Variant report

Variant	nsv1027781
Chromosome Location	chr4:142943485-143306567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2328)
CpG islands
(count:793)
Chromatin interactive
region (count:73)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2328 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:143012167-143013131	A549	lung:	n/a	n/a
2	ATF3	chr4:143012057-143013268	A549	lung:	n/a	n/a
3	BATF	chr4:143186776-143187022	GM12878	blood:	n/a	chr4:143186896-143186907
4	BCL3	chr4:143012112-143013373	A549	lung:	n/a	n/a
5	BCL3	chr4:143011959-143013454	A549	lung:	n/a	n/a
6	BCL3	chr4:143016875-143017712	A549	lung:	n/a	chr4:143017228-143017237
7	BCL3	chr4:143186705-143187107	A549	lung:	n/a	n/a
8	BCLAF1	chr4:143274272-143274612	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:143274328-143274365	K562	blood:	n/a	n/a
10	BHLHE40	chr4:143085907-143086265	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:143215733-143216068	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:143186231-143186650	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:143066381-143066422	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:143080277-143080336	GM12878	blood:	n/a	n/a
15	BRCA1	chr4:143017113-143017529	Hela-S3	cervix:	n/a	chr4:143017466-143017473
16	BRCA1	chr4:143012116-143013359	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr4:143186538-143187040	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:143062502-143062550	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:143274375-143274623	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr4:142957947-142958330	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:143012729-143013372	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:143186576-143187184	HCT-116	colon:	n/a	n/a
23	CBX3	chr4:143012341-143013416	HCT-116	colon:	n/a	n/a
24	CBX3	chr4:143186676-143187202	HCT-116	colon:	n/a	n/a
25	CBX3	chr4:143017018-143017642	HCT-116	colon:	n/a	n/a
26	CBX3	chr4:143016883-143017689	HCT-116	colon:	n/a	n/a
27	CCNT2	chr4:142970568-142970768	K562	blood:	n/a	n/a
28	CEBPB	chr4:143227822-143228047	HepG2	liver:	n/a	chr4:143227978-143227989
29	CEBPB	chr4:143164432-143164751	HepG2	liver:	n/a	chr4:143164596-143164607
30	CEBPB	chr4:143186185-143187094	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:143214583-143215439	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:143300396-143301136	ECC-1	luminal epithelium:	n/a	chr4:143300882-143300893
33	CEBPB	chr4:143078632-143078904	A549	lung:	n/a	chr4:143078737-143078748 chr4:143078735-143078746
34	CEBPB	chr4:143012219-143013372	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:143186821-143187384	A549	lung:	n/a	n/a
36	CEBPB	chr4:143120819-143121035	A549	lung:	n/a	chr4:143120911-143120922
37	CEBPB	chr4:143186205-143187315	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:143305214-143305665	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr4:143291297-143291590	IMR90	lung:	n/a	chr4:143291454-143291465 chr4:143291456-143291465 chr4:143291456-143291465 chr4:143291456-143291465 chr4:143291454-143291467 chr4:143291456-143291465 chr4:143291454-143291467 chr4:143291456-143291467
40	CEBPB	chr4:143016855-143017808	HCT-116	colon:	n/a	chr4:143017638-143017649 chr4:143017531-143017542
41	CEBPB	chr4:143158737-143158992	IMR90	lung:	n/a	chr4:143158916-143158927 chr4:143158898-143158909
42	CEBPB	chr4:143268224-143268786	IMR90	lung:	n/a	chr4:143268592-143268603
43	CEBPB	chr4:142967254-142967471	HepG2	liver:	n/a	chr4:142967320-142967333 chr4:142967320-142967331 chr4:142967322-142967333
44	CEBPB	chr4:142967190-142967414	A549	lung:	n/a	chr4:142967320-142967333 chr4:142967320-142967331 chr4:142967322-142967333
45	CEBPB	chr4:143186625-143187120	HCT-116	colon:	n/a	n/a
46	CEBPB	chr4:142955330-142955582	K562	blood:	n/a	chr4:142955479-142955490
47	CEBPB	chr4:143012131-143013352	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:143195351-143196043	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:143012275-143013259	HCT-116	colon:	n/a	n/a
50	CEBPB	chr4:143268318-143268885	HCT-116	colon:	n/a	chr4:143268592-143268603

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:142956467-142956517	AG10803	skin:	n/a
2	chr4:143160459-143160509	LNCaP	prostate:	n/a
3	chr4:143184270-143184320	PFSK-1	brain:	n/a
4	chr4:143275181-143275231	Hepatocyte	liver:	n/a
5	chr4:143191281-143191331	GM12891	blood:	n/a
6	chr4:143160459-143160509	RPTEC	kidney:	n/a
7	chr4:143269319-143269369	HRCEpiC	kidney:	n/a
8	chr4:143275181-143275231	GM12878	blood:	n/a
9	chr4:143192375-143192425	AG09309	skin:	n/a
10	chr4:143170236-143170286	HNPCEpiC	eye:	n/a
11	chr4:143275181-143275231	PFSK-1	brain:	n/a
12	chr4:143160459-143160509	HEEpiC	esophagus:	n/a
13	chr4:143301382-143301432	NH-A	brain:	n/a
14	chr4:143217765-143217815	HCPEpiC	choroid plexus:	n/a
15	chr4:143160459-143160509	NHDF-neo	bronchial:	n/a
16	chr4:143192375-143192425	HRCEpiC	kidney:	n/a
17	chr4:143050435-143050485	AG09319	gingival:	n/a
18	chr4:143217765-143217815	HMEC	breast:	n/a
19	chr4:143184270-143184320	AG10803	skin:	n/a
20	chr4:142956467-142956517	CMK	blood:	n/a
21	chr4:142965608-142965658	NB4	blood:	n/a
22	chr4:143192375-143192425	RPTEC	kidney:	n/a
23	chr4:143192375-143192425	CMK	blood:	n/a
24	chr4:142965608-142965658	HepG2	liver:	n/a
25	chr4:143191281-143191331	NT2-D1	testis:	n/a
26	chr4:143160459-143160509	HUVEC	blood vessel:	n/a
27	chr4:143192375-143192425	GM19239	blood:	n/a
28	chr4:142956467-142956517	LNCaP	prostate:	n/a
29	chr4:142956467-142956517	HEK293	kidney:	embryo
30	chr4:143217765-143217815	MCF-7	breast:	n/a
31	chr4:143050435-143050485	GM06990	blood:	n/a
32	chr4:143217765-143217815	NH-A	brain:	n/a
33	chr4:143269319-143269369	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:143275181-143275231	SAEC	small airway:	n/a
35	chr4:143217765-143217815	HIPEpiC	eye:	n/a
36	chr4:142956467-142956517	HEEpiC	esophagus:	n/a
37	chr4:143170236-143170286	ProgFib	skin:	n/a
38	chr4:143286770-143286820	AG09309	skin:	n/a
39	chr4:143301382-143301432	PrEC	prostate:	n/a
40	chr4:143301382-143301432	NHBE	bronchial:	n/a
41	chr4:143301382-143301432	AG04450	lung:	fetal
42	chr4:143050435-143050485	GM12891	blood:	n/a
43	chr4:142956467-142956517	AG04450	lung:	fetal
44	chr4:143050435-143050485	NHDF-neo	bronchial:	n/a
45	chr4:143192375-143192425	MCF10A-Er-Src	breast:	n/a
46	chr4:143170236-143170286	ECC-1	luminal epithelium:	n/a
47	chr4:143160459-143160509	HCM	heart:	n/a
48	chr4:143301382-143301432	RPTEC	kidney:	n/a
49	chr4:143192375-143192425	HCPEpiC	choroid plexus:	n/a
50	chr4:143050435-143050485	HCT-116	colon:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:142950691..142953607-chr4:142965020..142967110,2	MCF-7	breast:
2	chr4:143122005..143123779-chr4:143127335..143129791,2	MCF-7	breast:
3	chr4:143248197..143251091-chr4:143251124..143253025,2	MCF-7	breast:
4	chr4:143266134..143268951-chr4:143395227..143397611,2	MCF-7	breast:
5	chr4:143130801..143132443-chr4:143135559..143138476,2	MCF-7	breast:
6	chr4:143254956..143256541-chr4:143392223..143394166,2	MCF-7	breast:
7	chr4:143086848..143088594-chr4:143091146..143093660,2	K562	blood:
8	chr4:143276856..143278860-chr4:143299385..143301357,2	MCF-7	breast:
9	chr4:143122005..143123779-chr4:143127335..143129791,2	MCF-7	breast:
10	chr4:143018754..143020846-chr4:143024197..143025698,2	MCF-7	breast:
11	chr4:143272607..143274373-chr4:143277065..143279303,2	MCF-7	breast:
12	chr4:143117327..143119027-chr4:143120300..143122539,2	MCF-7	breast:
13	chr4:143006661..143009015-chr4:143011228..143013827,2	MCF-7	breast:
14	chr4:143118041..143120721-chr4:143123483..143126182,2	MCF-7	breast:
15	chr4:143161536..143163187-chr4:143167916..143169950,2	MCF-7	breast:
16	chr4:142781808..142782795-chr4:143048083..143048829,2	MCF-7	breast:
17	chr4:143086848..143088594-chr4:143091146..143093660,2	K562	blood:
18	chr4:143087448..143089184-chr4:143091466..143093701,2	MCF-7	breast:
19	chr4:143248197..143251091-chr4:143251124..143253025,2	MCF-7	breast:
20	chr4:143246175..143247898-chr4:143247988..143249905,2	MCF-7	breast:
21	chr4:142951947..142953584-chr4:142957347..142959849,2	MCF-7	breast:
22	chr4:143110474..143112646-chr4:143112812..143114459,2	MCF-7	breast:
23	chr4:143277710..143279872-chr4:143280001..143282986,2	K562	blood:
24	chr4:142942418..142944888-chr4:142957295..142959081,2	MCF-7	breast:
25	chr4:143181530..143183042-chr4:143183086..143185031,2	MCF-7	breast:
26	chr4:142946395..142950633-chr4:142951002..142956006,4	MCF-7	breast:
27	chr4:143120582..143123051-chr4:143127171..143130077,2	MCF-7	breast:
28	chr4:142946395..142950633-chr4:142951002..142956006,4	MCF-7	breast:
29	chr4:143020271..143023015-chr4:143028673..143031244,3	MCF-7	breast:
30	chr4:143018754..143020846-chr4:143024197..143025698,2	MCF-7	breast:
31	chr4:143232269..143234234-chr4:143236195..143238233,2	K562	blood:
32	chr4:143272659..143276206-chr4:143392332..143397078,7	MCF-7	breast:
33	chr4:143023344..143025371-chr4:143034137..143035895,2	MCF-7	breast:
34	chr4:143277710..143279872-chr4:143280001..143282986,2	K562	blood:
35	chr4:142993302..142997726-chr4:142999331..143002418,4	MCF-7	breast:
36	chr4:143276856..143278860-chr4:143299385..143301357,2	MCF-7	breast:
37	chr4:143048538..143050644-chr4:143051888..143053940,2	MCF-7	breast:
38	chr4:143048538..143050644-chr4:143051888..143053940,2	MCF-7	breast:
39	chr4:143110474..143112646-chr4:143112812..143114459,2	MCF-7	breast:
40	chr4:142993302..142997726-chr4:142999331..143002418,4	MCF-7	breast:
41	chr4:143074063..143075563-chr4:143078201..143080746,2	MCF-7	breast:
42	chr4:143117327..143119027-chr4:143120300..143122539,2	MCF-7	breast:
43	chr15:65596725..65597394-chr4:143092760..143093280,2	Hela-S3	cervix:
44	chr4:143087448..143089184-chr4:143091466..143093701,2	MCF-7	breast:
45	chr4:143272607..143274373-chr4:143277065..143279303,2	MCF-7	breast:
46	chr4:143181530..143183042-chr4:143183086..143185031,2	MCF-7	breast:
47	chr4:143118041..143120721-chr4:143123483..143126182,2	MCF-7	breast:
48	chr4:142961970..142965946-chr4:142968550..142971585,4	MCF-7	breast:
49	chr4:142961970..142965946-chr4:142968550..142971585,4	MCF-7	breast:
50	chr4:143145988..143147916-chr4:143150196..143152200,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL15-1	chr4:143238391-143238699	NONHSAT098533

No data

Variant related genes	Relation type
INPP4B	TF binding region
RPL5P13	TF binding region
LSM3P4	TF binding region
INPP4B	CpG island
RPL5P13	CpG island
LSM3P4	CpG island
ENSG00000109452	chromatin interactions
ENSG00000200156	chromatin interactions

Extended variants
information (count: 14020 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:14020 , 50 per page) page: 1 2 3 4 5 6 7 ... 281

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2667120	chr4:142943485-142943486	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6829094	chr4:142943554-142943555	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs375673485	chr4:142943576-142943577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559731137	chr4:142943587-142943588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80261614	chr4:142943739-142943740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529274188	chr4:142943749-142943750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185352743	chr4:142943767-142943768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528045309	chr4:142943788-142943789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562814868	chr4:142943825-142943826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577974653	chr4:142943840-142943841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540159348	chr4:142943865-142943866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190900153	chr4:142943890-142943891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566234873	chr4:142943897-142943898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367919421	chr4:142943928-142943929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546199383	chr4:142943949-142943950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183975468	chr4:142943950-142943951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558183430	chr4:142943977-142943978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2645828	chr4:142944000-142944001	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556516392	chr4:142944025-142944026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538843921	chr4:142944029-142944030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529149883	chr4:142944047-142944048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376248850	chr4:142944053-142944054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553960964	chr4:142944057-142944058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189176290	chr4:142944070-142944071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11736202	chr4:142944080-142944081	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs79058486	chr4:142944170-142944171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75938847	chr4:142944183-142944184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151316909	chr4:142944212-142944213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573972755	chr4:142944305-142944306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531087601	chr4:142944317-142944318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544168460	chr4:142944322-142944323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562854347	chr4:142944353-142944354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533402478	chr4:142944379-142944380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192876585	chr4:142944496-142944497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149384926	chr4:142944515-142944516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527868616	chr4:142944553-142944554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548830686	chr4:142944586-142944587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549637607	chr4:142944653-142944654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72716481	chr4:142944681-142944682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529024275	chr4:142944684-142944685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539647984	chr4:142944745-142944746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549757543	chr4:142944768-142944769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17381004	chr4:142944769-142944770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs336363	chr4:142944773-142944774	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554093203	chr4:142944788-142944789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565765313	chr4:142944796-142944797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539772286	chr4:142944801-142944802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77825665	chr4:142944803-142944804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115649589	chr4:142944805-142944806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574040198	chr4:142944823-142944824	Weak transcription Enhancers	n/a	n/a	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
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
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	20952505	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:5206 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142940600-142948400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:142941800-142957800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr4:142942000-142953200	Weak transcription	Right Ventricle	heart
4	chr4:142942200-142949000	Weak transcription	Primary T cells from cord blood	blood
5	chr4:142942200-142949000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:142942400-142949200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:142942800-142945000	Enhancers	Stomach Mucosa	stomach
8	chr4:142943000-142944000	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr4:142943000-142944200	Enhancers	Fetal Intestine Small	intestine
10	chr4:142943200-142944000	Enhancers	Fetal Intestine Large	intestine
11	chr4:142943200-142945600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:142943400-142949000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr4:142943800-142944000	Enhancers	Duodenum Mucosa	Duodenum
14	chr4:142943800-142944200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:142943800-142944200	Enhancers	Pancreas	Pancrea
16	chr4:142943800-142965400	Weak transcription	Aorta	Aorta
17	chr4:142944000-142948800	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr4:142944200-142948400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr4:142944200-142955600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:142944200-142958600	Weak transcription	Fetal Intestine Small	intestine
21	chr4:142944200-142962800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr4:142945200-142946800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:142945400-142951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:142945400-142954800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr4:142945400-142983200	Weak transcription	Left Ventricle	heart
26	chr4:142945600-142948000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr4:142945600-142948200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr4:142945600-142949000	Weak transcription	NHEK	skin
29	chr4:142945600-142953400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:142945600-142955800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr4:142945800-142949800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr4:142946800-142947600	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr4:142947000-142948600	Weak transcription	HMEC	breast
34	chr4:142947000-142948600	Weak transcription	HSMM	muscle
35	chr4:142947400-142958000	Weak transcription	HSMMtube	muscle
36	chr4:142947600-142949000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr4:142947600-142949200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:142947800-142949400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:142947800-142977200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr4:142948000-142948200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:142948000-142950800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr4:142948200-142948400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:142948200-142951800	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr4:142948200-142959800	Weak transcription	Dnd41	blood
45	chr4:142948400-142948600	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr4:142948400-142949400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:142948400-142949600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:142948400-142950000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:142948400-142951800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:142948400-143029200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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