Variant report

Variant	esv2753640
Chromosome Location	chr4:147538395-147641395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147558227-147558300	HepG2	liver:	n/a	n/a
2	ATF2	chr4:147558048-147558348	H1-hESC	embryonic stem cell:	n/a	chr4:147558317-147558331
3	BACH1	chr4:147554984-147555098	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:147558034-147558061	K562	blood:	n/a	n/a
5	CEBPB	chr4:147619350-147619516	K562	blood:	n/a	n/a
6	CEBPB	chr4:147596352-147596700	IMR90	lung:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
7	CEBPB	chr4:147595644-147595933	Hela-S3	cervix:	n/a	chr4:147595791-147595808 chr4:147595793-147595804 chr4:147595757-147595770 chr4:147595792-147595805
8	CEBPB	chr4:147619331-147619531	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:147596345-147596690	K562	blood:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
10	CEBPB	chr4:147610925-147611158	A549	lung:	n/a	chr4:147611067-147611078
11	CEBPB	chr4:147595663-147595937	IMR90	lung:	n/a	chr4:147595791-147595808 chr4:147595793-147595804 chr4:147595757-147595770 chr4:147595792-147595805
12	CEBPB	chr4:147610968-147611231	HepG2	liver:	n/a	chr4:147611067-147611078
13	CEBPB	chr4:147596427-147596671	H1-hESC	embryonic stem cell:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
14	CEBPB	chr4:147595673-147595958	HepG2	liver:	n/a	chr4:147595791-147595808 chr4:147595793-147595804 chr4:147595757-147595770 chr4:147595792-147595805
15	CEBPB	chr4:147596336-147596711	HepG2	liver:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
16	CEBPB	chr4:147596338-147596672	A549	lung:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
17	CHD1	chr4:147569671-147569802	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr4:147568761-147569083	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr4:147576502-147576844	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr4:147560154-147560352	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:147559720-147560281	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr4:147561612-147561851	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr4:147569561-147569855	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr4:147561608-147561962	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr4:147561500-147562057	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr4:147559162-147562308	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr4:147568407-147569909	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTBP2	chr4:147557997-147558703	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr4:147575952-147576857	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:147558200-147558470	HAc	cerebellar:	n/a	n/a
31	CTCF	chr4:147576380-147576530	HMF	breast:	n/a	chr4:147576397-147576410 chr4:147576398-147576408 chr4:147576418-147576431
32	CTCF	chr4:147548059-147548090	Lung_OC	lung:	n/a	n/a
33	CTCF	chr4:147558120-147558270	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr4:147558213-147558296	Gliobla	brain:	n/a	n/a
35	CTCF	chr4:147584595-147584605	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:147558213-147558270	K562	blood:	n/a	n/a
37	CTCF	chr4:147558220-147558370	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr4:147558182-147558286	A549	lung:	n/a	n/a
39	CTCF	chr4:147558160-147558310	HPF	lung:	n/a	n/a
40	CTCF	chr4:147558160-147558310	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr4:147584583-147584584	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:147558174-147558329	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:147558340-147558490	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr4:147576369-147576536	ProgFib	skin:	n/a	chr4:147576397-147576410 chr4:147576398-147576408 chr4:147576418-147576431
45	CTCF	chr4:147558100-147558250	AG09319	gingival:	n/a	n/a
46	CTCF	chr4:147558160-147558310	AG10803	skin:	n/a	n/a
47	CTCF	chr4:147558160-147558310	HCM	heart:	n/a	n/a
48	CTCF	chr4:147568786-147568883	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:147576260-147576410	GM12875	blood:	n/a	chr4:147576397-147576410 chr4:147576398-147576408
50	CTCF	chr4:147558180-147558330	NHLF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147579200-147579250	CMK	blood:	n/a
2	chr4:147557774-147557824	AG10803	skin:	n/a
3	chr4:147554527-147554577	HepG2	liver:	n/a
4	chr4:147579200-147579250	CMK	blood:	n/a
5	chr4:147557774-147557824	AG10803	skin:	n/a
6	chr4:147554527-147554577	HepG2	liver:	n/a
7	chr4:147561203-147561253	GM19239	blood:	n/a
8	chr4:147568715-147568765	GM06990	blood:	n/a
9	chr4:147560770-147560820	HCM	heart:	n/a
10	chr4:147569185-147569235	HNPCEpiC	eye:	n/a
11	chr4:147559648-147559698	A549	lung:	n/a
12	chr4:147560770-147560820	BE2_C	brain:	n/a
13	chr4:147554527-147554577	NB4	blood:	n/a
14	chr4:147568715-147568765	MCF10A-Er-Src	breast:	n/a
15	chr4:147558435-147558485	NB4	blood:	n/a
16	chr4:147560286-147560336	HAEpiC	amniotic membrane:	n/a
17	chr4:147576547-147576597	SK-N-MC	brain:	n/a
18	chr4:147559423-147559473	HNPCEpiC	eye:	n/a
19	chr4:147556288-147556338	ProgFib	skin:	n/a
20	chr4:147576227-147576277	NB4	blood:	n/a
21	chr4:147559423-147559473	AG09319	gingival:	n/a
22	chr4:147561775-147561825	SKMC	muscle:	n/a
23	chr4:147560126-147560176	MCF-7	breast:	n/a
24	chr4:147554210-147554260	NHDF-neo	bronchial:	n/a
25	chr4:147558239-147558289	HCT-116	colon:	n/a
26	chr4:147561203-147561253	SK-N-MC	brain:	n/a
27	chr4:147576227-147576277	Caco-2	colon:	n/a
28	chr4:147575999-147576049	SAEC	small airway:	n/a
29	chr4:147575999-147576049	GM12878	blood:	n/a
30	chr4:147561900-147561950	CMK	blood:	n/a
31	chr4:147554144-147554194	AG04449	skin:	fetal
32	chr4:147558435-147558485	H1-hESC	embryonic stem cell:	embryo
33	chr4:147558089-147558139	GM19239	blood:	n/a
34	chr4:147561339-147561389	NB4	blood:	n/a
35	chr4:147558435-147558485	HAEpiC	amniotic membrane:	n/a
36	chr4:147559579-147559629	ECC-1	luminal epithelium:	n/a
37	chr4:147573410-147573460	PrEC	prostate:	n/a
38	chr4:147576227-147576277	HCF	heart:	n/a
39	chr4:147558544-147558594	LNCaP	prostate:	n/a
40	chr4:147561669-147561719	MCF10A-Er-Src	breast:	n/a
41	chr4:147558544-147558594	GM12878	blood:	n/a
42	chr4:147560282-147560332	SK-N-MC	brain:	n/a
43	chr4:147561669-147561719	NHDF-neo	bronchial:	n/a
44	chr4:147577630-147577680	HNPCEpiC	eye:	n/a
45	chr4:147558239-147558289	ECC-1	luminal epithelium:	n/a
46	chr4:147568715-147568765	CMK	blood:	n/a
47	chr4:147561775-147561825	HCF	heart:	n/a
48	chr4:147560282-147560332	AG10803	skin:	n/a
49	chr4:147557859-147557909	AG04449	skin:	fetal
50	chr4:147561339-147561389	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:147569383..147571342-chr4:147575306..147577219,2	MCF-7	breast:
2	chr4:147570143..147572498-chr4:147573319..147574831,2	K562	blood:
3	chr4:147569955..147572256-chr4:147575383..147578342,2	K562	blood:
4	chr4:147603707..147604442-chr5:15685536..15686251,2	MCF-7	breast:
5	chr4:147534574..147536794-chr4:147536840..147539665,2	MCF-7	breast:
6	chr4:147570143..147572498-chr4:147573319..147574831,2	K562	blood:
7	chr4:147569955..147572256-chr4:147575383..147578342,2	K562	blood:
8	chr4:147569383..147571342-chr4:147575306..147577219,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A7-3	chr4:147628637-147628703	NONHSAT098674
2	lnc-SLC10A7-3	chr4:147628339-147628340	NONHSAT098674

No.	miRNA target gene	miRNA name	Chromosome Location
1	POU4F2	hsa-miR-23a-3p	chr4:147562062-147562069
2	POU4F2	hsa-miR-23a-3p	chr4:147562049-147562069
3	POU4F2	hsa-miR-214-3p	chr4:147562560-147562581
4	POU4F2	hsa-miR-23a-3p	chr4:147562120-147562140
5	POU4F2	hsa-miR-23a-3p	chr4:147562409-147562430
6	POU4F2	hsa-miR-214-3p	chr4:147562574-147562580

Variant related genes	Relation type
POU4F2	TF binding region
ENSG00000264323	TF binding region
POU4F2	CpG island
ENSG00000264323	CpG island

Extended variants
information (count: 814 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10011145	chr4:147553803-147553804	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74938169	chr4:147553844-147553845	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs537692814	chr4:147553869-147553870	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs557159745	chr4:147553935-147553936	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs577295295	chr4:147553967-147553968	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs117928174	chr4:147553974-147553975	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs538309988	chr4:147553984-147553985	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs557134298	chr4:147553990-147553991	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs76834995	chr4:147554009-147554010	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs189155394	chr4:147554027-147554028	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs550817006	chr4:147554061-147554062	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs574281530	chr4:147554127-147554128	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs543634261	chr4:147554210-147554211	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs566397812	chr4:147554216-147554217	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs569100714	chr4:147554261-147554262	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs71593783	chr4:147554269-147554270	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs149281723	chr4:147554270-147554271	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs375858983	chr4:147554271-147554272	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs532251981	chr4:147554276-147554277	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs185574845	chr4:147554280-147554281	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs34844786	chr4:147554283-147554284	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs114258073	chr4:147554284-147554285	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs559395300	chr4:147554299-147554300	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs116441614	chr4:147554339-147554340	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs17021726	chr4:147554354-147554355	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs142031434	chr4:147554407-147554408	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs188765974	chr4:147554417-147554418	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs551176001	chr4:147554462-147554463	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs370773360	chr4:147554503-147554504	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566602247	chr4:147554560-147554561	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs77525277	chr4:147554561-147554562	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181367546	chr4:147554570-147554571	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs186697826	chr4:147554575-147554576	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs72956269	chr4:147554593-147554594	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540206632	chr4:147554606-147554607	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs535496043	chr4:147554636-147554637	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs10024327	chr4:147554684-147554685	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs372301597	chr4:147554714-147554715	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs574416745	chr4:147554715-147554716	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs543220994	chr4:147554738-147554739	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs182103735	chr4:147554748-147554749	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs576819182	chr4:147554765-147554766	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs187413906	chr4:147554839-147554840	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs559532073	chr4:147554841-147554842	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs150666739	chr4:147554905-147554906	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs367740540	chr4:147554998-147554999	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs116070384	chr4:147555014-147555015	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs531250525	chr4:147555020-147555021	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs112527580	chr4:147555023-147555024	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs190615351	chr4:147555038-147555039	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147553800-147554000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
2	chr4:147553800-147554000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:147554000-147554200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
4	chr4:147554000-147554200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:147554000-147554200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr4:147554000-147554200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr4:147554000-147554200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:147554000-147554200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
9	chr4:147554000-147554200	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:147554000-147554400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
11	chr4:147554000-147554400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
12	chr4:147554000-147554600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:147554000-147554600	Bivalent Enhancer	Fetal Brain Male	brain
14	chr4:147554000-147555000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
15	chr4:147554000-147555200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
16	chr4:147554200-147554400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
17	chr4:147554200-147554400	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:147554200-147554400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
19	chr4:147554200-147554400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:147554200-147554400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:147554200-147554400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:147554200-147554400	Bivalent Enhancer	Fetal Brain Female	brain
23	chr4:147554200-147554600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:147554200-147554600	Bivalent Enhancer	Fetal Heart	heart
25	chr4:147554200-147554800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:147554200-147555000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
27	chr4:147554200-147555000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
28	chr4:147554200-147555000	Bivalent Enhancer	Brain Hippocampus Middle	brain
29	chr4:147554200-147555200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
30	chr4:147554400-147554600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
31	chr4:147554400-147554600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
32	chr4:147554400-147554600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:147554400-147554600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:147554400-147554600	Bivalent Enhancer	Adipose Nuclei	Adipose
35	chr4:147554400-147554600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
36	chr4:147554400-147554800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
37	chr4:147554400-147555000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
38	chr4:147554600-147554800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:147554600-147554800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
40	chr4:147554600-147554800	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:147554600-147554800	Bivalent Enhancer	Brain Germinal Matrix	brain
42	chr4:147554600-147555000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
43	chr4:147554600-147555200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:147554800-147555000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:147554800-147555000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
46	chr4:147554800-147555200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:147555000-147555200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
48	chr4:147555000-147555400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
49	chr4:147555000-147555400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
50	chr4:147557800-147558200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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