Variant report

Variant	nsv1030613
Chromosome Location	chr5:119980213-120301205
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	ATF1	chr5:120192153-120192218	K562	blood:	n/a	n/a
2	ATF2	chr5:120033417-120033942	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:120042500-120043085	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:120042574-120042977	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:120031373-120031760	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:120030827-120031258	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:120032153-120033315	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:120179170-120179494	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:120026709-120027291	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:120023318-120023332	K562	blood:	n/a	n/a
11	BHLHE40	chr5:119991637-119991644	K562	blood:	n/a	n/a
12	BRCA1	chr5:120039223-120039493	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr5:120188276-120188363	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr5:120289176-120289482	K562	blood:	n/a	n/a
15	CCNT2	chr5:120010812-120011012	K562	blood:	n/a	n/a
16	CEBPB	chr5:120203111-120203312	H1-hESC	embryonic stem cell:	n/a	chr5:120203173-120203184
17	CEBPB	chr5:120054932-120055285	IMR90	lung:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
18	CEBPB	chr5:120141819-120142096	ECC-1	luminal epithelium:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
19	CEBPB	chr5:119984458-119984709	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:120141809-120142192	IMR90	lung:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
21	CEBPB	chr5:120141820-120142183	K562	blood:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
22	CEBPB	chr5:120260572-120260815	K562	blood:	n/a	chr5:120260680-120260691
23	CEBPB	chr5:120103253-120103501	H1-hESC	embryonic stem cell:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
24	CEBPB	chr5:120103071-120103392	K562	blood:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
25	CEBPB	chr5:120039460-120039708	H1-hESC	embryonic stem cell:	n/a	chr5:120039507-120039520
26	CEBPB	chr5:120206319-120206613	HepG2	liver:	n/a	chr5:120206461-120206472
27	CEBPB	chr5:120103021-120103545	Hela-S3	cervix:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
28	CEBPB	chr5:120030269-120030469	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr5:120254687-120255099	A549	lung:	n/a	n/a
30	CEBPB	chr5:120141909-120142165	MCF-7	breast:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141994-120142007 chr5:120141994-120142005 chr5:120141994-120142007
31	CEBPB	chr5:120141819-120142169	A549	lung:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
32	CEBPB	chr5:120208128-120208204	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr5:120141822-120142185	HepG2	liver:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141832-120141843 chr5:120141994-120142005 chr5:120141994-120142007
34	CEBPB	chr5:120260548-120260826	HepG2	liver:	n/a	chr5:120260680-120260691
35	CEBPB	chr5:120141910-120142172	A549	lung:	n/a	chr5:120141996-120142005 chr5:120141996-120142005 chr5:120141996-120142007 chr5:120141996-120142005 chr5:120141996-120142005 chr5:120142157-120142169 chr5:120141994-120142007 chr5:120141994-120142005 chr5:120141994-120142007
36	CEBPB	chr5:120054977-120055190	A549	lung:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
37	CEBPB	chr5:120038927-120039237	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr5:120124187-120124543	K562	blood:	n/a	n/a
39	CEBPB	chr5:119984469-119984716	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:120054965-120055296	HepG2	liver:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
41	CEBPB	chr5:120181066-120181326	IMR90	lung:	n/a	chr5:120181218-120181229 chr5:120181216-120181229 chr5:120181218-120181229 chr5:120181216-120181229 chr5:120181216-120181227
42	CEBPB	chr5:120102949-120103507	HepG2	liver:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
43	CEBPB	chr5:120254653-120255046	HCT-116	colon:	n/a	n/a
44	CEBPB	chr5:119993776-119994043	HepG2	liver:	n/a	chr5:119993879-119993890
45	CEBPB	chr5:120179183-120179476	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr5:120254721-120255092	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:120102971-120103502	A549	lung:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
48	CEBPB	chr5:120203027-120203285	HepG2	liver:	n/a	chr5:120203173-120203184
49	CEBPB	chr5:120254719-120255091	A549	lung:	n/a	n/a
50	CEBPB	chr5:120208117-120208321	A549	lung:	n/a	chr5:120208234-120208245 chr5:120208236-120208247 chr5:120208236-120208245

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120038247-120038297	SK-N-MC	brain:	n/a
2	chr5:120115250-120115300	AG10803	skin:	n/a
3	chr5:120179610-120179660	AG09309	skin:	n/a
4	chr5:120167319-120167369	Caco-2	colon:	n/a
5	chr5:120038247-120038297	SK-N-MC	brain:	n/a
6	chr5:120115250-120115300	AG10803	skin:	n/a
7	chr5:120179610-120179660	AG09309	skin:	n/a
8	chr5:120167319-120167369	Caco-2	colon:	n/a
9	chr5:120278165-120278215	HCT-116	colon:	n/a
10	chr5:120167415-120167465	HCT-116	colon:	n/a
11	chr5:120272625-120272675	HNPCEpiC	eye:	n/a
12	chr5:120167415-120167465	H1-hESC	embryonic stem cell:	embryo
13	chr5:120115250-120115300	U87	brain:	n/a
14	chr5:120254714-120254764	Jurkat	blood:	n/a
15	chr5:120069936-120069986	ECC-1	luminal epithelium:	n/a
16	chr5:120038342-120038392	HNPCEpiC	eye:	n/a
17	chr5:120272574-120272624	HEK293	kidney:	embryo
18	chr5:120040283-120040333	Jurkat	blood:	n/a
19	chr5:120278165-120278215	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:120254714-120254764	SKMC	muscle:	n/a
21	chr5:120278165-120278215	PANC-1	pancreas:	n/a
22	chr5:120026632-120026682	Caco-2	colon:	n/a
23	chr5:120192115-120192165	GM19239	blood:	n/a
24	chr5:120069936-120069986	U87	brain:	n/a
25	chr5:120115250-120115300	Jurkat	blood:	n/a
26	chr5:120254714-120254764	HIPEpiC	eye:	n/a
27	chr5:120188118-120188168	AG10803	skin:	n/a
28	chr5:120191823-120191873	NHBE	bronchial:	n/a
29	chr5:120254714-120254764	AoSMC	blood vessel:	n/a
30	chr5:120097654-120097704	AG04450	lung:	fetal
31	chr5:120254714-120254764	H1-hESC	embryonic stem cell:	embryo
32	chr5:120192115-120192165	HEEpiC	esophagus:	n/a
33	chr5:120081741-120081791	H1-hESC	embryonic stem cell:	embryo
34	chr5:120254714-120254764	HCPEpiC	choroid plexus:	n/a
35	chr5:120040283-120040333	MCF-7	breast:	n/a
36	chr5:120040283-120040333	AG10803	skin:	n/a
37	chr5:120191823-120191873	AG04449	skin:	fetal
38	chr5:120272574-120272624	AG10803	skin:	n/a
39	chr5:120272574-120272624	HCT-116	colon:	n/a
40	chr5:120081741-120081791	GM12892	blood:	n/a
41	chr5:120040283-120040333	HUVEC	blood vessel:	n/a
42	chr5:120026632-120026682	K562	blood:	n/a
43	chr5:120081741-120081791	NB4	blood:	n/a
44	chr5:120018164-120018214	AG09309	skin:	n/a
45	chr5:120040283-120040333	HL-60	blood:	n/a
46	chr5:120254714-120254764	AG10803	skin:	n/a
47	chr5:120272574-120272624	T-47D	breast:	n/a
48	chr5:120167319-120167369	HRE	kidney:	n/a
49	chr5:120018164-120018214	Hepatocyte	liver:	n/a
50	chr5:120018164-120018214	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:120211985..120214324-chr5:120217571..120220442,2	K562	blood:
2	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
3	chr5:119991420..119991957-chr5:121285300..121286207,2	MCF-7	breast:
4	chr5:120182804..120185937-chr5:120188813..120191326,3	K562	blood:
5	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:
6	chr5:119990484..119993004-chr5:119995293..119997349,2	K562	blood:
7	chr5:119990484..119993004-chr5:119995293..119997349,2	K562	blood:
8	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
9	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
10	chr5:120009986..120011754-chr5:120014103..120015876,2	K562	blood:
11	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
12	chr5:120182804..120185937-chr5:120188813..120191326,3	K562	blood:
13	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
14	chr5:119852123..119854010-chr5:120038446..120041236,2	K562	blood:
15	chr5:120211985..120214324-chr5:120217571..120220442,2	K562	blood:
16	chr5:120040953..120043952-chr5:120045648..120047608,2	K562	blood:
17	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
18	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
19	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
20	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
21	chr5:119991277..119991777-chr5:120137719..120138239,2	MCF-7	breast:
22	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
23	chr5:119991257..119992549-chr5:121285272..121286241,6	MCF-7	breast:
24	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
25	chr5:120023459..120026241-chr5:120030447..120032911,2	K562	blood:
26	chr5:120009986..120011754-chr5:120014103..120015876,2	K562	blood:
27	chr5:119991478..119992421-chr5:120138412..120139232,3	MCF-7	breast:
28	chr5:119991277..119991777-chr5:120137719..120138239,2	MCF-7	breast:
29	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
30	chr5:120023459..120026241-chr5:120030447..120032911,2	K562	blood:
31	chr5:119991478..119992421-chr5:120138412..120139232,3	MCF-7	breast:
32	chr5:120300949..120302956-chr5:121296548..121298304,2	K562	blood:
33	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
34	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
35	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-1	chr5:120125649-120126473	XLOC_004528
2	lnc-LOX-9	chr5:119993772-119994066	NONHSAT103445
3	lnc-PRR16-1	chr5:120115791-120115896	XLOC_004528
4	lnc-PRR16-1	chr5:120115735-120115896	XLOC_004528
5	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528
6	lnc-PRR16-1	chr5:120118132-120118267	XLOC_004528
7	lnc-PRR16-1	chr5:120116913-120117106	XLOC_004528
8	lnc-PRR16-1	chr5:120109041-120109070	XLOC_004528
9	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528

Variant related genes	Relation type
ENSG00000270741	TF binding region
RNU4-69P	TF binding region
ENSG00000248927	TF binding region
ENSG00000270741	CpG island
RNU4-69P	CpG island
ENSG00000248927	CpG island
ENSG00000222609	chromatin interactions
ENSG00000151304	chromatin interactions
UAP1	miRNA target sites
PSIP1	miRNA target sites

Extended variants
information (count: 9909 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9909 , 50 per page) page: 1 2 3 4 5 6 7 ... 199

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548324352	chr5:119980265-119980266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374036837	chr5:119980279-119980280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs62377787	chr5:119980297-119980298	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556668024	chr5:119980313-119980314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577518227	chr5:119980314-119980315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369075536	chr5:119980315-119980316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538489198	chr5:119980333-119980334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556807439	chr5:119980492-119980493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77643641	chr5:119980527-119980528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542201521	chr5:119980531-119980532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542584979	chr5:119980635-119980636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182197718	chr5:119980641-119980642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560742453	chr5:119980642-119980643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572568191	chr5:119980643-119980644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185209409	chr5:119980655-119980656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75098978	chr5:119980811-119980812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532170644	chr5:119980821-119980822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550539268	chr5:119980828-119980829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562783265	chr5:119980885-119980886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375905784	chr5:119980920-119980921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139346893	chr5:119980928-119980929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7722755	chr5:119980959-119980960	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7708737	chr5:119981007-119981008	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs201192469	chr5:119981032-119981033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111616442	chr5:119981047-119981048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534240721	chr5:119981064-119981065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552702955	chr5:119981078-119981079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577466246	chr5:119981081-119981082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111613654	chr5:119981084-119981085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112311242	chr5:119981085-119981086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59100348	chr5:119981086-119981087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs575049545	chr5:119981088-119981089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7726615	chr5:119981089-119981090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560078423	chr5:119981100-119981101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554102377	chr5:119981113-119981114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10074952	chr5:119981136-119981137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145401395	chr5:119981140-119981141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564625033	chr5:119981147-119981148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576561357	chr5:119981170-119981171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544370137	chr5:119981179-119981180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112857511	chr5:119981180-119981181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562559512	chr5:119981325-119981326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529961622	chr5:119981328-119981329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148809122	chr5:119981382-119981383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114980551	chr5:119981395-119981396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7709440	chr5:119981411-119981412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs552637870	chr5:119981431-119981432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377281666	chr5:119981473-119981474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141742228	chr5:119981504-119981505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375498973	chr5:119981506-119981507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119953000-120021800	Weak transcription	HSMMtube	muscle
2	chr5:119962200-119980400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr5:119967800-120012800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:119977400-119983800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:119978000-119980400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:119978600-120004600	Weak transcription	HSMM	muscle
7	chr5:119979600-119980600	Enhancers	Osteobl	bone
8	chr5:119979600-119984000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr5:119980200-119981000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:119980400-119980800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:119980400-119980800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:119980400-119980800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr5:119980400-119981000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:119980600-119981000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:119980600-119984000	Weak transcription	Osteobl	bone
16	chr5:119980800-119983600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr5:119981000-119983400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:119983400-119984200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:119983600-119985400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr5:119983800-119984200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:119984000-119984600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:119984000-119985200	Enhancers	Osteobl	bone
23	chr5:119984200-119984800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr5:119984200-119984800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:119984600-119992800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:119984800-119985200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:119984800-119985200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:119984800-119985400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:119985200-119993000	Weak transcription	Osteobl	bone
30	chr5:119985400-120004600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr5:119985400-120011200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr5:119987800-119993000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr5:119989400-119990000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr5:119989400-119990200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:119989400-119990400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr5:119989400-119990800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr5:119989600-119990000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr5:119989600-119990000	Enhancers	H9 Cell Line	embryonic stem cell
39	chr5:119989600-119990200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:119989600-119990400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr5:119989600-119990600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:119989800-119990000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr5:119990000-119991400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr5:119990000-119993000	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr5:119990000-119993000	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr5:119990200-119991800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr5:119990200-119993000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr5:119990400-119993000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr5:119990400-119993000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr5:119990600-119993000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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