Variant report

Variant	nsv880802
Chromosome Location	chr5:28682246-28853116
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	ATF1	chr5:28727124-28727126	K562	blood:	n/a	n/a
3	ATF1	chr5:28748273-28748340	K562	blood:	n/a	n/a
4	ATF1	chr5:28710259-28710312	K562	blood:	n/a	n/a
5	BHLHE40	chr5:28816335-28816476	K562	blood:	n/a	n/a
6	BHLHE40	chr5:28808920-28809724	K562	blood:	n/a	n/a
7	BHLHE40	chr5:28748213-28748330	K562	blood:	n/a	n/a
8	BHLHE40	chr5:28810355-28810693	K562	blood:	n/a	chr5:28810481-28810497 chr5:28810394-28810410
9	BHLHE40	chr5:28751531-28751557	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:28814502-28814623	K562	blood:	n/a	n/a
11	BRCA1	chr5:28815213-28815234	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr5:28766717-28767229	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr5:28727024-28727297	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr5:28823321-28823730	K562	blood:	n/a	n/a
15	CBX3	chr5:28823373-28823651	K562	blood:	n/a	n/a
16	CBX3	chr5:28809015-28809399	K562	blood:	n/a	n/a
17	CCNT2	chr5:28810313-28810825	K562	blood:	n/a	chr5:28810357-28810366
18	CCNT2	chr5:28816425-28816641	K562	blood:	n/a	n/a
19	CCNT2	chr5:28809192-28810112	K562	blood:	n/a	n/a
20	CEBPB	chr5:28834515-28834730	K562	blood:	n/a	chr5:28834587-28834598
21	CEBPB	chr5:28831177-28831503	A549	lung:	n/a	chr5:28831343-28831354
22	CEBPB	chr5:28743173-28743511	HepG2	liver:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334
23	CEBPB	chr5:28703848-28703955	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:28818678-28818966	HepG2	liver:	n/a	chr5:28818791-28818802
25	CEBPB	chr5:28828802-28828896	A549	lung:	n/a	n/a
26	CEBPB	chr5:28831182-28831450	H1-hESC	embryonic stem cell:	n/a	chr5:28831343-28831354
27	CEBPB	chr5:28834436-28834676	HepG2	liver:	n/a	chr5:28834587-28834598
28	CEBPB	chr5:28743140-28743512	IMR90	lung:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334
29	CEBPB	chr5:28763630-28763938	K562	blood:	n/a	chr5:28763789-28763800
30	CEBPB	chr5:28703785-28704059	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:28809192-28809322	K562	blood:	n/a	n/a
32	CEBPB	chr5:28743189-28743489	A549	lung:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334
33	CEBPB	chr5:28763690-28763856	A549	lung:	n/a	chr5:28763789-28763800
34	CEBPB	chr5:28713573-28713854	A549	lung:	n/a	n/a
35	CEBPB	chr5:28763672-28763927	IMR90	lung:	n/a	chr5:28763789-28763800
36	CEBPB	chr5:28726780-28727310	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:28818648-28818936	K562	blood:	n/a	chr5:28818791-28818802
38	CEBPB	chr5:28708665-28708964	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:28763632-28764408	HepG2	liver:	n/a	chr5:28764292-28764305 chr5:28763789-28763800
40	CEBPB	chr5:28708674-28708931	MCF-7	breast:	n/a	n/a
41	CEBPB	chr5:28763702-28764332	Hela-S3	cervix:	n/a	chr5:28764292-28764305 chr5:28763789-28763800
42	CEBPB	chr5:28743140-28743713	Hela-S3	cervix:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334
43	CEBPB	chr5:28686057-28686307	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:28743208-28743405	H1-hESC	embryonic stem cell:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334
45	CEBPB	chr5:28737268-28738143	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr5:28831210-28831505	K562	blood:	n/a	chr5:28831343-28831354
47	CEBPB	chr5:28743153-28743495	K562	blood:	n/a	chr5:28743323-28743332 chr5:28743323-28743332 chr5:28743322-28743333 chr5:28743323-28743332 chr5:28743321-28743332 chr5:28743321-28743334 chr5:28743323-28743332 chr5:28743321-28743334 chr5:28743321-28743334
48	CEBPB	chr5:28708731-28708929	A549	lung:	n/a	n/a
49	CEBPB	chr5:28831202-28831533	HepG2	liver:	n/a	chr5:28831343-28831354
50	CEBPB	chr5:28850602-28850862	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:28810402-28810452	NT2-D1	testis:	n/a
2	chr5:28810645-28810695	MCF-7	breast:	n/a
3	chr5:28809997-28810047	K562	blood:	n/a
4	chr5:28809121-28809171	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:28809622-28809672	PrEC	prostate:	n/a
6	chr5:28810402-28810452	IMR90	lung:	fetal
7	chr5:28810402-28810452	HRPEpiC	eye:	n/a
8	chr5:28809037-28809087	NT2-D1	testis:	n/a
9	chr5:28810402-28810452	GM12892	blood:	n/a
10	chr5:28809997-28810047	BJ	skin:	n/a
11	chr5:28810645-28810695	PANC-1	pancreas:	n/a
12	chr5:28799238-28799288	ProgFib	skin:	n/a
13	chr5:28809037-28809087	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:28809997-28810047	PrEC	prostate:	n/a
15	chr5:28810148-28810198	PFSK-1	brain:	n/a
16	chr5:28809997-28810047	ECC-1	luminal epithelium:	n/a
17	chr5:28810148-28810198	U87	brain:	n/a
18	chr5:28799238-28799288	LNCaP	prostate:	n/a
19	chr5:28810645-28810695	K562	blood:	n/a
20	chr5:28809121-28809171	HCF	heart:	n/a
21	chr5:28799238-28799288	SK-N-MC	brain:	n/a
22	chr5:28809121-28809171	U87	brain:	n/a
23	chr5:28810402-28810452	PANC-1	pancreas:	n/a
24	chr5:28809121-28809171	HUVEC	blood vessel:	n/a
25	chr5:28809121-28809171	LNCaP	prostate:	n/a
26	chr5:28809997-28810047	H1-hESC	embryonic stem cell:	embryo
27	chr5:28810402-28810452	NHBE	bronchial:	n/a
28	chr5:28809037-28809087	AG10803	skin:	n/a
29	chr5:28810402-28810452	SKMC	muscle:	n/a
30	chr5:28810645-28810695	SK-N-SH	brain:	n/a
31	chr5:28809037-28809087	AG09309	skin:	n/a
32	chr5:28809121-28809171	SK-N-SH	brain:	n/a
33	chr5:28799238-28799288	HAEpiC	amniotic membrane:	n/a
34	chr5:28809037-28809087	NHDF-neo	bronchial:	n/a
35	chr5:28809121-28809171	GM12891	blood:	n/a
36	chr5:28810645-28810695	T-47D	breast:	n/a
37	chr5:28809997-28810047	AG04450	lung:	fetal
38	chr5:28799238-28799288	AG04450	lung:	fetal
39	chr5:28809121-28809171	GM19239	blood:	n/a
40	chr5:28799238-28799288	Caco-2	colon:	n/a
41	chr5:28809997-28810047	Hepatocyte	liver:	n/a
42	chr5:28809997-28810047	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:28810402-28810452	SK-N-SH	brain:	n/a
44	chr5:28809622-28809672	NH-A	brain:	n/a
45	chr5:28799238-28799288	A549	lung:	n/a
46	chr5:28809997-28810047	BE2_C	brain:	n/a
47	chr5:28809037-28809087	U87	brain:	n/a
48	chr5:28810402-28810452	HL-60	blood:	n/a
49	chr5:28809037-28809087	HRCEpiC	kidney:	n/a
50	chr5:28809121-28809171	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:28743630..28746249-chr5:28809920..28812616,2	K562	blood:
2	chr5:27139047..27140972-chr5:28754402..28756411,2	MCF-7	breast:
3	chr5:28777228..28779572-chr5:28784624..28787544,2	K562	blood:
4	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
5	chr5:28805922..28808420-chr5:28809202..28811186,4	K562	blood:
6	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
7	chr5:28708085..28710925-chr5:28712121..28714327,2	K562	blood:
8	chr5:28743512..28746337-chr5:28749369..28752061,2	K562	blood:
9	chr5:28473383..28474265-chr5:28734098..28735113,3	MCF-7	breast:
10	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
11	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
12	chr5:28344204..28345499-chr5:28766065..28767256,3	MCF-7	breast:
13	chr5:28808032..28811102-chr5:28813971..28817710,5	K562	blood:
14	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
15	chr5:28851055..28851753-chr7:86185395..86186230,2	MCF-7	breast:
16	chr5:28763389..28766520-chr5:28808448..28811312,3	K562	blood:
17	chr5:28786798..28789363-chr5:28791647..28793398,2	K562	blood:
18	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
19	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
20	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
21	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
22	chr5:28708085..28710925-chr5:28712121..28714327,2	K562	blood:
23	chr5:28779022..28779987-chr5:28896759..28897898,5	MCF-7	breast:
24	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
25	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
26	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
27	chr5:28743512..28746337-chr5:28749369..28752061,2	K562	blood:
28	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
29	chr5:28771345..28773063-chr5:28782403..28784396,2	K562	blood:
30	chr5:28473399..28474025-chr5:28710323..28711039,2	MCF-7	breast:
31	chr5:28786798..28789363-chr5:28791647..28793398,2	K562	blood:
32	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
33	chr5:28665183..28667336-chr5:28683760..28686377,2	K562	blood:
34	chr1:121484566..121485406-chr5:28783478..28783978,2	MCF-7	breast:
35	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
36	chr5:28770203..28772237-chr6:49079734..49082291,2	MCF-7	breast:
37	chr5:28771345..28773063-chr5:28782403..28784396,2	K562	blood:
38	chr5:28473336..28474039-chr5:28734455..28735092,2	MCF-7	breast:
39	chr5:28743630..28746249-chr5:28809920..28812616,2	K562	blood:
40	chr5:28777228..28779572-chr5:28784624..28787544,2	K562	blood:
41	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
42	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
43	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
44	chr5:28809387..28811298-chr5:29193650..29195834,2	K562	blood:
45	chr17:57913887..57916844-chr5:28684524..28686984,2	MCF-7	breast:
46	chr5:28344669..28345343-chr5:28766345..28767141,3	MCF-7	breast:

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

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
ENSG00000062716	chromatin interactions

Extended variants
information (count: 1586 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13157069	chr5:28684536-28684537	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs56351346	chr5:28684570-28684571	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs13174824	chr5:28684634-28684635	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563598156	chr5:28684636-28684637	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530756165	chr5:28684637-28684638	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545355537	chr5:28684672-28684673	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563744543	chr5:28684678-28684679	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528138693	chr5:28684693-28684694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs202086166	chr5:28684726-28684727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs6899278	chr5:28684735-28684736	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188017462	chr5:28684742-28684743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565153816	chr5:28684743-28684744	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568089261	chr5:28684748-28684749	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530311081	chr5:28684754-28684755	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374188199	chr5:28684764-28684765	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570289070	chr5:28684798-28684799	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537743967	chr5:28684800-28684801	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs180943218	chr5:28684810-28684811	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541046437	chr5:28684870-28684871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113435527	chr5:28684874-28684875	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2042320	chr5:28684889-28684890	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553415067	chr5:28684899-28684900	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574875816	chr5:28684959-28684960	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146825008	chr5:28684965-28684966	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556878140	chr5:28684981-28684982	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189477855	chr5:28684991-28684992	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373859186	chr5:28684992-28684993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545704968	chr5:28684994-28684995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545660401	chr5:28685024-28685025	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs564070065	chr5:28685046-28685047	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546279629	chr5:28685096-28685097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564125291	chr5:28685110-28685111	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528064208	chr5:28685125-28685126	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539884679	chr5:28685134-28685135	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs116654727	chr5:28685145-28685146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2042321	chr5:28685156-28685157	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148951117	chr5:28685160-28685161	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143678619	chr5:28685177-28685178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570171071	chr5:28685307-28685308	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140551056	chr5:28685312-28685313	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201428794	chr5:28685313-28685314	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs74958340	chr5:28685472-28685473	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552881193	chr5:28685528-28685529	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs151036052	chr5:28685547-28685548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571195708	chr5:28685558-28685559	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535006615	chr5:28685580-28685581	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76337649	chr5:28685593-28685594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182158751	chr5:28685626-28685627	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34173992	chr5:28685628-28685629	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141102110	chr5:28685656-28685657	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:28685600-28686200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr5:28703600-28704600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:28703800-28704400	Enhancers	H9 Cell Line	embryonic stem cell
4	chr5:28703800-28704400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:28703800-28704600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:28703800-28705200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:28704000-28704200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:28704000-28704600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr5:28704200-28704600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:28704200-28704600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:28704200-28704600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:28704200-28704600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:28711200-28711600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:28711600-28715000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:28715000-28715400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:28723800-28724200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:28726400-28727600	Enhancers	Hela-S3	cervix
18	chr5:28726600-28727600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:28728600-28728800	Enhancers	Liver	Liver
20	chr5:28728800-28729000	Flanking Active TSS	Liver	Liver
21	chr5:28729000-28729400	Active TSS	Liver	Liver
22	chr5:28729400-28730600	Enhancers	Liver	Liver
23	chr5:28732000-28732400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:28733800-28735000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr5:28734000-28734800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr5:28734400-28734800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:28734400-28735000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:28734600-28735000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:28734800-28735000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:28736800-28737800	Enhancers	Hela-S3	cervix
31	chr5:28737800-28743200	Weak transcription	Hela-S3	cervix
32	chr5:28743200-28743600	Enhancers	Fetal Heart	heart
33	chr5:28743200-28743800	Enhancers	Hela-S3	cervix
34	chr5:28743200-28744000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:28743400-28743800	Enhancers	Fetal Stomach	stomach
36	chr5:28743400-28744200	Enhancers	NH-A	brain
37	chr5:28752800-28753000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:28763200-28763600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr5:28763200-28763800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:28764200-28765000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:28764200-28765200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:28764400-28765200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr5:28765200-28767600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:28767000-28767400	Enhancers	A549	lung
45	chr5:28767600-28768200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr5:28777400-28778600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:28781800-28784200	Weak transcription	K562	blood
48	chr5:28789200-28790200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:28789600-28790200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:28806200-28813200	Active TSS	K562	blood

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