Variant report

Variant	nsv537081
Chromosome Location	chr4:47493552-47863354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3848)
CpG islands
(count:1953)
Chromatin interactive
region (count:93)
LncRNA
region (count:8)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:3848 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:47707563-47707945	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:47566310-47566738	K562	blood:	n/a	n/a
3	ARID3A	chr4:47688376-47688645	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:47665081-47665333	K562	blood:	n/a	n/a
5	ARID3A	chr4:47566343-47566703	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:47838667-47838904	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:47751721-47752471	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:47563328-47563680	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:47670805-47671245	K562	blood:	n/a	chr4:47671147-47671163
10	ARID3A	chr4:47735208-47736035	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:47717974-47718536	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:47788705-47789130	HepG2	liver:	n/a	n/a
13	ATF1	chr4:47567261-47567600	K562	blood:	n/a	n/a
14	ATF2	chr4:47500864-47501370	GM12878	blood:	n/a	n/a
15	ATF2	chr4:47495167-47495817	GM12878	blood:	n/a	n/a
16	ATF2	chr4:47495837-47496260	GM12878	blood:	n/a	n/a
17	ATF2	chr4:47521386-47522151	GM12878	blood:	n/a	n/a
18	ATF2	chr4:47788986-47789548	GM12878	blood:	n/a	n/a
19	ATF2	chr4:47841134-47841615	GM12878	blood:	n/a	n/a
20	ATF2	chr4:47512313-47512968	GM12878	blood:	n/a	n/a
21	ATF2	chr4:47533555-47534185	GM12878	blood:	n/a	n/a
22	ATF2	chr4:47533593-47534069	GM12878	blood:	n/a	n/a
23	ATF2	chr4:47521233-47522006	GM12878	blood:	n/a	n/a
24	ATF2	chr4:47512406-47513246	GM12878	blood:	n/a	n/a
25	BACH1	chr4:47567297-47567657	K562	blood:	n/a	n/a
26	BACH1	chr4:47688351-47688734	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:47567278-47567639	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr4:47838507-47839363	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:47588673-47588680	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:47578860-47578906	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr4:47732634-47732828	GM12878	blood:	n/a	n/a
32	BATF	chr4:47495830-47496135	GM12878	blood:	n/a	n/a
33	BATF	chr4:47512488-47512846	GM12878	blood:	n/a	n/a
34	BATF	chr4:47841192-47841573	GM12878	blood:	n/a	n/a
35	BATF	chr4:47512447-47512805	GM12878	blood:	n/a	n/a
36	BATF	chr4:47619700-47619940	GM12878	blood:	n/a	n/a
37	BATF	chr4:47567227-47567642	GM12878	blood:	n/a	chr4:47567444-47567455
38	BATF	chr4:47619695-47619918	GM12878	blood:	n/a	n/a
39	BATF	chr4:47567258-47567627	GM12878	blood:	n/a	chr4:47567444-47567455
40	BATF	chr4:47692635-47692950	GM12878	blood:	n/a	n/a
41	BATF	chr4:47732587-47732811	GM12878	blood:	n/a	n/a
42	BATF	chr4:47500843-47501151	GM12878	blood:	n/a	chr4:47500950-47500961
43	BATF	chr4:47500935-47501204	GM12878	blood:	n/a	chr4:47500950-47500961
44	BATF	chr4:47521527-47521876	GM12878	blood:	n/a	chr4:47521702-47521713
45	BATF	chr4:47521506-47521847	GM12878	blood:	n/a	chr4:47521702-47521713
46	BCL11A	chr4:47533703-47533967	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:47521529-47521803	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:47788971-47789411	GM12878	blood:	n/a	chr4:47789308-47789317
49	BCL11A	chr4:47774153-47774426	GM12878	blood:	n/a	n/a
50	BCL11A	chr4:47567257-47567596	GM12878	blood:	n/a	n/a

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:47597617-47597667	HepG2	liver:	n/a
2	chr4:47597617-47597667	HepG2	liver:	n/a
3	chr4:47710147-47710197	GM06990	blood:	n/a
4	chr4:47839218-47839268	BE2_C	brain:	n/a
5	chr4:47840050-47840100	HRCEpiC	kidney:	n/a
6	chr4:47769337-47769387	HL-60	blood:	n/a
7	chr4:47843915-47843965	GM06990	blood:	n/a
8	chr4:47708675-47708725	Caco-2	colon:	n/a
9	chr4:47597617-47597667	HCT-116	colon:	n/a
10	chr4:47769337-47769387	U87	brain:	n/a
11	chr4:47854334-47854384	U87	brain:	n/a
12	chr4:47513375-47513425	K562	blood:	n/a
13	chr4:47513375-47513425	HepG2	liver:	n/a
14	chr4:47840162-47840212	HCPEpiC	choroid plexus:	n/a
15	chr4:47708590-47708640	HMEC	breast:	n/a
16	chr4:47710147-47710197	HMEC	breast:	n/a
17	chr4:47839218-47839268	HMEC	breast:	n/a
18	chr4:47839876-47839926	H1-hESC	embryonic stem cell:	embryo
19	chr4:47710820-47710870	Hepatocyte	liver:	n/a
20	chr4:47838670-47838720	HCPEpiC	choroid plexus:	n/a
21	chr4:47838169-47838219	U87	brain:	n/a
22	chr4:47841314-47841364	GM06990	blood:	n/a
23	chr4:47838616-47838666	T-47D	breast:	n/a
24	chr4:47839218-47839268	AoSMC	blood vessel:	n/a
25	chr4:47840050-47840100	IMR90	lung:	fetal
26	chr4:47837775-47837825	HMEC	breast:	n/a
27	chr4:47840050-47840100	PFSK-1	brain:	n/a
28	chr4:47840011-47840061	Hepatocyte	liver:	n/a
29	chr4:47843915-47843965	HCPEpiC	choroid plexus:	n/a
30	chr4:47837775-47837825	T-47D	breast:	n/a
31	chr4:47839876-47839926	SKMC	muscle:	n/a
32	chr4:47719380-47719430	BJ	skin:	n/a
33	chr4:47707064-47707114	PrEC	prostate:	n/a
34	chr4:47840050-47840100	SKMC	muscle:	n/a
35	chr4:47597617-47597667	ovcar-3	ovarian:	n/a
36	chr4:47840136-47840186	MCF10A-Er-Src	breast:	n/a
37	chr4:47838616-47838666	GM12892	blood:	n/a
38	chr4:47841314-47841364	NB4	blood:	n/a
39	chr4:47854334-47854384	PANC-1	pancreas:	n/a
40	chr4:47839218-47839268	NHDF-neo	bronchial:	n/a
41	chr4:47838616-47838666	HRE	kidney:	n/a
42	chr4:47719380-47719430	AG09319	gingival:	n/a
43	chr4:47840683-47840733	Caco-2	colon:	n/a
44	chr4:47839283-47839333	HCPEpiC	choroid plexus:	n/a
45	chr4:47840162-47840212	HRE	kidney:	n/a
46	chr4:47769337-47769387	GM12892	blood:	n/a
47	chr4:47839218-47839268	HCPEpiC	choroid plexus:	n/a
48	chr4:47840095-47840145	AG10803	skin:	n/a
49	chr4:47708509-47708559	MCF-7	breast:	n/a
50	chr4:47708590-47708640	HCT-116	colon:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:47784622..47786268-chr4:47828748..47830719,2	K562	blood:
2	chr4:47707683..47708302-chr4:47841300..47841809,2	MCF-7	breast:
3	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
4	chr4:47825378..47827547-chr4:47837462..47840177,2	K562	blood:
5	chr4:47681469..47683085-chr4:47695089..47697198,2	MCF-7	breast:
6	chr4:47851196..47853833-chr4:47870828..47872465,2	K562	blood:
7	chr4:47464391..47466758-chr4:47562914..47565162,3	MCF-7	breast:
8	chr4:47706456..47708112-chr4:47838146..47839411,13	MCF-7	breast:
9	chr4:47500151..47502308-chr4:47567247..47568908,2	MCF-7	breast:
10	chr4:47688063..47688915-chr4:47838342..47839484,4	MCF-7	breast:
11	chr4:47686925..47689964-chr4:47690624..47694621,3	K562	blood:
12	chr4:47856515..47858025-chr4:47868614..47870377,2	K562	blood:
13	chr4:47648571..47650880-chr4:47653230..47655335,2	K562	blood:
14	chr4:47833491..47836348-chr4:47838465..47840542,2	K562	blood:
15	chr4:47830877..47834399-chr4:47836493..47839965,4	MCF-7	breast:
16	chr4:47562873..47564467-chr4:47565898..47568483,2	K562	blood:
17	chr4:47670607..47671485-chr4:47706644..47707642,3	MCF-7	breast:
18	chr4:47551527..47553990-chr4:47565971..47567988,2	K562	blood:
19	chr4:47523458..47525968-chr4:47532454..47534503,2	K562	blood:
20	chr4:47635495..47638462-chr4:47640474..47643094,3	K562	blood:
21	chr4:47749490..47752397-chr4:47755183..47756959,2	K562	blood:
22	chr4:47707683..47708302-chr4:47841300..47841809,2	MCF-7	breast:
23	chr4:47845768..47847720-chr4:47850595..47852586,2	MCF-7	breast:
24	chr4:47565772..47567712-chr4:47570354..47573060,2	K562	blood:
25	chr4:47830463..47833080-chr4:47836939..47838798,2	K562	blood:
26	chr4:47681469..47683085-chr4:47695089..47697198,2	MCF-7	breast:
27	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
28	chr4:47664704..47666852-chr4:47669426..47672146,2	K562	blood:
29	chr4:47688906..47691612-chr4:47692853..47694990,2	K562	blood:
30	chr4:47582229..47585198-chr4:47587871..47590442,2	K562	blood:
31	chr4:47707242..47709385-chr4:47710417..47712148,2	MCF-7	breast:
32	chr4:47635495..47638462-chr4:47640474..47643094,3	K562	blood:
33	chr4:47555618..47557283-chr4:47565873..47568060,2	K562	blood:
34	chr4:47664704..47666852-chr4:47669426..47672146,2	K562	blood:
35	chr4:47559378..47560960-chr4:47564050..47565557,2	K562	blood:
36	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:
37	chr4:47688906..47691612-chr4:47692853..47694990,2	K562	blood:
38	chr12:29705422..29705972-chr4:47631907..47632427,2	K562	blood:
39	chr4:47555618..47557283-chr4:47565873..47568060,2	K562	blood:
40	chr4:47706419..47708274-chr4:47838366..47839313,9	MCF-7	breast:
41	chr4:47843029..47844670-chr4:47907030..47909401,2	K562	blood:
42	chr4:47567303..47570218-chr4:47578983..47580542,2	K562	blood:
43	chr4:47818744..47821029-chr4:47839898..47842458,2	K562	blood:
44	chr4:47706546..47707227-chr4:48088499..48089380,2	MCF-7	breast:
45	chr4:47706836..47707551-chr4:47840198..47840747,2	MCF-7	breast:
46	chr4:47706456..47708112-chr4:47838146..47839411,13	MCF-7	breast:
47	chr4:47830463..47833080-chr4:47836939..47838798,2	K562	blood:
48	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:
49	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
50	chr4:47784622..47786268-chr4:47828748..47830719,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CORIN-2	chr4:47562219-47562276	ENSG00000248254.1
2	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096263
3	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096264
4	lnc-NIPAL1-3	chr4:47833186-47833525	NONHSAT096265
5	lnc-CORIN-2	chr4:47558748-47559020	ENSG00000248254.1
6	lnc-CORIN-1	chr4:47842139-47846356	ENSG00000259959.1
7	lnc-CORIN-2	chr4:47559659-47559928	ENSG00000248254.1
8	lnc-NIPAL1-2	chr4:47841939-47846867	NONHSAT096267

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
ENSG00000242431	TF binding region
ENSG00000259959	TF binding region
ATP10D	TF binding region
NFXL1	TF binding region
RN7SKP215	TF binding region
ENSG00000242262	TF binding region
ENSG00000248254	TF binding region
CORIN	TF binding region
ENSG00000242431	CpG island
ENSG00000259959	CpG island
ATP10D	CpG island
NFXL1	CpG island
RN7SKP215	CpG island
ENSG00000242262	CpG island
ENSG00000248254	CpG island
CORIN	CpG island
ENSG00000169019	chromatin interactions
ENSG00000259959	chromatin interactions
ENSG00000242431	chromatin interactions
ENSG00000242262	chromatin interactions
ENSG00000145246	chromatin interactions
ENSG00000248254	chromatin interactions
ENSG00000145244	chromatin interactions

Extended variants
information (count: 13361 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:13361 , 50 per page) page: 1 2 3 4 5 6 7 ... 268

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73813572	chr4:47493553-47493554	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566813865	chr4:47493610-47493611	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs576611533	chr4:47493614-47493615	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs140396407	chr4:47493652-47493653	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs34553226	chr4:47493684-47493685	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377256042	chr4:47493707-47493708	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs561910079	chr4:47493746-47493747	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs533988198	chr4:47493830-47493831	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs528976287	chr4:47493842-47493843	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs6815132	chr4:47493907-47493908	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs114504100	chr4:47493908-47493909	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532802156	chr4:47493926-47493927	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs551083961	chr4:47493953-47493954	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149921167	chr4:47493969-47493970	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs73138052	chr4:47493979-47493980	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs549184330	chr4:47493980-47493981	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs77326234	chr4:47493986-47493987	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs367627288	chr4:47493993-47493994	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs534795356	chr4:47494068-47494069	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs34200884	chr4:47494090-47494091	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs566175267	chr4:47494091-47494092	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539824752	chr4:47494100-47494101	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs185093595	chr4:47494135-47494136	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201801574	chr4:47494158-47494159	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189989858	chr4:47494171-47494172	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs570485162	chr4:47494200-47494201	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs555618693	chr4:47494253-47494254	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs181170830	chr4:47494309-47494310	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs35103500	chr4:47494332-47494333	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs556888929	chr4:47494404-47494405	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs7681768	chr4:47494483-47494484	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs185261288	chr4:47494484-47494485	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs7681783	chr4:47494496-47494497	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs563112767	chr4:47494525-47494526	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs530506405	chr4:47494631-47494632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549043359	chr4:47494636-47494637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7680740	chr4:47494637-47494638	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs528341746	chr4:47494663-47494664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116256504	chr4:47494749-47494750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371969708	chr4:47494831-47494832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566187325	chr4:47494837-47494838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188171386	chr4:47494842-47494843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539513459	chr4:47494914-47494915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180703767	chr4:47494953-47494954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555709453	chr4:47494976-47494977	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375428500	chr4:47494992-47494993	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569977928	chr4:47494997-47494998	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537435102	chr4:47495032-47495033	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs140588821	chr4:47495100-47495101	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs573989469	chr4:47495119-47495120	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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

Chromatin state (count:4383 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47488000-47533800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:47488600-47495400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:47488600-47495600	Weak transcription	Small Intestine	intestine
4	chr4:47488600-47500000	Weak transcription	Fetal Brain Male	brain
5	chr4:47488600-47514400	Weak transcription	Lung	lung
6	chr4:47488600-47524600	Weak transcription	Fetal Intestine Small	intestine
7	chr4:47488800-47495200	Weak transcription	Fetal Kidney	kidney
8	chr4:47488800-47495400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr4:47488800-47495600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:47488800-47495600	Weak transcription	Fetal Lung	lung
11	chr4:47488800-47500800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr4:47488800-47502400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr4:47488800-47502600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr4:47488800-47559800	Weak transcription	Right Ventricle	heart
15	chr4:47489000-47495400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr4:47489000-47495400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:47489000-47495800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr4:47489000-47500600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr4:47489000-47512000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr4:47489000-47514400	Weak transcription	Fetal Stomach	stomach
21	chr4:47489000-47514600	Weak transcription	Fetal Muscle Leg	muscle
22	chr4:47489200-47493600	Weak transcription	HSMM	muscle
23	chr4:47489200-47533600	Weak transcription	Esophagus	oesophagus
24	chr4:47489400-47495800	Weak transcription	Brain Angular Gyrus	brain
25	chr4:47489600-47511800	Weak transcription	HMEC	breast
26	chr4:47490000-47493600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:47490000-47495800	Weak transcription	Osteobl	bone
28	chr4:47490000-47501800	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr4:47490000-47502600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:47490000-47511800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr4:47490000-47512200	Weak transcription	HSMMtube	muscle
32	chr4:47490000-47514800	Weak transcription	Placenta	Placenta
33	chr4:47490200-47514200	Weak transcription	NH-A	brain
34	chr4:47491000-47494600	Weak transcription	Pancreas	Pancrea
35	chr4:47491000-47495600	Weak transcription	Left Ventricle	heart
36	chr4:47491000-47495600	Weak transcription	Psoas Muscle	Psoas
37	chr4:47491200-47500400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:47492200-47494400	Enhancers	NHEK	skin
39	chr4:47492800-47494000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:47492800-47494600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:47492800-47495200	Weak transcription	Brain Substantia Nigra	brain
42	chr4:47492800-47495400	Weak transcription	Brain Anterior Caudate	brain
43	chr4:47492800-47495400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr4:47492800-47495600	Weak transcription	Ovary	ovary
45	chr4:47492800-47495600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr4:47492800-47495800	Weak transcription	Spleen	Spleen
47	chr4:47492800-47496200	Enhancers	Dnd41	blood
48	chr4:47492800-47499400	Weak transcription	Liver	Liver
49	chr4:47492800-47514400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr4:47493000-47493600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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