Variant report

Variant	nsv829923
Chromosome Location	chr4:47436139-47678443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3209)
CpG islands
(count:1892)
Chromatin interactive
region (count:68)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:3209 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:47665081-47665333	K562	blood:	n/a	n/a
2	ARID3A	chr4:47465478-47465975	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:47670805-47671245	K562	blood:	n/a	chr4:47671147-47671163
4	ARID3A	chr4:47566310-47566738	K562	blood:	n/a	n/a
5	ARID3A	chr4:47563328-47563680	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:47487095-47487417	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:47566343-47566703	HepG2	liver:	n/a	n/a
8	ATF1	chr4:47484127-47484287	K562	blood:	n/a	n/a
9	ATF1	chr4:47487087-47487619	K562	blood:	n/a	n/a
10	ATF1	chr4:47567261-47567600	K562	blood:	n/a	n/a
11	ATF2	chr4:47486877-47487724	GM12878	blood:	n/a	n/a
12	ATF2	chr4:47465150-47466061	GM12878	blood:	n/a	n/a
13	ATF2	chr4:47500864-47501370	GM12878	blood:	n/a	n/a
14	ATF2	chr4:47495837-47496260	GM12878	blood:	n/a	n/a
15	ATF2	chr4:47465413-47465867	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:47465468-47465825	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:47521386-47522151	GM12878	blood:	n/a	n/a
18	ATF2	chr4:47533593-47534069	GM12878	blood:	n/a	n/a
19	ATF2	chr4:47533555-47534185	GM12878	blood:	n/a	n/a
20	ATF2	chr4:47521233-47522006	GM12878	blood:	n/a	n/a
21	ATF2	chr4:47495167-47495817	GM12878	blood:	n/a	n/a
22	ATF2	chr4:47486956-47487848	GM12878	blood:	n/a	n/a
23	ATF2	chr4:47512313-47512968	GM12878	blood:	n/a	n/a
24	ATF2	chr4:47512406-47513246	GM12878	blood:	n/a	n/a
25	ATF2	chr4:47466935-47467507	GM12878	blood:	n/a	n/a
26	ATF3	chr4:47465491-47465867	H1-hESC	embryonic stem cell:	n/a	chr4:47465570-47465579
27	ATF3	chr4:47465515-47465976	A549	lung:	n/a	chr4:47465570-47465579
28	ATF3	chr4:47465562-47465919	K562	blood:	n/a	chr4:47465570-47465579
29	ATF3	chr4:47465468-47466025	GM12878	blood:	n/a	chr4:47465570-47465579
30	ATF3	chr4:47465456-47465941	HepG2	liver:	n/a	chr4:47465570-47465579
31	ATF3	chr4:47465535-47465868	K562	blood:	n/a	chr4:47465570-47465579
32	ATF3	chr4:47465578-47465836	GM12878	blood:	n/a	n/a
33	ATF3	chr4:47465427-47465908	H1-hESC	embryonic stem cell:	n/a	chr4:47465570-47465579
34	ATF3	chr4:47465525-47465870	HepG2	liver:	n/a	chr4:47465570-47465579
35	BACH1	chr4:47578860-47578906	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr4:47567278-47567639	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr4:47487301-47487818	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr4:47567297-47567657	K562	blood:	n/a	n/a
39	BACH1	chr4:47588673-47588680	H1-hESC	embryonic stem cell:	n/a	n/a
40	BATF	chr4:47495830-47496135	GM12878	blood:	n/a	n/a
41	BATF	chr4:47521527-47521876	GM12878	blood:	n/a	chr4:47521702-47521713
42	BATF	chr4:47521506-47521847	GM12878	blood:	n/a	chr4:47521702-47521713
43	BATF	chr4:47567258-47567627	GM12878	blood:	n/a	chr4:47567444-47567455
44	BATF	chr4:47484414-47484698	GM12878	blood:	n/a	chr4:47484565-47484576 chr4:47484566-47484576 chr4:47484601-47484612
45	BATF	chr4:47619695-47619918	GM12878	blood:	n/a	n/a
46	BATF	chr4:47567227-47567642	GM12878	blood:	n/a	chr4:47567444-47567455
47	BATF	chr4:47484427-47484735	GM12878	blood:	n/a	chr4:47484565-47484576 chr4:47484566-47484576 chr4:47484601-47484612
48	BATF	chr4:47500843-47501151	GM12878	blood:	n/a	chr4:47500950-47500961
49	BATF	chr4:47512488-47512846	GM12878	blood:	n/a	n/a
50	BATF	chr4:47619700-47619940	GM12878	blood:	n/a	n/a

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:47465763-47465813	K562	blood:	n/a
2	chr4:47465763-47465813	K562	blood:	n/a
3	chr4:47488375-47488425	HCT-116	colon:	n/a
4	chr4:47487307-47487357	SAEC	small airway:	n/a
5	chr4:47465676-47465726	A549	lung:	n/a
6	chr4:47487301-47487351	T-47D	breast:	n/a
7	chr4:47465011-47465061	HL-60	blood:	n/a
8	chr4:47487088-47487138	A549	lung:	n/a
9	chr4:47465727-47465777	GM06990	blood:	n/a
10	chr4:47465578-47465628	HMEC	breast:	n/a
11	chr4:47487181-47487231	PANC-1	pancreas:	n/a
12	chr4:47487088-47487138	U87	brain:	n/a
13	chr4:47487301-47487351	HNPCEpiC	eye:	n/a
14	chr4:47488620-47488670	HCF	heart:	n/a
15	chr4:47465578-47465628	HUVEC	blood vessel:	n/a
16	chr4:47465763-47465813	MCF-7	breast:	n/a
17	chr4:47465676-47465726	HEK293	kidney:	embryo
18	chr4:47465763-47465813	PFSK-1	brain:	n/a
19	chr4:47533905-47533955	HCM	heart:	n/a
20	chr4:47469644-47469694	ovcar-3	ovarian:	n/a
21	chr4:47465578-47465628	Jurkat	blood:	n/a
22	chr4:47513375-47513425	NHDF-neo	bronchial:	n/a
23	chr4:47465732-47465782	GM12891	blood:	n/a
24	chr4:47465732-47465782	SK-N-MC	brain:	n/a
25	chr4:47487587-47487637	IMR90	lung:	fetal
26	chr4:47487181-47487231	ovcar-3	ovarian:	n/a
27	chr4:47465578-47465628	HCPEpiC	choroid plexus:	n/a
28	chr4:47465732-47465782	GM12878	blood:	n/a
29	chr4:47465606-47465656	NHBE	bronchial:	n/a
30	chr4:47465887-47465937	MCF10A-Er-Src	breast:	n/a
31	chr4:47466696-47466746	SK-N-MC	brain:	n/a
32	chr4:47487307-47487357	HEEpiC	esophagus:	n/a
33	chr4:47465732-47465782	HUVEC	blood vessel:	n/a
34	chr4:47488375-47488425	SK-N-SH_RA	brain:	n/a
35	chr4:47595089-47595139	A549	lung:	n/a
36	chr4:47487181-47487231	HRE	kidney:	n/a
37	chr4:47487081-47487131	SK-N-MC	brain:	n/a
38	chr4:47513375-47513425	GM12891	blood:	n/a
39	chr4:47463168-47463218	SKMC	muscle:	n/a
40	chr4:47487235-47487285	HCF	heart:	n/a
41	chr4:47465727-47465777	PANC-1	pancreas:	n/a
42	chr4:47533905-47533955	U87	brain:	n/a
43	chr4:47463168-47463218	HMEC	breast:	n/a
44	chr4:47487307-47487357	HRPEpiC	eye:	n/a
45	chr4:47469644-47469694	IMR90	lung:	fetal
46	chr4:47513375-47513425	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:47465887-47465937	HRCEpiC	kidney:	n/a
48	chr4:47487081-47487131	HEK293	kidney:	embryo
49	chr4:47465011-47465061	SK-N-SH	brain:	n/a
50	chr4:47463168-47463218	HL-60	blood:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:47648571..47650880-chr4:47653230..47655335,2	K562	blood:
2	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
3	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
4	chr4:47459303..47460947-chr4:47464140..47467077,2	K562	blood:
5	chr4:47467618..47470444-chr4:47476083..47477741,2	MCF-7	breast:
6	chr4:47533452..47535756-chr4:47565106..47567780,2	K562	blood:
7	chr4:47536442..47538388-chr4:47538970..47540735,2	K562	blood:
8	chr4:47437562..47440498-chr4:47441242..47443779,2	K562	blood:
9	chr4:47523458..47525968-chr4:47532454..47534503,2	K562	blood:
10	chr4:47468877..47471001-chr4:47471871..47473913,2	K562	blood:
11	chr4:47464387..47467062-chr4:47485314..47486834,2	MCF-7	breast:
12	chr4:47464211..47465735-chr4:47501718..47503942,2	MCF-7	breast:
13	chr4:47437562..47440498-chr4:47441242..47443779,2	K562	blood:
14	chr4:47492804..47494644-chr4:47499606..47501616,2	K562	blood:
15	chr4:47465829..47468286-chr4:47470252..47472768,2	K562	blood:
16	chr4:47447254..47449925-chr4:47463916..47465485,2	MCF-7	breast:
17	chr4:47467618..47470444-chr4:47476083..47477741,2	MCF-7	breast:
18	chr4:47664704..47666852-chr4:47669426..47672146,2	K562	blood:
19	chr4:47523458..47525968-chr4:47532454..47534503,2	K562	blood:
20	chr4:47386562..47388237-chr4:47450427..47451934,2	K562	blood:
21	chr4:47472104..47474705-chr4:47476405..47478497,2	K562	blood:
22	chr4:47465829..47468286-chr4:47470252..47472768,2	K562	blood:
23	chr4:47565772..47567712-chr4:47570354..47573060,2	K562	blood:
24	chr4:47562873..47564467-chr4:47565898..47568483,2	K562	blood:
25	chr4:47500151..47502308-chr4:47567247..47568908,2	MCF-7	breast:
26	chr1:36983678..36984348-chr4:47541449..47542413,2	MCF-7	breast:
27	chr4:47559378..47560960-chr4:47564050..47565557,2	K562	blood:
28	chr4:47635495..47638462-chr4:47640474..47643094,3	K562	blood:
29	chr4:47551465..47554055-chr4:47561436..47564386,2	K562	blood:
30	chr4:47664704..47666852-chr4:47669426..47672146,2	K562	blood:
31	chr4:47477491..47479859-chr4:47486626..47489619,2	MCF-7	breast:
32	chr4:47455346..47457832-chr4:47566680..47568849,2	K562	blood:
33	chr4:47551527..47553990-chr4:47565971..47567988,2	K562	blood:
34	chr4:47579042..47580858-chr4:47586979..47588587,2	K562	blood:
35	chr4:47460523..47463508-chr4:47463640..47467389,5	MCF-7	breast:
36	chr4:47447345..47449625-chr4:47449993..47452895,2	K562	blood:
37	chr4:47565772..47567712-chr4:47570354..47573060,2	K562	blood:
38	chr4:47460857..47463494-chr4:47464329..47466944,2	MCF-7	breast:
39	chr4:47494690..47496480-chr4:47498763..47501727,2	K562	blood:
40	chr4:47468877..47471001-chr4:47471871..47473913,2	K562	blood:
41	chr4:47567303..47570218-chr4:47578983..47580542,2	K562	blood:
42	chr4:47551527..47553990-chr4:47565795..47567988,3	K562	blood:
43	chr4:47397863..47399973-chr4:47459020..47461928,2	K562	blood:
44	chr4:47670607..47671485-chr4:47706644..47707642,3	MCF-7	breast:
45	chr4:47447254..47449925-chr4:47463916..47465485,2	MCF-7	breast:
46	chr4:47447345..47449625-chr4:47449993..47452895,2	K562	blood:
47	chr4:47465270..47466239-chr4:47566493..47567056,2	MCF-7	breast:
48	chr4:47551527..47553990-chr4:47565971..47567988,2	K562	blood:
49	chr4:47555618..47557283-chr4:47565873..47568060,2	K562	blood:
50	chr4:47533452..47535756-chr4:47565106..47567780,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CORIN-2	chr4:47559659-47559928	ENSG00000248254.1
2	lnc-CORIN-2	chr4:47558748-47559020	ENSG00000248254.1
3	lnc-COMMD8-1	chr4:47492984-47493488	NONHSAT096253
4	lnc-GABRB1-1	chr4:47433977-47440976	ENSG00000260918.1
5	lnc-GABRB1-1	chr4:47438484-47440426	NONHSAT096250
6	lnc-CORIN-2	chr4:47562219-47562276	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
COMMD8	TF binding region
ENSG00000242431	TF binding region
ENSG00000248254	TF binding region
CORIN	TF binding region
ATP10D	CpG island
COMMD8	CpG island
ENSG00000242431	CpG island
ENSG00000248254	CpG island
CORIN	CpG island
ENSG00000169019	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000145246	chromatin interactions
ENSG00000242431	chromatin interactions
ENSG00000248254	chromatin interactions

Extended variants
information (count: 8895 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:8895 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185408371	chr4:47436231-47436232	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs144658307	chr4:47436236-47436237	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534463655	chr4:47436247-47436248	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs4450898	chr4:47436404-47436405	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs577238819	chr4:47436406-47436407	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs572171327	chr4:47436434-47436435	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs374087895	chr4:47436462-47436463	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs545874985	chr4:47436477-47436478	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs4388055	chr4:47436489-47436490	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556366134	chr4:47436529-47436530	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs116852989	chr4:47436552-47436553	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs544108093	chr4:47436553-47436554	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs10470771	chr4:47436571-47436572	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529514949	chr4:47436572-47436573	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs78557373	chr4:47436621-47436622	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs559972922	chr4:47436623-47436624	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs189986931	chr4:47436637-47436638	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs559868767	chr4:47436688-47436689	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs551499524	chr4:47436695-47436696	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs569673823	chr4:47436699-47436700	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs530385212	chr4:47436730-47436731	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs181573989	chr4:47436737-47436738	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs28564999	chr4:47436804-47436805	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs73813529	chr4:47436832-47436833	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552781368	chr4:47436844-47436845	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs139535945	chr4:47436868-47436869	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs539589309	chr4:47436873-47436874	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs557933264	chr4:47436971-47436972	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs533872045	chr4:47437071-47437072	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs576390236	chr4:47437077-47437078	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs527275488	chr4:47437131-47437132	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs144480987	chr4:47437148-47437149	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs73813530	chr4:47437155-47437156	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574422080	chr4:47437187-47437188	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs143425607	chr4:47437188-47437189	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs541723530	chr4:47437240-47437241	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs185517371	chr4:47437276-47437277	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs189989408	chr4:47437285-47437286	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs545134609	chr4:47437318-47437319	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs563188417	chr4:47437327-47437328	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs530548721	chr4:47437352-47437353	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs146162902	chr4:47437459-47437460	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs564433822	chr4:47437509-47437510	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs574158627	chr4:47437511-47437512	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs140124157	chr4:47437552-47437553	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs113003183	chr4:47437582-47437583	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs546484292	chr4:47437712-47437713	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs142428893	chr4:47437737-47437738	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs77711879	chr4:47437841-47437842	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs558255549	chr4:47437870-47437871	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19214233	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

Chromatin state (count:4276 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47404000-47439000	Weak transcription	Brain Anterior Caudate	brain
2	chr4:47433000-47437000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr4:47433800-47436200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:47435200-47436200	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:47436200-47444800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:47436800-47465000	Weak transcription	Gastric	stomach
7	chr4:47437000-47441800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr4:47438200-47438400	Enhancers	Small Intestine	intestine
9	chr4:47438600-47464200	Weak transcription	Small Intestine	intestine
10	chr4:47441000-47442400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr4:47441000-47456000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr4:47441400-47444600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr4:47441800-47442400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr4:47442200-47464000	Weak transcription	Left Ventricle	heart
15	chr4:47442400-47443400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:47442400-47443600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr4:47442800-47445000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:47442800-47451800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr4:47443400-47445000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr4:47443600-47443800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr4:47443600-47464000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:47443800-47444200	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr4:47444000-47453600	Weak transcription	HSMMtube	muscle
24	chr4:47444200-47445000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr4:47444200-47445000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:47444400-47445000	Enhancers	GM12878-XiMat	blood
27	chr4:47444600-47445000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr4:47444600-47446400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr4:47444800-47445200	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr4:47445000-47445200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr4:47445000-47445200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr4:47445000-47445200	Flanking Active TSS	GM12878-XiMat	blood
33	chr4:47445000-47445600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr4:47445000-47445600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:47445000-47445600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:47445000-47445600	Enhancers	Thymus	Thymus
37	chr4:47445000-47446000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr4:47445000-47446200	Enhancers	Primary B cells from peripheral blood	blood
39	chr4:47445000-47446200	Enhancers	Dnd41	blood
40	chr4:47445000-47454800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr4:47445200-47445400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr4:47445200-47445400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:47445200-47445400	Enhancers	GM12878-XiMat	blood
44	chr4:47445200-47446000	Enhancers	Primary B cells from cord blood	blood
45	chr4:47445200-47446800	Enhancers	Primary hematopoietic stem cells	blood
46	chr4:47445200-47453600	Weak transcription	NHDF-Ad	bronchial
47	chr4:47445200-47454600	Weak transcription	Fetal Intestine Small	intestine
48	chr4:47445400-47445600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
49	chr4:47445400-47445600	Enhancers	Primary T cells from cord blood	blood
50	chr4:47445400-47445600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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