Variant report

Variant	nsv882466
Chromosome Location	chr5:99936090-100029620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:183)
Chromatin interactive
region (count:37)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:99990630-99990941	K562	blood:	n/a	n/a
2	ARID3A	chr5:99977601-99977922	K562	blood:	n/a	n/a
3	ARID3A	chr5:99982017-99982085	K562	blood:	n/a	n/a
4	ARID3A	chr5:99983489-99983958	K562	blood:	n/a	n/a
5	ATF1	chr5:99990201-99990376	K562	blood:	n/a	n/a
6	BACH1	chr5:99963124-99963144	K562	blood:	n/a	n/a
7	BACH1	chr5:100000078-100000111	K562	blood:	n/a	n/a
8	BHLHE40	chr5:99970745-99970938	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:99990719-99990919	K562	blood:	n/a	n/a
10	BHLHE40	chr5:99980080-99980171	HepG2	liver:	n/a	n/a
11	BHLHE40	chr5:99978352-99978517	K562	blood:	n/a	n/a
12	BHLHE40	chr5:100029390-100029416	K562	blood:	n/a	n/a
13	BHLHE40	chr5:99983105-99983921	K562	blood:	n/a	n/a
14	BRCA1	chr5:100013835-100013910	GM12878	blood:	n/a	n/a
15	BRCA1	chr5:99983490-99983559	GM12878	blood:	n/a	n/a
16	BRCA1	chr5:99981848-99981913	GM12878	blood:	n/a	n/a
17	CBX3	chr5:99977588-99977872	K562	blood:	n/a	n/a
18	CCNT2	chr5:99990726-99991000	K562	blood:	n/a	chr5:99990744-99990764
19	CCNT2	chr5:100029224-100029637	K562	blood:	n/a	n/a
20	CCNT2	chr5:99977656-99977879	K562	blood:	n/a	n/a
21	CEBPB	chr5:99961086-99961376	A549	lung:	n/a	chr5:99961208-99961219
22	CEBPB	chr5:100027332-100027587	A549	lung:	n/a	chr5:100027474-100027487 chr5:100027476-100027487 chr5:100027476-100027487 chr5:100027474-100027487
23	CEBPB	chr5:99970744-99971140	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:100002888-100003324	K562	blood:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
25	CEBPB	chr5:100003105-100003224	H1-hESC	embryonic stem cell:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
26	CEBPB	chr5:100027264-100027695	MCF-7	breast:	n/a	chr5:100027474-100027487 chr5:100027476-100027487 chr5:100027476-100027487 chr5:100027474-100027487
27	CEBPB	chr5:99980653-99981420	HepG2	liver:	n/a	chr5:99981235-99981246
28	CEBPB	chr5:100002957-100003342	HepG2	liver:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
29	CEBPB	chr5:100002876-100003404	A549	lung:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
30	CEBPB	chr5:100019242-100019442	HepG2	liver:	n/a	chr5:100019320-100019331
31	CEBPB	chr5:99983195-99983759	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr5:100013050-100013447	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:100002822-100003462	Hela-S3	cervix:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
34	CEBPB	chr5:100027477-100027483	K562	blood:	n/a	n/a
35	CEBPB	chr5:100002966-100003372	MCF-7	breast:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
36	CEBPB	chr5:99954347-99954606	HepG2	liver:	n/a	chr5:99954478-99954489
37	CEBPB	chr5:100027316-100027616	IMR90	lung:	n/a	chr5:100027474-100027487 chr5:100027476-100027487 chr5:100027476-100027487 chr5:100027474-100027487
38	CEBPB	chr5:99959471-99959780	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:99983315-99983876	K562	blood:	n/a	n/a
40	CEBPB	chr5:99979154-99979484	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:100027207-100027763	MCF-7	breast:	n/a	chr5:100027474-100027487 chr5:100027476-100027487 chr5:100027476-100027487 chr5:100027474-100027487
42	CEBPB	chr5:99979829-99980250	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr5:99979129-99979560	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr5:100002888-100003406	HCT-116	colon:	n/a	chr5:100003132-100003145 chr5:100003133-100003144 chr5:100003132-100003143
45	CEBPB	chr5:99983312-99983748	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr5:99936825-99937072	HepG2	liver:	n/a	chr5:99936937-99936948
47	CEBPB	chr5:100027279-100027618	A549	lung:	n/a	chr5:100027474-100027487 chr5:100027476-100027487 chr5:100027476-100027487 chr5:100027474-100027487
48	CEBPB	chr5:99980650-99981422	A549	lung:	n/a	chr5:99981235-99981246
49	CEBPB	chr5:99961061-99961265	HepG2	liver:	n/a	chr5:99961208-99961219
50	CEBPB	chr5:100027104-100028125	Hela-S3	cervix:	n/a	chr5:100027474-100027487 chr5:100027476-100027487 chr5:100027476-100027487 chr5:100027474-100027487

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99979316-99979366	NH-A	brain:	n/a
2	chr5:99979316-99979366	HCM	heart:	n/a
3	chr5:99979316-99979366	AG04449	skin:	fetal
4	chr5:99979316-99979366	AG04450	lung:	fetal
5	chr5:99993323-99993373	ovcar-3	ovarian:	n/a
6	chr5:99979316-99979366	PrEC	prostate:	n/a
7	chr5:99979316-99979366	HL-60	blood:	n/a
8	chr5:99979316-99979366	NHDF-neo	bronchial:	n/a
9	chr5:100024634-100024684	SK-N-SH_RA	brain:	n/a
10	chr5:99993323-99993373	HCM	heart:	n/a
11	chr5:99979316-99979366	PANC-1	pancreas:	n/a
12	chr5:99979316-99979366	AG10803	skin:	n/a
13	chr5:99993323-99993373	SKMC	muscle:	n/a
14	chr5:99979316-99979366	MCF10A-Er-Src	breast:	n/a
15	chr5:99993323-99993373	T-47D	breast:	n/a
16	chr5:100024634-100024684	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:99979316-99979366	HIPEpiC	eye:	n/a
18	chr5:99979316-99979366	RPTEC	kidney:	n/a
19	chr5:99979316-99979366	CMK	blood:	n/a
20	chr5:99993323-99993373	HAEpiC	amniotic membrane:	n/a
21	chr5:100024634-100024684	AG04450	lung:	fetal
22	chr5:99979316-99979366	Jurkat	blood:	n/a
23	chr5:99979316-99979366	HNPCEpiC	eye:	n/a
24	chr5:100024634-100024684	HRPEpiC	eye:	n/a
25	chr5:99993323-99993373	SK-N-SH	brain:	n/a
26	chr5:99993323-99993373	AG04450	lung:	fetal
27	chr5:99979316-99979366	U87	brain:	n/a
28	chr5:99979316-99979366	Caco-2	colon:	n/a
29	chr5:99979316-99979366	HCPEpiC	choroid plexus:	n/a
30	chr5:100024634-100024684	GM12892	blood:	n/a
31	chr5:100024634-100024684	Jurkat	blood:	n/a
32	chr5:99979316-99979366	HRE	kidney:	n/a
33	chr5:99993323-99993373	GM12878	blood:	n/a
34	chr5:99993323-99993373	GM12892	blood:	n/a
35	chr5:100024634-100024684	PFSK-1	brain:	n/a
36	chr5:99993323-99993373	AoSMC	blood vessel:	n/a
37	chr5:99979316-99979366	HMEC	breast:	n/a
38	chr5:99979316-99979366	ECC-1	luminal epithelium:	n/a
39	chr5:100024634-100024684	CMK	blood:	n/a
40	chr5:100024634-100024684	PrEC	prostate:	n/a
41	chr5:99979316-99979366	GM06990	blood:	n/a
42	chr5:99993323-99993373	MCF10A-Er-Src	breast:	n/a
43	chr5:99993323-99993373	AG09319	gingival:	n/a
44	chr5:99993323-99993373	AG10803	skin:	n/a
45	chr5:99979316-99979366	LNCaP	prostate:	n/a
46	chr5:99979316-99979366	H1-hESC	embryonic stem cell:	embryo
47	chr5:99993323-99993373	GM06990	blood:	n/a
48	chr5:99979316-99979366	A549	lung:	n/a
49	chr5:100024634-100024684	K562	blood:	n/a
50	chr5:99993323-99993373	Hepatocyte	liver:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:99969436..99971759-chr5:99981835..99984130,2	MCF-7	breast:
2	chr5:99983206..99984911-chr8:101906981..101908614,2	MCF-7	breast:
3	chr5:99968617..99971336-chr5:99974828..99976431,2	K562	blood:
4	chr5:25503170..25504042-chr5:99982844..99983480,2	MCF-7	breast:
5	chr5:99978477..99981448-chr5:99989522..99992251,2	MCF-7	breast:
6	chr5:99983058..99983589-chr5:100699944..100700904,2	MCF-7	breast:
7	chr5:99969436..99971759-chr5:99981835..99984130,2	MCF-7	breast:
8	chr5:99994840..99996773-chr5:99998173..100000130,2	K562	blood:
9	chr5:99984054..99985811-chr5:99989132..99991041,2	K562	blood:
10	chr5:99993129..99995264-chr5:100001992..100004177,2	K562	blood:
11	chr5:99948806..99952463-chr5:99954515..99956491,4	K562	blood:
12	chr5:99983166..99984736-chr5:100011479..100013209,2	MCF-7	breast:
13	chr5:100010051..100013908-chr5:100016704..100018840,3	K562	blood:
14	chr5:99975585..99977874-chr5:99980709..99983188,3	K562	blood:
15	chr5:99979051..99981832-chr5:99981912..99985691,4	MCF-7	breast:
16	chr5:99959582..99960217-chr5:100683267..100683815,2	MCF-7	breast:
17	chr5:99978477..99981448-chr5:99989522..99992251,2	MCF-7	breast:
18	chr5:100010051..100013908-chr5:100016704..100018840,3	K562	blood:
19	chr5:99948806..99952463-chr5:99954515..99956491,4	K562	blood:
20	chr5:99983166..99984736-chr5:100011479..100013209,2	MCF-7	breast:
21	chr5:99989812..99991852-chr5:99993776..99996637,2	K562	blood:
22	chr5:99943979..99946598-chr5:99951467..99953484,2	K562	blood:
23	chr5:99983062..99983901-chr5:100090730..100091412,3	MCF-7	breast:
24	chr5:99989812..99991852-chr5:99993776..99996637,2	K562	blood:
25	chr5:99978017..99980273-chr5:99982713..99984242,2	MCF-7	breast:
26	chr5:99982908..99983980-chr5:100090394..100091716,11	MCF-7	breast:
27	chr5:99943979..99946598-chr5:99951467..99953484,2	K562	blood:
28	chr5:99979324..99981672-chr5:99983886..99985398,2	K562	blood:
29	chr5:99968617..99971336-chr5:99974828..99976431,2	K562	blood:
30	chr5:99982875..99983980-chr5:100090231..100091716,20	MCF-7	breast:
31	chr5:99979324..99981672-chr5:99983886..99985398,2	K562	blood:
32	chr5:99994840..99996773-chr5:99998173..100000130,2	K562	blood:
33	chr5:99978017..99980273-chr5:99982713..99984242,2	MCF-7	breast:
34	chr5:99979051..99981832-chr5:99981912..99985691,4	MCF-7	breast:
35	chr5:99975585..99977874-chr5:99980709..99983188,3	K562	blood:
36	chr5:99983045..99983930-chr5:100117214..100117742,2	MCF-7	breast:
37	chr5:99984054..99985811-chr5:99989132..99991041,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-2	chr5:99993523-99993674	XLOC_004939
2	lnc-ST8SIA4-2	chr5:99991144-99991179	XLOC_004939
3	lnc-ST8SIA4-2	chr5:99989816-99990096	XLOC_004939
4	lnc-ST8SIA4-2	chr5:99992117-99992230	XLOC_004939
5	lnc-ST8SIA4-2	chr5:99993523-99993674	XLOC_004939
6	lnc-ST8SIA4-2	chr5:99991144-99991208	XLOC_004939
7	lnc-ST8SIA4-2	chr5:99989792-99990096	XLOC_004939

No data

Variant related genes	Relation type
ENSG00000250806	TF binding region
ENSG00000250806	CpG island
ENSG00000250806	chromatin interactions
ENSG00000212994	chromatin interactions
RBFOX2	miRNA target sites

Extended variants
information (count: 1983 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1983 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2036562	chr5:99936090-99936091	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190927377	chr5:99936109-99936110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561167485	chr5:99936111-99936112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550553785	chr5:99936117-99936118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562469483	chr5:99936122-99936123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530010831	chr5:99936133-99936134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73774463	chr5:99936171-99936172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116695292	chr5:99936178-99936179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374059057	chr5:99936206-99936207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140073180	chr5:99936245-99936246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552111926	chr5:99936276-99936277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111879924	chr5:99936301-99936302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374594093	chr5:99936320-99936321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148901503	chr5:99936321-99936322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182591924	chr5:99936324-99936325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80145288	chr5:99936332-99936333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143749055	chr5:99936367-99936368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116591255	chr5:99936394-99936395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532539296	chr5:99936442-99936443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141546799	chr5:99936499-99936500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575283067	chr5:99936515-99936516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536608509	chr5:99936549-99936550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536536328	chr5:99936550-99936551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73152936	chr5:99936593-99936594	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573335434	chr5:99936684-99936685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532296059	chr5:99936687-99936688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540786157	chr5:99936691-99936692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188901977	chr5:99936830-99936831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547364854	chr5:99936831-99936832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73152939	chr5:99936840-99936841	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544369068	chr5:99936879-99936880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191943890	chr5:99936884-99936885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183370451	chr5:99936885-99936886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529747530	chr5:99936904-99936905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559355948	chr5:99936984-99936985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575885078	chr5:99938807-99938808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150523965	chr5:99938891-99938892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543358350	chr5:99938914-99938915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530062559	chr5:99938930-99938931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561910849	chr5:99939003-99939004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181605086	chr5:99939041-99939042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542284134	chr5:99939042-99939043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560352467	chr5:99939069-99939070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73774478	chr5:99939075-99939076	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541873194	chr5:99939080-99939081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185586751	chr5:99939110-99939111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532041863	chr5:99939119-99939120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368752891	chr5:99939123-99939124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372541780	chr5:99939160-99939161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563773658	chr5:99939191-99939192	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99932200-99936600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr5:99935600-99936400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:99935600-99936400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:99936000-99936200	Enhancers	Primary hematopoietic stem cells	blood
5	chr5:99936000-99936200	Enhancers	Psoas Muscle	Psoas
6	chr5:99936000-99937000	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr5:99936200-99936800	Weak transcription	Psoas Muscle	Psoas
8	chr5:99936600-99937000	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr5:99936800-99937000	Enhancers	Psoas Muscle	Psoas
10	chr5:99938800-99939600	Enhancers	Fetal Lung	lung
11	chr5:99939000-99941000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:99939400-99939600	Enhancers	NHDF-Ad	bronchial
13	chr5:99939600-99940600	Weak transcription	Fetal Lung	lung
14	chr5:99939600-99940600	Weak transcription	NHDF-Ad	bronchial
15	chr5:99940600-99941200	Enhancers	Fetal Lung	lung
16	chr5:99940800-99941000	Enhancers	NHDF-Ad	bronchial
17	chr5:99947600-99948800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:99951000-99951400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:99951000-99951800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:99951200-99951600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:99951200-99951600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:99951200-99951600	Enhancers	Fetal Kidney	kidney
23	chr5:99951200-99951600	Enhancers	Fetal Lung	lung
24	chr5:99955000-99955400	Enhancers	HUVEC	blood vessel
25	chr5:99955800-99956200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr5:99959400-99959600	Enhancers	GM12878-XiMat	blood
27	chr5:99959800-99960200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:99961400-99962200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:99961800-99962400	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr5:99971000-99971200	Enhancers	GM12878-XiMat	blood
31	chr5:99972800-99974200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:99973000-99973400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:99973000-99973400	Enhancers	Fetal Lung	lung
34	chr5:99973400-99978400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:99976800-99978600	Enhancers	K562	blood
36	chr5:99977600-99977800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:99977600-99978000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:99977600-99978000	Enhancers	Placenta	Placenta
39	chr5:99977600-99978200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr5:99977800-99978000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr5:99977800-99978400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:99977800-99979200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:99977800-99980000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr5:99978000-99979600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:99978000-99980200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:99978000-99983000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:99978000-99983200	Weak transcription	Placenta	Placenta
48	chr5:99978200-99979200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr5:99978200-99979400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr5:99978400-99980200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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