Variant report

Variant	nsv883040
Chromosome Location	chr5:151471642-151596273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:367)
Chromatin interactive
region (count:61)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:151496451-151496467	K562	blood:	n/a	n/a
2	BACH1	chr5:151531635-151531831	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr5:151472243-151472406	GM12878	blood:	n/a	chr5:151472314-151472325
4	BHLHE40	chr5:151522455-151522770	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:151522443-151522736	K562	blood:	n/a	n/a
6	BRCA1	chr5:151522462-151522623	GM12878	blood:	n/a	n/a
7	BRCA1	chr5:151494104-151494108	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr5:151559492-151559699	K562	blood:	n/a	n/a
9	CBX3	chr5:151559476-151559719	K562	blood:	n/a	n/a
10	CEBPB	chr5:151593039-151593101	H1-hESC	embryonic stem cell:	n/a	chr5:151593067-151593078
11	CEBPB	chr5:151565117-151565415	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:151565070-151565491	MCF-7	breast:	n/a	n/a
13	CEBPB	chr5:151505398-151505598	H1-hESC	embryonic stem cell:	n/a	chr5:151505476-151505484
14	CEBPB	chr5:151560988-151561558	MCF-7	breast:	n/a	chr5:151561253-151561264
15	CEBPB	chr5:151592928-151593198	K562	blood:	n/a	chr5:151593067-151593078
16	CEBPB	chr5:151592933-151593211	A549	lung:	n/a	chr5:151593067-151593078
17	CEBPB	chr5:151556672-151556902	HepG2	liver:	n/a	chr5:151556771-151556782
18	CEBPB	chr5:151565144-151565281	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:151481747-151482004	HepG2	liver:	n/a	chr5:151481862-151481873
20	CEBPB	chr5:151592919-151593237	IMR90	lung:	n/a	chr5:151593067-151593078
21	CEBPB	chr5:151481822-151481973	IMR90	lung:	n/a	chr5:151481862-151481873
22	CEBPB	chr5:151561175-151561371	A549	lung:	n/a	chr5:151561253-151561264
23	CEBPB	chr5:151560889-151561532	MCF-7	breast:	n/a	chr5:151561253-151561264
24	CEBPB	chr5:151565171-151565283	K562	blood:	n/a	n/a
25	CEBPB	chr5:151561155-151561390	HepG2	liver:	n/a	chr5:151561253-151561264
26	CEBPB	chr5:151556706-151556863	H1-hESC	embryonic stem cell:	n/a	chr5:151556771-151556782
27	CEBPB	chr5:151571729-151571772	A549	lung:	n/a	n/a
28	CEBPB	chr5:151565033-151565499	MCF-7	breast:	n/a	n/a
29	CEBPB	chr5:151592910-151593235	HepG2	liver:	n/a	chr5:151593067-151593078
30	CEBPD	chr5:151522412-151522807	K562	blood:	n/a	n/a
31	CTCF	chr5:151522520-151522670	GM12875	blood:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
32	CTCF	chr5:151544540-151544690	GM12872	blood:	n/a	chr5:151544616-151544625
33	CTCF	chr5:151522540-151522690	HRPEpiC	eye:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
34	CTCF	chr5:151522560-151522710	GM12865	blood:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
35	CTCF	chr5:151522520-151522670	GM12870	blood:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
36	CTCF	chr5:151544460-151544610	GM12866	blood:	n/a	n/a
37	CTCF	chr5:151544463-151544773	H1-hESC	embryonic stem cell:	n/a	chr5:151544616-151544625
38	CTCF	chr5:151544603-151544626	Medullo	brain:	n/a	chr5:151544616-151544625
39	CTCF	chr5:151544560-151544660	GM12878	blood:	n/a	chr5:151544616-151544625
40	CTCF	chr5:151522458-151522740	MCF-7	breast:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
41	CTCF	chr5:151550099-151550188	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:151544520-151544670	Caco-2	colon:	n/a	chr5:151544616-151544625
43	CTCF	chr5:151522520-151522670	MCF-7	breast:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
44	CTCF	chr5:151544580-151544730	Caco-2	colon:	n/a	chr5:151544616-151544625
45	CTCF	chr5:151522452-151522773	MCF-7	breast:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
46	CTCF	chr5:151522400-151522833	A549	lung:	n/a	chr5:151522589-151522607 chr5:151522584-151522605 chr5:151522590-151522606 chr5:151522591-151522604
47	CTCF	chr5:151523160-151523310	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr5:151523000-151523150	GM12865	blood:	n/a	n/a
49	CTCF	chr5:151523007-151523111	GM13977	blood:	n/a	n/a
50	CTCF	chr5:151544540-151544690	HEK293	kidney:	n/a	chr5:151544616-151544625

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:151557407-151557457	AG04449	skin:	fetal
2	chr5:151557407-151557457	AG04449	skin:	fetal
3	chr5:151504455-151504505	IMR90	lung:	fetal
4	chr5:151504455-151504505	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:151486992-151487042	NB4	blood:	n/a
6	chr5:151551810-151551860	HMEC	breast:	n/a
7	chr5:151557407-151557457	HCT-116	colon:	n/a
8	chr5:151551810-151551860	MCF-7	breast:	n/a
9	chr5:151486992-151487042	HUVEC	blood vessel:	n/a
10	chr5:151504455-151504505	SKMC	muscle:	n/a
11	chr5:151557407-151557457	GM19239	blood:	n/a
12	chr5:151551810-151551860	T-47D	breast:	n/a
13	chr5:151476553-151476603	ECC-1	luminal epithelium:	n/a
14	chr5:151551810-151551860	H1-hESC	embryonic stem cell:	embryo
15	chr5:151504425-151504475	IMR90	lung:	fetal
16	chr5:151476553-151476603	HUVEC	blood vessel:	n/a
17	chr5:151504425-151504475	H1-hESC	embryonic stem cell:	embryo
18	chr5:151476553-151476603	GM12878	blood:	n/a
19	chr5:151486992-151487042	AG04450	lung:	fetal
20	chr5:151504425-151504475	HL-60	blood:	n/a
21	chr5:151476553-151476603	CMK	blood:	n/a
22	chr5:151476553-151476603	SK-N-MC	brain:	n/a
23	chr5:151486992-151487042	Caco-2	colon:	n/a
24	chr5:151476553-151476603	NB4	blood:	n/a
25	chr5:151557407-151557457	IMR90	lung:	fetal
26	chr5:151504425-151504475	MCF-7	breast:	n/a
27	chr5:151476553-151476603	K562	blood:	n/a
28	chr5:151504425-151504475	PrEC	prostate:	n/a
29	chr5:151486992-151487042	GM12892	blood:	n/a
30	chr5:151504455-151504505	HCPEpiC	choroid plexus:	n/a
31	chr5:151504425-151504475	HIPEpiC	eye:	n/a
32	chr5:151476553-151476603	GM12892	blood:	n/a
33	chr5:151486992-151487042	MCF10A-Er-Src	breast:	n/a
34	chr5:151551810-151551860	GM12878	blood:	n/a
35	chr5:151486992-151487042	LNCaP	prostate:	n/a
36	chr5:151486992-151487042	ECC-1	luminal epithelium:	n/a
37	chr5:151504425-151504475	SKMC	muscle:	n/a
38	chr5:151504455-151504505	MCF10A-Er-Src	breast:	n/a
39	chr5:151476553-151476603	SKMC	muscle:	n/a
40	chr5:151486992-151487042	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:151504455-151504505	AG04449	skin:	fetal
42	chr5:151476553-151476603	SAEC	small airway:	n/a
43	chr5:151476553-151476603	AG04449	skin:	fetal
44	chr5:151551810-151551860	AG04449	skin:	fetal
45	chr5:151551810-151551860	HNPCEpiC	eye:	n/a
46	chr5:151476553-151476603	GM19239	blood:	n/a
47	chr5:151504455-151504505	K562	blood:	n/a
48	chr5:151486992-151487042	SAEC	small airway:	n/a
49	chr5:151476553-151476603	PFSK-1	brain:	n/a
50	chr5:151486992-151487042	HEEpiC	esophagus:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:151204677..151205872-chr5:151522532..151523052,3	MCF-7	breast:
2	chr5:151509815..151512281-chr5:151517345..151519719,2	MCF-7	breast:
3	chr5:151471064..151473858-chr5:151493966..151496756,2	MCF-7	breast:
4	chr5:151471064..151473858-chr5:151493966..151496756,2	MCF-7	breast:
5	chr5:151520907..151523004-chr5:151546531..151548901,2	K562	blood:
6	chr5:151523917..151524489-chr5:151572860..151573489,2	MCF-7	breast:
7	chr5:151523242..151525301-chr5:151526406..151528109,3	MCF-7	breast:
8	chr5:151471420..151474359-chr5:151488636..151491340,2	K562	blood:
9	chr5:151204595..151205535-chr5:151522142..151523020,2	K562	blood:
10	chr5:151523912..151524811-chr5:151568652..151569394,2	MCF-7	breast:
11	chr5:151513671..151516215-chr5:151517705..151520059,3	K562	blood:
12	chr5:151556665..151558861-chr5:151565595..151567114,2	MCF-7	breast:
13	chr5:151303407..151303946-chr5:151522386..151523026,2	MCF-7	breast:
14	chr5:151523874..151524765-chr5:151668143..151669088,3	MCF-7	breast:
15	chr5:151523886..151524850-chr5:151572559..151573494,21	MCF-7	breast:
16	chr5:151471420..151474359-chr5:151488636..151491340,2	K562	blood:
17	chr5:151580655..151582436-chr5:151582503..151585024,2	MCF-7	breast:
18	chr5:151560448..151561140-chr5:151651042..151651572,2	MCF-7	breast:
19	chr5:151303110..151303991-chr5:151522441..151523040,2	MCF-7	breast:
20	chr5:151565435..151567795-chr5:151572722..151574311,2	MCF-7	breast:
21	chr5:151491359..151493092-chr5:151503050..151505750,2	K562	blood:
22	chr5:151160169..151163153-chr5:151522448..151524598,2	K562	blood:
23	chr5:151523886..151524850-chr5:151572559..151573494,21	MCF-7	breast:
24	chr5:151523874..151524433-chr5:151668425..151669088,2	MCF-7	breast:
25	chr5:151524627..151526976-chr5:151527410..151529295,2	K562	blood:
26	chr5:151522076..151522840-chr5:151650800..151651429,3	MCF-7	breast:
27	chr5:151204736..151205618-chr5:151521905..151522989,3	MCF-7	breast:
28	chr5:151513919..151516215-chr5:151517657..151519224,2	K562	blood:
29	chr5:151524627..151526976-chr5:151527410..151529295,2	K562	blood:
30	chr5:151572609..151573576-chr5:151667738..151668966,3	MCF-7	breast:
31	chr5:151204659..151205617-chr5:151544194..151544853,2	MCF-7	breast:
32	chr5:151523917..151524489-chr5:151572860..151573489,2	MCF-7	breast:
33	chr5:151497548..151500233-chr5:151502295..151503821,2	MCF-7	breast:
34	chr5:151150191..151152730-chr5:151495520..151497974,2	MCF-7	breast:
35	chr5:151484112..151485634-chr5:151524575..151526562,2	K562	blood:
36	chr5:151565435..151567795-chr5:151572722..151574311,2	MCF-7	breast:
37	chr5:151565369..151567098-chr5:151571552..151573119,2	MCF-7	breast:
38	chr5:151522014..151522696-chr5:151729134..151730175,3	MCF-7	breast:
39	chr5:151523925..151524850-chr5:151572610..151573431,6	MCF-7	breast:
40	chr5:151484112..151485634-chr5:151524575..151526562,2	K562	blood:
41	chr5:151523912..151524811-chr5:151568652..151569394,2	MCF-7	breast:
42	chr5:151509815..151512281-chr5:151517345..151519719,2	MCF-7	breast:
43	chr5:151538414..151540360-chr5:151542767..151545602,2	MCF-7	breast:
44	chr5:151549711..151550252-chr5:151650725..151651679,2	MCF-7	breast:
45	chr5:151523879..151524822-chr5:151665463..151666473,3	MCF-7	breast:
46	chr5:151513671..151516215-chr5:151517705..151520059,3	K562	blood:
47	chr5:151513919..151516215-chr5:151517657..151519224,2	K562	blood:
48	chr5:151150270..151152142-chr5:151561847..151563500,2	MCF-7	breast:
49	chr19:49651763..49653325-chr5:151564551..151567335,2	MCF-7	breast:
50	chr5:151542542..151543442-chr6:76603129..76603708,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-G3BP1-4	chr5:151575009-151575091	ENSG00000254226
2	lnc-G3BP1-6	chr5:151554478-151554558	ucscGeneNc_uc003luu_1
3	lnc-G3BP1-4	chr5:151574285-151574365	XLOC_004607
4	lnc-G3BP1-6	chr5:151555195-151555284	ucscGeneNc_uc003luu_1
5	lnc-G3BP1-6	chr5:151591017-151591053	ucscGeneNc_uc003luu_1
6	lnc-G3BP1-4	chr5:151575002-151575091	XLOC_004607

No data

Variant related genes	Relation type
ENSG00000254226	TF binding region
ENSG00000254226	CpG island
ENSG00000145907	chromatin interactions
ENSG00000177380	chromatin interactions
ENSG00000177556	chromatin interactions

Extended variants
information (count: 3518 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3518 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10477008	chr5:151471642-151471643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145428492	chr5:151471657-151471658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533772732	chr5:151471675-151471676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs499767	chr5:151471748-151471749	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534607	chr5:151471753-151471754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs545414722	chr5:151471759-151471760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557345185	chr5:151471785-151471786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549873731	chr5:151471800-151471801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575559547	chr5:151471837-151471838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76840974	chr5:151471847-151471848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386405337	chr5:151471848-151471849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397807311	chr5:151471853-151471854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543270507	chr5:151471864-151471865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561444021	chr5:151471869-151471870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535232419	chr5:151471949-151471950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528670876	chr5:151472011-151472012	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7737106	chr5:151472048-151472049	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189782266	chr5:151472056-151472057	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145232575	chr5:151472114-151472115	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550272580	chr5:151472123-151472124	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115024323	chr5:151472162-151472163	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114072336	chr5:151472165-151472166	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs303989	chr5:151472189-151472190	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs557075112	chr5:151472232-151472233	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566685655	chr5:151472237-151472238	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74656275	chr5:151472275-151472276	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558830822	chr5:151472343-151472344	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75788569	chr5:151472357-151472358	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557504244	chr5:151472391-151472392	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575564999	chr5:151472418-151472419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367622726	chr5:151472435-151472436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79330318	chr5:151472485-151472486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555236115	chr5:151472494-151472495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs303990	chr5:151472553-151472554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533042444	chr5:151472600-151472601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540528186	chr5:151472604-151472605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565098929	chr5:151472638-151472639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532585752	chr5:151472644-151472645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543877992	chr5:151472681-151472682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562474166	chr5:151472703-151472704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs303991	chr5:151472734-151472735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs518297	chr5:151472827-151472828	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566753378	chr5:151472831-151472832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543226172	chr5:151472857-151472858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370396577	chr5:151472894-151472895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528415792	chr5:151472904-151472905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs891164	chr5:151472918-151472919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375249467	chr5:151472934-151472935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367967366	chr5:151473001-151473002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs695205	chr5:151473021-151473022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Parkinson disease	21829596	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151471200-151475800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:151472000-151472200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr5:151472000-151472400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:151472200-151476000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr5:151473200-151474000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:151473200-151474000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:151473200-151474800	Enhancers	Fetal Lung	lung
8	chr5:151473400-151474400	Enhancers	Fetal Kidney	kidney
9	chr5:151474000-151474600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr5:151474200-151474400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:151474400-151475000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:151474800-151475200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:151475000-151475200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:151475200-151475600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:151475200-151476400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:151475600-151477000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:151475600-151477400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr5:151475600-151477800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:151475800-151476200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:151475800-151476600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr5:151475800-151477200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr5:151475800-151477200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:151476000-151477200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:151476000-151477200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:151476200-151476600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:151476400-151476800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr5:151476400-151476800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:151476400-151477200	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr5:151476400-151477400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:151476600-151476800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:151476600-151477400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:151476800-151477600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr5:151476800-151480600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:151480600-151480800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:151480800-151486200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:151483400-151483600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr5:151483400-151484600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:151483800-151486400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr5:151484000-151484400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:151484600-151486200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:151486000-151487400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:151486000-151487400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:151486000-151487400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:151486000-151487600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:151486200-151487000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:151486200-151487400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:151486200-151487800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr5:151486400-151487000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:151486400-151487400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:151486400-151487600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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