Variant report

Variant	nsv890057
Chromosome Location	chr8:6317165-6427868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1191)
CpG islands
(count:2015)
Chromatin interactive
region (count:49)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6427716-6428410	K562	blood:	n/a	n/a
2	ARID3A	chr8:6417196-6417729	K562	blood:	n/a	n/a
3	ARID3A	chr8:6374235-6374891	K562	blood:	n/a	n/a
4	ARID3A	chr8:6321256-6321847	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:6415330-6415515	K562	blood:	n/a	n/a
6	ARID3A	chr8:6417121-6417672	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:6373920-6374092	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:6418017-6418400	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:6383927-6384127	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:6323049-6323486	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:6421737-6422437	HepG2	liver:	n/a	chr8:6422337-6422353
12	ARID3A	chr8:6405106-6405302	HepG2	liver:	n/a	n/a
13	ATF1	chr8:6415244-6415561	K562	blood:	n/a	n/a
14	ATF1	chr8:6417229-6417543	K562	blood:	n/a	n/a
15	ATF2	chr8:6405258-6405595	GM12878	blood:	n/a	n/a
16	ATF2	chr8:6405137-6405557	GM12878	blood:	n/a	n/a
17	BACH1	chr8:6404986-6405345	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:6407692-6407728	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:6427498-6427624	K562	blood:	n/a	n/a
20	BATF	chr8:6405280-6405568	GM12878	blood:	n/a	chr8:6405388-6405399
21	BATF	chr8:6405070-6405630	GM12878	blood:	n/a	chr8:6405388-6405399
22	BATF	chr8:6399759-6399979	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:6405193-6405571	GM12878	blood:	n/a	n/a
24	BCL3	chr8:6406977-6407373	GM12878	blood:	n/a	n/a
25	BCL3	chr8:6351266-6351531	GM12878	blood:	n/a	n/a
26	BCL3	chr8:6404997-6405370	GM12878	blood:	n/a	n/a
27	BCL3	chr8:6417222-6417592	GM12878	blood:	n/a	n/a
28	BHLHE40	chr8:6405065-6405319	HepG2	liver:	n/a	n/a
29	BHLHE40	chr8:6321267-6321818	HepG2	liver:	n/a	n/a
30	BHLHE40	chr8:6321392-6321688	HepG2	liver:	n/a	n/a
31	BHLHE40	chr8:6399745-6399948	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:6321381-6321736	HepG2	liver:	n/a	n/a
33	BRCA1	chr8:6344592-6344952	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr8:6351090-6351120	Hela-S3	cervix:	n/a	n/a
35	CCNT2	chr8:6415315-6415510	K562	blood:	n/a	n/a
36	CEBPB	chr8:6390918-6390982	K562	blood:	n/a	n/a
37	CEBPB	chr8:6338927-6339192	IMR90	lung:	n/a	n/a
38	CEBPB	chr8:6321429-6321720	A549	lung:	n/a	chr8:6321560-6321571
39	CEBPB	chr8:6387240-6387587	A549	lung:	n/a	chr8:6387420-6387431
40	CEBPB	chr8:6321392-6321716	HepG2	liver:	n/a	chr8:6321560-6321571
41	CEBPB	chr8:6338179-6338319	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:6343211-6343297	K562	blood:	n/a	n/a
43	CEBPB	chr8:6321383-6321746	HepG2	liver:	n/a	chr8:6321560-6321571
44	CEBPB	chr8:6395560-6395756	HepG2	liver:	n/a	chr8:6395596-6395607 chr8:6395595-6395608 chr8:6395595-6395606
45	CEBPB	chr8:6409734-6409970	A549	lung:	n/a	chr8:6409850-6409861
46	CEBPB	chr8:6371173-6371490	A549	lung:	n/a	n/a
47	CEBPB	chr8:6321351-6321748	Hela-S3	cervix:	n/a	chr8:6321560-6321571
48	CEBPB	chr8:6387243-6387602	IMR90	lung:	n/a	chr8:6387420-6387431
49	CEBPB	chr8:6387236-6387518	ECC-1	luminal epithelium:	n/a	chr8:6387420-6387431
50	CEBPB	chr8:6371146-6371481	HepG2	liver:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6366994-6367044	SK-N-SH_RA	brain:	n/a
2	chr8:6420726-6420776	SK-N-SH_RA	brain:	n/a
3	chr8:6366994-6367044	SK-N-SH_RA	brain:	n/a
4	chr8:6420726-6420776	SK-N-SH_RA	brain:	n/a
5	chr8:6400815-6400865	HRPEpiC	eye:	n/a
6	chr8:6424726-6424776	HNPCEpiC	eye:	n/a
7	chr8:6419483-6419533	BE2_C	brain:	n/a
8	chr8:6323131-6323181	MCF10A-Er-Src	breast:	n/a
9	chr8:6400815-6400865	HUVEC	blood vessel:	n/a
10	chr8:6420242-6420292	CMK	blood:	n/a
11	chr8:6405105-6405155	ProgFib	skin:	n/a
12	chr8:6407997-6408047	HRPEpiC	eye:	n/a
13	chr8:6419438-6419488	AG09309	skin:	n/a
14	chr8:6420242-6420292	U87	brain:	n/a
15	chr8:6424636-6424686	H1-hESC	embryonic stem cell:	embryo
16	chr8:6419438-6419488	H1-hESC	embryonic stem cell:	embryo
17	chr8:6386150-6386200	RPTEC	kidney:	n/a
18	chr8:6405105-6405155	HCT-116	colon:	n/a
19	chr8:6401045-6401095	AG04450	lung:	fetal
20	chr8:6420726-6420776	MCF10A-Er-Src	breast:	n/a
21	chr8:6419483-6419533	SK-N-MC	brain:	n/a
22	chr8:6366994-6367044	ECC-1	luminal epithelium:	n/a
23	chr8:6386150-6386200	HUVEC	blood vessel:	n/a
24	chr8:6407273-6407323	AG09309	skin:	n/a
25	chr8:6366994-6367044	Hepatocyte	liver:	n/a
26	chr8:6424636-6424686	NB4	blood:	n/a
27	chr8:6407676-6407726	HIPEpiC	eye:	n/a
28	chr8:6418978-6419028	Hepatocyte	liver:	n/a
29	chr8:6419570-6419620	K562	blood:	n/a
30	chr8:6328807-6328857	GM19239	blood:	n/a
31	chr8:6345256-6345306	HepG2	liver:	n/a
32	chr8:6401045-6401095	SAEC	small airway:	n/a
33	chr8:6420242-6420292	LNCaP	prostate:	n/a
34	chr8:6323131-6323181	GM19239	blood:	n/a
35	chr8:6407134-6407184	NB4	blood:	n/a
36	chr8:6420858-6420908	ovcar-3	ovarian:	n/a
37	chr8:6328807-6328857	PFSK-1	brain:	n/a
38	chr8:6423908-6423958	PrEC	prostate:	n/a
39	chr8:6407273-6407323	HRE	kidney:	n/a
40	chr8:6419483-6419533	BJ	skin:	n/a
41	chr8:6407812-6407862	HRPEpiC	eye:	n/a
42	chr8:6321006-6321056	NB4	blood:	n/a
43	chr8:6424636-6424686	AoSMC	blood vessel:	n/a
44	chr8:6407134-6407184	Hepatocyte	liver:	n/a
45	chr8:6401045-6401095	GM12892	blood:	n/a
46	chr8:6424269-6424319	Caco-2	colon:	n/a
47	chr8:6407997-6408047	LNCaP	prostate:	n/a
48	chr8:6323131-6323181	ECC-1	luminal epithelium:	n/a
49	chr8:6386114-6386164	SK-N-MC	brain:	n/a
50	chr8:6321006-6321056	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:6339705..6342364-chr8:6348069..6350911,2	K562	blood:
2	chr8:6394442..6396969-chr8:6403020..6405358,2	K562	blood:
3	chr8:6386091..6387814-chr8:6394957..6397917,2	K562	blood:
4	chr8:6404729..6406920-chr8:6412870..6416150,3	K562	blood:
5	chr8:6350753..6353576-chr8:6355217..6356986,2	K562	blood:
6	chr8:6427802..6430187-chr8:6431703..6433459,2	K562	blood:
7	chr8:6407291..6408244-chr8:6417821..6418628,2	MCF-7	breast:
8	chr8:6405547..6408006-chr8:6408375..6411218,3	K562	blood:
9	chr8:6414044..6416927-chr8:6417837..6419892,2	K562	blood:
10	chr8:6405547..6408006-chr8:6408375..6411218,3	K562	blood:
11	chr8:6339705..6342364-chr8:6348069..6350911,2	K562	blood:
12	chr8:6366887..6369432-chr8:6372035..6375805,3	K562	blood:
13	chr8:6357189..6359349-chr8:6362649..6365411,2	K562	blood:
14	chr8:6404729..6406920-chr8:6412870..6416150,3	K562	blood:
15	chr8:6340740..6344062-chr8:6345418..6348031,3	K562	blood:
16	chr8:6417306..6418909-chr8:6419114..6421148,2	K562	blood:
17	chr8:6286838..6288405-chr8:6317627..6319306,2	K562	blood:
18	chr8:6411074..6413407-chr8:6413898..6415617,2	K562	blood:
19	chr8:6426332..6429176-chr8:6564535..6567216,2	MCF-7	breast:
20	chr8:6326969..6329620-chr8:6343917..6345900,2	K562	blood:
21	chr8:6285464..6288077-chr8:6414656..6417304,2	K562	blood:
22	chr8:6366887..6369432-chr8:6372035..6375805,3	K562	blood:
23	chr8:6411074..6413407-chr8:6413898..6415617,2	K562	blood:
24	chr8:6340740..6344062-chr8:6345418..6348031,3	K562	blood:
25	chr8:6373777..6375573-chr8:6376126..6378974,2	K562	blood:
26	chr8:6340740..6343384-chr8:6345418..6348031,2	K562	blood:
27	chr8:6407403..6409815-chr8:6410671..6412901,2	K562	blood:
28	chr8:6340740..6343384-chr8:6345418..6348031,2	K562	blood:
29	chr8:6405224..6409336-chr8:6413306..6416659,4	K562	blood:
30	chr8:6327001..6332096-chr8:6332476..6335725,6	K562	blood:
31	chr8:6350753..6353576-chr8:6355217..6356986,2	K562	blood:
32	chr8:6280960..6282945-chr8:6426818..6429637,2	K562	blood:
33	chr8:6386091..6387814-chr8:6394957..6397917,2	K562	blood:
34	chr8:6393677..6395465-chr8:6397894..6400469,2	K562	blood:
35	chr8:6357189..6359349-chr8:6362649..6365411,2	K562	blood:
36	chr8:6308680..6311330-chr8:6317325..6320400,3	K562	blood:
37	chr8:6407291..6408244-chr8:6417821..6418628,2	MCF-7	breast:
38	chr8:6311610..6314385-chr8:6324095..6326791,2	K562	blood:
39	chr8:6393775..6396969-chr8:6403020..6405358,3	K562	blood:
40	chr8:6313067..6315249-chr8:6315975..6317705,2	MCF-7	breast:
41	chr8:6373777..6375573-chr8:6376126..6378974,2	K562	blood:
42	chr8:6405224..6409336-chr8:6413306..6416659,4	K562	blood:
43	chr8:6393677..6395465-chr8:6397894..6400469,2	K562	blood:
44	chr8:6414044..6416927-chr8:6417837..6419892,2	K562	blood:
45	chr8:6394442..6396969-chr8:6403020..6405358,2	K562	blood:
46	chr8:6326969..6329620-chr8:6343917..6345900,2	K562	blood:
47	chr8:6327001..6332096-chr8:6332476..6335725,6	K562	blood:
48	chr8:6393775..6396969-chr8:6403020..6405358,3	K562	blood:
49	chr8:6407403..6409815-chr8:6410671..6412901,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPAT5-3	chr8:6351645-6352063	NONHSAT124773
2	lnc-DEFB1-3	chr8:6369418-6369852	NONHSAT124774

No data

Variant related genes	Relation type
ENSG00000253550	TF binding region
ANGPT2	TF binding region
MCPH1	TF binding region
ENSG00000253550	CpG island
ANGPT2	CpG island
MCPH1	CpG island
ENSG00000249898	chromatin interactions
ENSG00000091879	chromatin interactions
ENSG00000147316	chromatin interactions
ENSG00000253550	chromatin interactions
ENSG00000155189	chromatin interactions

Extended variants
information (count: 6818 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:6818 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2922820	chr8:6317165-6317166	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185726450	chr8:6317166-6317167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs17076982	chr8:6317183-6317184	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs145428169	chr8:6317217-6317218	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3020279	chr8:6317220-6317221	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs149190301	chr8:6317227-6317228	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550775305	chr8:6317228-6317229	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567770789	chr8:6317255-6317256	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2916746	chr8:6317267-6317268	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs143341808	chr8:6317308-6317309	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190584403	chr8:6317321-6317322	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114069679	chr8:6317335-6317336	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558854310	chr8:6317345-6317346	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569328634	chr8:6317366-6317367	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576211084	chr8:6317367-6317368	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139096106	chr8:6317377-6317378	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141671818	chr8:6317420-6317421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78797069	chr8:6317425-6317426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542600436	chr8:6317432-6317433	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553003547	chr8:6317436-6317437	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561048791	chr8:6317445-6317446	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147070414	chr8:6317459-6317460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529866599	chr8:6317465-6317466	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565206013	chr8:6317467-6317468	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141862746	chr8:6317468-6317469	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544403721	chr8:6317489-6317490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561177768	chr8:6317491-6317492	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530207231	chr8:6317492-6317493	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180943986	chr8:6317495-6317496	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183497268	chr8:6317505-6317506	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188573439	chr8:6317549-6317550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529056130	chr8:6317555-6317556	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58453720	chr8:6317556-6317557	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2440405	chr8:6317567-6317568	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs569547645	chr8:6317579-6317580	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181033715	chr8:6317582-6317583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569688396	chr8:6317634-6317635	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150588489	chr8:6317635-6317636	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138646450	chr8:6317669-6317670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149287039	chr8:6317701-6317702	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553138750	chr8:6317708-6317709	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146247769	chr8:6317714-6317715	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572856358	chr8:6317716-6317717	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75413153	chr8:6317722-6317723	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558539140	chr8:6317730-6317731	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575496957	chr8:6317752-6317753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544227495	chr8:6317764-6317765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561125656	chr8:6317788-6317789	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552191145	chr8:6317818-6317819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565712050	chr8:6317835-6317836	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD
Tetralogy of Fallot	22912587	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:2775 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6265000-6339200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:6287600-6344400	Weak transcription	Small Intestine	intestine
3	chr8:6301000-6338400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr8:6302800-6339800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:6303000-6317200	Weak transcription	Brain Substantia Nigra	brain
6	chr8:6303000-6317800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:6303000-6319400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:6303000-6321000	Weak transcription	Psoas Muscle	Psoas
9	chr8:6303000-6321000	Weak transcription	Hela-S3	cervix
10	chr8:6303000-6322800	Weak transcription	Ovary	ovary
11	chr8:6303000-6322800	Weak transcription	Spleen	Spleen
12	chr8:6303000-6325000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:6303000-6325200	Weak transcription	Pancreas	Pancrea
14	chr8:6303000-6338200	Weak transcription	Gastric	stomach
15	chr8:6303000-6338200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr8:6303000-6338400	Weak transcription	Colonic Mucosa	Colon
17	chr8:6303000-6338400	Weak transcription	Right Ventricle	heart
18	chr8:6303000-6339400	Weak transcription	Placenta	Placenta
19	chr8:6303200-6318200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:6303200-6318800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:6303200-6320400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr8:6303200-6321000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr8:6303200-6322600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr8:6303200-6322800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:6303200-6339400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr8:6303200-6339400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr8:6303200-6340000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr8:6303400-6320600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr8:6303400-6320800	Weak transcription	Colon Smooth Muscle	Colon
30	chr8:6303400-6321000	Weak transcription	Brain Anterior Caudate	brain
31	chr8:6303400-6321200	Weak transcription	HUVEC	blood vessel
32	chr8:6303600-6321600	Weak transcription	Brain Germinal Matrix	brain
33	chr8:6303800-6338400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr8:6304000-6322600	Weak transcription	Fetal Brain Female	brain
35	chr8:6304000-6338000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr8:6304400-6318200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr8:6304400-6360200	Weak transcription	Esophagus	oesophagus
38	chr8:6304600-6317400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:6304600-6321200	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr8:6304800-6317200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:6304800-6323000	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr8:6305200-6320000	Weak transcription	Fetal Muscle Leg	muscle
43	chr8:6305800-6317200	Weak transcription	Brain Hippocampus Middle	brain
44	chr8:6305800-6319800	Weak transcription	Primary B cells from cord blood	blood
45	chr8:6305800-6322800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr8:6306000-6317400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:6306000-6317400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr8:6306200-6318200	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr8:6306200-6322800	Weak transcription	Fetal Intestine Large	intestine
50	chr8:6306200-6325400	Weak transcription	K562	blood

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