Variant report

Variant	nsv6294
Chromosome Location	chr8:90705780-90750101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:934)
CpG islands
(count:61)
Chromatin interactive
region (count:71)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90738052-90738327	K562	blood:	n/a	n/a
2	ARID3A	chr8:90738074-90738343	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:90732814-90733099	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:90741133-90741702	K562	blood:	n/a	n/a
5	ARID3A	chr8:90742157-90742510	K562	blood:	n/a	n/a
6	ARID3A	chr8:90730496-90730904	K562	blood:	n/a	n/a
7	ATF1	chr8:90740926-90741719	K562	blood:	n/a	n/a
8	ATF1	chr8:90738051-90738334	K562	blood:	n/a	n/a
9	ATF2	chr8:90741953-90742740	GM12878	blood:	n/a	n/a
10	ATF2	chr8:90737929-90738551	GM12878	blood:	n/a	n/a
11	ATF2	chr8:90741207-90741815	GM12878	blood:	n/a	n/a
12	ATF2	chr8:90738026-90738427	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr8:90732722-90733233	GM12878	blood:	n/a	n/a
14	ATF2	chr8:90732595-90733323	GM12878	blood:	n/a	n/a
15	ATF2	chr8:90741233-90741894	GM12878	blood:	n/a	n/a
16	ATF2	chr8:90741902-90742786	GM12878	blood:	n/a	n/a
17	ATF2	chr8:90737920-90738636	GM12878	blood:	n/a	n/a
18	BACH1	chr8:90738733-90738759	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:90738096-90738310	K562	blood:	n/a	n/a
20	BATF	chr8:90738011-90738449	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
21	BATF	chr8:90741444-90741729	GM12878	blood:	n/a	n/a
22	BATF	chr8:90742356-90742616	GM12878	blood:	n/a	n/a
23	BATF	chr8:90738003-90738500	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
24	BATF	chr8:90732830-90733137	GM12878	blood:	n/a	n/a
25	BATF	chr8:90742327-90742620	GM12878	blood:	n/a	n/a
26	BATF	chr8:90741449-90741737	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:90741404-90741705	GM12878	blood:	n/a	n/a
28	BCL3	chr8:90737989-90738504	GM12878	blood:	n/a	chr8:90738122-90738131
29	BCL3	chr8:90732736-90733192	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:90737861-90738551	GM12878	blood:	n/a	chr8:90738122-90738131 chr8:90737903-90737912
31	BCLAF1	chr8:90742189-90742602	GM12878	blood:	n/a	chr8:90742261-90742270
32	BCLAF1	chr8:90741285-90741840	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:90737957-90738469	GM12878	blood:	n/a	chr8:90738122-90738131
34	BHLHE40	chr8:90738028-90738733	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:90738026-90738384	K562	blood:	n/a	n/a
36	BHLHE40	chr8:90741068-90741648	K562	blood:	n/a	n/a
37	BHLHE40	chr8:90740597-90740708	GM12878	blood:	n/a	n/a
38	BHLHE40	chr8:90741301-90741779	GM12878	blood:	n/a	n/a
39	BHLHE40	chr8:90733984-90734101	K562	blood:	n/a	n/a
40	BRCA1	chr8:90741488-90741644	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr8:90717312-90717508	GM12878	blood:	n/a	n/a
42	CBX3	chr8:90748284-90748626	K562	blood:	n/a	n/a
43	CBX3	chr8:90740890-90741741	K562	blood:	n/a	n/a
44	CBX3	chr8:90737999-90738365	K562	blood:	n/a	n/a
45	CCNT2	chr8:90741406-90741610	K562	blood:	n/a	n/a
46	CEBPB	chr8:90709684-90710396	HCT-116	colon:	n/a	chr8:90710214-90710225
47	CEBPB	chr8:90710059-90710393	IMR90	lung:	n/a	chr8:90710214-90710225
48	CEBPB	chr8:90709827-90710408	Hela-S3	cervix:	n/a	chr8:90710214-90710225
49	CEBPB	chr8:90741065-90741667	Hela-S3	cervix:	n/a	chr8:90741231-90741240 chr8:90741231-90741242 chr8:90741229-90741242 chr8:90741229-90741240 chr8:90741229-90741242
50	CEBPB	chr8:90741102-90741585	K562	blood:	n/a	chr8:90741231-90741240 chr8:90741231-90741242 chr8:90741229-90741242 chr8:90741229-90741240 chr8:90741229-90741242

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90730638-90730688	U87	brain:	n/a
2	chr8:90730638-90730688	GM19239	blood:	n/a
3	chr8:90730638-90730688	ovcar-3	ovarian:	n/a
4	chr8:90730638-90730688	PFSK-1	brain:	n/a
5	chr8:90730638-90730688	GM12891	blood:	n/a
6	chr8:90730638-90730688	HNPCEpiC	eye:	n/a
7	chr8:90730638-90730688	HMEC	breast:	n/a
8	chr8:90730638-90730688	LNCaP	prostate:	n/a
9	chr8:90730638-90730688	PrEC	prostate:	n/a
10	chr8:90730638-90730688	SK-N-SH_RA	brain:	n/a
11	chr8:90730638-90730688	AG09319	gingival:	n/a
12	chr8:90730638-90730688	IMR90	lung:	fetal
13	chr8:90730638-90730688	A549	lung:	n/a
14	chr8:90730638-90730688	SKMC	muscle:	n/a
15	chr8:90730638-90730688	HCM	heart:	n/a
16	chr8:90730638-90730688	Hepatocyte	liver:	n/a
17	chr8:90730638-90730688	Hela-S3	cervix:	n/a
18	chr8:90730638-90730688	NH-A	brain:	n/a
19	chr8:90730638-90730688	GM06990	blood:	n/a
20	chr8:90730638-90730688	NT2-D1	testis:	n/a
21	chr8:90730638-90730688	SAEC	small airway:	n/a
22	chr8:90730638-90730688	NB4	blood:	n/a
23	chr8:90730638-90730688	BJ	skin:	n/a
24	chr8:90730638-90730688	HIPEpiC	eye:	n/a
25	chr8:90730638-90730688	HL-60	blood:	n/a
26	chr8:90730638-90730688	Caco-2	colon:	n/a
27	chr8:90730638-90730688	NHDF-neo	bronchial:	n/a
28	chr8:90730638-90730688	HRCEpiC	kidney:	n/a
29	chr8:90730638-90730688	GM12878	blood:	n/a
30	chr8:90730638-90730688	SK-N-SH	brain:	n/a
31	chr8:90730638-90730688	SK-N-MC	brain:	n/a
32	chr8:90730638-90730688	MCF-7	breast:	n/a
33	chr8:90730638-90730688	K562	blood:	n/a
34	chr8:90730638-90730688	ECC-1	luminal epithelium:	n/a
35	chr8:90730638-90730688	HRE	kidney:	n/a
36	chr8:90730638-90730688	RPTEC	kidney:	n/a
37	chr8:90730638-90730688	HEK293	kidney:	embryo
38	chr8:90730638-90730688	AG09309	skin:	n/a
39	chr8:90730638-90730688	HCF	heart:	n/a
40	chr8:90730638-90730688	T-47D	breast:	n/a
41	chr8:90730638-90730688	HRPEpiC	eye:	n/a
42	chr8:90730638-90730688	HEEpiC	esophagus:	n/a
43	chr8:90730638-90730688	HCT-116	colon:	n/a
44	chr8:90730638-90730688	AG04449	skin:	fetal
45	chr8:90730638-90730688	AG10803	skin:	n/a
46	chr8:90730638-90730688	HUVEC	blood vessel:	n/a
47	chr8:90730638-90730688	Jurkat	blood:	n/a
48	chr8:90730638-90730688	HAEpiC	amniotic membrane:	n/a
49	chr8:90730638-90730688	AG04450	lung:	fetal
50	chr8:90730638-90730688	HepG2	liver:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:90736651..90739528-chr8:90739958..90742509,3	MCF-7	breast:
2	chr8:90727781..90733734-chr8:90995200..90998684,11	MCF-7	breast:
3	chr8:90730418..90730960-chr8:90860233..90861169,2	MCF-7	breast:
4	chr8:90744391..90748036-chr8:90768454..90770594,4	MCF-7	breast:
5	chr8:90737820..90738670-chr8:90996630..90997353,4	K562	blood:
6	chr8:90741234..90743922-chr8:90995229..90998004,3	MCF-7	breast:
7	chr8:90737773..90739680-chr8:90867503..90870182,2	MCF-7	breast:
8	chr8:90730784..90732523-chr8:90913744..90915377,2	MCF-7	breast:
9	chr8:90701508..90704091-chr8:90704725..90706436,2	MCF-7	breast:
10	chr8:90707734..90710584-chr8:90712902..90714410,2	K562	blood:
11	chr8:90730992..90732620-chr8:90854047..90856090,2	MCF-7	breast:
12	chr8:90727118..90729538-chr8:90730165..90731877,3	MCF-7	breast:
13	chr17:65372095..65374964-chr8:90727575..90729422,2	MCF-7	breast:
14	chr8:90732834..90736227-chr8:90736670..90741646,5	MCF-7	breast:
15	chr8:90707734..90710584-chr8:90712902..90714410,2	K562	blood:
16	chr8:90737440..90740963-chr8:90912985..90916304,5	MCF-7	breast:
17	chr8:90742547..90745404-chr8:90995245..90998010,2	MCF-7	breast:
18	chr8:90738830..90741040-chr8:90913929..90916655,2	K562	blood:
19	chr8:90727118..90729538-chr8:90730165..90731877,3	MCF-7	breast:
20	chr8:90738336..90739847-chr8:90952483..90954708,2	MCF-7	breast:
21	chr8:90731255..90734229-chr8:90770926..90773381,2	MCF-7	breast:
22	chr8:90729414..90732733-chr8:91011369..91014401,3	MCF-7	breast:
23	chr8:90732834..90736227-chr8:90736670..90741646,5	MCF-7	breast:
24	chr8:90737750..90738653-chr8:90995891..90997375,11	MCF-7	breast:
25	chr8:90730473..90731451-chr8:90996501..90997250,3	K562	blood:
26	chr1:45195328..45196974-chr8:90708817..90711214,2	MCF-7	breast:
27	chr8:90718183..90720246-chr8:90997582..90999794,2	MCF-7	breast:
28	chr8:90740621..90743258-chr8:90763138..90765800,2	K562	blood:
29	chr8:90734630..90736246-chr8:90739978..90742912,2	K562	blood:
30	chr8:90730098..90733347-chr8:90733512..90737608,4	MCF-7	breast:
31	chr8:90735826..90740064-chr8:90995306..90998250,3	MCF-7	breast:
32	chr8:90740620..90742197-chr8:90743722..90745998,2	K562	blood:
33	chr8:90740620..90742197-chr8:90743722..90745998,2	K562	blood:
34	chr8:90730221..90731273-chr8:91007539..91008842,5	MCF-7	breast:
35	chr8:90740510..90743977-chr8:90993488..90997809,6	K562	blood:
36	chr8:90744716..90746435-chr8:90912838..90915687,2	MCF-7	breast:
37	chr8:90736815..90743993-chr8:90765696..90773918,18	MCF-7	breast:
38	chr8:90730206..90731189-chr8:90996034..90997277,6	MCF-7	breast:
39	chr8:90728791..90734507-chr8:90768671..90772991,6	MCF-7	breast:
40	chr8:90732925..90737686-chr8:90738407..90742912,6	K562	blood:
41	chr17:36869922..36870448-chr8:90717364..90718185,2	MCF-7	breast:
42	chr8:90742416..90744281-chr8:90745142..90746926,3	MCF-7	breast:
43	chr8:90730227..90732540-chr8:90735572..90739536,4	MCF-7	breast:
44	chr8:90727232..90729258-chr8:90996337..90998108,2	K562	blood:
45	chr8:90744912..90747575-chr8:90768585..90770314,2	MCF-7	breast:
46	chr8:90741497..90743886-chr8:90913667..90916372,2	MCF-7	breast:
47	chr8:90730601..90732192-chr8:90769579..90771493,2	K562	blood:
48	chr8:90728421..90731322-chr8:90768426..90770911,3	MCF-7	breast:
49	chr8:90735002..90740593-chr8:90994599..90998168,11	MCF-7	breast:
50	chr8:90707735..90710054-chr8:90995310..90996868,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90729627-90733428	ENSG00000251136
2	lnc-NBN-1	chr8:90733172-90733602	ENSG00000251136
3	lnc-NBN-1	chr8:90729656-90729956	ENSG00000251136
4	lnc-NBN-1	chr8:90734243-90734578	ENSG00000251136
5	lnc-NBN-1	chr8:90735244-90735764	NONHSAT127622
6	lnc-NBN-1	chr8:90736857-90737194	NONHSAT127622
7	lnc-NBN-1	chr8:90733132-90733602	ENSG00000251136
8	lnc-NBN-1	chr8:90737746-90737871	NONHSAT127622
9	lnc-NBN-1	chr8:90732820-90733604	NONHSAT127622
10	lnc-NBN-1	chr8:90737746-90737869	ENSG00000251136
11	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
12	lnc-NBN-1	chr8:90734243-90734578	NONHSAT127622
13	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
14	lnc-NBN-1	chr8:90736857-90737194	ENSG00000251136
15	lnc-NBN-1	chr8:90736857-90737158	ENSG00000251136

No data

Variant related genes	Relation type
ENSG00000251136	TF binding region
ENSG00000251136	CpG island
ENSG00000207359	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000154217	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000164823	chromatin interactions
TPM3	miRNA target sites
HMGA2	miRNA target sites
DPH1	miRNA target sites
TMEM214	miRNA target sites
BCL2	miRNA target sites
KLK6	miRNA target sites
CADM1	miRNA target sites
RGPD6	miRNA target sites

Extended variants
information (count: 1685 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186304181	chr8:90705851-90705852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531216832	chr8:90705858-90705859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189607188	chr8:90705874-90705875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549845324	chr8:90705876-90705877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181661003	chr8:90705901-90705902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527797432	chr8:90705923-90705924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13276489	chr8:90705949-90705950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567581927	chr8:90705958-90705959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538222905	chr8:90705974-90705975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550641336	chr8:90705979-90705980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186856344	chr8:90705990-90705991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs151125234	chr8:90705993-90705994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557991886	chr8:90705995-90705996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190808999	chr8:90706004-90706005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376799055	chr8:90706007-90706008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533669537	chr8:90706120-90706121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555416002	chr8:90706129-90706130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555329636	chr8:90706168-90706169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573598147	chr8:90706210-90706211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544195312	chr8:90706242-90706243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562100231	chr8:90706293-90706294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577928508	chr8:90706476-90706477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545263175	chr8:90706494-90706495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141092008	chr8:90706518-90706519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371318925	chr8:90706604-90706605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76420627	chr8:90706732-90706733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2132348	chr8:90706773-90706774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs149837270	chr8:90706807-90706808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553012323	chr8:90706910-90706911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544079806	chr8:90706919-90706920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372566475	chr8:90706966-90706967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs202101518	chr8:90706968-90706969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181993174	chr8:90707051-90707052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551670950	chr8:90707059-90707060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566697144	chr8:90707062-90707063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533983451	chr8:90707107-90707108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185049214	chr8:90707149-90707150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567360525	chr8:90707160-90707161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577731741	chr8:90707163-90707164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6999425	chr8:90707180-90707181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs141708737	chr8:90707226-90707227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577191582	chr8:90707229-90707230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545322766	chr8:90707303-90707304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146943557	chr8:90707374-90707375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562871746	chr8:90707388-90707389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199793324	chr8:90707389-90707390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201855440	chr8:90707391-90707392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373502816	chr8:90707510-90707511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554028663	chr8:90707533-90707534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572592668	chr8:90707536-90707537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90693200-90715600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90704400-90709600	Weak transcription	NH-A	brain
3	chr8:90709000-90720200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:90709400-90709600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr8:90709600-90709800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:90709600-90710200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:90709600-90710200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:90709600-90710200	Enhancers	Adipose Nuclei	Adipose
9	chr8:90709600-90710200	Enhancers	A549	lung
10	chr8:90709600-90710200	Enhancers	Hela-S3	cervix
11	chr8:90709600-90710200	Enhancers	NH-A	brain
12	chr8:90709600-90710200	Enhancers	Osteobl	bone
13	chr8:90709800-90710000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:90709800-90710000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr8:90709800-90710000	Enhancers	HSMMtube	muscle
16	chr8:90709800-90710200	Enhancers	NHEK	skin
17	chr8:90709800-90710600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:90710000-90710200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:90710000-90710200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:90710000-90716200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:90710000-90730000	Weak transcription	HSMMtube	muscle
22	chr8:90710200-90715800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:90710200-90716400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:90710200-90729600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:90710200-90730400	Weak transcription	A549	lung
26	chr8:90710200-90731200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr8:90710200-90736200	Weak transcription	Adipose Nuclei	Adipose
28	chr8:90710600-90715800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:90711200-90715400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:90711200-90733800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr8:90711400-90712800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:90711400-90720200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr8:90712200-90713000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:90712200-90715600	Weak transcription	Aorta	Aorta
35	chr8:90712400-90712800	Enhancers	K562	blood
36	chr8:90712600-90713200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:90712800-90713200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr8:90712800-90713200	Enhancers	Spleen	Spleen
39	chr8:90712800-90713400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:90713000-90713200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:90713000-90713200	Enhancers	Left Ventricle	heart
42	chr8:90713200-90713400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr8:90713200-90714200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:90713200-90715400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:90713200-90716400	Weak transcription	Spleen	Spleen
46	chr8:90713200-90717600	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr8:90713200-90741200	Weak transcription	Left Ventricle	heart
48	chr8:90713400-90715600	Weak transcription	Fetal Stomach	stomach
49	chr8:90713400-90715800	Weak transcription	Fetal Muscle Leg	muscle
50	chr8:90713400-90720400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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