr9:107444509..107445032,2	MCF-7	breast:
36	chr9:104437852..104440174-chr9:104442279..104444495,2	K562	blood:
37	chr9:104304678..104307406-chr9:104312351..104313863,2	MCF-7	breast:
38	chr9:104472870..104474526-chr9:104475820..104477413,2	K562	blood:
39	chr9:104210438..104213268-chr9:104328768..104330503,2	K562	blood:
40	chr9:104221002..104221801-chr9:104329610..104330484,3	MCF-7	breast:
41	chr9:104302143..104304850-chr9:104306401..104308642,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF20-3	chr9:104357347-104357370	NONHSAT133747
2	lnc-RNF20-3	chr9:104357625-104357790	NONHSAT133747
3	lnc-RNF20-3	chr9:104357879-104358148	NONHSAT133747

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNF20	hsa-miR-221-3p	chr9:104325139-104325161

Variant related genes	Relation type
RNF20	TF binding region
ENSG00000265068	TF binding region
GRIN3A	TF binding region
TMEM246	TF binding region
PPP3R2	TF binding region
RNF20	CpG island
ENSG00000265068	CpG island
GRIN3A	CpG island
TMEM246	CpG island
PPP3R2	CpG island
ENSG00000265068	chromatin interactions
ENSG00000188386	chromatin interactions
ENSG00000155827	chromatin interactions
ENSG00000165152	chromatin interactions
ENSG00000270982	chromatin interactions

Extended variants
information (count: 5855 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5855 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553341976	chr9:104300791-104300792	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs79232244	chr9:104300832-104300833	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34023527	chr9:104301083-104301084	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535688821	chr9:104301092-104301093	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140794843	chr9:104301100-104301101	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575440036	chr9:104301139-104301140	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376380880	chr9:104301194-104301195	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149716098	chr9:104301223-104301224	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188626508	chr9:104301227-104301228	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577266228	chr9:104301229-104301230	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545832533	chr9:104301249-104301250	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73503226	chr9:104301272-104301273	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs13296417	chr9:104301291-104301292	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529049556	chr9:104301293-104301294	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548925065	chr9:104301298-104301299	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562753115	chr9:104301316-104301317	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145587866	chr9:104301359-104301360	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192750184	chr9:104301409-104301410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570840971	chr9:104301418-104301419	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182172592	chr9:104301427-104301428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547083312	chr9:104301473-104301474	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566995170	chr9:104301475-104301476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35168482	chr9:104301506-104301507	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs75632424	chr9:104301508-104301509	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575835339	chr9:104301520-104301521	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148890328	chr9:104301535-104301536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147011984	chr9:104301556-104301557	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139008639	chr9:104301562-104301563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539856324	chr9:104301602-104301603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377723375	chr9:104301650-104301651	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573447954	chr9:104301702-104301703	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370388536	chr9:104301710-104301711	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187283066	chr9:104301750-104301751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372239294	chr9:104301766-104301767	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531578450	chr9:104301773-104301774	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561744004	chr9:104301796-104301797	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534076027	chr9:104301819-104301820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141524538	chr9:104301840-104301841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376552327	chr9:104301860-104301861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529545621	chr9:104301872-104301873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565195845	chr9:104301873-104301874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533338051	chr9:104301884-104301885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547022215	chr9:104301887-104301888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs59111885	chr9:104301943-104301944	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs529361119	chr9:104301998-104301999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7029878	chr9:104302165-104302166	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569330692	chr9:104302178-104302179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538466312	chr9:104302255-104302256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191730425	chr9:104302261-104302262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533458931	chr9:104302291-104302292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104296600-104301800	Weak transcription	Spleen	Spleen
2	chr9:104296800-104302600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:104296800-104302600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:104296800-104302600	Weak transcription	Lung	lung
5	chr9:104296800-104302800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:104296800-104302800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:104296800-104305800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:104296800-104334200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr9:104296800-104337400	Weak transcription	Stomach Mucosa	stomach
10	chr9:104297000-104302000	Weak transcription	Fetal Stomach	stomach
11	chr9:104297000-104302600	Weak transcription	Colonic Mucosa	Colon
12	chr9:104297000-104302600	Weak transcription	NH-A	brain
13	chr9:104297000-104302800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr9:104297000-104302800	Weak transcription	HSMMtube	muscle
15	chr9:104297000-104309200	Weak transcription	HUVEC	blood vessel
16	chr9:104297000-104317600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:104297200-104302400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr9:104297200-104302600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr9:104297200-104302800	Weak transcription	Fetal Intestine Small	intestine
20	chr9:104297200-104309200	Weak transcription	K562	blood
21	chr9:104297400-104301400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
22	chr9:104297600-104300800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
23	chr9:104297600-104300800	Strong transcription	Osteobl	bone
24	chr9:104297600-104301000	Genic enhancers	Brain Cingulate Gyrus	brain
25	chr9:104297600-104301000	Strong transcription	Fetal Muscle Trunk	muscle
26	chr9:104297600-104302800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr9:104297600-104304600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr9:104297600-104306000	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr9:104297600-104321200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr9:104297600-104330400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr9:104297600-104330400	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr9:104297800-104300800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:104297800-104300800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
34	chr9:104297800-104300800	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr9:104297800-104300800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr9:104297800-104300800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr9:104297800-104303800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr9:104297800-104303800	Strong transcription	Fetal Muscle Leg	muscle
39	chr9:104297800-104304800	Strong transcription	Fetal Lung	lung
40	chr9:104297800-104305800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr9:104297800-104311400	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr9:104297800-104317400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr9:104297800-104318400	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr9:104297800-104320400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:104297800-104320400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:104297800-104325400	Strong transcription	Duodenum Mucosa	Duodenum
47	chr9:104297800-104332600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:104297800-104333000	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr9:104298000-104301000	Strong transcription	Placenta	Placenta
50	chr9:104298000-104304200	Strong transcription	Fetal Thymus	thymus

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