Variant report

Variant	nsv1025734
Chromosome Location	chr8:6128828-6303511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2544)
CpG islands
(count:793)
Chromatin interactive
region (count:75)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2544 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6201384-6201656	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:6263882-6264269	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:6285833-6286815	K562	blood:	n/a	n/a
4	ARID3A	chr8:6263893-6264043	K562	blood:	n/a	n/a
5	ARID3A	chr8:6287029-6287220	K562	blood:	n/a	n/a
6	ARID3A	chr8:6281457-6281796	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:6281432-6281829	K562	blood:	n/a	n/a
8	ARID3A	chr8:6270786-6270943	K562	blood:	n/a	n/a
9	ATF1	chr8:6286138-6286688	K562	blood:	n/a	n/a
10	ATF2	chr8:6285699-6286950	GM12878	blood:	n/a	n/a
11	ATF2	chr8:6274564-6275935	GM12878	blood:	n/a	n/a
12	ATF2	chr8:6283712-6284449	GM12878	blood:	n/a	n/a
13	ATF2	chr8:6273689-6274273	GM12878	blood:	n/a	n/a
14	ATF2	chr8:6263711-6264270	GM12878	blood:	n/a	n/a
15	ATF2	chr8:6274572-6275754	GM12878	blood:	n/a	n/a
16	ATF2	chr8:6283513-6284264	GM12878	blood:	n/a	n/a
17	ATF2	chr8:6285679-6287065	GM12878	blood:	n/a	n/a
18	BACH1	chr8:6281726-6282075	K562	blood:	n/a	n/a
19	BACH1	chr8:6263916-6264157	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr8:6274761-6275058	GM12878	blood:	n/a	n/a
21	BATF	chr8:6286240-6286820	GM12878	blood:	n/a	n/a
22	BATF	chr8:6283891-6284144	GM12878	blood:	n/a	n/a
23	BATF	chr8:6275084-6275784	GM12878	blood:	n/a	n/a
24	BATF	chr8:6283796-6284188	GM12878	blood:	n/a	n/a
25	BATF	chr8:6274819-6275423	GM12878	blood:	n/a	n/a
26	BATF	chr8:6286244-6286758	GM12878	blood:	n/a	n/a
27	BATF	chr8:6285752-6286173	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:6275121-6275398	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:6285852-6286733	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:6285823-6286135	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:6286215-6286704	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:6274723-6275701	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:6283749-6284137	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:6283823-6284198	GM12878	blood:	n/a	n/a
35	BCL3	chr8:6286161-6286810	GM12878	blood:	n/a	n/a
36	BCL3	chr8:6286275-6286686	GM12878	blood:	n/a	n/a
37	BCLAF1	chr8:6263829-6264318	GM12878	blood:	n/a	chr8:6264126-6264139
38	BCLAF1	chr8:6285768-6287006	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:6283746-6284275	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:6275116-6275837	GM12878	blood:	n/a	n/a
41	BCLAF1	chr8:6286120-6286988	GM12878	blood:	n/a	n/a
42	BCLAF1	chr8:6274613-6275965	GM12878	blood:	n/a	n/a
43	BCLAF1	chr8:6283732-6284270	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:6263950-6264244	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:6285914-6286936	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:6287351-6287413	K562	blood:	n/a	n/a
47	BHLHE40	chr8:6281558-6281781	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:6264014-6264335	K562	blood:	n/a	n/a
49	BHLHE40	chr8:6285899-6287073	K562	blood:	n/a	n/a
50	BHLHE40	chr8:6281431-6281789	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6282955-6283005	HMEC	breast:	n/a
2	chr8:6264181-6264231	GM19239	blood:	n/a
3	chr8:6264171-6264221	SAEC	small airway:	n/a
4	chr8:6287904-6287954	HCT-116	colon:	n/a
5	chr8:6264181-6264231	GM12891	blood:	n/a
6	chr8:6282955-6283005	HCPEpiC	choroid plexus:	n/a
7	chr8:6264193-6264243	GM12891	blood:	n/a
8	chr8:6264959-6265009	GM12892	blood:	n/a
9	chr8:6259667-6259717	HRCEpiC	kidney:	n/a
10	chr8:6282955-6283005	AG09319	gingival:	n/a
11	chr8:6263623-6263673	SKMC	muscle:	n/a
12	chr8:6263789-6263839	HRCEpiC	kidney:	n/a
13	chr8:6264193-6264243	HRCEpiC	kidney:	n/a
14	chr8:6263363-6263413	AG04449	skin:	fetal
15	chr8:6287904-6287954	SK-N-SH	brain:	n/a
16	chr8:6287904-6287954	GM19239	blood:	n/a
17	chr8:6263268-6263318	GM12891	blood:	n/a
18	chr8:6189008-6189058	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:6263623-6263673	PFSK-1	brain:	n/a
20	chr8:6263623-6263673	BE2_C	brain:	n/a
21	chr8:6263623-6263673	HCPEpiC	choroid plexus:	n/a
22	chr8:6263363-6263413	K562	blood:	n/a
23	chr8:6263363-6263413	Jurkat	blood:	n/a
24	chr8:6264959-6265009	HCF	heart:	n/a
25	chr8:6264959-6265009	AG04450	lung:	fetal
26	chr8:6263363-6263413	HCT-116	colon:	n/a
27	chr8:6264181-6264231	SK-N-SH_RA	brain:	n/a
28	chr8:6287904-6287954	HEK293	kidney:	embryo
29	chr8:6263789-6263839	MCF10A-Er-Src	breast:	n/a
30	chr8:6263875-6263925	HRE	kidney:	n/a
31	chr8:6189008-6189058	U87	brain:	n/a
32	chr8:6263268-6263318	HPAEpiC	pulmonary alveolar:	n/a
33	chr8:6264181-6264231	Jurkat	blood:	n/a
34	chr8:6259667-6259717	MCF-7	breast:	n/a
35	chr8:6263875-6263925	AG09309	skin:	n/a
36	chr8:6263875-6263925	K562	blood:	n/a
37	chr8:6263875-6263925	SKMC	muscle:	n/a
38	chr8:6263623-6263673	IMR90	lung:	fetal
39	chr8:6264193-6264243	HIPEpiC	eye:	n/a
40	chr8:6263875-6263925	HMEC	breast:	n/a
41	chr8:6263623-6263673	GM12891	blood:	n/a
42	chr8:6263789-6263839	HRPEpiC	eye:	n/a
43	chr8:6189008-6189058	PrEC	prostate:	n/a
44	chr8:6259667-6259717	HAEpiC	amniotic membrane:	n/a
45	chr8:6189008-6189058	BE2_C	brain:	n/a
46	chr8:6282955-6283005	IMR90	lung:	fetal
47	chr8:6263623-6263673	HCM	heart:	n/a
48	chr8:6263789-6263839	HL-60	blood:	n/a
49	chr8:6282955-6283005	Hela-S3	cervix:	n/a
50	chr8:6264959-6265009	U87	brain:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:6280717..6283066-chr8:6285737..6287533,2	K562	blood:
2	chr8:6277995..6281670-chr8:6564311..6568348,3	MCF-7	breast:
3	chr8:6260743..6265726-chr8:6271007..6273930,5	K562	blood:
4	chr8:6283795..6285745-chr8:6287831..6290125,2	K562	blood:
5	chr8:6280706..6282253-chr8:6565976..6568022,2	K562	blood:
6	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
7	chr8:6286838..6288405-chr8:6317627..6319306,2	K562	blood:
8	chr8:6264145..6266520-chr8:6281324..6283294,2	K562	blood:
9	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
10	chr8:6286039..6288419-chr8:6293741..6296990,3	K562	blood:
11	chr8:6285374..6287527-chr8:6566715..6569546,2	K562	blood:
12	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
13	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
14	chr8:6260700..6262859-chr8:6263480..6266725,3	K562	blood:
15	chr8:6295181..6297550-chr8:6299786..6302300,2	K562	blood:
16	chr8:6286159..6289308-chr8:6294471..6296990,3	K562	blood:
17	chr8:6281135..6282131-chr8:6429461..6430416,3	K562	blood:
18	chr8:6281436..6282039-chr8:6539712..6540563,2	MCF-7	breast:
19	chr8:6281302..6282067-chr8:6658057..6658859,2	MCF-7	breast:
20	chr8:6295181..6297550-chr8:6299786..6302300,2	K562	blood:
21	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
22	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
23	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
24	chr8:6282319..6282937-chr8:6658301..6658907,2	MCF-7	breast:
25	chr8:6296050..6297803-chr8:6299786..6301470,2	K562	blood:
26	chr8:6257664..6260408-chr8:6262144..6263812,2	MCF-7	breast:
27	chr8:6275765..6277346-chr8:6279948..6281566,2	K562	blood:
28	chr8:6257269..6261482-chr8:6261737..6265749,8	MCF-7	breast:
29	chr8:6263561..6264353-chrX:135962392..135963076,2	NB4	blood:
30	chr8:6282250..6282973-chr8:6539904..6540599,2	MCF-7	breast:
31	chr8:6275765..6277346-chr8:6279948..6281566,2	K562	blood:
32	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
33	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
34	chr8:6281660..6282170-chr8:6637148..6637690,2	MCF-7	breast:
35	chr17:49196178..49198302-chr8:6264048..6265705,2	K562	blood:
36	chr8:6282837..6283344-chr8:6657975..6658871,2	K562	blood:
37	chr8:6262086..6265734-chr8:6266423..6270611,6	MCF-7	breast:
38	chr8:6264019..6265631-chr8:6276024..6277548,2	K562	blood:
39	chr8:6281170..6282061-chr8:6636804..6637878,7	K562	blood:
40	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
41	chr8:6274685..6276639-chr8:6565162..6567770,2	MCF-7	breast:
42	chr8:6286039..6288419-chr8:6293741..6296990,3	K562	blood:
43	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
44	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
45	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
46	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
47	chr8:6280318..6283443-chr8:6285224..6287821,3	MCF-7	breast:
48	chr8:6281453..6284315-chr8:6428967..6430752,3	K562	blood:
49	chr8:6262451..6265274-chr8:6277590..6279636,2	MCF-7	breast:
50	chr8:6257664..6260408-chr8:6262144..6263812,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-2	chr8:6263227-6264069	NR_040040
2	lnc-ANGPT2-2	chr8:6264049-6264055	XLOC_006985
3	lnc-ANGPT2-2	chr8:6263118-6263892	ENSG00000246089
4	lnc-ANGPT2-8	chr8:6250635-6251477	ucscGeneNc_uc003wqf_1
5	lnc-ANGPT2-2	chr8:6263227-6264069	XLOC_006985
6	lnc-ANGPT2-2	chr8:6262438-6264096	NONHSAT124771
7	lnc-ANGPT2-2	chr8:6262449-6263892	XLOC_006985
8	lnc-ANGPT2-8	chr8:6248485-6250049	ucscGeneNc_uc003wqf_1
9	lnc-ANGPT2-2	chr8:6261079-6262641	XLOC_006985
10	lnc-ANGPT2-2	chr8:6264049-6264229	ENSG00000246089
11	lnc-ANGPT2-2	chr8:6261077-6262641	NR_040040
12	lnc-ANGPT2-2	chr8:6262927-6264063	ENSG00000246089.3
13	lnc-ANGPT2-2	chr8:6264603-6264663	ENSG00000246089

No data

Variant related genes	Relation type
MCPH1	TF binding region
ENSG00000246089	TF binding region
MCPH1	CpG island
ENSG00000246089	CpG island
ENSG00000246089	chromatin interactions
ENSG00000008294	chromatin interactions
ENSG00000249898	chromatin interactions
ENSG00000147274	chromatin interactions
ENSG00000155189	chromatin interactions
ENSG00000147316	chromatin interactions

Extended variants
information (count: 9417 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:9417 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567849202	chr8:6132012-6132013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528901590	chr8:6132022-6132023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181781495	chr8:6132023-6132024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565773983	chr8:6132067-6132068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150388015	chr8:6132068-6132069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73192634	chr8:6132069-6132070	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571153715	chr8:6132087-6132088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536827691	chr8:6132090-6132091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557254348	chr8:6132135-6132136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144988264	chr8:6132139-6132140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536671388	chr8:6132173-6132174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187569754	chr8:6132180-6132181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573295612	chr8:6132190-6132191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545566508	chr8:6132192-6132193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565357072	chr8:6132230-6132231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563688017	chr8:6132250-6132251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575945008	chr8:6132262-6132263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544784679	chr8:6132300-6132301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148232808	chr8:6132320-6132321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561649809	chr8:6132326-6132327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530286976	chr8:6132351-6132352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536258150	chr8:6132353-6132354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112644001	chr8:6132361-6132362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75091977	chr8:6132391-6132392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528070022	chr8:6132415-6132416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372217532	chr8:6132426-6132427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117688018	chr8:6132476-6132477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536862667	chr8:6132506-6132507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114299394	chr8:6132508-6132509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs57084818	chr8:6132519-6132520	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536116440	chr8:6132549-6132550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190703600	chr8:6132560-6132561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573302261	chr8:6132570-6132571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539021068	chr8:6132595-6132596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112276107	chr8:6132608-6132609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575782955	chr8:6132627-6132628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544795196	chr8:6132641-6132642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561287732	chr8:6132642-6132643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574970470	chr8:6132662-6132663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540614368	chr8:6132673-6132674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61462536	chr8:6132677-6132678	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs534821698	chr8:6132693-6132694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528108070	chr8:6132706-6132707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7843093	chr8:6132709-6132710	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564658272	chr8:6132712-6132713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548431861	chr8:6132719-6132720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149094057	chr8:6132724-6132725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183003793	chr8:6132764-6132765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371689483	chr8:6132782-6132783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35222608	chr8:6132784-6132785	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:151)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
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
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
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	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
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
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2483 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:6132200-6132800	Enhancers	Spleen	Spleen
3	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
4	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
6	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:6147200-6148200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr8:6147200-6148200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells	blood
19	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:6147200-6148800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr8:6147600-6147800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr8:6147800-6148000	Enhancers	Duodenum Mucosa	Duodenum
24	chr8:6147800-6148200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:6147800-6148200	Enhancers	Adipose Nuclei	Adipose
26	chr8:6147800-6148200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:6147800-6148800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr8:6147800-6148800	Enhancers	Primary B cells from cord blood	blood
29	chr8:6148000-6149000	Enhancers	Primary B cells from peripheral blood	blood
30	chr8:6148000-6149000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr8:6148200-6148600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr8:6148200-6149000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr8:6148200-6149400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr8:6148200-6149600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr8:6148600-6149000	Enhancers	Brain Cingulate Gyrus	brain
36	chr8:6148600-6149400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr8:6148600-6149400	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr8:6148600-6149600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr8:6148600-6149800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:6148800-6149000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
41	chr8:6148800-6149000	Enhancers	GM12878-XiMat	blood
42	chr8:6148800-6149200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr8:6148800-6149200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr8:6148800-6149400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr8:6148800-6149400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
46	chr8:6148800-6149400	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr8:6148800-6149400	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr8:6148800-6149400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr8:6149000-6149200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
50	chr8:6149000-6149400	Flanking Active TSS	Primary B cells from peripheral blood	blood

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