Variant report

Variant	nsv829975
Chromosome Location	chr4:78426210-78565198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1534)
CpG islands
(count:549)
Chromatin interactive
region (count:50)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1534 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78459487-78459642	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:78557995-78558348	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:78558159-78558311	K562	blood:	n/a	n/a
4	ATF2	chr4:78507784-78508661	GM12878	blood:	n/a	n/a
5	ATF2	chr4:78550906-78551569	GM12878	blood:	n/a	n/a
6	ATF2	chr4:78551030-78551511	GM12878	blood:	n/a	n/a
7	ATF2	chr4:78507838-78508604	GM12878	blood:	n/a	n/a
8	ATF3	chr4:78538436-78538714	K562	blood:	n/a	n/a
9	BACH1	chr4:78558115-78558339	K562	blood:	n/a	n/a
10	BACH1	chr4:78558172-78558180	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:78539784-78540196	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:78502910-78503215	GM12878	blood:	n/a	chr4:78503126-78503136
13	BATF	chr4:78502874-78503256	GM12878	blood:	n/a	chr4:78503126-78503136
14	BATF	chr4:78426517-78427077	GM12878	blood:	n/a	n/a
15	BATF	chr4:78550972-78551452	GM12878	blood:	n/a	chr4:78551241-78551252
16	BATF	chr4:78507883-78508667	GM12878	blood:	n/a	n/a
17	BATF	chr4:78550905-78551525	GM12878	blood:	n/a	chr4:78551241-78551252
18	BATF	chr4:78507981-78508632	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:78507966-78508594	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:78514265-78514475	GM12878	blood:	n/a	chr4:78514342-78514351
21	BCL11A	chr4:78551047-78551453	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:78507904-78508619	GM12878	blood:	n/a	n/a
23	BCL3	chr4:78508078-78508553	GM12878	blood:	n/a	n/a
24	BCL3	chr4:78495532-78495756	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:78507887-78508631	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:78507951-78508501	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:78539876-78540051	K562	blood:	n/a	n/a
28	BHLHE40	chr4:78514242-78514566	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:78539858-78540151	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:78507974-78508748	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:78551096-78551411	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:78459389-78459628	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr4:78558034-78558192	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr4:78558006-78558469	K562	blood:	n/a	n/a
35	CBX3	chr4:78558092-78558392	K562	blood:	n/a	n/a
36	CBX3	chr4:78557948-78558460	HCT-116	colon:	n/a	n/a
37	CEBPB	chr4:78430250-78430382	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:78514377-78514641	HepG2	liver:	n/a	chr4:78514502-78514513
39	CEBPB	chr4:78562109-78562358	K562	blood:	n/a	chr4:78562222-78562233
40	CEBPB	chr4:78557286-78557385	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:78538469-78538685	H1-hESC	embryonic stem cell:	n/a	chr4:78538568-78538579
42	CEBPB	chr4:78538409-78538712	HepG2	liver:	n/a	chr4:78538568-78538579
43	CEBPB	chr4:78558088-78558385	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:78538433-78538630	K562	blood:	n/a	chr4:78538568-78538579
45	CEBPB	chr4:78518131-78518312	K562	blood:	n/a	chr4:78518225-78518236
46	CEBPB	chr4:78507984-78508764	GM12878	blood:	n/a	chr4:78508686-78508699
47	CEBPB	chr4:78538410-78538741	IMR90	lung:	n/a	chr4:78538568-78538579
48	CEBPB	chr4:78549677-78549804	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:78553841-78554032	K562	blood:	n/a	chr4:78553875-78553886
50	CEBPB	chr4:78538414-78538728	A549	lung:	n/a	chr4:78538568-78538579

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78432901-78432951	HRPEpiC	eye:	n/a
2	chr4:78432403-78432453	NB4	blood:	n/a
3	chr4:78432403-78432453	SK-N-MC	brain:	n/a
4	chr4:78492139-78492189	GM12892	blood:	n/a
5	chr4:78432011-78432061	GM06990	blood:	n/a
6	chr4:78484327-78484377	HAEpiC	amniotic membrane:	n/a
7	chr4:78432901-78432951	RPTEC	kidney:	n/a
8	chr4:78432403-78432453	PFSK-1	brain:	n/a
9	chr4:78432901-78432951	IMR90	lung:	fetal
10	chr4:78432204-78432254	AoSMC	blood vessel:	n/a
11	chr4:78431407-78431457	HAEpiC	amniotic membrane:	n/a
12	chr4:78432403-78432453	NH-A	brain:	n/a
13	chr4:78484327-78484377	AG09309	skin:	n/a
14	chr4:78532698-78532748	IMR90	lung:	fetal
15	chr4:78432011-78432061	AG10803	skin:	n/a
16	chr4:78432403-78432453	PrEC	prostate:	n/a
17	chr4:78432901-78432951	NHDF-neo	bronchial:	n/a
18	chr4:78529898-78529948	A549	lung:	n/a
19	chr4:78492139-78492189	SAEC	small airway:	n/a
20	chr4:78432204-78432254	NH-A	brain:	n/a
21	chr4:78532698-78532748	HUVEC	blood vessel:	n/a
22	chr4:78431407-78431457	T-47D	breast:	n/a
23	chr4:78492139-78492189	Caco-2	colon:	n/a
24	chr4:78432901-78432951	Caco-2	colon:	n/a
25	chr4:78432403-78432453	HEEpiC	esophagus:	n/a
26	chr4:78432403-78432453	BE2_C	brain:	n/a
27	chr4:78492139-78492189	NH-A	brain:	n/a
28	chr4:78431407-78431457	CMK	blood:	n/a
29	chr4:78432011-78432061	HCPEpiC	choroid plexus:	n/a
30	chr4:78432011-78432061	GM12892	blood:	n/a
31	chr4:78432403-78432453	U87	brain:	n/a
32	chr4:78484327-78484377	Hepatocyte	liver:	n/a
33	chr4:78484327-78484377	PrEC	prostate:	n/a
34	chr4:78529898-78529948	GM12891	blood:	n/a
35	chr4:78484327-78484377	HNPCEpiC	eye:	n/a
36	chr4:78432011-78432061	HCF	heart:	n/a
37	chr4:78532698-78532748	SK-N-MC	brain:	n/a
38	chr4:78492139-78492189	SK-N-SH	brain:	n/a
39	chr4:78431407-78431457	NHBE	bronchial:	n/a
40	chr4:78532698-78532748	HepG2	liver:	n/a
41	chr4:78532698-78532748	MCF10A-Er-Src	breast:	n/a
42	chr4:78431407-78431457	HCM	heart:	n/a
43	chr4:78432011-78432061	SK-N-SH	brain:	n/a
44	chr4:78432011-78432061	T-47D	breast:	n/a
45	chr4:78432204-78432254	H1-hESC	embryonic stem cell:	embryo
46	chr4:78432204-78432254	Caco-2	colon:	n/a
47	chr4:78432901-78432951	MCF-7	breast:	n/a
48	chr4:78432011-78432061	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:78431407-78431457	Hepatocyte	liver:	n/a
50	chr4:78529898-78529948	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:78522249..78524588-chr4:78525171..78527688,2	MCF-7	breast:
2	chr4:78540911..78543447-chr4:78545553..78547631,2	MCF-7	breast:
3	chr4:78538801..78540562-chr4:78562420..78564607,2	MCF-7	breast:
4	chr4:78446246..78448492-chr4:78458851..78460486,2	MCF-7	breast:
5	chr4:78306282..78306818-chr4:78539506..78540132,2	MCF-7	breast:
6	chr4:78521938..78522727-chr4:78539308..78540406,4	MCF-7	breast:
7	chr4:78498262..78499810-chr4:78506122..78508208,2	MCF-7	breast:
8	chr4:78521938..78522727-chr4:78539308..78540406,4	MCF-7	breast:
9	chr4:78354236..78354764-chr4:78521810..78522404,2	MCF-7	breast:
10	chr4:78394741..78395310-chr4:78522044..78522649,2	MCF-7	breast:
11	chr4:78473227..78475134-chr4:78486188..78487988,2	K562	blood:
12	chr4:78532722..78535241-chr4:78538489..78541830,3	MCF-7	breast:
13	chr4:78446246..78448492-chr4:78458851..78460486,2	MCF-7	breast:
14	chr4:78394433..78394946-chr4:78521807..78522340,2	MCF-7	breast:
15	chr4:78306302..78306941-chr4:78521930..78522730,3	MCF-7	breast:
16	chr4:78394658..78395254-chr4:78520671..78521209,2	MCF-7	breast:
17	chr4:78500488..78502218-chr4:78507307..78510203,2	K562	blood:
18	chr4:78306259..78307081-chr4:78539517..78540020,2	K562	blood:
19	chr4:78498262..78499810-chr4:78506122..78508208,2	MCF-7	breast:
20	chr4:78430923..78433836-chr4:78456770..78459197,2	K562	blood:
21	chr4:78386033..78387001-chr4:78522641..78523414,2	MCF-7	breast:
22	chr4:78428052..78429618-chr4:78431660..78434411,2	K562	blood:
23	chr4:78540911..78543447-chr4:78545553..78547631,2	MCF-7	breast:
24	chr4:78539680..78541728-chr4:78543487..78545525,2	MCF-7	breast:
25	chr4:78500488..78502218-chr4:78507307..78510203,2	K562	blood:
26	chr4:78532722..78535241-chr4:78538489..78541830,3	MCF-7	breast:
27	chr4:78504555..78506696-chr4:78507385..78508926,2	K562	blood:
28	chr4:78386143..78387109-chr4:78539081..78540489,9	MCF-7	breast:
29	chr4:78473227..78475134-chr4:78486188..78487988,2	K562	blood:
30	chr4:78521675..78522522-chr5:128453764..128454552,2	K562	blood:
31	chr4:78552964..78554952-chr4:78555723..78558165,2	MCF-7	breast:
32	chr4:78530875..78532515-chr4:78534945..78537935,2	K562	blood:
33	chr4:78386155..78387048-chr4:78520300..78520908,2	MCF-7	breast:
34	chr4:78521817..78522700-chr4:78619204..78620028,2	MCF-7	breast:
35	chr4:78528761..78530717-chr4:78532586..78534961,2	MCF-7	breast:
36	chr4:78386180..78387155-chr4:78519855..78521281,5	MCF-7	breast:
37	chr4:78515499..78517664-chr4:78519423..78521638,2	MCF-7	breast:
38	chr1:245028107..245028813-chr4:78427168..78428011,2	MCF-7	breast:
39	chr4:78385938..78387056-chr4:78521715..78522661,6	MCF-7	breast:
40	chr4:78530875..78532515-chr4:78534945..78537935,2	K562	blood:
41	chr4:78539512..78540036-chr4:78619176..78619985,2	MCF-7	breast:
42	chr4:78538801..78540562-chr4:78562420..78564607,2	MCF-7	breast:
43	chr4:78386426..78387105-chr4:78521722..78522272,2	MCF-7	breast:
44	chr4:78539680..78541728-chr4:78543487..78545525,2	MCF-7	breast:
45	chr4:78354631..78355201-chr4:78520510..78521240,2	MCF-7	breast:
46	chr4:78386121..78388787-chr4:78517468..78520191,2	MCF-7	breast:
47	chr4:78528761..78530717-chr4:78532586..78534961,2	MCF-7	breast:
48	chr4:78515499..78517664-chr4:78519423..78521638,2	MCF-7	breast:
49	chr4:78552964..78554952-chr4:78555723..78558165,2	MCF-7	breast:
50	chr4:78504555..78506696-chr4:78507385..78508926,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNG2-3	chr4:78526986-78527083	NONHSAT097055
2	lnc-CCNG2-3	chr4:78528857-78528989	NONHSAT097055
3	lnc-CCNG2-3	chr4:78531768-78532076	NONHSAT097055

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CXCL13	hsa-miR-26b-5p	chr4:78532460-78532483

Variant related genes	Relation type
CXCL13	TF binding region
CXCL13	CpG island
ENSG00000156234	chromatin interactions

Extended variants
information (count: 3759 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:3759 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200856336	chr4:78427937-78427938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs139730986	chr4:78427945-78427946	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs560474293	chr4:78428080-78428081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532416463	chr4:78428108-78428109	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184361786	chr4:78428114-78428115	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144826064	chr4:78428123-78428124	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531723937	chr4:78428130-78428131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79255221	chr4:78428135-78428136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561759858	chr4:78428219-78428220	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187596805	chr4:78428236-78428237	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs193033761	chr4:78428239-78428240	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571104073	chr4:78428254-78428255	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564375038	chr4:78428281-78428282	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550116256	chr4:78428341-78428342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs148590298	chr4:78428414-78428415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141925119	chr4:78428439-78428440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs185628499	chr4:78428448-78428449	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552784508	chr4:78428542-78428543	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554672085	chr4:78428556-78428557	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs114254766	chr4:78428561-78428562	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs150668418	chr4:78428562-78428563	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs77923578	chr4:78428610-78428611	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs577106449	chr4:78428630-78428631	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546040575	chr4:78428677-78428678	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140813791	chr4:78428706-78428707	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576150031	chr4:78428719-78428720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543573300	chr4:78428721-78428722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541606913	chr4:78428762-78428763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563255541	chr4:78428850-78428851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561872827	chr4:78428893-78428894	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527774924	chr4:78428945-78428946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs17002711	chr4:78428946-78428947	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564462888	chr4:78428965-78428966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533459101	chr4:78428986-78428987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550422902	chr4:78429022-78429023	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563523397	chr4:78429035-78429036	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs76777616	chr4:78429050-78429051	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562521051	chr4:78429060-78429061	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536092432	chr4:78429069-78429070	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144762558	chr4:78429115-78429116	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs534342247	chr4:78429116-78429117	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75767560	chr4:78429124-78429125	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147872865	chr4:78429131-78429132	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551067734	chr4:78429176-78429177	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190573263	chr4:78429190-78429191	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs139903071	chr4:78429193-78429194	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556453674	chr4:78429252-78429253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs373284056	chr4:78429269-78429270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529571000	chr4:78429291-78429292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575908545	chr4:78429313-78429314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
primary effusion lymphomas	17116491	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78428400-78429000	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:78429000-78429200	Enhancers	Fetal Muscle Leg	muscle
3	chr4:78429200-78431200	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:78429400-78429600	Enhancers	Fetal Muscle Trunk	muscle
5	chr4:78429600-78431600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr4:78431200-78431800	Enhancers	Fetal Muscle Leg	muscle
7	chr4:78431600-78432000	Flanking Active TSS	Fetal Muscle Trunk	muscle
8	chr4:78431800-78432200	Active TSS	Fetal Muscle Leg	muscle
9	chr4:78432000-78433800	Active TSS	Fetal Muscle Trunk	muscle
10	chr4:78432400-78433000	Enhancers	Fetal Heart	heart
11	chr4:78433200-78434000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:78447800-78448000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:78447800-78448200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:78447800-78448200	Enhancers	HSMM	muscle
15	chr4:78447800-78448200	Enhancers	HSMMtube	muscle
16	chr4:78447800-78448800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr4:78448000-78448800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:78448600-78448800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:78457600-78459000	Enhancers	Stomach Mucosa	stomach
20	chr4:78458200-78460200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr4:78458200-78460400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:78458400-78460800	Enhancers	Small Intestine	intestine
23	chr4:78458400-78461000	Enhancers	Pancreas	Pancrea
24	chr4:78458600-78459000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:78458600-78459000	Bivalent Enhancer	HMEC	breast
26	chr4:78458800-78459000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr4:78458800-78459800	Enhancers	Osteobl	bone
28	chr4:78458800-78460200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:78459000-78459200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
30	chr4:78459000-78459200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:78459000-78459200	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
32	chr4:78459000-78459400	Flanking Active TSS	Stomach Mucosa	stomach
33	chr4:78459000-78460000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:78459000-78460200	Enhancers	HSMM	muscle
35	chr4:78459000-78460400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:78459000-78460400	Enhancers	A549	lung
37	chr4:78459000-78460600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:78459000-78460800	Enhancers	HMEC	breast
39	chr4:78459000-78461000	Enhancers	Duodenum Mucosa	Duodenum
40	chr4:78459200-78459400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:78459200-78460000	Enhancers	Esophagus	oesophagus
42	chr4:78459200-78460200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr4:78459200-78460200	Enhancers	HSMMtube	muscle
44	chr4:78459200-78460200	Enhancers	NHDF-Ad	bronchial
45	chr4:78459200-78460400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:78459200-78460400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr4:78459200-78460400	Enhancers	NH-A	brain
48	chr4:78459200-78460400	Enhancers	NHEK	skin
49	chr4:78459200-78460800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr4:78459200-78460800	Enhancers	Sigmoid Colon	Sigmoid Colon

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