Variant report

Variant	esv3450815
Chromosome Location	chr3:179370008-179372006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:489)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:683 , 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	chr3:179370296-179370931	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:179371257-179371483	HepG2	liver:	n/a	n/a
3	ATF2	chr3:179370284-179370675	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:179370117-179370590	GM12878	blood:	n/a	n/a
5	BACH1	chr3:179370421-179370859	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr3:179370991-179371483	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:179370265-179371702	GM12878	blood:	n/a	chr3:179371226-179371235 chr3:179370781-179370797 chr3:179370749-179370765
8	BHLHE40	chr3:179371159-179371433	HepG2	liver:	n/a	chr3:179371226-179371235
9	BHLHE40	chr3:179370427-179370742	HepG2	liver:	n/a	n/a
10	BHLHE40	chr3:179370984-179371521	HepG2	liver:	n/a	chr3:179371226-179371235
11	BHLHE40	chr3:179371075-179371392	A549	lung:	n/a	chr3:179371226-179371235
12	BHLHE40	chr3:179371011-179371553	K562	blood:	n/a	chr3:179371226-179371235
13	BRCA1	chr3:179370218-179370651	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr3:179370469-179370617	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr3:179370402-179370471	HepG2	liver:	n/a	n/a
16	BRCA1	chr3:179371251-179371419	GM12878	blood:	n/a	n/a
17	CBX3	chr3:179371014-179371557	K562	blood:	n/a	n/a
18	CCNT2	chr3:179371058-179371392	K562	blood:	n/a	n/a
19	CCNT2	chr3:179370419-179370836	K562	blood:	n/a	chr3:179370763-179370772
20	CEBPB	chr3:179371040-179372602	Hela-S3	cervix:	n/a	chr3:179372296-179372313
21	CEBPB	chr3:179371186-179371263	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr3:179371674-179371888	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:179370243-179370639	Hela-S3	cervix:	n/a	n/a
24	CEBPD	chr3:179370482-179370921	HepG2	liver:	n/a	n/a
25	CHD1	chr3:179371037-179371761	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr3:179372005-179372467	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr3:179370991-179371641	GM12878	blood:	n/a	n/a
28	CHD1	chr3:179370160-179370465	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr3:179369863-179372616	IMR90	lung:	n/a	n/a
30	CHD2	chr3:179370994-179371562	GM12878	blood:	n/a	n/a
31	CHD2	chr3:179370420-179370665	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:179371196-179371525	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr3:179370103-179371714	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr3:179371489-179371647	HepG2	liver:	n/a	n/a
35	CHD2	chr3:179370467-179370543	K562	blood:	n/a	n/a
36	CREB1	chr3:179370352-179370896	A549	lung:	n/a	chr3:179370465-179370478
37	CREB1	chr3:179370555-179370996	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr3:179370194-179371707	HepG2	liver:	n/a	chr3:179370465-179370478
39	CREB1	chr3:179370228-179370880	GM12878	blood:	n/a	chr3:179370465-179370478
40	CTCF	chr3:179370320-179370470	GM12868	blood:	n/a	n/a
41	CTCF	chr3:179371260-179371410	HPF	lung:	n/a	n/a
42	CTCF	chr3:179371180-179371330	BE2_C	brain:	n/a	n/a
43	CTCF	chr3:179370980-179371130	HMEC	breast:	n/a	n/a
44	CTCF	chr3:179370719-179370758	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr3:179371234-179371329	Gliobla	brain:	n/a	n/a
46	CTCF	chr3:179370340-179370490	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr3:179371194-179371293	GM13976	blood:	n/a	n/a
48	CTCF	chr3:179371200-179371350	HMEC	breast:	n/a	n/a
49	CTCF	chr3:179371180-179371393	GM19240	blood:	n/a	n/a
50	CTCF	chr3:179370683-179370803	A549	lung:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:179370779-179370829	HCM	heart:	n/a
2	chr3:179370779-179370829	HCM	heart:	n/a
3	chr3:179370420-179370470	Jurkat	blood:	n/a
4	chr3:179370420-179370470	CMK	blood:	n/a
5	chr3:179370824-179370874	AG04450	lung:	fetal
6	chr3:179370465-179370515	AoSMC	blood vessel:	n/a
7	chr3:179371114-179371164	AG09319	gingival:	n/a
8	chr3:179370465-179370515	PFSK-1	brain:	n/a
9	chr3:179371510-179371560	HCF	heart:	n/a
10	chr3:179370821-179370871	SKMC	muscle:	n/a
11	chr3:179370779-179370829	A549	lung:	n/a
12	chr3:179370821-179370871	ProgFib	skin:	n/a
13	chr3:179371510-179371560	SAEC	small airway:	n/a
14	chr3:179371510-179371560	HAEpiC	amniotic membrane:	n/a
15	chr3:179370471-179370521	IMR90	lung:	fetal
16	chr3:179370471-179370521	GM12878	blood:	n/a
17	chr3:179371510-179371560	GM19239	blood:	n/a
18	chr3:179370465-179370515	HCM	heart:	n/a
19	chr3:179371114-179371164	HMEC	breast:	n/a
20	chr3:179370821-179370871	SAEC	small airway:	n/a
21	chr3:179370824-179370874	AoSMC	blood vessel:	n/a
22	chr3:179370779-179370829	HCT-116	colon:	n/a
23	chr3:179370821-179370871	HRCEpiC	kidney:	n/a
24	chr3:179370471-179370521	LNCaP	prostate:	n/a
25	chr3:179370465-179370515	ProgFib	skin:	n/a
26	chr3:179370471-179370521	PFSK-1	brain:	n/a
27	chr3:179370779-179370829	Hela-S3	cervix:	n/a
28	chr3:179371114-179371164	BE2_C	brain:	n/a
29	chr3:179370821-179370871	HEK293	kidney:	embryo
30	chr3:179370824-179370874	MCF10A-Er-Src	breast:	n/a
31	chr3:179370471-179370521	HAEpiC	amniotic membrane:	n/a
32	chr3:179371510-179371560	AG10803	skin:	n/a
33	chr3:179370779-179370829	AG09319	gingival:	n/a
34	chr3:179370821-179370871	A549	lung:	n/a
35	chr3:179370821-179370871	MCF10A-Er-Src	breast:	n/a
36	chr3:179370420-179370470	SK-N-SH	brain:	n/a
37	chr3:179370824-179370874	RPTEC	kidney:	n/a
38	chr3:179370465-179370515	GM06990	blood:	n/a
39	chr3:179370779-179370829	H1-hESC	embryonic stem cell:	embryo
40	chr3:179370420-179370470	ProgFib	skin:	n/a
41	chr3:179371114-179371164	T-47D	breast:	n/a
42	chr3:179371510-179371560	Hela-S3	cervix:	n/a
43	chr3:179370471-179370521	HPAEpiC	pulmonary alveolar:	n/a
44	chr3:179370821-179370871	HCPEpiC	choroid plexus:	n/a
45	chr3:179371114-179371164	LNCaP	prostate:	n/a
46	chr3:179370465-179370515	MCF10A-Er-Src	breast:	n/a
47	chr3:179370779-179370829	ovcar-3	ovarian:	n/a
48	chr3:179371114-179371164	HRE	kidney:	n/a
49	chr3:179370420-179370470	HEK293	kidney:	embryo
50	chr3:179370465-179370515	Caco-2	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:179369074..179371005-chr9:91932390..91934959,2	MCF-7	breast:
2	chr3:172467247..172468788-chr3:179370430..179372469,2	MCF-7	breast:
3	chr3:179279862..179282588-chr3:179370567..179372088,2	MCF-7	breast:
4	chr3:179371770..179374007-chr3:179377040..179379599,2	K562	blood:
5	chr3:179368583..179370477-chr3:179391121..179393841,2	MCF-7	breast:
6	chr3:179279377..179281917-chr3:179370859..179372461,2	K562	blood:
7	chr3:179062475..179065895-chr3:179368714..179370965,3	MCF-7	breast:

No data

Variant related genes	Relation type
USP13	TF binding region
ENSG00000243977	TF binding region
USP13	CpG island
ENSG00000243977	CpG island
ENSG00000114346	chromatin interactions
ENSG00000171109	chromatin interactions
ENSG00000136518	chromatin interactions
ENSG00000187742	chromatin interactions

Extended variants
information (count: 89 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13065067	chr3:179370014-179370015	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs13085070	chr3:179370015-179370016	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs13085079	chr3:179370034-179370035	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs13085080	chr3:179370038-179370039	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs9870194	chr3:179370059-179370060	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs532726360	chr3:179370066-179370067	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs13085212	chr3:179370098-179370099	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs13065229	chr3:179370100-179370101	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs13085536	chr3:179370123-179370124	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs143410176	chr3:179370144-179370145	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs371070156	chr3:179370186-179370187	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs113570177	chr3:179370191-179370192	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs538230358	chr3:179370201-179370202	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs183408353	chr3:179370263-179370264	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs113771858	chr3:179370288-179370289	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs201413474	chr3:179370298-179370299	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs9870283	chr3:179370310-179370311	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs534010876	chr3:179370364-179370365	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs553654434	chr3:179370366-179370367	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs115713539	chr3:179370415-179370416	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs76743370	chr3:179370437-179370438	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs556038643	chr3:179370505-179370506	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs151200653	chr3:179370508-179370509	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs187756168	chr3:179370521-179370522	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs9871045	chr3:179370599-179370600	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs561826326	chr3:179370643-179370644	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs369895968	chr3:179370649-179370650	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs527370183	chr3:179370720-179370721	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs541103197	chr3:179370725-179370726	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs560550942	chr3:179370780-179370781	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs111460997	chr3:179370907-179370908	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs532749978	chr3:179370921-179370922	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs572746005	chr3:179370942-179370943	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs552944493	chr3:179370958-179370959	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs569528329	chr3:179370967-179370968	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs370443197	chr3:179370995-179370996	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs200016596	chr3:179371008-179371009	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs374896625	chr3:179371024-179371025	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs368406240	chr3:179371029-179371030	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs193177026	chr3:179371049-179371050	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs534070013	chr3:179371054-179371055	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs373833022	chr3:179371074-179371075	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs144481641	chr3:179371088-179371089	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs147844491	chr3:179371108-179371109	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs372813389	chr3:179371142-179371143	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs2276803	chr3:179371154-179371155	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs376341612	chr3:179371177-179371178	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs570604627	chr3:179371181-179371182	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs202069129	chr3:179371182-179371183	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs368463855	chr3:179371195-179371196	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	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
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Esophageal squamous carcinoma	17470683	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179367800-179370200	Weak transcription	Placenta	Placenta
2	chr3:179369600-179370400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:179369600-179372400	Active TSS	NHDF-Ad	bronchial
4	chr3:179369600-179372600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr3:179369800-179370200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:179369800-179370200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr3:179369800-179370200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
8	chr3:179369800-179370200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr3:179369800-179370200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr3:179369800-179370200	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:179369800-179370200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:179369800-179370200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
13	chr3:179369800-179370200	Flanking Active TSS	Brain Anterior Caudate	brain
14	chr3:179369800-179370200	Flanking Active TSS	Brain Germinal Matrix	brain
15	chr3:179369800-179370200	Bivalent Enhancer	Fetal Thymus	thymus
16	chr3:179369800-179370200	Flanking Active TSS	A549	lung
17	chr3:179369800-179370200	Flanking Active TSS	GM12878-XiMat	blood
18	chr3:179369800-179370200	Flanking Active TSS	NH-A	brain
19	chr3:179369800-179370200	Flanking Active TSS	NHLF	lung
20	chr3:179369800-179370200	Flanking Active TSS	Osteobl	bone
21	chr3:179369800-179370400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:179369800-179370400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr3:179369800-179370400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:179369800-179370400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:179369800-179370400	Flanking Active TSS	Dnd41	blood
26	chr3:179369800-179370400	Flanking Active TSS	NHEK	skin
27	chr3:179369800-179370600	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr3:179369800-179370600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr3:179369800-179371800	Active TSS	Brain Cingulate Gyrus	brain
30	chr3:179369800-179372000	Active TSS	Stomach Smooth Muscle	stomach
31	chr3:179369800-179372200	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr3:179369800-179372200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:179369800-179372200	Active TSS	Fetal Brain Female	brain
34	chr3:179369800-179372400	Active TSS	H1 Cell Line	embryonic stem cell
35	chr3:179369800-179372400	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr3:179369800-179372400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr3:179369800-179372400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:179369800-179372400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:179369800-179372600	Active TSS	HSMMtube	muscle
40	chr3:179370000-179370200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
41	chr3:179370000-179370200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
42	chr3:179370000-179370200	Enhancers	Primary B cells from peripheral blood	blood
43	chr3:179370000-179370200	Enhancers	Primary T cells fromperipheralblood	blood
44	chr3:179370000-179370200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr3:179370000-179370200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:179370000-179370200	Enhancers	Colon Smooth Muscle	Colon
47	chr3:179370000-179370200	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr3:179370000-179370200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr3:179370000-179370200	Bivalent Enhancer	Fetal Intestine Large	intestine
50	chr3:179370000-179370200	Active TSS	Fetal Muscle Leg	muscle

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