Variant report

Variant	nsv881717
Chromosome Location	chr5:60141245-60372582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2159)
CpG islands
(count:1346)
Chromatin interactive
region (count:112)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60314308-60314387	K562	blood:	n/a	chr5:60314370-60314386
2	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
3	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
5	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
6	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
7	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
8	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
9	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
10	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
11	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
12	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
13	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
14	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
16	BATF	chr5:60347149-60347471	GM12878	blood:	n/a	chr5:60347322-60347333 chr5:60347323-60347333
17	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a
19	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
20	BHLHE40	chr5:60273867-60274075	K562	blood:	n/a	n/a
21	BHLHE40	chr5:60168934-60168938	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:60148834-60149083	K562	blood:	n/a	n/a
23	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
24	BHLHE40	chr5:60274319-60275283	K562	blood:	n/a	n/a
25	BRCA1	chr5:60242705-60242764	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:60306630-60306773	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr5:60240930-60241613	K562	blood:	n/a	n/a
28	CBX3	chr5:60251024-60251519	HCT-116	colon:	n/a	n/a
29	CBX3	chr5:60274796-60275180	K562	blood:	n/a	n/a
30	CBX3	chr5:60166733-60166960	K562	blood:	n/a	n/a
31	CBX3	chr5:60289190-60289610	K562	blood:	n/a	n/a
32	CBX3	chr5:60348517-60349283	HCT-116	colon:	n/a	n/a
33	CBX3	chr5:60348580-60349211	HCT-116	colon:	n/a	n/a
34	CBX3	chr5:60231541-60231761	K562	blood:	n/a	n/a
35	CBX3	chr5:60277815-60278245	K562	blood:	n/a	n/a
36	CBX3	chr5:60289206-60289789	K562	blood:	n/a	n/a
37	CBX3	chr5:60274711-60275276	K562	blood:	n/a	n/a
38	CBX3	chr5:60344265-60344917	HCT-116	colon:	n/a	n/a
39	CBX3	chr5:60344262-60344845	HCT-116	colon:	n/a	n/a
40	CBX3	chr5:60351230-60351719	HCT-116	colon:	n/a	n/a
41	CBX3	chr5:60289241-60289660	HCT-116	colon:	n/a	n/a
42	CCNT2	chr5:60273908-60274052	K562	blood:	n/a	n/a
43	CCNT2	chr5:60257762-60257798	K562	blood:	n/a	n/a
44	CCNT2	chr5:60274822-60275307	K562	blood:	n/a	n/a
45	CCNT2	chr5:60241747-60241947	K562	blood:	n/a	n/a
46	CCNT2	chr5:60240705-60241024	K562	blood:	n/a	n/a
47	CCNT2	chr5:60148817-60149120	K562	blood:	n/a	n/a
48	CCNT2	chr5:60336974-60337076	K562	blood:	n/a	n/a
49	CEBPB	chr5:60168749-60169059	IMR90	lung:	n/a	chr5:60168912-60168923
50	CEBPB	chr5:60249109-60249119	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60240952-60241002	HCT-116	colon:	n/a
2	chr5:60240568-60240618	GM12892	blood:	n/a
3	chr5:60241324-60241374	HRCEpiC	kidney:	n/a
4	chr5:60148273-60148323	LNCaP	prostate:	n/a
5	chr5:60240952-60241002	HCT-116	colon:	n/a
6	chr5:60240568-60240618	GM12892	blood:	n/a
7	chr5:60241324-60241374	HRCEpiC	kidney:	n/a
8	chr5:60148273-60148323	LNCaP	prostate:	n/a
9	chr5:60148273-60148323	HEEpiC	esophagus:	n/a
10	chr5:60325493-60325543	AG10803	skin:	n/a
11	chr5:60240952-60241002	HepG2	liver:	n/a
12	chr5:60241324-60241374	HRE	kidney:	n/a
13	chr5:60170058-60170108	HEEpiC	esophagus:	n/a
14	chr5:60240568-60240618	T-47D	breast:	n/a
15	chr5:60187211-60187261	HEK293	kidney:	embryo
16	chr5:60240670-60240720	CMK	blood:	n/a
17	chr5:60240952-60241002	ECC-1	luminal epithelium:	n/a
18	chr5:60240891-60240941	PrEC	prostate:	n/a
19	chr5:60240870-60240920	HNPCEpiC	eye:	n/a
20	chr5:60240952-60241002	GM06990	blood:	n/a
21	chr5:60241324-60241374	HepG2	liver:	n/a
22	chr5:60241424-60241474	IMR90	lung:	fetal
23	chr5:60241424-60241474	SK-N-SH	brain:	n/a
24	chr5:60170058-60170108	HEK293	kidney:	embryo
25	chr5:60240568-60240618	BE2_C	brain:	n/a
26	chr5:60241003-60241053	HIPEpiC	eye:	n/a
27	chr5:60240952-60241002	HCM	heart:	n/a
28	chr5:60240568-60240618	NHDF-neo	bronchial:	n/a
29	chr5:60187211-60187261	HepG2	liver:	n/a
30	chr5:60240670-60240720	ovcar-3	ovarian:	n/a
31	chr5:60241324-60241374	ProgFib	skin:	n/a
32	chr5:60142446-60142496	HEEpiC	esophagus:	n/a
33	chr5:60240926-60240976	ovcar-3	ovarian:	n/a
34	chr5:60346051-60346101	BE2_C	brain:	n/a
35	chr5:60240952-60241002	GM12891	blood:	n/a
36	chr5:60240670-60240720	HepG2	liver:	n/a
37	chr5:60346051-60346101	MCF-7	breast:	n/a
38	chr5:60240817-60240867	Hepatocyte	liver:	n/a
39	chr5:60142446-60142496	SK-N-SH_RA	brain:	n/a
40	chr5:60240568-60240618	PrEC	prostate:	n/a
41	chr5:60325493-60325543	GM06990	blood:	n/a
42	chr5:60240926-60240976	PFSK-1	brain:	n/a
43	chr5:60240926-60240976	Hela-S3	cervix:	n/a
44	chr5:60240938-60240988	HNPCEpiC	eye:	n/a
45	chr5:60240870-60240920	MCF10A-Er-Src	breast:	n/a
46	chr5:60170058-60170108	NHBE	bronchial:	n/a
47	chr5:60240938-60240988	HCT-116	colon:	n/a
48	chr5:60239580-60239630	RPTEC	kidney:	n/a
49	chr5:60325493-60325543	NHDF-neo	bronchial:	n/a
50	chr5:60240838-60240888	BJ	skin:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:60238110..60240722-chr5:60956482..60958434,2	MCF-7	breast:
2	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
3	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
4	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
5	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
6	chr5:60142106..60144527-chr5:60240837..60243388,2	K562	blood:
7	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
8	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
9	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
10	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
11	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
12	chr5:60274623..60276264-chr5:60290570..60293305,2	K562	blood:
13	chr5:60351342..60352964-chr5:60353710..60356675,2	K562	blood:
14	chr5:60150200..60152775-chr5:60153410..60154990,2	MCF-7	breast:
15	chr5:60365711..60368002-chr5:60369594..60371777,2	K562	blood:
16	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
17	chr5:60355470..60357785-chr5:60423437..60426318,2	K562	blood:
18	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
19	chr5:60320010..60322208-chr5:60331308..60333222,2	MCF-7	breast:
20	chr5:60311498..60313138-chr5:60318136..60319841,2	K562	blood:
21	chr5:60254798..60255532-chr5:60954065..60954863,2	K562	blood:
22	chr5:60321206..60323750-chr5:60323786..60326003,2	K562	blood:
23	chr1:156698013..156698560-chr5:60240745..60241454,2	Hela-S3	cervix:
24	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
25	chr5:60355839..60357550-chr5:60458247..60459791,2	MCF-7	breast:
26	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
27	chr5:60234534..60237256-chr5:60239004..60241956,3	K562	blood:
28	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
29	chr19:10314099..10314599-chr5:60155075..60155644,2	Hela-S3	cervix:
30	chr5:60143868..60145505-chr5:60146013..60148610,2	K562	blood:
31	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
32	chr5:60240835..60243505-chr5:60324746..60327313,2	MCF-7	breast:
33	chr5:59995891..59998683-chr5:60261062..60263658,2	K562	blood:
34	chr5:60318175..60320382-chr5:60629060..60630909,2	K562	blood:
35	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
36	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
37	chr5:60199382..60201400-chr5:60201974..60203709,2	MCF-7	breast:
38	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
39	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
40	chr5:60238903..60241711-chr5:60255745..60258195,2	K562	blood:
41	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
42	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
43	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
44	chr5:60324520..60326950-chr5:60332622..60334608,2	K562	blood:
45	chr5:60321206..60323750-chr5:60323786..60326003,2	K562	blood:
46	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
47	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
48	chr5:60334340..60336285-chr5:60341216..60344077,2	K562	blood:
49	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
50	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM6-4	chr5:60368953-60369018	NONHSAT101655
2	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1
3	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1
4	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
5	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655
6	lnc-ERCC8-1	chr5:60162284-60162762	ENSG00000272308.1

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
ELOVL7	TF binding region
ENSG00000272308	TF binding region
ERCC8	TF binding region
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
NDUFAF2	CpG island
ELOVL7	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000224165	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000112977	chromatin interactions
ENSG00000143319	chromatin interactions

Extended variants
information (count: 7957 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7957 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11740632	chr5:60141245-60141246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534990934	chr5:60141246-60141247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548620615	chr5:60141259-60141260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568401630	chr5:60141260-60141261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13171743	chr5:60141286-60141287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376800667	chr5:60141289-60141290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367644061	chr5:60141294-60141295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371500111	chr5:60141295-60141296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs397997938	chr5:60141323-60141324	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs13172273	chr5:60141381-60141382	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537276142	chr5:60141442-60141443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs557130004	chr5:60141447-60141448	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575773903	chr5:60141465-60141466	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75800468	chr5:60141467-60141468	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs376635297	chr5:60141508-60141509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369027517	chr5:60141509-60141510	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs568963230	chr5:60141510-60141511	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539587985	chr5:60141525-60141526	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs368414818	chr5:60141532-60141533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs574532869	chr5:60141565-60141566	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558574991	chr5:60141612-60141613	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs571966855	chr5:60141613-60141614	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147589775	chr5:60141617-60141618	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561201466	chr5:60141672-60141673	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574760063	chr5:60141684-60141685	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535669585	chr5:60141688-60141689	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs543686436	chr5:60141707-60141708	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563462601	chr5:60141760-60141761	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs141921741	chr5:60141836-60141837	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552414337	chr5:60141843-60141844	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs189304592	chr5:60141860-60141861	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs528513404	chr5:60141887-60141888	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs180721206	chr5:60141888-60141889	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs568461096	chr5:60141894-60141895	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs541345128	chr5:60141938-60141939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531102476	chr5:60141970-60141971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs550822668	chr5:60141973-60141974	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs72757159	chr5:60141988-60141989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs66982655	chr5:60141989-60141990	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570713341	chr5:60142013-60142014	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539993292	chr5:60142040-60142041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371881276	chr5:60142082-60142083	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113604220	chr5:60142208-60142209	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540197750	chr5:60142321-60142322	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565752067	chr5:60142354-60142355	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs75807973	chr5:60142396-60142397	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs80237771	chr5:60142397-60142398	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs564930489	chr5:60142424-60142425	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs576863927	chr5:60142446-60142447	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs375179907	chr5:60142481-60142482	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2419 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60141000-60141600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:60141200-60148000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:60142200-60142800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr5:60144400-60144600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:60146800-60147800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:60147600-60149200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr5:60147800-60148000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:60147800-60149000	Enhancers	Fetal Intestine Small	intestine
9	chr5:60147800-60149000	Enhancers	Placenta	Placenta
10	chr5:60147800-60149200	Enhancers	Fetal Intestine Large	intestine
11	chr5:60147800-60149600	Enhancers	K562	blood
12	chr5:60148000-60148200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:60148000-60148800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:60148000-60149000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:60148000-60149200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr5:60148000-60149400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:60148200-60148800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr5:60148200-60149000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr5:60148200-60149200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:60148400-60148800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr5:60148400-60149000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:60148400-60149000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr5:60148400-60149600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:60149000-60149200	Enhancers	HMEC	breast
25	chr5:60149000-60149600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:60149200-60150400	Weak transcription	Fetal Intestine Large	intestine
27	chr5:60149200-60151400	Weak transcription	HMEC	breast
28	chr5:60149400-60152000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:60149600-60150600	Weak transcription	K562	blood
30	chr5:60149600-60151600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:60150600-60150800	Enhancers	Fetal Intestine Large	intestine
32	chr5:60150600-60150800	Enhancers	K562	blood
33	chr5:60151400-60152600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:60151400-60152600	Enhancers	HMEC	breast
35	chr5:60151600-60152000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:60151600-60152000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:60151600-60152400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:60151800-60152200	Enhancers	Hela-S3	cervix
39	chr5:60151800-60152200	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr5:60151800-60152400	Enhancers	NHEK	skin
41	chr5:60152000-60152200	Enhancers	NHDF-Ad	bronchial
42	chr5:60152000-60152400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr5:60152200-60152400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr5:60162600-60166800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:60165400-60166600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:60165600-60166600	Weak transcription	Primary B cells from cord blood	blood
47	chr5:60165800-60167400	Weak transcription	Primary T cells from cord blood	blood
48	chr5:60165800-60167800	Weak transcription	Esophagus	oesophagus
49	chr5:60166600-60166800	ZNF genes & repeats	Primary B cells from cord blood	blood
50	chr5:60166600-60167200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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