Variant report

Variant	esv2754486
Chromosome Location	chr1:188731343-189181343
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	chr1:189118670-189118888	K562	blood:	n/a	n/a
2	ATF1	chr1:188818322-188818328	K562	blood:	n/a	n/a
3	ATF1	chr1:188967459-188967540	K562	blood:	n/a	n/a
4	ATF1	chr1:188884384-188884432	K562	blood:	n/a	n/a
5	ATF1	chr1:189118704-189119125	K562	blood:	n/a	n/a
6	BACH1	chr1:188957759-188958083	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr1:189118637-189119186	K562	blood:	n/a	n/a
8	BHLHE40	chr1:189118889-189119095	K562	blood:	n/a	n/a
9	BRCA1	chr1:188857430-188857935	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr1:189094793-189095258	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:189118641-189119561	K562	blood:	n/a	n/a
12	CBX3	chr1:188751264-188751748	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:189118747-189119060	K562	blood:	n/a	n/a
14	CEBPB	chr1:188984681-188984698	K562	blood:	n/a	n/a
15	CEBPB	chr1:188996676-188997003	MCF-7	breast:	n/a	chr1:188996869-188996880 chr1:188996869-188996882 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880
16	CEBPB	chr1:189149375-189149525	K562	blood:	n/a	chr1:189149432-189149443
17	CEBPB	chr1:188861151-188861446	A549	lung:	n/a	chr1:188861298-188861309
18	CEBPB	chr1:189038196-189038503	A549	lung:	n/a	chr1:189038330-189038343 chr1:189038331-189038342 chr1:189038332-189038341 chr1:189038332-189038341 chr1:189038332-189038341 chr1:189038332-189038341
19	CEBPB	chr1:188990601-188991154	A549	lung:	n/a	chr1:188990820-188990833
20	CEBPB	chr1:188795967-188796275	HepG2	liver:	n/a	chr1:188796129-188796140
21	CEBPB	chr1:188794707-188794885	A549	lung:	n/a	chr1:188794818-188794829
22	CEBPB	chr1:189149272-189149581	IMR90	lung:	n/a	chr1:189149525-189149536 chr1:189149432-189149443
23	CEBPB	chr1:188794612-188794962	MCF-7	breast:	n/a	chr1:188794818-188794829
24	CEBPB	chr1:189166341-189166619	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:189015259-189015572	A549	lung:	n/a	chr1:189015393-189015406 chr1:189015395-189015404 chr1:189015395-189015404 chr1:189015395-189015406 chr1:189015395-189015404 chr1:189015393-189015404 chr1:189015395-189015404 chr1:189015393-189015406
26	CEBPB	chr1:188996578-188997249	A549	lung:	n/a	chr1:188996869-188996880 chr1:188996869-188996882 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880
27	CEBPB	chr1:188749632-188750193	HepG2	liver:	n/a	chr1:188750018-188750031 chr1:188749997-188750008 chr1:188749997-188750010
28	CEBPB	chr1:189015228-189015573	IMR90	lung:	n/a	chr1:189015393-189015406 chr1:189015395-189015404 chr1:189015395-189015404 chr1:189015395-189015406 chr1:189015395-189015404 chr1:189015393-189015404 chr1:189015395-189015404 chr1:189015393-189015406
29	CEBPB	chr1:188998528-188998788	A549	lung:	n/a	n/a
30	CEBPB	chr1:188969376-188969576	K562	blood:	n/a	chr1:188969500-188969511
31	CEBPB	chr1:188996688-188997020	A549	lung:	n/a	chr1:188996869-188996880 chr1:188996869-188996882 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880
32	CEBPB	chr1:188733004-188733398	MCF-7	breast:	n/a	n/a
33	CEBPB	chr1:188795959-188796302	IMR90	lung:	n/a	chr1:188796129-188796140
34	CEBPB	chr1:188996669-188997064	H1-hESC	embryonic stem cell:	n/a	chr1:188996869-188996880 chr1:188996869-188996882 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880
35	CEBPB	chr1:189149263-189149576	HepG2	liver:	n/a	chr1:189149525-189149536 chr1:189149432-189149443
36	CEBPB	chr1:188743018-188743248	A549	lung:	n/a	chr1:188743109-188743120
37	CEBPB	chr1:188795984-188796250	A549	lung:	n/a	chr1:188796129-188796140
38	CEBPB	chr1:189166348-189166590	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:189118695-189119077	K562	blood:	n/a	n/a
40	CEBPB	chr1:188940509-188940936	A549	lung:	n/a	n/a
41	CEBPB	chr1:188996687-188997065	IMR90	lung:	n/a	chr1:188996869-188996880 chr1:188996869-188996882 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880
42	CEBPB	chr1:188861142-188861475	Hela-S3	cervix:	n/a	chr1:188861298-188861309
43	CEBPB	chr1:189015222-189015587	HepG2	liver:	n/a	chr1:189015393-189015406 chr1:189015395-189015404 chr1:189015395-189015404 chr1:189015395-189015406 chr1:189015395-189015404 chr1:189015393-189015404 chr1:189015395-189015404 chr1:189015393-189015406
44	CEBPB	chr1:188738866-188739491	MCF-7	breast:	n/a	n/a
45	CEBPB	chr1:188861237-188861445	H1-hESC	embryonic stem cell:	n/a	chr1:188861298-188861309
46	CEBPB	chr1:188861120-188861477	IMR90	lung:	n/a	chr1:188861298-188861309
47	CEBPB	chr1:188996604-188997110	MCF-7	breast:	n/a	chr1:188996869-188996880 chr1:188996869-188996882 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880 chr1:188996871-188996880
48	CEBPB	chr1:188918872-188919227	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:188908501-188909140	IMR90	lung:	n/a	chr1:188908639-188908650
50	CEBPB	chr1:188969322-188969657	IMR90	lung:	n/a	chr1:188969500-188969511

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:188826889-188826939	NHDF-neo	bronchial:	n/a
2	chr1:188826823-188826873	GM12892	blood:	n/a
3	chr1:188826823-188826873	H1-hESC	embryonic stem cell:	embryo
4	chr1:188826889-188826939	AG04450	lung:	fetal
5	chr1:188826889-188826939	RPTEC	kidney:	n/a
6	chr1:188826823-188826873	SKMC	muscle:	n/a
7	chr1:188826823-188826873	HCF	heart:	n/a
8	chr1:188826889-188826939	PANC-1	pancreas:	n/a
9	chr1:188826889-188826939	HCM	heart:	n/a
10	chr1:188826889-188826939	SAEC	small airway:	n/a
11	chr1:188826823-188826873	AG10803	skin:	n/a
12	chr1:188826889-188826939	Hela-S3	cervix:	n/a
13	chr1:188826823-188826873	HUVEC	blood vessel:	n/a
14	chr1:188826823-188826873	SK-N-SH	brain:	n/a
15	chr1:188826889-188826939	HMEC	breast:	n/a
16	chr1:188826889-188826939	GM12878	blood:	n/a
17	chr1:188826889-188826939	SK-N-MC	brain:	n/a
18	chr1:188826823-188826873	ECC-1	luminal epithelium:	n/a
19	chr1:188826889-188826939	NT2-D1	testis:	n/a
20	chr1:188826889-188826939	AG09319	gingival:	n/a
21	chr1:188826823-188826873	IMR90	lung:	fetal
22	chr1:188826889-188826939	HRPEpiC	eye:	n/a
23	chr1:188826823-188826873	A549	lung:	n/a
24	chr1:188826889-188826939	A549	lung:	n/a
25	chr1:188826889-188826939	AG10803	skin:	n/a
26	chr1:188826889-188826939	MCF-7	breast:	n/a
27	chr1:188826823-188826873	NHBE	bronchial:	n/a
28	chr1:188826889-188826939	HL-60	blood:	n/a
29	chr1:188826889-188826939	GM06990	blood:	n/a
30	chr1:188826889-188826939	NB4	blood:	n/a
31	chr1:188826823-188826873	MCF-7	breast:	n/a
32	chr1:188826823-188826873	PFSK-1	brain:	n/a
33	chr1:188826889-188826939	MCF10A-Er-Src	breast:	n/a
34	chr1:188826889-188826939	SK-N-SH	brain:	n/a
35	chr1:188826889-188826939	HEEpiC	esophagus:	n/a
36	chr1:188826823-188826873	HRCEpiC	kidney:	n/a
37	chr1:188826889-188826939	SKMC	muscle:	n/a
38	chr1:188826889-188826939	AG09309	skin:	n/a
39	chr1:188826823-188826873	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:188826889-188826939	NH-A	brain:	n/a
41	chr1:188826889-188826939	HCF	heart:	n/a
42	chr1:188826823-188826873	AoSMC	blood vessel:	n/a
43	chr1:188826823-188826873	ProgFib	skin:	n/a
44	chr1:188826823-188826873	HCM	heart:	n/a
45	chr1:188826823-188826873	HEK293	kidney:	embryo
46	chr1:188826823-188826873	PrEC	prostate:	n/a
47	chr1:188826823-188826873	SK-N-MC	brain:	n/a
48	chr1:188826823-188826873	HRE	kidney:	n/a
49	chr1:188826889-188826939	BJ	skin:	n/a
50	chr1:188826889-188826939	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:189078335..189080710-chr1:189084849..189087799,2	K562	blood:
2	chr1:188733061..188735226-chr1:188736574..188738238,2	K562	blood:
3	chr1:188762438..188765055-chr1:189455240..189458166,2	MCF-7	breast:
4	chr1:188899689..188901909-chr1:188904686..188906688,2	K562	blood:
5	chr1:189032912..189034690-chr1:189118689..189120245,2	K562	blood:
6	chr1:188846061..188848491-chr1:188851171..188853585,2	MCF-7	breast:
7	chr1:189118758..189120623-chr1:189121928..189123602,2	MCF-7	breast:
8	chr1:189009261..189011290-chr1:189013451..189014951,2	K562	blood:
9	chr1:189174928..189177287-chr1:189180109..189182692,2	K562	blood:
10	chr1:189027854..189030529-chr1:189039062..189041811,2	K562	blood:
11	chr1:188917480..188919329-chr1:188920804..188923130,2	MCF-7	breast:
12	chr1:189103992..189106373-chr1:189109756..189111271,2	MCF-7	breast:
13	chr1:188896826..188898736-chr1:188903150..188906844,3	MCF-7	breast:
14	chr1:188773169..188775117-chr1:188777054..188779991,2	K562	blood:
15	chr1:188751121..188751789-chr1:188907053..188907934,3	MCF-7	breast:
16	chr1:189110161..189112248-chr17:56736351..56738349,2	MCF-7	breast:
17	chr1:189067488..189069433-chr1:189071978..189073549,2	K562	blood:
18	chr1:188753407..188755924-chr1:188760366..188763242,2	K562	blood:
19	chr1:188788862..188791265-chr1:188817309..188819818,2	MCF-7	breast:
20	chr1:189129002..189131397-chr1:189134322..189136351,2	K562	blood:
21	chr1:189027854..189030529-chr1:189039062..189041811,2	K562	blood:
22	chr1:188866159..188868933-chr1:188870871..188872423,2	MCF-7	breast:
23	chr1:189116028..189120237-chr1:189160506..189163276,3	K562	blood:
24	chr1:189118996..189121109-chr1:189287929..189290792,2	K562	blood:
25	chr1:189167872..189169675-chr1:189171676..189174219,2	K562	blood:
26	chr1:189009261..189011290-chr1:189013451..189014951,2	K562	blood:
27	chr1:188432976..188433772-chr1:189118543..189119245,2	MCF-7	breast:
28	chr1:189148880..189151522-chr1:189151849..189154466,3	K562	blood:
29	chr1:189117678..189120245-chr1:189847842..189850269,2	K562	blood:
30	chr1:189051136..189054044-chr1:189118022..189120373,2	K562	blood:
31	chr1:189117456..189122192-chr1:189126377..189132093,10	K562	blood:
32	chr1:189117897..189121261-chr1:189121594..189126238,14	K562	blood:
33	chr1:189129002..189131397-chr1:189134322..189136351,2	K562	blood:
34	chr1:189078335..189080710-chr1:189084849..189087799,2	K562	blood:
35	chr1:188636854..188637418-chr1:188751018..188751851,2	MCF-7	breast:
36	chr1:189170367..189172924-chr1:189189578..189192081,2	K562	blood:
37	chr1:189067488..189069433-chr1:189071978..189073549,2	K562	blood:
38	chr1:188753407..188755924-chr1:188760366..188763242,2	K562	blood:
39	chr1:189109069..189111895-chr1:189118017..189120459,2	K562	blood:
40	chr1:188789143..188792283-chr1:188793641..188795538,3	K562	blood:
41	chr1:189112586..189116347-chr1:189117211..189120686,6	K562	blood:
42	chr1:188866159..188868933-chr1:188870871..188872423,2	MCF-7	breast:
43	chr1:188917480..188919329-chr1:188920804..188923130,2	MCF-7	breast:
44	chr1:188975384..188977741-chr1:188982777..188984574,2	K562	blood:
45	chr1:189145733..189147839-chr1:189155751..189158462,2	K562	blood:
46	chr1:188751072..188751772-chr1:189118548..189119200,2	MCF-7	breast:
47	chr1:188975384..188977741-chr1:188982777..188984574,2	K562	blood:
48	chr1:189167872..189169675-chr1:189171676..189174219,2	K562	blood:
49	chr1:189055283..189057511-chr1:189118631..189120197,2	K562	blood:
50	chr1:188899689..188901909-chr1:188904686..188906688,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA2G4A-17	chr1:189027267-189027316	refGeneNc_416_NR_033922
2	lnc-PLA2G4A-17	chr1:188974191-188974263	refGeneNc_416_NR_033922
3	lnc-PLA2G4A-17	chr1:189029259-189029349	refGeneNc_416_NR_033922
4	lnc-FAM5C-2	chr1:188856372-188856565	XLOC_001129
5	lnc-PLA2G4A-6	chr1:188874819-188875057	ENSG00000226486
6	lnc-PLA2G4A-7	chr1:189119674-189119918	NONHSAT008484
7	lnc-PLA2G4A-7	chr1:189118917-189119007	XLOC_000502
8	lnc-PLA2G4A-6	chr1:189005849-189006393	ENSG00000226486
9	lnc-PLA2G4A-17	chr1:188860643-188860786	refGeneNc_416_NR_033922
10	lnc-PLA2G4A-7	chr1:189119673-189119860	XLOC_000502
11	lnc-FAM5C-14	chr1:189005092-189005575	NONHSAT008482
12	lnc-FAM5C-2	chr1:188838608-188838879	XLOC_001129
13	lnc-PLA2G4A-17	chr1:189035554-189037410	refGeneNc_416_NR_033922

Variant related genes	Relation type
LINC01035	TF binding region
ENSG00000226196	TF binding region
CLPTM1LP1	TF binding region
ENSG00000238054	TF binding region
LINC01035	CpG island
ENSG00000226196	CpG island
CLPTM1LP1	CpG island
ENSG00000238054	CpG island
ENSG00000204569	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000202077	chromatin interactions
KIAA0494	miRNA target sites

Extended variants
information (count: 4098 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4098 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs118131659	chr1:188732625-188732626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546470808	chr1:188732647-188732648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116969326	chr1:188732657-188732658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142767023	chr1:188732663-188732664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559006961	chr1:188732708-188732709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs61066485	chr1:188732732-188732733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185856464	chr1:188732753-188732754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555259181	chr1:188732766-188732767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540997123	chr1:188732769-188732770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575020703	chr1:188732798-188732799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369826581	chr1:188732802-188732803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559584788	chr1:188732833-188732834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540870080	chr1:188732836-188732837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144943575	chr1:188732870-188732871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138807029	chr1:188732915-188732916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74758398	chr1:188732934-188732935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564561352	chr1:188732953-188732954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530379603	chr1:188732989-188732990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35413612	chr1:188734406-188734407	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs556338235	chr1:188734428-188734429	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs575027914	chr1:188734430-188734431	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs34865281	chr1:188734440-188734441	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192502574	chr1:188734442-188734443	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs574302221	chr1:188734451-188734452	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540530551	chr1:188734505-188734506	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs61578419	chr1:188734509-188734510	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs184856027	chr1:188734520-188734521	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs150804591	chr1:188734592-188734593	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs12071850	chr1:188734594-188734595	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs10922268	chr1:188734621-188734622	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4430332	chr1:188734625-188734626	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs73055076	chr1:188734700-188734701	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs568445532	chr1:188734701-188734702	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs199693366	chr1:188734749-188734750	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs527649156	chr1:188734758-188734759	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs547763305	chr1:188734780-188734781	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs570859500	chr1:188734830-188734831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187051536	chr1:188734897-188734898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4845308	chr1:188734908-188734909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569885333	chr1:188734936-188734937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537946242	chr1:188734945-188734946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554324558	chr1:188735021-188735022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191902773	chr1:188735025-188735026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184420041	chr1:188735050-188735051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553780664	chr1:188735064-188735065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577246779	chr1:188735068-188735069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563246604	chr1:188735074-188735075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546086711	chr1:188735122-188735123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562695659	chr1:188735166-188735167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76324070	chr1:188735200-188735201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:188732600-188733000	Enhancers	Hela-S3	cervix
2	chr1:188734400-188734800	Active TSS	Primary T killer memory cells from peripheral blood	blood
3	chr1:188734800-188738200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:188738000-188738400	Enhancers	H1 Cell Line	embryonic stem cell
5	chr1:188738000-188738800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:188738000-188739000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:188738200-188738400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:188738200-188738400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr1:188738200-188738800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:188738200-188739200	Enhancers	Placenta	Placenta
11	chr1:188742000-188742200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:188742200-188745000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:188744600-188745000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:188745000-188745400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:188749000-188749400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:188751400-188751600	Enhancers	Aorta	Aorta
17	chr1:188769000-188769600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:188769000-188769800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:188791000-188791400	Active TSS	Fetal Muscle Leg	muscle
20	chr1:188791200-188792000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:188791200-188792200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:188791400-188791600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:188791400-188791800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:188791400-188791800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr1:188791400-188791800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr1:188791400-188791800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:188791400-188792000	Enhancers	Fetal Muscle Leg	muscle
28	chr1:188791600-188792000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr1:188791800-188793200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr1:188793200-188793600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:188793400-188793800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:188812200-188812600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr1:188812200-188813000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr1:188812400-188813000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:188812800-188813000	Enhancers	Pancreas	Pancrea
36	chr1:188813000-188815600	Weak transcription	Pancreas	Pancrea
37	chr1:188815600-188816000	ZNF genes & repeats	Pancreas	Pancrea
38	chr1:188815800-188816000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:188819600-188820400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr1:188820400-188821400	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr1:188820600-188820800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr1:188823800-188824200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:188823800-188824600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:188824200-188824600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:188826600-188826800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr1:188826600-188827000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:188826600-188827200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:188826800-188827000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr1:188827000-188827200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:188835000-188835400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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