Variant report

Variant	nsv1011178
Chromosome Location	chr3:119437192-119589116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1486)
CpG islands
(count:1162)
Chromatin interactive
region (count:94)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:1486 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:119514818-119515071	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:119539949-119540175	K562	blood:	n/a	n/a
3	ARID3A	chr3:119539896-119540250	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:119500469-119500922	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:119513933-119514319	HepG2	liver:	n/a	n/a
6	ATF1	chr3:119513924-119514765	K562	blood:	n/a	n/a
7	ATF2	chr3:119528973-119529418	GM12878	blood:	n/a	n/a
8	ATF3	chr3:119513882-119514306	K562	blood:	n/a	n/a
9	ATF3	chr3:119513859-119514355	A549	lung:	n/a	n/a
10	ATF3	chr3:119513988-119514258	K562	blood:	n/a	n/a
11	ATF3	chr3:119513870-119514281	A549	lung:	n/a	n/a
12	BACH1	chr3:119513922-119514280	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:119502163-119502401	K562	blood:	n/a	n/a
14	BACH1	chr3:119516024-119516139	K562	blood:	n/a	n/a
15	BCLAF1	chr3:119528830-119529367	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:119539934-119540158	K562	blood:	n/a	n/a
17	BHLHE40	chr3:119529039-119529239	K562	blood:	n/a	n/a
18	BHLHE40	chr3:119528452-119529393	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:119513922-119514485	K562	blood:	n/a	n/a
20	BRCA1	chr3:119513926-119514561	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr3:119539845-119540329	HCT-116	colon:	n/a	n/a
22	CBX3	chr3:119513844-119514368	K562	blood:	n/a	n/a
23	CBX3	chr3:119539902-119540140	K562	blood:	n/a	n/a
24	CBX3	chr3:119513957-119514263	K562	blood:	n/a	n/a
25	CBX3	chr3:119539902-119540135	K562	blood:	n/a	n/a
26	CCNT2	chr3:119512238-119512368	K562	blood:	n/a	n/a
27	CCNT2	chr3:119513836-119514353	K562	blood:	n/a	n/a
28	CEBPB	chr3:119510137-119510415	HepG2	liver:	n/a	chr3:119510276-119510287
29	CEBPB	chr3:119502052-119502488	K562	blood:	n/a	n/a
30	CEBPB	chr3:119502148-119502465	IMR90	lung:	n/a	n/a
31	CEBPB	chr3:119502185-119502359	K562	blood:	n/a	n/a
32	CEBPB	chr3:119513839-119514322	Hela-S3	cervix:	n/a	chr3:119513840-119513851
33	CEBPB	chr3:119461226-119461302	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:119510237-119510308	K562	blood:	n/a	chr3:119510276-119510287
35	CEBPB	chr3:119502067-119502539	A549	lung:	n/a	n/a
36	CEBPB	chr3:119585550-119585834	A549	lung:	n/a	chr3:119585699-119585708 chr3:119585699-119585708 chr3:119585697-119585710 chr3:119585699-119585708 chr3:119585662-119585673 chr3:119585699-119585708 chr3:119585697-119585708 chr3:119585698-119585709
37	CEBPB	chr3:119580574-119580802	A549	lung:	n/a	n/a
38	CEBPB	chr3:119461104-119461384	A549	lung:	n/a	n/a
39	CEBPB	chr3:119513809-119514160	HepG2	liver:	n/a	chr3:119513840-119513851
40	CEBPB	chr3:119510281-119510304	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:119580559-119580874	IMR90	lung:	n/a	n/a
42	CEBPB	chr3:119540097-119540131	K562	blood:	n/a	n/a
43	CEBPB	chr3:119502126-119502474	A549	lung:	n/a	n/a
44	CEBPB	chr3:119502118-119502514	K562	blood:	n/a	n/a
45	CEBPB	chr3:119455494-119455634	A549	lung:	n/a	n/a
46	CEBPB	chr3:119455442-119455678	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:119539890-119540234	A549	lung:	n/a	n/a
48	CEBPB	chr3:119585531-119585866	IMR90	lung:	n/a	chr3:119585699-119585708 chr3:119585699-119585708 chr3:119585697-119585710 chr3:119585699-119585708 chr3:119585662-119585673 chr3:119585699-119585708 chr3:119585697-119585708 chr3:119585698-119585709
49	CEBPB	chr3:119585527-119585848	HepG2	liver:	n/a	chr3:119585699-119585708 chr3:119585699-119585708 chr3:119585697-119585710 chr3:119585699-119585708 chr3:119585662-119585673 chr3:119585699-119585708 chr3:119585697-119585708 chr3:119585698-119585709
50	CEBPB	chr3:119502120-119502488	HepG2	liver:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:119500929-119500979	NH-A	brain:	n/a
2	chr3:119528956-119529006	AG04450	lung:	fetal
3	chr3:119500902-119500952	Hela-S3	cervix:	n/a
4	chr3:119500929-119500979	NH-A	brain:	n/a
5	chr3:119528956-119529006	AG04450	lung:	fetal
6	chr3:119500902-119500952	Hela-S3	cervix:	n/a
7	chr3:119498036-119498086	IMR90	lung:	fetal
8	chr3:119526221-119526271	HepG2	liver:	n/a
9	chr3:119536718-119536768	BJ	skin:	n/a
10	chr3:119500902-119500952	SKMC	muscle:	n/a
11	chr3:119529148-119529198	H1-hESC	embryonic stem cell:	embryo
12	chr3:119500902-119500952	AoSMC	blood vessel:	n/a
13	chr3:119526221-119526271	HCM	heart:	n/a
14	chr3:119514395-119514445	AG10803	skin:	n/a
15	chr3:119500902-119500952	GM12878	blood:	n/a
16	chr3:119529290-119529340	AG04449	skin:	fetal
17	chr3:119528656-119528706	RPTEC	kidney:	n/a
18	chr3:119500902-119500952	Hepatocyte	liver:	n/a
19	chr3:119500929-119500979	HIPEpiC	eye:	n/a
20	chr3:119500929-119500979	SK-N-MC	brain:	n/a
21	chr3:119498036-119498086	HUVEC	blood vessel:	n/a
22	chr3:119536718-119536768	Hepatocyte	liver:	n/a
23	chr3:119527255-119527305	CMK	blood:	n/a
24	chr3:119528656-119528706	NH-A	brain:	n/a
25	chr3:119514395-119514445	SKMC	muscle:	n/a
26	chr3:119529290-119529340	RPTEC	kidney:	n/a
27	chr3:119529290-119529340	HCPEpiC	choroid plexus:	n/a
28	chr3:119528956-119529006	A549	lung:	n/a
29	chr3:119531385-119531435	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:119536718-119536768	AG04450	lung:	fetal
31	chr3:119529148-119529198	ovcar-3	ovarian:	n/a
32	chr3:119536718-119536768	H1-hESC	embryonic stem cell:	embryo
33	chr3:119514395-119514445	BJ	skin:	n/a
34	chr3:119547934-119547984	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:119527255-119527305	GM06990	blood:	n/a
36	chr3:119528956-119529006	BJ	skin:	n/a
37	chr3:119529158-119529208	AG09319	gingival:	n/a
38	chr3:119527255-119527305	HEK293	kidney:	embryo
39	chr3:119542274-119542324	SK-N-MC	brain:	n/a
40	chr3:119529158-119529208	BE2_C	brain:	n/a
41	chr3:119529148-119529198	AoSMC	blood vessel:	n/a
42	chr3:119500929-119500979	AG09309	skin:	n/a
43	chr3:119547934-119547984	AG10803	skin:	n/a
44	chr3:119527255-119527305	AG04449	skin:	fetal
45	chr3:119531385-119531435	ovcar-3	ovarian:	n/a
46	chr3:119498036-119498086	BJ	skin:	n/a
47	chr3:119499190-119499240	SK-N-SH_RA	brain:	n/a
48	chr3:119526221-119526271	HEK293	kidney:	embryo
49	chr3:119528956-119529006	HRCEpiC	kidney:	n/a
50	chr3:119529148-119529198	A549	lung:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:119532575..119536291-chr3:119538231..119540719,3	K562	blood:
2	chr3:119517202..119519135-chr3:119522391..119525138,2	K562	blood:
3	chr3:119527283..119529245-chr3:119900596..119902132,2	MCF-7	breast:
4	chr3:119539576..119540526-chr3:119901251..119902442,9	MCF-7	breast:
5	chr3:119539097..119541500-chr3:119541978..119544255,2	MCF-7	breast:
6	chr3:119548336..119550894-chr3:119551910..119554571,2	K562	blood:
7	chr3:119532575..119536291-chr3:119538231..119540719,3	K562	blood:
8	chr3:119559434..119561964-chr3:119812906..119815374,2	MCF-7	breast:
9	chr3:119514298..119516694-chr3:119519777..119521864,2	K562	blood:
10	chr3:119498195..119499801-chr3:119500089..119502246,2	K562	blood:
11	chr3:119542022..119546217-chr3:119548294..119552137,4	K562	blood:
12	chr3:119501588..119503583-chr3:119503958..119505707,2	MCF-7	breast:
13	chr3:119499565..119502247-chr3:119518347..119520866,2	MCF-7	breast:
14	chr3:119517202..119519135-chr3:119522391..119525138,2	K562	blood:
15	chr3:119533302..119535583-chr3:119535890..119538879,2	MCF-7	breast:
16	chr3:119501588..119503583-chr3:119503958..119505707,2	MCF-7	breast:
17	chr3:119549294..119550907-chr3:119812741..119814521,3	MCF-7	breast:
18	chr3:119464205..119467034-chr3:119468589..119471044,2	K562	blood:
19	chr3:119581923..119584726-chr3:119588066..119590624,3	MCF-7	breast:
20	chr3:119586172..119587789-chr3:119594184..119596483,2	MCF-7	breast:
21	chr3:119041713..119043287-chr3:119530571..119533210,2	MCF-7	breast:
22	chr3:119549554..119552189-chr3:119554613..119556599,3	MCF-7	breast:
23	chr3:119440802..119443470-chr3:119448061..119449825,2	K562	blood:
24	chr3:119512757..119515605-chr3:119516397..119518859,2	MCF-7	breast:
25	chr3:119531732..119533815-chr3:119534255..119536418,2	MCF-7	breast:
26	chr3:119548336..119550894-chr3:119551910..119554571,2	K562	blood:
27	chr3:119550948..119553209-chr3:119569939..119572570,3	MCF-7	breast:
28	chr3:119553090..119555920-chr3:119558108..119560664,3	MCF-7	breast:
29	chr3:119527025..119528584-chr3:119529180..119532030,2	MCF-7	breast:
30	chr3:119217125..119218663-chr3:119514473..119516155,2	K562	blood:
31	chr20:52685889..52686408-chr3:119539503..119540491,2	MCF-7	breast:
32	chr3:119550948..119553209-chr3:119569939..119572570,3	MCF-7	breast:
33	chr3:119498195..119499801-chr3:119500089..119502246,2	K562	blood:
34	chr3:119498195..119499776-chr3:119500089..119502545,2	K562	blood:
35	chr3:119440802..119443470-chr3:119448061..119449825,2	K562	blood:
36	chr3:119497497..119499606-chr3:119513242..119515425,2	K562	blood:
37	chr3:119540139..119541748-chr3:119811552..119813131,2	MCF-7	breast:
38	chr3:119532575..119535119-chr3:119538231..119540719,2	K562	blood:
39	chr3:119420317..119422309-chr3:119504669..119506842,2	MCF-7	breast:
40	chr3:119513257..119518482-chr3:119518835..119521864,6	K562	blood:
41	chr3:119215696..119217904-chr3:119512821..119515742,3	K562	blood:
42	chr3:119531331..119533784-chr3:119534969..119537956,2	K562	blood:
43	chr3:119533302..119535583-chr3:119535890..119538879,2	MCF-7	breast:
44	chr3:119549554..119552189-chr3:119554613..119556599,3	MCF-7	breast:
45	chr3:119523169..119526379-chr3:119529849..119532497,4	MCF-7	breast:
46	chr3:119546502..119549235-chr3:119813550..119815465,2	MCF-7	breast:
47	chr3:119539565..119540086-chr3:119901520..119902156,2	MCF-7	breast:
48	chr3:119534052..119535744-chr3:119538553..119540497,2	MCF-7	breast:
49	chr3:119513257..119518482-chr3:119518835..119521864,6	K562	blood:
50	chr3:119534052..119535744-chr3:119538553..119540497,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR1I2-2	chr3:119469784-119469945	NONHSAT091409
2	lnc-NR1I2-2	chr3:119469320-119469467	NONHSAT091410
3	lnc-NR1I2-2	chr3:119483899-119484543	NONHSAT091408
4	lnc-NR1I2-2	chr3:119471148-119471223	NONHSAT091409
5	lnc-NR1I2-2	chr3:119471148-119471223	NONHSAT091407
6	lnc-NR1I2-2	chr3:119483899-119484433	NONHSAT091410
7	lnc-NR1I2-2	chr3:119483899-119484087	NONHSAT091409
8	lnc-NR1I2-2	chr3:119469305-119469446	NONHSAT091408
9	lnc-COX17-1	chr3:119469053-119469197	ENSG00000239994.2
10	lnc-COX17-1	chr3:119462986-119463013	ENSG00000239994.1
11	lnc-NR1I2-2	chr3:119469784-119469945	NONHSAT091410
12	lnc-COX17-1	chr3:119462986-119463013	ENSG00000239994.2
13	lnc-COX17-1	chr3:119467945-119468040	ENSG00000239994.1
14	lnc-NR1I2-2	chr3:119483899-119484088	NONHSAT091407
15	lnc-NR1I2-2	chr3:119469784-119469945	NONHSAT091407
16	lnc-NR1I2-2	chr3:119469311-119469446	NONHSAT091409
17	lnc-COX17-1	chr3:119467945-119468037	ENSG00000239994.2
18	lnc-NR1I2-2	chr3:119469290-119469315	NONHSAT091407
19	lnc-NR1I2-2	chr3:119469784-119469945	NONHSAT091408

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GSK3B	hsa-miR-26a-5p	chr3:119544029-119544023
2	GSK3B	hsa-miR-26a-5p	chr3:119540998-119540991
3	GSK3B	hsa-miR-92a-3p	chr3:119542245-119542266
4	GSK3B	hsa-miR-26a-5p	chr3:119545593-119545587
5	GSK3B	hsa-miR-26a-5p	chr3:119541322-119541344
6	GSK3B	hsa-miR-425-5p	chr3:119541903-119541929
7	GSK3B	hsa-miR-26a-5p	chr3:119540992-119541012
8	GSK3B	hsa-miR-155-5p	chr3:119540835-119540857
9	NR1I2	hsa-let-7a-5p	chr3:119536478-119536497
10	NR1I2	hsa-miR-148a-3p	chr3:119536280-119536301
11	GSK3B	hsa-miR-155-5p	chr3:119540840-119540834

Variant related genes	Relation type
PHBP8	TF binding region
NR1I2	TF binding region
MAATS1	TF binding region
ENSG00000239994	TF binding region
GSK3B	TF binding region
PHBP8	CpG island
NR1I2	CpG island
MAATS1	CpG island
ENSG00000239994	CpG island
GSK3B	CpG island
ENSG00000242622	chromatin interactions
ENSG00000183833	chromatin interactions
ENSG00000272662	chromatin interactions
ENSG00000144852	chromatin interactions
ENSG00000113845	chromatin interactions
ENSG00000144840	chromatin interactions
ENSG00000112893	chromatin interactions
ENSG00000082701	chromatin interactions
ENSG00000119231	chromatin interactions
ENSG00000239994	chromatin interactions
ENSG00000153767	chromatin interactions

Extended variants
information (count: 5671 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5671 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4687878	chr3:119437286-119437287	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183975763	chr3:119437326-119437327	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145978506	chr3:119437348-119437349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545754964	chr3:119437361-119437362	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535333674	chr3:119437420-119437421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188955824	chr3:119437572-119437573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79788033	chr3:119437630-119437631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539151710	chr3:119437651-119437652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs193031911	chr3:119437667-119437668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79392545	chr3:119437715-119437716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540249941	chr3:119437757-119437758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542668939	chr3:119437791-119437792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138590411	chr3:119437800-119437801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572840446	chr3:119437802-119437803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553614521	chr3:119437803-119437804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185618410	chr3:119437842-119437843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564763840	chr3:119437895-119437896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532195463	chr3:119437915-119437916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115930352	chr3:119437949-119437950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562452889	chr3:119437955-119437956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75911026	chr3:119437998-119437999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182020097	chr3:119438004-119438005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4687879	chr3:119438007-119438008	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs535376956	chr3:119438009-119438010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534338191	chr3:119438047-119438048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373864556	chr3:119438057-119438058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185458585	chr3:119438063-119438064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4687880	chr3:119438085-119438086	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs4234665	chr3:119438135-119438136	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs557491439	chr3:119438188-119438189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35108219	chr3:119438253-119438254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71325399	chr3:119438255-119438256	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs559688427	chr3:119438263-119438264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188258838	chr3:119438283-119438284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10934497	chr3:119438290-119438291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181433160	chr3:119438343-119438344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540204286	chr3:119438413-119438414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558442650	chr3:119438452-119438453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576685223	chr3:119438597-119438598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185537270	chr3:119438599-119438600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6778570	chr3:119438608-119438609	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs76166263	chr3:119438610-119438611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529793260	chr3:119438664-119438665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541894300	chr3:119438724-119438725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560220108	chr3:119438778-119438779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527307768	chr3:119438786-119438787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191637680	chr3:119438832-119438833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571981609	chr3:119438834-119438835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532796981	chr3:119438917-119438918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71293248	chr3:119438941-119438942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2022 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119422200-119458200	Weak transcription	Aorta	Aorta
2	chr3:119422800-119440000	Weak transcription	Brain Angular Gyrus	brain
3	chr3:119423000-119463000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:119423000-119464400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr3:119423200-119464200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:119423200-119471600	Weak transcription	Fetal Kidney	kidney
7	chr3:119423400-119458200	Weak transcription	Brain Substantia Nigra	brain
8	chr3:119423800-119449000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr3:119428800-119469200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr3:119431200-119470400	Weak transcription	Gastric	stomach
11	chr3:119433800-119437200	Enhancers	Liver	Liver
12	chr3:119434000-119437400	Enhancers	Fetal Intestine Large	intestine
13	chr3:119434200-119438200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:119434800-119438000	Weak transcription	Fetal Stomach	stomach
15	chr3:119435000-119438800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr3:119435200-119437200	Enhancers	Fetal Intestine Small	intestine
17	chr3:119435400-119478200	Weak transcription	Colon Smooth Muscle	Colon
18	chr3:119435600-119437200	Enhancers	Stomach Mucosa	stomach
19	chr3:119436600-119444000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr3:119436800-119444600	Weak transcription	Ovary	ovary
21	chr3:119436800-119450200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:119436800-119450600	Weak transcription	Brain Anterior Caudate	brain
23	chr3:119436800-119462800	Weak transcription	Pancreas	Pancrea
24	chr3:119437200-119442400	Weak transcription	Stomach Mucosa	stomach
25	chr3:119438200-119449200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:119442400-119443000	Enhancers	Stomach Mucosa	stomach
27	chr3:119443800-119444000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:119444000-119444200	Enhancers	Spleen	Spleen
29	chr3:119444000-119453000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr3:119444200-119447000	Weak transcription	Spleen	Spleen
31	chr3:119444600-119446000	Strong transcription	Ovary	ovary
32	chr3:119444800-119445000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr3:119446000-119446800	Weak transcription	Ovary	ovary
34	chr3:119446800-119449000	Strong transcription	Ovary	ovary
35	chr3:119447000-119447800	Enhancers	Spleen	Spleen
36	chr3:119447400-119447800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:119447800-119450400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:119448400-119449800	Enhancers	Fetal Brain Male	brain
39	chr3:119448600-119449000	Enhancers	Fetal Brain Female	brain
40	chr3:119448800-119450400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr3:119449000-119449200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr3:119449000-119450400	Weak transcription	Fetal Brain Female	brain
43	chr3:119449000-119450600	Weak transcription	Ovary	ovary
44	chr3:119449200-119450400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr3:119449400-119450400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:119449800-119450200	Weak transcription	Fetal Brain Male	brain
47	chr3:119450000-119450800	Enhancers	Psoas Muscle	Psoas
48	chr3:119450200-119450400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:119450200-119451200	Enhancers	Fetal Brain Male	brain
50	chr3:119450400-119450600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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