Variant report

Variant	nsv1008515
Chromosome Location	chr4:47488431-47906835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4205)
CpG islands
(count:2139)
Chromatin interactive
region (count:132)
LncRNA
region (count:15)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:4205 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:47688376-47688645	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:47566343-47566703	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:47735208-47736035	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:47878677-47879238	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:47707563-47707945	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:47665081-47665333	K562	blood:	n/a	n/a
7	ARID3A	chr4:47788705-47789130	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:47751721-47752471	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:47899720-47899842	K562	blood:	n/a	n/a
10	ARID3A	chr4:47670805-47671245	K562	blood:	n/a	chr4:47671147-47671163
11	ARID3A	chr4:47884399-47884605	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:47838667-47838904	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:47717974-47718536	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:47566310-47566738	K562	blood:	n/a	n/a
15	ARID3A	chr4:47563328-47563680	HepG2	liver:	n/a	n/a
16	ARID3A	chr4:47881529-47882008	HepG2	liver:	n/a	n/a
17	ATF1	chr4:47567261-47567600	K562	blood:	n/a	n/a
18	ATF2	chr4:47500864-47501370	GM12878	blood:	n/a	n/a
19	ATF2	chr4:47512313-47512968	GM12878	blood:	n/a	n/a
20	ATF2	chr4:47841134-47841615	GM12878	blood:	n/a	n/a
21	ATF2	chr4:47495837-47496260	GM12878	blood:	n/a	n/a
22	ATF2	chr4:47533555-47534185	GM12878	blood:	n/a	n/a
23	ATF2	chr4:47788986-47789548	GM12878	blood:	n/a	n/a
24	ATF2	chr4:47533593-47534069	GM12878	blood:	n/a	n/a
25	ATF2	chr4:47521233-47522006	GM12878	blood:	n/a	n/a
26	ATF2	chr4:47495167-47495817	GM12878	blood:	n/a	n/a
27	ATF2	chr4:47521386-47522151	GM12878	blood:	n/a	n/a
28	ATF2	chr4:47512406-47513246	GM12878	blood:	n/a	n/a
29	BACH1	chr4:47567278-47567639	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:47588673-47588680	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:47567297-47567657	K562	blood:	n/a	n/a
32	BACH1	chr4:47578860-47578906	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr4:47688351-47688734	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr4:47838507-47839363	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr4:47495830-47496135	GM12878	blood:	n/a	n/a
36	BATF	chr4:47732634-47732828	GM12878	blood:	n/a	n/a
37	BATF	chr4:47567258-47567627	GM12878	blood:	n/a	chr4:47567444-47567455
38	BATF	chr4:47619700-47619940	GM12878	blood:	n/a	n/a
39	BATF	chr4:47512488-47512846	GM12878	blood:	n/a	n/a
40	BATF	chr4:47876259-47876454	GM12878	blood:	n/a	n/a
41	BATF	chr4:47500843-47501151	GM12878	blood:	n/a	chr4:47500950-47500961
42	BATF	chr4:47692635-47692950	GM12878	blood:	n/a	n/a
43	BATF	chr4:47619695-47619918	GM12878	blood:	n/a	n/a
44	BATF	chr4:47732587-47732811	GM12878	blood:	n/a	n/a
45	BATF	chr4:47500935-47501204	GM12878	blood:	n/a	chr4:47500950-47500961
46	BATF	chr4:47841192-47841573	GM12878	blood:	n/a	n/a
47	BATF	chr4:47521527-47521876	GM12878	blood:	n/a	chr4:47521702-47521713
48	BATF	chr4:47567227-47567642	GM12878	blood:	n/a	chr4:47567444-47567455
49	BATF	chr4:47512447-47512805	GM12878	blood:	n/a	n/a
50	BATF	chr4:47521506-47521847	GM12878	blood:	n/a	chr4:47521702-47521713

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:47840683-47840733	HAEpiC	amniotic membrane:	n/a
2	chr4:47840162-47840212	CMK	blood:	n/a
3	chr4:47840050-47840100	U87	brain:	n/a
4	chr4:47513375-47513425	HCPEpiC	choroid plexus:	n/a
5	chr4:47840683-47840733	HAEpiC	amniotic membrane:	n/a
6	chr4:47840162-47840212	CMK	blood:	n/a
7	chr4:47840050-47840100	U87	brain:	n/a
8	chr4:47513375-47513425	HCPEpiC	choroid plexus:	n/a
9	chr4:47843915-47843965	HNPCEpiC	eye:	n/a
10	chr4:47840162-47840212	AoSMC	blood vessel:	n/a
11	chr4:47708590-47708640	AoSMC	blood vessel:	n/a
12	chr4:47719380-47719430	AG04449	skin:	fetal
13	chr4:47840683-47840733	HEK293	kidney:	embryo
14	chr4:47488620-47488670	HUVEC	blood vessel:	n/a
15	chr4:47706142-47706192	NB4	blood:	n/a
16	chr4:47839876-47839926	ECC-1	luminal epithelium:	n/a
17	chr4:47708590-47708640	SKMC	muscle:	n/a
18	chr4:47708675-47708725	AG04449	skin:	fetal
19	chr4:47806451-47806501	NHBE	bronchial:	n/a
20	chr4:47710820-47710870	GM12892	blood:	n/a
21	chr4:47706142-47706192	AG09319	gingival:	n/a
22	chr4:47839283-47839333	HCT-116	colon:	n/a
23	chr4:47597617-47597667	AG10803	skin:	n/a
24	chr4:47708590-47708640	T-47D	breast:	n/a
25	chr4:47837775-47837825	AG04450	lung:	fetal
26	chr4:47708590-47708640	GM19239	blood:	n/a
27	chr4:47841314-47841364	HEEpiC	esophagus:	n/a
28	chr4:47708590-47708640	ovcar-3	ovarian:	n/a
29	chr4:47840095-47840145	Caco-2	colon:	n/a
30	chr4:47597617-47597667	HMEC	breast:	n/a
31	chr4:47839876-47839926	SK-N-SH_RA	brain:	n/a
32	chr4:47708590-47708640	K562	blood:	n/a
33	chr4:47840011-47840061	HEK293	kidney:	embryo
34	chr4:47838616-47838666	HUVEC	blood vessel:	n/a
35	chr4:47840011-47840061	ECC-1	luminal epithelium:	n/a
36	chr4:47595089-47595139	SK-N-SH	brain:	n/a
37	chr4:47710820-47710870	GM06990	blood:	n/a
38	chr4:47840011-47840061	HL-60	blood:	n/a
39	chr4:47885045-47885095	HRCEpiC	kidney:	n/a
40	chr4:47806451-47806501	MCF-7	breast:	n/a
41	chr4:47839218-47839268	HUVEC	blood vessel:	n/a
42	chr4:47839283-47839333	Jurkat	blood:	n/a
43	chr4:47840683-47840733	T-47D	breast:	n/a
44	chr4:47710820-47710870	CMK	blood:	n/a
45	chr4:47488620-47488670	A549	lung:	n/a
46	chr4:47840050-47840100	SKMC	muscle:	n/a
47	chr4:47838616-47838666	NHDF-neo	bronchial:	n/a
48	chr4:47708675-47708725	RPTEC	kidney:	n/a
49	chr4:47839876-47839926	GM12878	blood:	n/a
50	chr4:47865430-47865480	HRCEpiC	kidney:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:47681469..47683085-chr4:47695089..47697198,2	MCF-7	breast:
2	chr4:47851196..47853833-chr4:47870828..47872465,2	K562	blood:
3	chr4:47873831..47876676-chr4:47876808..47878387,2	K562	blood:
4	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:
5	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:
6	chr4:47902868..47906438-chr4:47914868..47916859,4	K562	blood:
7	chr4:47464211..47465735-chr4:47501718..47503942,2	MCF-7	breast:
8	chr4:47830463..47833080-chr4:47836939..47838798,2	K562	blood:
9	chr12:29705422..29705972-chr4:47631907..47632427,2	K562	blood:
10	chr4:47871619..47873479-chr4:47875359..47877345,2	K562	blood:
11	chr4:47856515..47858025-chr4:47868614..47870377,2	K562	blood:
12	chr4:47706458..47708260-chr4:47841005..47842113,10	MCF-7	breast:
13	chr4:47792582..47794260-chr4:47794493..47796071,2	K562	blood:
14	chr4:47464391..47466758-chr4:47562914..47565162,3	MCF-7	breast:
15	chr4:47523458..47525968-chr4:47532454..47534503,2	K562	blood:
16	chr4:47648571..47651518-chr4:47651849..47655335,3	K562	blood:
17	chr4:47906567..47911619-chr4:47914438..47917527,8	K562	blood:
18	chr4:47635495..47638462-chr4:47640474..47643094,3	K562	blood:
19	chr4:47551527..47553990-chr4:47565971..47567988,2	K562	blood:
20	chr4:47851196..47853833-chr4:47870828..47872465,2	K562	blood:
21	chr4:47706836..47707551-chr4:47840198..47840747,2	MCF-7	breast:
22	chr4:47533452..47535756-chr4:47565106..47567780,2	K562	blood:
23	chr4:47551465..47554055-chr4:47561436..47564386,2	K562	blood:
24	chr1:36983678..36984348-chr4:47541449..47542413,2	MCF-7	breast:
25	chr4:47664704..47666852-chr4:47669426..47672146,2	K562	blood:
26	chr4:47792582..47794260-chr4:47794493..47796071,2	K562	blood:
27	chr4:47888142..47889697-chr4:47892947..47895362,2	K562	blood:
28	chr4:47877148..47879313-chr4:47882721..47884841,2	MCF-7	breast:
29	chr4:47688052..47688948-chr4:48088860..48089367,2	K562	blood:
30	chr4:47500151..47502308-chr4:47567247..47568908,2	MCF-7	breast:
31	chr4:47899421..47901723-chr4:47910092..47913165,3	K562	blood:
32	chr4:47898704..47900928-chr4:47903159..47905423,2	MCF-7	breast:
33	chr4:47899350..47902171-chr4:47914955..47917482,2	K562	blood:
34	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
35	chr4:47833491..47836348-chr4:47838465..47840542,2	K562	blood:
36	chr4:47898704..47900928-chr4:47903159..47905423,2	MCF-7	breast:
37	chr4:47579042..47580858-chr4:47586979..47588587,2	K562	blood:
38	chr4:47681357..47683442-chr4:47686923..47688767,2	K562	blood:
39	chr4:47465270..47466239-chr4:47566493..47567056,2	MCF-7	breast:
40	chr4:47707242..47709385-chr4:47710417..47712148,2	MCF-7	breast:
41	chr4:47567303..47570218-chr4:47578983..47580542,2	K562	blood:
42	chr4:47648571..47650880-chr4:47653230..47655335,2	K562	blood:
43	chr4:47894034..47895961-chr4:47915600..47918104,2	K562	blood:
44	chr4:47830463..47833080-chr4:47836939..47838798,2	K562	blood:
45	chr4:47899340..47901037-chr4:47915084..47917889,2	MCF-7	breast:
46	chr4:47688611..47689443-chr4:47936530..47937494,2	K562	blood:
47	chr4:47902691..47906376-chr4:47913835..47916673,3	K562	blood:
48	chr4:47881002..47883818-chr4:47884414..47887354,2	K562	blood:
49	chr4:47845768..47847720-chr4:47850595..47852586,2	MCF-7	breast:
50	chr4:47784622..47786268-chr4:47828748..47830719,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CORIN-1	chr4:47842139-47846356	ENSG00000259959.1
2	lnc-NIPAL1-3	chr4:47877194-47877348	NONHSAT096265
3	lnc-CORIN-2	chr4:47562219-47562276	ENSG00000248254.1
4	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096263
5	lnc-NIPAL1-3	chr4:47877223-47877348	NONHSAT096264
6	lnc-NIPAL1-3	chr4:47898559-47898946	NONHSAT096263
7	lnc-NIPAL1-2	chr4:47841939-47846867	NONHSAT096267
8	lnc-COMMD8-1	chr4:47492984-47493488	NONHSAT096253
9	lnc-NIPAL1-3	chr4:47877194-47877348	NONHSAT096263
10	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096265
11	lnc-NIPAL1-3	chr4:47884259-47884595	NONHSAT096265
12	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096264
13	lnc-NIPAL1-3	chr4:47898559-47898630	NONHSAT096264
14	lnc-CORIN-2	chr4:47559659-47559928	ENSG00000248254.1
15	lnc-CORIN-2	chr4:47558748-47559020	ENSG00000248254.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-8053	chr4:47654696-47654719	MIMAT0030980

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATP10D	hsa-miR-192-5p	chr4:47548938-47548960

Variant related genes	Relation type
ATP10D	TF binding region
NFXL1	TF binding region
RN7SKP215	TF binding region
ENSG00000242262	TF binding region
ENSG00000242431	TF binding region
ENSG00000248254	TF binding region
ENSG00000259959	TF binding region
CORIN	TF binding region
ATP10D	CpG island
NFXL1	CpG island
RN7SKP215	CpG island
ENSG00000242262	CpG island
ENSG00000242431	CpG island
ENSG00000248254	CpG island
ENSG00000259959	CpG island
CORIN	CpG island
ENSG00000259959	chromatin interactions
ENSG00000242262	chromatin interactions
ENSG00000169019	chromatin interactions
ENSG00000163293	chromatin interactions
ENSG00000248254	chromatin interactions
ENSG00000170448	chromatin interactions
ENSG00000242431	chromatin interactions
ENSG00000145244	chromatin interactions
ENSG00000145246	chromatin interactions

Extended variants
information (count: 15054 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:15054 , 50 per page) page: 1 2 3 4 5 6 7 ... 302

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4695238	chr4:47488431-47488432	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11945442	chr4:47488480-47488481	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs35760816	chr4:47488548-47488549	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139737899	chr4:47488554-47488555	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143078787	chr4:47488559-47488560	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144323598	chr4:47488563-47488564	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs118113351	chr4:47488581-47488582	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148778373	chr4:47488621-47488622	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs575203720	chr4:47488641-47488642	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs111424345	chr4:47488642-47488643	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs560687270	chr4:47488816-47488817	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187808898	chr4:47488861-47488862	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190823175	chr4:47488905-47488906	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565161763	chr4:47488913-47488914	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532387440	chr4:47488951-47488952	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563193886	chr4:47488974-47488975	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550790937	chr4:47489008-47489009	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6851361	chr4:47489048-47489049	Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs373859287	chr4:47489053-47489054	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183009189	chr4:47489076-47489077	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6829370	chr4:47489135-47489136	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567584135	chr4:47489138-47489139	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188627226	chr4:47489139-47489140	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553294973	chr4:47489142-47489143	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139561405	chr4:47489170-47489171	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538852396	chr4:47489171-47489172	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557233380	chr4:47489235-47489236	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569514895	chr4:47489242-47489243	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146861690	chr4:47489244-47489245	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13146884	chr4:47489247-47489248	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11339753	chr4:47489248-47489249	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112976134	chr4:47489269-47489270	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572909725	chr4:47489294-47489295	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530574382	chr4:47489303-47489304	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73237014	chr4:47489308-47489309	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs545081210	chr4:47489323-47489324	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192799583	chr4:47489338-47489339	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183288624	chr4:47489345-47489346	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550759617	chr4:47489443-47489444	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562506914	chr4:47489461-47489462	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144984840	chr4:47489538-47489539	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187820369	chr4:47489583-47489584	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192746031	chr4:47489624-47489625	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs534744909	chr4:47489630-47489631	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546543831	chr4:47489655-47489656	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs571618267	chr4:47489716-47489717	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs10010745	chr4:47489726-47489727	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs557554040	chr4:47489727-47489728	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs183682131	chr4:47489734-47489735	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs189570578	chr4:47489750-47489751	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19214233	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Renal cell carcinoma	20952505	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:5783 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47486600-47488600	Active TSS	Brain Anterior Caudate	brain
2	chr4:47486800-47488600	Active TSS	Brain Germinal Matrix	brain
3	chr4:47486800-47488600	Active TSS	Fetal Intestine Small	intestine
4	chr4:47486800-47488800	Active TSS	Brain Cingulate Gyrus	brain
5	chr4:47486800-47488800	Active TSS	Brain Hippocampus Middle	brain
6	chr4:47486800-47488800	Active TSS	Brain Substantia Nigra	brain
7	chr4:47486800-47489000	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr4:47486800-47489000	Active TSS	Colon Smooth Muscle	Colon
9	chr4:47486800-47489000	Active TSS	Right Atrium	heart
10	chr4:47486800-47489400	Active TSS	Brain Angular Gyrus	brain
11	chr4:47486800-47489600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:47486800-47490000	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr4:47487000-47488600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:47487000-47488600	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr4:47487000-47488600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr4:47487000-47488600	Active TSS	Esophagus	oesophagus
17	chr4:47487000-47488600	Active TSS	Fetal Intestine Large	intestine
18	chr4:47487000-47488600	Active TSS	Fetal Muscle Trunk	muscle
19	chr4:47487000-47488600	Active TSS	Left Ventricle	heart
20	chr4:47487000-47488600	Active TSS	Lung	lung
21	chr4:47487000-47488600	Active TSS	A549	lung
22	chr4:47487000-47488800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr4:47487000-47488800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr4:47487000-47488800	Active TSS	Fetal Kidney	kidney
25	chr4:47487000-47488800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr4:47487000-47488800	Active TSS	Rectal Mucosa Donor 31	rectum
27	chr4:47487000-47488800	Active TSS	Rectal Smooth Muscle	rectum
28	chr4:47487000-47488800	Active TSS	Right Ventricle	heart
29	chr4:47487000-47488800	Active TSS	NHDF-Ad	bronchial
30	chr4:47487000-47489000	Active TSS	Aorta	Aorta
31	chr4:47487000-47489000	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr4:47487000-47489000	Active TSS	Ovary	ovary
33	chr4:47487000-47489000	Active TSS	Psoas Muscle	Psoas
34	chr4:47487000-47489200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:47487000-47489200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:47487000-47489600	Active TSS	HSMMtube	muscle
37	chr4:47487200-47488600	Active TSS	Pancreas	Pancrea
38	chr4:47487200-47488600	Active TSS	Small Intestine	intestine
39	chr4:47487200-47488600	Active TSS	Thymus	Thymus
40	chr4:47487200-47488600	Active TSS	GM12878-XiMat	blood
41	chr4:47487200-47488800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:47487200-47488800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:47487200-47488800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:47487200-47488800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:47487200-47488800	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr4:47487200-47488800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr4:47487200-47488800	Active TSS	Stomach Smooth Muscle	stomach
48	chr4:47487200-47488800	Active TSS	NHLF	lung
49	chr4:47487200-47489000	Active TSS	Muscle Satellite Cultured Cells	--
50	chr4:47487200-47489000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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