Variant report

Variant	esv3373675
Chromosome Location	chr1:10489565-10491863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:751)
CpG islands
(count:854)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10490317-10490659	K562	blood:	n/a	n/a
2	ARID3A	chr1:10490879-10490979	K562	blood:	n/a	n/a
3	ARID3A	chr1:10490255-10490607	HepG2	liver:	n/a	n/a
4	ATF2	chr1:10490050-10491090	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:10490282-10490712	GM12878	blood:	n/a	n/a
6	ATF2	chr1:10490155-10491320	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:10490203-10491114	GM12878	blood:	n/a	n/a
8	ATF3	chr1:10490192-10490693	A549	lung:	n/a	n/a
9	ATF3	chr1:10490184-10490591	K562	blood:	n/a	n/a
10	ATF3	chr1:10490272-10490947	A549	lung:	n/a	n/a
11	ATF3	chr1:10490604-10490917	K562	blood:	n/a	n/a
12	BACH1	chr1:10490297-10490653	K562	blood:	n/a	n/a
13	BACH1	chr1:10490911-10490917	K562	blood:	n/a	n/a
14	BACH1	chr1:10490385-10490644	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:10490274-10490567	GM12878	blood:	n/a	n/a
16	BCL3	chr1:10490241-10490664	A549	lung:	n/a	n/a
17	BCLAF1	chr1:10490079-10490957	GM12878	blood:	n/a	chr1:10490694-10490707
18	BCLAF1	chr1:10490157-10490753	GM12878	blood:	n/a	chr1:10490694-10490707
19	BCLAF1	chr1:10490169-10490750	K562	blood:	n/a	chr1:10490694-10490707
20	BCLAF1	chr1:10490759-10491165	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:10490035-10491296	K562	blood:	n/a	chr1:10490694-10490710
22	BHLHE40	chr1:10490364-10490665	A549	lung:	n/a	n/a
23	BHLHE40	chr1:10490256-10490917	GM12878	blood:	n/a	chr1:10490694-10490710
24	BRCA1	chr1:10491201-10491451	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr1:10490198-10490589	HepG2	liver:	n/a	n/a
26	BRCA1	chr1:10490280-10490580	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr1:10490935-10491285	HepG2	liver:	n/a	n/a
28	BRCA1	chr1:10490084-10490605	GM12878	blood:	n/a	n/a
29	BRCA1	chr1:10490329-10490980	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr1:10490825-10491474	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr1:10490024-10491355	K562	blood:	n/a	n/a
32	CBX3	chr1:10490266-10490883	K562	blood:	n/a	n/a
33	CCNT2	chr1:10490212-10491004	K562	blood:	n/a	n/a
34	CEBPB	chr1:10490284-10490982	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:10490332-10491001	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:10490360-10490576	K562	blood:	n/a	n/a
37	CEBPB	chr1:10490312-10490495	HepG2	liver:	n/a	n/a
38	CEBPD	chr1:10490434-10491037	HepG2	liver:	n/a	n/a
39	CHD1	chr1:10490254-10491126	GM12878	blood:	n/a	n/a
40	CHD1	chr1:10490205-10490658	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:10490179-10491510	GM12878	blood:	n/a	n/a
42	CHD2	chr1:10490193-10490980	HepG2	liver:	n/a	n/a
43	CHD2	chr1:10490256-10491475	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr1:10491195-10491445	K562	blood:	n/a	n/a
45	CHD2	chr1:10490269-10491405	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr1:10491199-10491399	HepG2	liver:	n/a	n/a
47	CHD2	chr1:10490257-10490930	K562	blood:	n/a	n/a
48	CREB1	chr1:10490020-10491169	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr1:10489834-10491148	GM12878	blood:	n/a	n/a
50	CREB1	chr1:10490134-10490663	A549	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10490236-10490286	SK-N-SH_RA	brain:	n/a
2	chr1:10489962-10490012	NT2-D1	testis:	n/a
3	chr1:10490985-10491035	NHBE	bronchial:	n/a
4	chr1:10490496-10490546	GM19239	blood:	n/a
5	chr1:10490637-10490687	NH-A	brain:	n/a
6	chr1:10490236-10490286	A549	lung:	n/a
7	chr1:10490985-10491035	AG09309	skin:	n/a
8	chr1:10490667-10490717	HepG2	liver:	n/a
9	chr1:10490025-10490075	AG09309	skin:	n/a
10	chr1:10489962-10490012	Hela-S3	cervix:	n/a
11	chr1:10490043-10490093	HRCEpiC	kidney:	n/a
12	chr1:10490667-10490717	HEK293	kidney:	embryo
13	chr1:10490985-10491035	PANC-1	pancreas:	n/a
14	chr1:10490025-10490075	K562	blood:	n/a
15	chr1:10490124-10490174	GM12891	blood:	n/a
16	chr1:10489962-10490012	MCF-7	breast:	n/a
17	chr1:10490943-10490993	HRPEpiC	eye:	n/a
18	chr1:10490063-10490113	RPTEC	kidney:	n/a
19	chr1:10490637-10490687	HRPEpiC	eye:	n/a
20	chr1:10490124-10490174	SK-N-SH	brain:	n/a
21	chr1:10490025-10490075	HEEpiC	esophagus:	n/a
22	chr1:10490058-10490108	AoSMC	blood vessel:	n/a
23	chr1:10490667-10490717	RPTEC	kidney:	n/a
24	chr1:10490236-10490286	NH-A	brain:	n/a
25	chr1:10490637-10490687	AG04450	lung:	fetal
26	chr1:10489962-10490012	ovcar-3	ovarian:	n/a
27	chr1:10490637-10490687	AG09319	gingival:	n/a
28	chr1:10491304-10491354	SK-N-SH	brain:	n/a
29	chr1:10490344-10490394	AG04449	skin:	fetal
30	chr1:10491304-10491354	BJ	skin:	n/a
31	chr1:10490985-10491035	H1-hESC	embryonic stem cell:	embryo
32	chr1:10489962-10490012	A549	lung:	n/a
33	chr1:10490124-10490174	NHDF-neo	bronchial:	n/a
34	chr1:10491304-10491354	HAEpiC	amniotic membrane:	n/a
35	chr1:10490496-10490546	HIPEpiC	eye:	n/a
36	chr1:10490124-10490174	RPTEC	kidney:	n/a
37	chr1:10490058-10490108	HCF	heart:	n/a
38	chr1:10490667-10490717	HIPEpiC	eye:	n/a
39	chr1:10490124-10490174	AoSMC	blood vessel:	n/a
40	chr1:10490063-10490113	HRCEpiC	kidney:	n/a
41	chr1:10490344-10490394	Caco-2	colon:	n/a
42	chr1:10490943-10490993	AG09309	skin:	n/a
43	chr1:10490043-10490093	IMR90	lung:	fetal
44	chr1:10490236-10490286	PANC-1	pancreas:	n/a
45	chr1:10490236-10490286	RPTEC	kidney:	n/a
46	chr1:10489962-10490012	SK-N-SH_RA	brain:	n/a
47	chr1:10489962-10490012	AG10803	skin:	n/a
48	chr1:10490043-10490093	GM12891	blood:	n/a
49	chr1:10490058-10490108	HCT-116	colon:	n/a
50	chr1:10490985-10491035	NB4	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10473791..10476777-chr1:10490511..10492354,2	K562	blood:
2	chr1:10488008..10492443-chr1:10531123..10534892,8	K562	blood:
3	chr1:10457794..10460664-chr1:10487844..10492697,5	K562	blood:
4	chr1:10490607..10494447-chr1:10532445..10535163,5	K562	blood:
5	chr1:10488905..10491611-chr1:10518532..10520834,2	MCF-7	breast:
6	chr1:10483316..10484984-chr1:10487772..10489866,2	K562	blood:
7	chr1:10489448..10493967-chr1:10494423..10498103,7	K562	blood:
8	chr1:10002273..10004549-chr1:10490535..10492203,2	MCF-7	breast:
9	chr1:10457794..10461321-chr1:10487053..10491931,7	K562	blood:
10	chr1:10490864..10493248-chr1:10508230..10510272,2	K562	blood:
11	chr1:10489993..10493018-chr1:10531254..10535234,5	MCF-7	breast:
12	chr1:10490187..10490687-chr12:52449617..52450158,2	Hela-S3	cervix:
13	chr1:10457881..10459696-chr1:10491385..10493588,2	MCF-7	breast:
14	chr1:10475041..10475642-chr1:10489986..10490702,2	K562	blood:
15	chr1:10270585..10272249-chr1:10490197..10491890,2	K562	blood:
16	chr1:10490085..10492364-chr1:10508772..10511442,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DFFA-1	chr1:10489938-10490734	ENSG00000271989.1

No data

Variant related genes	Relation type
APITD1	TF binding region
ENSG00000271989	TF binding region
APITD1-CORT	TF binding region
APITD1	CpG island
ENSG00000271989	CpG island
APITD1-CORT	CpG island
ENSG00000054523	chromatin interactions
ENSG00000160049	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000142657	chromatin interactions
ENSG00000241563	chromatin interactions
ENSG00000162441	chromatin interactions
ENSG00000173614	chromatin interactions
ENSG00000203469	chromatin interactions
ENSG00000142655	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000228150	chromatin interactions

Extended variants
information (count: 98 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372041697	chr1:10489588-10489589	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs140868958	chr1:10489664-10489665	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs146197720	chr1:10489667-10489668	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs539801751	chr1:10489686-10489687	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs558203903	chr1:10489698-10489699	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs111900407	chr1:10489710-10489711	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs536757182	chr1:10489731-10489732	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs186647420	chr1:10489770-10489771	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs534177822	chr1:10489789-10489790	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs375156861	chr1:10489808-10489809	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs577002243	chr1:10489849-10489850	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs556000149	chr1:10489854-10489855	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs574246198	chr1:10489863-10489864	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs138957413	chr1:10489922-10489923	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs562542927	chr1:10489931-10489932	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs142802859	chr1:10489938-10489939	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
17	rs147415571	chr1:10489949-10489950	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
18	rs138764035	chr1:10489988-10489989	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
19	rs191293298	chr1:10489995-10489996	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
20	rs527586952	chr1:10489998-10489999	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
21	rs143993690	chr1:10489999-10490000	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
22	rs149377338	chr1:10490004-10490005	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
23	rs560762432	chr1:10490012-10490013	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
24	rs540845900	chr1:10490059-10490060	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
25	rs531373303	chr1:10490063-10490064	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
26	rs550688600	chr1:10490064-10490065	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
27	rs553265750	chr1:10490073-10490074	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
28	rs577882794	chr1:10490079-10490080	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs539492607	chr1:10490100-10490101	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
30	rs649101	chr1:10490111-10490112	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs566706183	chr1:10490130-10490131	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
32	rs144662034	chr1:10490211-10490212	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
33	rs554024579	chr1:10490245-10490246	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
34	rs556063628	chr1:10490270-10490271	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
35	rs34266391	chr1:10490282-10490283	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
36	rs649639	chr1:10490285-10490286	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148511711	chr1:10490350-10490351	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
38	rs200229439	chr1:10490383-10490384	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
39	rs556332764	chr1:10490385-10490386	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
40	rs552013045	chr1:10490387-10490388	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
41	rs545745253	chr1:10490436-10490437	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
42	rs544729355	chr1:10490475-10490476	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
43	rs553739349	chr1:10490518-10490519	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
44	rs116395144	chr1:10490522-10490523	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
45	rs661256	chr1:10490539-10490540	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs661272	chr1:10490550-10490551	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs570419369	chr1:10490633-10490634	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
48	rs372438339	chr1:10490636-10490637	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
49	rs547690900	chr1:10490655-10490656	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
50	rs371207642	chr1:10490683-10490684	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10460000-10490200	Weak transcription	Psoas Muscle	Psoas
2	chr1:10461200-10490000	Weak transcription	Right Atrium	heart
3	chr1:10468800-10489800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr1:10472000-10490000	Weak transcription	Stomach Mucosa	stomach
5	chr1:10475600-10489600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:10475800-10490000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:10477800-10490000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:10477800-10490000	Weak transcription	Fetal Heart	heart
9	chr1:10478200-10490000	Weak transcription	Fetal Brain Male	brain
10	chr1:10479800-10490200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:10480200-10490000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:10480200-10490000	Weak transcription	Pancreas	Pancrea
13	chr1:10480200-10490400	Weak transcription	Aorta	Aorta
14	chr1:10480400-10489600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr1:10480400-10489800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr1:10480400-10490000	Weak transcription	Colonic Mucosa	Colon
17	chr1:10480400-10490000	Weak transcription	Small Intestine	intestine
18	chr1:10480400-10490000	Weak transcription	NH-A	brain
19	chr1:10480600-10489600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr1:10480600-10489800	Weak transcription	Hela-S3	cervix
21	chr1:10480800-10489600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr1:10480800-10489600	Weak transcription	HUVEC	blood vessel
23	chr1:10480800-10490000	Weak transcription	Placenta	Placenta
24	chr1:10480800-10490200	Weak transcription	Left Ventricle	heart
25	chr1:10481000-10489600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr1:10481000-10489600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr1:10481000-10489800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr1:10481000-10490000	Weak transcription	Right Ventricle	heart
29	chr1:10481200-10489600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:10481200-10489800	Weak transcription	Osteobl	bone
31	chr1:10481200-10490000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr1:10481400-10490200	Weak transcription	Ovary	ovary
33	chr1:10481600-10489800	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr1:10481600-10489800	Weak transcription	HMEC	breast
35	chr1:10481600-10490000	Weak transcription	Gastric	stomach
36	chr1:10481600-10490000	Weak transcription	HSMM	muscle
37	chr1:10481800-10489600	Weak transcription	Primary T cells from cord blood	blood
38	chr1:10481800-10489800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:10481800-10489800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr1:10481800-10490000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr1:10481800-10490000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr1:10481800-10490000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:10481800-10490000	Weak transcription	HSMMtube	muscle
44	chr1:10482000-10489800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:10482000-10490000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr1:10482000-10490000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:10482000-10490000	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr1:10482000-10490000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:10482000-10490000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr1:10482000-10490000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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