Variant report

Variant	esv3397896
Chromosome Location	chr3:141120287-141122835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:141120698-141120886	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr3:141120953-141121746	GM12878	blood:	n/a	chr3:141121210-141121223 chr3:141121034-141121047 chr3:141121423-141121432 chr3:141120953-141120966 chr3:141121027-141121040 chr3:141121096-141121109 chr3:141121033-141121042 chr3:141121173-141121186
3	BCLAF1	chr3:141120656-141121228	GM12878	blood:	n/a	chr3:141121210-141121223 chr3:141121034-141121047 chr3:141120953-141120966 chr3:141121027-141121040 chr3:141121096-141121109 chr3:141121033-141121042 chr3:141121173-141121186
4	BCLAF1	chr3:141121325-141122127	GM12878	blood:	n/a	chr3:141121956-141121965 chr3:141121423-141121432
5	BHLHE40	chr3:141120917-141123230	GM12878	blood:	n/a	chr3:141121087-141121103
6	BRCA1	chr3:141121434-141121598	HepG2	liver:	n/a	n/a
7	BRCA1	chr3:141121112-141121118	HepG2	liver:	n/a	n/a
8	CEBPB	chr3:141121627-141121882	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:141121452-141121937	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:141121613-141121847	A549	lung:	n/a	n/a
11	CEBPB	chr3:141121615-141121932	IMR90	lung:	n/a	n/a
12	CEBPD	chr3:141121051-141121304	HepG2	liver:	n/a	n/a
13	CHD1	chr3:141120719-141120911	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr3:141120680-141123252	GM12878	blood:	n/a	n/a
15	CHD1	chr3:141121429-141121460	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr3:141119815-141123440	IMR90	lung:	n/a	n/a
17	CHD2	chr3:141120813-141121041	GM12878	blood:	n/a	n/a
18	CHD2	chr3:141121644-141121883	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr3:141121422-141122036	GM12878	blood:	n/a	n/a
20	CHD2	chr3:141120943-141121350	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr3:141121417-141121538	HepG2	liver:	n/a	n/a
22	CHD2	chr3:141120615-141120920	HepG2	liver:	n/a	n/a
23	CREB1	chr3:141120725-141121730	A549	lung:	n/a	n/a
24	CTBP2	chr3:141120800-141121820	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:141121720-141121870	GM12864	blood:	n/a	chr3:141121819-141121828
26	CTCF	chr3:141121306-141121781	H1-hESC	embryonic stem cell:	n/a	chr3:141121488-141121501
27	CTCF	chr3:141121780-141121930	GM12864	blood:	n/a	chr3:141121819-141121828
28	CTCF	chr3:141121740-141121890	GM12873	blood:	n/a	chr3:141121819-141121828
29	CTCF	chr3:141121740-141121890	GM12869	blood:	n/a	chr3:141121819-141121828
30	CTCF	chr3:141121760-141121910	GM12878	blood:	n/a	chr3:141121819-141121828
31	CTCF	chr3:141121700-141121850	AG10803	skin:	n/a	chr3:141121819-141121828
32	CTCF	chr3:141121660-141121810	GM12874	blood:	n/a	n/a
33	CTCF	chr3:141121720-141121870	AG04449	skin:	n/a	chr3:141121819-141121828
34	CTCF	chr3:141121760-141121910	GM12868	blood:	n/a	chr3:141121819-141121828
35	CTCF	chr3:141120400-141120550	HMEC	breast:	n/a	n/a
36	CTCF	chr3:141121700-141121850	GM12878	blood:	n/a	chr3:141121819-141121828
37	CTCF	chr3:141120460-141120610	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr3:141121620-141121770	GM12865	blood:	n/a	n/a
39	CTCF	chr3:141120520-141120670	AG04449	skin:	n/a	n/a
40	CTCF	chr3:141120520-141120670	Caco-2	colon:	n/a	n/a
41	CTCF	chr3:141121740-141121890	AG04450	lung:	n/a	chr3:141121819-141121828
42	CTCF	chr3:141121720-141121870	AG10803	skin:	n/a	chr3:141121819-141121828
43	CTCF	chr3:141121680-141121830	HA-sp	spinal cord:	n/a	chr3:141121819-141121828
44	CTCF	chr3:141120480-141120630	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr3:141121440-141121590	GM12867	blood:	n/a	chr3:141121488-141121501
46	CTCF	chr3:141120480-141120630	HMEC	breast:	n/a	n/a
47	CTCF	chr3:141121840-141121990	GM12866	blood:	n/a	n/a
48	CTCF	chr3:141122800-141122950	NB4	blood:	n/a	n/a
49	CTCF	chr3:141121400-141121550	GM12866	blood:	n/a	chr3:141121488-141121501
50	CTCF	chr3:141120620-141120770	HMEC	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141121016-141121066	Hepatocyte	liver:	n/a
2	chr3:141122632-141122682	HL-60	blood:	n/a
3	chr3:141122632-141122682	NHDF-neo	bronchial:	n/a
4	chr3:141121677-141121727	CMK	blood:	n/a
5	chr3:141121417-141121467	RPTEC	kidney:	n/a
6	chr3:141121897-141121947	IMR90	lung:	fetal
7	chr3:141120919-141120969	H1-hESC	embryonic stem cell:	embryo
8	chr3:141121417-141121467	SKMC	muscle:	n/a
9	chr3:141121417-141121467	T-47D	breast:	n/a
10	chr3:141121677-141121727	NB4	blood:	n/a
11	chr3:141121417-141121467	SAEC	small airway:	n/a
12	chr3:141121677-141121727	GM12892	blood:	n/a
13	chr3:141120919-141120969	SK-N-MC	brain:	n/a
14	chr3:141121677-141121727	GM06990	blood:	n/a
15	chr3:141122632-141122682	IMR90	lung:	fetal
16	chr3:141121897-141121947	AG04450	lung:	fetal
17	chr3:141121016-141121066	PFSK-1	brain:	n/a
18	chr3:141121897-141121947	U87	brain:	n/a
19	chr3:141121897-141121947	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:141121016-141121066	AoSMC	blood vessel:	n/a
21	chr3:141121897-141121947	HRPEpiC	eye:	n/a
22	chr3:141121016-141121066	AG04450	lung:	fetal
23	chr3:141121677-141121727	HCM	heart:	n/a
24	chr3:141121897-141121947	ovcar-3	ovarian:	n/a
25	chr3:141120919-141120969	GM12891	blood:	n/a
26	chr3:141121897-141121947	AG09319	gingival:	n/a
27	chr3:141121417-141121467	HRE	kidney:	n/a
28	chr3:141122632-141122682	ProgFib	skin:	n/a
29	chr3:141121897-141121947	HCF	heart:	n/a
30	chr3:141121417-141121467	MCF-7	breast:	n/a
31	chr3:141122632-141122682	U87	brain:	n/a
32	chr3:141121417-141121467	ProgFib	skin:	n/a
33	chr3:141121677-141121727	HMEC	breast:	n/a
34	chr3:141121897-141121947	NT2-D1	testis:	n/a
35	chr3:141121677-141121727	HAEpiC	amniotic membrane:	n/a
36	chr3:141121677-141121727	ovcar-3	ovarian:	n/a
37	chr3:141120919-141120969	HAEpiC	amniotic membrane:	n/a
38	chr3:141121897-141121947	BE2_C	brain:	n/a
39	chr3:141121897-141121947	PANC-1	pancreas:	n/a
40	chr3:141122632-141122682	HAEpiC	amniotic membrane:	n/a
41	chr3:141121677-141121727	NT2-D1	testis:	n/a
42	chr3:141121016-141121066	SAEC	small airway:	n/a
43	chr3:141121897-141121947	K562	blood:	n/a
44	chr3:141121417-141121467	HEK293	kidney:	embryo
45	chr3:141121677-141121727	HEK293	kidney:	embryo
46	chr3:141121677-141121727	Hepatocyte	liver:	n/a
47	chr3:141121897-141121947	T-47D	breast:	n/a
48	chr3:141120919-141120969	HCM	heart:	n/a
49	chr3:141121897-141121947	HIPEpiC	eye:	n/a
50	chr3:141121417-141121467	NT2-D1	testis:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:141084785..141090037-chr3:141119214..141123075,16	MCF-7	breast:
2	chr3:141110266..141112911-chr3:141118799..141121045,2	K562	blood:
3	chr3:141106008..141109150-chr3:141119369..141122507,3	MCF-7	breast:
4	chr3:141103343..141105459-chr3:141119625..141122357,2	MCF-7	breast:
5	chr3:141086056..141088881-chr3:141120759..141122855,2	K562	blood:
6	chr3:141115976..141119088-chr3:141122527..141125160,3	MCF-7	breast:
7	chr3:141122791..141124629-chr3:141128045..141130082,2	K562	blood:
8	chr3:141085384..141087888-chr3:141119776..141122327,3	MCF-7	breast:
9	chr3:141120069..141122089-chr3:141143062..141145117,2	MCF-7	breast:
10	chr22:32145985..32146538-chr3:141121041..141121604,2	HCT-116	colon:
11	chr3:141110266..141112261-chr3:141118799..141120629,2	K562	blood:
12	chr3:141091574..141093729-chr3:141119134..141120872,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACPL2-3	chr3:141122769-141122873	NONHSAT092428
2	lnc-ACPL2-3	chr3:141122769-141122858	NONHSAT092432
3	lnc-ACPL2-3	chr3:141122769-141122848	NONHSAT092431

No data

Variant related genes	Relation type
ZBTB38	TF binding region
ZBTB38	CpG island
ENSG00000177311	chromatin interactions
ENSG00000183530	chromatin interactions
ENSG00000249417	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566470423	chr3:141120383-141120384	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs527290989	chr3:141120419-141120420	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs10935429	chr3:141120453-141120454	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs397694094	chr3:141120467-141120468	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs201166975	chr3:141120468-141120469	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs200539876	chr3:141120470-141120471	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs73872712	chr3:141120481-141120482	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191290933	chr3:141120550-141120551	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs73872713	chr3:141120591-141120592	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571160078	chr3:141120592-141120593	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs543966854	chr3:141120683-141120684	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs562666096	chr3:141120684-141120685	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs530163329	chr3:141120772-141120773	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs574811617	chr3:141120835-141120836	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs139444224	chr3:141120893-141120894	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs527685896	chr3:141120898-141120899	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs552600936	chr3:141120969-141120970	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs144222867	chr3:141120996-141120997	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs538458915	chr3:141121002-141121003	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs550423959	chr3:141121011-141121012	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs9871858	chr3:141121041-141121042	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs568652489	chr3:141121136-141121137	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs536390500	chr3:141121224-141121225	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs554642633	chr3:141121294-141121295	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs531972730	chr3:141121324-141121325	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs370968468	chr3:141121325-141121326	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs566347840	chr3:141121330-141121331	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs184258346	chr3:141121336-141121337	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs550094177	chr3:141121341-141121342	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs112469434	chr3:141121352-141121353	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs533740191	chr3:141121379-141121380	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs558592941	chr3:141121434-141121435	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs147365702	chr3:141121493-141121494	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs193165206	chr3:141121504-141121505	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs555975162	chr3:141121525-141121526	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs117589471	chr3:141121557-141121558	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs542007921	chr3:141121592-141121593	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs139565641	chr3:141121740-141121741	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs527697710	chr3:141121742-141121743	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546146918	chr3:141121780-141121781	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564300217	chr3:141121804-141121805	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2871960	chr3:141121814-141121815	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs550484261	chr3:141121828-141121829	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs115219969	chr3:141121855-141121856	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs529461471	chr3:141121872-141121873	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547988390	chr3:141121892-141121893	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs80058072	chr3:141121898-141121899	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538015717	chr3:141121904-141121905	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568607284	chr3:141121913-141121914	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201369692	chr3:141121914-141121915	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141111600-141120800	Weak transcription	Gastric	stomach
2	chr3:141112600-141120400	Weak transcription	Fetal Stomach	stomach
3	chr3:141112600-141120600	Weak transcription	Lung	lung
4	chr3:141112800-141120400	Weak transcription	Hela-S3	cervix
5	chr3:141112800-141120600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr3:141112800-141120600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr3:141112800-141120800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:141116000-141120600	Weak transcription	Right Ventricle	heart
9	chr3:141116200-141120600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:141116200-141120600	Weak transcription	Fetal Kidney	kidney
11	chr3:141116400-141120400	Weak transcription	HSMMtube	muscle
12	chr3:141116400-141120600	Weak transcription	Fetal Brain Female	brain
13	chr3:141116400-141120600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr3:141116400-141120800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr3:141116800-141120600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:141116800-141120600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:141116800-141120800	Weak transcription	Fetal Lung	lung
18	chr3:141116800-141121600	Weak transcription	Fetal Brain Male	brain
19	chr3:141116800-141122600	Weak transcription	K562	blood
20	chr3:141117000-141120600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:141117200-141120600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr3:141117200-141120800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:141117400-141120400	Weak transcription	NH-A	brain
24	chr3:141117400-141120600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:141117400-141120600	Enhancers	Fetal Intestine Small	intestine
26	chr3:141117800-141120400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:141117800-141120400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:141117800-141120400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr3:141117800-141120400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr3:141117800-141120600	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr3:141117800-141120600	Enhancers	NHDF-Ad	bronchial
32	chr3:141117800-141120600	Enhancers	NHLF	lung
33	chr3:141118000-141120600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:141118000-141120600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr3:141118200-141120400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr3:141118200-141120600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr3:141118200-141120600	Weak transcription	Primary hematopoietic stem cells	blood
38	chr3:141118200-141120600	Enhancers	Adipose Nuclei	Adipose
39	chr3:141118400-141120400	Weak transcription	Psoas Muscle	Psoas
40	chr3:141118400-141120400	Weak transcription	Right Atrium	heart
41	chr3:141118400-141120400	Enhancers	Stomach Smooth Muscle	stomach
42	chr3:141118400-141120600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr3:141118600-141120600	Enhancers	Fetal Intestine Large	intestine
44	chr3:141118600-141120800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr3:141118800-141120400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:141118800-141120600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr3:141118800-141120600	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr3:141118800-141120600	Weak transcription	Aorta	Aorta
49	chr3:141118800-141120600	Enhancers	Brain Hippocampus Middle	brain
50	chr3:141118800-141120600	Enhancers	Rectal Mucosa Donor 29	rectum

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