Variant report

Variant	nsv881704
Chromosome Location	chr5:58653383-58675538
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:58667411-58667779	GM12878	blood:	n/a	n/a
2	ATF2	chr5:58663693-58663944	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:58667352-58667796	GM12878	blood:	n/a	n/a
4	ATF3	chr5:58652777-58654067	A549	lung:	n/a	n/a
5	BATF	chr5:58667359-58667749	GM12878	blood:	n/a	chr5:58667586-58667597 chr5:58667587-58667597
6	BATF	chr5:58667396-58667737	GM12878	blood:	n/a	chr5:58667586-58667597 chr5:58667587-58667597
7	BCL3	chr5:58657154-58657767	A549	lung:	n/a	n/a
8	BCL3	chr5:58653155-58654805	A549	lung:	n/a	chr5:58654065-58654072
9	BCL3	chr5:58655859-58656666	A549	lung:	n/a	n/a
10	BCL3	chr5:58652380-58654882	A549	lung:	n/a	chr5:58654065-58654072
11	CBX3	chr5:58663710-58664021	HCT-116	colon:	n/a	n/a
12	CEBPB	chr5:58658453-58658601	A549	lung:	n/a	n/a
13	CEBPB	chr5:58655968-58656493	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
14	CEBPB	chr5:58653597-58653845	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:58659381-58659514	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:58663663-58664162	A549	lung:	n/a	n/a
17	CEBPB	chr5:58657316-58657613	MCF-7	breast:	n/a	n/a
18	CEBPB	chr5:58652378-58654781	A549	lung:	n/a	chr5:58654387-58654404 chr5:58653463-58653476
19	CEBPB	chr5:58655870-58656886	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
20	CEBPB	chr5:58655980-58656547	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
21	CEBPB	chr5:58653216-58653932	A549	lung:	n/a	chr5:58653463-58653476
22	CEBPB	chr5:58652711-58653861	A549	lung:	n/a	chr5:58653463-58653476
23	CEBPB	chr5:58658471-58658649	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:58654293-58654492	A549	lung:	n/a	chr5:58654387-58654404
25	CREB1	chr5:58653258-58653846	A549	lung:	n/a	n/a
26	CREB1	chr5:58653318-58653866	A549	lung:	n/a	n/a
27	CREB1	chr5:58667434-58667800	GM12878	blood:	n/a	n/a
28	CREB1	chr5:58654387-58654602	A549	lung:	n/a	n/a
29	CREB1	chr5:58667475-58667763	GM12878	blood:	n/a	n/a
30	CREB1	chr5:58663700-58663957	A549	lung:	n/a	n/a
31	CTCF	chr5:58663720-58663870	BJ	skin:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
32	CTCF	chr5:58663720-58663870	GM12875	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
33	CTCF	chr5:58663720-58663870	GM12873	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
34	CTCF	chr5:58663740-58663890	GM12868	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
35	CTCF	chr5:58663620-58663770	A549	lung:	n/a	n/a
36	CTCF	chr5:58663618-58663926	GM13977	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
37	CTCF	chr5:58663760-58663910	HFF-Myc	foreskin:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
38	CTCF	chr5:58663605-58664008	H1-hESC	embryonic stem cell:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
39	CTCF	chr5:58663705-58663911	MCF-7	breast:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
40	CTCF	chr5:58663720-58663880	GM12891	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
41	CTCF	chr5:58665920-58665924	GM10248	blood:	n/a	n/a
42	CTCF	chr5:58663400-58663550	GM12864	blood:	n/a	n/a
43	CTCF	chr5:58663697-58663925	Hela-S3	cervix:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
44	CTCF	chr5:58663760-58663910	HCFaa	heart:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
45	CTCF	chr5:58663720-58663870	HBMEC	blood vessel:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
46	CTCF	chr5:58663681-58663921	GM19238	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
47	CTCF	chr5:58663368-58664180	SK-N-SH	brain:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
48	CTCF	chr5:58663648-58663958	Gliobla	brain:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814
49	CTCF	chr5:58663320-58663470	SAEC	small airway:	n/a	n/a
50	CTCF	chr5:58663695-58663914	GM13976	blood:	n/a	chr5:58663798-58663816 chr5:58663799-58663815 chr5:58663793-58663814

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58653624-58653674	HAEpiC	amniotic membrane:	n/a
2	chr5:58653624-58653674	PANC-1	pancreas:	n/a
3	chr5:58653624-58653674	HUVEC	blood vessel:	n/a
4	chr5:58653624-58653674	IMR90	lung:	fetal
5	chr5:58653624-58653674	GM12891	blood:	n/a
6	chr5:58653624-58653674	U87	brain:	n/a
7	chr5:58653624-58653674	ovcar-3	ovarian:	n/a
8	chr5:58653624-58653674	AG04450	lung:	fetal
9	chr5:58653624-58653674	AG04449	skin:	fetal
10	chr5:58653624-58653674	CMK	blood:	n/a
11	chr5:58653624-58653674	MCF-7	breast:	n/a
12	chr5:58653624-58653674	SKMC	muscle:	n/a
13	chr5:58653624-58653674	Hela-S3	cervix:	n/a
14	chr5:58653624-58653674	HMEC	breast:	n/a
15	chr5:58653624-58653674	BJ	skin:	n/a
16	chr5:58653624-58653674	HIPEpiC	eye:	n/a
17	chr5:58653624-58653674	HCM	heart:	n/a
18	chr5:58653624-58653674	NHBE	bronchial:	n/a
19	chr5:58653624-58653674	GM12892	blood:	n/a
20	chr5:58653624-58653674	HRCEpiC	kidney:	n/a
21	chr5:58653624-58653674	AG09319	gingival:	n/a
22	chr5:58653624-58653674	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:58653624-58653674	Caco-2	colon:	n/a
24	chr5:58653624-58653674	RPTEC	kidney:	n/a
25	chr5:58653624-58653674	PrEC	prostate:	n/a
26	chr5:58653624-58653674	AG09309	skin:	n/a
27	chr5:58653624-58653674	MCF10A-Er-Src	breast:	n/a
28	chr5:58653624-58653674	HNPCEpiC	eye:	n/a
29	chr5:58653624-58653674	HL-60	blood:	n/a
30	chr5:58653624-58653674	H1-hESC	embryonic stem cell:	embryo
31	chr5:58653624-58653674	GM06990	blood:	n/a
32	chr5:58653624-58653674	AG10803	skin:	n/a
33	chr5:58653624-58653674	A549	lung:	n/a
34	chr5:58653624-58653674	PFSK-1	brain:	n/a
35	chr5:58653624-58653674	HRE	kidney:	n/a
36	chr5:58653624-58653674	GM12878	blood:	n/a
37	chr5:58653624-58653674	LNCaP	prostate:	n/a
38	chr5:58653624-58653674	HCPEpiC	choroid plexus:	n/a
39	chr5:58653624-58653674	NB4	blood:	n/a
40	chr5:58653624-58653674	GM19239	blood:	n/a
41	chr5:58653624-58653674	HEEpiC	esophagus:	n/a
42	chr5:58653624-58653674	Hepatocyte	liver:	n/a
43	chr5:58653624-58653674	Jurkat	blood:	n/a
44	chr5:58653624-58653674	HEK293	kidney:	embryo
45	chr5:58653624-58653674	SK-N-SH	brain:	n/a
46	chr5:58653624-58653674	AoSMC	blood vessel:	n/a
47	chr5:58653624-58653674	SK-N-MC	brain:	n/a
48	chr5:58653624-58653674	HCT-116	colon:	n/a
49	chr5:58653624-58653674	BE2_C	brain:	n/a
50	chr5:58653624-58653674	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:58517841..58518362-chr5:58663716..58664223,2	MCF-7	breast:
2	chr5:58483931..58484785-chr5:58663381..58664456,4	MCF-7	breast:
3	chr5:58513952..58514913-chr5:58663432..58664673,5	MCF-7	breast:
4	chr5:58657123..58657869-chr5:58676349..58676935,2	MCF-7	breast:
5	chr5:58651518..58653116-chr5:58654954..58657664,2	K562	blood:
6	chr5:58631024..58631593-chr5:58663326..58663872,2	MCF-7	breast:

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island
ENSG00000113448	chromatin interactions

Extended variants
information (count: 775 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11959801	chr5:58653383-58653384	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143092892	chr5:58653392-58653393	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116526629	chr5:58653408-58653409	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs190789746	chr5:58653423-58653424	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553050851	chr5:58653492-58653493	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572968334	chr5:58653583-58653584	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs144330587	chr5:58653592-58653593	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs555517849	chr5:58653624-58653625	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs148780853	chr5:58653625-58653626	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs575320401	chr5:58653649-58653650	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs544409534	chr5:58653664-58653665	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs115754550	chr5:58653676-58653677	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs531495522	chr5:58653700-58653701	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs568572835	chr5:58653707-58653708	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs116071027	chr5:58653719-58653720	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs560154533	chr5:58653745-58653746	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs183341413	chr5:58653785-58653786	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs549237050	chr5:58653794-58653795	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs185716595	chr5:58653795-58653796	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531773400	chr5:58653798-58653799	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs191895151	chr5:58653883-58653884	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs6877927	chr5:58653917-58653918	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs554187713	chr5:58653975-58653976	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs114773135	chr5:58654077-58654078	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs375720190	chr5:58654106-58654107	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs376658948	chr5:58654124-58654125	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs566504111	chr5:58654129-58654130	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs35280	chr5:58654168-58654169	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188390716	chr5:58654181-58654182	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555137630	chr5:58654206-58654207	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs142338896	chr5:58654239-58654240	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs150851368	chr5:58654251-58654252	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs16889696	chr5:58654399-58654400	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534438105	chr5:58654401-58654402	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs139229993	chr5:58654418-58654419	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs540169751	chr5:58654427-58654428	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs192227493	chr5:58654456-58654457	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs80262158	chr5:58654461-58654462	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs145360442	chr5:58654480-58654481	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182159512	chr5:58654495-58654496	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs562795821	chr5:58654514-58654515	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs61048373	chr5:58654528-58654529	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs6897015	chr5:58654531-58654532	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565515873	chr5:58654591-58654592	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs146743022	chr5:58654626-58654627	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527969356	chr5:58654663-58654664	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs9292205	chr5:58654684-58654685	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs567977712	chr5:58654703-58654704	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs528839708	chr5:58654712-58654713	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548963380	chr5:58654725-58654726	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Acute myeloid leukemia	21251322	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
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58646200-58654400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:58648000-58654200	Weak transcription	Ovary	ovary
3	chr5:58648600-58653400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:58648600-58653800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:58649400-58653600	Weak transcription	Brain Anterior Caudate	brain
6	chr5:58649400-58653600	Weak transcription	Brain Substantia Nigra	brain
7	chr5:58649400-58654000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr5:58649400-58654200	Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr5:58649600-58653600	Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr5:58652000-58653400	Flanking Active TSS	A549	lung
11	chr5:58652000-58654400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:58652200-58653400	Enhancers	Primary hematopoietic stem cells	blood
13	chr5:58652200-58653600	Enhancers	Rectal Smooth Muscle	rectum
14	chr5:58652200-58654400	Enhancers	Fetal Lung	lung
15	chr5:58652200-58654800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:58652200-58654800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:58652200-58655000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:58652200-58655000	Enhancers	Fetal Intestine Small	intestine
19	chr5:58652200-58656200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr5:58652200-58656600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:58652400-58653400	Enhancers	Colon Smooth Muscle	Colon
22	chr5:58652400-58653800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr5:58652400-58653800	Enhancers	Primary T cells from cord blood	blood
24	chr5:58652400-58654400	Enhancers	Fetal Intestine Large	intestine
25	chr5:58652400-58654800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:58652400-58655000	Enhancers	Stomach Mucosa	stomach
27	chr5:58652400-58655200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:58652400-58655200	Enhancers	Fetal Kidney	kidney
29	chr5:58652400-58655800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:58652400-58656400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr5:58652600-58653800	Enhancers	Placenta	Placenta
32	chr5:58652600-58654200	Enhancers	Brain Angular Gyrus	brain
33	chr5:58652600-58654600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:58652600-58654600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:58652600-58654600	Enhancers	Fetal Muscle Leg	muscle
36	chr5:58652600-58654600	Enhancers	Fetal Stomach	stomach
37	chr5:58652600-58654600	Enhancers	Fetal Thymus	thymus
38	chr5:58652600-58654600	Enhancers	Pancreas	Pancrea
39	chr5:58652600-58654800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr5:58652600-58654800	Enhancers	Gastric	stomach
41	chr5:58652600-58654800	Enhancers	Placenta Amnion	Placenta Amnion
42	chr5:58652600-58655000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:58652600-58655000	Enhancers	Brain Hippocampus Middle	brain
44	chr5:58652600-58655000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr5:58652600-58655200	Enhancers	Fetal Brain Male	brain
46	chr5:58652600-58655800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:58652800-58653400	Enhancers	Psoas Muscle	Psoas
48	chr5:58652800-58653400	Active TSS	Stomach Smooth Muscle	stomach
49	chr5:58652800-58653800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr5:58652800-58654600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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