Variant report

Variant	nsv1031453
Chromosome Location	chr5:119843593-120393038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2786)
CpG islands
(count:1588)
Chromatin interactive
region (count:90)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2786 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120321426-120321583	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:119845695-119846337	K562	blood:	n/a	n/a
3	ARID3A	chr5:119848349-119848986	K562	blood:	n/a	n/a
4	ARID3A	chr5:119853390-119853829	K562	blood:	n/a	n/a
5	ATF1	chr5:120192153-120192218	K562	blood:	n/a	n/a
6	ATF1	chr5:119899838-119899993	K562	blood:	n/a	n/a
7	ATF1	chr5:119848381-119848909	K562	blood:	n/a	n/a
8	ATF1	chr5:119853689-119853917	K562	blood:	n/a	n/a
9	ATF2	chr5:120042574-120042977	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:120032153-120033315	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:120031373-120031760	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:120033417-120033942	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:120042500-120043085	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr5:119847523-119848070	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:120030827-120031258	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr5:119848349-119848681	K562	blood:	n/a	n/a
17	BACH1	chr5:120026709-120027291	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:120179170-120179494	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:119959300-119959328	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:120023318-120023332	K562	blood:	n/a	n/a
21	BHLHE40	chr5:119991637-119991644	K562	blood:	n/a	n/a
22	BHLHE40	chr5:119845855-119845896	K562	blood:	n/a	n/a
23	BHLHE40	chr5:120355613-120355776	K562	blood:	n/a	n/a
24	BRCA1	chr5:120039223-120039493	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr5:120188276-120188363	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr5:119974391-119974481	GM12878	blood:	n/a	n/a
27	BRCA1	chr5:119940521-119941137	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr5:120289176-120289482	K562	blood:	n/a	n/a
29	CBX3	chr5:119848317-119849007	K562	blood:	n/a	n/a
30	CCNT2	chr5:119927724-119927859	K562	blood:	n/a	n/a
31	CCNT2	chr5:119852471-119852671	K562	blood:	n/a	n/a
32	CCNT2	chr5:120010812-120011012	K562	blood:	n/a	n/a
33	CCNT2	chr5:119891204-119891275	K562	blood:	n/a	n/a
34	CCNT2	chr5:119845998-119846328	K562	blood:	n/a	chr5:119846139-119846159
35	CCNT2	chr5:119868130-119868256	K562	blood:	n/a	n/a
36	CCNT2	chr5:119848506-119848843	K562	blood:	n/a	n/a
37	CEBPB	chr5:120254719-120255091	A549	lung:	n/a	n/a
38	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
39	CEBPB	chr5:120254718-120255097	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
41	CEBPB	chr5:119873912-119874713	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:120208105-120208305	HepG2	liver:	n/a	chr5:120208234-120208245 chr5:120208236-120208247 chr5:120208236-120208245
43	CEBPB	chr5:119848584-119849065	K562	blood:	n/a	n/a
44	CEBPB	chr5:120315991-120316249	HepG2	liver:	n/a	chr5:120316125-120316136
45	CEBPB	chr5:120052477-120052610	K562	blood:	n/a	n/a
46	CEBPB	chr5:119854898-119855148	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:120218188-120218329	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:120124235-120124536	K562	blood:	n/a	n/a
49	CEBPB	chr5:119857162-119857394	HepG2	liver:	n/a	chr5:119857273-119857284
50	CEBPB	chr5:119984469-119984716	HepG2	liver:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120081741-120081791	A549	lung:	n/a
2	chr5:120040283-120040333	SK-N-SH_RA	brain:	n/a
3	chr5:120081741-120081791	A549	lung:	n/a
4	chr5:120040283-120040333	SK-N-SH_RA	brain:	n/a
5	chr5:120040283-120040333	HIPEpiC	eye:	n/a
6	chr5:120097654-120097704	GM19239	blood:	n/a
7	chr5:119942454-119942504	SK-N-SH	brain:	n/a
8	chr5:119942454-119942504	HEEpiC	esophagus:	n/a
9	chr5:120115250-120115300	AG09309	skin:	n/a
10	chr5:120188118-120188168	HL-60	blood:	n/a
11	chr5:120038247-120038297	HUVEC	blood vessel:	n/a
12	chr5:120038342-120038392	NB4	blood:	n/a
13	chr5:120018164-120018214	SK-N-SH_RA	brain:	n/a
14	chr5:120097654-120097704	LNCaP	prostate:	n/a
15	chr5:120272625-120272675	HRCEpiC	kidney:	n/a
16	chr5:120272625-120272675	HNPCEpiC	eye:	n/a
17	chr5:120167319-120167369	HCPEpiC	choroid plexus:	n/a
18	chr5:119846291-119846341	HNPCEpiC	eye:	n/a
19	chr5:119952679-119952729	ovcar-3	ovarian:	n/a
20	chr5:119951527-119951577	Hela-S3	cervix:	n/a
21	chr5:120188118-120188168	HUVEC	blood vessel:	n/a
22	chr5:119852385-119852435	AG09309	skin:	n/a
23	chr5:119852385-119852435	GM19239	blood:	n/a
24	chr5:120192115-120192165	AoSMC	blood vessel:	n/a
25	chr5:120081741-120081791	RPTEC	kidney:	n/a
26	chr5:120167319-120167369	HRE	kidney:	n/a
27	chr5:120097654-120097704	HIPEpiC	eye:	n/a
28	chr5:119951527-119951577	Jurkat	blood:	n/a
29	chr5:120188118-120188168	HRE	kidney:	n/a
30	chr5:120038247-120038297	NT2-D1	testis:	n/a
31	chr5:120191823-120191873	HCPEpiC	choroid plexus:	n/a
32	chr5:120272574-120272624	Hela-S3	cervix:	n/a
33	chr5:120115250-120115300	NB4	blood:	n/a
34	chr5:120038342-120038392	SK-N-MC	brain:	n/a
35	chr5:119942454-119942504	HRCEpiC	kidney:	n/a
36	chr5:120272574-120272624	RPTEC	kidney:	n/a
37	chr5:119951527-119951577	AG04449	skin:	fetal
38	chr5:120026632-120026682	GM12878	blood:	n/a
39	chr5:120191823-120191873	HCF	heart:	n/a
40	chr5:119846291-119846341	NHBE	bronchial:	n/a
41	chr5:120040283-120040333	HepG2	liver:	n/a
42	chr5:119864497-119864547	NH-A	brain:	n/a
43	chr5:120167415-120167465	HRPEpiC	eye:	n/a
44	chr5:120040283-120040333	HRE	kidney:	n/a
45	chr5:119852385-119852435	SK-N-SH_RA	brain:	n/a
46	chr5:119952679-119952729	HCF	heart:	n/a
47	chr5:120191823-120191873	SK-N-SH	brain:	n/a
48	chr5:120191823-120191873	PrEC	prostate:	n/a
49	chr5:120018164-120018214	AG09309	skin:	n/a
50	chr5:120097654-120097704	NHBE	bronchial:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
2	chr5:120182804..120185937-chr5:120188813..120191326,3	K562	blood:
3	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
4	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
5	chr5:119797915..119802369-chr5:119845575..119850142,8	K562	blood:
6	chr5:119851956..119853481-chr5:119862285..119864209,2	K562	blood:
7	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
8	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:
9	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
10	chr5:119849515..119851535-chr5:119903167..119905944,2	K562	blood:
11	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
12	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
13	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
14	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
15	chr5:119926337..119929229-chr5:119929732..119932370,2	K562	blood:
16	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
17	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
18	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
19	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
20	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
21	chr5:119799024..119803543-chr5:119846360..119850142,7	K562	blood:
22	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
23	chr5:119801016..119803100-chr5:119851238..119853983,3	K562	blood:
24	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
25	chr5:119852123..119854010-chr5:120038446..120041236,2	K562	blood:
26	chr5:119799492..119801330-chr5:119860595..119862492,2	K562	blood:
27	chr5:119858416..119860878-chr5:119871767..119873808,2	K562	blood:
28	chr5:120193977..120195872-chr5:120199617..120202112,2	K562	blood:
29	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
30	chr5:119851956..119854339-chr5:119862015..119863785,2	K562	blood:
31	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:
32	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
33	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
34	chr5:120009986..120011754-chr5:120014103..120015876,2	K562	blood:
35	chr5:119847102..119848643-chr5:119877942..119880653,2	K562	blood:
36	chr5:120211985..120214324-chr5:120217571..120220442,2	K562	blood:
37	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
38	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
39	chr5:119848832..119850459-chr5:119850972..119852496,2	K562	blood:
40	chr5:119852641..119855403-chr5:119858663..119861465,3	K562	blood:
41	chr5:119848883..119851465-chr5:119858913..119862355,3	K562	blood:
42	chr5:119991478..119992421-chr5:120138412..120139232,3	MCF-7	breast:
43	chr5:119991257..119992549-chr5:121285272..121286241,6	MCF-7	breast:
44	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
45	chr5:119851956..119854339-chr5:119862015..119863785,2	K562	blood:
46	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
47	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
48	chr5:119891736..119894093-chr5:119898854..119902222,3	K562	blood:
49	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
50	chr5:119848832..119850459-chr5:119850972..119852496,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-1	chr5:120125649-120126473	XLOC_004528
2	lnc-PRR16-1	chr5:120115791-120115896	XLOC_004528
3	lnc-LOX-9	chr5:119993772-119994066	NONHSAT103445
4	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
5	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528
6	lnc-PRR16-1	chr5:120118132-120118267	XLOC_004528
7	lnc-PRR16-1	chr5:120116913-120117106	XLOC_004528
8	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528
9	lnc-PRR16-1	chr5:120115735-120115896	XLOC_004528
10	lnc-PRR16-1	chr5:120109041-120109070	XLOC_004528
11	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
12	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450

No data

Variant related genes	Relation type
ENSG00000270741	TF binding region
ENSG00000251135	TF binding region
RNU4-69P	TF binding region
PRR16	TF binding region
ENSG00000248853	TF binding region
ENSG00000248927	TF binding region
ENSG00000270741	CpG island
ENSG00000251135	CpG island
RNU4-69P	CpG island
PRR16	CpG island
ENSG00000248853	CpG island
ENSG00000248927	CpG island
ENSG00000151304	chromatin interactions
ENSG00000222609	chromatin interactions
ENSG00000184838	chromatin interactions
PSIP1	miRNA target sites
UAP1	miRNA target sites

Extended variants
information (count: 18824 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:18824 , 50 per page) page: 1 2 3 4 5 6 7 ... 377

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543146135	chr5:119843653-119843654	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77016475	chr5:119843661-119843662	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73264192	chr5:119843716-119843717	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs149293336	chr5:119843727-119843728	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76501260	chr5:119843729-119843730	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538075598	chr5:119843750-119843751	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541606702	chr5:119843756-119843757	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9327146	chr5:119843757-119843758	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs180827525	chr5:119843766-119843767	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548693576	chr5:119843831-119843832	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550355290	chr5:119843867-119843868	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564150800	chr5:119843887-119843888	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144562246	chr5:119843894-119843895	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369175522	chr5:119843931-119843932	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532789763	chr5:119843977-119843978	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552865025	chr5:119844038-119844039	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139406633	chr5:119844042-119844043	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185103630	chr5:119844055-119844056	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368968144	chr5:119844057-119844058	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76189361	chr5:119844065-119844066	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568623910	chr5:119844101-119844102	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142703568	chr5:119844106-119844107	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146032169	chr5:119844119-119844120	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139786939	chr5:119844143-119844144	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539429203	chr5:119844147-119844148	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534436372	chr5:119844149-119844150	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552882276	chr5:119844165-119844166	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572814165	chr5:119844275-119844276	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs189294839	chr5:119844280-119844281	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs561546563	chr5:119844304-119844305	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs575338920	chr5:119844305-119844306	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544342751	chr5:119844314-119844315	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181634815	chr5:119844317-119844318	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs13360299	chr5:119844351-119844352	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142072266	chr5:119844375-119844376	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs151160911	chr5:119844382-119844383	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs139113223	chr5:119844389-119844390	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs185967678	chr5:119844401-119844402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548860541	chr5:119844434-119844435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568677973	chr5:119844466-119844467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373867802	chr5:119844562-119844563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537081668	chr5:119844599-119844600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551081501	chr5:119844654-119844655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570841582	chr5:119844657-119844658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539886057	chr5:119844658-119844659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190338410	chr5:119844661-119844662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10064623	chr5:119844663-119844664	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs147943413	chr5:119844671-119844672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367595710	chr5:119844682-119844683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575426148	chr5:119844700-119844701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2002 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119818200-119845600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:119834400-119843600	Weak transcription	HSMMtube	muscle
3	chr5:119836400-119852400	Weak transcription	HSMM	muscle
4	chr5:119838800-119843600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr5:119839800-119879800	Weak transcription	Psoas Muscle	Psoas
6	chr5:119842400-119844000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:119842400-119844000	Enhancers	Osteobl	bone
8	chr5:119842600-119843800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr5:119842600-119852400	Weak transcription	Aorta	Aorta
10	chr5:119842800-119843600	Weak transcription	K562	blood
11	chr5:119842800-119844200	Enhancers	Fetal Lung	lung
12	chr5:119843000-119844000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:119843000-119844000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:119843000-119844200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr5:119843000-119844400	Flanking Active TSS	NHDF-Ad	bronchial
16	chr5:119843200-119843800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:119843200-119844200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:119843200-119844400	Enhancers	NHLF	lung
19	chr5:119843400-119843800	Enhancers	Dnd41	blood
20	chr5:119843400-119844800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr5:119843400-119845200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:119843400-119848000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr5:119843600-119843800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:119843600-119843800	Enhancers	HSMMtube	muscle
25	chr5:119843600-119844000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:119843600-119844000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:119843600-119844000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr5:119843600-119844200	Enhancers	K562	blood
29	chr5:119843600-119844400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr5:119843600-119844600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr5:119843600-119845200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr5:119843600-119845200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:119843600-119845400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr5:119843800-119844200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr5:119843800-119844200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr5:119843800-119846200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:119844000-119845000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:119844000-119845000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:119844000-119845800	Weak transcription	Osteobl	bone
40	chr5:119844000-119846000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr5:119844000-119846600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:119844000-119847800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr5:119844200-119844600	Weak transcription	K562	blood
44	chr5:119844200-119844800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr5:119844200-119845000	Weak transcription	Fetal Lung	lung
46	chr5:119844200-119846000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr5:119844200-119846600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr5:119844200-119847400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:119844200-119864200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr5:119844400-119844800	Weak transcription	H1 Cell Line	embryonic stem cell

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