Variant report

Variant	nsv881525
Chromosome Location	chr5:28806256-28921260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:428)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr5:28810355-28810693	K562	blood:	n/a	chr5:28810481-28810497 chr5:28810394-28810410
6	BHLHE40	chr5:28816335-28816476	K562	blood:	n/a	n/a
7	BRCA1	chr5:28815213-28815234	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr5:28823373-28823651	K562	blood:	n/a	n/a
9	CBX3	chr5:28809015-28809399	K562	blood:	n/a	n/a
10	CBX3	chr5:28823321-28823730	K562	blood:	n/a	n/a
11	CCNT2	chr5:28816425-28816641	K562	blood:	n/a	n/a
12	CCNT2	chr5:28809192-28810112	K562	blood:	n/a	n/a
13	CCNT2	chr5:28810313-28810825	K562	blood:	n/a	chr5:28810357-28810366
14	CEBPB	chr5:28809192-28809322	K562	blood:	n/a	n/a
15	CEBPB	chr5:28915431-28915546	Hela-S3	cervix:	n/a	chr5:28915458-28915471 chr5:28915458-28915471
16	CEBPB	chr5:28818678-28818966	HepG2	liver:	n/a	chr5:28818791-28818802
17	CEBPB	chr5:28914557-28914757	A549	lung:	n/a	chr5:28914660-28914673
18	CEBPB	chr5:28831210-28831505	K562	blood:	n/a	chr5:28831343-28831354
19	CEBPB	chr5:28896561-28896803	K562	blood:	n/a	n/a
20	CEBPB	chr5:28831202-28831533	HepG2	liver:	n/a	chr5:28831343-28831354
21	CEBPB	chr5:28834436-28834676	HepG2	liver:	n/a	chr5:28834587-28834598
22	CEBPB	chr5:28818648-28818936	K562	blood:	n/a	chr5:28818791-28818802
23	CEBPB	chr5:28862960-28863277	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:28850602-28850862	K562	blood:	n/a	n/a
25	CEBPB	chr5:28831182-28831450	H1-hESC	embryonic stem cell:	n/a	chr5:28831343-28831354
26	CEBPB	chr5:28834515-28834730	K562	blood:	n/a	chr5:28834587-28834598
27	CEBPB	chr5:28828802-28828896	A549	lung:	n/a	n/a
28	CEBPB	chr5:28831177-28831503	A549	lung:	n/a	chr5:28831343-28831354
29	CHD2	chr5:28810617-28810817	K562	blood:	n/a	n/a
30	CHD2	chr5:28810281-28810330	K562	blood:	n/a	n/a
31	CHD2	chr5:28809029-28809592	K562	blood:	n/a	n/a
32	CTCF	chr5:28810930-28811187	K562	blood:	n/a	chr5:28811027-28811040
33	CTCF	chr5:28903904-28903995	LNCaP	prostate:	n/a	n/a
34	CTCF	chr5:28810900-28811050	Hela-S3	cervix:	n/a	chr5:28811027-28811040
35	CTCF	chr5:28897200-28897350	HA-sp	spinal cord:	n/a	chr5:28897255-28897273 chr5:28897250-28897271 chr5:28897256-28897272
36	CTCF	chr5:28897180-28897330	HRPEpiC	eye:	n/a	chr5:28897255-28897273 chr5:28897250-28897271 chr5:28897256-28897272
37	CTCF	chr5:28897180-28897330	HCPEpiC	choroid plexus:	n/a	chr5:28897255-28897273 chr5:28897250-28897271 chr5:28897256-28897272
38	CTCF	chr5:28810880-28811030	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr5:28810960-28811110	MCF-7	breast:	n/a	chr5:28811027-28811040
40	CTCF	chr5:28897140-28897290	Hela-S3	cervix:	n/a	chr5:28897255-28897273 chr5:28897250-28897271 chr5:28897256-28897272
41	CTCF	chr5:28810880-28811030	HEK293	kidney:	n/a	n/a
42	CTCF	chr5:28809845-28809945	K562	blood:	n/a	n/a
43	CTCF	chr5:28810425-28810488	K562	blood:	n/a	n/a
44	CTCF	chr5:28810960-28811110	HBMEC	blood vessel:	n/a	chr5:28811027-28811040
45	CTCF	chr5:28810940-28811090	HEK293	kidney:	n/a	chr5:28811027-28811040
46	CTCF	chr5:28810400-28810550	HVMF	connective:	n/a	n/a
47	CTCF	chr5:28903808-28904068	GM12878	blood:	n/a	n/a
48	CTCF	chr5:28903880-28904030	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr5:28897380-28897530	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr5:28903860-28904010	Hela-S3	cervix:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:28809997-28810047	HMEC	breast:	n/a
2	chr5:28809997-28810047	HMEC	breast:	n/a
3	chr5:28810148-28810198	AG09319	gingival:	n/a
4	chr5:28809121-28809171	AoSMC	blood vessel:	n/a
5	chr5:28809037-28809087	HRCEpiC	kidney:	n/a
6	chr5:28810148-28810198	A549	lung:	n/a
7	chr5:28809622-28809672	SK-N-SH	brain:	n/a
8	chr5:28810148-28810198	HEK293	kidney:	embryo
9	chr5:28809037-28809087	HAEpiC	amniotic membrane:	n/a
10	chr5:28810148-28810198	HMEC	breast:	n/a
11	chr5:28809037-28809087	BJ	skin:	n/a
12	chr5:28809121-28809171	ovcar-3	ovarian:	n/a
13	chr5:28809037-28809087	ovcar-3	ovarian:	n/a
14	chr5:28810402-28810452	PFSK-1	brain:	n/a
15	chr5:28810148-28810198	AG04450	lung:	fetal
16	chr5:28809997-28810047	SK-N-SH	brain:	n/a
17	chr5:28809121-28809171	MCF-7	breast:	n/a
18	chr5:28809997-28810047	ovcar-3	ovarian:	n/a
19	chr5:28809997-28810047	Hela-S3	cervix:	n/a
20	chr5:28809997-28810047	GM12891	blood:	n/a
21	chr5:28809037-28809087	K562	blood:	n/a
22	chr5:28810645-28810695	HEK293	kidney:	embryo
23	chr5:28810402-28810452	H1-hESC	embryonic stem cell:	embryo
24	chr5:28809622-28809672	CMK	blood:	n/a
25	chr5:28810645-28810695	MCF-7	breast:	n/a
26	chr5:28809121-28809171	SKMC	muscle:	n/a
27	chr5:28809037-28809087	SAEC	small airway:	n/a
28	chr5:28809997-28810047	NH-A	brain:	n/a
29	chr5:28809037-28809087	ProgFib	skin:	n/a
30	chr5:28810148-28810198	ECC-1	luminal epithelium:	n/a
31	chr5:28809622-28809672	SK-N-MC	brain:	n/a
32	chr5:28809622-28809672	HEEpiC	esophagus:	n/a
33	chr5:28810645-28810695	SK-N-MC	brain:	n/a
34	chr5:28810148-28810198	HRCEpiC	kidney:	n/a
35	chr5:28810645-28810695	HL-60	blood:	n/a
36	chr5:28809037-28809087	HCT-116	colon:	n/a
37	chr5:28809037-28809087	GM06990	blood:	n/a
38	chr5:28809121-28809171	K562	blood:	n/a
39	chr5:28810148-28810198	Caco-2	colon:	n/a
40	chr5:28810148-28810198	MCF10A-Er-Src	breast:	n/a
41	chr5:28809121-28809171	GM12878	blood:	n/a
42	chr5:28809121-28809171	AG10803	skin:	n/a
43	chr5:28810645-28810695	HCT-116	colon:	n/a
44	chr5:28810148-28810198	HEEpiC	esophagus:	n/a
45	chr5:28809037-28809087	PFSK-1	brain:	n/a
46	chr5:28809622-28809672	Hepatocyte	liver:	n/a
47	chr5:28809121-28809171	HCF	heart:	n/a
48	chr5:28810645-28810695	CMK	blood:	n/a
49	chr5:28809121-28809171	A549	lung:	n/a
50	chr5:28810148-28810198	PFSK-1	brain:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:28809387..28811298-chr5:29193650..29195834,2	K562	blood:
2	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
3	chr5:28898397..28901228-chr5:28905919..28907829,2	K562	blood:
4	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
5	chr5:28808352..28811830-chr5:28882168..28885526,3	K562	blood:
6	chr5:28805922..28808420-chr5:28809202..28811186,4	K562	blood:
7	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
8	chr5:28851055..28851753-chr7:86185395..86186230,2	MCF-7	breast:
9	chr5:28914551..28916336-chr5:28918425..28920411,2	MCF-7	breast:
10	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
11	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
12	chr5:28878210..28880658-chr5:28883353..28885115,2	K562	blood:
13	chr5:28878210..28880658-chr5:28883353..28885115,2	K562	blood:
14	chr5:28898397..28901228-chr5:28905919..28907829,2	K562	blood:
15	chr5:28808032..28811102-chr5:28813971..28817710,5	K562	blood:
16	chr5:28903483..28905347-chr5:28915457..28917454,2	K562	blood:
17	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
18	chr5:28779022..28779987-chr5:28896759..28897898,5	MCF-7	breast:
19	chr5:28910494..28912517-chr5:28913196..28915967,2	MCF-7	breast:
20	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
21	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
22	chr5:28906947..28909506-chr5:29049292..29051622,2	K562	blood:
23	chr5:28882757..28885638-chr5:28890766..28893255,2	K562	blood:
24	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
25	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
26	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
27	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
28	chr5:28882757..28885638-chr5:28890766..28893255,2	K562	blood:
29	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
30	chr5:28914551..28916336-chr5:28918425..28920411,2	MCF-7	breast:
31	chr5:28903483..28905347-chr5:28915457..28917454,2	K562	blood:
32	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
33	chr5:28892844..28895321-chr5:28897758..28899346,2	K562	blood:
34	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
35	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
36	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
37	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
38	chr5:28743630..28746249-chr5:28809920..28812616,2	K562	blood:
39	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
40	chr5:28910494..28912517-chr5:28913196..28915967,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH9-6	chr5:28809063-28809356	ENSG00000250453
2	lnc-CDH9-12	chr5:28897892-28898381	NONHSAT100823
3	lnc-CDH6-15	chr5:28900872-28902541	NONHSAT100824
4	lnc-CDH6-16	chr5:28808645-28809362	NONHSAT100821

No data

Variant related genes	Relation type
LSP1P3	TF binding region
ENSG00000250453	TF binding region
ENSG00000270495	TF binding region
ENSG00000271035	TF binding region
LSP1P3	CpG island
ENSG00000250453	CpG island
ENSG00000270495	CpG island
ENSG00000271035	CpG island
ENSG00000271035	chromatin interactions
ENSG00000270495	chromatin interactions
ENSG00000250453	chromatin interactions

Extended variants
information (count: 1299 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1299 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2548005	chr5:28806256-28806257	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551186705	chr5:28806284-28806285	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563109734	chr5:28806312-28806313	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs193192287	chr5:28806321-28806322	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376383516	chr5:28806328-28806329	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184560921	chr5:28806332-28806333	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566521445	chr5:28806343-28806344	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533980934	chr5:28806367-28806368	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555421789	chr5:28806414-28806415	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188484449	chr5:28806443-28806444	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs72758537	chr5:28806489-28806490	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146665005	chr5:28806618-28806619	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138773380	chr5:28806622-28806623	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545246215	chr5:28806649-28806650	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181341454	chr5:28806674-28806675	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572067334	chr5:28806709-28806710	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200288764	chr5:28806719-28806720	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566164333	chr5:28806733-28806734	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542671915	chr5:28806762-28806763	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs16898167	chr5:28806780-28806781	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142746889	chr5:28806782-28806783	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549630885	chr5:28806828-28806829	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2554914	chr5:28806835-28806836	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569683999	chr5:28806861-28806862	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377143232	chr5:28806867-28806868	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551657542	chr5:28806977-28806978	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368384422	chr5:28807006-28807007	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs78640654	chr5:28807015-28807016	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185170412	chr5:28807040-28807041	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs147361360	chr5:28807143-28807144	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375820588	chr5:28807203-28807204	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374137560	chr5:28807232-28807233	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs147974981	chr5:28807267-28807268	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141613718	chr5:28807345-28807346	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538291149	chr5:28807400-28807401	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs112345849	chr5:28807412-28807413	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs566552982	chr5:28807426-28807427	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577757535	chr5:28807453-28807454	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7726657	chr5:28807460-28807461	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572404588	chr5:28807487-28807488	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542955914	chr5:28807488-28807489	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs560836466	chr5:28807491-28807492	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575949885	chr5:28807498-28807499	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543463622	chr5:28807541-28807542	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189590174	chr5:28807559-28807560	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs535493095	chr5:28807643-28807644	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182004772	chr5:28807674-28807675	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs72758538	chr5:28807695-28807696	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs551594647	chr5:28807700-28807701	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs73749816	chr5:28807742-28807743	Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:28806200-28813200	Active TSS	K562	blood
2	chr5:28807200-28807800	Enhancers	Hela-S3	cervix
3	chr5:28808400-28808600	Enhancers	Placenta	Placenta
4	chr5:28808400-28809200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:28808600-28810800	ZNF genes & repeats	Placenta	Placenta
6	chr5:28809000-28810600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:28809200-28809400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:28809400-28809800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:28809800-28810400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:28810800-28811400	Active TSS	Placenta	Placenta
11	chr5:28813200-28816600	Weak transcription	K562	blood
12	chr5:28822200-28822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:28823200-28823800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:28825600-28827000	Enhancers	Fetal Heart	heart
15	chr5:28857600-28859800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:28859800-28860000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:28860000-28861600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:28861400-28862600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:28861600-28862000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:28862000-28862400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:28862200-28863000	Enhancers	HepG2	liver
22	chr5:28862400-28863600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:28863600-28864200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:28876800-28877400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:28884200-28889600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:28897400-28898600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:28913400-28914800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:28913600-28914800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:28914200-28914600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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