Variant report

Variant	nsv879504
Chromosome Location	chr4:79759796-79874275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1458)
CpG islands
(count:855)
Chromatin interactive
region (count:100)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79785579-79785957	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:79848133-79848210	K562	blood:	n/a	n/a
3	ARID3A	chr4:79861092-79861293	K562	blood:	n/a	n/a
4	ARID3A	chr4:79873063-79873300	K562	blood:	n/a	n/a
5	ARID3A	chr4:79783432-79784100	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:79785292-79785904	K562	blood:	n/a	n/a
7	ARID3A	chr4:79819756-79819877	K562	blood:	n/a	n/a
8	ATF1	chr4:79860428-79860778	K562	blood:	n/a	chr4:79860588-79860602
9	ATF2	chr4:79766511-79767010	GM12878	blood:	n/a	n/a
10	ATF3	chr4:79860298-79860756	K562	blood:	n/a	chr4:79860592-79860599 chr4:79860460-79860469 chr4:79860589-79860599 chr4:79860589-79860599
11	ATF3	chr4:79860353-79860754	H1-hESC	embryonic stem cell:	n/a	chr4:79860592-79860599 chr4:79860460-79860469 chr4:79860589-79860599 chr4:79860589-79860599
12	BACH1	chr4:79833071-79833432	K562	blood:	n/a	n/a
13	BACH1	chr4:79860390-79860553	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:79809144-79809314	K562	blood:	n/a	n/a
15	BATF	chr4:79861939-79862235	GM12878	blood:	n/a	n/a
16	BATF	chr4:79873713-79873907	GM12878	blood:	n/a	n/a
17	BCL3	chr4:79834012-79834662	K562	blood:	n/a	n/a
18	BCL3	chr4:79830474-79831147	K562	blood:	n/a	n/a
19	BCL3	chr4:79832653-79833335	K562	blood:	n/a	n/a
20	BCL3	chr4:79835256-79836579	K562	blood:	n/a	n/a
21	BCL3	chr4:79831208-79832389	K562	blood:	n/a	n/a
22	BCLAF1	chr4:79860302-79860806	GM12878	blood:	n/a	chr4:79860501-79860514 chr4:79860388-79860397 chr4:79860558-79860567 chr4:79860459-79860468 chr4:79860569-79860582 chr4:79860389-79860402 chr4:79860392-79860405 chr4:79860557-79860570 chr4:79860448-79860461
23	BHLHE40	chr4:79860381-79861177	GM12878	blood:	n/a	chr4:79860385-79860401 chr4:79860450-79860466 chr4:79860679-79860695
24	BHLHE40	chr4:79785583-79785928	K562	blood:	n/a	n/a
25	BHLHE40	chr4:79785560-79785921	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:79847698-79847707	K562	blood:	n/a	n/a
27	BHLHE40	chr4:79860453-79861141	K562	blood:	n/a	chr4:79860679-79860695
28	BHLHE40	chr4:79861371-79861378	K562	blood:	n/a	n/a
29	BHLHE40	chr4:79844804-79844893	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:79860373-79860797	HepG2	liver:	n/a	chr4:79860385-79860401 chr4:79860450-79860466 chr4:79860679-79860695
31	BHLHE40	chr4:79873063-79873329	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:79856171-79856233	HepG2	liver:	n/a	chr4:79856201-79856222
33	BHLHE40	chr4:79859982-79860084	HepG2	liver:	n/a	n/a
34	BHLHE40	chr4:79844764-79844888	K562	blood:	n/a	n/a
35	BHLHE40	chr4:79785696-79785848	A549	lung:	n/a	n/a
36	BHLHE40	chr4:79785593-79785894	HepG2	liver:	n/a	n/a
37	BRCA1	chr4:79860429-79860674	HepG2	liver:	n/a	n/a
38	BRCA1	chr4:79860568-79860768	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr4:79860441-79861108	K562	blood:	n/a	n/a
40	CBX3	chr4:79783417-79783810	K562	blood:	n/a	n/a
41	CCNT2	chr4:79860285-79860852	K562	blood:	n/a	n/a
42	CCNT2	chr4:79832937-79833033	K562	blood:	n/a	n/a
43	CCNT2	chr4:79826725-79826982	K562	blood:	n/a	n/a
44	CCNT2	chr4:79827679-79827879	K562	blood:	n/a	n/a
45	CCNT2	chr4:79808044-79808157	K562	blood:	n/a	n/a
46	CCNT2	chr4:79789916-79790022	K562	blood:	n/a	n/a
47	CCNT2	chr4:79836216-79836416	K562	blood:	n/a	n/a
48	CCNT2	chr4:79784481-79784683	K562	blood:	n/a	n/a
49	CEBPB	chr4:79785600-79785965	IMR90	lung:	n/a	chr4:79785779-79785790
50	CEBPB	chr4:79783366-79783842	A549	lung:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79861272-79861322	LNCaP	prostate:	n/a
2	chr4:79861272-79861322	LNCaP	prostate:	n/a
3	chr4:79860764-79860814	ECC-1	luminal epithelium:	n/a
4	chr4:79861064-79861114	NH-A	brain:	n/a
5	chr4:79861272-79861322	SK-N-SH_RA	brain:	n/a
6	chr4:79860731-79860781	BE2_C	brain:	n/a
7	chr4:79857189-79857239	SK-N-SH_RA	brain:	n/a
8	chr4:79861064-79861114	HRPEpiC	eye:	n/a
9	chr4:79861398-79861448	PANC-1	pancreas:	n/a
10	chr4:79860227-79860277	GM06990	blood:	n/a
11	chr4:79861272-79861322	HRPEpiC	eye:	n/a
12	chr4:79860764-79860814	HUVEC	blood vessel:	n/a
13	chr4:79861272-79861322	HIPEpiC	eye:	n/a
14	chr4:79860764-79860814	AG10803	skin:	n/a
15	chr4:79860706-79860756	CMK	blood:	n/a
16	chr4:79860686-79860736	ovcar-3	ovarian:	n/a
17	chr4:79861064-79861114	HCF	heart:	n/a
18	chr4:79861398-79861448	LNCaP	prostate:	n/a
19	chr4:79863439-79863489	Hela-S3	cervix:	n/a
20	chr4:79861064-79861114	MCF-7	breast:	n/a
21	chr4:79860731-79860781	SAEC	small airway:	n/a
22	chr4:79860507-79860557	AoSMC	blood vessel:	n/a
23	chr4:79863439-79863489	PrEC	prostate:	n/a
24	chr4:79833206-79833256	AG10803	skin:	n/a
25	chr4:79860764-79860814	HEEpiC	esophagus:	n/a
26	chr4:79861064-79861114	HAEpiC	amniotic membrane:	n/a
27	chr4:79861272-79861322	NH-A	brain:	n/a
28	chr4:79861284-79861334	SKMC	muscle:	n/a
29	chr4:79861284-79861334	AG04449	skin:	fetal
30	chr4:79860379-79860429	RPTEC	kidney:	n/a
31	chr4:79833206-79833256	HUVEC	blood vessel:	n/a
32	chr4:79860507-79860557	NH-A	brain:	n/a
33	chr4:79863439-79863489	AG09319	gingival:	n/a
34	chr4:79860686-79860736	A549	lung:	n/a
35	chr4:79861064-79861114	HepG2	liver:	n/a
36	chr4:79863439-79863489	AG04449	skin:	fetal
37	chr4:79861398-79861448	SK-N-MC	brain:	n/a
38	chr4:79861398-79861448	A549	lung:	n/a
39	chr4:79860227-79860277	U87	brain:	n/a
40	chr4:79860706-79860756	GM06990	blood:	n/a
41	chr4:79861284-79861334	PrEC	prostate:	n/a
42	chr4:79860686-79860736	Hela-S3	cervix:	n/a
43	chr4:79860731-79860781	ECC-1	luminal epithelium:	n/a
44	chr4:79861398-79861448	BJ	skin:	n/a
45	chr4:79861064-79861114	HEK293	kidney:	embryo
46	chr4:79860764-79860814	NT2-D1	testis:	n/a
47	chr4:79860731-79860781	ovcar-3	ovarian:	n/a
48	chr4:79857189-79857239	PrEC	prostate:	n/a
49	chr4:79857189-79857239	SAEC	small airway:	n/a
50	chr4:79857189-79857239	Hela-S3	cervix:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:79801022..79805808-chr4:79807726..79811074,5	K562	blood:
2	chr4:79825919..79829336-chr4:79829339..79831601,4	K562	blood:
3	chr4:79831058..79832655-chr4:79840506..79842015,2	K562	blood:
4	chr4:79760812..79762742-chr4:79764884..79766656,2	K562	blood:
5	chr4:79822536..79825441-chr4:79835440..79838269,2	K562	blood:
6	chr4:79769174..79772080-chr4:79784280..79787147,3	K562	blood:
7	chr4:79829059..79831029-chr4:79832192..79834992,2	MCF-7	breast:
8	chr4:79778433..79779969-chr4:79781094..79783460,2	MCF-7	breast:
9	chr4:79697257..79699576-chr4:79770892..79773352,2	MCF-7	breast:
10	chr4:79696515..79698358-chr4:79778442..79780983,2	K562	blood:
11	chr4:79844612..79846577-chr4:79849709..79851536,2	K562	blood:
12	chr4:79781020..79783476-chr4:79785688..79788652,2	K562	blood:
13	chr4:79530033..79532299-chr4:79783489..79785388,2	K562	blood:
14	chr4:79862625..79864770-chr4:79868680..79870409,2	K562	blood:
15	chr4:79851616..79853186-chr4:79857040..79859204,2	K562	blood:
16	chr4:79837404..79838979-chr4:79854322..79856124,2	K562	blood:
17	chr4:79829830..79832841-chr4:79834364..79837824,5	K562	blood:
18	chr4:79761242..79763220-chr4:79764884..79767301,3	K562	blood:
19	chr4:79829059..79831029-chr4:79832192..79834992,2	MCF-7	breast:
20	chr4:79801022..79805808-chr4:79807726..79811074,5	K562	blood:
21	chr4:79695272..79698029-chr4:79784745..79787185,2	K562	blood:
22	chr4:79873242..79873800-chr4:81973211..81973738,2	MCF-7	breast:
23	chr4:79782620..79784445-chr4:79794037..79795842,2	K562	blood:
24	chr4:79471198..79473938-chr4:79857809..79860687,2	MCF-7	breast:
25	chr4:79770645..79772901-chr4:79776506..79779680,4	K562	blood:
26	chr4:79847059..79848626-chr4:79851803..79854574,2	MCF-7	breast:
27	chr4:79805887..79807602-chr4:79818996..79821641,2	K562	blood:
28	chr4:79805590..79808034-chr4:79829365..79831567,2	K562	blood:
29	chr4:79830154..79832739-chr4:79833941..79836867,6	K562	blood:
30	chr4:79873164..79873769-chr4:81257744..81258254,2	K562	blood:
31	chr4:79774563..79776854-chr4:79782145..79784064,2	K562	blood:
32	chr4:79862625..79864770-chr4:79868680..79870409,2	K562	blood:
33	chr4:79805590..79808034-chr4:79829365..79831567,2	K562	blood:
34	chr4:79785946..79789478-chr4:79791153..79794900,4	K562	blood:
35	chr4:79837404..79838979-chr4:79854322..79856124,2	K562	blood:
36	chr4:79791678..79793828-chr4:79794814..79796919,2	K562	blood:
37	chr4:79779277..79780895-chr4:79788393..79790584,2	K562	blood:
38	chr4:79833011..79834569-chr4:79834648..79836357,2	K562	blood:
39	chr4:79773476..79776467-chr4:79776731..79781526,5	K562	blood:
40	chr4:79762332..79763887-chr4:79767751..79769373,2	K562	blood:
41	chr4:79873154..79873710-chr4:81104976..81105506,2	MCF-7	breast:
42	chr4:79696491..79698405-chr4:79800839..79803388,2	MCF-7	breast:
43	chr4:79855106..79856905-chr4:79860204..79861714,2	MCF-7	breast:
44	chr4:79530799..79532363-chr4:79783489..79785979,2	K562	blood:
45	chr4:79846006..79848197-chr4:79849339..79851682,3	MCF-7	breast:
46	chr4:79700005..79702087-chr4:79782609..79785586,2	MCF-7	breast:
47	chr4:79791387..79793798-chr4:79797474..79798989,2	K562	blood:
48	chr4:79873114..79873664-chr4:81910812..81911504,2	K562	blood:
49	chr4:79855400..79857526-chr4:79859371..79861316,2	MCF-7	breast:
50	chr4:79762332..79763887-chr4:79767751..79769373,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANXA3-8	chr4:79834384-79837517	NONHSAT097093
2	lnc-ANXA3-7	chr4:79789779-79789887	ucscGeneNc_uc003hlh_2
3	lnc-ANXA3-7	chr4:79820939-79823361	ucscGeneNc_uc003hlh_2
4	lnc-ANXA3-7	chr4:79786362-79786441	ucscGeneNc_uc003hlh_2
5	lnc-ANXA3-6	chr4:79820009-79820306	NONHSAT097090
6	lnc-ANXA3-7	chr4:79803096-79803189	ucscGeneNc_uc003hlh_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PAQR3	hsa-miR-16-5p	chr4:79841493-79841487
2	PAQR3	hsa-miR-16-5p	chr4:79841487-79841508

Variant related genes	Relation type
RN7SL127P	TF binding region
PAQR3	TF binding region
BMP2K	TF binding region
RN7SL127P	CpG island
PAQR3	CpG island
BMP2K	CpG island
ENSG00000260278	chromatin interactions
ENSG00000138756	chromatin interactions
ENSG00000242175	chromatin interactions
ENSG00000138772	chromatin interactions
ENSG00000163291	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000152784	chromatin interactions

Extended variants
information (count: 3722 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3722 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13122868	chr4:79759796-79759797	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77315690	chr4:79759802-79759803	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs531976637	chr4:79759824-79759825	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs547966991	chr4:79759828-79759829	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs568183892	chr4:79759853-79759854	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs17003464	chr4:79759857-79759858	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148400605	chr4:79759872-79759873	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs142993835	chr4:79759873-79759874	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs529894667	chr4:79759876-79759877	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs181360143	chr4:79759918-79759919	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs556453646	chr4:79759925-79759926	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs186844170	chr4:79759926-79759927	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs150687250	chr4:79759938-79759939	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs555434149	chr4:79759942-79759943	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs560051109	chr4:79759943-79759944	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs72659101	chr4:79760072-79760073	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541023869	chr4:79760075-79760076	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs570382254	chr4:79760102-79760103	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs564519864	chr4:79760108-79760109	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs532276908	chr4:79760133-79760134	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs190133391	chr4:79760197-79760198	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs181909779	chr4:79760268-79760269	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs186555222	chr4:79760324-79760325	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs548452502	chr4:79760325-79760326	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs144782625	chr4:79760342-79760343	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs527392887	chr4:79760363-79760364	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs191060342	chr4:79760401-79760402	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570450377	chr4:79760406-79760407	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539092256	chr4:79760407-79760408	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs367694113	chr4:79760437-79760438	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556803422	chr4:79760466-79760467	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182101116	chr4:79760483-79760484	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528603802	chr4:79760546-79760547	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10022801	chr4:79760693-79760694	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs535195482	chr4:79760720-79760721	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369880978	chr4:79760730-79760731	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs207464825	chr4:79760735-79760736	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555547524	chr4:79760760-79760761	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554130359	chr4:79760768-79760769	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78687158	chr4:79760794-79760795	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147903968	chr4:79760799-79760800	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557996794	chr4:79760811-79760812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577954502	chr4:79760841-79760842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186039195	chr4:79761037-79761038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28542833	chr4:79761045-79761046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576155044	chr4:79761061-79761062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35961308	chr4:79761116-79761117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562768248	chr4:79761130-79761131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115387358	chr4:79761202-79761203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542005440	chr4:79761206-79761207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2554 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79738800-79793200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:79744600-79793800	Weak transcription	Psoas Muscle	Psoas
3	chr4:79745400-79760400	Strong transcription	K562	blood
4	chr4:79745800-79786400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr4:79746600-79761000	Strong transcription	Primary B cells from cord blood	blood
6	chr4:79746800-79760400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:79746800-79761000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:79746800-79783400	Weak transcription	A549	lung
9	chr4:79747200-79815600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr4:79748800-79823600	Weak transcription	Small Intestine	intestine
11	chr4:79749200-79773800	Weak transcription	Esophagus	oesophagus
12	chr4:79749200-79793600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr4:79749400-79780000	Weak transcription	HUVEC	blood vessel
14	chr4:79749400-79782000	Weak transcription	HepG2	liver
15	chr4:79749400-79792400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr4:79749400-79793800	Weak transcription	Gastric	stomach
17	chr4:79749600-79762200	Weak transcription	Pancreas	Pancrea
18	chr4:79749600-79766000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr4:79749600-79781000	Weak transcription	Ovary	ovary
20	chr4:79749600-79784600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:79749600-79793000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:79749600-79793600	Weak transcription	Brain Germinal Matrix	brain
23	chr4:79749600-79793800	Weak transcription	Fetal Brain Female	brain
24	chr4:79749800-79760000	Weak transcription	Spleen	Spleen
25	chr4:79749800-79761800	Weak transcription	Fetal Brain Male	brain
26	chr4:79749800-79762200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr4:79749800-79766200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr4:79749800-79772200	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr4:79749800-79773600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:79749800-79781400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr4:79749800-79786800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr4:79749800-79788000	Weak transcription	Lung	lung
33	chr4:79749800-79793400	Weak transcription	Thymus	Thymus
34	chr4:79749800-79793600	Weak transcription	Colonic Mucosa	Colon
35	chr4:79750000-79766800	Weak transcription	Brain Substantia Nigra	brain
36	chr4:79750200-79762200	Weak transcription	Aorta	Aorta
37	chr4:79750200-79772200	Weak transcription	Placenta	Placenta
38	chr4:79750200-79786600	Weak transcription	Left Ventricle	heart
39	chr4:79750200-79787600	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr4:79750400-79763800	Weak transcription	Brain Anterior Caudate	brain
41	chr4:79750400-79764200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr4:79750400-79772600	Weak transcription	Dnd41	blood
43	chr4:79750400-79777800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr4:79750400-79783400	Weak transcription	NHEK	skin
45	chr4:79750400-79786800	Weak transcription	NH-A	brain
46	chr4:79750400-79791400	Weak transcription	Colon Smooth Muscle	Colon
47	chr4:79750400-79792200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr4:79750400-79792600	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr4:79750400-79793600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr4:79750400-79797000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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