Variant report

Variant	nsv430566
Chromosome Location	chr13:49945247-50089844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2135)
CpG islands
(count:2748)
Chromatin interactive
region (count:105)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2135 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50018824-50019531	K562	blood:	n/a	n/a
2	ARID3A	chr13:50038795-50039574	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:50017884-50018589	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:49995639-49995842	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:50022201-50022473	K562	blood:	n/a	n/a
6	ARID3A	chr13:50040074-50041075	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:50018043-50018342	K562	blood:	n/a	n/a
8	ATF1	chr13:49948735-49949011	K562	blood:	n/a	n/a
9	ATF2	chr13:50069871-50070277	GM12878	blood:	n/a	n/a
10	ATF2	chr13:50017921-50018315	GM12878	blood:	n/a	n/a
11	ATF2	chr13:50028547-50029303	GM12878	blood:	n/a	n/a
12	ATF2	chr13:50017799-50018696	GM12878	blood:	n/a	n/a
13	ATF2	chr13:50069823-50070213	GM12878	blood:	n/a	n/a
14	ATF2	chr13:50017524-50018660	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr13:50028627-50029260	GM12878	blood:	n/a	n/a
16	ATF2	chr13:50017722-50018650	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:49974206-49974216	K562	blood:	n/a	n/a
18	BACH1	chr13:50070386-50070773	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr13:50069852-50070221	GM12878	blood:	n/a	n/a
20	BATF	chr13:50028580-50029122	GM12878	blood:	n/a	n/a
21	BATF	chr13:50069835-50070194	GM12878	blood:	n/a	n/a
22	BATF	chr13:50028595-50029091	GM12878	blood:	n/a	n/a
23	BATF	chr13:50033761-50033980	GM12878	blood:	n/a	n/a
24	BATF	chr13:50033735-50034011	GM12878	blood:	n/a	n/a
25	BCL11A	chr13:50069845-50070179	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:50069906-50070213	GM12878	blood:	n/a	n/a
27	BCLAF1	chr13:50017854-50018762	GM12878	blood:	n/a	chr13:50018730-50018743
28	BCLAF1	chr13:50017479-50018901	GM12878	blood:	n/a	chr13:50018730-50018743
29	BCLAF1	chr13:50069804-50070564	GM12878	blood:	n/a	n/a
30	BHLHE40	chr13:50040050-50040053	HepG2	liver:	n/a	n/a
31	BHLHE40	chr13:50070022-50070675	HepG2	liver:	n/a	n/a
32	BHLHE40	chr13:50017572-50017700	HepG2	liver:	n/a	n/a
33	BHLHE40	chr13:50019167-50019537	HepG2	liver:	n/a	n/a
34	BHLHE40	chr13:50017924-50019861	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:50069894-50070748	GM12878	blood:	n/a	n/a
36	BHLHE40	chr13:49995589-49995906	HepG2	liver:	n/a	n/a
37	BHLHE40	chr13:49984789-49984955	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:50019165-50019509	A549	lung:	n/a	n/a
39	BHLHE40	chr13:49946064-49946407	HepG2	liver:	n/a	n/a
40	BHLHE40	chr13:50070011-50070578	K562	blood:	n/a	n/a
41	BHLHE40	chr13:50028754-50029257	GM12878	blood:	n/a	n/a
42	BHLHE40	chr13:50017907-50019581	K562	blood:	n/a	n/a
43	BRCA1	chr13:50017958-50018595	HepG2	liver:	n/a	n/a
44	BRCA1	chr13:49948748-49949109	Hela-S3	cervix:	n/a	chr13:49949075-49949082
45	BRCA1	chr13:50017797-50019617	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:50017808-50018576	GM12878	blood:	n/a	n/a
47	BRCA1	chr13:50017752-50018443	H1-hESC	embryonic stem cell:	n/a	n/a
48	CBX3	chr13:49978764-49979124	K562	blood:	n/a	n/a
49	CBX3	chr13:50037345-50037712	K562	blood:	n/a	n/a
50	CBX3	chr13:50017739-50018627	K562	blood:	n/a	n/a

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50070045-50070095	RPTEC	kidney:	n/a
2	chr13:50021335-50021385	Hepatocyte	liver:	n/a
3	chr13:50018171-50018221	Hepatocyte	liver:	n/a
4	chr13:50070045-50070095	RPTEC	kidney:	n/a
5	chr13:50021335-50021385	Hepatocyte	liver:	n/a
6	chr13:50018171-50018221	Hepatocyte	liver:	n/a
7	chr13:50070504-50070554	HAEpiC	amniotic membrane:	n/a
8	chr13:50018531-50018581	GM12891	blood:	n/a
9	chr13:50021335-50021385	T-47D	breast:	n/a
10	chr13:50070718-50070768	GM12891	blood:	n/a
11	chr13:50021335-50021385	MCF-7	breast:	n/a
12	chr13:50018355-50018405	PrEC	prostate:	n/a
13	chr13:50018171-50018221	PANC-1	pancreas:	n/a
14	chr13:50018044-50018094	GM06990	blood:	n/a
15	chr13:50062611-50062661	AG04449	skin:	fetal
16	chr13:50062611-50062661	PANC-1	pancreas:	n/a
17	chr13:50069489-50069539	A549	lung:	n/a
18	chr13:50074189-50074239	MCF-7	breast:	n/a
19	chr13:50018352-50018402	Hela-S3	cervix:	n/a
20	chr13:50070045-50070095	CMK	blood:	n/a
21	chr13:50074189-50074239	SKMC	muscle:	n/a
22	chr13:49990767-49990817	NB4	blood:	n/a
23	chr13:50070045-50070095	U87	brain:	n/a
24	chr13:50069705-50069755	BE2_C	brain:	n/a
25	chr13:50070504-50070554	HCPEpiC	choroid plexus:	n/a
26	chr13:50069489-50069539	AG04449	skin:	fetal
27	chr13:50056284-50056334	HUVEC	blood vessel:	n/a
28	chr13:50070504-50070554	AG09309	skin:	n/a
29	chr13:50070045-50070095	AG10803	skin:	n/a
30	chr13:50068486-50068536	GM12892	blood:	n/a
31	chr13:50025780-50025830	Hela-S3	cervix:	n/a
32	chr13:50069705-50069755	MCF-7	breast:	n/a
33	chr13:50062611-50062661	GM12878	blood:	n/a
34	chr13:50070045-50070095	SAEC	small airway:	n/a
35	chr13:50018157-50018207	NB4	blood:	n/a
36	chr13:50018531-50018581	HEEpiC	esophagus:	n/a
37	chr13:50018636-50018686	Jurkat	blood:	n/a
38	chr13:50070482-50070532	IMR90	lung:	fetal
39	chr13:50070045-50070095	PrEC	prostate:	n/a
40	chr13:50069509-50069559	MCF10A-Er-Src	breast:	n/a
41	chr13:50074189-50074239	RPTEC	kidney:	n/a
42	chr13:50021335-50021385	CMK	blood:	n/a
43	chr13:50070102-50070152	HIPEpiC	eye:	n/a
44	chr13:50018352-50018402	H1-hESC	embryonic stem cell:	embryo
45	chr13:50070499-50070549	SAEC	small airway:	n/a
46	chr13:49977110-49977160	ProgFib	skin:	n/a
47	chr13:50070482-50070532	NB4	blood:	n/a
48	chr13:50062611-50062661	GM19239	blood:	n/a
49	chr13:50018137-50018187	HUVEC	blood vessel:	n/a
50	chr13:50069705-50069755	AG09319	gingival:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
2	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
3	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
4	chr13:50033311..50035354-chr13:50074002..50076664,2	MCF-7	breast:
5	chr13:50011471..50014414-chr13:50018159..50020318,3	K562	blood:
6	chr13:49874986..49875912-chr13:49995476..49996152,3	MCF-7	breast:
7	chr13:50017920..50018425-chr3:127317278..127318186,2	NB4	blood:
8	chr13:49993633..49996417-chr13:50068251..50070383,2	K562	blood:
9	chr13:49980803..49985123-chr13:49985194..49988213,3	MCF-7	breast:
10	chr13:49993633..49996417-chr13:50068251..50070383,2	K562	blood:
11	chr13:50013502..50016015-chr13:50068967..50071697,2	K562	blood:
12	chr13:50068457..50070652-chr13:50081260..50083175,3	MCF-7	breast:
13	chr13:50038641..50040451-chr13:50143314..50145864,2	MCF-7	breast:
14	chr13:50063834..50065648-chr13:50067086..50070077,2	MCF-7	breast:
15	chr13:50029751..50032528-chr13:50034704..50037567,2	MCF-7	breast:
16	chr13:50060291..50062533-chr13:50067429..50069545,2	K562	blood:
17	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
18	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
19	chr13:50016483..50020444-chr13:50068529..50072853,4	MCF-7	breast:
20	chr13:50069004..50071273-chr13:50075738..50077658,2	MCF-7	breast:
21	chr13:50085860..50087945-chr13:50089850..50091816,2	MCF-7	breast:
22	chr13:50016895..50018613-chr13:50024420..50026981,2	MCF-7	breast:
23	chr13:50019424..50021164-chr13:50065782..50068488,2	MCF-7	breast:
24	chr13:50064832..50068654-chr13:50068754..50072882,4	K562	blood:
25	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
26	chr13:50068795..50071828-chr13:50072712..50075254,3	K562	blood:
27	chr10:75173616..75174305-chr13:50017762..50018728,2	HCT-116	colon:
28	chr13:49948746..49951030-chr13:49963060..49965178,2	K562	blood:
29	chr13:50045650..50047733-chr13:50190939..50192914,2	MCF-7	breast:
30	chr13:49875221..49876253-chr13:50010820..50011928,3	K562	blood:
31	chr13:50071647..50073472-chr13:50180377..50183221,3	MCF-7	breast:
32	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
33	chr13:49820441..49822930-chr13:50018500..50020473,2	K562	blood:
34	chr13:50072605..50075983-chr13:50085931..50088388,3	MCF-7	breast:
35	chr13:49874978..49875489-chr13:50010786..50011661,2	MCF-7	breast:
36	chr13:50033311..50035354-chr13:50074002..50076664,2	MCF-7	breast:
37	chr13:49937629..49939824-chr13:49947316..49949983,2	MCF-7	breast:
38	chr13:49959574..49961755-chr13:50016698..50018510,2	MCF-7	breast:
39	chr13:50068585..50069355-chr13:50091395..50092213,3	MCF-7	breast:
40	chr13:50022863..50025187-chr13:50116857..50119478,2	K562	blood:
41	chr13:50072641..50077099-chr13:50079863..50082927,4	MCF-7	breast:
42	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
43	chr13:50020071..50022197-chr13:50067941..50070115,2	K562	blood:
44	chr13:49961570..49963263-chr13:49972646..49974956,2	MCF-7	breast:
45	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
46	chr13:50016481..50018378-chr13:50070335..50072171,3	K562	blood:
47	chr13:50064483..50067847-chr13:50070204..50072747,3	K562	blood:
48	chr13:50017638..50018206-chr6:35436122..35436718,2	NB4	blood:
49	chr13:49961570..49963263-chr13:49972646..49974956,2	MCF-7	breast:
50	chr13:50072605..50075983-chr13:50085931..50088388,3	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETDB2-1	chr13:50080771-50080892	NONHSAT033746
2	lnc-SETDB2-1	chr13:50070372-50070584	NONHSAT033747
3	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033747
4	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033746
5	lnc-SETDB2-1	chr13:50087195-50087302	NONHSAT033747
6	lnc-AL136218.1-2	chr13:49956643-49957077	NONHSAT033740
7	lnc-SETDB2-1	chr13:50070120-50070231	NONHSAT033746
8	lnc-AL136218.1-1	chr13:49999416-49999586	NONHSAT033742
9	lnc-AL136218.1-2	chr13:50018122-50018200	NONHSAT033741
10	lnc-AL136218.1-2	chr13:49975269-49975406	NONHSAT033740
11	lnc-AL136218.1-2	chr13:49975531-49975723	NONHSAT033740
12	lnc-PHF11-1	chr13:50063106-50063206	NONHSAT033745
13	lnc-AL136218.1-1	chr13:49998089-49998144	NONHSAT033742
14	lnc-AL136218.1-2	chr13:49988140-49988335	NONHSAT033741
15	lnc-PHF11-2	chr13:50019689-50020088	NONHSAT033744
16	lnc-AL136218.1-1	chr13:49993070-49993573	NONHSAT033742
17	lnc-AL136218.1-1	chr13:49999396-49999977	NONHSAT033743
18	lnc-AL136218.1-2	chr13:49975632-49975723	NONHSAT033741
19	lnc-PHF11-1	chr13:50063383-50063500	NONHSAT033745
20	lnc-AL136218.1-1	chr13:49999345-49999351	NONHSAT033743
21	lnc-AL136218.1-2	chr13:50008222-50008359	NONHSAT033741
22	lnc-AL136218.1-2	chr13:50007454-50007529	NONHSAT033741
23	lnc-SETDB2-1	chr13:50087195-50087302	NONHSAT033746
24	lnc-PHF11-2	chr13:50018820-50018993	NONHSAT033744
25	lnc-AL136218.1-2	chr13:49987048-49987176	NONHSAT033740

No data

Variant related genes	Relation type
PHF11	TF binding region
SNRPGP14	TF binding region
CAB39L	TF binding region
SETDB2	TF binding region
ENSG00000215462	TF binding region
PHF11	CpG island
SNRPGP14	CpG island
CAB39L	CpG island
SETDB2	CpG island
ENSG00000215462	CpG island
ENSG00000136144	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000236577	chromatin interactions
ENSG00000215462	chromatin interactions
ENSG00000006194	chromatin interactions
ENSG00000136147	chromatin interactions
ENSG00000136169	chromatin interactions
ENSG00000073111	chromatin interactions
ENSG00000199788	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000116863	chromatin interactions
ENSG00000102547	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000125753	chromatin interactions
ENSG00000138279	chromatin interactions

Extended variants
information (count: 4939 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4939 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9783555	chr13:49945247-49945248	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542335674	chr13:49945307-49945308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202093835	chr13:49945321-49945322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35211288	chr13:49945324-49945325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs386379129	chr13:49945325-49945326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111542246	chr13:49945326-49945327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574337779	chr13:49945334-49945335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563558893	chr13:49945385-49945386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184970214	chr13:49945395-49945396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527500710	chr13:49945402-49945403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7998955	chr13:49945410-49945411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112734655	chr13:49945427-49945428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188635215	chr13:49945437-49945438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367865951	chr13:49945483-49945484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7998999	chr13:49945501-49945502	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192247436	chr13:49945528-49945529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530196303	chr13:49945545-49945546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116792251	chr13:49945546-49945547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547866784	chr13:49945566-49945567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564335253	chr13:49945583-49945584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142007371	chr13:49945588-49945589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184625181	chr13:49945627-49945628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34627506	chr13:49945631-49945632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535041663	chr13:49945706-49945707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531968984	chr13:49945769-49945770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556179198	chr13:49945785-49945786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568437607	chr13:49945881-49945882	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs9596088	chr13:49945901-49945902	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs200305728	chr13:49945902-49945903	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs189409697	chr13:49945949-49945950	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs4942819	chr13:49946000-49946001	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs575602186	chr13:49946054-49946055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs180724493	chr13:49946055-49946056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs554429794	chr13:49946086-49946087	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs564374032	chr13:49946121-49946122	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs183652677	chr13:49946226-49946227	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs565198612	chr13:49946258-49946259	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189356480	chr13:49946282-49946283	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs540238408	chr13:49946291-49946292	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs150088431	chr13:49946339-49946340	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs73485494	chr13:49946395-49946396	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548368499	chr13:49946453-49946454	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs74072542	chr13:49946482-49946483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs181265549	chr13:49946495-49946496	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200850096	chr13:49946506-49946507	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs201382802	chr13:49946507-49946508	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs368853192	chr13:49946512-49946513	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs368178747	chr13:49946549-49946550	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs186495731	chr13:49946627-49946628	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs56041650	chr13:49946640-49946641	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3511 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49889000-49947600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr13:49912600-49948800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr13:49922400-49946600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:49922400-49947800	Weak transcription	Right Ventricle	heart
5	chr13:49922800-49951400	Weak transcription	Gastric	stomach
6	chr13:49923200-49951200	Weak transcription	Pancreas	Pancrea
7	chr13:49929400-49950000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:49934200-49957400	Weak transcription	Left Ventricle	heart
9	chr13:49938600-49961000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:49941600-49946200	Weak transcription	HSMMtube	muscle
11	chr13:49942600-49946000	Weak transcription	NH-A	brain
12	chr13:49942600-49946200	Weak transcription	Fetal Lung	lung
13	chr13:49942600-49946400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:49942600-49947600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:49942600-49947800	Weak transcription	NHDF-Ad	bronchial
16	chr13:49942800-49945800	Weak transcription	Primary B cells from cord blood	blood
17	chr13:49942800-49946000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr13:49942800-49946600	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr13:49942800-49947800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr13:49942800-49948000	Weak transcription	NHLF	lung
21	chr13:49942800-49952800	Weak transcription	Aorta	Aorta
22	chr13:49943000-49946200	Weak transcription	Osteobl	bone
23	chr13:49943000-49946400	Weak transcription	Placenta	Placenta
24	chr13:49943000-49947000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr13:49943000-49947800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:49943000-49947800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr13:49943000-49947800	Weak transcription	Ovary	ovary
28	chr13:49943000-49948000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr13:49943600-49945400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr13:49944400-49951400	Enhancers	Fetal Heart	heart
31	chr13:49944600-49945400	Enhancers	Rectal Smooth Muscle	rectum
32	chr13:49944800-49945800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr13:49944800-49946200	Weak transcription	Stomach Smooth Muscle	stomach
34	chr13:49945000-49945400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr13:49945000-49946000	Weak transcription	Adipose Nuclei	Adipose
36	chr13:49945000-49946000	Weak transcription	Brain Hippocampus Middle	brain
37	chr13:49945000-49946000	Weak transcription	Colon Smooth Muscle	Colon
38	chr13:49945000-49946000	Weak transcription	Stomach Mucosa	stomach
39	chr13:49945000-49947400	Weak transcription	Brain Angular Gyrus	brain
40	chr13:49945000-49947600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr13:49945000-49948000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr13:49945000-49948800	Weak transcription	Brain Anterior Caudate	brain
43	chr13:49945000-49952000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr13:49945200-49946200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr13:49945200-49946200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr13:49945200-49948800	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr13:49945200-49949000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr13:49945200-49950200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr13:49945200-49973000	Weak transcription	Brain Substantia Nigra	brain
50	chr13:49945400-49945800	Weak transcription	Rectal Smooth Muscle	rectum

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