Variant report

Variant	nsv598653
Chromosome Location	chr5:73992881-74095542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1442)
CpG islands
(count:1343)
Chromatin interactive
region (count:70)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1442 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74060976-74061176	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74062264-74062558	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:74068351-74068551	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74062781-74063161	HepG2	liver:	n/a	n/a
5	ATF1	chr5:74062825-74063165	K562	blood:	n/a	n/a
6	ATF2	chr5:74062812-74063262	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:74062771-74063234	GM12878	blood:	n/a	n/a
8	ATF2	chr5:74062753-74063236	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:74062674-74063296	GM12878	blood:	n/a	n/a
10	ATF3	chr5:74058322-74058905	HCT-116	colon:	n/a	n/a
11	ATF3	chr5:74062702-74063269	A549	lung:	n/a	n/a
12	ATF3	chr5:74058322-74058912	HCT-116	colon:	n/a	n/a
13	ATF3	chr5:74062606-74063251	A549	lung:	n/a	n/a
14	BACH1	chr5:74062862-74063483	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr5:74062816-74063104	GM12878	blood:	n/a	n/a
16	BCL3	chr5:74062551-74063442	A549	lung:	n/a	chr5:74062947-74062956 chr5:74063287-74063296
17	BCL3	chr5:74062369-74063397	A549	lung:	n/a	chr5:74062947-74062956 chr5:74063287-74063296
18	BCLAF1	chr5:74062635-74063521	GM12878	blood:	n/a	chr5:74062947-74062956 chr5:74063287-74063296
19	BCLAF1	chr5:74062658-74063277	GM12878	blood:	n/a	chr5:74062947-74062956
20	BCLAF1	chr5:74062732-74063294	K562	blood:	n/a	chr5:74062947-74062956
21	BCLAF1	chr5:74062776-74063288	K562	blood:	n/a	chr5:74062947-74062956
22	BHLHE40	chr5:74095221-74095392	HepG2	liver:	n/a	n/a
23	BHLHE40	chr5:74014067-74014096	A549	lung:	n/a	n/a
24	BHLHE40	chr5:74062707-74063677	K562	blood:	n/a	n/a
25	BHLHE40	chr5:74062807-74063452	GM12878	blood:	n/a	n/a
26	BHLHE40	chr5:74062487-74062687	A549	lung:	n/a	n/a
27	BRCA1	chr5:74062800-74063419	GM12878	blood:	n/a	n/a
28	BRCA1	chr5:74062845-74063164	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr5:74062838-74063395	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr5:74002349-74002641	K562	blood:	n/a	n/a
31	CBX3	chr5:74062626-74063428	HCT-116	colon:	n/a	n/a
32	CBX3	chr5:74062817-74063177	K562	blood:	n/a	n/a
33	CBX3	chr5:74062758-74063258	K562	blood:	n/a	n/a
34	CCNT2	chr5:74062657-74063298	K562	blood:	n/a	chr5:74063261-74063270
35	CCNT2	chr5:74018893-74019050	K562	blood:	n/a	n/a
36	CEBPB	chr5:74038660-74039015	IMR90	lung:	n/a	chr5:74038835-74038846
37	CEBPB	chr5:74067851-74068564	HepG2	liver:	n/a	chr5:74068338-74068349
38	CEBPB	chr5:74038706-74039011	Hela-S3	cervix:	n/a	chr5:74038835-74038846
39	CEBPB	chr5:74038655-74039034	HepG2	liver:	n/a	chr5:74038835-74038846
40	CEBPB	chr5:74058411-74058822	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:74038684-74039019	K562	blood:	n/a	chr5:74038835-74038846
42	CEBPB	chr5:74053821-74053976	Hela-S3	cervix:	n/a	chr5:74053833-74053844
43	CEBPB	chr5:74088645-74088722	A549	lung:	n/a	n/a
44	CEBPB	chr5:74068201-74068532	A549	lung:	n/a	chr5:74068338-74068349
45	CEBPB	chr5:74062721-74063316	GM12878	blood:	n/a	n/a
46	CEBPB	chr5:74039773-74040021	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:74062759-74063259	A549	lung:	n/a	n/a
48	CEBPB	chr5:74058275-74058833	HCT-116	colon:	n/a	n/a
49	CEBPB	chr5:74039760-74040043	A549	lung:	n/a	n/a
50	CEBPB	chr5:74034459-74034751	HepG2	liver:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74062831-74062881	LNCaP	prostate:	n/a
2	chr5:74062831-74062881	LNCaP	prostate:	n/a
3	chr5:74062824-74062874	ProgFib	skin:	n/a
4	chr5:74076752-74076802	H1-hESC	embryonic stem cell:	embryo
5	chr5:74060291-74060341	HCF	heart:	n/a
6	chr5:74066522-74066572	HepG2	liver:	n/a
7	chr5:74063144-74063194	Jurkat	blood:	n/a
8	chr5:74063324-74063374	ECC-1	luminal epithelium:	n/a
9	chr5:74076752-74076802	AoSMC	blood vessel:	n/a
10	chr5:74062824-74062874	H1-hESC	embryonic stem cell:	embryo
11	chr5:74062053-74062103	MCF10A-Er-Src	breast:	n/a
12	chr5:74063363-74063413	MCF-7	breast:	n/a
13	chr5:74060291-74060341	PFSK-1	brain:	n/a
14	chr5:74063010-74063060	K562	blood:	n/a
15	chr5:74063095-74063145	AoSMC	blood vessel:	n/a
16	chr5:74063626-74063676	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:74062824-74062874	HNPCEpiC	eye:	n/a
18	chr5:74002437-74002487	GM12891	blood:	n/a
19	chr5:74063125-74063175	ProgFib	skin:	n/a
20	chr5:74063138-74063188	AG04450	lung:	fetal
21	chr5:74063324-74063374	Jurkat	blood:	n/a
22	chr5:74063095-74063145	PFSK-1	brain:	n/a
23	chr5:74062831-74062881	H1-hESC	embryonic stem cell:	embryo
24	chr5:74002437-74002487	SK-N-MC	brain:	n/a
25	chr5:74062956-74063006	Jurkat	blood:	n/a
26	chr5:74063363-74063413	HIPEpiC	eye:	n/a
27	chr5:74061999-74062049	HCF	heart:	n/a
28	chr5:74061999-74062049	MCF-7	breast:	n/a
29	chr5:74062053-74062103	PANC-1	pancreas:	n/a
30	chr5:74061999-74062049	A549	lung:	n/a
31	chr5:74066522-74066572	Jurkat	blood:	n/a
32	chr5:74063010-74063060	ProgFib	skin:	n/a
33	chr5:74062053-74062103	RPTEC	kidney:	n/a
34	chr5:74002417-74002467	A549	lung:	n/a
35	chr5:74062053-74062103	HRE	kidney:	n/a
36	chr5:74063144-74063194	HCPEpiC	choroid plexus:	n/a
37	chr5:74062846-74062896	BJ	skin:	n/a
38	chr5:74066522-74066572	HRE	kidney:	n/a
39	chr5:74063138-74063188	HEK293	kidney:	embryo
40	chr5:74002417-74002467	PFSK-1	brain:	n/a
41	chr5:74063690-74063740	GM12891	blood:	n/a
42	chr5:74062956-74063006	HCPEpiC	choroid plexus:	n/a
43	chr5:74062846-74062896	NHBE	bronchial:	n/a
44	chr5:74002417-74002467	PANC-1	pancreas:	n/a
45	chr5:74063363-74063413	HAEpiC	amniotic membrane:	n/a
46	chr5:74062831-74062881	GM12892	blood:	n/a
47	chr5:74060291-74060341	K562	blood:	n/a
48	chr5:74062956-74063006	GM06990	blood:	n/a
49	chr5:74061999-74062049	SKMC	muscle:	n/a
50	chr5:74063125-74063175	RPTEC	kidney:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:74035458..74037434-chr5:74062225..74064378,2	K562	blood:
2	chr5:73981038..73983852-chr5:73999852..74002635,2	MCF-7	breast:
3	chr5:74040354..74042046-chr5:74045118..74047151,2	MCF-7	breast:
4	chr5:74079316..74081474-chr5:74083129..74085276,2	K562	blood:
5	chr5:74079316..74081474-chr5:74083129..74085276,2	K562	blood:
6	chr5:74015011..74017827-chr5:74019863..74023018,4	K562	blood:
7	chr5:72801428..72802038-chr5:74073569..74074403,2	MCF-7	breast:
8	chr5:74017557..74019398-chr5:74064773..74067311,2	K562	blood:
9	chr5:74011710..74014183-chr5:74028234..74030055,2	K562	blood:
10	chr5:73981324..73983563-chr5:74077397..74079724,2	K562	blood:
11	chr5:74030380..74033334-chr5:74036247..74039853,3	K562	blood:
12	chr5:73995760..73997460-chr5:73998842..74001561,2	K562	blood:
13	chr5:74062787..74065047-chr5:74073990..74076959,3	MCF-7	breast:
14	chr5:73986659..73988888-chr5:73994649..73997081,2	MCF-7	breast:
15	chr5:74072325..74074602-chr5:74076186..74079025,2	K562	blood:
16	chr5:74055753..74057505-chr5:74061220..74062838,2	K562	blood:
17	chr5:74072325..74074602-chr5:74076186..74079025,2	K562	blood:
18	chr5:74062619..74065180-chr5:74065672..74068766,3	K562	blood:
19	chr5:74070152..74072138-chr5:74074887..74076433,2	K562	blood:
20	chr5:74018853..74021864-chr5:74023433..74025995,4	K562	blood:
21	chr5:74073102..74074762-chr5:74077525..74079360,2	K562	blood:
22	chr5:74073102..74074762-chr5:74077525..74079360,2	K562	blood:
23	chr16:33965082..33965611-chr5:74062938..74063440,2	K562	blood:
24	chr5:74022416..74025189-chr5:74034895..74036734,2	K562	blood:
25	chr5:73980026..73982895-chr5:74017239..74018833,2	K562	blood:
26	chr5:74061790..74063907-chr5:74068318..74070016,2	MCF-7	breast:
27	chr5:74023027..74024562-chr5:74031417..74033252,2	MCF-7	breast:
28	chr5:74054567..74056927-chr5:74071615..74073229,2	MCF-7	breast:
29	chr5:74068532..74070395-chr5:74082418..74084693,2	K562	blood:
30	chr5:74040810..74043802-chr5:74045296..74047358,2	K562	blood:
31	chr5:74050706..74053641-chr5:74055711..74057646,2	K562	blood:
32	chr5:74040810..74043802-chr5:74045296..74047358,2	K562	blood:
33	chr5:74045315..74047772-chr5:74062616..74065560,2	MCF-7	breast:
34	chr5:73980885..73983030-chr5:74062980..74064496,2	MCF-7	breast:
35	chr5:74011922..74013768-chr5:74017287..74019015,2	K562	blood:
36	chr5:74050706..74053641-chr5:74055711..74057646,2	K562	blood:
37	chr5:74040810..74043898-chr5:74045296..74047358,3	K562	blood:
38	chr5:74070106..74071963-chr5:74087987..74090742,2	K562	blood:
39	chr5:74022416..74025189-chr5:74034895..74036734,2	K562	blood:
40	chr5:73980953..73983731-chr5:74012002..74014571,3	MCF-7	breast:
41	chr5:74068761..74070273-chr5:74071485..74073703,2	K562	blood:
42	chr5:74015011..74017827-chr5:74019863..74023018,4	K562	blood:
43	chr5:73978938..73982006-chr5:74061565..74064417,3	K562	blood:
44	chr5:74082489..74083391-chr5:74199247..74199809,4	MCF-7	breast:
45	chr5:74070106..74071963-chr5:74087987..74090742,2	K562	blood:
46	chr5:73980260..73982470-chr5:74054627..74056426,2	MCF-7	breast:
47	chr5:73995760..73997460-chr5:73998842..74001561,2	K562	blood:
48	chr5:74011710..74014183-chr5:74028234..74030055,2	K562	blood:
49	chr5:74011922..74013768-chr5:74017287..74019347,3	K562	blood:
50	chr5:73979747..73982608-chr5:73994043..73996170,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM169A-3	chr5:74056718-74056928	expReg_chr5_3584_-

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GFM2	hsa-miR-375	chr5:74017417-74017438

Variant related genes	Relation type
ENSG00000250071	TF binding region
RNU6-1330P	TF binding region
RNU6-658P	TF binding region
NSA2	TF binding region
GFM2	TF binding region
HEXB	TF binding region
ENSG00000250071	CpG island
RNU6-1330P	CpG island
RNU6-658P	CpG island
NSA2	CpG island
GFM2	CpG island
HEXB	CpG island
ENSG00000200434	chromatin interactions
ENSG00000049860	chromatin interactions
ENSG00000164346	chromatin interactions
ENSG00000207336	chromatin interactions
ENSG00000199645	chromatin interactions
ENSG00000164347	chromatin interactions

Extended variants
information (count: 3849 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3849 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10805890	chr5:73992881-73992882	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141175812	chr5:73992919-73992920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367963796	chr5:73992930-73992931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371656792	chr5:73992943-73992944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537451266	chr5:73992998-73992999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555415247	chr5:73993009-73993010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371546460	chr5:73993084-73993085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567245998	chr5:73993152-73993153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114583040	chr5:73993212-73993213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187670002	chr5:73993218-73993219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549207452	chr5:73993219-73993220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191288272	chr5:73993260-73993261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11959392	chr5:73993279-73993280	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529099962	chr5:73993305-73993306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111456757	chr5:73993308-73993309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183042052	chr5:73993322-73993323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188471494	chr5:73993330-73993331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539365241	chr5:73993411-73993412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192139365	chr5:73993412-73993413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62368222	chr5:73993419-73993420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11749435	chr5:73993420-73993421	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557588915	chr5:73993422-73993423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559557520	chr5:73993423-73993424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533329098	chr5:73993483-73993484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528354785	chr5:73993502-73993503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563794026	chr5:73993507-73993508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149681251	chr5:73993544-73993545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34363294	chr5:73993553-73993554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397998153	chr5:73993571-73993572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184686156	chr5:73993651-73993652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549364402	chr5:73993668-73993669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115812712	chr5:73993693-73993694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534934773	chr5:73993764-73993765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116257380	chr5:73993778-73993779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111992538	chr5:73993800-73993801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538823627	chr5:73993846-73993847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2442041	chr5:73993871-73993872	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112416350	chr5:73993880-73993881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535938405	chr5:73993932-73993933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148900920	chr5:73993933-73993934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537404669	chr5:73993949-73993950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187825697	chr5:73993971-73993972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192598365	chr5:73994043-73994044	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183675493	chr5:73994059-73994060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143556449	chr5:73994064-73994065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545207575	chr5:73994090-73994091	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577732102	chr5:73994095-73994096	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189219520	chr5:73994129-73994130	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181110788	chr5:73994188-73994189	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74206453	chr5:73994204-73994205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Sandhoff disease	22848519	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3121 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:73982000-73994400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:73982000-74002200	Weak transcription	Fetal Brain Female	brain
3	chr5:73982000-74017400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:73982000-74061800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:73982200-74020600	Weak transcription	Fetal Brain Male	brain
6	chr5:73982400-73993000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr5:73982400-73994600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:73982400-73998200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr5:73982400-73999400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:73982400-74002200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:73982600-73999400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr5:73983000-74001000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr5:73983000-74001600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:73983000-74017400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr5:73983000-74027000	Weak transcription	Fetal Heart	heart
16	chr5:73983200-73993000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr5:73983200-73993000	Weak transcription	GM12878-XiMat	blood
18	chr5:73983200-73994800	Weak transcription	Gastric	stomach
19	chr5:73983200-74002200	Weak transcription	Esophagus	oesophagus
20	chr5:73983200-74030200	Weak transcription	Small Intestine	intestine
21	chr5:73983400-73999000	Weak transcription	Colonic Mucosa	Colon
22	chr5:73983400-73999200	Weak transcription	Psoas Muscle	Psoas
23	chr5:73983400-74016000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr5:73984400-74002200	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr5:73984600-74000400	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr5:73984600-74001000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:73984600-74001600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr5:73984600-74002600	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr5:73984800-73995200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr5:73984800-73995200	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr5:73985000-73994000	Strong transcription	Placenta	Placenta
32	chr5:73985000-74002600	Strong transcription	Duodenum Mucosa	Duodenum
33	chr5:73985200-73995400	Strong transcription	Liver	Liver
34	chr5:73985200-74002600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr5:73987200-74017400	Weak transcription	Fetal Kidney	kidney
36	chr5:73987400-73998200	Weak transcription	HSMM	muscle
37	chr5:73987600-74014800	Weak transcription	Fetal Lung	lung
38	chr5:73987800-73998200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr5:73987800-73999400	Weak transcription	Hela-S3	cervix
40	chr5:73988000-73997000	Strong transcription	Left Ventricle	heart
41	chr5:73988200-73995800	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr5:73988400-74021000	Weak transcription	Right Ventricle	heart
43	chr5:73988800-73997000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr5:73989200-73998600	Weak transcription	Fetal Muscle Leg	muscle
45	chr5:73989400-73998200	Weak transcription	K562	blood
46	chr5:73989600-74001000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:73989800-74000600	Weak transcription	HUVEC	blood vessel
48	chr5:73989800-74002200	Weak transcription	Brain Angular Gyrus	brain
49	chr5:73989800-74002600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:73990000-73993000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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