Variant report

Variant	nsv879486
Chromosome Location	chr4:74031423-74114322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:306)
Chromatin interactive
region (count:115)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:74111830-74112051	K562	blood:	n/a	n/a
2	ARID3A	chr4:74098327-74098361	K562	blood:	n/a	n/a
3	ARID3A	chr4:74096860-74097556	K562	blood:	n/a	n/a
4	ARID3A	chr4:74053144-74053255	K562	blood:	n/a	n/a
5	ARID3A	chr4:74055386-74055525	K562	blood:	n/a	n/a
6	ARID3A	chr4:74088179-74089111	K562	blood:	n/a	chr4:74088412-74088428
7	ARID3A	chr4:74088637-74088954	HepG2	liver:	n/a	n/a
8	ATF1	chr4:74088642-74089046	K562	blood:	n/a	n/a
9	ATF2	chr4:74088491-74089048	GM12878	blood:	n/a	n/a
10	ATF2	chr4:74088448-74089073	GM12878	blood:	n/a	n/a
11	ATF3	chr4:74088565-74089120	K562	blood:	n/a	n/a
12	BACH1	chr4:74078840-74079040	K562	blood:	n/a	n/a
13	BATF	chr4:74088639-74088976	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:74088420-74089071	K562	blood:	n/a	n/a
15	BCLAF1	chr4:74046849-74047376	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:74088715-74089013	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:74088555-74089111	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:74088581-74089061	K562	blood:	n/a	n/a
19	BRCA1	chr4:74088635-74089113	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:74090500-74090501	GM12878	blood:	n/a	n/a
21	CBX3	chr4:74088641-74089117	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:74088524-74089058	K562	blood:	n/a	n/a
23	CBX3	chr4:74055032-74055417	K562	blood:	n/a	n/a
24	CBX3	chr4:74111569-74112016	K562	blood:	n/a	n/a
25	CBX3	chr4:74088575-74089030	K562	blood:	n/a	n/a
26	CBX3	chr4:74069559-74069966	K562	blood:	n/a	n/a
27	CBX3	chr4:74088578-74089172	HCT-116	colon:	n/a	n/a
28	CCNT2	chr4:74058936-74059136	K562	blood:	n/a	n/a
29	CCNT2	chr4:74059942-74060113	K562	blood:	n/a	n/a
30	CCNT2	chr4:74088629-74088829	K562	blood:	n/a	n/a
31	CCNT2	chr4:74111518-74112034	K562	blood:	n/a	n/a
32	CCNT2	chr4:74097005-74097205	K562	blood:	n/a	n/a
33	CCNT2	chr4:74046840-74047040	K562	blood:	n/a	n/a
34	CCNT2	chr4:74087518-74087724	K562	blood:	n/a	n/a
35	CEBPB	chr4:74063037-74063275	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:74063002-74063304	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:74059460-74059730	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:74062953-74063321	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:74062964-74063250	MCF-7	breast:	n/a	n/a
40	CEBPB	chr4:74059296-74059766	K562	blood:	n/a	n/a
41	CEBPB	chr4:74059374-74059787	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:74092408-74092511	HepG2	liver:	n/a	chr4:74092486-74092497
43	CEBPB	chr4:74059440-74059695	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:74062959-74063316	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:74059433-74059785	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:74092449-74092516	A549	lung:	n/a	chr4:74092486-74092497
47	CEBPB	chr4:74092435-74092522	IMR90	lung:	n/a	chr4:74092486-74092497
48	CEBPB	chr4:74096482-74096687	HepG2	liver:	n/a	chr4:74096601-74096612
49	CEBPB	chr4:74059435-74059838	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:74055921-74056073	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74047370-74047420	PFSK-1	brain:	n/a
2	chr4:74047370-74047420	PFSK-1	brain:	n/a
3	chr4:74065349-74065399	U87	brain:	n/a
4	chr4:74103157-74103207	Caco-2	colon:	n/a
5	chr4:74103157-74103207	HL-60	blood:	n/a
6	chr4:74088730-74088780	ProgFib	skin:	n/a
7	chr4:74047370-74047420	AG09309	skin:	n/a
8	chr4:74047370-74047420	HNPCEpiC	eye:	n/a
9	chr4:74088730-74088780	H1-hESC	embryonic stem cell:	embryo
10	chr4:74111455-74111505	AG09309	skin:	n/a
11	chr4:74111455-74111505	GM12892	blood:	n/a
12	chr4:74047370-74047420	H1-hESC	embryonic stem cell:	embryo
13	chr4:74111455-74111505	LNCaP	prostate:	n/a
14	chr4:74065349-74065399	HEK293	kidney:	embryo
15	chr4:74103157-74103207	BJ	skin:	n/a
16	chr4:74111455-74111505	U87	brain:	n/a
17	chr4:74103157-74103207	MCF-7	breast:	n/a
18	chr4:74065349-74065399	BJ	skin:	n/a
19	chr4:74088730-74088780	HCF	heart:	n/a
20	chr4:74088730-74088780	HL-60	blood:	n/a
21	chr4:74065349-74065399	SK-N-MC	brain:	n/a
22	chr4:74111455-74111505	HIPEpiC	eye:	n/a
23	chr4:74111455-74111505	HCPEpiC	choroid plexus:	n/a
24	chr4:74103157-74103207	NB4	blood:	n/a
25	chr4:74103157-74103207	SK-N-SH	brain:	n/a
26	chr4:74088730-74088780	SK-N-SH_RA	brain:	n/a
27	chr4:74047370-74047420	T-47D	breast:	n/a
28	chr4:74103157-74103207	U87	brain:	n/a
29	chr4:74065349-74065399	NHBE	bronchial:	n/a
30	chr4:74111455-74111505	HUVEC	blood vessel:	n/a
31	chr4:74111455-74111505	AG10803	skin:	n/a
32	chr4:74088730-74088780	Caco-2	colon:	n/a
33	chr4:74047370-74047420	GM12878	blood:	n/a
34	chr4:74065349-74065399	Hela-S3	cervix:	n/a
35	chr4:74111455-74111505	ovcar-3	ovarian:	n/a
36	chr4:74088730-74088780	U87	brain:	n/a
37	chr4:74088730-74088780	HAEpiC	amniotic membrane:	n/a
38	chr4:74088730-74088780	NH-A	brain:	n/a
39	chr4:74047370-74047420	AG04449	skin:	fetal
40	chr4:74103157-74103207	PrEC	prostate:	n/a
41	chr4:74111455-74111505	NH-A	brain:	n/a
42	chr4:74065349-74065399	LNCaP	prostate:	n/a
43	chr4:74088730-74088780	HIPEpiC	eye:	n/a
44	chr4:74047370-74047420	HCM	heart:	n/a
45	chr4:74103157-74103207	BE2_C	brain:	n/a
46	chr4:74103157-74103207	HRE	kidney:	n/a
47	chr4:74103157-74103207	GM12891	blood:	n/a
48	chr4:74065349-74065399	AG09309	skin:	n/a
49	chr4:74065349-74065399	IMR90	lung:	fetal
50	chr4:74065349-74065399	AG04449	skin:	fetal

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:74049747..74053903-chr4:74055413..74060187,5	K562	blood:
2	chr4:74092974..74095435-chr4:74123584..74125368,2	K562	blood:
3	chr4:73970811..73973172-chr4:74028857..74031698,2	K562	blood:
4	chr4:74050887..74052868-chr4:74066183..74068472,2	K562	blood:
5	chr4:74044682..74047650-chr4:74072993..74074617,2	K562	blood:
6	chr4:74068748..74071542-chr4:74072724..74077034,4	K562	blood:
7	chr4:74061445..74063140-chr4:74117099..74120021,2	K562	blood:
8	chr4:74099672..74104982-chr4:74123482..74126181,5	MCF-7	breast:
9	chr4:74036315..74038802-chr4:74124243..74126453,4	MCF-7	breast:
10	chr4:74046445..74048807-chr4:74084717..74087260,2	K562	blood:
11	chr4:74103163..74106414-chr4:74122698..74126217,3	MCF-7	breast:
12	chr4:74085378..74089938-chr4:74109585..74113346,7	K562	blood:
13	chr4:74054562..74057067-chr4:74057401..74060235,2	K562	blood:
14	chr4:74094714..74099476-chr4:74109744..74111749,4	K562	blood:
15	chr4:74072374..74074564-chr4:74074721..74076887,2	K562	blood:
16	chr4:74090826..74092875-chr4:74092966..74095699,2	MCF-7	breast:
17	chr4:74107320..74110128-chr4:74122442..74124984,2	MCF-7	breast:
18	chr4:74094116..74095692-chr4:74117214..74119409,2	K562	blood:
19	chr4:74037406..74040137-chr4:74042759..74046162,3	MCF-7	breast:
20	chr4:74086142..74089038-chr4:74090611..74092346,2	MCF-7	breast:
21	chr4:74042367..74044250-chr4:74088386..74090139,2	K562	blood:
22	chr4:74030522..74032070-chr4:74034879..74036523,2	MCF-7	breast:
23	chr4:74044444..74046783-chr4:74088415..74090635,2	K562	blood:
24	chr4:74087106..74090351-chr4:74123421..74126445,9	K562	blood:
25	chr4:73983376..73985757-chr4:74044958..74047334,2	K562	blood:
26	chr4:74041420..74044364-chr4:74048787..74051206,3	K562	blood:
27	chr4:74078580..74080113-chr4:74115423..74117254,2	K562	blood:
28	chr4:74048549..74051354-chr4:74053215..74054751,2	K562	blood:
29	chr4:73998911..74001287-chr4:74095013..74097048,2	K562	blood:
30	chr4:74067827..74069350-chr4:74117043..74119731,2	K562	blood:
31	chr4:74051359..74054338-chr4:74122904..74126621,3	K562	blood:
32	chr4:74065951..74068812-chr4:74070946..74073291,3	K562	blood:
33	chr4:74069384..74072019-chr4:74086100..74088780,2	K562	blood:
34	chr4:74060240..74062620-chr4:74065043..74067696,2	K562	blood:
35	chr4:74030840..74033690-chr4:74081965..74083470,2	K562	blood:
36	chr4:74041420..74044364-chr4:74048787..74051206,3	K562	blood:
37	chr4:74066592..74068413-chr4:74122719..74124463,3	K562	blood:
38	chr4:74108645..74112551-chr4:74114263..74118175,3	MCF-7	breast:
39	chr4:74052236..74053936-chr4:74063244..74066174,3	K562	blood:
40	chr4:74028581..74032881-chr4:74033688..74038120,5	K562	blood:
41	chr4:74029082..74031220-chr4:74040346..74042692,2	MCF-7	breast:
42	chr4:74030522..74032070-chr4:74034879..74036523,2	MCF-7	breast:
43	chr4:74056365..74058810-chr4:74121522..74124421,2	K562	blood:
44	chr4:74054562..74057067-chr4:74057401..74060235,2	K562	blood:
45	chr4:74046445..74048807-chr4:74084717..74087260,2	K562	blood:
46	chr4:74028962..74031937-chr4:74045669..74047435,2	K562	blood:
47	chr4:74054729..74058685-chr4:74124246..74126441,3	MCF-7	breast:
48	chr4:73933887..73935834-chr4:74035566..74037820,2	MCF-7	breast:
49	chr4:74070251..74073029-chr4:74074120..74076871,2	MCF-7	breast:
50	chr4:74029391..74031667-chr4:74035341..74038120,3	K562	blood:

No data

Variant related genes	Relation type
ANKRD17	TF binding region
ANKRD17	CpG island
ENSG00000132466	chromatin interactions
ENSG00000163626	chromatin interactions
ENSG00000250220	chromatin interactions
ENSG00000169155	chromatin interactions
ENSG00000156140	chromatin interactions

Extended variants
information (count: 2786 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2786 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13113551	chr4:74031423-74031424	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201035589	chr4:74031439-74031440	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534573351	chr4:74031472-74031473	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs552873994	chr4:74031492-74031493	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs552406877	chr4:74031567-74031568	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs75798026	chr4:74031571-74031572	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563559633	chr4:74031670-74031671	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs539832885	chr4:74031707-74031708	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557965752	chr4:74031721-74031722	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576507528	chr4:74031777-74031778	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs117246399	chr4:74031778-74031779	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562226333	chr4:74031819-74031820	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs574305269	chr4:74031821-74031822	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541698721	chr4:74031840-74031841	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527996541	chr4:74031884-74031885	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs556339220	chr4:74031893-74031894	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs150102953	chr4:74031896-74031897	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552253217	chr4:74031899-74031900	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563216226	chr4:74031948-74031949	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs530553890	chr4:74031975-74031976	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548685523	chr4:74031983-74031984	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs567097599	chr4:74031989-74031990	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534515454	chr4:74031994-74031995	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546451482	chr4:74032013-74032014	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542148343	chr4:74032025-74032026	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564526147	chr4:74032046-74032047	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs116369395	chr4:74032085-74032086	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569221621	chr4:74032095-74032096	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538017206	chr4:74032153-74032154	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377277784	chr4:74032229-74032230	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180813075	chr4:74032317-74032318	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185845715	chr4:74032390-74032391	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558163779	chr4:74032407-74032408	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576372573	chr4:74032411-74032412	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191099280	chr4:74032455-74032456	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555900171	chr4:74032464-74032465	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs13115366	chr4:74032465-74032466	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557490181	chr4:74032476-74032477	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375054160	chr4:74032477-74032478	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs13115373	chr4:74032481-74032482	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112873599	chr4:74032491-74032492	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183257405	chr4:74032558-74032559	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs13121051	chr4:74032564-74032565	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13121064	chr4:74032585-74032586	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559793689	chr4:74032590-74032591	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554148519	chr4:74032591-74032592	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs578218390	chr4:74032603-74032604	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544662282	chr4:74032647-74032648	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs13116001	chr4:74032711-74032712	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs13121485	chr4:74032727-74032728	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2573 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:73940400-74043400	Strong transcription	Fetal Thymus	thymus
2	chr4:73970800-74040800	Weak transcription	Stomach Mucosa	stomach
3	chr4:73971800-74032200	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:74004800-74031600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:74005600-74034400	Weak transcription	Esophagus	oesophagus
6	chr4:74005800-74035000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:74006800-74031600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr4:74006800-74034400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:74006800-74043400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:74008000-74039000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr4:74008600-74034800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:74008800-74059600	Weak transcription	Fetal Brain Male	brain
13	chr4:74009800-74034400	Weak transcription	Gastric	stomach
14	chr4:74014600-74046400	Weak transcription	Hela-S3	cervix
15	chr4:74015600-74031600	Weak transcription	Fetal Kidney	kidney
16	chr4:74018400-74055200	Weak transcription	Psoas Muscle	Psoas
17	chr4:74018600-74031800	Weak transcription	Brain Anterior Caudate	brain
18	chr4:74018600-74034400	Weak transcription	Colonic Mucosa	Colon
19	chr4:74018600-74034400	Weak transcription	Pancreas	Pancrea
20	chr4:74018600-74034400	Weak transcription	Spleen	Spleen
21	chr4:74018600-74034400	Weak transcription	NHLF	lung
22	chr4:74018800-74034400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr4:74019200-74043400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr4:74021000-74031600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr4:74021000-74032000	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr4:74021200-74035000	Strong transcription	K562	blood
27	chr4:74022200-74034200	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr4:74022400-74034400	Weak transcription	Brain Substantia Nigra	brain
29	chr4:74022400-74035000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:74022600-74031600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr4:74024000-74031800	Strong transcription	Dnd41	blood
32	chr4:74024000-74032200	Strong transcription	Fetal Intestine Large	intestine
33	chr4:74024200-74032400	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr4:74024200-74043200	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr4:74024800-74034400	Weak transcription	Aorta	Aorta
36	chr4:74025400-74034200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr4:74025600-74031600	Strong transcription	Primary B cells from peripheral blood	blood
38	chr4:74025600-74040800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:74026000-74031800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr4:74026600-74031600	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr4:74027200-74031800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr4:74027200-74032200	Weak transcription	HUVEC	blood vessel
43	chr4:74027200-74035600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:74027400-74031800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr4:74027400-74031800	Weak transcription	A549	lung
46	chr4:74027400-74032000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr4:74027800-74033400	Strong transcription	NH-A	brain
48	chr4:74027800-74035400	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr4:74027800-74043600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:74028000-74031600	Strong transcription	HMEC	breast

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