Variant report

Variant	nsv598750
Chromosome Location	chr5:80503528-80599578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1478)
CpG islands
(count:2078)
Chromatin interactive
region (count:44)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1478 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:80599488-80599712	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:80597116-80597580	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:80564444-80565018	HepG2	liver:	n/a	chr5:80564660-80564676 chr5:80564661-80564677
4	ARID3A	chr5:80597171-80597472	K562	blood:	n/a	n/a
5	ATF1	chr5:80597083-80597744	K562	blood:	n/a	n/a
6	ATF2	chr5:80597143-80597676	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:80507878-80508462	GM12878	blood:	n/a	n/a
8	ATF2	chr5:80597099-80597655	GM12878	blood:	n/a	n/a
9	ATF2	chr5:80508010-80508458	GM12878	blood:	n/a	n/a
10	ATF2	chr5:80597145-80597642	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:80597146-80597802	GM12878	blood:	n/a	n/a
12	ATF3	chr5:80597184-80597611	K562	blood:	n/a	n/a
13	ATF3	chr5:80596970-80597605	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr5:80597158-80597502	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr5:80597085-80597629	A549	lung:	n/a	n/a
16	ATF3	chr5:80597216-80597471	GM12878	blood:	n/a	n/a
17	BACH1	chr5:80597227-80597607	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:80531333-80531367	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:80529155-80529491	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr5:80583811-80584207	GM12878	blood:	n/a	n/a
21	BATF	chr5:80510611-80510996	GM12878	blood:	n/a	n/a
22	BATF	chr5:80510697-80510958	GM12878	blood:	n/a	n/a
23	BATF	chr5:80538117-80538420	GM12878	blood:	n/a	n/a
24	BATF	chr5:80580622-80580983	GM12878	blood:	n/a	chr5:80580782-80580793
25	BATF	chr5:80538032-80538387	GM12878	blood:	n/a	n/a
26	BATF	chr5:80508048-80508377	GM12878	blood:	n/a	n/a
27	BATF	chr5:80505682-80506044	GM12878	blood:	n/a	chr5:80505898-80505908 chr5:80505897-80505908
28	BATF	chr5:80507611-80507881	GM12878	blood:	n/a	n/a
29	BATF	chr5:80580700-80580926	GM12878	blood:	n/a	chr5:80580782-80580793
30	BCL11A	chr5:80538140-80538470	GM12878	blood:	n/a	n/a
31	BCL11A	chr5:80538097-80538443	GM12878	blood:	n/a	n/a
32	BCL3	chr5:80596980-80597635	A549	lung:	n/a	chr5:80597382-80597391
33	BCL3	chr5:80597053-80597807	A549	lung:	n/a	chr5:80597382-80597391
34	BCLAF1	chr5:80597040-80597858	GM12878	blood:	n/a	chr5:80597382-80597391
35	BCLAF1	chr5:80597019-80597810	GM12878	blood:	n/a	chr5:80597382-80597391
36	BHLHE40	chr5:80528359-80528491	K562	blood:	n/a	n/a
37	BHLHE40	chr5:80598282-80598589	HepG2	liver:	n/a	n/a
38	BHLHE40	chr5:80538684-80538916	GM12878	blood:	n/a	n/a
39	BHLHE40	chr5:80597079-80597909	K562	blood:	n/a	chr5:80597683-80597699
40	BHLHE40	chr5:80507685-80508520	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:80583719-80584282	GM12878	blood:	n/a	n/a
42	BHLHE40	chr5:80597236-80597630	GM12878	blood:	n/a	n/a
43	BRCA1	chr5:80596869-80597584	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr5:80597007-80597629	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr5:80597044-80597792	GM12878	blood:	n/a	n/a
46	BRCA1	chr5:80597210-80597925	HepG2	liver:	n/a	n/a
47	BRCA1	chr5:80537441-80537502	GM12878	blood:	n/a	n/a
48	CBX3	chr5:80597025-80597890	K562	blood:	n/a	n/a
49	CBX3	chr5:80597084-80597650	K562	blood:	n/a	n/a
50	CCNT2	chr5:80528899-80529331	K562	blood:	n/a	n/a

(count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80595275-80595325	ECC-1	luminal epithelium:	n/a
2	chr5:80529100-80529150	GM06990	blood:	n/a
3	chr5:80596277-80596327	AG04450	lung:	fetal
4	chr5:80542999-80543049	NH-A	brain:	n/a
5	chr5:80595275-80595325	ECC-1	luminal epithelium:	n/a
6	chr5:80529100-80529150	GM06990	blood:	n/a
7	chr5:80596277-80596327	AG04450	lung:	fetal
8	chr5:80542999-80543049	NH-A	brain:	n/a
9	chr5:80594700-80594750	BE2_C	brain:	n/a
10	chr5:80542999-80543049	SK-N-MC	brain:	n/a
11	chr5:80529340-80529390	Hela-S3	cervix:	n/a
12	chr5:80597718-80597768	HRPEpiC	eye:	n/a
13	chr5:80597384-80597434	T-47D	breast:	n/a
14	chr5:80521615-80521665	PANC-1	pancreas:	n/a
15	chr5:80529340-80529390	PANC-1	pancreas:	n/a
16	chr5:80597196-80597246	GM19239	blood:	n/a
17	chr5:80597482-80597532	CMK	blood:	n/a
18	chr5:80550291-80550341	GM12891	blood:	n/a
19	chr5:80550841-80550891	GM19239	blood:	n/a
20	chr5:80529340-80529390	AG09309	skin:	n/a
21	chr5:80597551-80597601	NHDF-neo	bronchial:	n/a
22	chr5:80597384-80597434	PFSK-1	brain:	n/a
23	chr5:80597143-80597193	HEK293	kidney:	embryo
24	chr5:80597196-80597246	PFSK-1	brain:	n/a
25	chr5:80597551-80597601	Hela-S3	cervix:	n/a
26	chr5:80595354-80595404	Hela-S3	cervix:	n/a
27	chr5:80521615-80521665	GM12878	blood:	n/a
28	chr5:80529121-80529171	HRCEpiC	kidney:	n/a
29	chr5:80596277-80596327	NHDF-neo	bronchial:	n/a
30	chr5:80529340-80529390	H1-hESC	embryonic stem cell:	embryo
31	chr5:80596475-80596525	Caco-2	colon:	n/a
32	chr5:80595275-80595325	RPTEC	kidney:	n/a
33	chr5:80597143-80597193	PFSK-1	brain:	n/a
34	chr5:80597288-80597338	HRCEpiC	kidney:	n/a
35	chr5:80597551-80597601	IMR90	lung:	fetal
36	chr5:80597509-80597559	SK-N-SH_RA	brain:	n/a
37	chr5:80550841-80550891	Hela-S3	cervix:	n/a
38	chr5:80529121-80529171	HUVEC	blood vessel:	n/a
39	chr5:80596277-80596327	AG04449	skin:	fetal
40	chr5:80596475-80596525	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:80529187-80529237	GM19239	blood:	n/a
42	chr5:80597482-80597532	HMEC	breast:	n/a
43	chr5:80596475-80596525	A549	lung:	n/a
44	chr5:80595275-80595325	PFSK-1	brain:	n/a
45	chr5:80597143-80597193	SK-N-MC	brain:	n/a
46	chr5:80529135-80529185	HepG2	liver:	n/a
47	chr5:80528698-80528748	HUVEC	blood vessel:	n/a
48	chr5:80597509-80597559	AoSMC	blood vessel:	n/a
49	chr5:80597395-80597445	HCPEpiC	choroid plexus:	n/a
50	chr5:80596277-80596327	HNPCEpiC	eye:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:80488093..80488779-chr5:80595082..80595655,2	MCF-7	breast:
2	chr5:80596931..80597570-chr5:148205888..148206610,2	NB4	blood:
3	chr5:80530046..80533018-chr5:80537820..80540645,2	MCF-7	breast:
4	chr5:80559870..80562227-chr5:80563019..80565306,2	MCF-7	breast:
5	chr5:80571971..80574840-chr5:80577272..80579024,2	K562	blood:
6	chr17:79369420..79370958-chr5:80594929..80596916,2	MCF-7	breast:
7	chr5:80547726..80550284-chr5:80550387..80553255,3	K562	blood:
8	chr5:80579977..80582427-chr5:80582466..80585104,2	K562	blood:
9	chr5:80533844..80536662-chr5:80539256..80543290,4	K562	blood:
10	chr5:80535144..80535935-chr5:80595128..80595851,2	MCF-7	breast:
11	chr5:80543196..80545536-chr5:80550500..80552357,2	K562	blood:
12	chr5:80599288..80602129-chr5:80607036..80608849,2	K562	blood:
13	chr5:80580034..80582470-chr5:80593982..80596791,2	K562	blood:
14	chr5:80598755..80600911-chr5:80604785..80606382,2	K562	blood:
15	chr5:80540741..80543266-chr5:80561744..80563838,2	K562	blood:
16	chr5:80592174..80595605-chr5:80595635..80599173,5	MCF-7	breast:
17	chr5:80509061..80510857-chr5:80523692..80526084,2	K562	blood:
18	chr5:80531823..80533359-chr5:80535137..80538128,2	K562	blood:
19	chr21:43236982..43237531-chr5:80503397..80503897,2	MCF-7	breast:
20	chr5:80543196..80546159-chr5:80550500..80552357,3	K562	blood:
21	chr5:80533835..80535952-chr5:80536358..80538969,2	K562	blood:
22	chr5:80514079..80517036-chr5:80522834..80524358,2	K562	blood:
23	chr5:80514079..80517036-chr5:80522834..80524358,2	K562	blood:
24	chr5:80540741..80543266-chr5:80561744..80563838,2	K562	blood:
25	chr5:80547726..80550284-chr5:80550387..80553255,3	K562	blood:
26	chr5:80571971..80574840-chr5:80577272..80579024,2	K562	blood:
27	chr5:80533844..80536662-chr5:80539256..80543290,4	K562	blood:
28	chr5:80583580..80587936-chr5:80595683..80598863,3	MCF-7	breast:
29	chr5:80546433..80550284-chr5:80550387..80553828,5	K562	blood:
30	chr5:80537672..80539759-chr5:80539987..80541535,2	MCF-7	breast:
31	chr5:80527933..80529757-chr5:80532503..80536137,3	K562	blood:
32	chr5:80579977..80582427-chr5:80582466..80585104,2	K562	blood:
33	chr5:80509061..80510857-chr5:80523692..80526084,2	K562	blood:
34	chr17:58001323..58002216-chr5:80511299..80512148,2	MCF-7	breast:
35	chr5:80562714..80564322-chr5:80589942..80591670,2	K562	blood:
36	chr5:80580034..80582470-chr5:80593982..80596791,2	K562	blood:
37	chr5:80546433..80550284-chr5:80550387..80553828,5	K562	blood:
38	chr1:87793815..87794355-chr5:80596988..80597951,2	HCT-116	colon:
39	chr5:80538494..80540112-chr5:80595834..80598511,2	MCF-7	breast:
40	chr5:80535144..80535935-chr5:80595128..80595851,2	MCF-7	breast:
41	chr5:80531823..80533359-chr5:80535137..80538128,2	K562	blood:
42	chr5:80559870..80562227-chr5:80563019..80565306,2	MCF-7	breast:
43	chr5:80562714..80564322-chr5:80589942..80591670,2	K562	blood:
44	chr5:80590488..80592952-chr5:80595910..80597883,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOT12-1	chr5:80540563-80540598	NONHSAT102444
2	lnc-ACOT12-8	chr5:80528125-80529661	NONHSAT102437
3	lnc-ACOT12-8	chr5:80521955-80529138	NONHSAT102436
4	lnc-ACOT12-6	chr5:80569140-80570930	ucscGeneNc_uc003khg_1
5	lnc-ACOT12-1	chr5:80534255-80535179	NONHSAT102444

No data

Variant related genes	Relation type
ZCCHC9	TF binding region
ENSG00000248794	TF binding region
CKMT2-AS1	TF binding region
CKMT2	TF binding region
ZCCHC9	CpG island
ENSG00000248794	CpG island
CKMT2-AS1	CpG island
CKMT2	CpG island
ENSG00000131730	chromatin interactions
ENSG00000143013	chromatin interactions
ENSG00000248794	chromatin interactions
ENSG00000169252	chromatin interactions
ENSG00000247572	chromatin interactions
ENSG00000131732	chromatin interactions

Extended variants
information (count: 3616 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3616 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7732064	chr5:80503528-80503529	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73130845	chr5:80503567-80503568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554654878	chr5:80503575-80503576	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193248840	chr5:80503589-80503590	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7712754	chr5:80503596-80503597	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs553387110	chr5:80503615-80503616	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576400311	chr5:80503623-80503624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78760882	chr5:80503630-80503631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73768042	chr5:80503647-80503648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17294084	chr5:80503676-80503677	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs558265015	chr5:80503716-80503717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561523399	chr5:80503750-80503751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373804002	chr5:80503821-80503822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530251748	chr5:80503848-80503849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547093238	chr5:80503861-80503862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116961679	chr5:80503871-80503872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147248183	chr5:80503876-80503877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375063383	chr5:80503926-80503927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369372039	chr5:80503960-80503961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569009894	chr5:80504005-80504006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538142805	chr5:80504009-80504010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548128529	chr5:80504013-80504014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568232102	chr5:80504057-80504058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533671117	chr5:80504070-80504071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553415497	chr5:80504123-80504124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576436759	chr5:80504185-80504186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185703808	chr5:80504191-80504192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372222879	chr5:80504212-80504213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556120453	chr5:80504213-80504214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149879297	chr5:80504222-80504223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374914135	chr5:80504231-80504232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61759867	chr5:80504257-80504258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372162559	chr5:80504268-80504269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11957258	chr5:80504282-80504283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs575887895	chr5:80504287-80504288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs16878536	chr5:80504288-80504289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373058229	chr5:80504292-80504293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376291498	chr5:80504297-80504298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551821872	chr5:80504301-80504302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575060228	chr5:80504312-80504313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188869653	chr5:80504328-80504329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559712513	chr5:80504354-80504355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71000806	chr5:80504375-80504376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540746856	chr5:80504401-80504402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560530759	chr5:80504402-80504403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551419905	chr5:80504431-80504432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10805937	chr5:80504440-80504441	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539614823	chr5:80504476-80504477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139747197	chr5:80504493-80504494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369394267	chr5:80504533-80504534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80464200-80528400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:80465200-80528200	Weak transcription	Ovary	ovary
3	chr5:80466000-80512600	Weak transcription	Gastric	stomach
4	chr5:80485200-80516200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:80491000-80505600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr5:80491000-80508600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:80491000-80520200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:80491000-80528400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr5:80491200-80504600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr5:80491200-80505600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr5:80491200-80530000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr5:80491400-80505400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr5:80491400-80528400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:80491600-80505400	Weak transcription	NHLF	lung
15	chr5:80491600-80505800	Weak transcription	Brain Angular Gyrus	brain
16	chr5:80491800-80504800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr5:80491800-80505000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr5:80492000-80510800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr5:80492000-80528600	Weak transcription	Left Ventricle	heart
20	chr5:80496400-80511000	Strong transcription	Primary T cells from cord blood	blood
21	chr5:80496600-80513200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr5:80497000-80517000	Weak transcription	Right Atrium	heart
23	chr5:80498000-80528800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr5:80498200-80504800	Weak transcription	Brain Substantia Nigra	brain
25	chr5:80498800-80530000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr5:80499800-80505200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr5:80499800-80505800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr5:80500000-80507200	Weak transcription	Fetal Intestine Small	intestine
29	chr5:80501000-80508800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:80501400-80505000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr5:80502000-80511400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr5:80502200-80503800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr5:80502200-80506000	Strong transcription	HepG2	liver
34	chr5:80502400-80510600	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr5:80502600-80503800	Strong transcription	Brain Hippocampus Middle	brain
36	chr5:80502600-80508600	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr5:80502800-80503800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr5:80503200-80506000	Strong transcription	Adipose Nuclei	Adipose
39	chr5:80503200-80506600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:80503400-80503800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:80503800-80504600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr5:80503800-80504600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr5:80503800-80505400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:80503800-80505400	Weak transcription	Brain Hippocampus Middle	brain
45	chr5:80503800-80507800	Weak transcription	Fetal Brain Female	brain
46	chr5:80504400-80512200	Weak transcription	Right Ventricle	heart
47	chr5:80504600-80505400	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr5:80504600-80505400	Enhancers	NHEK	skin
49	chr5:80504600-80505600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:80504600-80505600	Weak transcription	Brain Anterior Caudate	brain

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