Variant report

Variant	nsv869522
Chromosome Location	chr4:20724433-20938248
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	ARID3A	chr4:20775077-20775342	HepG2	liver:	n/a	n/a
2	ATF1	chr4:20865610-20865795	K562	blood:	n/a	n/a
3	BACH1	chr4:20817391-20817392	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:20775048-20775386	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:20726709-20727073	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:20811465-20811810	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:20733794-20734144	A549	lung:	n/a	chr4:20733957-20733968
8	CEBPB	chr4:20797177-20797386	A549	lung:	n/a	chr4:20797259-20797272 chr4:20797259-20797270
9	CEBPB	chr4:20733820-20734122	IMR90	lung:	n/a	chr4:20733957-20733968
10	CEBPB	chr4:20798521-20798728	HepG2	liver:	n/a	chr4:20798642-20798653
11	CEBPB	chr4:20733786-20734123	H1-hESC	embryonic stem cell:	n/a	chr4:20733957-20733968
12	CEBPB	chr4:20926759-20926809	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:20814036-20814312	IMR90	lung:	n/a	chr4:20814155-20814166
14	CEBPB	chr4:20733795-20734145	K562	blood:	n/a	chr4:20733957-20733968
15	CEBPB	chr4:20814041-20814294	HepG2	liver:	n/a	chr4:20814155-20814166
16	CEBPB	chr4:20733795-20734141	HepG2	liver:	n/a	chr4:20733957-20733968
17	CEBPB	chr4:20741677-20741914	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:20836373-20836591	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:20741679-20741991	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:20800556-20800817	HepG2	liver:	n/a	chr4:20800688-20800699 chr4:20800653-20800664
21	CEBPB	chr4:20797109-20797407	HepG2	liver:	n/a	chr4:20797259-20797272 chr4:20797259-20797270
22	CEBPB	chr4:20836338-20836538	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:20842371-20842617	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:20937960-20938160	HepG2	liver:	n/a	chr4:20938070-20938081
25	CEBPB	chr4:20741665-20741893	K562	blood:	n/a	n/a
26	CEBPB	chr4:20741643-20741951	A549	lung:	n/a	n/a
27	CEBPB	chr4:20788544-20788846	HepG2	liver:	n/a	chr4:20788712-20788723 chr4:20788714-20788723 chr4:20788713-20788724 chr4:20788714-20788723 chr4:20788714-20788723 chr4:20788714-20788723
28	CEBPD	chr4:20725081-20725411	K562	blood:	n/a	n/a
29	CHD2	chr4:20775018-20775331	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:20912316-20912408	Lung_OC	lung:	n/a	n/a
31	CTCF	chr4:20775114-20775373	ECC-1	luminal epithelium:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
32	CTCF	chr4:20775120-20775270	HMEC	breast:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
33	CTCF	chr4:20775140-20775290	HVMF	connective:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
34	CTCF	chr4:20775140-20775290	HPAF	blood vessel:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
35	CTCF	chr4:20774976-20775459	HCT-116	colon:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
36	CTCF	chr4:20761780-20761930	AG09309	skin:	n/a	chr4:20761860-20761876
37	CTCF	chr4:20775100-20775250	AG09309	skin:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
38	CTCF	chr4:20761774-20761972	GM12878	blood:	n/a	chr4:20761860-20761876
39	CTCF	chr4:20761760-20761910	HEK293	kidney:	n/a	chr4:20761860-20761876
40	CTCF	chr4:20888220-20888370	Caco-2	colon:	n/a	n/a
41	CTCF	chr4:20775054-20775309	ProgFib	skin:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
42	CTCF	chr4:20761780-20761930	BE2_C	brain:	n/a	chr4:20761860-20761876
43	CTCF	chr4:20761740-20761890	GM12878	blood:	n/a	chr4:20761860-20761876
44	CTCF	chr4:20775077-20775275	MCF-7	breast:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
45	CTCF	chr4:20775160-20775310	GM12871	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
46	CTCF	chr4:20761800-20761950	K562	blood:	n/a	chr4:20761860-20761876
47	CTCF	chr4:20775120-20775270	AG09309	skin:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
48	CTCF	chr4:20761780-20761930	GM12864	blood:	n/a	chr4:20761860-20761876
49	CTCF	chr4:20761800-20761950	HMF	breast:	n/a	chr4:20761860-20761876
50	CTCF	chr4:20761780-20761930	MCF-7	breast:	n/a	chr4:20761860-20761876

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20885246-20885296	AG09319	gingival:	n/a
2	chr4:20884431-20884481	Hela-S3	cervix:	n/a
3	chr4:20852366-20852416	HRPEpiC	eye:	n/a
4	chr4:20885246-20885296	T-47D	breast:	n/a
5	chr4:20884321-20884371	NHBE	bronchial:	n/a
6	chr4:20811042-20811092	GM06990	blood:	n/a
7	chr4:20852337-20852387	GM19239	blood:	n/a
8	chr4:20884321-20884371	AG04450	lung:	fetal
9	chr4:20885246-20885296	RPTEC	kidney:	n/a
10	chr4:20885019-20885069	GM12891	blood:	n/a
11	chr4:20852672-20852722	NHBE	bronchial:	n/a
12	chr4:20730493-20730543	AG04450	lung:	fetal
13	chr4:20885246-20885296	AG10803	skin:	n/a
14	chr4:20811042-20811092	A549	lung:	n/a
15	chr4:20884385-20884435	GM12892	blood:	n/a
16	chr4:20884321-20884371	HRCEpiC	kidney:	n/a
17	chr4:20885246-20885296	HUVEC	blood vessel:	n/a
18	chr4:20729211-20729261	ECC-1	luminal epithelium:	n/a
19	chr4:20884321-20884371	T-47D	breast:	n/a
20	chr4:20730493-20730543	AG09319	gingival:	n/a
21	chr4:20811042-20811092	PFSK-1	brain:	n/a
22	chr4:20811042-20811092	AG09309	skin:	n/a
23	chr4:20885536-20885586	AG09319	gingival:	n/a
24	chr4:20730493-20730543	HRPEpiC	eye:	n/a
25	chr4:20884321-20884371	PANC-1	pancreas:	n/a
26	chr4:20852672-20852722	BE2_C	brain:	n/a
27	chr4:20884431-20884481	GM12891	blood:	n/a
28	chr4:20884321-20884371	MCF10A-Er-Src	breast:	n/a
29	chr4:20884321-20884371	GM12891	blood:	n/a
30	chr4:20811042-20811092	SK-N-SH	brain:	n/a
31	chr4:20811042-20811092	RPTEC	kidney:	n/a
32	chr4:20885536-20885586	HCM	heart:	n/a
33	chr4:20885246-20885296	HEEpiC	esophagus:	n/a
34	chr4:20730493-20730543	SAEC	small airway:	n/a
35	chr4:20730493-20730543	AG04449	skin:	fetal
36	chr4:20885246-20885296	HIPEpiC	eye:	n/a
37	chr4:20730493-20730543	NB4	blood:	n/a
38	chr4:20852672-20852722	HL-60	blood:	n/a
39	chr4:20729211-20729261	HRE	kidney:	n/a
40	chr4:20811042-20811092	AG04449	skin:	fetal
41	chr4:20852337-20852387	HRE	kidney:	n/a
42	chr4:20852337-20852387	HIPEpiC	eye:	n/a
43	chr4:20885019-20885069	HAEpiC	amniotic membrane:	n/a
44	chr4:20885019-20885069	SKMC	muscle:	n/a
45	chr4:20852672-20852722	AG04450	lung:	fetal
46	chr4:20852337-20852387	BE2_C	brain:	n/a
47	chr4:20885246-20885296	AG04449	skin:	fetal
48	chr4:20852337-20852387	AoSMC	blood vessel:	n/a
49	chr4:20729211-20729261	HRCEpiC	kidney:	n/a
50	chr4:20730493-20730543	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
2	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
3	chr4:20733613..20735469-chr4:20737753..20739786,2	K562	blood:
4	chr4:20774939..20775520-chr4:21136553..21137202,2	MCF-7	breast:
5	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
6	chr18:10317211..10317949-chr4:20836718..20837659,2	MCF-7	breast:
7	chr4:20733613..20735469-chr4:20737753..20739786,2	K562	blood:
8	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
9	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
10	chr4:20736248..20737799-chr4:20738056..20739802,2	MCF-7	breast:
11	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
12	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
13	chr4:20736150..20738048-chr4:20747130..20748840,2	K562	blood:
14	chr4:20700788..20703573-chr4:20723140..20724857,2	MCF-7	breast:
15	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
16	chr4:20701205..20703695-chr4:20723209..20725454,2	MCF-7	breast:
17	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
18	chr4:20736248..20737799-chr4:20738056..20739802,2	MCF-7	breast:
19	chr4:20736150..20738048-chr4:20747130..20748840,2	K562	blood:
20	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
21	chr4:20774749..20775678-chr4:21136384..21137379,5	MCF-7	breast:
22	chr4:20849276..20852275-chr6:109770823..109773619,2	K562	blood:
23	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
24	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:
25	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
26	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
27	chr4:20702290..20703806-chr4:20728599..20731005,2	K562	blood:
28	chr4:20700229..20702940-chr4:20728046..20730028,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-6	chr4:20768431-20768995	ENSG00000272995.1
2	lnc-SLIT2-3	chr4:20731428-20733259	NONHSAT095738
3	lnc-SLIT2-3	chr4:20733323-20734177	NONHSAT095738

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PACRGL	hsa-miR-373-3p	chr4:20754297-20754319

Variant related genes	Relation type
KCNIP4	TF binding region
ENSG00000272995	TF binding region
KCNIP4	CpG island
ENSG00000272995	CpG island
ENSG00000135596	chromatin interactions
ENSG00000163138	chromatin interactions

Extended variants
information (count: 6381 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:6381 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568174409	chr4:20724433-20724434	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535377000	chr4:20724453-20724454	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535576578	chr4:20724483-20724484	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555292112	chr4:20724489-20724490	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553878751	chr4:20724505-20724506	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565724283	chr4:20724537-20724538	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112251681	chr4:20724563-20724564	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539401431	chr4:20724580-20724581	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558432194	chr4:20724600-20724601	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576635463	chr4:20724606-20724607	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544011542	chr4:20724671-20724672	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555719154	chr4:20724679-20724680	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575133601	chr4:20724730-20724731	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7688592	chr4:20724731-20724732	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs554216775	chr4:20724771-20724772	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs386672348	chr4:20724773-20724774	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541175435	chr4:20724774-20724775	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557493037	chr4:20724784-20724785	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576073823	chr4:20724916-20724917	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559410754	chr4:20724926-20724927	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577624167	chr4:20724932-20724933	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs75140723	chr4:20724952-20724953	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191223879	chr4:20724996-20724997	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564760289	chr4:20725002-20725003	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531470392	chr4:20725005-20725006	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550031712	chr4:20725036-20725037	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs142101499	chr4:20725061-20725062	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs201922123	chr4:20725066-20725067	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142305792	chr4:20725078-20725079	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565735356	chr4:20725167-20725168	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180780535	chr4:20725224-20725225	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185439597	chr4:20725232-20725233	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113890597	chr4:20725287-20725288	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537374100	chr4:20725307-20725308	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191030079	chr4:20725333-20725334	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573937361	chr4:20725340-20725341	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534848353	chr4:20725372-20725373	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553053684	chr4:20725375-20725376	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183354909	chr4:20725381-20725382	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545399159	chr4:20725383-20725384	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563564201	chr4:20725390-20725391	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112299421	chr4:20725399-20725400	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs61013057	chr4:20725403-20725404	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543396744	chr4:20725449-20725450	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141879365	chr4:20725478-20725479	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147866913	chr4:20725496-20725497	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150416221	chr4:20725528-20725529	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145287814	chr4:20725536-20725537	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2052775	chr4:20725548-20725549	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76392954	chr4:20725549-20725550	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	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
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20703000-20741400	Weak transcription	Stomach Mucosa	stomach
2	chr4:20703200-20741000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr4:20706800-20738600	Weak transcription	Psoas Muscle	Psoas
4	chr4:20707200-20739400	Weak transcription	HepG2	liver
5	chr4:20708200-20733600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:20715400-20738600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr4:20715400-20739400	Weak transcription	Osteobl	bone
8	chr4:20718000-20738600	Weak transcription	NHDF-Ad	bronchial
9	chr4:20718200-20738400	Weak transcription	Fetal Heart	heart
10	chr4:20721600-20727600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:20721800-20724800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:20721800-20724800	Strong transcription	Rectal Smooth Muscle	rectum
13	chr4:20721800-20725200	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr4:20721800-20725600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:20721800-20736000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:20721800-20736400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:20721800-20737200	Strong transcription	Liver	Liver
18	chr4:20722000-20724600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:20722000-20724600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:20722000-20724600	Strong transcription	Fetal Kidney	kidney
21	chr4:20722000-20724800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr4:20722000-20724800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr4:20722000-20724800	Strong transcription	Primary T cells from cord blood	blood
24	chr4:20722000-20724800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:20722000-20724800	ZNF genes & repeats	Fetal Muscle Leg	muscle
26	chr4:20722000-20725000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:20722000-20725000	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr4:20722000-20725200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr4:20722000-20725400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr4:20722000-20725600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr4:20722000-20726000	Strong transcription	Brain Inferior Temporal Lobe	brain
32	chr4:20722000-20727000	Strong transcription	Brain Cingulate Gyrus	brain
33	chr4:20722000-20727800	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr4:20722200-20724800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr4:20722200-20724800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr4:20722200-20725400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr4:20722200-20727600	Strong transcription	Brain Hippocampus Middle	brain
38	chr4:20722600-20724600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:20722600-20724800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr4:20722600-20724800	Strong transcription	Brain Substantia Nigra	brain
41	chr4:20722800-20724600	ZNF genes & repeats	Brain Germinal Matrix	brain
42	chr4:20722800-20724600	Strong transcription	Pancreatic Islets	Pancreatic Islet
43	chr4:20722800-20725000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:20722800-20725000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr4:20722800-20725000	Strong transcription	Skeletal Muscle Male	skeletal muscle
46	chr4:20722800-20725200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:20722800-20735800	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr4:20723000-20726000	Strong transcription	Right Ventricle	heart
49	chr4:20723000-20738400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr4:20723200-20727200	Strong transcription	Sigmoid Colon	Sigmoid Colon

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