Variant report

Variant	nsv538863
Chromosome Location	chr7:56307057-56677865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1154)
CpG islands
(count:4093)
Chromatin interactive
region (count:6)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:56396037-56396404	K562	blood:	n/a	n/a
2	ATF1	chr7:56317868-56318068	K562	blood:	n/a	n/a
3	ATF1	chr7:56392870-56393144	K562	blood:	n/a	n/a
4	BATF	chr7:56438226-56439458	GM12878	blood:	n/a	n/a
5	BATF	chr7:56439524-56440756	GM12878	blood:	n/a	n/a
6	BATF	chr7:56439727-56440134	GM12878	blood:	n/a	n/a
7	BATF	chr7:56442645-56442830	GM12878	blood:	n/a	n/a
8	BATF	chr7:56441464-56441866	GM12878	blood:	n/a	n/a
9	BATF	chr7:56450946-56451228	GM12878	blood:	n/a	n/a
10	BATF	chr7:56394887-56395134	GM12878	blood:	n/a	n/a
11	BATF	chr7:56463577-56463911	GM12878	blood:	n/a	n/a
12	BATF	chr7:56437428-56437607	GM12878	blood:	n/a	n/a
13	BATF	chr7:56438872-56439456	GM12878	blood:	n/a	n/a
14	BATF	chr7:56440976-56442496	GM12878	blood:	n/a	n/a
15	BATF	chr7:56440170-56440754	GM12878	blood:	n/a	n/a
16	BATF	chr7:56438429-56438836	GM12878	blood:	n/a	n/a
17	BATF	chr7:56441021-56441428	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:56437865-56440812	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:56435572-56435743	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:56440912-56442515	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:56437350-56437622	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:56440941-56442557	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:56437836-56440868	GM12878	blood:	n/a	chr7:56437839-56437852
24	BHLHE40	chr7:56439495-56440612	HepG2	liver:	n/a	n/a
25	BHLHE40	chr7:56438197-56439314	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:56440907-56441906	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:56541864-56541898	A549	lung:	n/a	n/a
28	BHLHE40	chr7:56442086-56442477	HepG2	liver:	n/a	n/a
29	BHLHE40	chr7:56396053-56396246	K562	blood:	n/a	n/a
30	BRCA1	chr7:56536519-56536621	GM12878	blood:	n/a	n/a
31	BRCA1	chr7:56566718-56566802	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:56441064-56441264	GM12878	blood:	n/a	n/a
33	BRCA1	chr7:56606505-56606701	GM12878	blood:	n/a	n/a
34	BRCA1	chr7:56559961-56560030	GM12878	blood:	n/a	n/a
35	CBX3	chr7:56437915-56438800	K562	blood:	n/a	n/a
36	CBX3	chr7:56440971-56442559	K562	blood:	n/a	n/a
37	CBX3	chr7:56437959-56440105	K562	blood:	n/a	n/a
38	CBX3	chr7:56440162-56440822	K562	blood:	n/a	n/a
39	CBX3	chr7:56440964-56441418	K562	blood:	n/a	n/a
40	CBX3	chr7:56438827-56440837	K562	blood:	n/a	n/a
41	CBX3	chr7:56441554-56442520	K562	blood:	n/a	n/a
42	CEBPB	chr7:56331752-56331815	HepG2	liver:	n/a	chr7:56331776-56331787
43	CEBPB	chr7:56361446-56361522	HepG2	liver:	n/a	chr7:56361484-56361495
44	CEBPB	chr7:56629964-56630176	IMR90	lung:	n/a	chr7:56630010-56630021
45	CEBPB	chr7:56307103-56307194	A549	lung:	n/a	chr7:56307153-56307166 chr7:56307153-56307164
46	CEBPB	chr7:56331758-56331766	K562	blood:	n/a	n/a
47	CEBPB	chr7:56629968-56630102	HepG2	liver:	n/a	chr7:56630010-56630021
48	CEBPB	chr7:56436638-56436845	K562	blood:	n/a	n/a
49	CEBPB	chr7:56635681-56635783	HepG2	liver:	n/a	chr7:56635719-56635730
50	CEBPB	chr7:56354384-56354589	HepG2	liver:	n/a	n/a

(count:4093 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56515601-56515651	CMK	blood:	n/a
2	chr7:56606663-56606713	PANC-1	pancreas:	n/a
3	chr7:56672774-56672824	A549	lung:	n/a
4	chr7:56446385-56446435	RPTEC	kidney:	n/a
5	chr7:56515752-56515802	HEEpiC	esophagus:	n/a
6	chr7:56515601-56515651	HNPCEpiC	eye:	n/a
7	chr7:56515601-56515651	CMK	blood:	n/a
8	chr7:56606663-56606713	PANC-1	pancreas:	n/a
9	chr7:56672774-56672824	A549	lung:	n/a
10	chr7:56446385-56446435	RPTEC	kidney:	n/a
11	chr7:56515752-56515802	HEEpiC	esophagus:	n/a
12	chr7:56515601-56515651	HNPCEpiC	eye:	n/a
13	chr7:56551640-56551690	HCT-116	colon:	n/a
14	chr7:56553709-56553759	SK-N-SH_RA	brain:	n/a
15	chr7:56563742-56563792	HIPEpiC	eye:	n/a
16	chr7:56673189-56673239	HUVEC	blood vessel:	n/a
17	chr7:56435424-56435474	PrEC	prostate:	n/a
18	chr7:56446176-56446226	SKMC	muscle:	n/a
19	chr7:56563152-56563202	GM06990	blood:	n/a
20	chr7:56434239-56434289	AG09319	gingival:	n/a
21	chr7:56606663-56606713	SK-N-SH_RA	brain:	n/a
22	chr7:56450073-56450123	HCPEpiC	choroid plexus:	n/a
23	chr7:56439703-56439753	K562	blood:	n/a
24	chr7:56357732-56357782	AoSMC	blood vessel:	n/a
25	chr7:56606663-56606713	AG04449	skin:	fetal
26	chr7:56555482-56555532	GM12878	blood:	n/a
27	chr7:56673049-56673099	ECC-1	luminal epithelium:	n/a
28	chr7:56358512-56358562	IMR90	lung:	fetal
29	chr7:56435424-56435474	IMR90	lung:	fetal
30	chr7:56605325-56605375	HNPCEpiC	eye:	n/a
31	chr7:56605835-56605885	ProgFib	skin:	n/a
32	chr7:56549234-56549284	AG04450	lung:	fetal
33	chr7:56605835-56605885	NH-A	brain:	n/a
34	chr7:56550751-56550801	HAEpiC	amniotic membrane:	n/a
35	chr7:56550751-56550801	LNCaP	prostate:	n/a
36	chr7:56551492-56551542	NHDF-neo	bronchial:	n/a
37	chr7:56551590-56551640	HL-60	blood:	n/a
38	chr7:56434951-56435001	AG04449	skin:	fetal
39	chr7:56357732-56357782	HCPEpiC	choroid plexus:	n/a
40	chr7:56551640-56551690	HRE	kidney:	n/a
41	chr7:56515752-56515802	SKMC	muscle:	n/a
42	chr7:56516129-56516179	SAEC	small airway:	n/a
43	chr7:56551112-56551162	HEEpiC	esophagus:	n/a
44	chr7:56605830-56605880	PFSK-1	brain:	n/a
45	chr7:56605830-56605880	AG09309	skin:	n/a
46	chr7:56551112-56551162	NHBE	bronchial:	n/a
47	chr7:56563018-56563068	BJ	skin:	n/a
48	chr7:56356698-56356748	LNCaP	prostate:	n/a
49	chr7:56563018-56563068	HCM	heart:	n/a
50	chr7:56605325-56605375	SK-N-SH	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:56593770..56596285-chr7:56602462..56604093,2	K562	blood:
2	chr7:56171801..56173788-chr7:56307425..56310338,2	K562	blood:
3	chr7:56587375..56589819-chr7:56607783..56609780,2	K562	blood:
4	chr7:56587375..56589819-chr7:56607783..56609780,2	K562	blood:
5	chr7:56545109..56547428-chr7:56558350..56560610,2	K562	blood:
6	chr6:88665773..88666293-chr7:56605897..56606515,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUMF2-13	chr7:56448669-56449005	NONHSAT120750
2	lnc-RP4-725G10.1.1-8	chr7:56500181-56500394	NONHSAT147555
3	lnc-RP4-725G10.1.1-3	chr7:56549800-56550149	XLOC_006456
4	lnc-RP4-725G10.1.1-2	chr7:56446322-56446398	XLOC_006455
5	lnc-SUMF2-11	chr7:56391008-56391294	NONHSAT120741
6	lnc-RP4-725G10.1.1-8	chr7:56493828-56493956	NR_029420
7	lnc-RP4-725G10.1.1-3	chr7:56550668-56550988	ENSG00000225488
8	lnc-RP4-725G10.1.1-8	chr7:56496078-56496134	NONHSAT147555
9	lnc-RP4-725G10.1.1-8	chr7:56515912-56516068	NR_029420
10	lnc-RP4-725G10.1.1-8	chr7:56489550-56489702	NONHSAT120753
11	lnc-RP4-725G10.1.1-8	chr7:56493828-56493956	NONHSAT120753
12	lnc-RP4-725G10.1.1-8	chr7:56491383-56492330	NONHSAT120753
13	lnc-RP4-725G10.1.1-2	chr7:56446010-56446229	XLOC_006455
14	lnc-RP4-725G10.1.1-9	chr7:56569977-56570737	NONHSAT120762
15	lnc-SUMF2-2	chr7:56560817-56564978	ENSG00000261275.1
16	lnc-RP4-725G10.1.1-3	chr7:56549977-56550149	XLOC_006456
17	lnc-SUMF2-2	chr7:56563916-56564977	NONHSAT120761
18	lnc-RP4-725G10.1.1-3	chr7:56551405-56551606	NONHSAT120756
19	lnc-RP4-725G10.1.1-8	chr7:56494528-56494703	NONHSAT120753
20	lnc-RP4-725G10.1.1-8	chr7:56491397-56492330	NR_029420
21	lnc-RP4-725G10.1.1-3	chr7:56545289-56545525	XLOC_006456
22	lnc-SUMF2-15	chr7:56646470-56646559	NONHSAT120770
23	lnc-RP4-725G10.1.1-10	chr7:56593121-56593806	NONHSAT120763
24	lnc-RP4-725G10.1.1-8	chr7:56500181-56500395	NONHSAT120753
25	lnc-RP4-725G10.1.1-8	chr7:56515912-56516068	NONHSAT147555
26	lnc-RP4-725G10.1.1-8	chr7:56494528-56494703	NR_029420
27	lnc-RP4-725G10.1.1-3	chr7:56550668-56551012	NR_108095
28	lnc-RP4-725G10.1.1-4	chr7:56605742-56605823	XLOC_006457
29	lnc-RP4-725G10.1.1-4	chr7:56601923-56604581	XLOC_006457
30	lnc-RP4-725G10.1.1-8	chr7:56496078-56496134	NR_029420
31	lnc-RP4-725G10.1.1-3	chr7:56550668-56550988	XLOC_006456
32	lnc-SUMF2-10	chr7:56357589-56359118	NONHSAT120740
33	lnc-RP4-725G10.1.1-3	chr7:56551406-56551606	XLOC_006456
34	lnc-SUMF2-10	chr7:56355923-56357276	NONHSAT120740
35	lnc-SUMF2-14	chr7:56626914-56627651	NONHSAT120768
36	lnc-RP4-725G10.1.1-3	chr7:56549798-56550149	ENSG00000225488
37	lnc-RP4-725G10.1.1-3	chr7:56545288-56545525	NONHSAT120756
38	lnc-RP4-725G10.1.1-8	chr7:56500181-56500394	NR_029420
39	lnc-SUMF2-2	chr7:56558375-56559328	NONHSAT120759
40	lnc-SUMF2-11	chr7:56390497-56390549	NONHSAT120741
41	lnc-RP4-725G10.1.1-2	chr7:56446340-56446379	XLOC_006455
42	lnc-RP4-725G10.1.1-8	chr7:56494552-56494703	NONHSAT147555
43	lnc-SUMF2-15	chr7:56645541-56645660	NONHSAT120770
44	lnc-RP4-725G10.1.1-3	chr7:56549976-56550149	NONHSAT120756
45	lnc-RP4-725G10.1.1-3	chr7:56549798-56550149	NR_108095
46	lnc-RP4-725G10.1.1-2	chr7:56448433-56448602	XLOC_006455

No data

Variant related genes	Relation type
RNU6-1335P	TF binding region
ENSG00000213067	TF binding region
ENSG00000203462	TF binding region
ENSG00000223740	TF binding region
ENSG00000223559	TF binding region
ENSG00000234716	TF binding region
CICP8	TF binding region
ENSG00000237268	TF binding region
ENSG00000232944	TF binding region
NMD3P2	TF binding region
ENSG00000271047	TF binding region
RBM22P3	TF binding region
ENSG00000261275	TF binding region
ENSG00000224370	TF binding region
ENSG00000213650	TF binding region
ENSG00000231299	TF binding region
ENSG00000225488	TF binding region
ENSG00000233288	TF binding region
ENSG00000265887	TF binding region
ENSG00000224155	TF binding region
VN1R25P	TF binding region
RNU6-1052P	TF binding region
RNU6-1335P	CpG island
ENSG00000213067	CpG island
ENSG00000203462	CpG island
ENSG00000223740	CpG island
ENSG00000223559	CpG island
ENSG00000234716	CpG island
CICP8	CpG island
ENSG00000237268	CpG island
ENSG00000232944	CpG island
NMD3P2	CpG island
ENSG00000271047	CpG island
RBM22P3	CpG island
ENSG00000261275	CpG island
ENSG00000224370	CpG island
ENSG00000213650	CpG island
ENSG00000231299	CpG island
ENSG00000225488	CpG island
ENSG00000233288	CpG island
ENSG00000265887	CpG island
ENSG00000224155	CpG island
VN1R25P	CpG island
RNU6-1052P	CpG island
ENSG00000223740	chromatin interactions
ENSG00000226485	chromatin interactions

Extended variants
information (count: 4724 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4724 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74519481	chr7:56323649-56323650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs73353577	chr7:56323650-56323651	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs184781195	chr7:56323651-56323652	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs375585150	chr7:56323658-56323659	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs80008186	chr7:56323671-56323672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs548206599	chr7:56323684-56323685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs78232800	chr7:56323687-56323688	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs138541329	chr7:56323701-56323702	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs187895590	chr7:56323738-56323739	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs74558281	chr7:56323768-56323769	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs138909557	chr7:56323777-56323778	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs556317941	chr7:56323784-56323785	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs574627505	chr7:56323796-56323797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs144090339	chr7:56323808-56323809	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554186588	chr7:56323882-56323883	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78745751	chr7:56323899-56323900	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540534731	chr7:56323916-56323917	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555053182	chr7:56323973-56323974	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147362472	chr7:56323978-56323979	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565148964	chr7:56323994-56323995	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200569895	chr7:56324004-56324005	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544450646	chr7:56324047-56324048	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79012627	chr7:56324051-56324052	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74317026	chr7:56324056-56324057	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547928724	chr7:56324063-56324064	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371404102	chr7:56324091-56324092	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558591628	chr7:56324133-56324134	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193189919	chr7:56324135-56324136	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11980255	chr7:56324136-56324137	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552859458	chr7:56324236-56324237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139435909	chr7:56324253-56324254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79736090	chr7:56324306-56324307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550002517	chr7:56324358-56324359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568314215	chr7:56324382-56324383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535948596	chr7:56324397-56324398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537588131	chr7:56324408-56324409	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184296028	chr7:56324424-56324425	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75221443	chr7:56324479-56324480	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558168117	chr7:56324550-56324551	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77598622	chr7:56324584-56324585	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544513750	chr7:56324700-56324701	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10268280	chr7:56324728-56324729	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs115425428	chr7:56324744-56324745	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141696748	chr7:56324784-56324785	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17172518	chr7:56324798-56324799	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs371033903	chr7:56324816-56324817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147305290	chr7:56324817-56324818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35900866	chr7:56324819-56324820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530714975	chr7:56324820-56324821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs66607649	chr7:56324833-56324834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56323600-56324200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:56323800-56324600	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr7:56323800-56324800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr7:56324400-56324800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr7:56324600-56325600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:56325600-56325800	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr7:56334000-56336600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:56336000-56336400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr7:56355000-56355200	Enhancers	Brain Anterior Caudate	brain
10	chr7:56355000-56355200	Enhancers	Brain Cingulate Gyrus	brain
11	chr7:56355000-56355800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:56355000-56355800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:56355000-56356000	Active TSS	Aorta	Aorta
14	chr7:56355000-56356000	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr7:56355000-56356000	Active TSS	Right Atrium	heart
16	chr7:56355000-56356000	Active TSS	Stomach Smooth Muscle	stomach
17	chr7:56355200-56355400	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr7:56355200-56355600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:56355200-56355600	Active TSS	Colon Smooth Muscle	Colon
20	chr7:56355200-56355600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr7:56355200-56355600	Active TSS	Fetal Stomach	stomach
22	chr7:56355200-56355600	Bivalent Enhancer	Left Ventricle	heart
23	chr7:56355200-56355800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:56355200-56355800	Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr7:56355200-56355800	Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr7:56355200-56355800	Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr7:56355200-56355800	Active TSS	Fetal Muscle Leg	muscle
28	chr7:56355200-56355800	Active TSS	Rectal Smooth Muscle	rectum
29	chr7:56355200-56355800	Active TSS	NHEK	skin
30	chr7:56355200-56356000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:56355200-56356000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:56355200-56356000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:56355200-56356000	Enhancers	Liver	Liver
34	chr7:56355200-56356000	Active TSS	Brain Angular Gyrus	brain
35	chr7:56355200-56356000	Active TSS	Brain Anterior Caudate	brain
36	chr7:56355200-56356000	Active TSS	Brain Cingulate Gyrus	brain
37	chr7:56355200-56356000	Active TSS	Brain Hippocampus Middle	brain
38	chr7:56355200-56356000	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr7:56355200-56356000	Active TSS	Brain Substantia Nigra	brain
40	chr7:56355200-56356000	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr7:56355200-56356000	Active TSS	Fetal Brain Female	brain
42	chr7:56355200-56356000	Active TSS	Ovary	ovary
43	chr7:56355200-56356000	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr7:56355200-56356200	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr7:56355400-56355600	Active TSS	Adipose Nuclei	Adipose
46	chr7:56355400-56355800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:56355400-56355800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:56355400-56355800	Active TSS	Brain Germinal Matrix	brain
49	chr7:56355400-56355800	Active TSS	Psoas Muscle	Psoas
50	chr7:56355400-56355800	Active TSS	Right Ventricle	heart

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