Variant report

Variant	nsv913670
Chromosome Location	chr21:29022265-29525767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2068)
CpG islands
(count:366)
Chromatin interactive
region (count:19)
LncRNA
region (count:63)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:29391845-29392013	HepG2	liver:	n/a	n/a
2	ATF1	chr21:29029380-29029433	K562	blood:	n/a	n/a
3	ATF1	chr21:29110010-29110027	K562	blood:	n/a	n/a
4	ATF2	chr21:29073346-29073703	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr21:29073392-29073757	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr21:29440893-29441210	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr21:29462221-29462505	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr21:29301101-29301296	GM12878	blood:	n/a	chr21:29301204-29301215 chr21:29301205-29301215
9	BATF	chr21:29265811-29266074	GM12878	blood:	n/a	n/a
10	BATF	chr21:29217974-29218258	GM12878	blood:	n/a	n/a
11	BATF	chr21:29216892-29217092	GM12878	blood:	n/a	n/a
12	BATF	chr21:29301074-29301306	GM12878	blood:	n/a	chr21:29301204-29301215 chr21:29301205-29301215
13	BATF	chr21:29233154-29233409	GM12878	blood:	n/a	chr21:29233254-29233263
14	BCL11A	chr21:29265809-29266067	GM12878	blood:	n/a	n/a
15	BCL11A	chr21:29216799-29217050	GM12878	blood:	n/a	n/a
16	BCL11A	chr21:29265670-29266117	GM12878	blood:	n/a	n/a
17	BCL11A	chr21:29217980-29218268	GM12878	blood:	n/a	n/a
18	BHLHE40	chr21:29073430-29073632	HepG2	liver:	n/a	n/a
19	BRCA1	chr21:29423979-29424171	Hela-S3	cervix:	n/a	chr21:29424073-29424080
20	BRCA1	chr21:29505457-29505529	HepG2	liver:	n/a	n/a
21	BRCA1	chr21:29073324-29073714	Hela-S3	cervix:	n/a	n/a
22	CCNT2	chr21:29025478-29025823	K562	blood:	n/a	n/a
23	CEBPB	chr21:29290375-29290580	IMR90	lung:	n/a	n/a
24	CEBPB	chr21:29479113-29479347	A549	lung:	n/a	n/a
25	CEBPB	chr21:29441231-29441535	IMR90	lung:	n/a	chr21:29441383-29441394 chr21:29441383-29441396 chr21:29441431-29441444
26	CEBPB	chr21:29492171-29492261	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr21:29116343-29116435	HepG2	liver:	n/a	n/a
28	CEBPB	chr21:29046243-29046729	IMR90	lung:	n/a	n/a
29	CEBPB	chr21:29310870-29311008	H1-hESC	embryonic stem cell:	n/a	chr21:29310977-29310988
30	CEBPB	chr21:29280334-29280411	IMR90	lung:	n/a	n/a
31	CEBPB	chr21:29184627-29184943	IMR90	lung:	n/a	n/a
32	CEBPB	chr21:29204205-29204838	IMR90	lung:	n/a	chr21:29204683-29204694 chr21:29204683-29204694 chr21:29204681-29204694 chr21:29204681-29204694
33	CEBPB	chr21:29478951-29479406	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr21:29425313-29425640	IMR90	lung:	n/a	n/a
35	CEBPB	chr21:29353316-29353408	A549	lung:	n/a	chr21:29353346-29353357
36	CEBPB	chr21:29073252-29073904	IMR90	lung:	n/a	chr21:29073413-29073424
37	CEBPB	chr21:29073319-29073793	HepG2	liver:	n/a	chr21:29073413-29073424
38	CEBPB	chr21:29077177-29077377	HepG2	liver:	n/a	chr21:29077309-29077320
39	CEBPB	chr21:29202745-29202976	K562	blood:	n/a	chr21:29202854-29202865 chr21:29202853-29202864
40	CEBPB	chr21:29471433-29471586	K562	blood:	n/a	n/a
41	CEBPB	chr21:29310828-29311071	HepG2	liver:	n/a	chr21:29310977-29310988
42	CEBPB	chr21:29084470-29084512	IMR90	lung:	n/a	n/a
43	CEBPB	chr21:29073307-29073727	H1-hESC	embryonic stem cell:	n/a	chr21:29073413-29073424
44	CEBPB	chr21:29136389-29136701	IMR90	lung:	n/a	chr21:29136550-29136561
45	CEBPB	chr21:29073256-29073935	Hela-S3	cervix:	n/a	chr21:29073413-29073424
46	CEBPB	chr21:29474460-29474657	IMR90	lung:	n/a	chr21:29474564-29474577 chr21:29474564-29474575 chr21:29474564-29474577
47	CEBPB	chr21:29353299-29353489	IMR90	lung:	n/a	chr21:29353346-29353357
48	CEBPB	chr21:29027226-29027313	IMR90	lung:	n/a	n/a
49	CEBPB	chr21:29159437-29159735	IMR90	lung:	n/a	chr21:29159609-29159620
50	CEBPB	chr21:29524144-29524362	HepG2	liver:	n/a	chr21:29524267-29524278

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:29093202-29093252	SKMC	muscle:	n/a
2	chr21:29384327-29384377	SK-N-MC	brain:	n/a
3	chr21:29093202-29093252	Jurkat	blood:	n/a
4	chr21:29385056-29385106	GM12878	blood:	n/a
5	chr21:29391771-29391821	GM19239	blood:	n/a
6	chr21:29391726-29391776	ECC-1	luminal epithelium:	n/a
7	chr21:29385056-29385106	NHBE	bronchial:	n/a
8	chr21:29384327-29384377	HCT-116	colon:	n/a
9	chr21:29093202-29093252	HMEC	breast:	n/a
10	chr21:29391726-29391776	HRCEpiC	kidney:	n/a
11	chr21:29391771-29391821	HPAEpiC	pulmonary alveolar:	n/a
12	chr21:29093202-29093252	AG04449	skin:	fetal
13	chr21:29093202-29093252	SK-N-SH	brain:	n/a
14	chr21:29391771-29391821	GM06990	blood:	n/a
15	chr21:29391726-29391776	HRE	kidney:	n/a
16	chr21:29385056-29385106	HIPEpiC	eye:	n/a
17	chr21:29385056-29385106	Hela-S3	cervix:	n/a
18	chr21:29391726-29391776	AoSMC	blood vessel:	n/a
19	chr21:29093202-29093252	BE2_C	brain:	n/a
20	chr21:29385056-29385106	ovcar-3	ovarian:	n/a
21	chr21:29385056-29385106	HCF	heart:	n/a
22	chr21:29391726-29391776	RPTEC	kidney:	n/a
23	chr21:29391726-29391776	HepG2	liver:	n/a
24	chr21:29093202-29093252	GM12892	blood:	n/a
25	chr21:29391771-29391821	Jurkat	blood:	n/a
26	chr21:29384327-29384377	SAEC	small airway:	n/a
27	chr21:29385056-29385106	U87	brain:	n/a
28	chr21:29384327-29384377	SK-N-SH_RA	brain:	n/a
29	chr21:29385056-29385106	H1-hESC	embryonic stem cell:	embryo
30	chr21:29099379-29099429	SKMC	muscle:	n/a
31	chr21:29391771-29391821	HRCEpiC	kidney:	n/a
32	chr21:29099379-29099429	HIPEpiC	eye:	n/a
33	chr21:29099379-29099429	AG04450	lung:	fetal
34	chr21:29385056-29385106	BJ	skin:	n/a
35	chr21:29391726-29391776	CMK	blood:	n/a
36	chr21:29099379-29099429	A549	lung:	n/a
37	chr21:29093202-29093252	NH-A	brain:	n/a
38	chr21:29099379-29099429	AG10803	skin:	n/a
39	chr21:29391771-29391821	AG04450	lung:	fetal
40	chr21:29384327-29384377	GM12892	blood:	n/a
41	chr21:29099379-29099429	T-47D	breast:	n/a
42	chr21:29099379-29099429	AG09319	gingival:	n/a
43	chr21:29099379-29099429	HNPCEpiC	eye:	n/a
44	chr21:29099379-29099429	HEK293	kidney:	embryo
45	chr21:29093202-29093252	MCF10A-Er-Src	breast:	n/a
46	chr21:29093202-29093252	HUVEC	blood vessel:	n/a
47	chr21:29099379-29099429	HCT-116	colon:	n/a
48	chr21:29384327-29384377	SK-N-SH	brain:	n/a
49	chr21:29385056-29385106	HCM	heart:	n/a
50	chr21:29391771-29391821	HIPEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:29386666..29389295-chr21:29400358..29402509,2	K562	blood:
2	chr21:29203444..29205390-chr21:29209699..29212332,2	K562	blood:
3	chr21:29423938..29424536-chr21:29708144..29709031,2	MCF-7	breast:
4	chr21:29130365..29132734-chr21:29133407..29135689,2	K562	blood:
5	chr21:29130365..29132734-chr21:29133407..29135689,2	K562	blood:
6	chr21:29386666..29389295-chr21:29400358..29402509,2	K562	blood:
7	chr21:29446065..29447620-chr21:29453105..29455058,2	K562	blood:
8	chr21:28221528..28222669-chr21:29423576..29424576,3	MCF-7	breast:
9	chr21:28222055..28222830-chr21:29073096..29074079,2	K562	blood:
10	chr1:113346446..113346980-chr21:29107601..29108558,2	MCF-7	breast:
11	chr21:29131169..29131808-chr21:29708353..29709051,2	MCF-7	breast:
12	chr21:28141720..28142490-chr21:29073373..29073879,2	MCF-7	breast:
13	chr21:28104973..28105545-chr21:29073049..29073643,2	MCF-7	breast:
14	chr21:29446065..29447620-chr21:29453105..29455058,2	K562	blood:
15	chr21:28221528..28223154-chr21:29072525..29074611,26	MCF-7	breast:
16	chr21:28222266..28223005-chr21:29072932..29073598,4	MCF-7	breast:
17	chr21:29203444..29205390-chr21:29209699..29212332,2	K562	blood:
18	chr21:28221585..28222726-chr21:29073735..29074729,3	MCF-7	breast:
19	chr21:28221411..28222029-chr21:29073057..29074050,3	K562	blood:

(count:63 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP16-6	chr21:29118137-29118355	ENSG00000225298
2	lnc-USP16-6	chr21:29094698-29094732	XLOC_013897
3	lnc-USP16-3	chr21:29502849-29502891	XLOC_013900
4	lnc-USP16-4	chr21:29395016-29395552	ENSG00000178457
5	lnc-USP16-6	chr21:29118137-29118351	ENSG00000225298
6	lnc-USP16-4	chr21:29385682-29385751	XLOC_013899
7	lnc-USP16-3	chr21:29509009-29509930	ENSG00000232079
8	lnc-USP16-6	chr21:29097118-29097200	ENSG00000225298
9	lnc-USP16-7	chr21:29047026-29047091	NONHSAT081577
10	lnc-USP16-4	chr21:29385682-29385751	ENSG00000178457
11	lnc-USP16-6	chr21:29123391-29123524	FPKM1_group_20009_transcript_1
12	lnc-USP16-6	chr21:29115712-29115823	XLOC_013897
13	lnc-USP16-6	chr21:29118137-29118351	XLOC_013897
14	lnc-USP16-5	chr21:29357359-29357614	XLOC_013898
15	lnc-USP16-6	chr21:29123391-29123552	ENSG00000225298
16	lnc-USP16-3	chr21:29507633-29508027	XLOC_013900
17	lnc-USP16-7	chr21:29025675-29025810	XLOC_013896
18	lnc-USP16-3	chr21:29474869-29475559	XLOC_013900
19	lnc-USP16-7	chr21:29044308-29044503	NONHSAT081577
20	lnc-USP16-3	chr21:29474869-29475088	XLOC_013900
21	lnc-USP16-6	chr21:29118675-29118913	FPKM1_group_20009_transcript_1
22	lnc-USP16-3	chr21:29462558-29462840	XLOC_013900
23	lnc-USP16-7	chr21:29044309-29044465	XLOC_013896
24	lnc-USP16-6	chr21:29094717-29094732	ENSG00000225298
25	lnc-USP16-7	chr21:29047027-29047091	XLOC_013896
26	lnc-USP16-3	chr21:29502849-29502886	NONHSAT081589
27	lnc-USP16-6	chr21:29115712-29115823	ENSG00000225298
28	lnc-USP16-3	chr21:29473453-29473638	XLOC_013900
29	lnc-N6AMT1-4	chr21:29481865-29481987	NONHSAT081594
30	lnc-USP16-6	chr21:29118617-29118913	NONHSAT081584
31	lnc-USP16-6	chr21:29123391-29123552	XLOC_013897
32	lnc-USP16-6	chr21:29123391-29123552	ENSG00000225298
33	lnc-USP16-3	chr21:29473585-29473638	XLOC_013900
34	lnc-USP16-3	chr21:29502849-29502941	XLOC_013900
35	lnc-USP16-3	chr21:29502438-29502941	ENSG00000232079.2
36	lnc-USP16-12	chr21:29287270-29287303	l_2190_chr21:29287269-29288399_testes
37	lnc-USP16-3	chr21:29507633-29507891	ENSG00000232079.2
38	lnc-USP16-3	chr21:29462525-29462840	NONHSAT081589
39	lnc-USP16-3	chr21:29474869-29475899	XLOC_013900
40	lnc-USP16-3	chr21:29474869-29475088	XLOC_013900
41	lnc-USP16-3	chr21:29462633-29462840	XLOC_013900
42	lnc-USP16-3	chr21:29420733-29420856	ENSG00000232079
43	lnc-USP16-3	chr21:29420844-29420856	XLOC_013900
44	lnc-USP16-5	chr21:29327240-29327341	XLOC_013898
45	lnc-USP16-3	chr21:29462764-29462840	XLOC_013900
46	lnc-USP16-7	chr21:29025674-29025810	NONHSAT081577
47	lnc-USP16-3	chr21:29474869-29475088	ENSG00000232079
48	lnc-USP16-4	chr21:29395016-29395528	XLOC_013899
49	lnc-USP16-3	chr21:29420766-29420856	XLOC_013900
50	lnc-USP16-3	chr21:29468200-29468238	XLOC_013900

No data

Variant related genes	Relation type
ENSG00000232079	TF binding region
LINC00113	TF binding region
ENSG00000234083	TF binding region
LINC00314	TF binding region
ENSG00000232079	CpG island
LINC00113	CpG island
ENSG00000234083	CpG island
LINC00314	CpG island
RARG	miRNA target sites
LIMCH1	miRNA target sites
VPS13B	miRNA target sites
CYP7A1	miRNA target sites
KIAA1328	miRNA target sites
LONRF1	miRNA target sites
PROSC	miRNA target sites
GPATCH8	miRNA target sites
PROX1	miRNA target sites
CMTM7	miRNA target sites
SPATA2	miRNA target sites
PDE3A	miRNA target sites
SUV420H1	miRNA target sites

Extended variants
information (count: 13895 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:13895 , 50 per page) page: 1 2 3 4 5 6 7 ... 278

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2831040	chr21:29022265-29022266	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576271665	chr21:29022266-29022267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367904351	chr21:29022288-29022289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10482986	chr21:29022289-29022290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs537431790	chr21:29022296-29022297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537704977	chr21:29022313-29022314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555703378	chr21:29022324-29022325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140012325	chr21:29022350-29022351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34072513	chr21:29022387-29022388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574663576	chr21:29022415-29022416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572224812	chr21:29022416-29022417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149810580	chr21:29022432-29022433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145740656	chr21:29022447-29022448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192784511	chr21:29022462-29022463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552526539	chr21:29022487-29022488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185520425	chr21:29022521-29022522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190834381	chr21:29022522-29022523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548549942	chr21:29022540-29022541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568420255	chr21:29022542-29022543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148982063	chr21:29022559-29022560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181381902	chr21:29022575-29022576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374719582	chr21:29022597-29022598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184374767	chr21:29022633-29022634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539195286	chr21:29022634-29022635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188420511	chr21:29022636-29022637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575919670	chr21:29022697-29022698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535436232	chr21:29022749-29022750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142909293	chr21:29022750-29022751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17716530	chr21:29022751-29022752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541204648	chr21:29022772-29022773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142663127	chr21:29022777-29022778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs928273	chr21:29022810-29022811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545952173	chr21:29022813-29022814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562999544	chr21:29022817-29022818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531563687	chr21:29022818-29022819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548221187	chr21:29022924-29022925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562043334	chr21:29022933-29022934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528008192	chr21:29022957-29022958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547571550	chr21:29022974-29022975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11909433	chr21:29023078-29023079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs181103627	chr21:29023079-29023080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540047657	chr21:29023106-29023107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549565439	chr21:29023177-29023178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77671154	chr21:29023178-29023179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535101207	chr21:29023185-29023186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112205117	chr21:29023191-29023192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555430701	chr21:29023299-29023300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565963885	chr21:29023321-29023322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146898785	chr21:29023325-29023326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558103155	chr21:29023337-29023338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	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
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	21251322	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	22174824	CNVD
Renal cell carcinoma	18765545	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	18160780	CNVD
Mental retardation	17621639	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Williams-beuren syndrome	16826523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1501 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:29017600-29022400	Enhancers	NHDF-Ad	bronchial
2	chr21:29017600-29022400	Enhancers	NHEK	skin
3	chr21:29017800-29022400	Enhancers	HMEC	breast
4	chr21:29019000-29022400	Enhancers	HUVEC	blood vessel
5	chr21:29019400-29022400	Enhancers	Osteobl	bone
6	chr21:29019800-29022400	Enhancers	HSMM	muscle
7	chr21:29020800-29022400	Enhancers	NH-A	brain
8	chr21:29021000-29022400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr21:29021600-29022400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr21:29021600-29022600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr21:29021800-29022400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr21:29021800-29025800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr21:29022000-29025400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr21:29022400-29025400	Weak transcription	HMEC	breast
15	chr21:29022400-29025600	Weak transcription	NHEK	skin
16	chr21:29025400-29026200	Enhancers	HMEC	breast
17	chr21:29025400-29026400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr21:29025600-29026400	Enhancers	NHEK	skin
19	chr21:29025800-29026200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr21:29025800-29026400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr21:29026000-29026400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr21:29026200-29029000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr21:29026400-29046200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr21:29029000-29029200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr21:29029200-29029600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr21:29029600-29030000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr21:29032800-29033200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr21:29032800-29033400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr21:29033000-29033400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr21:29039200-29039600	Enhancers	NHDF-Ad	bronchial
31	chr21:29039400-29039800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr21:29039600-29043600	Weak transcription	NHDF-Ad	bronchial
33	chr21:29039800-29040200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr21:29040200-29040400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr21:29040400-29043600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr21:29042200-29043200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr21:29043600-29043800	Enhancers	Psoas Muscle	Psoas
38	chr21:29043600-29044000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr21:29043600-29044800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr21:29043600-29044800	Enhancers	NHDF-Ad	bronchial
41	chr21:29043600-29045000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr21:29043600-29045000	Enhancers	Osteobl	bone
43	chr21:29043600-29046200	Enhancers	Brain Germinal Matrix	brain
44	chr21:29043800-29044000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr21:29043800-29044600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr21:29043800-29044600	Weak transcription	Psoas Muscle	Psoas
47	chr21:29044000-29046200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr21:29044200-29044400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr21:29044200-29046200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr21:29044600-29044800	Enhancers	Psoas Muscle	Psoas

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