Variant report

Variant	nsv831121
Chromosome Location	chr7:126593363-126774413
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:715)
CpG islands
(count:610)
Chromatin interactive
region (count:40)
LncRNA
region (count:11)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:126646619-126646698	K562	blood:	n/a	n/a
2	ATF1	chr7:126698009-126698276	K562	blood:	n/a	n/a
3	ATF3	chr7:126698103-126698234	K562	blood:	n/a	n/a
4	BCLAF1	chr7:126747776-126748061	GM12878	blood:	n/a	chr7:126747977-126747986
5	BHLHE40	chr7:126747718-126748132	K562	blood:	n/a	n/a
6	CBX3	chr7:126747686-126748104	K562	blood:	n/a	n/a
7	CBX3	chr7:126747633-126748162	K562	blood:	n/a	n/a
8	CCNT2	chr7:126598491-126598668	K562	blood:	n/a	n/a
9	CEBPB	chr7:126714252-126714589	HepG2	liver:	n/a	chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714417-126714428 chr7:126714417-126714428 chr7:126714417-126714430 chr7:126714417-126714430 chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714418-126714429 chr7:126714417-126714430
10	CEBPB	chr7:126729684-126729737	K562	blood:	n/a	chr7:126729719-126729730
11	CEBPB	chr7:126651754-126652063	H1-hESC	embryonic stem cell:	n/a	chr7:126652025-126652038
12	CEBPB	chr7:126664292-126664492	HepG2	liver:	n/a	chr7:126664371-126664382
13	CEBPB	chr7:126640794-126641172	A549	lung:	n/a	chr7:126640988-126640999
14	CEBPB	chr7:126675667-126675895	HepG2	liver:	n/a	chr7:126675790-126675801
15	CEBPB	chr7:126698005-126698340	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:126714292-126714568	A549	lung:	n/a	chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714417-126714428 chr7:126714417-126714428 chr7:126714417-126714430 chr7:126714417-126714430 chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714418-126714429 chr7:126714417-126714430
17	CEBPB	chr7:126729643-126729857	HepG2	liver:	n/a	chr7:126729719-126729730
18	CEBPB	chr7:126651787-126651946	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:126640722-126641110	K562	blood:	n/a	chr7:126640988-126640999
20	CEBPB	chr7:126723318-126723628	A549	lung:	n/a	chr7:126723476-126723487
21	CEBPB	chr7:126611438-126611726	HepG2	liver:	n/a	chr7:126611572-126611583
22	CEBPB	chr7:126698048-126698309	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:126698002-126698351	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:126640817-126641170	IMR90	lung:	n/a	chr7:126640988-126640999
25	CEBPB	chr7:126697990-126698356	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:126723317-126723623	HepG2	liver:	n/a	chr7:126723476-126723487
27	CEBPB	chr7:126619889-126620141	A549	lung:	n/a	chr7:126619992-126620003
28	CEBPB	chr7:126593940-126594250	HepG2	liver:	n/a	chr7:126594091-126594100 chr7:126594089-126594100 chr7:126594089-126594102
29	CEBPB	chr7:126650410-126650534	HepG2	liver:	n/a	chr7:126650447-126650458
30	CEBPB	chr7:126697994-126698353	A549	lung:	n/a	n/a
31	CEBPB	chr7:126698015-126698343	K562	blood:	n/a	n/a
32	CEBPB	chr7:126619872-126620171	HepG2	liver:	n/a	chr7:126619992-126620003
33	CEBPB	chr7:126698067-126698370	MCF-7	breast:	n/a	n/a
34	CEBPB	chr7:126640645-126641176	HepG2	liver:	n/a	chr7:126640988-126640999
35	CEBPB	chr7:126651805-126652002	A549	lung:	n/a	n/a
36	CEBPB	chr7:126714285-126714566	IMR90	lung:	n/a	chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714417-126714428 chr7:126714417-126714428 chr7:126714417-126714430 chr7:126714417-126714430 chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714418-126714429 chr7:126714417-126714430
37	CHD2	chr7:126692575-126692577	K562	blood:	n/a	n/a
38	CREB1	chr7:126697948-126698411	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr7:126698067-126698390	HepG2	liver:	n/a	n/a
40	CREB1	chr7:126698046-126698253	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr7:126697894-126698463	K562	blood:	n/a	n/a
42	CREB1	chr7:126698047-126698285	A549	lung:	n/a	n/a
43	CTCF	chr7:126748040-126748190	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:126707080-126707230	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr7:126687720-126687870	HRE	kidney:	n/a	n/a
46	CTCF	chr7:126707140-126707290	GM12864	blood:	n/a	chr7:126707229-126707247 chr7:126707235-126707244 chr7:126707228-126707241 chr7:126707231-126707244 chr7:126707224-126707245
47	CTCF	chr7:126747640-126747790	HCT-116	colon:	n/a	n/a
48	CTCF	chr7:126747700-126747850	GM12878	blood:	n/a	n/a
49	CTCF	chr7:126687680-126687830	RPTEC	kidney:	n/a	n/a
50	CTCF	chr7:126707148-126707279	GM12892	blood:	n/a	chr7:126707229-126707247 chr7:126707235-126707244 chr7:126707228-126707241 chr7:126707231-126707244 chr7:126707224-126707245

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126675358-126675408	NB4	blood:	n/a
2	chr7:126675358-126675408	IMR90	lung:	fetal
3	chr7:126698829-126698879	ECC-1	luminal epithelium:	n/a
4	chr7:126698344-126698394	HRCEpiC	kidney:	n/a
5	chr7:126765549-126765599	ovcar-3	ovarian:	n/a
6	chr7:126698156-126698206	HRPEpiC	eye:	n/a
7	chr7:126675358-126675408	HNPCEpiC	eye:	n/a
8	chr7:126752911-126752961	ProgFib	skin:	n/a
9	chr7:126675528-126675578	BJ	skin:	n/a
10	chr7:126675528-126675578	CMK	blood:	n/a
11	chr7:126675358-126675408	ovcar-3	ovarian:	n/a
12	chr7:126752911-126752961	LNCaP	prostate:	n/a
13	chr7:126675358-126675408	K562	blood:	n/a
14	chr7:126698451-126698501	RPTEC	kidney:	n/a
15	chr7:126698829-126698879	HIPEpiC	eye:	n/a
16	chr7:126675528-126675578	Hepatocyte	liver:	n/a
17	chr7:126615786-126615836	HNPCEpiC	eye:	n/a
18	chr7:126698344-126698394	HIPEpiC	eye:	n/a
19	chr7:126675528-126675578	SK-N-SH	brain:	n/a
20	chr7:126765549-126765599	HCF	heart:	n/a
21	chr7:126675528-126675578	HepG2	liver:	n/a
22	chr7:126752911-126752961	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:126615786-126615836	ECC-1	luminal epithelium:	n/a
24	chr7:126698156-126698206	HepG2	liver:	n/a
25	chr7:126615786-126615836	HUVEC	blood vessel:	n/a
26	chr7:126765549-126765599	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:126698344-126698394	PrEC	prostate:	n/a
28	chr7:126675528-126675578	BE2_C	brain:	n/a
29	chr7:126615786-126615836	SK-N-SH	brain:	n/a
30	chr7:126698156-126698206	HMEC	breast:	n/a
31	chr7:126752816-126752866	RPTEC	kidney:	n/a
32	chr7:126675528-126675578	NT2-D1	testis:	n/a
33	chr7:126675358-126675408	Caco-2	colon:	n/a
34	chr7:126675528-126675578	A549	lung:	n/a
35	chr7:126698344-126698394	HUVEC	blood vessel:	n/a
36	chr7:126698451-126698501	HRE	kidney:	n/a
37	chr7:126675528-126675578	Hela-S3	cervix:	n/a
38	chr7:126698344-126698394	SK-N-SH	brain:	n/a
39	chr7:126752911-126752961	HepG2	liver:	n/a
40	chr7:126615786-126615836	SK-N-MC	brain:	n/a
41	chr7:126698156-126698206	GM12891	blood:	n/a
42	chr7:126698829-126698879	HAEpiC	amniotic membrane:	n/a
43	chr7:126698451-126698501	GM12891	blood:	n/a
44	chr7:126698829-126698879	PrEC	prostate:	n/a
45	chr7:126698829-126698879	GM19239	blood:	n/a
46	chr7:126698344-126698394	Jurkat	blood:	n/a
47	chr7:126752816-126752866	HCPEpiC	choroid plexus:	n/a
48	chr7:126698156-126698206	PrEC	prostate:	n/a
49	chr7:126675528-126675578	HNPCEpiC	eye:	n/a
50	chr7:126752911-126752961	BJ	skin:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126701730..126703955-chr7:126708628..126710434,2	MCF-7	breast:
2	chr7:126747293..126748237-chr7:126893164..126894608,6	MCF-7	breast:
3	chr7:126634749..126637802-chr7:126647798..126650684,3	K562	blood:
4	chr10:97065210..97065763-chr7:126649354..126650093,2	MCF-7	breast:
5	chr7:126612202..126614471-chr7:126617154..126618998,2	K562	blood:
6	chr7:126747689..126748223-chr7:126982959..126983570,2	MCF-7	breast:
7	chr7:126748685..126750706-chr7:126758876..126761407,2	K562	blood:
8	7:126593467-126596179..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
9	chr7:126586006..126588015-chr7:126594826..126596374,2	MCF-7	breast:
10	chr7:126634749..126636430-chr7:126647798..126650007,2	K562	blood:
11	chr7:126747288..126748236-chr7:126893729..126894723,2	K562	blood:
12	chr7:126643620..126647077-chr7:126648157..126650582,3	K562	blood:
13	7:126085913-126088095..7:126662926-126671620	K562	blood:
14	chr7:126612202..126614471-chr7:126617154..126618998,2	K562	blood:
15	chr7:126719826..126721988-chr7:126731679..126734281,2	K562	blood:
16	chr7:126727758..126729748-chr7:126749664..126752422,2	K562	blood:
17	chr7:126762824..126764890-chr7:126769812..126771409,2	K562	blood:
18	chr7:126714682..126717546-chr7:126724506..126726256,2	K562	blood:
19	chr7:126714682..126717546-chr7:126724506..126726256,2	K562	blood:
20	chr7:126709768..126712072-chr7:126713094..126716180,3	K562	blood:
21	chr7:126746979..126748949-chr7:126761231..126762876,2	K562	blood:
22	chr7:126719826..126721988-chr7:126731679..126734281,2	K562	blood:
23	chr7:126643620..126647077-chr7:126648157..126650582,3	K562	blood:
24	chr7:126634749..126636430-chr7:126647798..126650007,2	K562	blood:
25	chr7:126746979..126748949-chr7:126761231..126762876,2	K562	blood:
26	chr7:126744151..126746757-chr7:126749061..126750994,2	K562	blood:
27	7:126085913-126088095..7:126639464-126642359	K562	blood:
28	chr7:126709768..126712072-chr7:126713094..126716180,3	K562	blood:
29	chr7:126748685..126750706-chr7:126758876..126761407,2	K562	blood:
30	chr7:126718359..126720333-chr7:126729809..126731677,2	K562	blood:
31	chr7:126634749..126637802-chr7:126647798..126650684,3	K562	blood:
32	chr7:126762824..126764890-chr7:126769812..126771409,2	K562	blood:
33	7:126085913-126088095..7:126678600-126685844	K562	blood:
34	chr7:126747301..126748195-chr7:127154353..127155146,2	MCF-7	breast:
35	7:126678600-126685844..7:127233104-127239235	H1-hESC	embryonic stem cell:	embryo
36	7:126678600-126685844..7:127009457-127018926	H1-hESC	embryonic stem cell:	embryo
37	7:126651745-126656082..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
38	chr7:126701730..126703955-chr7:126708628..126710434,2	MCF-7	breast:
39	7:126651745-126656082..7:126756671-126761022	H1-hESC	embryonic stem cell:	embryo
40	7:126678600-126685844..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF800-1	chr7:126730963-126731067	NONHSAT123126
2	lnc-ZNF800-1	chr7:126730963-126730972	ENSG00000230206.1
3	lnc-ARF5-15	chr7:126642417-126642543	ucscGeneNc_uc003vlv_2
4	lnc-ZNF800-1	chr7:126722158-126722228	ENSG00000230206.1
5	lnc-ZNF800-1	chr7:126724745-126724843	ENSG00000230206.1
6	lnc-ZNF800-1	chr7:126724343-126724469	NONHSAT123126
7	lnc-ARF5-15	chr7:126646757-126646992	ucscGeneNc_uc003vlv_2
8	lnc-ZNF800-1	chr7:126720747-126720931	ENSG00000230206.1
9	lnc-ZNF800-1	chr7:126724745-126724843	NONHSAT123126
10	lnc-ZNF800-1	chr7:126735719-126735864	NONHSAT123126
11	lnc-ARF5-15	chr7:126655663-126657210	ucscGeneNc_uc003vlv_2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-592	chr7:126698202-126698223	MIMAT0003260

No data

Variant related genes	Relation type
MIR592	TF binding region
ENSG00000230820	TF binding region
GRM8	TF binding region
MIR592	CpG island
ENSG00000230820	CpG island
GRM8	CpG island
ENSG00000179603	chromatin interactions
ENSG00000106328	chromatin interactions
ENSG00000179562	chromatin interactions
ENSG00000048405	chromatin interactions

Extended variants
information (count: 2434 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2434 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17863168	chr7:126593467-126593468	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139735016	chr7:126593468-126593469	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564642854	chr7:126593471-126593472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528996585	chr7:126593482-126593483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150605736	chr7:126593510-126593511	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528657546	chr7:126593512-126593513	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547503862	chr7:126593583-126593584	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144621010	chr7:126593609-126593610	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs147456856	chr7:126593612-126593613	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192627868	chr7:126593614-126593615	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201563638	chr7:126593640-126593641	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549137501	chr7:126593641-126593642	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77158999	chr7:126593649-126593650	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs76070690	chr7:126593650-126593651	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs17865260	chr7:126593708-126593709	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs1204569	chr7:126593774-126593775	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184662344	chr7:126593805-126593806	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs570651278	chr7:126593811-126593812	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534499840	chr7:126593843-126593844	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140235991	chr7:126593856-126593857	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs17867199	chr7:126593867-126593868	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs187561878	chr7:126593869-126593870	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535863075	chr7:126593889-126593890	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74699905	chr7:126593924-126593925	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17869313	chr7:126593952-126593953	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546548385	chr7:126594016-126594017	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs17867375	chr7:126594029-126594030	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558153119	chr7:126594030-126594031	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145647448	chr7:126594046-126594047	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540467843	chr7:126594051-126594052	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559401858	chr7:126594063-126594064	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs17869208	chr7:126594069-126594070	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs541439195	chr7:126594070-126594071	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551355688	chr7:126594125-126594126	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192530808	chr7:126594156-126594157	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147727188	chr7:126594215-126594216	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552085888	chr7:126594257-126594258	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375798969	chr7:126594331-126594332	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570644212	chr7:126594416-126594417	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528333073	chr7:126594429-126594430	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184524897	chr7:126594521-126594522	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs17865026	chr7:126594522-126594523	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535926967	chr7:126594527-126594528	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs17867043	chr7:126594549-126594550	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs569309251	chr7:126594581-126594582	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs7782188	chr7:126594592-126594593	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs558476338	chr7:126594604-126594605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189022166	chr7:126594606-126594607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573410434	chr7:126594609-126594610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540831022	chr7:126594678-126594679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
early-passage human iPS cells	21368824	CNVD
Malignant melanoma	17260012	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Chordoma	21215367	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126593600-126594600	Enhancers	Fetal Kidney	kidney
2	chr7:126594600-126595000	Weak transcription	Fetal Kidney	kidney
3	chr7:126595000-126595400	Enhancers	Fetal Kidney	kidney
4	chr7:126597600-126598400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:126598200-126598800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:126601000-126601600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:126613000-126613400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr7:126618200-126618600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:126619800-126620200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr7:126634200-126635400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:126645800-126646800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:126646000-126646800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:126646200-126646800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:126646200-126646800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:126646200-126647000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:126646400-126646800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr7:126646400-126646800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:126658600-126659000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr7:126660800-126661200	Enhancers	Fetal Intestine Large	intestine
20	chr7:126661400-126661600	Enhancers	Fetal Intestine Small	intestine
21	chr7:126671400-126674000	Weak transcription	Fetal Kidney	kidney
22	chr7:126673800-126674600	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr7:126674000-126674400	Enhancers	Liver	Liver
24	chr7:126674000-126676000	Enhancers	Fetal Kidney	kidney
25	chr7:126674200-126674400	Enhancers	Pancreas	Pancrea
26	chr7:126674200-126675800	Enhancers	Fetal Intestine Large	intestine
27	chr7:126674400-126674800	Flanking Active TSS	Liver	Liver
28	chr7:126674400-126675400	Weak transcription	Pancreas	Pancrea
29	chr7:126674400-126675800	Enhancers	Fetal Intestine Small	intestine
30	chr7:126674600-126675600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr7:126674600-126676000	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr7:126674800-126675200	Enhancers	Liver	Liver
33	chr7:126675200-126675400	Flanking Active TSS	Liver	Liver
34	chr7:126675400-126675800	Enhancers	Liver	Liver
35	chr7:126675400-126675800	Enhancers	Gastric	stomach
36	chr7:126675400-126675800	Enhancers	Pancreas	Pancrea
37	chr7:126675600-126675800	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr7:126675800-126676200	Flanking Active TSS	Liver	Liver
39	chr7:126675800-126676200	Weak transcription	Fetal Intestine Small	intestine
40	chr7:126676200-126676600	Enhancers	Liver	Liver
41	chr7:126676200-126676600	Enhancers	Fetal Intestine Small	intestine
42	chr7:126676600-126682000	Weak transcription	Liver	Liver
43	chr7:126682000-126682400	Enhancers	Liver	Liver
44	chr7:126695400-126696600	Enhancers	Fetal Intestine Large	intestine
45	chr7:126695800-126696800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:126696200-126696600	Enhancers	Liver	Liver
47	chr7:126696200-126697200	Enhancers	Fetal Intestine Small	intestine
48	chr7:126696800-126697000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:126708600-126709000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:126720200-126721600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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