Variant report

Variant	nsv975360
Chromosome Location	chr11:57466716-57480320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:874)
CpG islands
(count:1282)
Chromatin interactive
region (count:42)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:57479334-57480399	HepG2	liver:	n/a	chr11:57480242-57480257
2	ARID3A	chr11:57479671-57480063	K562	blood:	n/a	n/a
3	ATF1	chr11:57479607-57480234	K562	blood:	n/a	n/a
4	ATF2	chr11:57479408-57480328	GM12878	blood:	n/a	n/a
5	ATF2	chr11:57479583-57480248	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr11:57479668-57479873	K562	blood:	n/a	n/a
7	ATF3	chr11:57479620-57480096	A549	lung:	n/a	n/a
8	BACH1	chr11:57479780-57479849	K562	blood:	n/a	n/a
9	BACH1	chr11:57480073-57480419	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr11:57477321-57477659	GM12878	blood:	n/a	chr11:57477455-57477466
11	BATF	chr11:57477248-57477636	GM12878	blood:	n/a	chr11:57477455-57477466
12	BCL3	chr11:57479293-57480159	GM12878	blood:	n/a	chr11:57479657-57479666
13	BCL3	chr11:57479121-57480476	A549	lung:	n/a	chr11:57479210-57479223 chr11:57479657-57479666
14	BCL3	chr11:57479260-57480481	A549	lung:	n/a	chr11:57479657-57479666
15	BHLHE40	chr11:57479433-57480316	K562	blood:	n/a	n/a
16	BHLHE40	chr11:57479417-57480351	GM12878	blood:	n/a	n/a
17	BRCA1	chr11:57479254-57479696	HepG2	liver:	n/a	n/a
18	BRCA1	chr11:57479220-57480636	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr11:57479004-57480334	K562	blood:	n/a	n/a
20	CCNT2	chr11:57479223-57480307	K562	blood:	n/a	n/a
21	CEBPB	chr11:57477479-57477789	A549	lung:	n/a	n/a
22	CEBPB	chr11:57479594-57480240	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:57477459-57477825	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:57477468-57477809	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:57477445-57477951	A549	lung:	n/a	n/a
26	CEBPB	chr11:57477454-57477810	MCF-7	breast:	n/a	n/a
27	CEBPB	chr11:57477432-57477813	K562	blood:	n/a	n/a
28	CEBPB	chr11:57477458-57477836	K562	blood:	n/a	n/a
29	CEBPB	chr11:57477466-57477812	A549	lung:	n/a	n/a
30	CEBPB	chr11:57478956-57479586	H1-hESC	embryonic stem cell:	n/a	chr11:57479401-57479409
31	CEBPB	chr11:57479800-57480442	K562	blood:	n/a	n/a
32	CEBPB	chr11:57477514-57477718	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr11:57478959-57479132	K562	blood:	n/a	n/a
34	CEBPB	chr11:57479764-57480250	K562	blood:	n/a	n/a
35	CEBPB	chr11:57473007-57473175	HepG2	liver:	n/a	chr11:57473076-57473087
36	CEBPB	chr11:57477453-57477818	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:57479511-57479579	K562	blood:	n/a	n/a
38	CEBPZ	chr11:57479658-57480118	HepG2	liver:	n/a	n/a
39	CHD1	chr11:57479412-57479770	GM12878	blood:	n/a	n/a
40	CHD2	chr11:57479248-57480322	K562	blood:	n/a	n/a
41	CHD2	chr11:57467155-57467168	GM12878	blood:	n/a	n/a
42	CHD2	chr11:57479260-57480424	GM12878	blood:	n/a	n/a
43	CHD2	chr11:57479318-57480205	HepG2	liver:	n/a	n/a
44	CHD2	chr11:57479185-57480373	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr11:57479261-57480434	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr11:57479512-57480271	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr11:57479151-57480394	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr11:57479176-57480456	GM12878	blood:	n/a	n/a
49	CREB1	chr11:57479163-57480519	K562	blood:	n/a	n/a
50	CREB1	chr11:57479156-57480471	GM12878	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:57479678-57479728	CMK	blood:	n/a
2	chr11:57479678-57479728	CMK	blood:	n/a
3	chr11:57479818-57479868	HNPCEpiC	eye:	n/a
4	chr11:57480004-57480054	MCF10A-Er-Src	breast:	n/a
5	chr11:57479604-57479654	K562	blood:	n/a
6	chr11:57479805-57479855	PFSK-1	brain:	n/a
7	chr11:57480176-57480226	HepG2	liver:	n/a
8	chr11:57480041-57480091	LNCaP	prostate:	n/a
9	chr11:57479802-57479852	GM12891	blood:	n/a
10	chr11:57480024-57480074	HAEpiC	amniotic membrane:	n/a
11	chr11:57480024-57480074	NHBE	bronchial:	n/a
12	chr11:57479895-57479945	NH-A	brain:	n/a
13	chr11:57479895-57479945	SAEC	small airway:	n/a
14	chr11:57479895-57479945	Hela-S3	cervix:	n/a
15	chr11:57479323-57479373	SK-N-SH_RA	brain:	n/a
16	chr11:57471957-57472007	Hepatocyte	liver:	n/a
17	chr11:57471957-57472007	HCPEpiC	choroid plexus:	n/a
18	chr11:57480307-57480357	NHDF-neo	bronchial:	n/a
19	chr11:57480041-57480091	SAEC	small airway:	n/a
20	chr11:57479687-57479737	HCPEpiC	choroid plexus:	n/a
21	chr11:57479818-57479868	GM19239	blood:	n/a
22	chr11:57479687-57479737	HAEpiC	amniotic membrane:	n/a
23	chr11:57476216-57476266	PFSK-1	brain:	n/a
24	chr11:57479895-57479945	Hepatocyte	liver:	n/a
25	chr11:57467618-57467668	SK-N-SH	brain:	n/a
26	chr11:57476216-57476266	HCT-116	colon:	n/a
27	chr11:57480041-57480091	T-47D	breast:	n/a
28	chr11:57479652-57479702	HCM	heart:	n/a
29	chr11:57480307-57480357	Jurkat	blood:	n/a
30	chr11:57479802-57479852	PANC-1	pancreas:	n/a
31	chr11:57480004-57480054	SK-N-SH_RA	brain:	n/a
32	chr11:57479604-57479654	HCPEpiC	choroid plexus:	n/a
33	chr11:57479895-57479945	HepG2	liver:	n/a
34	chr11:57479994-57480044	ECC-1	luminal epithelium:	n/a
35	chr11:57479818-57479868	U87	brain:	n/a
36	chr11:57479895-57479945	T-47D	breast:	n/a
37	chr11:57480024-57480074	NHDF-neo	bronchial:	n/a
38	chr11:57467618-57467668	AoSMC	blood vessel:	n/a
39	chr11:57479981-57480031	MCF-7	breast:	n/a
40	chr11:57479805-57479855	NHDF-neo	bronchial:	n/a
41	chr11:57480041-57480091	HRCEpiC	kidney:	n/a
42	chr11:57479323-57479373	MCF10A-Er-Src	breast:	n/a
43	chr11:57467618-57467668	T-47D	breast:	n/a
44	chr11:57479637-57479687	PANC-1	pancreas:	n/a
45	chr11:57480004-57480054	HEK293	kidney:	embryo
46	chr11:57480024-57480074	SK-N-SH_RA	brain:	n/a
47	chr11:57480307-57480357	HepG2	liver:	n/a
48	chr11:57480307-57480357	NT2-D1	testis:	n/a
49	chr11:57479687-57479737	HRPEpiC	eye:	n/a
50	chr11:57479687-57479737	HIPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:57470955..57473359-chr11:57567861..57570027,2	K562	blood:
2	chr11:57469323..57472017-chr11:57472443..57474700,2	K562	blood:
3	chr11:57416825..57418474-chr11:57477020..57479617,2	K562	blood:
4	chr11:57433884..57439071-chr11:57477629..57483930,15	K562	blood:
5	chr11:57471016..57472571-chr11:57477897..57479622,2	MCF-7	breast:
6	chr11:57469550..57472113-chr11:57477517..57480022,2	K562	blood:
7	chr11:57466742..57469032-chr11:57508887..57511436,2	K562	blood:
8	chr11:57296138..57298827-chr11:57479075..57481840,2	K562	blood:
9	chr11:57479619..57480126-chr4:174255691..174256370,2	Hela-S3	cervix:
10	chr11:57478095..57482223-chr11:57507421..57512003,5	K562	blood:
11	chr11:57433936..57437289-chr11:57477964..57482818,9	K562	blood:
12	chr11:57465162..57467138-chr11:57508721..57511292,2	MCF-7	breast:
13	chr11:57447901..57451282-chr11:57477513..57480655,3	K562	blood:
14	chr11:57478095..57481312-chr11:57507421..57511942,8	K562	blood:
15	chr11:57469323..57472017-chr11:57472443..57474700,2	K562	blood:
16	chr11:57448539..57450852-chr11:57471944..57474684,2	K562	blood:
17	chr11:57467968..57471169-chr11:57473477..57476394,3	MCF-7	breast:
18	chr11:57463417..57465032-chr11:57465221..57467463,2	K562	blood:
19	chr11:57464857..57467583-chr11:57469531..57471627,4	K562	blood:
20	chr11:57433212..57437810-chr11:57477098..57481918,8	MCF-7	breast:
21	chr11:57436045..57439920-chr11:57463580..57467800,3	K562	blood:
22	chr11:57479298..57481073-chr11:57485511..57487387,2	MCF-7	breast:
23	chr11:57461028..57463369-chr11:57466408..57468235,2	MCF-7	breast:
24	chr11:57477767..57479895-chr11:57568305..57570936,2	K562	blood:
25	chr11:57464857..57467583-chr11:57469531..57471627,4	K562	blood:
26	chr11:57432810..57435746-chr11:57470332..57472894,2	MCF-7	breast:
27	chr11:57467690..57470283-chr11:57473431..57475034,2	MCF-7	breast:
28	chr11:57469769..57472099-chr11:57500346..57502166,2	K562	blood:
29	chr11:57478792..57480294-chr11:57529805..57532617,2	K562	blood:
30	chr11:57467968..57471169-chr11:57473477..57476394,3	MCF-7	breast:
31	chr11:57473781..57477362-chr11:57478566..57481637,6	K562	blood:
32	chr11:57433359..57435481-chr11:57466980..57468619,2	K562	blood:
33	chr11:57478057..57480948-chr11:57506438..57510938,4	MCF-7	breast:
34	chr11:57464857..57467583-chr11:57469531..57471287,2	K562	blood:
35	chr11:57464857..57467583-chr11:57469531..57471287,2	K562	blood:
36	chr11:57478395..57480567-chr11:57567397..57569805,2	K562	blood:
37	chr11:57467690..57470283-chr11:57473431..57475034,2	MCF-7	breast:
38	chr11:57478353..57481972-chr11:57506953..57510365,5	MCF-7	breast:
39	chr11:57465191..57468347-chr11:57478149..57481711,3	K562	blood:
40	chr11:57471016..57472571-chr11:57477897..57479622,2	MCF-7	breast:
41	chr11:57459870..57462694-chr11:57476257..57478537,2	MCF-7	breast:
42	chr11:57435266..57437517-chr11:57478547..57480108,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMX2-1	chr11:57467953-57468629	NONHSAT021435

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ZDHHC5	hsa-miR-32-5p	chr11:57467767-57467773
2	MED19	hsa-miR-32-5p	chr11:57471246-57471267
3	ZDHHC5	hsa-miR-32-5p	chr11:57467748-57467774

Variant related genes	Relation type
TMX2-CTNND1	TF binding region
MED19	TF binding region
TMX2	TF binding region
TMX2-CTNND1	CpG island
MED19	CpG island
TMX2	CpG island
ENSG00000198561	chromatin interactions
ENSG00000254462	chromatin interactions
ENSG00000166793	chromatin interactions
ENSG00000156599	chromatin interactions
ENSG00000211450	chromatin interactions
ENSG00000164104	chromatin interactions
ENSG00000134809	chromatin interactions
ENSG00000213592	chromatin interactions
ENSG00000156603	chromatin interactions
ENSG00000213593	chromatin interactions
ENSG00000254732	chromatin interactions

Extended variants
information (count: 539 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375000419	chr11:57466723-57466724	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs180768308	chr11:57466728-57466729	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs138138603	chr11:57466757-57466758	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs545902836	chr11:57466780-57466781	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs141172250	chr11:57466799-57466800	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs201530882	chr11:57466806-57466807	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs117135042	chr11:57466809-57466810	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs540728880	chr11:57466834-57466835	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs375528385	chr11:57466898-57466899	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs371465389	chr11:57466917-57466918	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs374908974	chr11:57466918-57466919	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs372927555	chr11:57466936-57466937	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs2969940	chr11:57466978-57466979	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187274989	chr11:57466993-57466994	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs11604333	chr11:57467035-57467036	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs563213176	chr11:57467053-57467054	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs373802306	chr11:57467094-57467095	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs533645928	chr11:57467129-57467130	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs2911725	chr11:57467144-57467145	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560085540	chr11:57467150-57467151	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs76062648	chr11:57467166-57467167	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs192133351	chr11:57467179-57467180	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs566987986	chr11:57467183-57467184	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs537683024	chr11:57467228-57467229	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs549542713	chr11:57467245-57467246	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs377608497	chr11:57467274-57467275	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs538911983	chr11:57467288-57467289	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs376011671	chr11:57467310-57467311	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs201514417	chr11:57467317-57467318	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs183454851	chr11:57467318-57467319	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs573191349	chr11:57467400-57467401	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs374080912	chr11:57467402-57467403	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs150286584	chr11:57467411-57467412	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs377763198	chr11:57467417-57467418	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs555914167	chr11:57467434-57467435	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs371222737	chr11:57467443-57467444	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs199525387	chr11:57467497-57467498	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs530650676	chr11:57467510-57467511	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs200117655	chr11:57467513-57467514	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs376192237	chr11:57467526-57467527	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs370314176	chr11:57467528-57467529	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs374038596	chr11:57467529-57467530	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs367986917	chr11:57467536-57467537	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs544848422	chr11:57467547-57467548	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs113438323	chr11:57467556-57467557	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs563072034	chr11:57467574-57467575	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs578260699	chr11:57467586-57467587	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs545695706	chr11:57467670-57467671	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs186968752	chr11:57467671-57467672	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs371268180	chr11:57467703-57467704	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57436600-57479000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:57438600-57469400	Strong transcription	Rectal Mucosa Donor 29	rectum
3	chr11:57438600-57478200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:57438800-57469600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr11:57438800-57473800	Strong transcription	Fetal Muscle Trunk	muscle
6	chr11:57439000-57469400	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr11:57439000-57473400	Strong transcription	Fetal Thymus	thymus
8	chr11:57439000-57477400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:57439200-57469600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:57439400-57473000	Strong transcription	Placenta	Placenta
11	chr11:57439800-57473400	Strong transcription	Fetal Muscle Leg	muscle
12	chr11:57442800-57472800	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr11:57443200-57472600	Strong transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:57446600-57474200	Strong transcription	Fetal Intestine Large	intestine
15	chr11:57447000-57473800	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr11:57447800-57474200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:57448000-57472800	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr11:57448000-57473200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:57448200-57474400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:57448400-57472600	Strong transcription	Liver	Liver
21	chr11:57448400-57472600	Strong transcription	Lung	lung
22	chr11:57448400-57472600	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr11:57448400-57472800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:57448400-57472800	Strong transcription	Duodenum Mucosa	Duodenum
25	chr11:57448400-57473800	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr11:57448600-57469800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:57448600-57476400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr11:57448800-57468600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:57449000-57476000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:57449200-57469200	Strong transcription	Adipose Nuclei	Adipose
31	chr11:57449400-57469200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr11:57449400-57474200	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr11:57449800-57469600	Strong transcription	Stomach Smooth Muscle	stomach
34	chr11:57449800-57474200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr11:57450000-57469600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr11:57450200-57466800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:57450400-57473800	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr11:57450800-57469600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:57451000-57469800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:57451200-57474200	Strong transcription	Fetal Stomach	stomach
41	chr11:57451400-57472600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:57451400-57472800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr11:57453000-57475200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:57455600-57469400	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr11:57455600-57472800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr11:57455600-57472800	Strong transcription	Left Ventricle	heart
47	chr11:57458000-57472600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:57458000-57474600	Strong transcription	Fetal Intestine Small	intestine
49	chr11:57458000-57475800	Strong transcription	Thymus	Thymus
50	chr11:57458200-57469600	Strong transcription	Primary B cells from peripheral blood	blood

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