Variant report

Variant	nsv1024103
Chromosome Location	chr8:6124125-6303511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2555)
CpG islands
(count:794)
Chromatin interactive
region (count:75)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2555 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6285833-6286815	K562	blood:	n/a	n/a
2	ARID3A	chr8:6263893-6264043	K562	blood:	n/a	n/a
3	ARID3A	chr8:6201384-6201656	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:6287029-6287220	K562	blood:	n/a	n/a
5	ARID3A	chr8:6263882-6264269	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:6281432-6281829	K562	blood:	n/a	n/a
7	ARID3A	chr8:6270786-6270943	K562	blood:	n/a	n/a
8	ARID3A	chr8:6281457-6281796	HepG2	liver:	n/a	n/a
9	ATF1	chr8:6286138-6286688	K562	blood:	n/a	n/a
10	ATF2	chr8:6274572-6275754	GM12878	blood:	n/a	n/a
11	ATF2	chr8:6274564-6275935	GM12878	blood:	n/a	n/a
12	ATF2	chr8:6273689-6274273	GM12878	blood:	n/a	n/a
13	ATF2	chr8:6283712-6284449	GM12878	blood:	n/a	n/a
14	ATF2	chr8:6263711-6264270	GM12878	blood:	n/a	n/a
15	ATF2	chr8:6285679-6287065	GM12878	blood:	n/a	n/a
16	ATF2	chr8:6285699-6286950	GM12878	blood:	n/a	n/a
17	ATF2	chr8:6283513-6284264	GM12878	blood:	n/a	n/a
18	BACH1	chr8:6263916-6264157	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:6281726-6282075	K562	blood:	n/a	n/a
20	BATF	chr8:6274819-6275423	GM12878	blood:	n/a	n/a
21	BATF	chr8:6283891-6284144	GM12878	blood:	n/a	n/a
22	BATF	chr8:6275084-6275784	GM12878	blood:	n/a	n/a
23	BATF	chr8:6283796-6284188	GM12878	blood:	n/a	n/a
24	BATF	chr8:6274761-6275058	GM12878	blood:	n/a	n/a
25	BATF	chr8:6125905-6126127	GM12878	blood:	n/a	n/a
26	BATF	chr8:6286240-6286820	GM12878	blood:	n/a	n/a
27	BATF	chr8:6285752-6286173	GM12878	blood:	n/a	n/a
28	BATF	chr8:6286244-6286758	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:6286215-6286704	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:6275121-6275398	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:6283823-6284198	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:6285852-6286733	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:6283749-6284137	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:6274723-6275701	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:6285823-6286135	GM12878	blood:	n/a	n/a
36	BCL3	chr8:6286161-6286810	GM12878	blood:	n/a	n/a
37	BCL3	chr8:6286275-6286686	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:6283732-6284270	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:6286120-6286988	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:6275116-6275837	GM12878	blood:	n/a	n/a
41	BCLAF1	chr8:6285768-6287006	GM12878	blood:	n/a	n/a
42	BCLAF1	chr8:6274613-6275965	GM12878	blood:	n/a	n/a
43	BCLAF1	chr8:6263829-6264318	GM12878	blood:	n/a	chr8:6264126-6264139
44	BCLAF1	chr8:6283746-6284275	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:6263973-6264241	HepG2	liver:	n/a	n/a
46	BHLHE40	chr8:6264014-6264335	K562	blood:	n/a	n/a
47	BHLHE40	chr8:6285914-6286936	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:6285899-6287073	K562	blood:	n/a	n/a
49	BHLHE40	chr8:6274528-6275764	GM12878	blood:	n/a	n/a
50	BHLHE40	chr8:6281431-6281789	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6264171-6264221	HRCEpiC	kidney:	n/a
2	chr8:6264171-6264221	HRCEpiC	kidney:	n/a
3	chr8:6264959-6265009	AG10803	skin:	n/a
4	chr8:6189008-6189058	NT2-D1	testis:	n/a
5	chr8:6264181-6264231	T-47D	breast:	n/a
6	chr8:6259667-6259717	BJ	skin:	n/a
7	chr8:6263623-6263673	GM12891	blood:	n/a
8	chr8:6287904-6287954	AG04450	lung:	fetal
9	chr8:6264959-6265009	SK-N-SH_RA	brain:	n/a
10	chr8:6263268-6263318	HCM	heart:	n/a
11	chr8:6264181-6264231	HCT-116	colon:	n/a
12	chr8:6263875-6263925	HCT-116	colon:	n/a
13	chr8:6263789-6263839	HCM	heart:	n/a
14	chr8:6259667-6259717	SK-N-MC	brain:	n/a
15	chr8:6263875-6263925	PFSK-1	brain:	n/a
16	chr8:6264171-6264221	HCPEpiC	choroid plexus:	n/a
17	chr8:6263789-6263839	NHBE	bronchial:	n/a
18	chr8:6263363-6263413	HCT-116	colon:	n/a
19	chr8:6264959-6265009	PFSK-1	brain:	n/a
20	chr8:6263789-6263839	NB4	blood:	n/a
21	chr8:6263875-6263925	HRE	kidney:	n/a
22	chr8:6264181-6264231	HMEC	breast:	n/a
23	chr8:6263363-6263413	LNCaP	prostate:	n/a
24	chr8:6263789-6263839	NH-A	brain:	n/a
25	chr8:6263875-6263925	HNPCEpiC	eye:	n/a
26	chr8:6263268-6263318	AG04449	skin:	fetal
27	chr8:6263363-6263413	PFSK-1	brain:	n/a
28	chr8:6264193-6264243	T-47D	breast:	n/a
29	chr8:6264181-6264231	Jurkat	blood:	n/a
30	chr8:6189008-6189058	Jurkat	blood:	n/a
31	chr8:6189008-6189058	HUVEC	blood vessel:	n/a
32	chr8:6264181-6264231	PANC-1	pancreas:	n/a
33	chr8:6263363-6263413	H1-hESC	embryonic stem cell:	embryo
34	chr8:6287904-6287954	ProgFib	skin:	n/a
35	chr8:6263623-6263673	HRCEpiC	kidney:	n/a
36	chr8:6264181-6264231	HRE	kidney:	n/a
37	chr8:6263789-6263839	AG09309	skin:	n/a
38	chr8:6263789-6263839	HNPCEpiC	eye:	n/a
39	chr8:6287904-6287954	U87	brain:	n/a
40	chr8:6263623-6263673	RPTEC	kidney:	n/a
41	chr8:6189008-6189058	AG09309	skin:	n/a
42	chr8:6287904-6287954	MCF10A-Er-Src	breast:	n/a
43	chr8:6263623-6263673	BJ	skin:	n/a
44	chr8:6189008-6189058	AoSMC	blood vessel:	n/a
45	chr8:6263623-6263673	HNPCEpiC	eye:	n/a
46	chr8:6264959-6265009	HRE	kidney:	n/a
47	chr8:6264959-6265009	PANC-1	pancreas:	n/a
48	chr8:6263363-6263413	A549	lung:	n/a
49	chr8:6264171-6264221	HMEC	breast:	n/a
50	chr8:6264959-6265009	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
2	chr8:6264019..6265631-chr8:6276024..6277548,2	K562	blood:
3	chr8:6286159..6289308-chr8:6294471..6296990,3	K562	blood:
4	chr8:6262974..6265715-chr8:6564962..6567789,4	MCF-7	breast:
5	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
6	chr8:6257269..6261482-chr8:6261737..6265749,8	MCF-7	breast:
7	chr8:6264145..6266520-chr8:6281324..6283294,2	K562	blood:
8	chr8:6262086..6265734-chr8:6266423..6270611,6	MCF-7	breast:
9	chr8:6261231..6262782-chr8:6268049..6270486,2	K562	blood:
10	chr8:6281453..6284315-chr8:6428967..6430752,3	K562	blood:
11	chr8:6286159..6289308-chr8:6294471..6296990,3	K562	blood:
12	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
13	chr8:6280960..6282945-chr8:6426818..6429637,2	K562	blood:
14	chr8:6285374..6287527-chr8:6566715..6569546,2	K562	blood:
15	chr8:6282447..6283252-chr8:6539685..6540602,2	K562	blood:
16	chr8:6295181..6297550-chr8:6299786..6302300,2	K562	blood:
17	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
18	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
19	chr8:6283795..6285745-chr8:6287831..6290125,2	K562	blood:
20	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
21	chr8:6283795..6285745-chr8:6287831..6290125,2	K562	blood:
22	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
23	chr8:6286039..6288419-chr8:6293741..6296990,3	K562	blood:
24	chr8:6281660..6282170-chr8:6637148..6637690,2	MCF-7	breast:
25	chr8:6261231..6262782-chr8:6268049..6270486,2	K562	blood:
26	chr8:6277995..6281670-chr8:6564311..6568348,3	MCF-7	breast:
27	chr8:6280706..6282253-chr8:6565976..6568022,2	K562	blood:
28	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:
29	chr8:6280717..6283066-chr8:6285737..6287533,2	K562	blood:
30	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
31	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
32	chr8:6275765..6277346-chr8:6279948..6281566,2	K562	blood:
33	chr8:6281170..6282061-chr8:6636804..6637878,7	K562	blood:
34	chr8:6257664..6260408-chr8:6262144..6263812,2	MCF-7	breast:
35	chr8:6282250..6282973-chr8:6539904..6540599,2	MCF-7	breast:
36	chr8:6253865..6260422-chr8:6262184..6266042,7	K562	blood:
37	chr8:6280318..6283443-chr8:6285224..6287821,3	MCF-7	breast:
38	chr8:6262451..6265274-chr8:6277590..6279636,2	MCF-7	breast:
39	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
40	chr8:6286039..6288419-chr8:6293741..6296990,3	K562	blood:
41	chr8:6277390..6279333-chr8:6576770..6578776,2	K562	blood:
42	chr8:6263426..6264997-chr8:6273721..6275248,2	MCF-7	breast:
43	chr8:6281302..6282067-chr8:6658057..6658859,2	MCF-7	breast:
44	chr8:6296050..6297803-chr8:6299786..6301470,2	K562	blood:
45	chr8:6282319..6282937-chr8:6658301..6658907,2	MCF-7	breast:
46	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
47	chr8:6262444..6265412-chr8:6565205..6567179,2	K562	blood:
48	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
49	chr8:6263561..6264353-chrX:135962392..135963076,2	NB4	blood:
50	chr8:6286384..6290104-chr8:6563339..6566818,4	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 9448 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:9448 , 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	rs543354517	chr8:6128222-6128223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531209264	chr8:6128227-6128228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563237410	chr8:6128234-6128235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187863466	chr8:6128249-6128250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191223075	chr8:6128274-6128275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559607819	chr8:6128285-6128286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528557336	chr8:6128298-6128299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375184459	chr8:6128312-6128313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551684815	chr8:6128320-6128321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552018496	chr8:6128327-6128328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537639638	chr8:6128336-6128337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182338718	chr8:6128369-6128370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567944854	chr8:6128392-6128393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149445758	chr8:6128398-6128399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187010635	chr8:6128423-6128424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367814290	chr8:6128433-6128434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572052622	chr8:6128436-6128437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534676316	chr8:6128464-6128465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62505529	chr8:6128474-6128475	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs201906184	chr8:6128507-6128508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113464227	chr8:6128520-6128521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543189281	chr8:6128525-6128526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563275641	chr8:6128541-6128542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4240685	chr8:6128542-6128543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542633581	chr8:6128550-6128551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73192627	chr8:6128562-6128563	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs528585225	chr8:6128565-6128566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545524068	chr8:6128578-6128579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565214862	chr8:6128580-6128581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531165330	chr8:6128584-6128585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376070276	chr8:6128588-6128589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567849202	chr8:6132012-6132013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528901590	chr8:6132022-6132023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181781495	chr8:6132023-6132024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565773983	chr8:6132067-6132068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150388015	chr8:6132068-6132069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73192634	chr8:6132069-6132070	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs571153715	chr8:6132087-6132088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536827691	chr8:6132090-6132091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557254348	chr8:6132135-6132136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144988264	chr8:6132139-6132140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536671388	chr8:6132173-6132174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187569754	chr8:6132180-6132181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573295612	chr8:6132190-6132191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545566508	chr8:6132192-6132193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565357072	chr8:6132230-6132231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563688017	chr8:6132250-6132251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575945008	chr8:6132262-6132263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544784679	chr8:6132300-6132301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148232808	chr8:6132320-6132321	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:2484 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:6132200-6132800	Enhancers	Spleen	Spleen
4	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
5	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
7	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr8:6147200-6148200	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr8:6147200-6148200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells	blood
20	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:6147200-6148800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr8:6147600-6147800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr8:6147800-6148000	Enhancers	Duodenum Mucosa	Duodenum
25	chr8:6147800-6148200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:6147800-6148200	Enhancers	Adipose Nuclei	Adipose
27	chr8:6147800-6148200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr8:6147800-6148800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:6147800-6148800	Enhancers	Primary B cells from cord blood	blood
30	chr8:6148000-6149000	Enhancers	Primary B cells from peripheral blood	blood
31	chr8:6148000-6149000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr8:6148200-6148600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr8:6148200-6149000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr8:6148200-6149400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr8:6148200-6149600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr8:6148600-6149000	Enhancers	Brain Cingulate Gyrus	brain
37	chr8:6148600-6149400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:6148600-6149400	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr8:6148600-6149600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:6148600-6149800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:6148800-6149000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
42	chr8:6148800-6149000	Enhancers	GM12878-XiMat	blood
43	chr8:6148800-6149200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr8:6148800-6149200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr8:6148800-6149400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr8:6148800-6149400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
47	chr8:6148800-6149400	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr8:6148800-6149400	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr8:6148800-6149400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:6149000-6149200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose

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