Variant report

Variant	nsv873377
Chromosome Location	chr1:242607583-243114662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2454)
CpG islands
(count:2138)
Chromatin interactive
region (count:49)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2454 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF2	chr1:242976778-242977056	GM12878	blood:	n/a	n/a
3	ATF2	chr1:242749196-242749772	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:242765415-242765554	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:242802067-242802078	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:242686703-242687743	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:242908535-242908689	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:242618940-242618963	K562	blood:	n/a	n/a
9	BACH1	chr1:242996994-242996997	K562	blood:	n/a	n/a
10	BACH1	chr1:242918799-242919176	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:242907415-242907671	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:242848092-242848258	K562	blood:	n/a	n/a
13	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
14	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
15	BCL11A	chr1:242749309-242749565	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr1:242843343-242843676	GM12878	blood:	n/a	n/a
17	BCL3	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
19	BHLHE40	chr1:243031757-243031938	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:242976782-242977230	GM12878	blood:	n/a	n/a
21	BRCA1	chr1:242954012-242954043	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr1:242798548-242798608	HepG2	liver:	n/a	n/a
23	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr1:242749358-242749729	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
26	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
27	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
28	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
29	CCNT2	chr1:242687442-242687642	K562	blood:	n/a	n/a
30	CCNT2	chr1:242654129-242654329	K562	blood:	n/a	n/a
31	CEBPB	chr1:242874257-242874306	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:242731714-242731926	IMR90	lung:	n/a	chr1:242731782-242731793 chr1:242731783-242731794
33	CEBPB	chr1:242689119-242689436	A549	lung:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
34	CEBPB	chr1:242689089-242689448	H1-hESC	embryonic stem cell:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
35	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
36	CEBPB	chr1:242899978-242900301	A549	lung:	n/a	chr1:242900141-242900152
37	CEBPB	chr1:242774541-242774804	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:242899993-242900287	HepG2	liver:	n/a	chr1:242900141-242900152
39	CEBPB	chr1:242815292-242815888	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:242933600-242934106	A549	lung:	n/a	n/a
41	CEBPB	chr1:242766651-242766980	A549	lung:	n/a	n/a
42	CEBPB	chr1:242815630-242815862	A549	lung:	n/a	n/a
43	CEBPB	chr1:242731638-242731932	A549	lung:	n/a	chr1:242731782-242731793 chr1:242731783-242731794
44	CEBPB	chr1:242890951-242891053	A549	lung:	n/a	n/a
45	CEBPB	chr1:242687508-242687635	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
47	CEBPB	chr1:242749263-242749763	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:242615991-242616182	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:242689091-242689451	K562	blood:	n/a	chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689264-242689275 chr1:242689264-242689277 chr1:242689266-242689275 chr1:242689266-242689275 chr1:242689265-242689276
50	CEBPB	chr1:242695775-242696035	HepG2	liver:	n/a	chr1:242695864-242695873 chr1:242695862-242695873 chr1:242695863-242695874

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242686709-242686759	NHDF-neo	bronchial:	n/a
2	chr1:242874219-242874269	T-47D	breast:	n/a
3	chr1:242688591-242688641	BJ	skin:	n/a
4	chr1:242686709-242686759	NHDF-neo	bronchial:	n/a
5	chr1:242874219-242874269	T-47D	breast:	n/a
6	chr1:242688591-242688641	BJ	skin:	n/a
7	chr1:243053934-243053984	PrEC	prostate:	n/a
8	chr1:243053673-243053723	HRCEpiC	kidney:	n/a
9	chr1:242653362-242653412	ProgFib	skin:	n/a
10	chr1:242874219-242874269	NT2-D1	testis:	n/a
11	chr1:242688144-242688194	A549	lung:	n/a
12	chr1:242688523-242688573	PrEC	prostate:	n/a
13	chr1:242767942-242767992	BE2_C	brain:	n/a
14	chr1:242688523-242688573	HEEpiC	esophagus:	n/a
15	chr1:242686709-242686759	MCF-7	breast:	n/a
16	chr1:242613203-242613253	SK-N-SH	brain:	n/a
17	chr1:242683142-242683192	AG04449	skin:	fetal
18	chr1:242687465-242687515	HCPEpiC	choroid plexus:	n/a
19	chr1:242688591-242688641	AG10803	skin:	n/a
20	chr1:242612849-242612899	PrEC	prostate:	n/a
21	chr1:242612849-242612899	NB4	blood:	n/a
22	chr1:242613245-242613295	T-47D	breast:	n/a
23	chr1:243053934-243053984	AG09319	gingival:	n/a
24	chr1:242683142-242683192	NT2-D1	testis:	n/a
25	chr1:242687018-242687068	GM19239	blood:	n/a
26	chr1:242688226-242688276	CMK	blood:	n/a
27	chr1:242874219-242874269	HIPEpiC	eye:	n/a
28	chr1:243053865-243053915	IMR90	lung:	fetal
29	chr1:242767727-242767777	NHDF-neo	bronchial:	n/a
30	chr1:242688591-242688641	U87	brain:	n/a
31	chr1:242612787-242612837	NHBE	bronchial:	n/a
32	chr1:242683142-242683192	IMR90	lung:	fetal
33	chr1:242767942-242767992	GM12891	blood:	n/a
34	chr1:242613245-242613295	HRPEpiC	eye:	n/a
35	chr1:243053934-243053984	NH-A	brain:	n/a
36	chr1:242613203-242613253	BE2_C	brain:	n/a
37	chr1:242613245-242613295	ProgFib	skin:	n/a
38	chr1:242687465-242687515	BJ	skin:	n/a
39	chr1:242690593-242690643	SK-N-SH	brain:	n/a
40	chr1:243053934-243053984	Hepatocyte	liver:	n/a
41	chr1:242687018-242687068	T-47D	breast:	n/a
42	chr1:242688681-242688731	HIPEpiC	eye:	n/a
43	chr1:242688144-242688194	HRPEpiC	eye:	n/a
44	chr1:242767727-242767777	NT2-D1	testis:	n/a
45	chr1:242767727-242767777	MCF-7	breast:	n/a
46	chr1:243050875-243050925	SK-N-SH_RA	brain:	n/a
47	chr1:242612787-242612837	AG10803	skin:	n/a
48	chr1:242688226-242688276	ProgFib	skin:	n/a
49	chr1:242612849-242612899	MCF-7	breast:	n/a
50	chr1:242687412-242687462	ovcar-3	ovarian:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
2	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
3	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
4	chr1:242687461..242689938-chr1:242691020..242693615,2	K562	blood:
5	chr1:242616929..242619643-chr1:242629672..242631653,2	K562	blood:
6	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
7	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
8	chr1:242725284..242727359-chr1:242740097..242742633,2	K562	blood:
9	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
10	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
11	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
12	chr1:242630619..242631512-chr1:244436093..244436950,3	MCF-7	breast:
13	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
14	chr1:242725284..242727359-chr1:242740097..242742633,2	K562	blood:
15	chr1:242687074..242690257-chr1:242691020..242695095,4	K562	blood:
16	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
17	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
18	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
19	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
20	chr1:242690016..242691872-chr1:242693633..242696620,2	K562	blood:
21	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
22	chr1:242680127..242681627-chr2:114917951..114919998,2	K562	blood:
23	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
24	chr1:242182892..242183793-chr1:242638283..242638859,2	MCF-7	breast:
25	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
26	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
27	chr1:242608265..242609787-chr20:56286531..56288293,2	MCF-7	breast:
28	chr1:242731452..242733233-chr1:242737501..242739906,2	K562	blood:
29	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
30	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
31	chr1:242617811..242618559-chr1:242630673..242631426,2	MCF-7	breast:
32	chr1:242617811..242618559-chr1:242630673..242631426,2	MCF-7	breast:
33	chr1:242626775..242629510-chr1:242632318..242634678,2	K562	blood:
34	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
35	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
36	chr1:242626775..242629510-chr1:242632318..242634678,2	K562	blood:
37	chr1:242731452..242733233-chr1:242737501..242739906,2	K562	blood:
38	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
39	chr1:242616929..242619643-chr1:242629672..242631653,2	K562	blood:
40	chr1:242692263..242693064-chr17:56708576..56709248,2	MCF-7	breast:
41	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
42	chr1:242690016..242691872-chr1:242693633..242696620,2	K562	blood:
43	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
44	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
45	chr1:242687782..242688282-chr7:140396130..140396992,2	MCF-7	breast:
46	chr1:242617851..242618670-chr1:243488347..243489044,3	K562	blood:
47	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
48	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
49	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
2	lnc-MAP1LC3C-3	chr1:242654490-242654577	NONHSAT010568
3	lnc-PLD5-1	chr1:242693049-242693341	NONHSAT010569
4	lnc-MAP1LC3C-7	chr1:242681118-242681325	expReg_chr1_22661_-
5	lnc-PLD5-2	chr1:242717724-242718022	XLOC_001281
6	lnc-MAP1LC3C-4	chr1:242654836-242655140	expReg_chr1_22645_-
7	lnc-MAP1LC3C-5	chr1:242676012-242676332	expReg_chr1_22653_-
8	lnc-SDCCAG8-4	chr1:242834442-242834878	NONHSAT010573
9	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
10	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
11	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
12	lnc-PLD5-1	chr1:242692647-242692740	NONHSAT010569
13	lnc-PLD5-1	chr1:242690923-242691021	NONHSAT010569
14	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-
15	lnc-MAP1LC3C-6	chr1:242680432-242680918	expReg_chr1_22659_-
16	lnc-PLD5-2	chr1:242717038-242717147	XLOC_001281
17	lnc-MAP1LC3C-3	chr1:242652877-242653660	NONHSAT010568

No data

Variant related genes	Relation type
ENSG00000270859	TF binding region
ENSG00000270818	TF binding region
PLD5	TF binding region
RSL24D1P4	TF binding region
ENSG00000264972	TF binding region
ENSG00000270859	CpG island
ENSG00000270818	CpG island
PLD5	CpG island
RSL24D1P4	CpG island
ENSG00000264972	CpG island
ENSG00000212195	chromatin interactions
ENSG00000240889	chromatin interactions
ENSG00000124225	chromatin interactions
ENSG00000180287	chromatin interactions
ENSG00000090266	chromatin interactions
DAB2IP	miRNA target sites
DACT1	miRNA target sites

Extended variants
information (count: 15113 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:15113 , 50 per page) page: 1 2 3 4 5 6 7 ... 303

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2654882	chr1:242607583-242607584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527262528	chr1:242607634-242607635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79688609	chr1:242607637-242607638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371881675	chr1:242607651-242607652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533191757	chr1:242607655-242607656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386641271	chr1:242607683-242607684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182523180	chr1:242607684-242607685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544745994	chr1:242607689-242607690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373645856	chr1:242607761-242607762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529359505	chr1:242607770-242607771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549034196	chr1:242607771-242607772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367556475	chr1:242607796-242607797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6674594	chr1:242607800-242607801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534687065	chr1:242607816-242607817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149703131	chr1:242607834-242607835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571839874	chr1:242607853-242607854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200529170	chr1:242607918-242607919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs55885600	chr1:242607924-242607925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56032576	chr1:242607925-242607926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs56333389	chr1:242607929-242607930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12135439	chr1:242607940-242607941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12134677	chr1:242607948-242607949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12134678	chr1:242607949-242607950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373713007	chr1:242607955-242607956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377091506	chr1:242607956-242607957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368876947	chr1:242607959-242607960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188038412	chr1:242607960-242607961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371382075	chr1:242607962-242607963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs55802487	chr1:242607966-242607967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374667773	chr1:242607968-242607969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79869356	chr1:242607969-242607970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370111266	chr1:242607971-242607972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7414118	chr1:242607974-242607975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373962170	chr1:242607977-242607978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376891680	chr1:242607978-242607979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373294279	chr1:242607979-242607980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61677955	chr1:242607983-242607984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371436198	chr1:242607984-242607985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374374662	chr1:242607985-242607986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377492993	chr1:242607987-242607988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369716880	chr1:242607988-242607989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10522983	chr1:242607994-242607995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374099317	chr1:242607997-242607998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71176762	chr1:242607998-242607999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377585815	chr1:242607999-242608000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376196692	chr1:242608000-242608001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58769277	chr1:242608001-242608002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370528973	chr1:242608002-242608003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373284186	chr1:242608004-242608005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370582595	chr1:242608005-242608006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1393 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242590400-242610200	Weak transcription	HMEC	breast
2	chr1:242594400-242610600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:242597200-242610600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:242597600-242610000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:242597600-242612400	Weak transcription	Aorta	Aorta
6	chr1:242597800-242619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:242599600-242612600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:242604000-242611000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:242605800-242609800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:242606000-242609800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:242606400-242609800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr1:242606400-242610000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr1:242606400-242610800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:242609800-242610000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:242609800-242610000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:242609800-242610800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:242609800-242613200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr1:242609800-242613200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:242609800-242613400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr1:242609800-242613600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:242610000-242610400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:242610000-242610600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:242610000-242610800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr1:242610000-242611000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:242610000-242611400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr1:242610000-242613400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr1:242610200-242611000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:242610200-242611000	Enhancers	HMEC	breast
29	chr1:242610200-242613400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:242610400-242610800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr1:242610400-242611400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:242610600-242610800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:242610600-242611200	Enhancers	NHEK	skin
34	chr1:242610600-242611400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:242610600-242612000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:242610600-242612200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:242610800-242611000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr1:242610800-242611200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr1:242610800-242611400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:242610800-242611800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:242610800-242612200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:242610800-242613000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:242611000-242611200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:242611000-242611400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:242611000-242611600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:242611000-242612000	Active TSS	Brain Germinal Matrix	brain
47	chr1:242611000-242613000	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr1:242611000-242613600	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr1:242611000-242632200	Weak transcription	HMEC	breast
50	chr1:242611200-242613200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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