Variant report

Variant	nsv1027070
Chromosome Location	chr8:112490160-112844323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:112576305-112577602	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:112809453-112809783	HepG2	liver:	n/a	n/a
3	BACH1	chr8:112692464-112692870	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:112691006-112691050	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:112565168-112565174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr8:112809530-112809825	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:112576576-112576903	HepG2	liver:	n/a	n/a
8	BHLHE40	chr8:112716680-112716782	GM12878	blood:	n/a	n/a
9	BRCA1	chr8:112691833-112692033	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr8:112678378-112678702	K562	blood:	n/a	n/a
11	CCNT2	chr8:112730529-112730729	K562	blood:	n/a	n/a
12	CEBPB	chr8:112631993-112632244	HepG2	liver:	n/a	chr8:112632167-112632180
13	CEBPB	chr8:112526420-112526708	ECC-1	luminal epithelium:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
14	CEBPB	chr8:112618812-112619060	HepG2	liver:	n/a	chr8:112618953-112618964 chr8:112618955-112618964
15	CEBPB	chr8:112526372-112526696	K562	blood:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
16	CEBPB	chr8:112818835-112819234	MCF-7	breast:	n/a	n/a
17	CEBPB	chr8:112753993-112754235	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:112648825-112649214	HepG2	liver:	n/a	chr8:112649115-112649126 chr8:112649115-112649126
19	CEBPB	chr8:112780227-112780716	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr8:112603408-112603661	H1-hESC	embryonic stem cell:	n/a	chr8:112603525-112603536
21	CEBPB	chr8:112526378-112526701	A549	lung:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
22	CEBPB	chr8:112589943-112590245	HepG2	liver:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
23	CEBPB	chr8:112704205-112704474	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:112809439-112809764	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:112809471-112809708	A549	lung:	n/a	n/a
26	CEBPB	chr8:112575228-112575538	HepG2	liver:	n/a	chr8:112575342-112575355 chr8:112575342-112575353 chr8:112575343-112575354 chr8:112575342-112575355
27	CEBPB	chr8:112722332-112722588	HepG2	liver:	n/a	chr8:112722472-112722483
28	CEBPB	chr8:112656695-112656966	IMR90	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
29	CEBPB	chr8:112711608-112711664	A549	lung:	n/a	chr8:112711627-112711640
30	CEBPB	chr8:112829171-112829427	MCF-7	breast:	n/a	n/a
31	CEBPB	chr8:112656674-112657002	HepG2	liver:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
32	CEBPB	chr8:112519386-112519549	A549	lung:	n/a	n/a
33	CEBPB	chr8:112809479-112809785	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:112656669-112656973	A549	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
35	CEBPB	chr8:112795764-112796069	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:112578664-112578920	HepG2	liver:	n/a	chr8:112578719-112578732
37	CEBPB	chr8:112495005-112495321	IMR90	lung:	n/a	n/a
38	CEBPB	chr8:112576445-112576921	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:112722331-112722655	ECC-1	luminal epithelium:	n/a	chr8:112722472-112722483
40	CEBPB	chr8:112578688-112578901	A549	lung:	n/a	chr8:112578719-112578732
41	CEBPB	chr8:112795741-112796043	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:112526403-112526670	H1-hESC	embryonic stem cell:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
43	CEBPB	chr8:112526364-112526721	HepG2	liver:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
44	CEBPB	chr8:112658465-112658728	MCF-7	breast:	n/a	n/a
45	CEBPB	chr8:112565892-112566140	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:112603419-112603617	HepG2	liver:	n/a	chr8:112603525-112603536
47	CEBPB	chr8:112576541-112576791	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:112722343-112722717	ECC-1	luminal epithelium:	n/a	chr8:112722472-112722483
49	CEBPB	chr8:112526367-112526717	IMR90	lung:	n/a	chr8:112526527-112526536 chr8:112526527-112526536 chr8:112526525-112526536 chr8:112526527-112526536 chr8:112526525-112526538 chr8:112526527-112526536 chr8:112526527-112526538
50	CEBPB	chr8:112589952-112590235	A549	lung:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112655155-112655205	NB4	blood:	n/a
2	chr8:112655155-112655205	NB4	blood:	n/a
3	chr8:112835665-112835715	SAEC	small airway:	n/a
4	chr8:112835665-112835715	SKMC	muscle:	n/a
5	chr8:112612368-112612418	Caco-2	colon:	n/a
6	chr8:112612368-112612418	GM12891	blood:	n/a
7	chr8:112612368-112612418	HL-60	blood:	n/a
8	chr8:112636613-112636663	GM12891	blood:	n/a
9	chr8:112612368-112612418	Jurkat	blood:	n/a
10	chr8:112636625-112636675	Caco-2	colon:	n/a
11	chr8:112655155-112655205	U87	brain:	n/a
12	chr8:112636613-112636663	AG04449	skin:	fetal
13	chr8:112636625-112636675	IMR90	lung:	fetal
14	chr8:112636613-112636663	CMK	blood:	n/a
15	chr8:112655155-112655205	HL-60	blood:	n/a
16	chr8:112636613-112636663	HIPEpiC	eye:	n/a
17	chr8:112636625-112636675	PFSK-1	brain:	n/a
18	chr8:112636625-112636675	MCF10A-Er-Src	breast:	n/a
19	chr8:112655155-112655205	HIPEpiC	eye:	n/a
20	chr8:112835665-112835715	HNPCEpiC	eye:	n/a
21	chr8:112612368-112612418	GM12878	blood:	n/a
22	chr8:112636613-112636663	GM12878	blood:	n/a
23	chr8:112612368-112612418	Hepatocyte	liver:	n/a
24	chr8:112655155-112655205	ovcar-3	ovarian:	n/a
25	chr8:112612368-112612418	HRE	kidney:	n/a
26	chr8:112636625-112636675	SAEC	small airway:	n/a
27	chr8:112636625-112636675	LNCaP	prostate:	n/a
28	chr8:112655155-112655205	Caco-2	colon:	n/a
29	chr8:112655155-112655205	GM12892	blood:	n/a
30	chr8:112655155-112655205	MCF-7	breast:	n/a
31	chr8:112835665-112835715	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:112612368-112612418	U87	brain:	n/a
33	chr8:112691450-112691500	ProgFib	skin:	n/a
34	chr8:112636613-112636663	Jurkat	blood:	n/a
35	chr8:112691450-112691500	MCF10A-Er-Src	breast:	n/a
36	chr8:112612368-112612418	HUVEC	blood vessel:	n/a
37	chr8:112655155-112655205	HCT-116	colon:	n/a
38	chr8:112612368-112612418	BE2_C	brain:	n/a
39	chr8:112612368-112612418	HRPEpiC	eye:	n/a
40	chr8:112636625-112636675	AG09309	skin:	n/a
41	chr8:112612368-112612418	ovcar-3	ovarian:	n/a
42	chr8:112636625-112636675	BE2_C	brain:	n/a
43	chr8:112636625-112636675	NT2-D1	testis:	n/a
44	chr8:112655155-112655205	HNPCEpiC	eye:	n/a
45	chr8:112612368-112612418	ECC-1	luminal epithelium:	n/a
46	chr8:112691450-112691500	NHBE	bronchial:	n/a
47	chr8:112655155-112655205	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:112612368-112612418	ProgFib	skin:	n/a
49	chr8:112612368-112612418	NH-A	brain:	n/a
50	chr8:112835665-112835715	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
2	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
3	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
4	chr8:112753150..112755193-chr8:112756669..112758806,2	MCF-7	breast:
5	chr8:112765107..112767231-chr8:112771782..112773764,2	K562	blood:
6	chr8:112438643..112439991-chr8:112809151..112809703,4	MCF-7	breast:
7	chr8:112455862..112457106-chr8:112809020..112809893,6	MCF-7	breast:
8	chr8:112456153..112457084-chr8:112809101..112810085,7	MCF-7	breast:
9	chr8:112570236..112571107-chr8:139584283..139585016,2	MCF-7	breast:
10	chr8:112456214..112456969-chr8:112758072..112758694,3	MCF-7	breast:
11	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
12	chr8:112248265..112249043-chr8:112809213..112809738,2	MCF-7	breast:
13	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
14	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
15	chr8:112765107..112767231-chr8:112771782..112773764,2	K562	blood:
16	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
17	chr8:112841029..112843004-chr8:112843259..112845025,2	MCF-7	breast:
18	chr8:112471086..112471839-chr8:112809518..112810102,2	MCF-7	breast:
19	chr8:112439221..112439930-chr8:112809136..112809948,2	MCF-7	breast:
20	chr8:112721723..112722542-chr9:119005808..119006308,2	MCF-7	breast:
21	chr8:112841029..112843004-chr8:112843259..112845025,2	MCF-7	breast:
22	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
23	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
24	chr8:112753150..112755193-chr8:112756669..112758806,2	MCF-7	breast:
25	chr8:112437770..112438280-chr8:112809131..112809707,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-67H2.1.1-2	chr8:112768739-112768861	ENSG00000254262
2	lnc-CSMD3-4	chr8:112633687-112634026	NONHSAT128329
3	lnc-RP11-67H2.1.1-3	chr8:112712239-112712497	NONHSAT128330
4	lnc-RP11-67H2.1.1-3	chr8:112711744-112711881	XLOC_006902
5	lnc-RP11-67H2.1.1-3	chr8:112711743-112711881	NONHSAT128330
6	lnc-RP11-67H2.1.1-3	chr8:112712240-112712497	XLOC_006902
7	lnc-RP11-67H2.1.1-2	chr8:112754241-112754312	ENSG00000254262
8	lnc-RP11-67H2.1.1-2	chr8:112768535-112768629	ENSG00000254262
9	lnc-RP11-67H2.1.1-2	chr8:112754207-112754312	XLOC_006903
10	lnc-RP11-67H2.1.1-2	chr8:112757671-112757836	ENSG00000254262
11	lnc-RP11-67H2.1.1-7	chr8:112837712-112837805	l_3669_chr8:112823382-112827015_testes
12	lnc-RP11-67H2.1.1-2	chr8:112754224-112754312	NONHSAT128333
13	lnc-RP11-422N16.3.1-4	chr8:112525276-112525364	ENSG00000253434.1
14	lnc-RP11-67H2.1.1-2	chr8:112757671-112757916	XLOC_006903
15	lnc-RP11-67H2.1.1-2	chr8:112768536-112768629	XLOC_006903
16	lnc-RP11-422N16.3.1-4	chr8:112554278-112554452	ENSG00000253434.1
17	lnc-RP11-67H2.1.1-7	chr8:112837915-112838389	l_3669_chr8:112823382-112827015_testes
18	lnc-RP11-67H2.1.1-2	chr8:112768739-112770625	XLOC_006903
19	lnc-RP11-67H2.1.1-2	chr8:112757670-112757836	NONHSAT128333
20	lnc-RP11-67H2.1.1-7	chr8:112823383-112823488	l_3669_chr8:112823382-112827015_testes
21	lnc-RP11-422N16.3.1-4	chr8:112555148-112555202	ENSG00000253434.1
22	lnc-RP11-422N16.3.1-4	chr8:112527241-112527565	ENSG00000253434.1
23	lnc-RP11-67H2.1.1-2	chr8:112754225-112754312	XLOC_006903
24	lnc-RP11-67H2.1.1-2	chr8:112757671-112757836	XLOC_006903
25	lnc-RP11-67H2.1.1-2	chr8:112768738-112770625	NONHSAT128333
26	lnc-RP11-67H2.1.1-2	chr8:112768739-112769213	XLOC_006903
27	lnc-RP11-422N16.3.1-4	chr8:112525276-112525364	ENSG00000253434.1
28	lnc-RP11-67H2.1.1-7	chr8:112826847-112827015	l_3669_chr8:112823382-112827015_testes

Variant related genes	Relation type
ENSG00000253156	TF binding region
ENSG00000254262	TF binding region
ENSG00000253156	CpG island
ENSG00000254262	CpG island
ENSG00000254262	chromatin interactions
ENSG00000253103	chromatin interactions
ACSL1	miRNA target sites
RPRD1A	miRNA target sites
ACPL2	miRNA target sites

Extended variants
information (count: 4143 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4143 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7830277	chr8:112498274-112498275	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151331427	chr8:112498286-112498287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75770691	chr8:112498322-112498323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2717184	chr8:112498376-112498377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140589683	chr8:112498387-112498388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74718232	chr8:112498409-112498410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572370028	chr8:112498436-112498437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111411167	chr8:112498450-112498451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186134523	chr8:112498472-112498473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150457048	chr8:112498475-112498476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541006091	chr8:112498490-112498491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371670925	chr8:112498541-112498542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375364678	chr8:112498554-112498555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368005355	chr8:112498563-112498564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565202694	chr8:112498583-112498584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs67811760	chr8:112498587-112498588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368124021	chr8:112498588-112498589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201080547	chr8:112498594-112498595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77732038	chr8:112498595-112498596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531159774	chr8:112498629-112498630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374963383	chr8:112498681-112498682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550712288	chr8:112498689-112498690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567625575	chr8:112498701-112498702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554891212	chr8:112498710-112498711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536535893	chr8:112498724-112498725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546234826	chr8:112498738-112498739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566440658	chr8:112498747-112498748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538388553	chr8:112498759-112498760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200351912	chr8:112498798-112498799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558635138	chr8:112498811-112498812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575221789	chr8:112498825-112498826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538047375	chr8:112498835-112498836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147709017	chr8:112498857-112498858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367544176	chr8:112498875-112498876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142476643	chr8:112498877-112498878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2606198	chr8:112498885-112498886	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563861428	chr8:112498886-112498887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559523744	chr8:112498974-112498975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13253875	chr8:112499000-112499001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545049336	chr8:112499023-112499024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189773800	chr8:112499041-112499042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565379220	chr8:112499077-112499078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182070191	chr8:112499107-112499108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187989333	chr8:112499116-112499117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146546554	chr8:112499118-112499119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191403059	chr8:112499132-112499133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139065654	chr8:112499161-112499162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201151289	chr8:112499175-112499176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13252204	chr8:112499179-112499180	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs183581396	chr8:112499181-112499182	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112498200-112498600	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr8:112498200-112499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:112538600-112539000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:112539000-112544000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:112539200-112540000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:112544000-112544600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:112551400-112552000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:112552800-112557800	Weak transcription	Adipose Nuclei	Adipose
9	chr8:112557200-112558800	Enhancers	Fetal Lung	lung
10	chr8:112557800-112558400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:112557800-112558600	Strong transcription	Adipose Nuclei	Adipose
12	chr8:112558600-112560200	Weak transcription	Adipose Nuclei	Adipose
13	chr8:112575200-112577600	Enhancers	Liver	Liver
14	chr8:112575800-112578400	Enhancers	HepG2	liver
15	chr8:112578200-112578400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:112593600-112593800	Enhancers	Pancreas	Pancrea
17	chr8:112597000-112598400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:112611000-112611800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:112611400-112612000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:112611600-112611800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr8:112611600-112612200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr8:112611800-112612000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr8:112611800-112612800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr8:112615400-112615800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:112623600-112624000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:112623800-112624200	ZNF genes & repeats	Spleen	Spleen
27	chr8:112624000-112624200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:112624000-112624200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
29	chr8:112624000-112627600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:112624200-112633800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:112627200-112628000	Enhancers	Brain Germinal Matrix	brain
32	chr8:112627600-112628200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:112633800-112634000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:112633800-112634000	Bivalent Enhancer	Aorta	Aorta
35	chr8:112655000-112655200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:112655200-112655400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:112665400-112666000	Enhancers	Fetal Muscle Leg	muscle
38	chr8:112688200-112689400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:112688200-112690400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr8:112689400-112689800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:112689600-112690400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr8:112689600-112690400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:112689800-112690200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:112690000-112690400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:112690000-112690600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr8:112690000-112690600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr8:112690000-112690800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr8:112690200-112691400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:112690200-112692200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr8:112690200-112692400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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