Variant report

Variant	nsv897191
Chromosome Location	chr11:32805169-32903263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32851965-32852404	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:32814471-32814880	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:32850824-32851272	HepG2	liver:	n/a	n/a
4	ATF1	chr11:32878012-32878101	K562	blood:	n/a	n/a
5	ATF1	chr11:32888538-32888562	K562	blood:	n/a	n/a
6	ATF2	chr11:32850594-32851339	GM12878	blood:	n/a	n/a
7	ATF2	chr11:32850720-32851321	GM12878	blood:	n/a	n/a
8	BACH1	chr11:32862150-32862517	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr11:32902869-32903255	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:32830791-32831195	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:32846405-32846534	K562	blood:	n/a	n/a
12	BRCA1	chr11:32897267-32897327	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:32850715-32851268	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr11:32851524-32851531	GM12878	blood:	n/a	n/a
15	BRCA1	chr11:32851255-32851263	H1-hESC	embryonic stem cell:	n/a	n/a
16	CCNT2	chr11:32860829-32861008	K562	blood:	n/a	n/a
17	CCNT2	chr11:32808701-32808880	K562	blood:	n/a	n/a
18	CEBPB	chr11:32851907-32852432	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
19	CEBPB	chr11:32860372-32860755	HepG2	liver:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
20	CEBPB	chr11:32860402-32860698	K562	blood:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
21	CEBPB	chr11:32860071-32860812	HCT-116	colon:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
22	CEBPB	chr11:32860125-32861051	MCF-7	breast:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
23	CEBPB	chr11:32851813-32852506	MCF-7	breast:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
24	CEBPB	chr11:32873859-32874214	Hela-S3	cervix:	n/a	chr11:32874038-32874049
25	CEBPB	chr11:32860503-32860617	HepG2	liver:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
26	CEBPB	chr11:32851855-32852473	ECC-1	luminal epithelium:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
27	CEBPB	chr11:32873897-32874252	K562	blood:	n/a	chr11:32874038-32874049
28	CEBPB	chr11:32873949-32874191	IMR90	lung:	n/a	chr11:32874038-32874049
29	CEBPB	chr11:32851052-32852610	HCT-116	colon:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
30	CEBPB	chr11:32851939-32852391	HepG2	liver:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
31	CEBPB	chr11:32892240-32892584	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:32845218-32845505	HepG2	liver:	n/a	chr11:32845341-32845352
33	CEBPB	chr11:32852047-32852201	K562	blood:	n/a	chr11:32852133-32852144
34	CEBPB	chr11:32851943-32852334	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
35	CEBPB	chr11:32892292-32892633	MCF-7	breast:	n/a	n/a
36	CEBPB	chr11:32865173-32865425	A549	lung:	n/a	chr11:32865248-32865259 chr11:32865290-32865301
37	CEBPB	chr11:32860374-32860765	A549	lung:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
38	CEBPB	chr11:32851807-32852532	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
39	CEBPB	chr11:32892291-32892555	K562	blood:	n/a	n/a
40	CEBPB	chr11:32845248-32845397	HepG2	liver:	n/a	chr11:32845341-32845352
41	CEBPB	chr11:32860134-32860823	ECC-1	luminal epithelium:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
42	CEBPB	chr11:32860171-32860840	ECC-1	luminal epithelium:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
43	CEBPB	chr11:32851962-32852298	K562	blood:	n/a	chr11:32852133-32852144
44	CEBPB	chr11:32892363-32892495	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:32851833-32852432	HCT-116	colon:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
46	CEBPB	chr11:32840508-32840570	A549	lung:	n/a	chr11:32840539-32840550
47	CEBPB	chr11:32851793-32852346	H1-hESC	embryonic stem cell:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
48	CEBPB	chr11:32860368-32860760	H1-hESC	embryonic stem cell:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
49	CEBPB	chr11:32892285-32892603	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr11:32860212-32860926	A549	lung:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32854320-32854370	HAEpiC	amniotic membrane:	n/a
2	chr11:32854320-32854370	Hela-S3	cervix:	n/a
3	chr11:32854320-32854370	NHDF-neo	bronchial:	n/a
4	chr11:32851356-32851406	ovcar-3	ovarian:	n/a
5	chr11:32854320-32854370	HAEpiC	amniotic membrane:	n/a
6	chr11:32854320-32854370	Hela-S3	cervix:	n/a
7	chr11:32854320-32854370	NHDF-neo	bronchial:	n/a
8	chr11:32851356-32851406	ovcar-3	ovarian:	n/a
9	chr11:32875930-32875980	SK-N-SH_RA	brain:	n/a
10	chr11:32851260-32851310	HCF	heart:	n/a
11	chr11:32816211-32816261	A549	lung:	n/a
12	chr11:32851240-32851290	MCF10A-Er-Src	breast:	n/a
13	chr11:32815865-32815915	U87	brain:	n/a
14	chr11:32851356-32851406	U87	brain:	n/a
15	chr11:32816080-32816130	AG09319	gingival:	n/a
16	chr11:32851531-32851581	A549	lung:	n/a
17	chr11:32816080-32816130	GM06990	blood:	n/a
18	chr11:32851361-32851411	NHDF-neo	bronchial:	n/a
19	chr11:32851240-32851290	HL-60	blood:	n/a
20	chr11:32816885-32816935	HCT-116	colon:	n/a
21	chr11:32851346-32851396	BJ	skin:	n/a
22	chr11:32851371-32851421	PANC-1	pancreas:	n/a
23	chr11:32851361-32851411	GM19239	blood:	n/a
24	chr11:32815896-32815946	T-47D	breast:	n/a
25	chr11:32851950-32852000	AG10803	skin:	n/a
26	chr11:32851378-32851428	PANC-1	pancreas:	n/a
27	chr11:32815896-32815946	GM06990	blood:	n/a
28	chr11:32816227-32816277	HCF	heart:	n/a
29	chr11:32851087-32851137	H1-hESC	embryonic stem cell:	embryo
30	chr11:32816254-32816304	HepG2	liver:	n/a
31	chr11:32816885-32816935	SKMC	muscle:	n/a
32	chr11:32816227-32816277	AG09319	gingival:	n/a
33	chr11:32816885-32816935	HUVEC	blood vessel:	n/a
34	chr11:32851950-32852000	NT2-D1	testis:	n/a
35	chr11:32875930-32875980	AG09319	gingival:	n/a
36	chr11:32851087-32851137	HEK293	kidney:	embryo
37	chr11:32847480-32847530	HCT-116	colon:	n/a
38	chr11:32851240-32851290	SK-N-SH	brain:	n/a
39	chr11:32851361-32851411	HEK293	kidney:	embryo
40	chr11:32851346-32851396	AG09309	skin:	n/a
41	chr11:32815968-32816018	HUVEC	blood vessel:	n/a
42	chr11:32816080-32816130	GM12891	blood:	n/a
43	chr11:32851346-32851396	PANC-1	pancreas:	n/a
44	chr11:32851950-32852000	HUVEC	blood vessel:	n/a
45	chr11:32816211-32816261	HepG2	liver:	n/a
46	chr11:32851531-32851581	Jurkat	blood:	n/a
47	chr11:32851356-32851406	BJ	skin:	n/a
48	chr11:32875930-32875980	NB4	blood:	n/a
49	chr11:32851361-32851411	SK-N-SH_RA	brain:	n/a
50	chr11:32815865-32815915	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
2	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
3	chr11:32814796..32817275-chr11:32819869..32822707,2	MCF-7	breast:
4	chr11:32830572..32833021-chr11:32913903..32915593,2	MCF-7	breast:
5	chr11:32395477..32395997-chr11:32813804..32814649,2	K562	blood:
6	chr11:32830676..32831274-chr11:33709287..33709961,2	K562	blood:
7	chr11:32734959..32735691-chr11:32814406..32814938,2	MCF-7	breast:
8	chr11:32862183..32864294-chr11:32914218..32916079,2	K562	blood:
9	chr11:32851420..32852136-chr5:36606640..36607218,2	Hela-S3	cervix:
10	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
11	chr11:32734492..32735804-chr11:32813911..32815565,5	MCF-7	breast:
12	chr11:32892094..32893817-chr11:32914118..32916253,2	K562	blood:
13	chr11:32851187..32853645-chr11:32854709..32858523,6	MCF-7	breast:
14	chr11:32851076..32851981-chr12:123011655..123012268,2	Hela-S3	cervix:
15	chr11:32825967..32829445-chr11:32834509..32837119,3	K562	blood:
16	chr11:32825967..32829445-chr11:32834509..32837119,3	K562	blood:
17	chr11:32858756..32863139-chr11:32912593..32915314,4	MCF-7	breast:
18	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
19	chr11:32851461..32852210-chr3:49058647..49059440,2	NB4	blood:
20	chr11:32734751..32735852-chr11:32814047..32815123,4	K562	blood:
21	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
22	chr11:32892015..32892872-chr11:32914554..32915403,2	MCF-7	breast:
23	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
24	chr11:32850955..32851927-chr16:89752956..89753523,2	Hela-S3	cervix:
25	chr11:32344866..32345612-chr11:32814115..32815021,3	K562	blood:
26	chr11:32850121..32852277-chr11:33088797..33091531,2	MCF-7	breast:
27	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
28	chr11:32847589..32849311-chr11:32913725..32915620,2	K562	blood:
29	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
30	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
31	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
32	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
33	chr11:32850866..32853799-chr11:32862127..32863701,2	MCF-7	breast:
34	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
35	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
36	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
37	chr11:32789537..32792072-chr11:32812363..32815095,2	K562	blood:
38	chr11:32770910..32771799-chr11:32813954..32815012,4	MCF-7	breast:
39	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
40	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
41	chr11:32851440..32852221-chr2:173420119..173420696,2	Hela-S3	cervix:
42	chr11:32861977..32862713-chr14:65386776..65387380,2	MCF-7	breast:
43	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
44	chr11:32843099..32845929-chr11:32851383..32853799,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRRG4-2	chr11:32839485-32839664	NONHSAT018676
2	lnc-PRRG4-3	chr11:32823241-32823497	NONHSAT018675
3	lnc-PRRG4-2	chr11:32839176-32839252	NONHSAT018676
4	lnc-CCDC73-1	chr11:32878982-32879665	ENSG00000248689
5	lnc-PRRG4-1	chr11:32846016-32846832	NONHSAT018677
6	lnc-CCDC73-2	chr11:32817536-32817819	NONHSAT018674
7	lnc-QSER1-1	chr11:32875249-32875808	NONHSAT018678
8	lnc-CCDC73-1	chr11:32875249-32875810	ENSG00000248689
9	lnc-QSER1-1	chr11:32878980-32879666	NONHSAT018678

Variant related genes	Relation type
CCDC73	TF binding region
PRRG4	TF binding region
CCDC73	CpG island
PRRG4	CpG island
ENSG00000178149	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000260259	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000186714	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000185324	chromatin interactions
ENSG00000079215	chromatin interactions
ENSG00000184445	chromatin interactions
FBXW7	miRNA target sites
LMAN2L	miRNA target sites

Extended variants
information (count: 2556 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2556 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs198264	chr11:32805169-32805170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11031980	chr11:32805188-32805189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368120935	chr11:32805232-32805233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563064209	chr11:32805238-32805239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562282784	chr11:32805244-32805245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531795629	chr11:32805248-32805249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185779451	chr11:32805326-32805327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114579334	chr11:32805339-32805340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532802523	chr11:32805344-32805345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546145819	chr11:32805356-32805357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566230775	chr11:32805390-32805391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190298706	chr11:32805414-32805415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150704607	chr11:32805428-32805429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56695506	chr11:32805470-32805471	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs537644340	chr11:32805489-32805490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182564844	chr11:32805510-32805511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565368076	chr11:32805538-32805539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540635324	chr11:32805613-32805614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11031981	chr11:32805625-32805626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs149668509	chr11:32805663-32805664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543141088	chr11:32805695-32805696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562818422	chr11:32805702-32805703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187608040	chr11:32805732-32805733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192089106	chr11:32805737-32805738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565245547	chr11:32805740-32805741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533142310	chr11:32805764-32805765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144469327	chr11:32805774-32805775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546207521	chr11:32805790-32805791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566167601	chr11:32805832-32805833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10835971	chr11:32805836-32805837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs139221084	chr11:32805839-32805840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568851211	chr11:32805852-32805853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs36029585	chr11:32805876-32805877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77235323	chr11:32805886-32805887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397798589	chr11:32805887-32805888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183539238	chr11:32805896-32805897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557621105	chr11:32805900-32805901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571587402	chr11:32805940-32805941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534044178	chr11:32805963-32805964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554093014	chr11:32806099-32806100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570788534	chr11:32806103-32806104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144064158	chr11:32806148-32806149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542652577	chr11:32806160-32806161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189040827	chr11:32806171-32806172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184514386	chr11:32807039-32807040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150199006	chr11:32807074-32807075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115598757	chr11:32807106-32807107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116947215	chr11:32807135-32807136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117292362	chr11:32807230-32807231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539418560	chr11:32807278-32807279	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32798200-32806200	Weak transcription	Liver	Liver
2	chr11:32807000-32807400	Enhancers	HepG2	liver
3	chr11:32814000-32814200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr11:32814000-32814200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:32814000-32814200	Enhancers	Liver	Liver
6	chr11:32814000-32814200	Enhancers	Brain Substantia Nigra	brain
7	chr11:32814000-32814200	Enhancers	Dnd41	blood
8	chr11:32814000-32814200	Enhancers	GM12878-XiMat	blood
9	chr11:32814000-32815000	Active TSS	A549	lung
10	chr11:32814200-32814400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:32814200-32814400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr11:32814200-32814400	Bivalent Enhancer	Primary B cells from cord blood	blood
13	chr11:32814200-32814400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
14	chr11:32814200-32814400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
15	chr11:32814200-32814400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr11:32814200-32814400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr11:32814200-32814400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:32814200-32814400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:32814200-32814400	Active TSS	Adipose Nuclei	Adipose
20	chr11:32814200-32814400	Active TSS	Monocytes-CD14+_RO01746	blood
21	chr11:32814200-32814600	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr11:32814200-32814600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr11:32814200-32814600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr11:32814200-32814600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr11:32814200-32814600	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr11:32814200-32814600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr11:32814200-32814600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
28	chr11:32814200-32814600	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr11:32814200-32814600	Flanking Active TSS	Liver	Liver
30	chr11:32814200-32814600	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr11:32814200-32814600	Flanking Active TSS	GM12878-XiMat	blood
32	chr11:32814200-32814800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr11:32814200-32814800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:32814200-32814800	Active TSS	Brain Anterior Caudate	brain
35	chr11:32814200-32814800	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr11:32814200-32814800	Active TSS	Right Atrium	heart
37	chr11:32814200-32815000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:32814200-32815000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:32814200-32815000	Active TSS	Brain Hippocampus Middle	brain
40	chr11:32814200-32815000	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr11:32814200-32815000	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr11:32814200-32815000	Flanking Active TSS	Dnd41	blood
43	chr11:32814200-32815000	Enhancers	NHEK	skin
44	chr11:32814400-32814600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr11:32814400-32814600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:32814400-32814600	Enhancers	Primary B cells from cord blood	blood
47	chr11:32814400-32814600	Active TSS	Primary hematopoietic stem cells	blood
48	chr11:32814400-32814600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr11:32814400-32814600	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr11:32814400-32814600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood

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