Variant report

Variant	nsv587963
Chromosome Location	chr21:47592268-47603747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:489)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:174 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:47600273-47600541	K562	blood:	n/a	n/a
2	BHLHE40	chr21:47599878-47600783	K562	blood:	n/a	chr21:47600024-47600040
3	BHLHE40	chr21:47602670-47602874	K562	blood:	n/a	n/a
4	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
5	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
6	CCNT2	chr21:47602103-47602303	K562	blood:	n/a	n/a
7	CCNT2	chr21:47599662-47600295	K562	blood:	n/a	n/a
8	CCNT2	chr21:47601111-47601719	K562	blood:	n/a	chr21:47601532-47601541
9	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
10	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
11	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
12	CHD2	chr21:47600498-47600573	K562	blood:	n/a	n/a
13	CHD2	chr21:47602210-47602336	K562	blood:	n/a	n/a
14	CTCF	chr21:47596508-47596563	GM10248	blood:	n/a	n/a
15	CTCF	chr21:47602610-47602670	K562	blood:	n/a	n/a
16	CTCF	chr21:47597865-47597885	GM13976	blood:	n/a	n/a
17	CTCF	chr21:47602315-47602837	K562	blood:	n/a	n/a
18	CTCF	chr21:47602520-47602670	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr21:47602413-47602773	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr21:47602560-47602710	K562	blood:	n/a	n/a
21	CTCF	chr21:47602580-47602666	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr21:47593440-47593590	HepG2	liver:	n/a	n/a
23	CTCF	chr21:47602470-47602826	K562	blood:	n/a	n/a
24	CTCF	chr21:47602447-47602803	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr21:47603185-47603333	K562	blood:	n/a	chr21:47603201-47603214
26	CTCF	chr21:47602491-47602813	K562	blood:	n/a	n/a
27	CTCF	chr21:47599680-47599830	GM12873	blood:	n/a	n/a
28	CTCF	chr21:47595267-47595330	GM20000	blood:	n/a	n/a
29	CTCF	chr21:47603670-47603684	GM10248	blood:	n/a	n/a
30	CTCF	chr21:47603580-47603665	GM10248	blood:	n/a	n/a
31	CTCF	chr21:47602387-47602802	K562	blood:	n/a	n/a
32	CTCFL	chr21:47602553-47602755	K562	blood:	n/a	n/a
33	CTCFL	chr21:47602540-47602767	K562	blood:	n/a	n/a
34	E2F6	chr21:47602509-47602788	K562	blood:	n/a	n/a
35	E2F6	chr21:47592507-47592691	K562	blood:	n/a	n/a
36	EBF1	chr21:47603427-47603861	GM12878	blood:	n/a	n/a
37	EGR1	chr21:47603099-47603599	K562	blood:	n/a	chr21:47603156-47603180
38	EGR1	chr21:47603176-47603587	K562	blood:	n/a	n/a
39	EGR1	chr21:47599858-47600167	K562	blood:	n/a	chr21:47600012-47600021
40	EP300	chr21:47603146-47603581	K562	blood:	n/a	n/a
41	EP300	chr21:47599955-47600515	K562	blood:	n/a	chr21:47600032-47600041
42	FOSL1	chr21:47598927-47599155	K562	blood:	n/a	n/a
43	GABPA	chr21:47603074-47603630	K562	blood:	n/a	n/a
44	GATA1	chr21:47599973-47600327	K562	blood:	n/a	chr21:47600129-47600141 chr21:47600132-47600142 chr21:47600132-47600139 chr21:47600130-47600139 chr21:47600130-47600140
45	GATA2	chr21:47603217-47603972	K562	blood:	n/a	n/a
46	GATA2	chr21:47599690-47600373	K562	blood:	n/a	chr21:47600129-47600141 chr21:47600132-47600142 chr21:47600132-47600139 chr21:47600130-47600139 chr21:47600130-47600140
47	GATA2	chr21:47599905-47600260	K562	blood:	n/a	chr21:47600129-47600141 chr21:47600132-47600142 chr21:47600132-47600139 chr21:47600130-47600139 chr21:47600130-47600140
48	GTF2F1	chr21:47603238-47603276	K562	blood:	n/a	n/a
49	HCFC1	chr21:47599976-47600292	K562	blood:	n/a	n/a
50	HDAC2	chr21:47603103-47603465	K562	blood:	n/a	chr21:47603157-47603176

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47602702-47602752	AG09309	skin:	n/a
2	chr21:47602702-47602752	AG09309	skin:	n/a
3	chr21:47602432-47602482	NH-A	brain:	n/a
4	chr21:47601211-47601261	SK-N-MC	brain:	n/a
5	chr21:47601211-47601261	GM12878	blood:	n/a
6	chr21:47602486-47602536	SK-N-SH	brain:	n/a
7	chr21:47602432-47602482	NT2-D1	testis:	n/a
8	chr21:47602432-47602482	Caco-2	colon:	n/a
9	chr21:47602432-47602482	HCT-116	colon:	n/a
10	chr21:47602486-47602536	AG09319	gingival:	n/a
11	chr21:47602486-47602536	MCF10A-Er-Src	breast:	n/a
12	chr21:47602486-47602536	LNCaP	prostate:	n/a
13	chr21:47601150-47601200	AG09309	skin:	n/a
14	chr21:47602702-47602752	H1-hESC	embryonic stem cell:	embryo
15	chr21:47602486-47602536	Hela-S3	cervix:	n/a
16	chr21:47602486-47602536	HPAEpiC	pulmonary alveolar:	n/a
17	chr21:47602486-47602536	HNPCEpiC	eye:	n/a
18	chr21:47602486-47602536	BJ	skin:	n/a
19	chr21:47602486-47602536	Jurkat	blood:	n/a
20	chr21:47601211-47601261	U87	brain:	n/a
21	chr21:47601211-47601261	AG09309	skin:	n/a
22	chr21:47602148-47602198	HAEpiC	amniotic membrane:	n/a
23	chr21:47602486-47602536	PrEC	prostate:	n/a
24	chr21:47601211-47601261	BE2_C	brain:	n/a
25	chr21:47601150-47601200	Hela-S3	cervix:	n/a
26	chr21:47601047-47601097	MCF10A-Er-Src	breast:	n/a
27	chr21:47602702-47602752	HPAEpiC	pulmonary alveolar:	n/a
28	chr21:47601150-47601200	NB4	blood:	n/a
29	chr21:47602702-47602752	HAEpiC	amniotic membrane:	n/a
30	chr21:47601211-47601261	HepG2	liver:	n/a
31	chr21:47602148-47602198	SK-N-SH_RA	brain:	n/a
32	chr21:47602486-47602536	SK-N-MC	brain:	n/a
33	chr21:47601211-47601261	H1-hESC	embryonic stem cell:	embryo
34	chr21:47602486-47602536	HMEC	breast:	n/a
35	chr21:47601211-47601261	CMK	blood:	n/a
36	chr21:47601150-47601200	CMK	blood:	n/a
37	chr21:47602432-47602482	Hepatocyte	liver:	n/a
38	chr21:47602148-47602198	HEK293	kidney:	embryo
39	chr21:47601150-47601200	GM12892	blood:	n/a
40	chr21:47601211-47601261	Hela-S3	cervix:	n/a
41	chr21:47602148-47602198	SKMC	muscle:	n/a
42	chr21:47602486-47602536	HepG2	liver:	n/a
43	chr21:47601150-47601200	GM12878	blood:	n/a
44	chr21:47602486-47602536	NT2-D1	testis:	n/a
45	chr21:47602486-47602536	NHDF-neo	bronchial:	n/a
46	chr21:47602148-47602198	ovcar-3	ovarian:	n/a
47	chr21:47601211-47601261	HCM	heart:	n/a
48	chr21:47599972-47600022	HEEpiC	esophagus:	n/a
49	chr21:47601211-47601261	HRE	kidney:	n/a
50	chr21:47599972-47600022	HRCEpiC	kidney:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
2	chr21:47573796..47576021-chr21:47598325..47600385,2	K562	blood:
3	chr21:47600262..47602297-chr21:47602464..47604765,2	K562	blood:
4	chr21:47599317..47602217-chr21:47649153..47650672,2	K562	blood:
5	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
6	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
7	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
8	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
9	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
10	chr21:47599873..47602213-chr21:47649234..47651649,2	K562	blood:
11	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
12	chr21:47579510..47581260-chr21:47592233..47594320,2	K562	blood:
13	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
14	chr21:47540169..47542673-chr21:47591421..47593527,2	MCF-7	breast:
15	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
16	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
17	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
18	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
19	chr21:47598526..47600624-chr21:47604926..47607198,2	K562	blood:
20	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
21	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
22	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
23	chr21:47575014..47577674-chr21:47594867..47597205,2	K562	blood:
24	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
25	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
26	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
27	chr21:47598086..47600168-chr21:47602807..47604710,2	K562	blood:
28	chr21:47572549..47576001-chr21:47599228..47602499,3	MCF-7	breast:
29	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
30	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:
31	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
32	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
33	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228404	TF binding region
ENSG00000228404	CpG island
ENSG00000160285	chromatin interactions
ENSG00000160284	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160282	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000228404	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000142173	chromatin interactions

Extended variants
information (count: 479 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17293390	chr21:47592268-47592269	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147768262	chr21:47592287-47592288	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2839136	chr21:47592308-47592309	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs556273479	chr21:47592325-47592326	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573903173	chr21:47592332-47592333	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs113633185	chr21:47592344-47592345	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs76698352	chr21:47592345-47592346	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs541575372	chr21:47592357-47592358	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs193049460	chr21:47592366-47592367	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs78441905	chr21:47592410-47592411	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564536102	chr21:47592463-47592464	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531562172	chr21:47592466-47592467	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs62214053	chr21:47592494-47592495	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561996045	chr21:47592495-47592496	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2839137	chr21:47592524-47592525	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146963774	chr21:47592545-47592546	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376069452	chr21:47592587-47592588	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566137554	chr21:47592593-47592594	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533133943	chr21:47592594-47592595	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184961149	chr21:47592609-47592610	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs75222741	chr21:47592686-47592687	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs13051547	chr21:47592748-47592749	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs529358007	chr21:47592763-47592764	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537016496	chr21:47592788-47592789	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73144714	chr21:47592817-47592818	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs13051649	chr21:47592828-47592829	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs534908977	chr21:47592837-47592838	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553181915	chr21:47592866-47592867	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577744893	chr21:47592868-47592869	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539935950	chr21:47592884-47592885	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs13048940	chr21:47592897-47592898	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs540544540	chr21:47592898-47592899	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189294791	chr21:47592900-47592901	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561737249	chr21:47592905-47592906	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs75794974	chr21:47592906-47592907	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12482741	chr21:47592946-47592947	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs13051757	chr21:47592950-47592951	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs533330903	chr21:47592951-47592952	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs551476570	chr21:47592954-47592955	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs563327206	chr21:47592956-47592957	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs13046028	chr21:47592970-47592971	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs549043683	chr21:47592988-47592989	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34984641	chr21:47592990-47592991	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534948035	chr21:47593008-47593009	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181074880	chr21:47593009-47593010	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116295387	chr21:47593013-47593014	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538405527	chr21:47593036-47593037	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558239248	chr21:47593048-47593049	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576170093	chr21:47593098-47593099	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs70940596	chr21:47593109-47593110	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47573600-47600200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr21:47573600-47602000	Weak transcription	Gastric	stomach
3	chr21:47573800-47593400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr21:47573800-47593400	Weak transcription	Brain Anterior Caudate	brain
5	chr21:47573800-47602200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr21:47573800-47603800	Weak transcription	Right Atrium	heart
7	chr21:47581400-47602800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr21:47581600-47600000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr21:47581600-47600200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr21:47582000-47592800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr21:47582000-47602200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr21:47582000-47602800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr21:47582000-47602800	Weak transcription	Ovary	ovary
14	chr21:47582400-47600200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr21:47582400-47603800	Weak transcription	Thymus	Thymus
16	chr21:47583000-47602800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr21:47583600-47594000	Weak transcription	Fetal Lung	lung
18	chr21:47588600-47592400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr21:47588600-47593600	Weak transcription	Fetal Muscle Leg	muscle
20	chr21:47588600-47599800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr21:47588600-47602800	Weak transcription	Lung	lung
22	chr21:47588800-47594000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr21:47589000-47600400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr21:47589200-47593400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr21:47589400-47599400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr21:47590000-47592800	Strong transcription	Fetal Stomach	stomach
27	chr21:47591200-47592400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr21:47591200-47592800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr21:47591400-47600000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr21:47591600-47592400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr21:47591600-47593400	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr21:47591800-47593400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr21:47592000-47592600	Enhancers	Primary B cells from peripheral blood	blood
34	chr21:47592000-47593000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr21:47592200-47592400	Weak transcription	Right Ventricle	heart
36	chr21:47592200-47592600	Strong transcription	Fetal Intestine Small	intestine
37	chr21:47592200-47593200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr21:47592200-47593600	Genic enhancers	K562	blood
39	chr21:47592400-47592800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr21:47592400-47593200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr21:47592600-47593000	Weak transcription	Fetal Intestine Small	intestine
42	chr21:47592800-47593000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr21:47592800-47593000	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr21:47592800-47594200	ZNF genes & repeats	Fetal Stomach	stomach
45	chr21:47593000-47593400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr21:47593000-47594000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr21:47593000-47594200	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr21:47593200-47593800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr21:47593200-47594200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr21:47593400-47593600	Enhancers	Brain Anterior Caudate	brain

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