Variant report

Variant	nsv1013365
Chromosome Location	chr4:20834054-21609078
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	chr4:21409476-21409646	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:21409038-21409186	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:21207380-21208041	HepG2	liver:	n/a	chr4:21207685-21207701
4	ARID3A	chr4:21509115-21509312	HepG2	liver:	n/a	n/a
5	ATF1	chr4:20865610-20865795	K562	blood:	n/a	n/a
6	BACH1	chr4:20985747-20986024	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:21139642-21139925	H1-hESC	embryonic stem cell:	n/a	chr4:21139764-21139778
8	BACH1	chr4:21132290-21132590	K562	blood:	n/a	n/a
9	BACH1	chr4:21386733-21386848	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:21340833-21340873	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:21132270-21132579	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr4:21545162-21545418	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr4:21261355-21261732	HepG2	liver:	n/a	n/a
14	BHLHE40	chr4:21091805-21092242	GM12878	blood:	n/a	n/a
15	BRCA1	chr4:21471169-21471375	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr4:21514045-21514352	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr4:21473772-21473970	K562	blood:	n/a	n/a
18	CCNT2	chr4:21050255-21050426	K562	blood:	n/a	n/a
19	CEBPB	chr4:21427566-21427787	A549	lung:	n/a	chr4:21427718-21427729
20	CEBPB	chr4:21369524-21369702	A549	lung:	n/a	chr4:21369585-21369598 chr4:21369585-21369596 chr4:21369586-21369597
21	CEBPB	chr4:21155546-21155836	HepG2	liver:	n/a	chr4:21155691-21155702
22	CEBPB	chr4:21268311-21268585	H1-hESC	embryonic stem cell:	n/a	chr4:21268454-21268465 chr4:21268453-21268466
23	CEBPB	chr4:21389323-21389632	H1-hESC	embryonic stem cell:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
24	CEBPB	chr4:21575694-21575733	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:20842371-20842617	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:21283417-21283704	HepG2	liver:	n/a	chr4:21283560-21283571 chr4:21283560-21283573 chr4:21283557-21283574
27	CEBPB	chr4:21212159-21212371	K562	blood:	n/a	chr4:21212242-21212253 chr4:21212240-21212251
28	CEBPB	chr4:21528873-21529208	HepG2	liver:	n/a	chr4:21529040-21529051
29	CEBPB	chr4:21389446-21389557	K562	blood:	n/a	chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389459-21389468 chr4:21389457-21389470
30	CEBPB	chr4:21016036-21016344	K562	blood:	n/a	chr4:21016190-21016201
31	CEBPB	chr4:21331830-21332133	IMR90	lung:	n/a	chr4:21331975-21331986
32	CEBPB	chr4:21156044-21156243	HepG2	liver:	n/a	chr4:21156091-21156102 chr4:21156091-21156100 chr4:21156089-21156100 chr4:21156089-21156102
33	CEBPB	chr4:21449344-21449649	HepG2	liver:	n/a	chr4:21449511-21449522
34	CEBPB	chr4:21290298-21290413	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:21528872-21529203	IMR90	lung:	n/a	chr4:21529040-21529051
36	CEBPB	chr4:21331895-21332143	HepG2	liver:	n/a	chr4:21331975-21331986
37	CEBPB	chr4:21362771-21363035	A549	lung:	n/a	chr4:21362916-21362927
38	CEBPB	chr4:21400092-21400191	K562	blood:	n/a	chr4:21400158-21400169
39	CEBPB	chr4:21261375-21261746	HepG2	liver:	n/a	chr4:21261486-21261497 chr4:21261562-21261571 chr4:21261562-21261571 chr4:21261562-21261571 chr4:21261560-21261573 chr4:21261560-21261571 chr4:21261560-21261573 chr4:21261562-21261571 chr4:21261561-21261572
40	CEBPB	chr4:21449350-21449652	H1-hESC	embryonic stem cell:	n/a	chr4:21449511-21449522
41	CEBPB	chr4:21427707-21427907	K562	blood:	n/a	chr4:21427718-21427729
42	CEBPB	chr4:21432334-21432679	IMR90	lung:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
43	CEBPB	chr4:21007300-21007669	IMR90	lung:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
44	CEBPB	chr4:20941551-20941842	HepG2	liver:	n/a	chr4:20941702-20941715 chr4:20941704-20941713 chr4:20941704-20941713 chr4:20941704-20941713
45	CEBPB	chr4:21436283-21436393	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:21141966-21142222	K562	blood:	n/a	chr4:21142097-21142106 chr4:21142097-21142106 chr4:21142097-21142106 chr4:21142097-21142106 chr4:21142097-21142108 chr4:21142095-21142106 chr4:21142022-21142030
47	CEBPB	chr4:21016084-21016366	H1-hESC	embryonic stem cell:	n/a	chr4:21016190-21016201
48	CEBPB	chr4:20937960-20938160	HepG2	liver:	n/a	chr4:20938070-20938081
49	CEBPB	chr4:21528920-21529206	A549	lung:	n/a	chr4:21529040-21529051
50	CEBPB	chr4:21400056-21400228	A549	lung:	n/a	chr4:21400158-21400169

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:21305490-21305540	BE2_C	brain:	n/a
2	chr4:21305490-21305540	BE2_C	brain:	n/a
3	chr4:21546545-21546595	BJ	skin:	n/a
4	chr4:20986246-20986296	Caco-2	colon:	n/a
5	chr4:21546029-21546079	AG09319	gingival:	n/a
6	chr4:20852366-20852416	HIPEpiC	eye:	n/a
7	chr4:20884321-20884371	PANC-1	pancreas:	n/a
8	chr4:20885536-20885586	AG04450	lung:	fetal
9	chr4:20852672-20852722	RPTEC	kidney:	n/a
10	chr4:21546545-21546595	NB4	blood:	n/a
11	chr4:20985984-20986034	SKMC	muscle:	n/a
12	chr4:20885019-20885069	GM19239	blood:	n/a
13	chr4:21039877-21039927	HMEC	breast:	n/a
14	chr4:20985984-20986034	IMR90	lung:	fetal
15	chr4:21120300-21120350	PANC-1	pancreas:	n/a
16	chr4:21305941-21305991	PrEC	prostate:	n/a
17	chr4:20985623-20985673	ProgFib	skin:	n/a
18	chr4:21470137-21470187	GM12891	blood:	n/a
19	chr4:21470137-21470187	A549	lung:	n/a
20	chr4:20852672-20852722	IMR90	lung:	fetal
21	chr4:21305805-21305855	GM06990	blood:	n/a
22	chr4:21470137-21470187	HRE	kidney:	n/a
23	chr4:21305805-21305855	SK-N-SH_RA	brain:	n/a
24	chr4:20852366-20852416	RPTEC	kidney:	n/a
25	chr4:20960712-20960762	AG09309	skin:	n/a
26	chr4:20986246-20986296	NHDF-neo	bronchial:	n/a
27	chr4:20885536-20885586	BE2_C	brain:	n/a
28	chr4:21039877-21039927	NT2-D1	testis:	n/a
29	chr4:21305941-21305991	AG04449	skin:	fetal
30	chr4:21470137-21470187	MCF-7	breast:	n/a
31	chr4:20960712-20960762	Hela-S3	cervix:	n/a
32	chr4:20884385-20884435	T-47D	breast:	n/a
33	chr4:21305805-21305855	NH-A	brain:	n/a
34	chr4:20985696-20985746	NHBE	bronchial:	n/a
35	chr4:21004400-21004450	AG10803	skin:	n/a
36	chr4:20884431-20884481	GM06990	blood:	n/a
37	chr4:20885246-20885296	PANC-1	pancreas:	n/a
38	chr4:20885246-20885296	AG09319	gingival:	n/a
39	chr4:21546029-21546079	HRE	kidney:	n/a
40	chr4:20885019-20885069	Jurkat	blood:	n/a
41	chr4:20884321-20884371	ECC-1	luminal epithelium:	n/a
42	chr4:20985696-20985746	SK-N-SH_RA	brain:	n/a
43	chr4:20985623-20985673	MCF10A-Er-Src	breast:	n/a
44	chr4:21470137-21470187	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:21306051-21306101	T-47D	breast:	n/a
46	chr4:21546545-21546595	U87	brain:	n/a
47	chr4:20884431-20884481	BJ	skin:	n/a
48	chr4:20885019-20885069	NHDF-neo	bronchial:	n/a
49	chr4:20985696-20985746	NH-A	brain:	n/a
50	chr4:21305490-21305540	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:21186139..21187069-chr4:21470759..21471732,3	MCF-7	breast:
2	chr4:21513660..21514733-chr4:21769803..21771071,4	MCF-7	breast:
3	chr4:20940626..20942127-chr4:20945526..20948025,2	K562	blood:
4	chr4:21297051..21299486-chr4:21300587..21302226,2	MCF-7	breast:
5	chr4:21510988..21512730-chr4:21514428..21516962,2	K562	blood:
6	chr4:21099804..21101899-chr4:21102257..21105155,2	K562	blood:
7	chr4:21373360..21375651-chr4:21376032..21378469,2	MCF-7	breast:
8	chr4:21186139..21187069-chr4:21470759..21471732,3	MCF-7	breast:
9	chr1:147804723..147806420-chr4:20979153..20981320,2	MCF-7	breast:
10	chr4:21407818..21410530-chrX:40552943..40555484,2	MCF-7	breast:
11	chr20:61279326..61279889-chr4:21329070..21329892,2	Hela-S3	cervix:
12	chr4:21186540..21187139-chr4:21470730..21471606,2	MCF-7	breast:
13	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
14	chr4:21513547..21514492-chr4:21769669..21770605,6	MCF-7	breast:
15	chr4:21002667..21005415-chr4:21005443..21008347,2	K562	blood:
16	chr4:21373360..21375651-chr4:21376032..21378469,2	MCF-7	breast:
17	chr4:21497861..21500462-chr4:21501332..21503199,2	K562	blood:
18	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
19	chr4:21497861..21500462-chr4:21501332..21503199,2	K562	blood:
20	chr4:21159106..21161937-chr4:21165905..21168685,2	MCF-7	breast:
21	chr4:21510988..21512730-chr4:21514428..21516962,2	K562	blood:
22	chr4:21508722..21509309-chr4:21767490..21768052,2	MCF-7	breast:
23	chr1:217085881..217086616-chr4:21121511..21122023,2	MCF-7	breast:
24	chr4:21297051..21299486-chr4:21300587..21302226,2	MCF-7	breast:
25	chr18:10317211..10317949-chr4:20836718..20837659,2	MCF-7	breast:
26	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
27	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
28	chr4:21513432..21514751-chr4:21767040..21768803,10	MCF-7	breast:
29	chr4:20849276..20852275-chr6:109770823..109773619,2	K562	blood:
30	chr4:21513582..21515656-chr4:21764630..21766290,2	MCF-7	breast:
31	chr4:21372485..21375089-chr4:21376184..21378296,2	K562	blood:
32	chr4:20774749..20775678-chr4:21136384..21137379,5	MCF-7	breast:
33	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:
34	chr4:20940626..20942127-chr4:20945526..20948025,2	K562	blood:
35	chr4:21372485..21375089-chr4:21376184..21378296,2	K562	blood:
36	chr4:21002667..21005415-chr4:21005443..21008347,2	K562	blood:
37	chr4:21159106..21161937-chr4:21165905..21168685,2	MCF-7	breast:
38	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
39	chr4:20774939..20775520-chr4:21136553..21137202,2	MCF-7	breast:
40	chr4:21099804..21101899-chr4:21102257..21105155,2	K562	blood:
41	chr4:21186540..21187139-chr4:21470730..21471606,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR125-6	chr4:21454062-21463909	ucscGeneNc_uc003gqj_1
2	lnc-PACRGL-3	chr4:21583719-21583748	ENSG00000250092.2
3	lnc-PACRGL-2	chr4:21306165-21306236	ENSG00000250243.2
4	lnc-PACRGL-2	chr4:21317905-21318108	ENSG00000250243.2
5	lnc-PACRGL-3	chr4:21583841-21583998	ENSG00000250092.2
6	lnc-PACRGL-2	chr4:21316899-21316963	ENSG00000250243.2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7978	chr4:21466361-21466381	MIMAT0031181

Variant related genes	Relation type
KCNIP4	TF binding region
ENSG00000250092	TF binding region
ENSG00000250243	TF binding region
KCNIP4	CpG island
ENSG00000250092	CpG island
ENSG00000250243	CpG island
ENSG00000135596	chromatin interactions

Extended variants
information (count: 15876 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:15876 , 50 per page) page: 1 2 3 4 5 6 7 ... 318

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4988679	chr4:20834054-20834055	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187543556	chr4:20834116-20834117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192314495	chr4:20834144-20834145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577210805	chr4:20834165-20834166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538982867	chr4:20834166-20834167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183843337	chr4:20834167-20834168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575818243	chr4:20834174-20834175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543219511	chr4:20834175-20834176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571698835	chr4:20834193-20834194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147655511	chr4:20834229-20834230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540726495	chr4:20834233-20834234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141596260	chr4:20834269-20834270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs67155846	chr4:20834270-20834271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113234000	chr4:20834285-20834286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367686712	chr4:20834346-20834347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200280584	chr4:20834350-20834351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557458253	chr4:20834351-20834352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565318362	chr4:20834375-20834376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532533161	chr4:20834386-20834387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142377574	chr4:20834415-20834416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189157038	chr4:20834419-20834420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547931783	chr4:20834423-20834424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530676787	chr4:20834443-20834444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376175386	chr4:20834448-20834449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368451815	chr4:20834449-20834450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34434096	chr4:20834450-20834451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147128388	chr4:20834451-20834452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs3077701	chr4:20834454-20834455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201281634	chr4:20834455-20834456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549164165	chr4:20834470-20834471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10012893	chr4:20834473-20834474	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534759702	chr4:20834486-20834487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147913249	chr4:20834528-20834529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4391029	chr4:20834562-20834563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs67378217	chr4:20834563-20834564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377349466	chr4:20834620-20834621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10020916	chr4:20834659-20834660	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148976023	chr4:20834675-20834676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536497530	chr4:20834707-20834708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143749623	chr4:20834715-20834716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs902665	chr4:20834721-20834722	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573346917	chr4:20834753-20834754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184530221	chr4:20834764-20834765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565401847	chr4:20834794-20834795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148142261	chr4:20834807-20834808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11946996	chr4:20834810-20834811	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141071621	chr4:20834827-20834828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562693430	chr4:20834847-20834848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530884780	chr4:20834855-20834856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549000512	chr4:20834861-20834862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20819200-20834400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:20822800-20834600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:20832200-20838000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:20833400-20834800	Enhancers	HSMM	muscle
5	chr4:20833400-20835000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:20834000-20834200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:20834200-20834600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:20834400-20834800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:20834600-20834800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:20834800-20850800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:20835400-20835800	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr4:20835800-20841800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr4:20836800-20837400	Weak transcription	NHEK	skin
14	chr4:20837600-20838200	Enhancers	NHEK	skin
15	chr4:20837800-20838600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:20838000-20838200	Enhancers	HMEC	breast
17	chr4:20838000-20838800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:20838200-20840200	Weak transcription	HMEC	breast
19	chr4:20838200-20840200	Weak transcription	NHEK	skin
20	chr4:20838600-20841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:20838800-20841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:20839600-20843200	Enhancers	HUVEC	blood vessel
23	chr4:20840200-20840400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:20840200-20840400	Enhancers	HMEC	breast
25	chr4:20840200-20841400	Enhancers	NHEK	skin
26	chr4:20840400-20841000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:20840400-20841200	Weak transcription	HMEC	breast
28	chr4:20841000-20842400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:20841200-20842000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr4:20841200-20842400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr4:20841200-20842400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:20841200-20842400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:20841200-20842600	Enhancers	HMEC	breast
34	chr4:20841400-20841600	Flanking Active TSS	NHEK	skin
35	chr4:20841400-20841800	Enhancers	Rectal Smooth Muscle	rectum
36	chr4:20841400-20842200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr4:20841400-20842200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:20841400-20842200	Enhancers	NHLF	lung
39	chr4:20841400-20842400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:20841400-20842400	Enhancers	HSMM	muscle
41	chr4:20841400-20842400	Enhancers	NH-A	brain
42	chr4:20841600-20841800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:20841600-20841800	Enhancers	NHEK	skin
44	chr4:20841600-20842200	Enhancers	Colon Smooth Muscle	Colon
45	chr4:20841600-20842400	Enhancers	HSMMtube	muscle
46	chr4:20841800-20842000	Flanking Active TSS	NHEK	skin
47	chr4:20841800-20842200	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr4:20842000-20842400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr4:20842000-20842400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr4:20842000-20842600	Enhancers	NHEK	skin

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