Variant report

Variant	nsv949501
Chromosome Location	chr8:6081704-6303511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2799)
CpG islands
(count:917)
Chromatin interactive
region (count:86)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2799 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6263882-6264269	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:6281457-6281796	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:6201384-6201656	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:6285833-6286815	K562	blood:	n/a	n/a
5	ARID3A	chr8:6263893-6264043	K562	blood:	n/a	n/a
6	ARID3A	chr8:6287029-6287220	K562	blood:	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	chr8:6273689-6274273	GM12878	blood:	n/a	n/a
11	ATF2	chr8:6263711-6264270	GM12878	blood:	n/a	n/a
12	ATF2	chr8:6274572-6275754	GM12878	blood:	n/a	n/a
13	ATF2	chr8:6285679-6287065	GM12878	blood:	n/a	n/a
14	ATF2	chr8:6285699-6286950	GM12878	blood:	n/a	n/a
15	ATF2	chr8:6283513-6284264	GM12878	blood:	n/a	n/a
16	ATF2	chr8:6283712-6284449	GM12878	blood:	n/a	n/a
17	ATF2	chr8:6274564-6275935	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	chr8:6125905-6126127	GM12878	blood:	n/a	n/a
21	BATF	chr8:6283891-6284144	GM12878	blood:	n/a	n/a
22	BATF	chr8:6274819-6275423	GM12878	blood:	n/a	n/a
23	BATF	chr8:6283796-6284188	GM12878	blood:	n/a	n/a
24	BATF	chr8:6286244-6286758	GM12878	blood:	n/a	n/a
25	BATF	chr8:6274761-6275058	GM12878	blood:	n/a	n/a
26	BATF	chr8:6275084-6275784	GM12878	blood:	n/a	n/a
27	BATF	chr8:6286240-6286820	GM12878	blood:	n/a	n/a
28	BATF	chr8:6285752-6286173	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:6286215-6286704	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:6283823-6284198	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:6285823-6286135	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:6275121-6275398	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:6274723-6275701	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:6285852-6286733	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:6283749-6284137	GM12878	blood:	n/a	n/a
36	BCL3	chr8:6286275-6286686	GM12878	blood:	n/a	n/a
37	BCL3	chr8:6286161-6286810	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:6274613-6275965	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:6286120-6286988	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:6283732-6284270	GM12878	blood:	n/a	n/a
41	BCLAF1	chr8:6285768-6287006	GM12878	blood:	n/a	n/a
42	BCLAF1	chr8:6263829-6264318	GM12878	blood:	n/a	chr8:6264126-6264139
43	BCLAF1	chr8:6275116-6275837	GM12878	blood:	n/a	n/a
44	BCLAF1	chr8:6283746-6284275	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:6263973-6264241	HepG2	liver:	n/a	n/a
46	BHLHE40	chr8:6149426-6149734	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:6283569-6284269	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:6273910-6274154	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:6287351-6287413	K562	blood:	n/a	n/a
50	BHLHE40	chr8:6285899-6287073	K562	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6263789-6263839	T-47D	breast:	n/a
2	chr8:6263875-6263925	PrEC	prostate:	n/a
3	chr8:6263789-6263839	T-47D	breast:	n/a
4	chr8:6263875-6263925	PrEC	prostate:	n/a
5	chr8:6263789-6263839	PFSK-1	brain:	n/a
6	chr8:6263268-6263318	HAEpiC	amniotic membrane:	n/a
7	chr8:6282955-6283005	AG09309	skin:	n/a
8	chr8:6189008-6189058	HUVEC	blood vessel:	n/a
9	chr8:6263268-6263318	GM12891	blood:	n/a
10	chr8:6263268-6263318	NT2-D1	testis:	n/a
11	chr8:6118526-6118576	HIPEpiC	eye:	n/a
12	chr8:6264171-6264221	HRPEpiC	eye:	n/a
13	chr8:6263875-6263925	HRPEpiC	eye:	n/a
14	chr8:6263789-6263839	HEEpiC	esophagus:	n/a
15	chr8:6264171-6264221	NB4	blood:	n/a
16	chr8:6263875-6263925	NHBE	bronchial:	n/a
17	chr8:6259667-6259717	GM12892	blood:	n/a
18	chr8:6118526-6118576	NH-A	brain:	n/a
19	chr8:6263789-6263839	HepG2	liver:	n/a
20	chr8:6118526-6118576	GM06990	blood:	n/a
21	chr8:6263623-6263673	Hela-S3	cervix:	n/a
22	chr8:6264181-6264231	NHDF-neo	bronchial:	n/a
23	chr8:6263623-6263673	GM19239	blood:	n/a
24	chr8:6263268-6263318	AG04450	lung:	fetal
25	chr8:6118526-6118576	HRCEpiC	kidney:	n/a
26	chr8:6287904-6287954	SK-N-SH_RA	brain:	n/a
27	chr8:6263875-6263925	K562	blood:	n/a
28	chr8:6259667-6259717	MCF10A-Er-Src	breast:	n/a
29	chr8:6264171-6264221	SAEC	small airway:	n/a
30	chr8:6118575-6118625	HMEC	breast:	n/a
31	chr8:6263363-6263413	T-47D	breast:	n/a
32	chr8:6263268-6263318	SK-N-MC	brain:	n/a
33	chr8:6263363-6263413	Hela-S3	cervix:	n/a
34	chr8:6263363-6263413	ovcar-3	ovarian:	n/a
35	chr8:6259667-6259717	HCM	heart:	n/a
36	chr8:6259667-6259717	ECC-1	luminal epithelium:	n/a
37	chr8:6263789-6263839	NB4	blood:	n/a
38	chr8:6259667-6259717	GM12878	blood:	n/a
39	chr8:6264181-6264231	GM06990	blood:	n/a
40	chr8:6264193-6264243	AG10803	skin:	n/a
41	chr8:6282955-6283005	CMK	blood:	n/a
42	chr8:6263875-6263925	T-47D	breast:	n/a
43	chr8:6264181-6264231	HCT-116	colon:	n/a
44	chr8:6287904-6287954	AG10803	skin:	n/a
45	chr8:6263789-6263839	HNPCEpiC	eye:	n/a
46	chr8:6263623-6263673	HNPCEpiC	eye:	n/a
47	chr8:6264171-6264221	MCF-7	breast:	n/a
48	chr8:6263875-6263925	AG10803	skin:	n/a
49	chr8:6264959-6265009	SAEC	small airway:	n/a
50	chr8:6264181-6264231	LNCaP	prostate:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:6080157..6081666-chr8:6091415..6093477,2	MCF-7	breast:
2	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
3	chr8:6281302..6282067-chr8:6658057..6658859,2	MCF-7	breast:
4	chr8:6257664..6260408-chr8:6262144..6263812,2	MCF-7	breast:
5	chr8:6260700..6262859-chr8:6263480..6266725,3	K562	blood:
6	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
7	chr8:6285374..6287527-chr8:6566715..6569546,2	K562	blood:
8	chr8:6275765..6277346-chr8:6279948..6281566,2	K562	blood:
9	chr8:6263912..6265972-chr8:6565205..6568456,4	K562	blood:
10	chr8:6280318..6283443-chr8:6285224..6287821,3	MCF-7	breast:
11	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
12	chr8:6283795..6285745-chr8:6287831..6290125,2	K562	blood:
13	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
14	chr8:6262444..6265412-chr8:6565205..6567179,2	K562	blood:
15	chr8:6264145..6266520-chr8:6281324..6283294,2	K562	blood:
16	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
17	chr8:6263561..6264353-chrX:135962392..135963076,2	NB4	blood:
18	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
19	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
20	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
21	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
22	chr8:6282319..6282937-chr8:6658301..6658907,2	MCF-7	breast:
23	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
24	chr8:6277390..6279333-chr8:6576770..6578776,2	K562	blood:
25	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
26	chr8:6296050..6297803-chr8:6299786..6301470,2	K562	blood:
27	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
28	chr8:6079332..6082540-chr8:6084426..6086508,3	K562	blood:
29	chr8:6280706..6282253-chr8:6565976..6568022,2	K562	blood:
30	chr8:6281176..6281768-chr8:6657921..6658559,2	K562	blood:
31	chr8:6281453..6284315-chr8:6428967..6430752,3	K562	blood:
32	chr8:6295181..6297550-chr8:6299786..6302300,2	K562	blood:
33	chr8:6285464..6288077-chr8:6414656..6417304,2	K562	blood:
34	chr8:6281660..6282170-chr8:6637148..6637690,2	MCF-7	breast:
35	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
36	chr8:6282250..6282973-chr8:6539904..6540599,2	MCF-7	breast:
37	chr8:6282837..6283344-chr8:6657975..6658871,2	K562	blood:
38	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
39	chr8:6280717..6283066-chr8:6285737..6287533,2	K562	blood:
40	chr8:6274685..6276639-chr8:6565162..6567770,2	MCF-7	breast:
41	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:
42	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
43	chr8:6280960..6282945-chr8:6426818..6429637,2	K562	blood:
44	chr8:6115678..6116241-chr8:6687345..6688278,2	K562	blood:
45	chr8:6281170..6282061-chr8:6636804..6637878,7	K562	blood:
46	chr8:6286384..6290104-chr8:6563339..6566818,4	MCF-7	breast:
47	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:
48	chr8:6286838..6288405-chr8:6317627..6319306,2	K562	blood:
49	chr8:6286159..6289308-chr8:6294471..6296990,3	K562	blood:
50	chr8:6263426..6264997-chr8:6273721..6275248,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-2	chr8:6262927-6264063	ENSG00000246089.3
2	lnc-ANGPT2-2	chr8:6263227-6264069	XLOC_006985
3	lnc-ANGPT2-2	chr8:6264603-6264663	ENSG00000246089
4	lnc-ANGPT2-2	chr8:6264049-6264055	XLOC_006985
5	lnc-ANGPT2-2	chr8:6262449-6263892	XLOC_006985
6	lnc-ANGPT2-3	chr8:6114933-6115058	ENSG00000253880
7	lnc-ANGPT2-2	chr8:6262438-6264096	NONHSAT124771
8	lnc-ANGPT2-8	chr8:6250635-6251477	ucscGeneNc_uc003wqf_1
9	lnc-ANGPT2-2	chr8:6263227-6264069	NR_040040
10	lnc-ANGPT2-11	chr8:6082847-6083064	NONHSAT124769
11	lnc-ANGPT2-2	chr8:6261079-6262641	XLOC_006985
12	lnc-ANGPT2-2	chr8:6261077-6262641	NR_040040
13	lnc-ANGPT2-8	chr8:6248485-6250049	ucscGeneNc_uc003wqf_1
14	lnc-ANGPT2-2	chr8:6264049-6264229	ENSG00000246089
15	lnc-ANGPT2-2	chr8:6263118-6263892	ENSG00000246089

No data

Variant related genes	Relation type
MCPH1	TF binding region
ENSG00000246089	TF binding region
ENSG00000253880	TF binding region
MCPH1	CpG island
ENSG00000246089	CpG island
ENSG00000253880	CpG island
ENSG00000147316	chromatin interactions
ENSG00000155189	chromatin interactions
ENSG00000147274	chromatin interactions
ENSG00000246089	chromatin interactions
ENSG00000249898	chromatin interactions
ENSG00000253880	chromatin interactions
ENSG00000008294	chromatin interactions

Extended variants
information (count: 11493 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:11493 , 50 per page) page: 1 2 3 4 5 6 7 ... 230

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4504660	chr8:6081704-6081705	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529169835	chr8:6081718-6081719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548942316	chr8:6081726-6081727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145909687	chr8:6081744-6081745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534795912	chr8:6081747-6081748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558278070	chr8:6081788-6081789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140551780	chr8:6081806-6081807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73190723	chr8:6081813-6081814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4629890	chr8:6081834-6081835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71212881	chr8:6081836-6081837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537610250	chr8:6081842-6081843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557603548	chr8:6081859-6081860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369752032	chr8:6081860-6081861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543379221	chr8:6081881-6081882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555767844	chr8:6081898-6081899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3903108	chr8:6081917-6081918	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs540677119	chr8:6081918-6081919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564168678	chr8:6081927-6081928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370733339	chr8:6081933-6081934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532902650	chr8:6081934-6081935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374107568	chr8:6081974-6081975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4407895	chr8:6081981-6081982	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563168674	chr8:6081993-6081994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201838377	chr8:6081997-6081998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111563829	chr8:6081998-6081999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77467408	chr8:6082009-6082010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11422171	chr8:6082010-6082011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529133648	chr8:6082064-6082065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190714692	chr8:6082099-6082100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191183254	chr8:6082139-6082140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555407145	chr8:6082145-6082146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12682138	chr8:6082154-6082155	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571679192	chr8:6082155-6082156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537178362	chr8:6082214-6082215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6993405	chr8:6082233-6082234	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs138819084	chr8:6082237-6082238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141383232	chr8:6082254-6082255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183734984	chr8:6082267-6082268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553658401	chr8:6082270-6082271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6993439	chr8:6082279-6082280	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs146951769	chr8:6082284-6082285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375717403	chr8:6082311-6082312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138048935	chr8:6082335-6082336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577643494	chr8:6082346-6082347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543145947	chr8:6082354-6082355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563129876	chr8:6082389-6082390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573545110	chr8:6082394-6082395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542416291	chr8:6082396-6082397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559559142	chr8:6082405-6082406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528389524	chr8:6082449-6082450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

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
Melanoma	20688739	CNVD
early-passage human iPS cells	21368824	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
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2530 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6080800-6081800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:6080800-6082000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:6081400-6087800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr8:6081800-6082800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:6082000-6082400	Enhancers	Fetal Brain Male	brain
6	chr8:6082400-6084600	Weak transcription	Fetal Brain Male	brain
7	chr8:6084600-6087200	Enhancers	Fetal Brain Male	brain
8	chr8:6086800-6087800	Enhancers	Pancreas	Pancrea
9	chr8:6087000-6087800	Enhancers	Esophagus	oesophagus
10	chr8:6087000-6088400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr8:6087000-6089000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:6100200-6100600	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr8:6104000-6105600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:6104000-6106000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr8:6104400-6107400	Enhancers	Primary hematopoietic stem cells	blood
16	chr8:6104800-6105200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:6105000-6107400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr8:6105200-6105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:6105600-6106400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:6106000-6106400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:6107000-6107200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr8:6107400-6110200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr8:6107400-6110600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr8:6110200-6110600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr8:6110600-6111000	Enhancers	Primary hematopoietic stem cells	blood
28	chr8:6110600-6111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr8:6111000-6112400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:6111800-6112800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr8:6112200-6112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:6112200-6112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:6112400-6112600	Enhancers	Primary hematopoietic stem cells	blood
36	chr8:6112800-6114800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
40	chr8:6119400-6120000	Enhancers	Osteobl	bone
41	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
43	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
46	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:6132200-6132800	Enhancers	Spleen	Spleen
50	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea

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