Variant report

Variant	nsv998499
Chromosome Location	chr1:76361784-76598712
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1898)
CpG islands
(count:1343)
Chromatin interactive
region (count:44)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1898 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76457206-76457580	K562	blood:	n/a	n/a
2	ARID3A	chr1:76525298-76525542	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:76457207-76457579	HepG2	liver:	n/a	n/a
4	ATF1	chr1:76579247-76579370	K562	blood:	n/a	n/a
5	ATF1	chr1:76498047-76498053	K562	blood:	n/a	n/a
6	ATF2	chr1:76451406-76452104	GM12878	blood:	n/a	n/a
7	ATF2	chr1:76451366-76452138	GM12878	blood:	n/a	n/a
8	ATF2	chr1:76446837-76447332	GM12878	blood:	n/a	n/a
9	ATF3	chr1:76540117-76540372	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:76540149-76540437	K562	blood:	n/a	n/a
11	ATF3	chr1:76540224-76540336	GM12878	blood:	n/a	n/a
12	BACH1	chr1:76540156-76540223	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:76540813-76540973	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:76511892-76511893	K562	blood:	n/a	n/a
15	BACH1	chr1:76540453-76540565	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr1:76445574-76446122	GM12878	blood:	n/a	n/a
17	BATF	chr1:76446837-76447467	GM12878	blood:	n/a	n/a
18	BATF	chr1:76446894-76447376	GM12878	blood:	n/a	n/a
19	BATF	chr1:76451409-76451946	GM12878	blood:	n/a	n/a
20	BATF	chr1:76402769-76403052	GM12878	blood:	n/a	n/a
21	BATF	chr1:76451481-76451880	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:76451382-76451972	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:76451525-76451819	GM12878	blood:	n/a	n/a
24	BCL3	chr1:76451369-76451965	GM12878	blood:	n/a	n/a
25	BCL3	chr1:76525123-76525625	A549	lung:	n/a	n/a
26	BCL3	chr1:76517845-76518261	GM12878	blood:	n/a	n/a
27	BCL3	chr1:76451479-76451851	GM12878	blood:	n/a	n/a
28	BCL3	chr1:76402779-76403076	GM12878	blood:	n/a	n/a
29	BCL3	chr1:76446928-76447226	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:76451463-76451916	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:76451446-76451992	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:76540154-76540432	A549	lung:	n/a	chr1:76540284-76540300 chr1:76540311-76540320 chr1:76540309-76540318 chr1:76540194-76540210 chr1:76540287-76540303 chr1:76540310-76540319 chr1:76540281-76540297 chr1:76540310-76540319
33	BHLHE40	chr1:76408798-76409160	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:76539831-76540489	K562	blood:	n/a	chr1:76540284-76540300 chr1:76540311-76540320 chr1:76540309-76540318 chr1:76540194-76540210 chr1:76540287-76540303 chr1:76540310-76540319 chr1:76540281-76540297 chr1:76540310-76540319
35	BHLHE40	chr1:76540022-76540477	GM12878	blood:	n/a	chr1:76540284-76540300 chr1:76540311-76540320 chr1:76540309-76540318 chr1:76540194-76540210 chr1:76540287-76540303 chr1:76540310-76540319 chr1:76540281-76540297 chr1:76540310-76540319
36	BHLHE40	chr1:76540112-76540484	HepG2	liver:	n/a	chr1:76540284-76540300 chr1:76540311-76540320 chr1:76540309-76540318 chr1:76540194-76540210 chr1:76540287-76540303 chr1:76540310-76540319 chr1:76540281-76540297 chr1:76540310-76540319
37	BHLHE40	chr1:76432663-76432684	K562	blood:	n/a	n/a
38	BHLHE40	chr1:76457335-76457598	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:76408753-76409142	K562	blood:	n/a	n/a
40	BHLHE40	chr1:76457357-76457567	K562	blood:	n/a	n/a
41	BHLHE40	chr1:76451404-76451942	GM12878	blood:	n/a	n/a
42	BRCA1	chr1:76428003-76428170	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr1:76490205-76490683	HCT-116	colon:	n/a	n/a
44	CBX3	chr1:76534227-76534567	HCT-116	colon:	n/a	n/a
45	CCNT2	chr1:76540110-76540558	K562	blood:	n/a	n/a
46	CEBPB	chr1:76589860-76590334	A549	lung:	n/a	chr1:76590142-76590151 chr1:76590142-76590151 chr1:76590042-76590055 chr1:76590142-76590151 chr1:76590140-76590153 chr1:76590142-76590151
47	CEBPB	chr1:76589978-76590270	ECC-1	luminal epithelium:	n/a	chr1:76590142-76590151 chr1:76590142-76590151 chr1:76590042-76590055 chr1:76590142-76590151 chr1:76590140-76590153 chr1:76590142-76590151
48	CEBPB	chr1:76518638-76519295	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:76397180-76397391	HepG2	liver:	n/a	chr1:76397281-76397292
50	CEBPB	chr1:76589955-76590308	H1-hESC	embryonic stem cell:	n/a	chr1:76590142-76590151 chr1:76590142-76590151 chr1:76590042-76590055 chr1:76590142-76590151 chr1:76590140-76590153 chr1:76590142-76590151

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76537463-76537513	T-47D	breast:	n/a
2	chr1:76537463-76537513	T-47D	breast:	n/a
3	chr1:76540465-76540515	PANC-1	pancreas:	n/a
4	chr1:76540574-76540624	MCF-7	breast:	n/a
5	chr1:76540168-76540218	SKMC	muscle:	n/a
6	chr1:76543815-76543865	AG09319	gingival:	n/a
7	chr1:76489892-76489942	MCF10A-Er-Src	breast:	n/a
8	chr1:76540110-76540160	BE2_C	brain:	n/a
9	chr1:76396165-76396215	HCF	heart:	n/a
10	chr1:76540438-76540488	HEK293	kidney:	embryo
11	chr1:76540574-76540624	GM12891	blood:	n/a
12	chr1:76539186-76539236	HCT-116	colon:	n/a
13	chr1:76543815-76543865	ECC-1	luminal epithelium:	n/a
14	chr1:76543815-76543865	ovcar-3	ovarian:	n/a
15	chr1:76540168-76540218	MCF10A-Er-Src	breast:	n/a
16	chr1:76518896-76518946	Hepatocyte	liver:	n/a
17	chr1:76540641-76540691	SAEC	small airway:	n/a
18	chr1:76540148-76540198	AG04449	skin:	fetal
19	chr1:76518896-76518946	NHDF-neo	bronchial:	n/a
20	chr1:76540148-76540198	AG09319	gingival:	n/a
21	chr1:76543815-76543865	HEEpiC	esophagus:	n/a
22	chr1:76550508-76550558	HUVEC	blood vessel:	n/a
23	chr1:76543815-76543865	BE2_C	brain:	n/a
24	chr1:76537463-76537513	HRE	kidney:	n/a
25	chr1:76397847-76397897	BE2_C	brain:	n/a
26	chr1:76540641-76540691	AG04449	skin:	fetal
27	chr1:76574405-76574455	GM12891	blood:	n/a
28	chr1:76396165-76396215	HCT-116	colon:	n/a
29	chr1:76540222-76540272	ECC-1	luminal epithelium:	n/a
30	chr1:76550508-76550558	AoSMC	blood vessel:	n/a
31	chr1:76556226-76556276	HAEpiC	amniotic membrane:	n/a
32	chr1:76540148-76540198	SAEC	small airway:	n/a
33	chr1:76518896-76518946	T-47D	breast:	n/a
34	chr1:76540641-76540691	NH-A	brain:	n/a
35	chr1:76540641-76540691	HNPCEpiC	eye:	n/a
36	chr1:76540465-76540515	A549	lung:	n/a
37	chr1:76540148-76540198	ovcar-3	ovarian:	n/a
38	chr1:76547234-76547284	SK-N-MC	brain:	n/a
39	chr1:76539186-76539236	GM12878	blood:	n/a
40	chr1:76540999-76541049	MCF-7	breast:	n/a
41	chr1:76540148-76540198	HCF	heart:	n/a
42	chr1:76550508-76550558	IMR90	lung:	fetal
43	chr1:76540236-76540286	PANC-1	pancreas:	n/a
44	chr1:76572603-76572653	PFSK-1	brain:	n/a
45	chr1:76540641-76540691	GM12891	blood:	n/a
46	chr1:76537463-76537513	SK-N-SH	brain:	n/a
47	chr1:76540641-76540691	AG09319	gingival:	n/a
48	chr1:76550508-76550558	NB4	blood:	n/a
49	chr1:76540236-76540286	A549	lung:	n/a
50	chr1:76540236-76540286	HRPEpiC	eye:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76528266..76531083-chr1:76533694..76535257,2	MCF-7	breast:
2	chr1:76456960..76458188-chr1:76619791..76620471,4	MCF-7	breast:
3	chr1:76440537..76442638-chr1:76444032..76446733,2	K562	blood:
4	chr1:76437063..76439745-chr1:76450449..76452475,3	K562	blood:
5	chr1:76437063..76439745-chr1:76450449..76452475,3	K562	blood:
6	chr1:76440537..76442638-chr1:76444032..76446733,2	K562	blood:
7	chr1:76492764..76495132-chr1:76495850..76497868,2	K562	blood:
8	chr1:76469959..76472531-chr1:76473869..76475395,2	K562	blood:
9	chr1:76528266..76531083-chr1:76533694..76535257,2	MCF-7	breast:
10	chr1:76538798..76540470-chr1:76545089..76547752,3	K562	blood:
11	chr1:76434414..76437432-chr1:76439336..76442369,3	K562	blood:
12	chr1:76596952..76598504-chr1:76616645..76619490,2	K562	blood:
13	chr1:76559480..76561053-chr1:76563523..76565127,2	MCF-7	breast:
14	chr1:76438120..76439745-chr1:76450591..76452475,2	K562	blood:
15	chr1:76465512..76468433-chr1:76470100..76472168,2	K562	blood:
16	chr1:76430702..76432337-chr1:76445197..76447195,2	K562	blood:
17	chr1:76590552..76592977-chr1:76595661..76598388,2	K562	blood:
18	chr1:76383436..76384363-chr16:27389146..27390073,2	MCF-7	breast:
19	chr1:76456960..76457802-chr1:76619597..76620478,2	K562	blood:
20	chr1:76434414..76437432-chr1:76439336..76442369,3	K562	blood:
21	chr1:76451720..76454634-chr1:76455943..76457649,2	K562	blood:
22	chr1:76492764..76495132-chr1:76495850..76497868,2	K562	blood:
23	chr1:76540930..76543846-chr1:76546687..76549468,2	K562	blood:
24	chr1:76430702..76432337-chr1:76445197..76447195,2	K562	blood:
25	chr1:76392792..76394366-chr1:76397859..76400177,2	K562	blood:
26	chr1:76451720..76454634-chr1:76455943..76457649,2	K562	blood:
27	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
28	chr1:76584811..76587020-chr1:76588977..76591542,2	K562	blood:
29	chr1:76584811..76587020-chr1:76588977..76591542,2	K562	blood:
30	chr1:76380506..76383484-chr1:76388793..76390855,2	K562	blood:
31	chr1:76563429..76565224-chr1:76569257..76571060,2	K562	blood:
32	chr1:76465512..76468433-chr1:76470100..76472168,2	K562	blood:
33	chr1:76469959..76472531-chr1:76473869..76475395,2	K562	blood:
34	chr1:76540930..76543846-chr1:76546687..76549468,2	K562	blood:
35	chr1:76374124..76374771-chr1:76619576..76620091,2	MCF-7	breast:
36	chr1:76438120..76439745-chr1:76450591..76452475,2	K562	blood:
37	chr1:76590552..76592977-chr1:76595661..76598388,2	K562	blood:
38	chr1:76456932..76457512-chr1:76605708..76606546,2	MCF-7	breast:
39	chr1:76563429..76565224-chr1:76569257..76571060,2	K562	blood:
40	chr1:76380506..76383484-chr1:76388793..76390855,2	K562	blood:
41	chr1:76532586..76534644-chr1:76541569..76543185,2	K562	blood:
42	chr1:76532586..76534644-chr1:76541569..76543185,2	K562	blood:
43	chr1:76260266..76263027-chr1:76396916..76399571,2	K562	blood:
44	chr1:76559480..76561053-chr1:76563523..76565127,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST6GALNAC3-2	chr1:76478945-76479015	ENSG00000225605
2	lnc-MSH4-1	chr1:76398207-76398355	NONHSAT004007
3	lnc-MSH4-1	chr1:76400119-76400171	NONHSAT004007
4	lnc-ST6GALNAC3-2	chr1:76477009-76477083	ENSG00000225605
5	lnc-MSH4-1	chr1:76449130-76449245	NONHSAT004007
6	lnc-MSH4-1	chr1:76437905-76437950	NONHSAT004007
7	lnc-MSH4-1	chr1:76476425-76476466	NONHSAT004007
8	lnc-ST6GALNAC3-2	chr1:76484819-76485041	ENSG00000225605
9	lnc-ST6GALNAC3-1	chr1:76507405-76507583	NONHSAT004009
10	lnc-ST6GALNAC3-1	chr1:76507376-76507583	ENSG00000230027
11	lnc-ST6GALNAC3-1	chr1:76531723-76531913	ENSG00000230027
12	lnc-ST6GALNAC3-1	chr1:76507405-76507583	NONHSAT004010
13	lnc-ST6GALNAC3-1	chr1:76521433-76521898	NONHSAT004011
14	lnc-ST6GALNAC3-1	chr1:76531723-76531979	NONHSAT004011
15	lnc-ST6GALNAC3-1	chr1:76531723-76531979	NONHSAT004009
16	lnc-ST6GALNAC3-1	chr1:76521198-76521376	NONHSAT004010

No data

Variant related genes	Relation type
ENSG00000225605	TF binding region
ENSG00000230027	TF binding region
ST6GALNAC3	TF binding region
ASB17	TF binding region
ENSG00000225605	CpG island
ENSG00000230027	CpG island
ST6GALNAC3	CpG island
ASB17	CpG island
ENSG00000057468	chromatin interactions
ENSG00000154007	chromatin interactions
ENSG00000184005	chromatin interactions

Extended variants
information (count: 6914 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:6914 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114874674	chr1:76366435-76366436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74764793	chr1:76366456-76366457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538952393	chr1:76366460-76366461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142090223	chr1:76366487-76366488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569424801	chr1:76366620-76366621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183472838	chr1:76366631-76366632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555027093	chr1:76366634-76366635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188009044	chr1:76366640-76366641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527273238	chr1:76366730-76366731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540674180	chr1:76366766-76366767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559000892	chr1:76366771-76366772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34285781	chr1:76366822-76366823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577961067	chr1:76366859-76366860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1586936	chr1:76366877-76366878	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs61770550	chr1:76366966-76366967	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs143095529	chr1:76367006-76367007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148216710	chr1:76367011-76367012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192232041	chr1:76367045-76367046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528185702	chr1:76367058-76367059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183609338	chr1:76367132-76367133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564536746	chr1:76367213-76367214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549632867	chr1:76367244-76367245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188658158	chr1:76367259-76367260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76646808	chr1:76367316-76367317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112683167	chr1:76367358-76367359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530285911	chr1:76367365-76367366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569795878	chr1:76367374-76367375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10873786	chr1:76367419-76367420	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566929960	chr1:76367529-76367530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192724219	chr1:76367552-76367553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11161845	chr1:76367559-76367560	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs570847436	chr1:76367564-76367565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537885801	chr1:76367571-76367572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557198724	chr1:76367591-76367592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575466573	chr1:76367612-76367613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566023984	chr1:76367613-76367614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12079950	chr1:76367614-76367615	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs115849851	chr1:76367624-76367625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568470623	chr1:76367640-76367641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11161848	chr1:76367722-76367723	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs140135554	chr1:76367736-76367737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564676192	chr1:76367752-76367753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10873787	chr1:76367797-76367798	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs10873788	chr1:76367857-76367858	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs563161172	chr1:76367945-76367946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530334703	chr1:76367947-76367948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565584823	chr1:76367975-76367976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150296368	chr1:76367985-76367986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532701382	chr1:76374622-76374623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551305246	chr1:76374648-76374649	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20393555	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76366400-76368000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:76366800-76367800	Enhancers	Fetal Heart	heart
3	chr1:76374600-76374800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:76374600-76375000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr1:76374600-76375000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr1:76374600-76375000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr1:76374600-76375000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:76374600-76375000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:76374600-76375000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:76374600-76375000	Enhancers	HMEC	breast
11	chr1:76374600-76375000	Enhancers	NHLF	lung
12	chr1:76375000-76375800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:76375800-76378000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:76376600-76377000	Enhancers	Fetal Heart	heart
15	chr1:76393800-76394600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:76402200-76403200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:76402400-76402800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:76402400-76402800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:76402600-76403400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr1:76402800-76403600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:76402800-76420000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:76408800-76409200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:76408800-76409200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:76408800-76409400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:76408800-76409600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr1:76409000-76409400	Enhancers	HUVEC	blood vessel
27	chr1:76409000-76409600	Enhancers	Spleen	Spleen
28	chr1:76415000-76418600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:76415600-76415800	Enhancers	Brain Anterior Caudate	brain
30	chr1:76415600-76415800	Enhancers	A549	lung
31	chr1:76415800-76420400	Weak transcription	Brain Anterior Caudate	brain
32	chr1:76416200-76417400	Weak transcription	A549	lung
33	chr1:76416800-76417000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:76417400-76417800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:76417400-76417800	Enhancers	A549	lung
36	chr1:76417800-76419000	Weak transcription	A549	lung
37	chr1:76418600-76419000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:76418600-76419000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:76419000-76419200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:76419000-76420800	Enhancers	A549	lung
41	chr1:76419000-76421000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:76419200-76419600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:76419200-76419600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:76419200-76420800	Enhancers	HepG2	liver
45	chr1:76419200-76421000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr1:76419800-76421000	Enhancers	HMEC	breast
47	chr1:76420000-76420800	Enhancers	NHEK	skin
48	chr1:76420000-76421000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:76420200-76420800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:76420400-76420800	Enhancers	Brain Angular Gyrus	brain

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