Variant report

Variant	nsv872262
Chromosome Location	chr1:146767353-146901677
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:695)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:146851502-146852003	K562	blood:	n/a	n/a
2	ARID3A	chr1:146861769-146862001	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:146848855-146850777	K562	blood:	n/a	n/a
4	ATF1	chr1:146856653-146856731	K562	blood:	n/a	n/a
5	ATF1	chr1:146848936-146850093	K562	blood:	n/a	n/a
6	ATF1	chr1:146851640-146852020	K562	blood:	n/a	n/a
7	ATF1	chr1:146838281-146838313	K562	blood:	n/a	n/a
8	ATF3	chr1:146851605-146852038	K562	blood:	n/a	n/a
9	BACH1	chr1:146848828-146849217	K562	blood:	n/a	n/a
10	BHLHE40	chr1:146848904-146849288	K562	blood:	n/a	n/a
11	BRCA1	chr1:146809453-146809605	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:146861769-146861997	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr1:146810425-146810519	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr1:146849314-146850084	K562	blood:	n/a	n/a
15	CCNT2	chr1:146851714-146851966	K562	blood:	n/a	n/a
16	CCNT2	chr1:146848949-146850069	K562	blood:	n/a	n/a
17	CEBPB	chr1:146776093-146776292	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:146851674-146852010	K562	blood:	n/a	n/a
19	CEBPB	chr1:146826701-146826897	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:146774059-146774335	K562	blood:	n/a	chr1:146774175-146774186
21	CEBPB	chr1:146861745-146862014	K562	blood:	n/a	n/a
22	CEBPB	chr1:146849583-146850143	K562	blood:	n/a	n/a
23	CEBPB	chr1:146849497-146850196	K562	blood:	n/a	n/a
24	CEBPB	chr1:146826798-146826887	K562	blood:	n/a	n/a
25	CEBPB	chr1:146851596-146852074	K562	blood:	n/a	n/a
26	CEBPB	chr1:146774017-146774358	HepG2	liver:	n/a	chr1:146774175-146774186
27	CEBPB	chr1:146801401-146801445	A549	lung:	n/a	n/a
28	CEBPB	chr1:146851405-146852071	K562	blood:	n/a	chr1:146851508-146851521 chr1:146851510-146851521
29	CEBPB	chr1:146861690-146862028	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:146849641-146849999	K562	blood:	n/a	n/a
31	CEBPB	chr1:146774011-146774354	IMR90	lung:	n/a	chr1:146774175-146774186
32	CEBPB	chr1:146792919-146793071	A549	lung:	n/a	n/a
33	CEBPB	chr1:146774158-146774237	H1-hESC	embryonic stem cell:	n/a	chr1:146774175-146774186
34	CEBPB	chr1:146774019-146774307	A549	lung:	n/a	chr1:146774175-146774186
35	CEBPB	chr1:146891751-146891948	A549	lung:	n/a	n/a
36	CEBPB	chr1:146891745-146891945	HepG2	liver:	n/a	n/a
37	CEBPD	chr1:146849391-146850045	K562	blood:	n/a	n/a
38	CEBPD	chr1:146851473-146852055	K562	blood:	n/a	n/a
39	CEBPD	chr1:146849479-146850128	K562	blood:	n/a	n/a
40	CEBPD	chr1:146851557-146852128	K562	blood:	n/a	n/a
41	CHD1	chr1:146808199-146808588	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr1:146808807-146809266	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr1:146776706-146776779	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr1:146775472-146775477	HepG2	liver:	n/a	n/a
45	CHD2	chr1:146774219-146774483	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr1:146773328-146773534	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr1:146786721-146786945	K562	blood:	n/a	n/a
48	CTCF	chr1:146861698-146862007	Medullo	brain:	n/a	n/a
49	CTCF	chr1:146861663-146862000	K562	blood:	n/a	n/a
50	CTCF	chr1:146860520-146860670	WERI-Rb-1	eye:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146807706-146807756	SK-N-MC	brain:	n/a
2	chr1:146895247-146895297	Hela-S3	cervix:	n/a
3	chr1:146895247-146895297	MCF-7	breast:	n/a
4	chr1:146895247-146895297	SK-N-SH_RA	brain:	n/a
5	chr1:146807706-146807756	GM19239	blood:	n/a
6	chr1:146807706-146807756	NH-A	brain:	n/a
7	chr1:146807706-146807756	Caco-2	colon:	n/a
8	chr1:146895247-146895297	HMEC	breast:	n/a
9	chr1:146807706-146807756	AG09319	gingival:	n/a
10	chr1:146807706-146807756	U87	brain:	n/a
11	chr1:146807706-146807756	HCPEpiC	choroid plexus:	n/a
12	chr1:146807706-146807756	PFSK-1	brain:	n/a
13	chr1:146807706-146807756	GM12891	blood:	n/a
14	chr1:146895247-146895297	AG10803	skin:	n/a
15	chr1:146895247-146895297	PrEC	prostate:	n/a
16	chr1:146895247-146895297	LNCaP	prostate:	n/a
17	chr1:146807706-146807756	HCT-116	colon:	n/a
18	chr1:146895247-146895297	U87	brain:	n/a
19	chr1:146807706-146807756	T-47D	breast:	n/a
20	chr1:146895247-146895297	Hepatocyte	liver:	n/a
21	chr1:146807706-146807756	AoSMC	blood vessel:	n/a
22	chr1:146895247-146895297	PANC-1	pancreas:	n/a
23	chr1:146895247-146895297	GM19239	blood:	n/a
24	chr1:146807706-146807756	NHDF-neo	bronchial:	n/a
25	chr1:146895247-146895297	HCM	heart:	n/a
26	chr1:146895247-146895297	NB4	blood:	n/a
27	chr1:146807706-146807756	IMR90	lung:	fetal
28	chr1:146807706-146807756	NB4	blood:	n/a
29	chr1:146895247-146895297	HAEpiC	amniotic membrane:	n/a
30	chr1:146807706-146807756	SAEC	small airway:	n/a
31	chr1:146895247-146895297	HRE	kidney:	n/a
32	chr1:146895247-146895297	HCPEpiC	choroid plexus:	n/a
33	chr1:146807706-146807756	SK-N-SH_RA	brain:	n/a
34	chr1:146807706-146807756	BJ	skin:	n/a
35	chr1:146895247-146895297	GM12892	blood:	n/a
36	chr1:146895247-146895297	HL-60	blood:	n/a
37	chr1:146807706-146807756	HCM	heart:	n/a
38	chr1:146807706-146807756	Jurkat	blood:	n/a
39	chr1:146807706-146807756	HCF	heart:	n/a
40	chr1:146807706-146807756	AG04450	lung:	fetal
41	chr1:146807706-146807756	Hela-S3	cervix:	n/a
42	chr1:146807706-146807756	HRCEpiC	kidney:	n/a
43	chr1:146807706-146807756	HUVEC	blood vessel:	n/a
44	chr1:146807706-146807756	HNPCEpiC	eye:	n/a
45	chr1:146895247-146895297	AG09319	gingival:	n/a
46	chr1:146807706-146807756	Hepatocyte	liver:	n/a
47	chr1:146895247-146895297	HCT-116	colon:	n/a
48	chr1:146807706-146807756	LNCaP	prostate:	n/a
49	chr1:146807706-146807756	RPTEC	kidney:	n/a
50	chr1:146895247-146895297	SK-N-SH	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146763219..146764772-chr1:146768463..146770035,2	MCF-7	breast:
2	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
3	chr1:146829897..146832000-chr1:146834771..146837746,2	K562	blood:
4	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
5	chr1:146900267..146901994-chr1:146917876..146920490,2	MCF-7	breast:
6	chr1:146829897..146832000-chr1:146834771..146837746,2	K562	blood:
7	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
8	chr1:146553543..146556468-chr1:146848913..146851805,2	K562	blood:
9	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
10	chr1:146853507..146856418-chr1:146857817..146859989,2	MCF-7	breast:
11	chr1:146861647..146862210-chr1:146963967..146964711,2	MCF-7	breast:
12	chr1:146643870..146644650-chr1:146861592..146862107,2	MCF-7	breast:
13	chr1:146714335..146717266-chr1:146861810..146864638,2	K562	blood:
14	chr1:146745473..146746108-chr1:146861600..146862389,4	K562	blood:
15	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
16	chr1:146886806..146889082-chr1:146891750..146894750,3	K562	blood:
17	chr1:146851757..146854184-chr1:146855912..146857816,2	K562	blood:
18	chr1:146892606..146894867-chr1:146909100..146911293,2	MCF-7	breast:
19	chr1:146892685..146894306-chr1:146902333..146904733,2	K562	blood:
20	chr1:146889760..146891342-chr1:146892775..146894723,2	K562	blood:
21	chr1:146745161..146746194-chr1:146861354..146862246,9	MCF-7	breast:
22	chr1:146763180..146767980-chr1:146768468..146771849,4	MCF-7	breast:
23	chr1:146714725..146717432-chr1:146860214..146861781,2	MCF-7	breast:
24	chr1:146745103..146745868-chr1:146861342..146862193,4	MCF-7	breast:
25	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
26	chr1:146841177..146844214-chr1:146848195..146851017,3	K562	blood:
27	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
28	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
29	chr1:146785986..146788702-chr1:146789697..146791855,2	MCF-7	breast:
30	chr1:146763180..146767980-chr1:146768468..146771849,4	MCF-7	breast:
31	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
32	chr1:146857005..146859244-chr1:146860862..146863182,2	K562	blood:
33	chr1:146849091..146851989-chr1:146881100..146883319,2	K562	blood:
34	chr1:146899574..146902487-chr1:146902750..146904367,2	K562	blood:
35	chr1:146744019..146745756-chr1:146860547..146863397,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD1L-1	chr1:146767170-146767458	NONHSAT006031
2	lnc-ACP6-1	chr1:146880322-146880421	NONHSAT006008
3	lnc-ACP6-1	chr1:146856390-146856585	NONHSAT006008
4	lnc-ACP6-1	chr1:146880390-146880421	NONHSAT139896
5	lnc-ACP6-1	chr1:146853914-146856585	NONHSAT006032

No data

Variant related genes	Relation type
ENSG00000213226	TF binding region
OR13Z1P	TF binding region
ENSG00000207209	TF binding region
ENSG00000213226	CpG island
OR13Z1P	CpG island
ENSG00000207209	CpG island
ENSG00000237188	chromatin interactions
ENSG00000226653	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000131791	chromatin interactions
ENSG00000207209	chromatin interactions
ENSG00000213226	chromatin interactions
ENSG00000131778	chromatin interactions

Extended variants
information (count: 2480 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6538	chr1:146767353-146767354	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587774988	chr1:146767364-146767365	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs142513044	chr1:146767411-146767412	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs587741783	chr1:146767419-146767420	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs189028206	chr1:146767439-146767440	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs12566235	chr1:146767447-146767448	ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs3737850	chr1:146767486-146767487	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs41295831	chr1:146767490-146767491	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs3737849	chr1:146767494-146767495	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs189861246	chr1:146767514-146767515	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587739113	chr1:146767588-146767589	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587634689	chr1:146767662-146767663	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182128603	chr1:146767663-146767664	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587669443	chr1:146767718-146767719	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187093074	chr1:146767723-146767724	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587614799	chr1:146767752-146767753	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191544751	chr1:146767757-146767758	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587703335	chr1:146767766-146767767	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17356492	chr1:146767770-146767771	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs587650014	chr1:146767784-146767785	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146916443	chr1:146767814-146767815	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587774723	chr1:146767824-146767825	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115003388	chr1:146767829-146767830	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6659630	chr1:146767853-146767854	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs587752989	chr1:146767872-146767873	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587643065	chr1:146767886-146767887	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587706460	chr1:146767904-146767905	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11239968	chr1:146767908-146767909	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs587660980	chr1:146767950-146767951	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151323025	chr1:146767951-146767952	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587612850	chr1:146768002-146768003	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75021941	chr1:146768009-146768010	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140580817	chr1:146768027-146768028	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587620048	chr1:146768049-146768050	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587671833	chr1:146768053-146768054	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4284292	chr1:146768105-146768106	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs587651834	chr1:146768114-146768115	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376376168	chr1:146768126-146768127	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374421755	chr1:146768127-146768128	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150404328	chr1:146768138-146768139	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185326777	chr1:146768148-146768149	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587692550	chr1:146768158-146768159	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188183385	chr1:146768163-146768164	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587646550	chr1:146768172-146768173	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587676315	chr1:146768209-146768210	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587761685	chr1:146768255-146768256	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587658993	chr1:146768279-146768280	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587712552	chr1:146768284-146768285	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12407195	chr1:146768287-146768288	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs587635381	chr1:146768309-146768310	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:162)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146722800-146769800	Strong transcription	Dnd41	blood
2	chr1:146724200-146769800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr1:146726600-146769600	Strong transcription	Primary T helper cells PMA-I stimulated	--
4	chr1:146727000-146770000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:146727200-146767800	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:146727200-146770200	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr1:146727400-146767800	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:146727400-146767800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr1:146728200-146770800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:146729400-146769800	Strong transcription	Primary T cells from cord blood	blood
11	chr1:146733000-146770600	Strong transcription	HepG2	liver
12	chr1:146735600-146768600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr1:146735800-146769000	Strong transcription	Fetal Thymus	thymus
14	chr1:146736400-146770200	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr1:146742400-146767800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:146745200-146769400	Strong transcription	Fetal Muscle Trunk	muscle
17	chr1:146745600-146768200	Strong transcription	K562	blood
18	chr1:146746000-146769400	Strong transcription	Hela-S3	cervix
19	chr1:146746200-146770000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr1:146746200-146770000	Strong transcription	Brain Anterior Caudate	brain
21	chr1:146746400-146769400	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr1:146746400-146770000	Strong transcription	Stomach Smooth Muscle	stomach
23	chr1:146746600-146769800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr1:146746600-146770000	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr1:146746800-146769600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:146746800-146770000	Strong transcription	Duodenum Mucosa	Duodenum
27	chr1:146746800-146770000	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:146747000-146770000	Strong transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:146747600-146769000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr1:146749600-146769000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:146754800-146769600	Strong transcription	Left Ventricle	heart
32	chr1:146755200-146768400	Strong transcription	Fetal Muscle Leg	muscle
33	chr1:146755200-146769000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr1:146755200-146769600	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr1:146755400-146769400	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr1:146755400-146770800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:146755600-146768800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr1:146755600-146769000	Strong transcription	Fetal Intestine Large	intestine
39	chr1:146755600-146769600	Strong transcription	GM12878-XiMat	blood
40	chr1:146755600-146770000	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr1:146755800-146768400	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr1:146755800-146769000	Strong transcription	Brain Hippocampus Middle	brain
43	chr1:146755800-146770000	Strong transcription	Adipose Nuclei	Adipose
44	chr1:146755800-146770000	Strong transcription	Brain Substantia Nigra	brain
45	chr1:146755800-146770000	Strong transcription	Ovary	ovary
46	chr1:146756200-146769800	Strong transcription	Brain Angular Gyrus	brain
47	chr1:146756400-146769800	Strong transcription	Brain Cingulate Gyrus	brain
48	chr1:146756400-146770400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:146756800-146768400	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr1:146758400-146767800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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