Variant report

Variant	nsv872421
Chromosome Location	chr1:151055670-151098077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151072210-151072608	K562	blood:	n/a	n/a
2	ARID3A	chr1:151072242-151072566	HepG2	liver:	n/a	n/a
3	BACH1	chr1:151097168-151097195	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:151081420-151081660	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:151068392-151068588	HepG2	liver:	n/a	chr1:151068529-151068540
6	CEBPB	chr1:151071689-151071882	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:151062292-151062323	HepG2	liver:	n/a	chr1:151062298-151062311
8	CEBPB	chr1:151094719-151094954	A549	lung:	n/a	chr1:151094814-151094825
9	CEBPB	chr1:151094702-151094939	HepG2	liver:	n/a	chr1:151094814-151094825
10	CEBPB	chr1:151080848-151081225	HepG2	liver:	n/a	chr1:151081033-151081044
11	CEBPB	chr1:151068408-151068576	IMR90	lung:	n/a	chr1:151068529-151068540
12	CEBPB	chr1:151080906-151081199	HepG2	liver:	n/a	chr1:151081033-151081044
13	CEBPB	chr1:151079913-151080187	HepG2	liver:	n/a	chr1:151080033-151080044
14	CEBPB	chr1:151080880-151081090	HepG2	liver:	n/a	chr1:151081033-151081044
15	CHD2	chr1:151097659-151097795	HepG2	liver:	n/a	n/a
16	CHD2	chr1:151097694-151097773	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:151072340-151072490	GM12873	blood:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
18	CTCF	chr1:151072328-151072568	ECC-1	luminal epithelium:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
19	CTCF	chr1:151072380-151072530	HFF-Myc	foreskin:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
20	CTCF	chr1:151072340-151072490	AG09319	gingival:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
21	CTCF	chr1:151072320-151072470	HepG2	liver:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
22	CTCF	chr1:151072380-151072530	RPTEC	kidney:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
23	CTCF	chr1:151072362-151072515	MCF-7	breast:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
24	CTCF	chr1:151072420-151072570	HCT-116	colon:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
25	CTCF	chr1:151072380-151072530	HRPEpiC	eye:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
26	CTCF	chr1:151056320-151056470	HepG2	liver:	n/a	n/a
27	CTCF	chr1:151072360-151072510	SK-N-SH_RA	brain:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
28	CTCF	chr1:151072340-151072534	Gliobla	brain:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
29	CTCF	chr1:151072242-151072642	GM12878	blood:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
30	CTCF	chr1:151066400-151066550	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:151072987-151073009	LNCaP	prostate:	n/a	n/a
32	CTCF	chr1:151072360-151072510	HCFaa	heart:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
33	CTCF	chr1:151095047-151095110	GM20000	blood:	n/a	n/a
34	CTCF	chr1:151072396-151072472	MCF-7	breast:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
35	CTCF	chr1:151072360-151072510	NB4	blood:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
36	CTCF	chr1:151072273-151072604	SK-N-SH_RA	brain:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
37	CTCF	chr1:151072340-151072490	NHDF-neo	bronchial:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
38	CTCF	chr1:151074040-151074190	MCF-7	breast:	n/a	chr1:151074091-151074107
39	CTCF	chr1:151072141-151072604	A549	lung:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
40	CTCF	chr1:151072360-151072510	WERI-Rb-1	eye:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
41	CTCF	chr1:151072380-151072530	HMF	breast:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
42	CTCF	chr1:151056200-151056350	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:151072380-151072530	GM12878	blood:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
44	CTCF	chr1:151074084-151074169	Hela-S3	cervix:	n/a	chr1:151074091-151074107
45	CTCF	chr1:151072380-151072530	AG10803	skin:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
46	CTCF	chr1:151072340-151072490	GM12878	blood:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
47	CTCF	chr1:151072072-151072631	MCF-7	breast:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
48	CTCF	chr1:151074060-151074210	HPAF	blood vessel:	n/a	chr1:151074091-151074107
49	CTCF	chr1:151072340-151072490	GM12874	blood:	n/a	chr1:151072444-151072462 chr1:151072447-151072456 chr1:151072446-151072467 chr1:151072449-151072459
50	CTCF	chr1:151074040-151074190	NHDF-neo	bronchial:	n/a	chr1:151074091-151074107

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151089582-151089632	K562	blood:	n/a
2	chr1:151089582-151089632	SK-N-SH	brain:	n/a
3	chr1:151089582-151089632	ovcar-3	ovarian:	n/a
4	chr1:151089582-151089632	MCF10A-Er-Src	breast:	n/a
5	chr1:151089582-151089632	HCM	heart:	n/a
6	chr1:151089582-151089632	BJ	skin:	n/a
7	chr1:151089582-151089632	HRPEpiC	eye:	n/a
8	chr1:151089582-151089632	GM19239	blood:	n/a
9	chr1:151089582-151089632	HL-60	blood:	n/a
10	chr1:151089582-151089632	SAEC	small airway:	n/a
11	chr1:151089582-151089632	GM12878	blood:	n/a
12	chr1:151089582-151089632	HUVEC	blood vessel:	n/a
13	chr1:151089582-151089632	Jurkat	blood:	n/a
14	chr1:151089582-151089632	H1-hESC	embryonic stem cell:	embryo
15	chr1:151089582-151089632	ECC-1	luminal epithelium:	n/a
16	chr1:151089582-151089632	GM12891	blood:	n/a
17	chr1:151089582-151089632	T-47D	breast:	n/a
18	chr1:151089582-151089632	PrEC	prostate:	n/a
19	chr1:151089582-151089632	ProgFib	skin:	n/a
20	chr1:151089582-151089632	HepG2	liver:	n/a
21	chr1:151089582-151089632	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:151089582-151089632	NHDF-neo	bronchial:	n/a
23	chr1:151089582-151089632	Hela-S3	cervix:	n/a
24	chr1:151089582-151089632	U87	brain:	n/a
25	chr1:151089582-151089632	NT2-D1	testis:	n/a
26	chr1:151089582-151089632	HCF	heart:	n/a
27	chr1:151089582-151089632	SK-N-MC	brain:	n/a
28	chr1:151089582-151089632	HMEC	breast:	n/a
29	chr1:151089582-151089632	PFSK-1	brain:	n/a
30	chr1:151089582-151089632	PANC-1	pancreas:	n/a
31	chr1:151089582-151089632	HRCEpiC	kidney:	n/a
32	chr1:151089582-151089632	SKMC	muscle:	n/a
33	chr1:151089582-151089632	GM06990	blood:	n/a
34	chr1:151089582-151089632	HEEpiC	esophagus:	n/a
35	chr1:151089582-151089632	GM12892	blood:	n/a
36	chr1:151089582-151089632	HAEpiC	amniotic membrane:	n/a
37	chr1:151089582-151089632	A549	lung:	n/a
38	chr1:151089582-151089632	SK-N-SH_RA	brain:	n/a
39	chr1:151089582-151089632	HCT-116	colon:	n/a
40	chr1:151089582-151089632	HEK293	kidney:	embryo
41	chr1:151089582-151089632	AG09319	gingival:	n/a
42	chr1:151089582-151089632	HIPEpiC	eye:	n/a
43	chr1:151089582-151089632	AG04450	lung:	fetal
44	chr1:151089582-151089632	NH-A	brain:	n/a
45	chr1:151089582-151089632	MCF-7	breast:	n/a
46	chr1:151089582-151089632	NHBE	bronchial:	n/a
47	chr1:151089582-151089632	AG09309	skin:	n/a
48	chr1:151089582-151089632	HCPEpiC	choroid plexus:	n/a
49	chr1:151089582-151089632	AG10803	skin:	n/a
50	chr1:151089582-151089632	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:151056165..151058135-chr1:151058218..151060375,2	MCF-7	breast:
2	chr1:151072366..151073004-chr1:151224013..151224543,2	MCF-7	breast:
3	chr1:151043121..151046108-chr1:151097534..151100028,2	MCF-7	breast:
4	chr1:151093654..151096589-chr1:151098300..151100001,2	MCF-7	breast:
5	chr1:151056165..151058135-chr1:151058218..151060375,2	MCF-7	breast:
6	chr1:151094609..151096522-chr1:151105000..151107715,2	MCF-7	breast:
7	chr1:151095743..151100031-chr1:151101378..151107018,6	MCF-7	breast:
8	chr1:151079279..151081159-chr1:151117382..151120022,2	MCF-7	breast:
9	chr1:151071447..151073068-chr1:151128034..151129071,15	MCF-7	breast:
10	chr1:151061570..151063782-chr1:151170963..151173029,2	MCF-7	breast:
11	chr1:151071939..151072878-chr1:151128175..151129386,8	K562	blood:
12	chr1:151029066..151032043-chr1:151061557..151063897,2	MCF-7	breast:
13	chr1:151042351..151044409-chr1:151092761..151094633,2	K562	blood:
14	chr1:151022097..151024795-chr1:151070842..151073434,2	K562	blood:
15	chr1:150996791..150997291-chr1:151072097..151072918,2	MCF-7	breast:
16	chr1:151070545..151072421-chr1:151127566..151130439,2	K562	blood:
17	chr1:151096194..151098701-chr1:151116242..151118774,2	MCF-7	breast:
18	chr1:151072449..151072961-chr1:151118250..151119246,2	MCF-7	breast:
19	chr1:151040835..151043433-chr1:151088012..151090522,2	K562	blood:
20	chr1:151091415..151093045-chr1:151095396..151097246,2	MCF-7	breast:
21	chr1:151069957..151072629-chr1:151138588..151140280,2	MCF-7	breast:
22	chr1:151042902..151044640-chr1:151055874..151057918,2	MCF-7	breast:
23	chr1:151061580..151063442-chr1:151066054..151068144,2	MCF-7	breast:
24	chr1:151071098..151073489-chr1:151128242..151129745,2	K562	blood:
25	chr1:151093689..151096579-chr1:151097300..151100637,3	K562	blood:
26	chr1:151089435..151091250-chr1:151117616..151120097,2	MCF-7	breast:
27	chr1:151061509..151064311-chr1:151070878..151072701,2	MCF-7	breast:
28	chr1:151093689..151096579-chr1:151097300..151100637,3	K562	blood:
29	chr1:151097101..151099997-chr1:151109204..151110916,2	MCF-7	breast:
30	chr1:151072083..151072933-chr1:151128224..151129166,3	MCF-7	breast:
31	chr1:151075147..151078000-chr1:151127777..151130219,2	MCF-7	breast:
32	chr1:151043637..151045310-chr1:151061634..151063146,2	MCF-7	breast:
33	chr1:151060840..151064286-chr1:151064964..151068170,3	K562	blood:
34	chr1:151061509..151064311-chr1:151070878..151072701,2	MCF-7	breast:
35	chr1:151070659..151073129-chr1:151227300..151229103,2	K562	blood:
36	chr1:151091415..151093045-chr1:151095396..151097246,2	MCF-7	breast:
37	chr1:151065188..151067602-chr1:151069192..151070994,2	K562	blood:
38	chr1:151061580..151063442-chr1:151066054..151068144,2	MCF-7	breast:
39	chr1:151042955..151044667-chr1:151056758..151059730,2	K562	blood:
40	chr1:151060714..151063433-chr1:151121100..151123126,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GABPB2-1	chr1:151097701-151098018	NONHSAT006360
2	lnc-GABPB2-1	chr1:151097097-151097695	NONHSAT006360

Variant related genes	Relation type
GABPB2	TF binding region
ENSG00000233717	TF binding region
GABPB2	CpG island
ENSG00000233717	CpG island
ENSG00000213190	chromatin interactions
ENSG00000163154	chromatin interactions
ENSG00000163156	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000261168	chromatin interactions
ENSG00000143434	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000143363	chromatin interactions

Extended variants
information (count: 1442 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1442 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10788798	chr1:151055670-151055671	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144172495	chr1:151055676-151055677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587688664	chr1:151055713-151055714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375012862	chr1:151055736-151055737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587747640	chr1:151055769-151055770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116259980	chr1:151055785-151055786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587698277	chr1:151055823-151055824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587750600	chr1:151055833-151055834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587632426	chr1:151055834-151055835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146516635	chr1:151055835-151055836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141041537	chr1:151055836-151055837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587652822	chr1:151055845-151055846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587703628	chr1:151055850-151055851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587759520	chr1:151055868-151055869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189110357	chr1:151055874-151055875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs587629181	chr1:151055902-151055903	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587716816	chr1:151055927-151055928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144759189	chr1:151055981-151055982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587699074	chr1:151056028-151056029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10888403	chr1:151056041-151056042	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs587631673	chr1:151056051-151056052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116666233	chr1:151056058-151056059	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587738493	chr1:151056059-151056060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587619743	chr1:151056085-151056086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587669972	chr1:151056086-151056087	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148223774	chr1:151056104-151056105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192435919	chr1:151056112-151056113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587640005	chr1:151056130-151056131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs368501073	chr1:151056131-151056132	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374677828	chr1:151056132-151056133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs57774210	chr1:151056146-151056147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182407553	chr1:151056150-151056151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372586112	chr1:151056195-151056196	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12090912	chr1:151056243-151056244	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs150297207	chr1:151056262-151056263	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587680340	chr1:151056279-151056280	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs11204772	chr1:151056305-151056306	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs587638067	chr1:151056366-151056367	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587689358	chr1:151056377-151056378	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs6692296	chr1:151056378-151056379	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs587677198	chr1:151056432-151056433	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs374399310	chr1:151056504-151056505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587735588	chr1:151056522-151056523	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587631818	chr1:151056535-151056536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587635064	chr1:151056536-151056537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143408237	chr1:151056541-151056542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147338084	chr1:151056543-151056544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587677876	chr1:151056548-151056549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11204773	chr1:151056550-151056551	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
50	rs587597569	chr1:151056552-151056553	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151043800-151056200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:151044000-151062800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr1:151044000-151066800	Weak transcription	Ovary	ovary
4	chr1:151044000-151079600	Weak transcription	Spleen	Spleen
5	chr1:151044000-151080600	Weak transcription	Esophagus	oesophagus
6	chr1:151044200-151069800	Weak transcription	HSMM	muscle
7	chr1:151044200-151070800	Weak transcription	Fetal Lung	lung
8	chr1:151044200-151080200	Weak transcription	Aorta	Aorta
9	chr1:151044400-151061600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:151044400-151062200	Weak transcription	Liver	Liver
11	chr1:151044400-151079000	Weak transcription	Left Ventricle	heart
12	chr1:151044400-151079600	Weak transcription	Lung	lung
13	chr1:151044400-151090200	Weak transcription	Gastric	stomach
14	chr1:151044400-151090400	Weak transcription	Right Ventricle	heart
15	chr1:151044400-151103600	Weak transcription	Small Intestine	intestine
16	chr1:151044600-151061200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr1:151044600-151069600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr1:151044600-151069800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:151044600-151069800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:151044600-151070000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr1:151044600-151076000	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr1:151044600-151080400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:151044600-151080600	Weak transcription	Brain Anterior Caudate	brain
24	chr1:151044600-151081000	Weak transcription	Colon Smooth Muscle	Colon
25	chr1:151044800-151061400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr1:151044800-151062800	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:151044800-151065400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:151044800-151066200	Weak transcription	Brain Substantia Nigra	brain
29	chr1:151044800-151069800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:151044800-151070400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr1:151044800-151079600	Weak transcription	Primary B cells from peripheral blood	blood
32	chr1:151044800-151080200	Weak transcription	Fetal Brain Female	brain
33	chr1:151044800-151089400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:151044800-151098800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:151045000-151062800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr1:151045000-151065400	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr1:151045000-151065400	Weak transcription	Adipose Nuclei	Adipose
38	chr1:151045000-151070400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr1:151045000-151079400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr1:151045000-151080000	Weak transcription	Brain Angular Gyrus	brain
41	chr1:151045000-151080400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:151045200-151081000	Weak transcription	Placenta	Placenta
43	chr1:151045800-151062800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr1:151045800-151070400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr1:151046000-151069800	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr1:151047200-151058800	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr1:151047200-151090400	Weak transcription	Dnd41	blood
48	chr1:151047400-151060600	Weak transcription	Primary T cells from cord blood	blood
49	chr1:151047400-151069800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:151047400-151090400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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