Variant report

Variant	nsv587954
Chromosome Location	chr21:47582102-47603465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:612)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

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	chr21:47602670-47602874	K562	blood:	n/a	n/a
3	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
4	BHLHE40	chr21:47599878-47600783	K562	blood:	n/a	chr21:47600024-47600040
5	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
6	CCNT2	chr21:47599662-47600295	K562	blood:	n/a	n/a
7	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
8	CCNT2	chr21:47602103-47602303	K562	blood:	n/a	n/a
9	CCNT2	chr21:47601111-47601719	K562	blood:	n/a	chr21:47601532-47601541
10	CEBPB	chr21:47584218-47584328	HepG2	liver:	n/a	n/a
11	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
12	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
13	CHD2	chr21:47602210-47602336	K562	blood:	n/a	n/a
14	CHD2	chr21:47600498-47600573	K562	blood:	n/a	n/a
15	CTCF	chr21:47602610-47602670	K562	blood:	n/a	n/a
16	CTCF	chr21:47593440-47593590	HepG2	liver:	n/a	n/a
17	CTCF	chr21:47599680-47599830	GM12873	blood:	n/a	n/a
18	CTCF	chr21:47590271-47590287	GM10248	blood:	n/a	n/a
19	CTCF	chr21:47602447-47602803	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr21:47590539-47590619	GM10248	blood:	n/a	n/a
21	CTCF	chr21:47602387-47602802	K562	blood:	n/a	n/a
22	CTCF	chr21:47602470-47602826	K562	blood:	n/a	n/a
23	CTCF	chr21:47603185-47603333	K562	blood:	n/a	chr21:47603201-47603214
24	CTCF	chr21:47590535-47590671	Lung_OC	lung:	n/a	n/a
25	CTCF	chr21:47602580-47602666	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr21:47590294-47590358	GM10248	blood:	n/a	n/a
27	CTCF	chr21:47596508-47596563	GM10248	blood:	n/a	n/a
28	CTCF	chr21:47602491-47602813	K562	blood:	n/a	n/a
29	CTCF	chr21:47590390-47590450	GM13976	blood:	n/a	n/a
30	CTCF	chr21:47602315-47602837	K562	blood:	n/a	n/a
31	CTCF	chr21:47595267-47595330	GM20000	blood:	n/a	n/a
32	CTCF	chr21:47602520-47602670	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr21:47602560-47602710	K562	blood:	n/a	n/a
34	CTCF	chr21:47597865-47597885	GM13976	blood:	n/a	n/a
35	CTCF	chr21:47602413-47602773	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr21:47590514-47590527	GM13976	blood:	n/a	n/a
37	CTCFL	chr21:47602553-47602755	K562	blood:	n/a	n/a
38	CTCFL	chr21:47602540-47602767	K562	blood:	n/a	n/a
39	CUX1	chr21:47587940-47588030	K562	blood:	n/a	n/a
40	E2F6	chr21:47592507-47592691	K562	blood:	n/a	n/a
41	E2F6	chr21:47602509-47602788	K562	blood:	n/a	n/a
42	EBF1	chr21:47603427-47603861	GM12878	blood:	n/a	n/a
43	EGR1	chr21:47599858-47600167	K562	blood:	n/a	chr21:47600012-47600021
44	EGR1	chr21:47603176-47603587	K562	blood:	n/a	n/a
45	EGR1	chr21:47603099-47603599	K562	blood:	n/a	chr21:47603156-47603180
46	EP300	chr21:47599955-47600515	K562	blood:	n/a	chr21:47600032-47600041
47	EP300	chr21:47603146-47603581	K562	blood:	n/a	n/a
48	FOS	chr21:47591723-47591752	MCF10A-Er-Src	breast:	n/a	n/a
49	FOSL1	chr21:47598927-47599155	K562	blood:	n/a	n/a
50	GABPA	chr21:47603074-47603630	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47601150-47601200	PFSK-1	brain:	n/a
2	chr21:47599972-47600022	T-47D	breast:	n/a
3	chr21:47601150-47601200	PFSK-1	brain:	n/a
4	chr21:47599972-47600022	T-47D	breast:	n/a
5	chr21:47602486-47602536	LNCaP	prostate:	n/a
6	chr21:47599972-47600022	K562	blood:	n/a
7	chr21:47602148-47602198	HCF	heart:	n/a
8	chr21:47585850-47585900	HL-60	blood:	n/a
9	chr21:47601150-47601200	HIPEpiC	eye:	n/a
10	chr21:47602486-47602536	Hepatocyte	liver:	n/a
11	chr21:47599972-47600022	SK-N-SH	brain:	n/a
12	chr21:47601211-47601261	SK-N-MC	brain:	n/a
13	chr21:47602148-47602198	SK-N-MC	brain:	n/a
14	chr21:47601150-47601200	PANC-1	pancreas:	n/a
15	chr21:47602486-47602536	AG09319	gingival:	n/a
16	chr21:47599972-47600022	PANC-1	pancreas:	n/a
17	chr21:47582351-47582401	Hepatocyte	liver:	n/a
18	chr21:47602702-47602752	Caco-2	colon:	n/a
19	chr21:47602702-47602752	H1-hESC	embryonic stem cell:	embryo
20	chr21:47599972-47600022	HAEpiC	amniotic membrane:	n/a
21	chr21:47601047-47601097	U87	brain:	n/a
22	chr21:47601211-47601261	CMK	blood:	n/a
23	chr21:47602702-47602752	HRCEpiC	kidney:	n/a
24	chr21:47602432-47602482	Caco-2	colon:	n/a
25	chr21:47585850-47585900	HUVEC	blood vessel:	n/a
26	chr21:47602702-47602752	AG04449	skin:	fetal
27	chr21:47602702-47602752	HRE	kidney:	n/a
28	chr21:47602702-47602752	NT2-D1	testis:	n/a
29	chr21:47601150-47601200	SKMC	muscle:	n/a
30	chr21:47582351-47582401	AG10803	skin:	n/a
31	chr21:47585850-47585900	HCF	heart:	n/a
32	chr21:47601047-47601097	GM12892	blood:	n/a
33	chr21:47599972-47600022	GM19239	blood:	n/a
34	chr21:47582351-47582401	HCT-116	colon:	n/a
35	chr21:47601150-47601200	HPAEpiC	pulmonary alveolar:	n/a
36	chr21:47601150-47601200	MCF10A-Er-Src	breast:	n/a
37	chr21:47601211-47601261	BJ	skin:	n/a
38	chr21:47585850-47585900	RPTEC	kidney:	n/a
39	chr21:47601047-47601097	Hela-S3	cervix:	n/a
40	chr21:47602432-47602482	GM12878	blood:	n/a
41	chr21:47599972-47600022	NT2-D1	testis:	n/a
42	chr21:47602486-47602536	CMK	blood:	n/a
43	chr21:47582351-47582401	AG09309	skin:	n/a
44	chr21:47585850-47585900	Jurkat	blood:	n/a
45	chr21:47599972-47600022	HCT-116	colon:	n/a
46	chr21:47601047-47601097	GM12891	blood:	n/a
47	chr21:47602486-47602536	HNPCEpiC	eye:	n/a
48	chr21:47602702-47602752	NB4	blood:	n/a
49	chr21:47601150-47601200	HCPEpiC	choroid plexus:	n/a
50	chr21:47582351-47582401	A549	lung:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47583504..47585135-chr21:47586773..47588426,2	K562	blood:
2	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
3	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
4	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
5	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
6	chr21:47575923..47577951-chr21:47583383..47585806,2	K562	blood:
7	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
8	chr21:47573796..47576021-chr21:47598325..47600385,2	K562	blood:
9	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
10	chr21:47572189..47573895-chr21:47587183..47588702,2	K562	blood:
11	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
12	chr21:47563777..47566243-chr21:47580677..47583007,2	K562	blood:
13	chr21:47572328..47575443-chr21:47578503..47583188,4	MCF-7	breast:
14	chr21:47573565..47576139-chr21:47579614..47582261,4	K562	blood:
15	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
16	chr21:47578648..47581560-chr21:47583837..47585987,2	MCF-7	breast:
17	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
18	chr21:47583504..47585135-chr21:47586773..47588426,2	K562	blood:
19	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
20	chr21:47600262..47602297-chr21:47602464..47604765,2	K562	blood:
21	chr21:47579510..47581260-chr21:47592233..47594320,2	K562	blood:
22	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
23	chr21:47540169..47542673-chr21:47591421..47593527,2	MCF-7	breast:
24	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
25	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:
26	chr21:47598526..47600624-chr21:47604926..47607198,2	K562	blood:
27	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
28	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
29	chr21:47578880..47581848-chr21:47584809..47588383,3	K562	blood:
30	chr21:47598086..47600168-chr21:47602807..47604710,2	K562	blood:
31	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
32	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
33	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
34	chr21:47572549..47576001-chr21:47599228..47602499,3	MCF-7	breast:
35	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
36	chr21:47579366..47583740-chr21:47600501..47605706,6	K562	blood:
37	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
38	chr21:47572242..47575458-chr21:47578361..47583454,7	K562	blood:
39	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
40	chr21:47599873..47602213-chr21:47649234..47651649,2	K562	blood:
41	chr21:47575014..47577674-chr21:47594867..47597205,2	K562	blood:
42	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
43	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
44	chr21:47587472..47590076-chr21:47646984..47649833,2	MCF-7	breast:
45	chr21:47580435..47582947-chr21:47589052..47590591,2	K562	blood:
46	chr21:47580435..47582947-chr21:47589052..47590591,2	K562	blood:
47	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
48	chr21:47599317..47602217-chr21:47649153..47650672,2	K562	blood:

No data

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

Extended variants
information (count: 1061 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200412374	chr21:47582102-47582103	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs181141098	chr21:47582150-47582151	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs563975246	chr21:47582152-47582153	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs531034592	chr21:47582159-47582160	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs549509407	chr21:47582168-47582169	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs547261827	chr21:47582180-47582181	ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372920964	chr21:47582229-47582230	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs144073173	chr21:47582235-47582236	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs62214043	chr21:47582241-47582242	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs184437069	chr21:47582243-47582244	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs79530301	chr21:47582259-47582260	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs370890645	chr21:47582260-47582261	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs537893637	chr21:47582288-47582289	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs569084605	chr21:47582295-47582296	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536065318	chr21:47582361-47582362	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs554791804	chr21:47582369-47582370	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs558028829	chr21:47582373-47582374	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs189020220	chr21:47582387-47582388	ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs553035283	chr21:47582428-47582429	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs116575934	chr21:47582460-47582461	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs536722937	chr21:47582470-47582471	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs144378342	chr21:47582479-47582480	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs116089145	chr21:47582490-47582491	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs3057184	chr21:47582516-47582517	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs113792328	chr21:47582517-47582518	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs542949018	chr21:47582520-47582521	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs561556311	chr21:47582521-47582522	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs528679711	chr21:47582522-47582523	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs147434776	chr21:47582594-47582595	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs571335637	chr21:47582595-47582596	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs532145224	chr21:47582619-47582620	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs550507362	chr21:47582656-47582657	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs114783660	chr21:47582664-47582665	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs536598301	chr21:47582708-47582709	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs112851170	chr21:47582726-47582727	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs571485198	chr21:47582764-47582765	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs115654656	chr21:47582793-47582794	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566365986	chr21:47582836-47582837	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs534096059	chr21:47582880-47582881	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs139721896	chr21:47582902-47582903	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs77283605	chr21:47582909-47582910	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573088230	chr21:47582914-47582915	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs553983110	chr21:47582915-47582916	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs78072940	chr21:47582919-47582920	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs575527366	chr21:47582954-47582955	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs543340414	chr21:47582989-47582990	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs181418277	chr21:47582998-47582999	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs142796974	chr21:47582999-47583000	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs540779649	chr21:47583002-47583003	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs564979995	chr21:47583025-47583026	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 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:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47573400-47590200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr21:47573600-47583200	Weak transcription	Brain Substantia Nigra	brain
3	chr21:47573600-47589600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr21:47573600-47600200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr21:47573600-47602000	Weak transcription	Gastric	stomach
6	chr21:47573800-47583000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr21:47573800-47585400	Weak transcription	Brain Angular Gyrus	brain
8	chr21:47573800-47585600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr21:47573800-47588000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr21:47573800-47590800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr21:47573800-47591400	Weak transcription	Left Ventricle	heart
12	chr21:47573800-47592000	Weak transcription	Right Ventricle	heart
13	chr21:47573800-47593400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr21:47573800-47593400	Weak transcription	Brain Anterior Caudate	brain
15	chr21:47573800-47602200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr21:47573800-47603800	Weak transcription	Right Atrium	heart
17	chr21:47574000-47590400	Weak transcription	Placenta	Placenta
18	chr21:47574200-47590800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr21:47575800-47583800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr21:47577800-47582600	Strong transcription	Fetal Intestine Small	intestine
21	chr21:47579400-47582200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr21:47579600-47582400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr21:47579800-47582400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr21:47580000-47583600	ZNF genes & repeats	K562	blood
25	chr21:47580200-47588000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr21:47580800-47582400	ZNF genes & repeats	Thymus	Thymus
27	chr21:47580800-47582800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
28	chr21:47581000-47582200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr21:47581000-47582400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr21:47581000-47583000	ZNF genes & repeats	Fetal Stomach	stomach
31	chr21:47581200-47582200	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr21:47581200-47582400	Bivalent/Poised TSS	Fetal Brain Female	brain
33	chr21:47581400-47582400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
34	chr21:47581400-47585400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr21:47581400-47602800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr21:47581600-47588000	Weak transcription	Lung	lung
37	chr21:47581600-47588400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr21:47581600-47588800	Weak transcription	Spleen	Spleen
39	chr21:47581600-47590000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr21:47581600-47600000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr21:47581600-47600200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr21:47581800-47582200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr21:47581800-47588000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr21:47582000-47582800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr21:47582000-47583000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr21:47582000-47583400	Weak transcription	Colonic Mucosa	Colon
47	chr21:47582000-47585200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr21:47582000-47588000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr21:47582000-47588000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr21:47582000-47592800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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