Variant report

Variant	nsv539740
Chromosome Location	chr8:121501179-121620441
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	chr8:121618057-121618165	HepG2	liver:	n/a	n/a
2	BCL3	chr8:121612925-121613258	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:121566090-121566109	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:121553461-121553463	HepG2	liver:	n/a	n/a
5	BRCA1	chr8:121535055-121535064	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr8:121617857-121618166	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr8:121567489-121567888	K562	blood:	n/a	n/a
8	CEBPB	chr8:121553089-121553424	HepG2	liver:	n/a	chr8:121553236-121553247
9	CEBPB	chr8:121617837-121618172	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:121597777-121597938	HepG2	liver:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
11	CEBPB	chr8:121597618-121598088	MCF-7	breast:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
12	CEBPB	chr8:121615780-121615835	K562	blood:	n/a	chr8:121615788-121615799
13	CEBPB	chr8:121557057-121557358	HepG2	liver:	n/a	chr8:121557180-121557193 chr8:121557181-121557192
14	CEBPB	chr8:121557080-121557316	A549	lung:	n/a	chr8:121557180-121557193 chr8:121557181-121557192
15	CEBPB	chr8:121553109-121553414	IMR90	lung:	n/a	chr8:121553236-121553247
16	CEBPB	chr8:121520911-121521210	HepG2	liver:	n/a	chr8:121521033-121521044 chr8:121521035-121521046
17	CEBPB	chr8:121597660-121598064	Hela-S3	cervix:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
18	CEBPB	chr8:121540058-121540250	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:121581153-121581173	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:121577200-121577276	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:121520970-121521130	HepG2	liver:	n/a	chr8:121521033-121521044 chr8:121521035-121521046
22	CEBPB	chr8:121559228-121559457	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:121597510-121598124	MCF-7	breast:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
24	CEBPB	chr8:121615707-121615909	HepG2	liver:	n/a	chr8:121615788-121615799
25	CEBPB	chr8:121597596-121598167	HCT-116	colon:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
26	CEBPB	chr8:121577198-121577265	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:121553120-121553364	H1-hESC	embryonic stem cell:	n/a	chr8:121553236-121553247
28	CEBPB	chr8:121617943-121618183	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr8:121581014-121581295	HepG2	liver:	n/a	chr8:121581171-121581182
30	CEBPB	chr8:121557045-121557333	IMR90	lung:	n/a	chr8:121557180-121557193 chr8:121557181-121557192
31	CEBPB	chr8:121597702-121598052	HepG2	liver:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
32	CEBPB	chr8:121597673-121598065	IMR90	lung:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
33	CEBPB	chr8:121597745-121598138	A549	lung:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
34	CEBPB	chr8:121597639-121598124	A549	lung:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
35	CEBPB	chr8:121557047-121557318	Hela-S3	cervix:	n/a	chr8:121557180-121557193 chr8:121557181-121557192
36	CEBPB	chr8:121600186-121600289	K562	blood:	n/a	n/a
37	CEBPB	chr8:121597775-121598015	K562	blood:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
38	CEBPB	chr8:121539813-121540314	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:121581040-121581326	A549	lung:	n/a	chr8:121581171-121581182
40	CEBPB	chr8:121553148-121553385	A549	lung:	n/a	chr8:121553236-121553247
41	CEBPB	chr8:121597595-121598128	HCT-116	colon:	n/a	chr8:121597860-121597871 chr8:121597862-121597873 chr8:121597860-121597873 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597862-121597871 chr8:121597860-121597873 chr8:121597862-121597871
42	CEBPB	chr8:121607097-121607183	IMR90	lung:	n/a	n/a
43	CHD2	chr8:121540708-121540720	K562	blood:	n/a	n/a
44	CHD2	chr8:121581963-121582085	HepG2	liver:	n/a	n/a
45	CTCF	chr8:121605320-121605470	WI-38	lung:	n/a	n/a
46	CTCF	chr8:121618000-121618150	Hela-S3	cervix:	n/a	chr8:121618093-121618111 chr8:121618088-121618109 chr8:121618095-121618108 chr8:121618120-121618128
47	CTCF	chr8:121617960-121618110	HAc	cerebellar:	n/a	chr8:121618088-121618109 chr8:121618095-121618108
48	CTCF	chr8:121575633-121575742	LNCaP	prostate:	n/a	n/a
49	CTCF	chr8:121605520-121605670	SAEC	small airway:	n/a	n/a
50	CTCF	chr8:121618040-121618190	NHLF	lung:	n/a	chr8:121618093-121618111 chr8:121618088-121618109 chr8:121618095-121618108 chr8:121618120-121618128

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:121566699-121566749	ProgFib	skin:	n/a
2	chr8:121598484-121598534	BE2_C	brain:	n/a
3	chr8:121604940-121604990	PANC-1	pancreas:	n/a
4	chr8:121604940-121604990	A549	lung:	n/a
5	chr8:121575063-121575113	HMEC	breast:	n/a
6	chr8:121604940-121604990	Jurkat	blood:	n/a
7	chr8:121566699-121566749	IMR90	lung:	fetal
8	chr8:121598484-121598534	HRPEpiC	eye:	n/a
9	chr8:121604940-121604990	CMK	blood:	n/a
10	chr8:121598484-121598534	HIPEpiC	eye:	n/a
11	chr8:121575063-121575113	GM12892	blood:	n/a
12	chr8:121598484-121598534	IMR90	lung:	fetal
13	chr8:121575063-121575113	GM12878	blood:	n/a
14	chr8:121604940-121604990	SAEC	small airway:	n/a
15	chr8:121604940-121604990	AG10803	skin:	n/a
16	chr8:121604940-121604990	IMR90	lung:	fetal
17	chr8:121604940-121604990	HCT-116	colon:	n/a
18	chr8:121575063-121575113	BE2_C	brain:	n/a
19	chr8:121598484-121598534	Jurkat	blood:	n/a
20	chr8:121566699-121566749	AG10803	skin:	n/a
21	chr8:121604940-121604990	T-47D	breast:	n/a
22	chr8:121598484-121598534	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:121604940-121604990	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:121598484-121598534	AG04449	skin:	fetal
25	chr8:121575063-121575113	HRCEpiC	kidney:	n/a
26	chr8:121566699-121566749	HMEC	breast:	n/a
27	chr8:121598484-121598534	HCPEpiC	choroid plexus:	n/a
28	chr8:121566699-121566749	PANC-1	pancreas:	n/a
29	chr8:121575063-121575113	SK-N-SH	brain:	n/a
30	chr8:121604940-121604990	GM12878	blood:	n/a
31	chr8:121604940-121604990	H1-hESC	embryonic stem cell:	embryo
32	chr8:121604940-121604990	HIPEpiC	eye:	n/a
33	chr8:121598484-121598534	Caco-2	colon:	n/a
34	chr8:121598484-121598534	K562	blood:	n/a
35	chr8:121566699-121566749	GM12878	blood:	n/a
36	chr8:121566699-121566749	HRPEpiC	eye:	n/a
37	chr8:121598484-121598534	GM06990	blood:	n/a
38	chr8:121566699-121566749	GM06990	blood:	n/a
39	chr8:121575063-121575113	K562	blood:	n/a
40	chr8:121604940-121604990	U87	brain:	n/a
41	chr8:121575063-121575113	Jurkat	blood:	n/a
42	chr8:121604940-121604990	GM19239	blood:	n/a
43	chr8:121604940-121604990	NB4	blood:	n/a
44	chr8:121598484-121598534	PANC-1	pancreas:	n/a
45	chr8:121575063-121575113	Caco-2	colon:	n/a
46	chr8:121598484-121598534	SAEC	small airway:	n/a
47	chr8:121575063-121575113	ECC-1	luminal epithelium:	n/a
48	chr8:121598484-121598534	HepG2	liver:	n/a
49	chr8:121598484-121598534	ovcar-3	ovarian:	n/a
50	chr8:121566699-121566749	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:121493947..121495884-chr8:121507888..121510586,2	K562	blood:
2	chr8:121586914..121588422-chr9:132086514..132089138,2	MCF-7	breast:
3	chr8:121570203..121571845-chr8:121572153..121574124,2	K562	blood:
4	chr8:121619967..121621577-chr8:121621884..121624584,2	MCF-7	breast:
5	chr8:121532282..121534379-chr8:121535503..121538039,2	K562	blood:
6	chr8:121519851..121521480-chr8:121528320..121530323,2	K562	blood:
7	chr8:121513049..121516697-chr8:121519405..121522575,3	K562	blood:
8	chr8:112112573..112113471-chr8:121617637..121618420,2	MCF-7	breast:
9	chr8:121544486..121549968-chr8:121551053..121554339,4	K562	blood:
10	chr8:121608620..121610687-chr8:121614325..121616979,2	K562	blood:
11	chr8:121572609..121577050-chr8:121578389..121580916,4	MCF-7	breast:
12	chr8:121537988..121539624-chr8:121540366..121542658,2	K562	blood:
13	chr8:121510638..121513169-chr8:121514269..121517383,3	K562	blood:
14	chr8:121464608..121465642-chr8:121617640..121618545,4	MCF-7	breast:
15	chr8:121509906..121512045-chr8:121517322..121521467,3	MCF-7	breast:
16	chr8:121509906..121512045-chr8:121517322..121521467,3	MCF-7	breast:
17	chr8:112248281..112249195-chr8:121617648..121618574,4	MCF-7	breast:
18	chr8:121608620..121610687-chr8:121614325..121616979,2	K562	blood:
19	chr8:121464599..121465793-chr8:121617159..121618618,14	MCF-7	breast:
20	chr8:121572609..121577050-chr8:121578389..121580916,4	MCF-7	breast:
21	chr8:120879496..120880083-chr8:121617650..121618484,2	K562	blood:
22	chr8:121456487..121458997-chr8:121617348..121619898,2	MCF-7	breast:
23	chr8:121510638..121513169-chr8:121514269..121517383,3	K562	blood:
24	chr8:121544486..121549968-chr8:121551053..121554339,4	K562	blood:
25	chr8:121491951..121494314-chr8:121553949..121556742,2	K562	blood:
26	chr8:112248686..112249491-chr8:121617700..121618578,2	MCF-7	breast:
27	chr8:121590814..121592983-chr8:121597409..121599196,2	MCF-7	breast:
28	chr17:59489591..59490358-chr8:121600927..121601792,2	MCF-7	breast:
29	chr8:121548668..121550591-chr8:121568296..121570186,2	K562	blood:
30	chr8:121324471..121327293-chr8:121521096..121522811,2	MCF-7	breast:
31	chr8:121590814..121592983-chr8:121597409..121599196,2	MCF-7	breast:
32	chr8:121456070..121457664-chr8:121509055..121511130,2	K562	blood:
33	chr8:121532282..121534379-chr8:121535503..121538039,2	K562	blood:
34	chr8:121513049..121516697-chr8:121519405..121522575,3	K562	blood:
35	chr4:151571818..151572526-chr8:121510190..121511044,2	MCF-7	breast:
36	chr8:112152279..112153092-chr8:121617588..121618297,2	MCF-7	breast:
37	chr7:1451932..1452733-chr8:121617665..121618450,2	MCF-7	breast:
38	chr8:121455673..121457794-chr8:121503507..121505497,2	MCF-7	breast:
39	chr8:121570203..121571845-chr8:121572153..121574124,2	K562	blood:
40	chr8:121548668..121550591-chr8:121568296..121570186,2	K562	blood:
41	chr8:121537988..121539624-chr8:121540366..121542658,2	K562	blood:
42	chr8:121519851..121521480-chr8:121528320..121530323,2	K562	blood:
43	chr8:111842460..111843306-chr8:121617683..121618475,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTBP-4	chr8:121554234-121554373	NONHSAT128455
2	lnc-MTBP-4	chr8:121553402-121553459	NONHSAT128455
3	lnc-MTBP-4	chr8:121550935-121551103	NONHSAT128455

No.	miRNA target gene	miRNA name	Chromosome Location
1	SNTB1	hsa-miR-335-5p	chr8:121548574-121548600
2	SNTB1	hsa-miR-24-3p	chr8:121550437-121550430
3	SNTB1	hsa-miR-24-3p	chr8:121550431-121550454

Variant related genes	Relation type
MTBP	TF binding region
MTBP	CpG island
ENSG00000172172	chromatin interactions
ENSG00000253103	chromatin interactions
ENSG00000172167	chromatin interactions

Extended variants
information (count: 4190 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:4190 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143057153	chr8:121501206-121501207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190659653	chr8:121501233-121501234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143386927	chr8:121501281-121501282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199528191	chr8:121501284-121501285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375850616	chr8:121501285-121501286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs71306887	chr8:121501297-121501298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540148983	chr8:121501339-121501340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533556380	chr8:121501343-121501344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369513027	chr8:121501421-121501422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573030191	chr8:121501436-121501437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541938435	chr8:121501499-121501500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556328049	chr8:121501528-121501529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562258971	chr8:121501529-121501530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549218845	chr8:121501537-121501538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567603599	chr8:121501540-121501541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537902168	chr8:121501547-121501548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575021223	chr8:121501556-121501557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147140547	chr8:121501569-121501570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571244655	chr8:121501666-121501667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553656231	chr8:121501701-121501702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7826906	chr8:121501723-121501724	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
22	rs572665759	chr8:121501735-121501736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182719652	chr8:121501755-121501756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148261774	chr8:121501790-121501791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187327684	chr8:121501794-121501795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535901382	chr8:121501843-121501844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554371412	chr8:121501867-121501868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575985586	chr8:121501904-121501905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60062153	chr8:121501938-121501939	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs371181128	chr8:121501973-121501974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373756182	chr8:121501977-121501978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190241212	chr8:121502019-121502020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545732224	chr8:121502088-121502089	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141382658	chr8:121502113-121502114	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183140943	chr8:121502157-121502158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561267740	chr8:121502192-121502193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540205998	chr8:121502193-121502194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531718768	chr8:121502195-121502196	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549937920	chr8:121502203-121502204	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188318076	chr8:121502266-121502267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567080951	chr8:121502272-121502273	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369606589	chr8:121502339-121502340	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532237237	chr8:121502394-121502395	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs193270314	chr8:121502408-121502409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150770476	chr8:121502434-121502435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373089432	chr8:121502460-121502461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7839548	chr8:121502498-121502499	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554640158	chr8:121502521-121502522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569683830	chr8:121502569-121502570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576995247	chr8:121502571-121502572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121458000-121510400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:121458200-121505200	Weak transcription	Placenta	Placenta
3	chr8:121458600-121504200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr8:121458600-121516400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr8:121458800-121504000	Weak transcription	Fetal Heart	heart
6	chr8:121458800-121510200	Weak transcription	Brain Germinal Matrix	brain
7	chr8:121458800-121510400	Weak transcription	NHLF	lung
8	chr8:121458800-121539000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:121459000-121528600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:121468600-121501800	Weak transcription	HUVEC	blood vessel
11	chr8:121469200-121515200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:121470000-121502400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr8:121474600-121553600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr8:121477800-121503800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:121481800-121501600	Weak transcription	Fetal Stomach	stomach
16	chr8:121482600-121503800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:121483400-121501600	Weak transcription	Primary B cells from cord blood	blood
18	chr8:121484400-121541800	Weak transcription	Left Ventricle	heart
19	chr8:121487600-121512200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr8:121488400-121539200	Weak transcription	HSMM	muscle
21	chr8:121491400-121501600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr8:121491400-121541800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr8:121493600-121502200	Weak transcription	Gastric	stomach
24	chr8:121493600-121506400	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr8:121497200-121534200	Weak transcription	Small Intestine	intestine
26	chr8:121497400-121501600	Weak transcription	Fetal Intestine Large	intestine
27	chr8:121497800-121501800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:121498000-121507400	Weak transcription	Psoas Muscle	Psoas
29	chr8:121498200-121503800	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr8:121498200-121552400	Weak transcription	Pancreas	Pancrea
31	chr8:121498400-121502000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:121498600-121509800	Weak transcription	Right Ventricle	heart
33	chr8:121498600-121533200	Weak transcription	HMEC	breast
34	chr8:121498800-121501600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr8:121498800-121503600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr8:121498800-121505400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:121498800-121506000	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr8:121498800-121510200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:121498800-121530200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr8:121499000-121504400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr8:121499200-121501600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr8:121499400-121501400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:121499400-121503200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:121499400-121503200	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr8:121499400-121503800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr8:121499400-121504000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr8:121499400-121504000	Weak transcription	Stomach Smooth Muscle	stomach
48	chr8:121499400-121530600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:121499400-121550600	Weak transcription	Fetal Kidney	kidney
50	chr8:121499600-121501600	Weak transcription	Thymus	Thymus

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