Variant report

Variant	nsv4610
Chromosome Location	chr4:174217026-174252627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:983)
CpG islands
(count:122)
Chromatin interactive
region (count:68)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:174239814-174240417	K562	blood:	n/a	n/a
2	ARID3A	chr4:174239855-174240333	HepG2	liver:	n/a	n/a
3	BCL3	chr4:174241877-174242205	GM12878	blood:	n/a	n/a
4	BCL3	chr4:174251350-174252196	K562	blood:	n/a	n/a
5	BCL3	chr4:174238965-174239257	GM12878	blood:	n/a	n/a
6	BCL3	chr4:174251901-174252274	K562	blood:	n/a	n/a
7	BCL3	chr4:174241964-174242218	GM12878	blood:	n/a	n/a
8	BCLAF1	chr4:174251234-174252045	K562	blood:	n/a	n/a
9	BHLHE40	chr4:174238183-174238527	K562	blood:	n/a	n/a
10	BHLHE40	chr4:174238272-174238440	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:174222695-174222976	K562	blood:	n/a	n/a
12	CCNT2	chr4:174250703-174251101	K562	blood:	n/a	n/a
13	CCNT2	chr4:174244579-174244779	K562	blood:	n/a	n/a
14	CCNT2	chr4:174251822-174252113	K562	blood:	n/a	n/a
15	CEBPB	chr4:174243302-174243497	A549	lung:	n/a	n/a
16	CEBPB	chr4:174239793-174240392	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:174252087-174252096	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:174234042-174234227	K562	blood:	n/a	chr4:174234160-174234171
19	CEBPB	chr4:174240197-174240215	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:174240066-174240361	K562	blood:	n/a	n/a
21	CEBPB	chr4:174234036-174234224	HepG2	liver:	n/a	chr4:174234160-174234171
22	CEBPB	chr4:174225527-174225752	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:174240884-174241338	HepG2	liver:	n/a	chr4:174241053-174241064
24	CEBPB	chr4:174222776-174223117	K562	blood:	n/a	n/a
25	CEBPB	chr4:174225523-174225725	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:174225590-174225752	A549	lung:	n/a	n/a
27	CEBPB	chr4:174240874-174241230	IMR90	lung:	n/a	chr4:174241053-174241064
28	CHD1	chr4:174251956-174251958	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:174251631-174251999	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr4:174239607-174240224	GM12878	blood:	n/a	n/a
31	CREB1	chr4:174251083-174251972	K562	blood:	n/a	n/a
32	CTCF	chr4:174222900-174223050	NHDF-neo	bronchial:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
33	CTCF	chr4:174222840-174222990	GM12878	blood:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
34	CTCF	chr4:174222880-174223030	HRPEpiC	eye:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
35	CTCF	chr4:174238220-174238370	BJ	skin:	n/a	n/a
36	CTCF	chr4:174222840-174222990	NB4	blood:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
37	CTCF	chr4:174238180-174238330	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr4:174222860-174223010	AG09319	gingival:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
39	CTCF	chr4:174237960-174238110	GM12874	blood:	n/a	n/a
40	CTCF	chr4:174222820-174222970	GM12872	blood:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
41	CTCF	chr4:174222840-174222990	WERI-Rb-1	eye:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
42	CTCF	chr4:174222860-174223010	HBMEC	blood vessel:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
43	CTCF	chr4:174238320-174238470	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:174238320-174238470	HMF	breast:	n/a	n/a
45	CTCF	chr4:174222900-174223050	HA-sp	spinal cord:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
46	CTCF	chr4:174222880-174223030	GM12867	blood:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950
47	CTCF	chr4:174223196-174223198	GM10248	blood:	n/a	n/a
48	CTCF	chr4:174239800-174239950	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:174240080-174240230	BJ	skin:	n/a	chr4:174240119-174240140 chr4:174240117-174240135 chr4:174240120-174240128
50	CTCF	chr4:174222920-174223070	HepG2	liver:	n/a	chr4:174222935-174222951 chr4:174222934-174222952 chr4:174222929-174222950

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:174251028-174251078	ECC-1	luminal epithelium:	n/a
2	chr4:174251028-174251078	NB4	blood:	n/a
3	chr4:174240175-174240225	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:174240175-174240225	Jurkat	blood:	n/a
5	chr4:174251028-174251078	U87	brain:	n/a
6	chr4:174251028-174251078	HEEpiC	esophagus:	n/a
7	chr4:174240175-174240225	SAEC	small airway:	n/a
8	chr4:174240175-174240225	AG10803	skin:	n/a
9	chr4:174240175-174240225	NB4	blood:	n/a
10	chr4:174240175-174240225	HL-60	blood:	n/a
11	chr4:174240175-174240225	Hepatocyte	liver:	n/a
12	chr4:174240175-174240225	GM12892	blood:	n/a
13	chr4:174251028-174251078	NT2-D1	testis:	n/a
14	chr4:174251028-174251078	Hepatocyte	liver:	n/a
15	chr4:174240175-174240225	HCM	heart:	n/a
16	chr4:174240175-174240225	U87	brain:	n/a
17	chr4:174251028-174251078	GM06990	blood:	n/a
18	chr4:174251028-174251078	HUVEC	blood vessel:	n/a
19	chr4:174240175-174240225	NH-A	brain:	n/a
20	chr4:174251028-174251078	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:174251028-174251078	AG04449	skin:	fetal
22	chr4:174251028-174251078	Hela-S3	cervix:	n/a
23	chr4:174240175-174240225	HIPEpiC	eye:	n/a
24	chr4:174240175-174240225	MCF10A-Er-Src	breast:	n/a
25	chr4:174240175-174240225	T-47D	breast:	n/a
26	chr4:174251028-174251078	GM12878	blood:	n/a
27	chr4:174251028-174251078	Caco-2	colon:	n/a
28	chr4:174251028-174251078	HCF	heart:	n/a
29	chr4:174251028-174251078	PrEC	prostate:	n/a
30	chr4:174251028-174251078	HCM	heart:	n/a
31	chr4:174240175-174240225	A549	lung:	n/a
32	chr4:174251028-174251078	NHDF-neo	bronchial:	n/a
33	chr4:174240175-174240225	AG09319	gingival:	n/a
34	chr4:174251028-174251078	T-47D	breast:	n/a
35	chr4:174240175-174240225	BE2_C	brain:	n/a
36	chr4:174251028-174251078	Jurkat	blood:	n/a
37	chr4:174240175-174240225	NHBE	bronchial:	n/a
38	chr4:174240175-174240225	ECC-1	luminal epithelium:	n/a
39	chr4:174240175-174240225	HCT-116	colon:	n/a
40	chr4:174240175-174240225	Hela-S3	cervix:	n/a
41	chr4:174240175-174240225	MCF-7	breast:	n/a
42	chr4:174240175-174240225	PFSK-1	brain:	n/a
43	chr4:174251028-174251078	HAEpiC	amniotic membrane:	n/a
44	chr4:174240175-174240225	ovcar-3	ovarian:	n/a
45	chr4:174251028-174251078	CMK	blood:	n/a
46	chr4:174240175-174240225	NHDF-neo	bronchial:	n/a
47	chr4:174251028-174251078	AG10803	skin:	n/a
48	chr4:174240175-174240225	HRPEpiC	eye:	n/a
49	chr4:174240175-174240225	HCPEpiC	choroid plexus:	n/a
50	chr4:174251028-174251078	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:174168542..174170640-chr4:174252148..174254186,2	K562	blood:
2	chr4:174228695..174231199-chr4:174232859..174234793,2	K562	blood:
3	chr4:174248835..174250449-chr4:174326947..174329292,2	K562	blood:
4	chr4:174249343..174251576-chr4:174340147..174342867,2	MCF-7	breast:
5	chr4:174239681..174240332-chr4:174337877..174338420,2	MCF-7	breast:
6	chr4:174242458..174245436-chr4:174334949..174337241,2	MCF-7	breast:
7	chr4:174236553..174238246-chr4:174252256..174255758,3	MCF-7	breast:
8	chr4:174225337..174228056-chr4:174239161..174240941,2	K562	blood:
9	chr4:174226655..174230788-chr4:174237584..174240608,3	K562	blood:
10	chr4:174221776..174224319-chr4:174307795..174309389,2	K562	blood:
11	chr4:174240982..174243911-chr4:174245243..174249082,5	MCF-7	breast:
12	chr4:174211568..174213734-chr4:174230936..174233775,2	K562	blood:
13	chr4:174090877..174092412-chr4:174243600..174245281,2	K562	blood:
14	chr4:174248778..174262653-chr4:174278408..174298501,82	K562	blood:
15	chr11:62609021..62610572-chr4:174243392..174244912,2	MCF-7	breast:
16	chr4:174243466..174246218-chr4:174302181..174305054,2	K562	blood:
17	chr4:174236553..174238246-chr4:174252256..174255758,3	MCF-7	breast:
18	chr4:174220269..174222590-chr4:174244769..174248298,3	K562	blood:
19	chr4:174225665..174227645-chr4:174247160..174250931,3	K562	blood:
20	chr4:174229058..174231834-chr4:174254792..174257398,2	MCF-7	breast:
21	chr4:174213511..174216529-chr4:174219957..174222791,4	K562	blood:
22	chr4:173934707..173935259-chr4:174237986..174238803,2	MCF-7	breast:
23	chr4:174222819..174224476-chr4:174307676..174309389,2	K562	blood:
24	chr4:173934377..173935350-chr4:174222613..174223693,4	MCF-7	breast:
25	chr4:174246136..174247718-chr4:174281054..174283423,2	MCF-7	breast:
26	chr4:174226990..174229389-chr4:174231756..174233665,2	MCF-7	breast:
27	chr17:57913457..57915668-chr4:174228820..174230620,2	MCF-7	breast:
28	chr4:174235439..174238227-chr4:174247293..174248977,2	MCF-7	breast:
29	chr4:174223462..174225413-chr4:174233539..174235313,2	K562	blood:
30	chr4:174252529..174254237-chr4:174310710..174314064,3	K562	blood:
31	chr4:174124001..174126902-chr4:174251610..174253502,2	K562	blood:
32	chr4:174251329..174253900-chr4:174300222..174303986,3	K562	blood:
33	chr4:174229950..174233368-chr4:174235304..174239617,4	K562	blood:
34	chr4:174234558..174237246-chr4:174239051..174241442,2	K562	blood:
35	chr4:174220269..174222590-chr4:174244769..174248298,3	K562	blood:
36	chr4:174237145..174239591-chr4:174291515..174293393,2	MCF-7	breast:
37	chr4:174232325..174234632-chr4:174253098..174255865,2	K562	blood:
38	chr4:174225337..174228056-chr4:174239161..174240941,2	K562	blood:
39	chr4:174219838..174221713-chr4:174249456..174251462,2	K562	blood:
40	chr4:174250771..174257645-chr4:174286907..174294441,15	MCF-7	breast:
41	chr4:174246012..174248721-chr4:174319342..174321970,2	MCF-7	breast:
42	chr4:174233579..174235436-chr4:174347126..174349799,2	K562	blood:
43	chr4:174239770..174240332-chr4:174281552..174282055,2	MCF-7	breast:
44	chr4:173946331..173946965-chr4:174222418..174223019,3	K562	blood:
45	chr4:174228695..174231199-chr4:174232859..174234793,2	K562	blood:
46	chr4:174239461..174240574-chr4:174414785..174416197,3	K562	blood:
47	chr4:174228022..174232721-chr4:174253766..174256479,5	K562	blood:
48	chr4:174209246..174210060-chr4:174222776..174223385,2	MCF-7	breast:
49	chr4:174245727..174260507-chr4:174283013..174295498,65	K562	blood:
50	chr4:174239631..174240582-chr4:174341121..174341795,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGB2-1	chr4:174250771-174250845	ENSG00000248774.1
2	lnc-HMGB2-1	chr4:174247820-174247871	ENSG00000248774.1
3	lnc-HMGB2-5	chr4:174245758-174247299	NONHSAT099232
4	lnc-HMGB2-1	chr4:174243357-174243750	ENSG00000248774.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HMGB2	hsa-miR-374a-5p	chr4:174252551-174252576

Variant related genes	Relation type
GALNT7	TF binding region
ENSG00000248774	TF binding region
GALNT7	CpG island
ENSG00000248774	CpG island
ENSG00000242882	chromatin interactions
ENSG00000272870	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000164104	chromatin interactions
ENSG00000248774	chromatin interactions
ENSG00000164106	chromatin interactions
ENSG00000164105	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000109586	chromatin interactions

Extended variants
information (count: 1179 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542734579	chr4:174217052-174217053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186116573	chr4:174217053-174217054	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548744372	chr4:174217096-174217097	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4696055	chr4:174217122-174217123	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs550313285	chr4:174217220-174217221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538970243	chr4:174217228-174217229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73003339	chr4:174217282-174217283	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs533020476	chr4:174217291-174217292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546207478	chr4:174217301-174217302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578086484	chr4:174217321-174217322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374285420	chr4:174217334-174217335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573850958	chr4:174217403-174217404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140316583	chr4:174217405-174217406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528283556	chr4:174217443-174217444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73872541	chr4:174217444-174217445	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs574094439	chr4:174217477-174217478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551031203	chr4:174217566-174217567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538446970	chr4:174217572-174217573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115541084	chr4:174217588-174217589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73003342	chr4:174217634-174217635	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534469013	chr4:174217672-174217673	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs80064054	chr4:174217676-174217677	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534955225	chr4:174217791-174217792	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543153194	chr4:174217793-174217794	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73003345	chr4:174217798-174217799	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs73872542	chr4:174217807-174217808	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553014527	chr4:174217823-174217824	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563908047	chr4:174217833-174217834	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533083861	chr4:174217897-174217898	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550344883	chr4:174217898-174217899	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190945752	chr4:174217951-174217952	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560136602	chr4:174217992-174217993	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577691445	chr4:174218017-174218018	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139098110	chr4:174218049-174218050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73872543	chr4:174218078-174218079	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs182843974	chr4:174218171-174218172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531400567	chr4:174218322-174218323	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145502810	chr4:174218323-174218324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78114430	chr4:174218365-174218366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138118927	chr4:174218396-174218397	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76574674	chr4:174218399-174218400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199651887	chr4:174218400-174218401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567901657	chr4:174218425-174218426	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114149805	chr4:174218444-174218445	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375766612	chr4:174218478-174218479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556486674	chr4:174218482-174218483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576147354	chr4:174218502-174218503	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545107190	chr4:174218550-174218551	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73872544	chr4:174218565-174218566	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577407161	chr4:174218567-174218568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Prostate cancer	22341455	CNVD
Ovarian cancer	22355333	CNVD
Burkitt''s lymphoma	19759907	CNVD

Chromatin state (count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174206200-174229000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr4:174206400-174249400	Weak transcription	Fetal Kidney	kidney
3	chr4:174207800-174232600	Weak transcription	Ovary	ovary
4	chr4:174208800-174230400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:174209000-174218600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr4:174209000-174218800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:174209000-174220600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:174209000-174223000	Weak transcription	HSMM	muscle
9	chr4:174209000-174223600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr4:174209000-174225200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr4:174209000-174228600	Weak transcription	Esophagus	oesophagus
12	chr4:174209000-174233400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr4:174209000-174235000	Weak transcription	Colonic Mucosa	Colon
14	chr4:174209200-174217600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr4:174209200-174226800	Weak transcription	Fetal Muscle Trunk	muscle
16	chr4:174209800-174217200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr4:174210200-174219000	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr4:174210200-174221200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:174210400-174226600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr4:174210400-174235400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:174210400-174253000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr4:174210400-174253000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr4:174210600-174228600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr4:174210600-174235200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr4:174210600-174235200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr4:174210600-174240200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr4:174210600-174253000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr4:174210800-174217400	Weak transcription	GM12878-XiMat	blood
29	chr4:174210800-174218600	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr4:174210800-174223000	Weak transcription	Brain Anterior Caudate	brain
31	chr4:174210800-174228400	Weak transcription	Small Intestine	intestine
32	chr4:174210800-174236200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:174210800-174252000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:174211000-174217800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:174211200-174225000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:174212200-174228000	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr4:174212200-174228200	Weak transcription	Fetal Intestine Small	intestine
38	chr4:174212400-174228200	Weak transcription	Fetal Stomach	stomach
39	chr4:174213000-174220600	Strong transcription	Fetal Thymus	thymus
40	chr4:174213000-174222600	Weak transcription	A549	lung
41	chr4:174213600-174237200	Weak transcription	NHEK	skin
42	chr4:174213800-174235400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr4:174214600-174220200	Strong transcription	Primary hematopoietic stem cells	blood
44	chr4:174214800-174219200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr4:174214800-174219800	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:174214800-174220600	Strong transcription	Dnd41	blood
47	chr4:174214800-174220600	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr4:174214800-174235600	Weak transcription	Adipose Nuclei	Adipose
49	chr4:174215000-174228600	Weak transcription	Spleen	Spleen
50	chr4:174215000-174239400	Weak transcription	HUVEC	blood vessel

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