Variant report

Variant	nsv1022438
Chromosome Location	chr4:150066349-150196711
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:150182051-150182054	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:150085578-150085819	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr4:150103753-150104034	HepG2	liver:	n/a	chr4:150103910-150103923 chr4:150103911-150103922 chr4:150103912-150103921
4	CEBPB	chr4:150185335-150185599	MCF-7	breast:	n/a	n/a
5	CEBPB	chr4:150185371-150185633	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:150089819-150090159	HepG2	liver:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
7	CEBPB	chr4:150186827-150187183	HepG2	liver:	n/a	chr4:150187013-150187022 chr4:150187011-150187024 chr4:150187013-150187022 chr4:150187011-150187022 chr4:150186992-150187005 chr4:150186992-150187003 chr4:150187013-150187022
8	CEBPB	chr4:150186829-150187177	A549	lung:	n/a	chr4:150187013-150187022 chr4:150187011-150187024 chr4:150187013-150187022 chr4:150187011-150187022 chr4:150186992-150187005 chr4:150186992-150187003 chr4:150187013-150187022
9	CEBPB	chr4:150089964-150090273	H1-hESC	embryonic stem cell:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
10	CEBPB	chr4:150185274-150185698	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr4:150186857-150187167	Hela-S3	cervix:	n/a	chr4:150187013-150187022 chr4:150187011-150187024 chr4:150187013-150187022 chr4:150187011-150187022 chr4:150186992-150187005 chr4:150186992-150187003 chr4:150187013-150187022
12	CEBPB	chr4:150089802-150090171	IMR90	lung:	n/a	chr4:150089983-150089994 chr4:150089982-150089993 chr4:150089982-150089995
13	CEBPB	chr4:150081486-150081932	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr4:150130637-150130875	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:150186845-150187197	IMR90	lung:	n/a	chr4:150187013-150187022 chr4:150187011-150187024 chr4:150187013-150187022 chr4:150187011-150187022 chr4:150186992-150187005 chr4:150186992-150187003 chr4:150187013-150187022
16	CEBPB	chr4:150130695-150130739	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:150186885-150187139	H1-hESC	embryonic stem cell:	n/a	chr4:150187013-150187022 chr4:150187011-150187024 chr4:150187013-150187022 chr4:150187011-150187022 chr4:150186992-150187005 chr4:150186992-150187003 chr4:150187013-150187022
18	CEBPB	chr4:150155028-150155228	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:150109374-150109673	HepG2	liver:	n/a	chr4:150109488-150109499
20	CEBPB	chr4:150186874-150187170	K562	blood:	n/a	chr4:150187013-150187022 chr4:150187011-150187024 chr4:150187013-150187022 chr4:150187011-150187022 chr4:150186992-150187005 chr4:150186992-150187003 chr4:150187013-150187022
21	CEBPB	chr4:150185288-150185842	IMR90	lung:	n/a	chr4:150185760-150185773 chr4:150185762-150185773
22	CHD2	chr4:150126306-150126345	HepG2	liver:	n/a	n/a
23	CTCF	chr4:150185500-150185650	HEEpiC	esophagus:	n/a	chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
24	CTCF	chr4:150185420-150185570	HAc	cerebellar:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
25	CTCF	chr4:150185418-150185576	SK-N-SH_RA	brain:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
26	CTCF	chr4:150185800-150185950	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr4:150168871-150168892	Lung_OC	lung:	n/a	n/a
28	CTCF	chr4:150185440-150185590	HA-sp	spinal cord:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
29	CTCF	chr4:150185440-150185590	GM12864	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
30	CTCF	chr4:150085640-150085790	WI-38	lung:	n/a	n/a
31	CTCF	chr4:150185360-150185510	WI-38	lung:	n/a	n/a
32	CTCF	chr4:150185480-150185630	NHEK	skin:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
33	CTCF	chr4:150185460-150185610	GM12874	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
34	CTCF	chr4:150085592-150085787	Gliobla	brain:	n/a	n/a
35	CTCF	chr4:150185395-150185637	GM19240	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
36	CTCF	chr4:150075122-150075141	HepG2	liver:	n/a	n/a
37	CTCF	chr4:150185366-150185617	A549	lung:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
38	CTCF	chr4:150185176-150185814	A549	lung:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
39	CTCF	chr4:150185416-150185654	GM10248	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
40	CTCF	chr4:150185395-150185641	Pancreas_OC	pancreas:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
41	CTCF	chr4:150185351-150185622	H1-hESC	embryonic stem cell:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
42	CTCF	chr4:150085401-150085809	IMR90	lung:	n/a	n/a
43	CTCF	chr4:150185378-150185654	GM12878	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
44	CTCF	chr4:150185433-150185605	GM12891	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
45	CTCF	chr4:150185194-150185877	SK-N-SH	brain:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
46	CTCF	chr4:150185420-150185570	HPAF	blood vessel:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
47	CTCF	chr4:150101652-150101695	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:150185378-150185639	GM13977	blood:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
49	CTCF	chr4:150185351-150185613	HepG2	liver:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522
50	CTCF	chr4:150185440-150185590	BJ	skin:	n/a	chr4:150185499-150185520 chr4:150185505-150185521 chr4:150185506-150185519 chr4:150185507-150185517 chr4:150185504-150185522

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:150085703-150085753	GM12892	blood:	n/a
2	chr4:150087191-150087241	SK-N-MC	brain:	n/a
3	chr4:150085703-150085753	BE2_C	brain:	n/a
4	chr4:150067050-150067100	GM12892	blood:	n/a
5	chr4:150087191-150087241	NHBE	bronchial:	n/a
6	chr4:150085703-150085753	HNPCEpiC	eye:	n/a
7	chr4:150087191-150087241	MCF10A-Er-Src	breast:	n/a
8	chr4:150085703-150085753	GM12891	blood:	n/a
9	chr4:150085703-150085753	Jurkat	blood:	n/a
10	chr4:150067050-150067100	HNPCEpiC	eye:	n/a
11	chr4:150067050-150067100	HCPEpiC	choroid plexus:	n/a
12	chr4:150067050-150067100	HEK293	kidney:	embryo
13	chr4:150067050-150067100	HCF	heart:	n/a
14	chr4:150087191-150087241	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:150087191-150087241	H1-hESC	embryonic stem cell:	embryo
16	chr4:150067050-150067100	SKMC	muscle:	n/a
17	chr4:150087191-150087241	PFSK-1	brain:	n/a
18	chr4:150067050-150067100	ProgFib	skin:	n/a
19	chr4:150085703-150085753	Caco-2	colon:	n/a
20	chr4:150067050-150067100	GM06990	blood:	n/a
21	chr4:150067050-150067100	AG04450	lung:	fetal
22	chr4:150085703-150085753	NHDF-neo	bronchial:	n/a
23	chr4:150087191-150087241	HRCEpiC	kidney:	n/a
24	chr4:150067050-150067100	AG09319	gingival:	n/a
25	chr4:150085703-150085753	HMEC	breast:	n/a
26	chr4:150067050-150067100	LNCaP	prostate:	n/a
27	chr4:150087191-150087241	HAEpiC	amniotic membrane:	n/a
28	chr4:150087191-150087241	A549	lung:	n/a
29	chr4:150087191-150087241	HIPEpiC	eye:	n/a
30	chr4:150087191-150087241	BJ	skin:	n/a
31	chr4:150067050-150067100	ovcar-3	ovarian:	n/a
32	chr4:150085703-150085753	GM06990	blood:	n/a
33	chr4:150085703-150085753	A549	lung:	n/a
34	chr4:150085703-150085753	ProgFib	skin:	n/a
35	chr4:150067050-150067100	HUVEC	blood vessel:	n/a
36	chr4:150067050-150067100	MCF-7	breast:	n/a
37	chr4:150085703-150085753	HRE	kidney:	n/a
38	chr4:150085703-150085753	HCM	heart:	n/a
39	chr4:150067050-150067100	HRE	kidney:	n/a
40	chr4:150087191-150087241	GM19239	blood:	n/a
41	chr4:150067050-150067100	ECC-1	luminal epithelium:	n/a
42	chr4:150067050-150067100	CMK	blood:	n/a
43	chr4:150087191-150087241	AoSMC	blood vessel:	n/a
44	chr4:150085703-150085753	HUVEC	blood vessel:	n/a
45	chr4:150085703-150085753	NB4	blood:	n/a
46	chr4:150067050-150067100	RPTEC	kidney:	n/a
47	chr4:150067050-150067100	U87	brain:	n/a
48	chr4:150085703-150085753	AG04449	skin:	fetal
49	chr4:150067050-150067100	PrEC	prostate:	n/a
50	chr4:150067050-150067100	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:150107886..150110536-chr4:150111462..150113624,2	K562	blood:
2	chr4:149972225..149974391-chr4:150191500..150193608,2	MCF-7	breast:
3	chr4:150185022..150185571-chr4:150817333..150817853,2	MCF-7	breast:
4	chr4:150107886..150110536-chr4:150111462..150113624,2	K562	blood:
5	chr4:149971800..149972594-chr4:150185270..150185843,2	MCF-7	breast:
6	chr4:150074768..150075429-chr4:150185153..150186021,2	MCF-7	breast:
7	chr4:150074900..150075629-chr4:150185869..150186846,2	MCF-7	breast:
8	chr4:150179267..150181852-chr4:150198987..150201287,2	K562	blood:
9	chr4:149919606..149920568-chr4:150185026..150186002,4	MCF-7	breast:
10	chr4:150074768..150075429-chr4:150185153..150186021,2	MCF-7	breast:
11	chr4:150063409..150066191-chr4:150071536..150073450,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCLK2-3	chr4:150076604-150076877	NONHSAT098714
2	lnc-NR3C2-9	chr4:150183251-150183387	NONHSAT098715
3	lnc-DCLK2-3	chr4:150123515-150123708	NONHSAT098714
4	lnc-DCLK2-3	chr4:150135803-150136039	NONHSAT098714
5	lnc-NR3C2-4	chr4:150068965-150069197	XLOC_004120
6	lnc-DCLK2-3	chr4:150075447-150075771	NONHSAT098714
7	lnc-NR3C2-9	chr4:150185470-150185581	NONHSAT098715
8	lnc-DCLK2-3	chr4:150135596-150135683	NONHSAT098714
9	lnc-DCLK2-3	chr4:150125045-150125304	NONHSAT098714
10	lnc-DCLK2-3	chr4:150177385-150177550	NONHSAT098714
11	lnc-DCLK2-3	chr4:150126059-150126366	NONHSAT098714
12	lnc-NR3C2-4	chr4:150070701-150070932	XLOC_004120
13	lnc-NR3C2-9	chr4:150175507-150175629	NONHSAT098715
14	lnc-NR3C2-4	chr4:150070701-150070929	XLOC_004120
15	lnc-DCLK2-3	chr4:150139117-150139172	NONHSAT098714
16	lnc-DCLK2-3	chr4:150137555-150137729	NONHSAT098714
17	lnc-DCLK2-3	chr4:150181129-150181214	NONHSAT098714
18	lnc-NR3C2-4	chr4:150071377-150071438	XLOC_004120
19	lnc-NR3C2-4	chr4:150068954-150069197	XLOC_004120
20	lnc-DCLK2-3	chr4:150177156-150177247	NONHSAT098714

Variant related genes	Relation type
ENSG00000248210	TF binding region
ENSG00000250252	TF binding region
ENSG00000248210	CpG island
ENSG00000250252	CpG island
ENSG00000234828	chromatin interactions
ENSG00000248210	chromatin interactions

Extended variants
information (count: 1648 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185557770	chr4:150066352-150066353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562878696	chr4:150066353-150066354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141571947	chr4:150066355-150066356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572394874	chr4:150066365-150066366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565398280	chr4:150066385-150066386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191954641	chr4:150066424-150066425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6823955	chr4:150066438-150066439	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs183553002	chr4:150066440-150066441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1438783	chr4:150066611-150066612	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs75663559	chr4:150066642-150066643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147035005	chr4:150066709-150066710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188596668	chr4:150066745-150066746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552446597	chr4:150066768-150066769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565949962	chr4:150066800-150066801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544106029	chr4:150066810-150066811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1438785	chr4:150066829-150066830	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs370637226	chr4:150066841-150066842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1438786	chr4:150066868-150066869	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1438787	chr4:150066890-150066891	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs115481420	chr4:150066930-150066931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559299647	chr4:150066939-150066940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556321664	chr4:150067027-150067028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576392310	chr4:150067092-150067093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545047245	chr4:150067146-150067147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530155780	chr4:150067187-150067188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559219536	chr4:150067282-150067283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540639126	chr4:150067345-150067346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572389052	chr4:150067355-150067356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192094092	chr4:150067461-150067462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561145461	chr4:150067568-150067569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529783552	chr4:150067589-150067590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543516243	chr4:150067656-150067657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563192325	chr4:150067708-150067709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532152951	chr4:150067714-150067715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs33937700	chr4:150067723-150067724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs397792556	chr4:150067733-150067734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551852619	chr4:150067749-150067750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566011948	chr4:150067792-150067793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528370565	chr4:150067812-150067813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548450652	chr4:150067902-150067903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74327500	chr4:150067937-150067938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559517640	chr4:150067949-150067950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536804602	chr4:150067951-150067952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368363441	chr4:150067959-150067960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200357960	chr4:150067960-150067961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556621394	chr4:150067975-150067976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570019803	chr4:150067983-150067984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539057156	chr4:150067989-150067990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558507841	chr4:150068012-150068013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138231558	chr4:150068094-150068095	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150058600-150066600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:150062600-150066800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:150062600-150066800	Weak transcription	HSMM	muscle
4	chr4:150063200-150066800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr4:150066200-150068200	Enhancers	NHDF-Ad	bronchial
6	chr4:150066600-150068400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:150066800-150067200	Enhancers	HSMM	muscle
8	chr4:150066800-150067200	Enhancers	Osteobl	bone
9	chr4:150066800-150067400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr4:150066800-150067400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:150066800-150067400	Enhancers	NH-A	brain
12	chr4:150066800-150067400	Enhancers	NHLF	lung
13	chr4:150068400-150068800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:150068800-150069400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:150069000-150069600	Enhancers	Fetal Kidney	kidney
16	chr4:150078600-150080800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:150079400-150080200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:150079400-150081000	Enhancers	NHLF	lung
19	chr4:150079400-150083000	Enhancers	NHDF-Ad	bronchial
20	chr4:150079800-150080600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr4:150080200-150080400	Enhancers	HSMM	muscle
22	chr4:150080200-150080600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:150080400-150080600	Enhancers	Osteobl	bone
24	chr4:150080400-150081800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:150080400-150081800	Weak transcription	HSMM	muscle
26	chr4:150080600-150081600	Weak transcription	Osteobl	bone
27	chr4:150080600-150082000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr4:150080600-150085200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:150080800-150082200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:150081000-150084200	Weak transcription	NHLF	lung
31	chr4:150081400-150083600	Enhancers	Fetal Heart	heart
32	chr4:150081600-150083000	Enhancers	Osteobl	bone
33	chr4:150081600-150083200	Enhancers	HSMMtube	muscle
34	chr4:150081800-150082200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:150081800-150083200	Enhancers	HSMM	muscle
36	chr4:150082000-150083400	Enhancers	Muscle Satellite Cultured Cells	--
37	chr4:150082200-150083400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:150082200-150085000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:150082400-150082600	Enhancers	Left Ventricle	heart
40	chr4:150082400-150082800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr4:150082400-150082800	Enhancers	Adipose Nuclei	Adipose
42	chr4:150083000-150084200	Weak transcription	NHDF-Ad	bronchial
43	chr4:150083000-150084400	Weak transcription	Osteobl	bone
44	chr4:150083200-150084400	Weak transcription	HSMM	muscle
45	chr4:150083200-150085600	Weak transcription	HSMMtube	muscle
46	chr4:150083400-150084400	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr4:150083400-150092200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:150083600-150085200	Weak transcription	Fetal Heart	heart
49	chr4:150084200-150084600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:150084200-150086200	Enhancers	NHDF-Ad	bronchial

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