Variant report

Variant	esv3410570
Chromosome Location	chr4:74055180-74122498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:808)
CpG islands
(count:305)
Chromatin interactive
region (count:85)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:808 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:74096860-74097556	K562	blood:	n/a	n/a
2	ARID3A	chr4:74088179-74089111	K562	blood:	n/a	chr4:74088412-74088428
3	ARID3A	chr4:74111830-74112051	K562	blood:	n/a	n/a
4	ARID3A	chr4:74098327-74098361	K562	blood:	n/a	n/a
5	ARID3A	chr4:74116858-74116892	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:74088637-74088954	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:74055386-74055525	K562	blood:	n/a	n/a
8	ATF1	chr4:74088642-74089046	K562	blood:	n/a	n/a
9	ATF2	chr4:74088448-74089073	GM12878	blood:	n/a	n/a
10	ATF2	chr4:74088491-74089048	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	BHLHE40	chr4:74088555-74089111	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:74088581-74089061	K562	blood:	n/a	n/a
17	BHLHE40	chr4:74088715-74089013	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:74088635-74089113	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:74090500-74090501	GM12878	blood:	n/a	n/a
20	CBX3	chr4:74088524-74089058	K562	blood:	n/a	n/a
21	CBX3	chr4:74088641-74089117	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:74069559-74069966	K562	blood:	n/a	n/a
23	CBX3	chr4:74088575-74089030	K562	blood:	n/a	n/a
24	CBX3	chr4:74055032-74055417	K562	blood:	n/a	n/a
25	CBX3	chr4:74111569-74112016	K562	blood:	n/a	n/a
26	CBX3	chr4:74088578-74089172	HCT-116	colon:	n/a	n/a
27	CCNT2	chr4:74088629-74088829	K562	blood:	n/a	n/a
28	CCNT2	chr4:74097005-74097205	K562	blood:	n/a	n/a
29	CCNT2	chr4:74111518-74112034	K562	blood:	n/a	n/a
30	CCNT2	chr4:74058936-74059136	K562	blood:	n/a	n/a
31	CCNT2	chr4:74087518-74087724	K562	blood:	n/a	n/a
32	CCNT2	chr4:74059942-74060113	K562	blood:	n/a	n/a
33	CEBPB	chr4:74059435-74059738	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:74059440-74059695	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:74062964-74063250	MCF-7	breast:	n/a	n/a
36	CEBPB	chr4:74055921-74056073	K562	blood:	n/a	n/a
37	CEBPB	chr4:74096482-74096687	HepG2	liver:	n/a	chr4:74096601-74096612
38	CEBPB	chr4:74059430-74059779	A549	lung:	n/a	n/a
39	CEBPB	chr4:74092449-74092516	A549	lung:	n/a	chr4:74092486-74092497
40	CEBPB	chr4:74059435-74059838	MCF-7	breast:	n/a	n/a
41	CEBPB	chr4:74100579-74100647	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:74059502-74059686	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:74092408-74092511	HepG2	liver:	n/a	chr4:74092486-74092497
44	CEBPB	chr4:74088663-74088965	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:74059374-74059787	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:74059488-74059816	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr4:74062953-74063321	IMR90	lung:	n/a	n/a
48	CEBPB	chr4:74063003-74063307	K562	blood:	n/a	n/a
49	CEBPB	chr4:74059439-74059782	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:74059408-74059789	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74103157-74103207	AG10803	skin:	n/a
2	chr4:74121722-74121772	Hela-S3	cervix:	n/a
3	chr4:74103157-74103207	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:74088730-74088780	GM12892	blood:	n/a
5	chr4:74111455-74111505	HCPEpiC	choroid plexus:	n/a
6	chr4:74121722-74121772	HCF	heart:	n/a
7	chr4:74065349-74065399	Hela-S3	cervix:	n/a
8	chr4:74065349-74065399	GM12878	blood:	n/a
9	chr4:74103157-74103207	HCF	heart:	n/a
10	chr4:74088730-74088780	LNCaP	prostate:	n/a
11	chr4:74088730-74088780	HCPEpiC	choroid plexus:	n/a
12	chr4:74103157-74103207	AG09309	skin:	n/a
13	chr4:74111455-74111505	GM12891	blood:	n/a
14	chr4:74065349-74065399	SK-N-SH	brain:	n/a
15	chr4:74103157-74103207	LNCaP	prostate:	n/a
16	chr4:74065349-74065399	GM12892	blood:	n/a
17	chr4:74111455-74111505	HL-60	blood:	n/a
18	chr4:74111455-74111505	HIPEpiC	eye:	n/a
19	chr4:74121722-74121772	LNCaP	prostate:	n/a
20	chr4:74065349-74065399	HNPCEpiC	eye:	n/a
21	chr4:74103157-74103207	RPTEC	kidney:	n/a
22	chr4:74065349-74065399	ECC-1	luminal epithelium:	n/a
23	chr4:74065349-74065399	NT2-D1	testis:	n/a
24	chr4:74121722-74121772	GM12878	blood:	n/a
25	chr4:74103157-74103207	IMR90	lung:	fetal
26	chr4:74121722-74121772	HCM	heart:	n/a
27	chr4:74121722-74121772	HL-60	blood:	n/a
28	chr4:74111455-74111505	AG09309	skin:	n/a
29	chr4:74065349-74065399	IMR90	lung:	fetal
30	chr4:74111455-74111505	GM12878	blood:	n/a
31	chr4:74088730-74088780	K562	blood:	n/a
32	chr4:74111455-74111505	HRE	kidney:	n/a
33	chr4:74088730-74088780	AG09309	skin:	n/a
34	chr4:74121722-74121772	NH-A	brain:	n/a
35	chr4:74065349-74065399	RPTEC	kidney:	n/a
36	chr4:74065349-74065399	Jurkat	blood:	n/a
37	chr4:74121722-74121772	A549	lung:	n/a
38	chr4:74121722-74121772	NB4	blood:	n/a
39	chr4:74121722-74121772	GM12892	blood:	n/a
40	chr4:74088730-74088780	Jurkat	blood:	n/a
41	chr4:74121722-74121772	MCF-7	breast:	n/a
42	chr4:74088730-74088780	A549	lung:	n/a
43	chr4:74121722-74121772	ProgFib	skin:	n/a
44	chr4:74121722-74121772	GM06990	blood:	n/a
45	chr4:74111455-74111505	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:74065349-74065399	AG09309	skin:	n/a
47	chr4:74065349-74065399	HRCEpiC	kidney:	n/a
48	chr4:74111455-74111505	PrEC	prostate:	n/a
49	chr4:74103157-74103207	HEEpiC	esophagus:	n/a
50	chr4:74065349-74065399	AoSMC	blood vessel:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:74086780..74089405-chr4:74114803..74116855,3	K562	blood:
2	chr4:74067827..74069350-chr4:74117043..74119731,2	K562	blood:
3	chr4:74072374..74074564-chr4:74074721..74076887,2	K562	blood:
4	chr4:74086092..74089125-chr4:74123157..74126277,4	MCF-7	breast:
5	chr4:74094116..74095692-chr4:74117214..74119409,2	K562	blood:
6	chr4:73932268..73935243-chr4:74118599..74120212,2	K562	blood:
7	chr4:74103163..74106414-chr4:74122698..74126217,3	MCF-7	breast:
8	chr4:74086142..74089038-chr4:74090611..74092346,2	MCF-7	breast:
9	chr4:74030840..74033690-chr4:74081965..74083470,2	K562	blood:
10	chr4:74085682..74087798-chr4:74091964..74093705,2	K562	blood:
11	chr4:74110343..74113153-chr4:74121857..74126145,5	MCF-7	breast:
12	chr4:74088349..74088887-chr9:129566714..129567552,2	Hela-S3	cervix:
13	chr4:74085682..74087798-chr4:74091964..74093705,2	K562	blood:
14	chr4:74085378..74089938-chr4:74109585..74113346,7	K562	blood:
15	chr4:74082077..74085036-chr4:74123102..74125899,3	K562	blood:
16	chr4:74094714..74099476-chr4:74109744..74111749,4	K562	blood:
17	chr4:74065951..74068812-chr4:74070946..74073291,3	K562	blood:
18	chr4:74090826..74092875-chr4:74092966..74095699,2	MCF-7	breast:
19	chr4:74107320..74110128-chr4:74122442..74124984,2	MCF-7	breast:
20	chr4:74065003..74066606-chr4:74087400..74088901,2	K562	blood:
21	chr4:74099463..74102347-chr4:74103511..74105287,2	MCF-7	breast:
22	chr4:74050887..74052868-chr4:74066183..74068472,2	K562	blood:
23	chr4:73992240..73994706-chr4:74121884..74123760,2	MCF-7	breast:
24	chr4:74054562..74057067-chr4:74057401..74060235,2	K562	blood:
25	chr4:74099811..74102120-chr4:74103829..74105781,2	MCF-7	breast:
26	chr4:73918845..73921259-chr4:74116403..74118681,2	MCF-7	breast:
27	chr4:73932730..73938383-chr4:74120374..74126369,19	MCF-7	breast:
28	chr4:74046445..74048807-chr4:74084717..74087260,2	K562	blood:
29	chr4:74003190..74004710-chr4:74112693..74114696,2	MCF-7	breast:
30	chr4:74060240..74062620-chr4:74065043..74067696,2	K562	blood:
31	chr4:74054729..74058685-chr4:74124246..74126441,3	MCF-7	breast:
32	chr4:74065951..74068812-chr4:74070946..74073291,3	K562	blood:
33	chr4:74099654..74102966-chr4:74122579..74124991,5	MCF-7	breast:
34	chr4:74072374..74074564-chr4:74074721..74076887,2	K562	blood:
35	chr4:73998911..74001287-chr4:74095013..74097048,2	K562	blood:
36	chr4:74083386..74085370-chr4:74088578..74090685,2	MCF-7	breast:
37	chr4:74067827..74069350-chr4:74117043..74119731,2	K562	blood:
38	chr4:73433767..73436140-chr4:74111222..74113851,2	K562	blood:
39	chr4:74086715..74092062-chr4:74122892..74125871,6	MCF-7	breast:
40	chr4:74096213..74098237-chr4:74123373..74125010,2	K562	blood:
41	chr4:74023196..74024938-chr4:74114235..74116444,2	K562	blood:
42	chr4:73944396..73945924-chr4:74118345..74120655,2	K562	blood:
43	chr4:74108645..74112551-chr4:74114263..74118175,3	MCF-7	breast:
44	chr4:74030007..74032415-chr4:74070930..74073778,2	K562	blood:
45	chr4:74052236..74053936-chr4:74063244..74066174,3	K562	blood:
46	chr4:74070251..74073029-chr4:74074120..74076871,2	MCF-7	breast:
47	chr4:74099463..74102347-chr4:74103511..74105287,2	MCF-7	breast:
48	chr4:74094116..74095692-chr4:74117214..74119409,2	K562	blood:
49	chr4:73929823..73938112-chr4:74120693..74129342,27	K562	blood:
50	chr4:74092974..74095435-chr4:74123584..74125368,2	K562	blood:

No data

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

Extended variants
information (count: 2217 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2217 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539886507	chr4:74055241-74055242	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs540752252	chr4:74055256-74055257	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559088395	chr4:74055263-74055264	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs142088653	chr4:74055325-74055326	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558089558	chr4:74055333-74055334	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184702232	chr4:74055365-74055366	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563482770	chr4:74055487-74055488	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531720977	chr4:74055494-74055495	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs56261590	chr4:74055498-74055499	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574550471	chr4:74055550-74055551	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189491988	chr4:74055554-74055555	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs544135322	chr4:74055563-74055564	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs377731139	chr4:74055610-74055611	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs181494192	chr4:74055641-74055642	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548927049	chr4:74055689-74055690	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184422660	chr4:74055701-74055702	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs565895607	chr4:74055758-74055759	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534694033	chr4:74055780-74055781	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190066060	chr4:74055783-74055784	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs151171130	chr4:74055812-74055813	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551544696	chr4:74055813-74055814	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555038827	chr4:74055880-74055881	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs571262063	chr4:74055907-74055908	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537049377	chr4:74055920-74055921	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540710799	chr4:74055956-74055957	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535557778	chr4:74055986-74055987	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557595221	chr4:74055988-74055989	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577413782	chr4:74056010-74056011	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544913655	chr4:74056011-74056012	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370108631	chr4:74056020-74056021	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563506233	chr4:74056042-74056043	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553612803	chr4:74056043-74056044	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs530669414	chr4:74056172-74056173	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181141385	chr4:74056173-74056174	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574991065	chr4:74056264-74056265	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34241615	chr4:74056265-74056266	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140531351	chr4:74056271-74056272	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373606352	chr4:74056276-74056277	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186377023	chr4:74056286-74056287	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373122589	chr4:74056302-74056303	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536978784	chr4:74056312-74056313	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553273125	chr4:74056323-74056324	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184493841	chr4:74056345-74056346	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150041447	chr4:74056376-74056377	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577079127	chr4:74056383-74056384	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs566222420	chr4:74056472-74056473	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs533478346	chr4:74056487-74056488	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs551637915	chr4:74056534-74056535	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528603566	chr4:74056570-74056571	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573141455	chr4:74056622-74056623	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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

Chromatin state (count:2270 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74008800-74059600	Weak transcription	Fetal Brain Male	brain
2	chr4:74018400-74055200	Weak transcription	Psoas Muscle	Psoas
3	chr4:74031600-74066800	Weak transcription	HMEC	breast
4	chr4:74031600-74077200	Weak transcription	Small Intestine	intestine
5	chr4:74036600-74088200	Weak transcription	Colonic Mucosa	Colon
6	chr4:74036800-74055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:74036800-74055200	Weak transcription	Pancreas	Pancrea
8	chr4:74036800-74059400	Weak transcription	Spleen	Spleen
9	chr4:74036800-74062800	Weak transcription	Aorta	Aorta
10	chr4:74036800-74064800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:74037000-74055200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:74037000-74064800	Weak transcription	Brain Anterior Caudate	brain
13	chr4:74037000-74072200	Weak transcription	Gastric	stomach
14	chr4:74037200-74058800	Weak transcription	NHEK	skin
15	chr4:74037200-74064400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:74039400-74058000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr4:74039400-74062200	Weak transcription	HSMM	muscle
18	chr4:74039400-74064600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:74039400-74068800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:74039600-74055200	Weak transcription	Fetal Stomach	stomach
21	chr4:74039600-74062800	Weak transcription	Thymus	Thymus
22	chr4:74039600-74067600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr4:74039800-74055600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr4:74039800-74066000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr4:74039800-74074600	Weak transcription	Left Ventricle	heart
26	chr4:74040200-74064800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:74040200-74065800	Weak transcription	Fetal Muscle Leg	muscle
28	chr4:74040400-74056400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:74041200-74059800	Weak transcription	NHLF	lung
30	chr4:74041600-74055200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr4:74042200-74055200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr4:74042400-74064600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr4:74043000-74058400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:74043000-74063200	Weak transcription	Osteobl	bone
35	chr4:74043200-74055200	Weak transcription	K562	blood
36	chr4:74043200-74067800	Weak transcription	Fetal Intestine Large	intestine
37	chr4:74043200-74088200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr4:74043400-74056600	Weak transcription	Placenta	Placenta
39	chr4:74043400-74062800	Weak transcription	Fetal Thymus	thymus
40	chr4:74043400-74064400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr4:74043600-74059200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr4:74043800-74064400	Weak transcription	NHDF-Ad	bronchial
43	chr4:74044000-74072200	Weak transcription	Fetal Lung	lung
44	chr4:74044000-74078600	Weak transcription	Primary T cells from cord blood	blood
45	chr4:74044400-74059200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr4:74044400-74059200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:74044400-74065800	Weak transcription	Liver	Liver
48	chr4:74044400-74081400	Weak transcription	Dnd41	blood
49	chr4:74045000-74069000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr4:74046800-74087400	Weak transcription	Hela-S3	cervix

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