Variant report

Variant	nsv893507
Chromosome Location	chr9:84799537-85097651
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:989)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:102)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:84928716-84928934	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:85081980-85082088	HepG2	liver:	n/a	n/a
3	ATF2	chr9:84821834-84822235	GM12878	blood:	n/a	n/a
4	ATF2	chr9:84821828-84822200	GM12878	blood:	n/a	n/a
5	ATF2	chr9:85025221-85025581	GM12878	blood:	n/a	n/a
6	BATF	chr9:85025234-85025563	GM12878	blood:	n/a	chr9:85025416-85025427
7	BATF	chr9:84869899-84870226	GM12878	blood:	n/a	n/a
8	BATF	chr9:84821899-84822123	GM12878	blood:	n/a	n/a
9	BATF	chr9:85025194-85025607	GM12878	blood:	n/a	chr9:85025416-85025427
10	BATF	chr9:84998190-84998518	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:85025297-85025525	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:84821873-84822206	GM12878	blood:	n/a	n/a
13	BCL3	chr9:84921108-84921595	GM12878	blood:	n/a	n/a
14	CEBPB	chr9:84928643-84929010	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:84969093-84969621	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:85025165-85026460	MCF-7	breast:	n/a	chr9:85025991-85026004
17	CEBPB	chr9:84971835-84972116	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:85066671-85066891	A549	lung:	n/a	chr9:85066724-85066735
19	CEBPB	chr9:85051501-85051701	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:84818810-84818959	HepG2	liver:	n/a	chr9:84818876-84818887
21	CEBPB	chr9:84892866-84892936	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:84946942-84947541	A549	lung:	n/a	n/a
23	CEBPB	chr9:85072384-85072419	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:84922779-84923093	IMR90	lung:	n/a	chr9:84922935-84922946
25	CEBPB	chr9:84949211-84949536	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:85025807-85026283	MCF-7	breast:	n/a	chr9:85025991-85026004
27	CEBPB	chr9:84955789-84956093	IMR90	lung:	n/a	n/a
28	CEBPB	chr9:85066665-85066873	HepG2	liver:	n/a	chr9:85066724-85066735
29	CEBPB	chr9:84918517-84918689	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:84933029-84933258	IMR90	lung:	n/a	chr9:84933143-84933154 chr9:84933143-84933156 chr9:84933145-84933156
31	CEBPB	chr9:85090757-85091049	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:84818742-84818994	IMR90	lung:	n/a	chr9:84818876-84818887
33	CEBPB	chr9:84955847-84956110	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:84837570-84837821	HepG2	liver:	n/a	chr9:84837672-84837683
35	CEBPB	chr9:84991815-84992114	HepG2	liver:	n/a	chr9:84991960-84991971
36	CEBPB	chr9:84884963-84885287	HepG2	liver:	n/a	chr9:84885116-84885127 chr9:84885115-84885126
37	CEBPB	chr9:85025348-85025560	A549	lung:	n/a	n/a
38	CEBPB	chr9:84922816-84923082	HepG2	liver:	n/a	chr9:84922935-84922946
39	CEBPB	chr9:84928723-84928963	MCF-7	breast:	n/a	n/a
40	CEBPB	chr9:84817817-84818023	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:84971882-84972110	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:84946997-84947428	IMR90	lung:	n/a	n/a
43	CEBPB	chr9:84837586-84837850	IMR90	lung:	n/a	chr9:84837672-84837683
44	CEBPB	chr9:84933010-84933314	HepG2	liver:	n/a	chr9:84933143-84933154 chr9:84933143-84933156 chr9:84933145-84933156
45	CEBPB	chr9:84839466-84839534	H1-hESC	embryonic stem cell:	n/a	chr9:84839501-84839514
46	CEBPB	chr9:84971874-84971981	A549	lung:	n/a	n/a
47	CEBPB	chr9:84946986-84947419	A549	lung:	n/a	n/a
48	CEBPB	chr9:84946980-84947492	MCF-7	breast:	n/a	n/a
49	CEBPB	chr9:84884950-84885283	IMR90	lung:	n/a	chr9:84885116-84885127 chr9:84885115-84885126
50	CEBPB	chr9:84983769-84984253	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:85020050-85020100	Hela-S3	cervix:	n/a
2	chr9:85020050-85020100	BJ	skin:	n/a
3	chr9:85020050-85020100	HRE	kidney:	n/a
4	chr9:85020050-85020100	MCF-7	breast:	n/a
5	chr9:85020050-85020100	PANC-1	pancreas:	n/a
6	chr9:85020050-85020100	HepG2	liver:	n/a
7	chr9:85020050-85020100	NB4	blood:	n/a
8	chr9:85020050-85020100	SK-N-SH_RA	brain:	n/a
9	chr9:85020050-85020100	Hepatocyte	liver:	n/a
10	chr9:85020050-85020100	GM19239	blood:	n/a
11	chr9:85020050-85020100	HUVEC	blood vessel:	n/a
12	chr9:85020050-85020100	LNCaP	prostate:	n/a
13	chr9:85020050-85020100	SK-N-SH	brain:	n/a
14	chr9:85020050-85020100	CMK	blood:	n/a
15	chr9:85020050-85020100	ovcar-3	ovarian:	n/a
16	chr9:85020050-85020100	GM06990	blood:	n/a
17	chr9:85020050-85020100	NHDF-neo	bronchial:	n/a
18	chr9:85020050-85020100	HNPCEpiC	eye:	n/a
19	chr9:85020050-85020100	NT2-D1	testis:	n/a
20	chr9:85020050-85020100	HCM	heart:	n/a
21	chr9:85020050-85020100	GM12878	blood:	n/a
22	chr9:85020050-85020100	PFSK-1	brain:	n/a
23	chr9:85020050-85020100	HRPEpiC	eye:	n/a
24	chr9:85020050-85020100	NHBE	bronchial:	n/a
25	chr9:85020050-85020100	BE2_C	brain:	n/a
26	chr9:85020050-85020100	K562	blood:	n/a
27	chr9:85020050-85020100	HCPEpiC	choroid plexus:	n/a
28	chr9:85020050-85020100	AG10803	skin:	n/a
29	chr9:85020050-85020100	ProgFib	skin:	n/a
30	chr9:85020050-85020100	T-47D	breast:	n/a
31	chr9:85020050-85020100	Jurkat	blood:	n/a
32	chr9:85020050-85020100	HCF	heart:	n/a
33	chr9:85020050-85020100	AG09319	gingival:	n/a
34	chr9:85020050-85020100	PrEC	prostate:	n/a
35	chr9:85020050-85020100	SKMC	muscle:	n/a
36	chr9:85020050-85020100	IMR90	lung:	fetal
37	chr9:85020050-85020100	RPTEC	kidney:	n/a
38	chr9:85020050-85020100	HL-60	blood:	n/a
39	chr9:85020050-85020100	HEEpiC	esophagus:	n/a
40	chr9:85020050-85020100	AG09309	skin:	n/a
41	chr9:85020050-85020100	MCF10A-Er-Src	breast:	n/a
42	chr9:85020050-85020100	GM12891	blood:	n/a
43	chr9:85020050-85020100	HEK293	kidney:	embryo
44	chr9:85020050-85020100	HPAEpiC	pulmonary alveolar:	n/a
45	chr9:85020050-85020100	HIPEpiC	eye:	n/a
46	chr9:85020050-85020100	AG04449	skin:	fetal
47	chr9:85020050-85020100	HMEC	breast:	n/a
48	chr9:85020050-85020100	U87	brain:	n/a
49	chr9:85020050-85020100	HCT-116	colon:	n/a
50	chr9:85020050-85020100	Caco-2	colon:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:84876151..84877827-chr9:84878097..84880393,2	MCF-7	breast:
2	chr9:84983133..84986129-chr9:85021514..85023241,2	MCF-7	breast:
3	chr9:84917850..84920304-chr9:84921549..84923460,2	MCF-7	breast:
4	chr9:84935000..84936813-chr9:84942574..84944418,2	MCF-7	breast:
5	chr9:84983442..84984621-chr9:85025269..85026194,3	MCF-7	breast:
6	chr9:84950253..84952417-chr9:84953799..84956702,3	MCF-7	breast:
7	chr9:84876151..84877827-chr9:84878097..84880393,2	MCF-7	breast:
8	chr9:84983133..84986129-chr9:85021514..85023241,2	MCF-7	breast:
9	chr9:84975589..84977641-chr9:84987476..84989507,2	MCF-7	breast:
10	chr9:84970664..84973580-chr9:84975501..84978043,2	MCF-7	breast:
11	chr9:85009985..85011686-chr9:85015834..85018239,2	MCF-7	breast:
12	chr9:84928482..84930129-chr9:84931646..84933962,2	MCF-7	breast:
13	chr9:84975589..84977641-chr9:84987476..84989507,2	MCF-7	breast:
14	chr9:84817379..84819303-chr9:84823332..84825500,2	MCF-7	breast:
15	chr9:84803616..84804404-chr9:85119459..85120214,2	MCF-7	breast:
16	chr9:84950816..84952967-chr9:84985391..84988044,2	MCF-7	breast:
17	chr9:85092539..85095359-chr9:85099024..85100878,2	MCF-7	breast:
18	chr9:84935000..84936813-chr9:84942574..84944418,2	MCF-7	breast:
19	chr9:84803734..84804592-chr9:85378132..85378774,2	MCF-7	breast:
20	chr9:85009985..85011686-chr9:85015834..85018239,2	MCF-7	breast:
21	chr9:84997983..85000625-chr9:85039684..85042502,2	MCF-7	breast:
22	chr9:84950253..84952417-chr9:84953799..84956702,3	MCF-7	breast:
23	chr9:84888213..84889834-chr9:84897716..84899682,2	MCF-7	breast:
24	chr9:84983442..84984621-chr9:85025269..85026194,3	MCF-7	breast:
25	chr9:84917850..84920304-chr9:84921549..84923460,2	MCF-7	breast:
26	chr9:84950816..84952967-chr9:84985391..84988044,2	MCF-7	breast:
27	chr9:84970664..84973580-chr9:84975501..84978043,2	MCF-7	breast:
28	chr9:84928482..84930129-chr9:84931646..84933962,2	MCF-7	breast:
29	chr9:84877571..84879568-chr9:85156519..85158651,2	MCF-7	breast:
30	chr9:84817379..84819303-chr9:84823332..84825500,2	MCF-7	breast:
31	chr9:84997983..85000625-chr9:85039684..85042502,2	MCF-7	breast:

(count:102 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM75D1-4	chr9:84964719-84964763	ENSG00000228430.4
2	lnc-FAM75D1-4	chr9:85043114-85043208	ENSG00000228430.4
3	lnc-FAM75D1-4	chr9:85043114-85043208	ENSG00000228430.4
4	lnc-FAM75D1-4	chr9:84964719-84964763	ENSG00000228430.4
5	lnc-FAM75D1-4	chr9:85043114-85043208	ENSG00000228430.4
6	lnc-FAM75D1-4	chr9:84891964-84892042	ENSG00000228430.4
7	lnc-FAM75D1-4	chr9:84891964-84892077	ENSG00000228430.4
8	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
9	lnc-FAM75B-4	chr9:85051617-85052093	expReg_chr9_3630_-
10	lnc-FAM75D1-4	chr9:84891964-84892077	ENSG00000228430.4
11	lnc-FAM75D1-4	chr9:84891964-84892077	ENSG00000228430.4
12	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
13	lnc-FAM75D1-4	chr9:85068668-85068718	XLOC_007422
14	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
15	lnc-FAM75D1-4	chr9:85069822-85070140	XLOC_007422
16	lnc-FAM75D1-4	chr9:84964719-84964763	ENSG00000228430.4
17	lnc-FAM75D1-3	chr9:84888321-84888396	ENSG00000228430
18	lnc-FAM75D1-4	chr9:84888374-84888396	ENSG00000228430.4
19	lnc-FAM75D1-4	chr9:85011623-85011715	ENSG00000228430.4
20	lnc-FAM75D1-4	chr9:84888374-84888396	ENSG00000228430.4
21	lnc-FAM75D1-4	chr9:85043114-85043202	NONHSAT132704
22	lnc-FAM75D1-4	chr9:84964719-84964763	ENSG00000228430.4
23	lnc-FAM75D1-4	chr9:85068553-85068718	ENSG00000228430.4
24	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
25	lnc-FAM75D1-4	chr9:84887671-84888396	ENSG00000228430.4
26	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
27	lnc-FAM75D1-4	chr9:85068553-85068914	ENSG00000228430.4
28	lnc-FAM75D1-4	chr9:85041207-85041291	ENSG00000228430.4
29	lnc-FAM75D1-4	chr9:85066518-85066638	ENSG00000228430.4
30	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
31	lnc-FAM75D1-4	chr9:84888322-84888396	NONHSAT132704
32	lnc-FAM75D1-4	chr9:85041897-85041941	ENSG00000228430.4
33	lnc-FAM75D1-4	chr9:85068260-85068373	ENSG00000228430.4
34	lnc-FAM75D1-4	chr9:84888374-84888396	ENSG00000228430.4
35	lnc-FAM75D1-3	chr9:85043114-85043202	ENSG00000228430
36	lnc-FAM75D1-4	chr9:84891964-84892077	ENSG00000228430.4
37	lnc-FAM75D1-8	chr9:85038785-85038977	NONHSAT132718
38	lnc-FAM75D1-2	chr9:85020103-85020225	XLOC_007421
39	lnc-FAM75D1-4	chr9:84888374-84888396	ENSG00000228430.4
40	lnc-FAM75D1-4	chr9:85066518-85066644	ENSG00000228430.4
41	lnc-FAM75D1-4	chr9:85068553-85068718	XLOC_007422
42	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
43	lnc-FAM75D1-3	chr9:84964719-84964763	ENSG00000228430
44	lnc-FAM75D1-4	chr9:84896497-84896565	ENSG00000228430.4
45	lnc-FAM75D1-4	chr9:85043114-85043208	ENSG00000228430.4
46	lnc-FAM75D1-4	chr9:85068260-85068373	XLOC_007422
47	lnc-FAM75D1-2	chr9:85020823-85021154	XLOC_007421
48	lnc-FAM75D1-4	chr9:84964719-84964763	ENSG00000228430.4
49	lnc-FAM75D1-4	chr9:84891964-84892077	ENSG00000228430.4
50	lnc-FAM75D1-4	chr9:84891964-84892077	ENSG00000228430.4

No data

Variant related genes	Relation type
ENSG00000228046	TF binding region
ENSG00000228123	TF binding region
ENSG00000232749	TF binding region
ENSG00000225085	TF binding region
ENSG00000228430	TF binding region
ENSG00000228046	CpG island
ENSG00000228123	CpG island
ENSG00000232749	CpG island
ENSG00000225085	CpG island
ENSG00000228430	CpG island
ENSG00000228430	chromatin interactions

Extended variants
information (count: 6253 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6253 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2767713	chr9:84799537-84799538	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552284981	chr9:84799553-84799554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141180490	chr9:84799585-84799586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545657714	chr9:84799589-84799590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114021744	chr9:84799622-84799623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577259909	chr9:84799652-84799653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150748829	chr9:84799674-84799675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553048669	chr9:84799706-84799707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138020571	chr9:84799712-84799713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534369027	chr9:84799727-84799728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560598972	chr9:84799757-84799758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149504981	chr9:84799769-84799770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552486328	chr9:84799797-84799798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183625363	chr9:84799802-84799803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554353458	chr9:84799815-84799816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74538608	chr9:84799835-84799836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188566635	chr9:84799844-84799845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567684778	chr9:84799887-84799888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535069408	chr9:84800025-84800026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116857531	chr9:84800081-84800082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553758090	chr9:84800105-84800106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34880259	chr9:84800152-84800153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537397988	chr9:84800255-84800256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117091882	chr9:84800306-84800307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539763816	chr9:84800325-84800326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556951697	chr9:84800369-84800370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557631064	chr9:84800370-84800371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576309268	chr9:84800478-84800479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544691743	chr9:84800501-84800502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556677185	chr9:84800506-84800507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11139512	chr9:84800507-84800508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62576786	chr9:84800525-84800526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575013742	chr9:84800610-84800611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs60916051	chr9:84800621-84800622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140604176	chr9:84800638-84800639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377185309	chr9:84800656-84800657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576416168	chr9:84800686-84800687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367791774	chr9:84800688-84800689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377211491	chr9:84800692-84800693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368827713	chr9:84800723-84800724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192769960	chr9:84800731-84800732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373003024	chr9:84800745-84800746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546479654	chr9:84800753-84800754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74901087	chr9:84800787-84800788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564492654	chr9:84800808-84800809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60785980	chr9:84800938-84800939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531801893	chr9:84800952-84800953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182540066	chr9:84800978-84800979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186869191	chr9:84800999-84801000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75042635	chr9:84801025-84801026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Astrocytoma	22246337	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Epilepsy	20502679	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:84797400-84800600	Enhancers	Primary B cells from peripheral blood	blood
2	chr9:84797600-84800800	Enhancers	Primary B cells from cord blood	blood
3	chr9:84798200-84800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:84799400-84799800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:84799400-84800000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr9:84799600-84800000	Enhancers	Primary hematopoietic stem cells	blood
7	chr9:84800000-84800400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:84800000-84805200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr9:84800800-84806200	Weak transcription	Primary B cells from cord blood	blood
10	chr9:84803800-84804000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr9:84803800-84804400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr9:84804000-84804200	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr9:84804200-84805000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr9:84804400-84804800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:84804800-84805200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:84805200-84805400	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr9:84805200-84807800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr9:84805600-84806200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:84805800-84807400	Enhancers	Primary hematopoietic stem cells	blood
20	chr9:84805800-84808000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:84806200-84806600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:84806200-84806800	Enhancers	Primary B cells from cord blood	blood
23	chr9:84806200-84807400	Enhancers	Primary B cells from peripheral blood	blood
24	chr9:84806600-84807800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:84806800-84807400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr9:84807200-84807600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr9:84807400-84810000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr9:84809200-84812400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:84810600-84813600	Enhancers	Brain Germinal Matrix	brain
30	chr9:84810800-84814400	Weak transcription	Psoas Muscle	Psoas
31	chr9:84811400-84812800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr9:84811600-84812600	Enhancers	Fetal Brain Female	brain
33	chr9:84811600-84813400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:84811800-84812600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr9:84811800-84812600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr9:84811800-84812800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr9:84811800-84813400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr9:84812200-84812600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:84812200-84812600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:84812200-84812600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr9:84812200-84812600	Enhancers	Fetal Brain Male	brain
42	chr9:84812400-84812600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:84812400-84813200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr9:84812600-84814400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:84812600-84815400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr9:84812600-84815600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr9:84812600-84821200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr9:84812800-84815400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr9:84813400-84815200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr9:84815200-84816000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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