Variant report

Variant	nsv462029
Chromosome Location	chr5:28763652-28870503
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	ARID3A	chr5:28810841-28811178	K562	blood:	n/a	n/a
2	ARID3A	chr5:28862973-28863184	HepG2	liver:	n/a	n/a
3	BHLHE40	chr5:28814502-28814623	K562	blood:	n/a	n/a
4	BHLHE40	chr5:28808920-28809724	K562	blood:	n/a	n/a
5	BHLHE40	chr5:28816335-28816476	K562	blood:	n/a	n/a
6	BHLHE40	chr5:28810355-28810693	K562	blood:	n/a	chr5:28810481-28810497 chr5:28810394-28810410
7	BRCA1	chr5:28766717-28767229	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr5:28815213-28815234	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr5:28823373-28823651	K562	blood:	n/a	n/a
10	CBX3	chr5:28809015-28809399	K562	blood:	n/a	n/a
11	CBX3	chr5:28823321-28823730	K562	blood:	n/a	n/a
12	CCNT2	chr5:28816425-28816641	K562	blood:	n/a	n/a
13	CCNT2	chr5:28810313-28810825	K562	blood:	n/a	chr5:28810357-28810366
14	CCNT2	chr5:28809192-28810112	K562	blood:	n/a	n/a
15	CEBPB	chr5:28828802-28828896	A549	lung:	n/a	n/a
16	CEBPB	chr5:28818648-28818936	K562	blood:	n/a	chr5:28818791-28818802
17	CEBPB	chr5:28834436-28834676	HepG2	liver:	n/a	chr5:28834587-28834598
18	CEBPB	chr5:28763690-28763856	A549	lung:	n/a	chr5:28763789-28763800
19	CEBPB	chr5:28763632-28764408	HepG2	liver:	n/a	chr5:28764292-28764305 chr5:28763789-28763800
20	CEBPB	chr5:28831177-28831503	A549	lung:	n/a	chr5:28831343-28831354
21	CEBPB	chr5:28834515-28834730	K562	blood:	n/a	chr5:28834587-28834598
22	CEBPB	chr5:28831182-28831450	H1-hESC	embryonic stem cell:	n/a	chr5:28831343-28831354
23	CEBPB	chr5:28850602-28850862	K562	blood:	n/a	n/a
24	CEBPB	chr5:28763702-28764332	Hela-S3	cervix:	n/a	chr5:28764292-28764305 chr5:28763789-28763800
25	CEBPB	chr5:28763672-28763927	IMR90	lung:	n/a	chr5:28763789-28763800
26	CEBPB	chr5:28809192-28809322	K562	blood:	n/a	n/a
27	CEBPB	chr5:28862960-28863277	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:28818678-28818966	HepG2	liver:	n/a	chr5:28818791-28818802
29	CEBPB	chr5:28763630-28763938	K562	blood:	n/a	chr5:28763789-28763800
30	CEBPB	chr5:28831210-28831505	K562	blood:	n/a	chr5:28831343-28831354
31	CEBPB	chr5:28831202-28831533	HepG2	liver:	n/a	chr5:28831343-28831354
32	CHD2	chr5:28810281-28810330	K562	blood:	n/a	n/a
33	CHD2	chr5:28810617-28810817	K562	blood:	n/a	n/a
34	CHD2	chr5:28809029-28809592	K562	blood:	n/a	n/a
35	CTCF	chr5:28766740-28766890	SK-N-SH_RA	brain:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
36	CTCF	chr5:28809845-28809945	K562	blood:	n/a	n/a
37	CTCF	chr5:28766800-28766950	GM06990	blood:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
38	CTCF	chr5:28779300-28779450	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr5:28766689-28767012	IMR90	lung:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
40	CTCF	chr5:28779428-28779524	GM12878	blood:	n/a	n/a
41	CTCF	chr5:28779412-28779530	HepG2	liver:	n/a	n/a
42	CTCF	chr5:28766760-28766910	HVMF	connective:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
43	CTCF	chr5:28766753-28766938	HUVEC	blood vessel:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
44	CTCF	chr5:28766687-28766993	MCF-7	breast:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
45	CTCF	chr5:28766780-28766930	HMEC	breast:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
46	CTCF	chr5:28766700-28766850	HCM	heart:	n/a	n/a
47	CTCF	chr5:28810380-28810530	K562	blood:	n/a	n/a
48	CTCF	chr5:28779317-28779599	T-47D	breast:	n/a	n/a
49	CTCF	chr5:28766740-28766890	HEK293	kidney:	n/a	chr5:28766847-28766863 chr5:28766846-28766864 chr5:28766841-28766862 chr5:28766849-28766859 chr5:28766848-28766861
50	CTCF	chr5:28779380-28779530	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:28810148-28810198	GM12892	blood:	n/a
2	chr5:28809997-28810047	AG09309	skin:	n/a
3	chr5:28810148-28810198	GM06990	blood:	n/a
4	chr5:28799238-28799288	H1-hESC	embryonic stem cell:	embryo
5	chr5:28810148-28810198	CMK	blood:	n/a
6	chr5:28810645-28810695	PANC-1	pancreas:	n/a
7	chr5:28810645-28810695	GM12891	blood:	n/a
8	chr5:28809997-28810047	NB4	blood:	n/a
9	chr5:28809121-28809171	HepG2	liver:	n/a
10	chr5:28810402-28810452	GM12892	blood:	n/a
11	chr5:28810645-28810695	ECC-1	luminal epithelium:	n/a
12	chr5:28810402-28810452	GM12878	blood:	n/a
13	chr5:28810402-28810452	SKMC	muscle:	n/a
14	chr5:28809121-28809171	SK-N-SH_RA	brain:	n/a
15	chr5:28809037-28809087	HEK293	kidney:	embryo
16	chr5:28810402-28810452	SK-N-SH_RA	brain:	n/a
17	chr5:28809622-28809672	SKMC	muscle:	n/a
18	chr5:28810402-28810452	SK-N-MC	brain:	n/a
19	chr5:28809997-28810047	SK-N-SH	brain:	n/a
20	chr5:28809037-28809087	MCF-7	breast:	n/a
21	chr5:28799238-28799288	PFSK-1	brain:	n/a
22	chr5:28809997-28810047	Jurkat	blood:	n/a
23	chr5:28809121-28809171	GM12878	blood:	n/a
24	chr5:28810645-28810695	AG10803	skin:	n/a
25	chr5:28810402-28810452	SK-N-SH	brain:	n/a
26	chr5:28809121-28809171	Hepatocyte	liver:	n/a
27	chr5:28810645-28810695	SKMC	muscle:	n/a
28	chr5:28809997-28810047	SK-N-SH_RA	brain:	n/a
29	chr5:28810402-28810452	HAEpiC	amniotic membrane:	n/a
30	chr5:28809037-28809087	Hela-S3	cervix:	n/a
31	chr5:28810645-28810695	LNCaP	prostate:	n/a
32	chr5:28799238-28799288	HEK293	kidney:	embryo
33	chr5:28809997-28810047	GM12892	blood:	n/a
34	chr5:28799238-28799288	HRE	kidney:	n/a
35	chr5:28810402-28810452	ovcar-3	ovarian:	n/a
36	chr5:28809037-28809087	Caco-2	colon:	n/a
37	chr5:28810148-28810198	HRCEpiC	kidney:	n/a
38	chr5:28810148-28810198	SK-N-MC	brain:	n/a
39	chr5:28809037-28809087	MCF10A-Er-Src	breast:	n/a
40	chr5:28810402-28810452	K562	blood:	n/a
41	chr5:28810402-28810452	ProgFib	skin:	n/a
42	chr5:28810148-28810198	HAEpiC	amniotic membrane:	n/a
43	chr5:28809037-28809087	SK-N-MC	brain:	n/a
44	chr5:28809121-28809171	NH-A	brain:	n/a
45	chr5:28810148-28810198	HEEpiC	esophagus:	n/a
46	chr5:28799238-28799288	A549	lung:	n/a
47	chr5:28810148-28810198	HRPEpiC	eye:	n/a
48	chr5:28809121-28809171	NT2-D1	testis:	n/a
49	chr5:28809121-28809171	HCF	heart:	n/a
50	chr5:28810148-28810198	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:28770203..28772237-chr6:49079734..49082291,2	MCF-7	breast:
2	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
3	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
4	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
5	chr5:28763389..28766520-chr5:28808448..28811312,3	K562	blood:
6	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
7	chr5:28786798..28789363-chr5:28791647..28793398,2	K562	blood:
8	chr5:28786798..28789363-chr5:28791647..28793398,2	K562	blood:
9	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
10	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
11	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
12	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
13	chr5:28777228..28779572-chr5:28784624..28787544,2	K562	blood:
14	chr5:28743630..28746249-chr5:28809920..28812616,2	K562	blood:
15	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
16	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
17	chr1:121484566..121485406-chr5:28783478..28783978,2	MCF-7	breast:
18	chr5:28808032..28811102-chr5:28813971..28817710,5	K562	blood:
19	chr5:28344669..28345343-chr5:28766345..28767141,3	MCF-7	breast:
20	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
21	chr5:28809387..28811298-chr5:29193650..29195834,2	K562	blood:
22	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
23	chr5:28779022..28779987-chr5:28896759..28897898,5	MCF-7	breast:
24	chr5:28771345..28773063-chr5:28782403..28784396,2	K562	blood:
25	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
26	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
27	chr5:28771345..28773063-chr5:28782403..28784396,2	K562	blood:
28	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
29	chr5:28344204..28345499-chr5:28766065..28767256,3	MCF-7	breast:
30	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
31	chr5:28777228..28779572-chr5:28784624..28787544,2	K562	blood:
32	chr5:28805922..28808420-chr5:28809202..28811186,4	K562	blood:
33	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
34	chr5:28851055..28851753-chr7:86185395..86186230,2	MCF-7	breast:
35	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
36	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
37	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH9-6	chr5:28782785-28782942	ENSG00000250453
2	lnc-CDH9-6	chr5:28809063-28809356	ENSG00000250453
3	lnc-CDH6-16	chr5:28808645-28809362	NONHSAT100821

Variant related genes	Relation type
ENSG00000250453	TF binding region
ENSG00000270495	TF binding region
ENSG00000250453	CpG island
ENSG00000270495	CpG island
ENSG00000270495	chromatin interactions
ENSG00000250453	chromatin interactions

Extended variants
information (count: 1051 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1160444	chr5:28763652-28763653	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144120766	chr5:28763684-28763685	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145984998	chr5:28763693-28763694	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533648206	chr5:28763867-28763868	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562966351	chr5:28763933-28763934	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2876977	chr5:28763941-28763942	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs73749805	chr5:28764008-28764009	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550984482	chr5:28764070-28764071	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs35404382	chr5:28764098-28764099	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7711476	chr5:28764175-28764176	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184833209	chr5:28764176-28764177	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567604642	chr5:28764214-28764215	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532167265	chr5:28764218-28764219	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537996413	chr5:28764246-28764247	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551864656	chr5:28764263-28764264	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs559397510	chr5:28764294-28764295	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555930153	chr5:28764308-28764309	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571136961	chr5:28764313-28764314	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs7731931	chr5:28764323-28764324	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368321407	chr5:28764342-28764343	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs553750521	chr5:28764415-28764416	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560039694	chr5:28764499-28764500	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372929787	chr5:28764520-28764521	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs572316228	chr5:28764522-28764523	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140630634	chr5:28764608-28764609	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs528769883	chr5:28764610-28764611	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs16898100	chr5:28764627-28764628	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs554599307	chr5:28764630-28764631	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190163944	chr5:28764631-28764632	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs568620346	chr5:28764651-28764652	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563046509	chr5:28764672-28764673	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs533534575	chr5:28764692-28764693	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs181912808	chr5:28764738-28764739	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10461848	chr5:28764743-28764744	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs144256031	chr5:28764751-28764752	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547849108	chr5:28764771-28764772	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs527989661	chr5:28764787-28764788	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs72758522	chr5:28764796-28764797	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145595715	chr5:28764834-28764835	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567692281	chr5:28764845-28764846	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557544823	chr5:28764847-28764848	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs539851417	chr5:28764849-28764850	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575782059	chr5:28764853-28764854	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553091158	chr5:28764913-28764914	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs117186359	chr5:28764921-28764922	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs369300581	chr5:28764932-28764933	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111968548	chr5:28764990-28764991	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538406586	chr5:28765023-28765024	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532907941	chr5:28765058-28765059	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs111959589	chr5:28765062-28765063	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	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
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:28763200-28763800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr5:28764200-28765000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:28764200-28765200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr5:28764400-28765200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr5:28765200-28767600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:28767000-28767400	Enhancers	A549	lung
7	chr5:28767600-28768200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:28777400-28778600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:28781800-28784200	Weak transcription	K562	blood
10	chr5:28789200-28790200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:28789600-28790200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:28806200-28813200	Active TSS	K562	blood
13	chr5:28807200-28807800	Enhancers	Hela-S3	cervix
14	chr5:28808400-28808600	Enhancers	Placenta	Placenta
15	chr5:28808400-28809200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:28808600-28810800	ZNF genes & repeats	Placenta	Placenta
17	chr5:28809000-28810600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:28809200-28809400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:28809400-28809800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:28809800-28810400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:28810800-28811400	Active TSS	Placenta	Placenta
22	chr5:28813200-28816600	Weak transcription	K562	blood
23	chr5:28822200-28822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr5:28823200-28823800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:28825600-28827000	Enhancers	Fetal Heart	heart
26	chr5:28857600-28859800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:28859800-28860000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:28860000-28861600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:28861400-28862600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr5:28861600-28862000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:28862000-28862400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:28862200-28863000	Enhancers	HepG2	liver
33	chr5:28862400-28863600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:28863600-28864200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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