Variant report

Variant	nsv878605
Chromosome Location	chr4:8332057-8378959
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:538)
CpG islands
(count:2503)
Chromatin interactive
region (count:29)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8337663-8338676	K562	blood:	n/a	n/a
2	ATF1	chr4:8338113-8338723	K562	blood:	n/a	n/a
3	ATF2	chr4:8359490-8359857	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:8338259-8338488	K562	blood:	n/a	n/a
5	ATF3	chr4:8338200-8338505	K562	blood:	n/a	n/a
6	BACH1	chr4:8359436-8359516	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr4:8374921-8375373	GM12878	blood:	n/a	n/a
8	BCL3	chr4:8374852-8375403	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:8338007-8338840	K562	blood:	n/a	n/a
10	BHLHE40	chr4:8347666-8347969	HepG2	liver:	n/a	chr4:8347718-8347734
11	BHLHE40	chr4:8354399-8354611	K562	blood:	n/a	chr4:8354498-8354507 chr4:8354496-8354512
12	BHLHE40	chr4:8349894-8350191	HepG2	liver:	n/a	chr4:8350024-8350033
13	BHLHE40	chr4:8349739-8350219	K562	blood:	n/a	chr4:8350024-8350033
14	BHLHE40	chr4:8351624-8351692	K562	blood:	n/a	n/a
15	BHLHE40	chr4:8376765-8376915	K562	blood:	n/a	n/a
16	BHLHE40	chr4:8372628-8373087	K562	blood:	n/a	chr4:8372836-8372845 chr4:8372836-8372845
17	BHLHE40	chr4:8349911-8350172	GM12878	blood:	n/a	chr4:8350024-8350033
18	BHLHE40	chr4:8338352-8338392	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:8373374-8373615	K562	blood:	n/a	n/a
20	BHLHE40	chr4:8340380-8340596	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:8369879-8369917	K562	blood:	n/a	n/a
22	CBX3	chr4:8337628-8338021	K562	blood:	n/a	n/a
23	CBX3	chr4:8338094-8338489	K562	blood:	n/a	n/a
24	CCNT2	chr4:8337718-8338616	K562	blood:	n/a	n/a
25	CCNT2	chr4:8344651-8344753	K562	blood:	n/a	n/a
26	CEBPB	chr4:8353775-8353986	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:8348143-8348389	A549	lung:	n/a	n/a
28	CEBPB	chr4:8348205-8348405	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:8338104-8338538	K562	blood:	n/a	n/a
30	CEBPB	chr4:8338216-8338398	K562	blood:	n/a	n/a
31	CEBPB	chr4:8348129-8348326	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:8348127-8348308	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:8338135-8338513	K562	blood:	n/a	n/a
34	CEBPB	chr4:8336727-8337075	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:8338264-8338475	Hela-S3	cervix:	n/a	n/a
36	CEBPD	chr4:8338099-8338616	K562	blood:	n/a	n/a
37	CEBPD	chr4:8338177-8338663	K562	blood:	n/a	n/a
38	CHD1	chr4:8359330-8359337	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:8377263-8377280	K562	blood:	n/a	n/a
40	CHD2	chr4:8337198-8337253	HepG2	liver:	n/a	n/a
41	CHD2	chr4:8359488-8360184	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:8344540-8344690	HPF	lung:	n/a	chr4:8344624-8344642 chr4:8344630-8344639 chr4:8344626-8344639
43	CTCF	chr4:8377200-8377350	GM06990	blood:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
44	CTCF	chr4:8344600-8344750	HBMEC	blood vessel:	n/a	chr4:8344624-8344642 chr4:8344630-8344639 chr4:8344626-8344639
45	CTCF	chr4:8332720-8332870	BJ	skin:	n/a	chr4:8332779-8332792 chr4:8332782-8332795
46	CTCF	chr4:8340885-8340916	Lung_OC	lung:	n/a	n/a
47	CTCF	chr4:8340345-8340454	Lung_OC	lung:	n/a	n/a
48	CTCF	chr4:8348060-8348210	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr4:8344420-8344570	AG04450	lung:	n/a	n/a
50	CTCF	chr4:8344560-8344710	HMF	breast:	n/a	chr4:8344624-8344642 chr4:8344630-8344639 chr4:8344626-8344639

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8374561-8374611	MCF-7	breast:	n/a
2	chr4:8368486-8368536	ProgFib	skin:	n/a
3	chr4:8374561-8374611	MCF-7	breast:	n/a
4	chr4:8368486-8368536	ProgFib	skin:	n/a
5	chr4:8372840-8372890	A549	lung:	n/a
6	chr4:8374429-8374479	NT2-D1	testis:	n/a
7	chr4:8378947-8378997	HCM	heart:	n/a
8	chr4:8347266-8347316	HCPEpiC	choroid plexus:	n/a
9	chr4:8376764-8376814	AG04449	skin:	fetal
10	chr4:8359499-8359549	ECC-1	luminal epithelium:	n/a
11	chr4:8345406-8345456	ProgFib	skin:	n/a
12	chr4:8368575-8368625	SK-N-MC	brain:	n/a
13	chr4:8376254-8376304	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:8372691-8372741	CMK	blood:	n/a
15	chr4:8368486-8368536	ovcar-3	ovarian:	n/a
16	chr4:8372840-8372890	HCM	heart:	n/a
17	chr4:8346138-8346188	HMEC	breast:	n/a
18	chr4:8374697-8374747	HCPEpiC	choroid plexus:	n/a
19	chr4:8376764-8376814	Hela-S3	cervix:	n/a
20	chr4:8374697-8374747	SK-N-SH	brain:	n/a
21	chr4:8346138-8346188	SAEC	small airway:	n/a
22	chr4:8345406-8345456	U87	brain:	n/a
23	chr4:8375268-8375318	PFSK-1	brain:	n/a
24	chr4:8347832-8347882	PrEC	prostate:	n/a
25	chr4:8354138-8354188	Hela-S3	cervix:	n/a
26	chr4:8347832-8347882	GM12878	blood:	n/a
27	chr4:8359247-8359297	NHDF-neo	bronchial:	n/a
28	chr4:8345406-8345456	RPTEC	kidney:	n/a
29	chr4:8372840-8372890	K562	blood:	n/a
30	chr4:8348121-8348171	RPTEC	kidney:	n/a
31	chr4:8375240-8375290	AG04450	lung:	fetal
32	chr4:8372758-8372808	HCT-116	colon:	n/a
33	chr4:8376254-8376304	NHBE	bronchial:	n/a
34	chr4:8374182-8374232	AG04450	lung:	fetal
35	chr4:8359269-8359319	NT2-D1	testis:	n/a
36	chr4:8373516-8373566	HCM	heart:	n/a
37	chr4:8376835-8376885	AG04450	lung:	fetal
38	chr4:8359458-8359508	HepG2	liver:	n/a
39	chr4:8373438-8373488	SK-N-SH_RA	brain:	n/a
40	chr4:8359269-8359319	MCF10A-Er-Src	breast:	n/a
41	chr4:8376254-8376304	ECC-1	luminal epithelium:	n/a
42	chr4:8374561-8374611	NHDF-neo	bronchial:	n/a
43	chr4:8368575-8368625	HRPEpiC	eye:	n/a
44	chr4:8368601-8368651	AG09309	skin:	n/a
45	chr4:8345588-8345638	AG09319	gingival:	n/a
46	chr4:8378176-8378226	HCM	heart:	n/a
47	chr4:8347477-8347527	T-47D	breast:	n/a
48	chr4:8368575-8368625	GM06990	blood:	n/a
49	chr4:8354138-8354188	MCF10A-Er-Src	breast:	n/a
50	chr4:8378176-8378226	HAEpiC	amniotic membrane:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8338499..8340014-chr4:8350078..8351770,2	K562	blood:
2	chr4:8338499..8340014-chr4:8350078..8351770,2	K562	blood:
3	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
4	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
5	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
6	chr4:8370118..8372500-chr4:8374648..8377546,2	K562	blood:
7	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
8	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
9	chr4:8372807..8374828-chr4:8375470..8377502,2	K562	blood:
10	chr4:8358055..8360875-chr4:8366726..8369353,3	K562	blood:
11	chr4:8326199..8328705-chr4:8337836..8339581,2	K562	blood:
12	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
13	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
14	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:
15	chr4:8321399..8323453-chr4:8336725..8338364,2	K562	blood:
16	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
17	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
18	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
19	chr4:8337029..8339751-chr4:8340402..8342759,2	K562	blood:
20	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
21	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
22	chr4:8308134..8310233-chr4:8366379..8367956,2	K562	blood:
23	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
24	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
25	chr4:8327689..8329411-chr4:8330180..8333204,3	MCF-7	breast:
26	chr4:8315694..8318647-chr4:8336893..8339393,2	K562	blood:
27	chr4:8337029..8339751-chr4:8340402..8342759,2	K562	blood:
28	chr4:8372002..8373720-chr4:8374604..8376742,2	MCF-7	breast:
29	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOX3-5	chr4:8365860-8366475	NONHSAT095091
2	lnc-ACOX3-1	chr4:8356817-8360065	ENSG00000251615.3
3	lnc-ACOX3-5	chr4:8367183-8367485	NONHSAT095091
4	lnc-METTL19-5	chr4:8372787-8373149	l_2595_chr4:8372786-8374779_heart
5	lnc-HTRA3-4	chr4:8358805-8360149	NONHSAT095089
6	lnc-ACOX3-1	chr4:8356817-8359103	NONHSAT095088
7	lnc-ACOX3-1	chr4:8357038-8359103	ENSG00000251615
8	lnc-METTL19-5	chr4:8374584-8374779	l_2595_chr4:8372786-8374779_heart
9	lnc-HTRA3-4	chr4:8358049-8358702	NONHSAT095089
10	lnc-METTL19-5	chr4:8376346-8376594	l_2595_chr4:8372786-8374779_heart

No data

Variant related genes	Relation type
ENSG00000251615	TF binding region
ACOX3	TF binding region
ENSG00000251615	CpG island
ACOX3	CpG island
ENSG00000251615	chromatin interactions
ENSG00000248986	chromatin interactions
ENSG00000249145	chromatin interactions
ENSG00000087008	chromatin interactions

Extended variants
information (count: 2459 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2459 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2386219	chr4:8332057-8332058	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537010666	chr4:8332095-8332096	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs113193538	chr4:8332104-8332105	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs558271593	chr4:8332134-8332135	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs899493	chr4:8332135-8332136	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs534428832	chr4:8332143-8332144	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs149520191	chr4:8332147-8332148	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs574721385	chr4:8332162-8332163	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs576937950	chr4:8332181-8332182	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs188169637	chr4:8332191-8332192	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs564053144	chr4:8332194-8332195	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs575848763	chr4:8332218-8332219	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs546148921	chr4:8332233-8332234	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs191846167	chr4:8332238-8332239	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs753622	chr4:8332244-8332245	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547142577	chr4:8332256-8332257	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559583338	chr4:8332257-8332258	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs201449757	chr4:8332266-8332267	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs2386221	chr4:8332267-8332268	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2386222	chr4:8332270-8332271	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs183652987	chr4:8332302-8332303	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs551722958	chr4:8332303-8332304	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs899492	chr4:8332304-8332305	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs534393618	chr4:8332306-8332307	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552699964	chr4:8332318-8332319	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs753621	chr4:8332355-8332356	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536010449	chr4:8332369-8332370	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs557290370	chr4:8332395-8332396	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs5856010	chr4:8332400-8332401	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs186825021	chr4:8332401-8332402	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs546209878	chr4:8332458-8332459	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs564129897	chr4:8332490-8332491	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs371481414	chr4:8332522-8332523	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs528199331	chr4:8332528-8332529	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs546617632	chr4:8332563-8332564	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs192355521	chr4:8332572-8332573	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184900214	chr4:8332573-8332574	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs568090598	chr4:8332589-8332590	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs144729999	chr4:8332602-8332603	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs562117791	chr4:8332617-8332618	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs148521354	chr4:8332620-8332621	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs548330983	chr4:8332646-8332647	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs58909732	chr4:8332648-8332649	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs530810511	chr4:8332663-8332664	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs10014361	chr4:8332665-8332666	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570101319	chr4:8332684-8332685	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs77394230	chr4:8332692-8332693	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs114677162	chr4:8332711-8332712	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs568116864	chr4:8332771-8332772	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs142860497	chr4:8332812-8332813	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8325600-8338400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:8326400-8332600	Weak transcription	Spleen	Spleen
3	chr4:8326800-8332200	Weak transcription	Right Atrium	heart
4	chr4:8327200-8332600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr4:8327400-8332600	Weak transcription	Esophagus	oesophagus
6	chr4:8327600-8332400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:8330400-8334200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:8331000-8333600	Enhancers	Fetal Muscle Leg	muscle
9	chr4:8331000-8333600	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr4:8331000-8334200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:8331200-8333200	Enhancers	Fetal Heart	heart
12	chr4:8331200-8334600	Enhancers	Right Ventricle	heart
13	chr4:8331400-8332400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:8331400-8333400	Enhancers	Psoas Muscle	Psoas
15	chr4:8331400-8333600	Enhancers	Left Ventricle	heart
16	chr4:8331600-8333200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr4:8331600-8333200	Enhancers	Ovary	ovary
18	chr4:8331600-8333400	Enhancers	Brain Hippocampus Middle	brain
19	chr4:8331800-8332200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:8332000-8332800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr4:8332000-8333400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:8332000-8333600	Bivalent Enhancer	Fetal Stomach	stomach
23	chr4:8332200-8333000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:8332200-8333200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:8332200-8333400	Enhancers	Right Atrium	heart
26	chr4:8332200-8333600	Enhancers	Brain Cingulate Gyrus	brain
27	chr4:8332400-8332800	Enhancers	Stomach Smooth Muscle	stomach
28	chr4:8332400-8333000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:8332400-8333200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr4:8332400-8333200	Bivalent Enhancer	Placenta	Placenta
31	chr4:8332400-8333400	Enhancers	Brain Anterior Caudate	brain
32	chr4:8332400-8333400	Enhancers	Brain Substantia Nigra	brain
33	chr4:8332400-8333400	Enhancers	HSMM	muscle
34	chr4:8332400-8333600	Enhancers	Adipose Nuclei	Adipose
35	chr4:8332400-8335200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr4:8332600-8332800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr4:8332600-8333000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:8332600-8333000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:8332600-8333000	Enhancers	Brain Angular Gyrus	brain
40	chr4:8332600-8333200	Enhancers	Primary hematopoietic stem cells	blood
41	chr4:8332600-8333200	Enhancers	Spleen	Spleen
42	chr4:8332600-8333400	Enhancers	Esophagus	oesophagus
43	chr4:8332600-8333600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:8332800-8333200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:8332800-8333200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
46	chr4:8332800-8333400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr4:8332800-8333400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:8332800-8335800	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr4:8333000-8336800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:8333200-8333400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--

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