Variant report

Variant	nsv1026097
Chromosome Location	chr8:112382141-112714042
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	chr8:112456471-112456739	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:112576305-112577602	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:112449828-112449990	HepG2	liver:	n/a	n/a
4	BACH1	chr8:112692464-112692870	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:112565168-112565174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:112691006-112691050	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr8:112485985-112486203	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr8:112576576-112576903	HepG2	liver:	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	CEBPB	chr8:112404299-112404642	HepG2	liver:	n/a	chr8:112404467-112404478
12	CEBPB	chr8:112408312-112408657	H1-hESC	embryonic stem cell:	n/a	chr8:112408484-112408497 chr8:112408486-112408495 chr8:112408485-112408496 chr8:112408486-112408495 chr8:112408486-112408495
13	CEBPB	chr8:112575228-112575538	HepG2	liver:	n/a	chr8:112575342-112575355 chr8:112575342-112575353 chr8:112575343-112575354 chr8:112575342-112575355
14	CEBPB	chr8:112603408-112603661	H1-hESC	embryonic stem cell:	n/a	chr8:112603525-112603536
15	CEBPB	chr8:112408291-112408670	IMR90	lung:	n/a	chr8:112408484-112408497 chr8:112408486-112408495 chr8:112408485-112408496 chr8:112408486-112408495 chr8:112408486-112408495
16	CEBPB	chr8:112495005-112495321	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:112603419-112603617	HepG2	liver:	n/a	chr8:112603525-112603536
18	CEBPB	chr8:112656674-112657002	HepG2	liver:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
19	CEBPB	chr8:112711608-112711664	A549	lung:	n/a	chr8:112711627-112711640
20	CEBPB	chr8:112481791-112481991	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:112576541-112576791	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:112658465-112658728	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:112404307-112404589	A549	lung:	n/a	chr8:112404467-112404478
24	CEBPB	chr8:112519386-112519549	A549	lung:	n/a	n/a
25	CEBPB	chr8:112589943-112590245	HepG2	liver:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
26	CEBPB	chr8:112578664-112578920	HepG2	liver:	n/a	chr8:112578719-112578732
27	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
28	CEBPB	chr8:112408306-112408655	HepG2	liver:	n/a	chr8:112408484-112408497 chr8:112408486-112408495 chr8:112408485-112408496 chr8:112408486-112408495 chr8:112408486-112408495
29	CEBPB	chr8:112408330-112408661	Hela-S3	cervix:	n/a	chr8:112408484-112408497 chr8:112408486-112408495 chr8:112408485-112408496 chr8:112408486-112408495 chr8:112408486-112408495
30	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
31	CEBPB	chr8:112576445-112576921	HepG2	liver:	n/a	n/a
32	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
33	CEBPB	chr8:112408310-112408678	K562	blood:	n/a	chr8:112408484-112408497 chr8:112408486-112408495 chr8:112408485-112408496 chr8:112408486-112408495 chr8:112408486-112408495
34	CEBPB	chr8:112656669-112656973	A549	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
35	CEBPB	chr8:112396842-112396953	HepG2	liver:	n/a	chr8:112396875-112396886
36	CEBPB	chr8:112481807-112482030	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:112589952-112590235	A549	lung:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
38	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
39	CEBPB	chr8:112618812-112619060	HepG2	liver:	n/a	chr8:112618953-112618964 chr8:112618955-112618964
40	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
41	CEBPB	chr8:112578688-112578901	A549	lung:	n/a	chr8:112578719-112578732
42	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
43	CEBPB	chr8:112704205-112704474	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:112404307-112404637	IMR90	lung:	n/a	chr8:112404467-112404478
45	CEBPB	chr8:112656695-112656966	IMR90	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
46	CEBPB	chr8:112631993-112632244	HepG2	liver:	n/a	chr8:112632167-112632180
47	CEBPB	chr8:112404357-112404500	K562	blood:	n/a	chr8:112404467-112404478
48	CEBPB	chr8:112648825-112649214	HepG2	liver:	n/a	chr8:112649115-112649126 chr8:112649115-112649126
49	CEBPB	chr8:112408299-112408622	A549	lung:	n/a	chr8:112408484-112408497 chr8:112408486-112408495 chr8:112408485-112408496 chr8:112408486-112408495 chr8:112408486-112408495
50	CEBPB	chr8:112565892-112566140	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112482677-112482727	HIPEpiC	eye:	n/a
2	chr8:112482677-112482727	HIPEpiC	eye:	n/a
3	chr8:112691450-112691500	Hepatocyte	liver:	n/a
4	chr8:112691450-112691500	SKMC	muscle:	n/a
5	chr8:112612368-112612418	GM12892	blood:	n/a
6	chr8:112482695-112482745	HCT-116	colon:	n/a
7	chr8:112655155-112655205	HAEpiC	amniotic membrane:	n/a
8	chr8:112691450-112691500	AG04450	lung:	fetal
9	chr8:112636625-112636675	CMK	blood:	n/a
10	chr8:112612368-112612418	SK-N-SH	brain:	n/a
11	chr8:112636613-112636663	AG04449	skin:	fetal
12	chr8:112482677-112482727	Caco-2	colon:	n/a
13	chr8:112655155-112655205	AG09309	skin:	n/a
14	chr8:112636613-112636663	MCF-7	breast:	n/a
15	chr8:112636613-112636663	HMEC	breast:	n/a
16	chr8:112691450-112691500	NH-A	brain:	n/a
17	chr8:112482695-112482745	AG04450	lung:	fetal
18	chr8:112636625-112636675	PANC-1	pancreas:	n/a
19	chr8:112636613-112636663	ovcar-3	ovarian:	n/a
20	chr8:112612368-112612418	AG04450	lung:	fetal
21	chr8:112691450-112691500	GM12892	blood:	n/a
22	chr8:112636625-112636675	HCF	heart:	n/a
23	chr8:112655155-112655205	NB4	blood:	n/a
24	chr8:112482677-112482727	NB4	blood:	n/a
25	chr8:112612368-112612418	MCF-7	breast:	n/a
26	chr8:112655155-112655205	GM12891	blood:	n/a
27	chr8:112612368-112612418	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:112482677-112482727	HEK293	kidney:	embryo
29	chr8:112482695-112482745	Caco-2	colon:	n/a
30	chr8:112636613-112636663	ProgFib	skin:	n/a
31	chr8:112655155-112655205	BE2_C	brain:	n/a
32	chr8:112636613-112636663	HCT-116	colon:	n/a
33	chr8:112636613-112636663	HCPEpiC	choroid plexus:	n/a
34	chr8:112482695-112482745	SK-N-MC	brain:	n/a
35	chr8:112691450-112691500	AoSMC	blood vessel:	n/a
36	chr8:112636625-112636675	Hepatocyte	liver:	n/a
37	chr8:112691450-112691500	AG09309	skin:	n/a
38	chr8:112482677-112482727	Jurkat	blood:	n/a
39	chr8:112636625-112636675	SK-N-SH_RA	brain:	n/a
40	chr8:112636625-112636675	GM12891	blood:	n/a
41	chr8:112482695-112482745	AG10803	skin:	n/a
42	chr8:112482695-112482745	K562	blood:	n/a
43	chr8:112482677-112482727	MCF10A-Er-Src	breast:	n/a
44	chr8:112636625-112636675	BE2_C	brain:	n/a
45	chr8:112636613-112636663	A549	lung:	n/a
46	chr8:112636625-112636675	HMEC	breast:	n/a
47	chr8:112482677-112482727	AG04450	lung:	fetal
48	chr8:112612368-112612418	NT2-D1	testis:	n/a
49	chr8:112636613-112636663	SK-N-SH_RA	brain:	n/a
50	chr8:112691450-112691500	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:112427186..112429388-chr8:112430940..112432715,2	K562	blood:
2	chr8:112438643..112439991-chr8:112809151..112809703,4	MCF-7	breast:
3	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
4	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
5	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
6	chr8:112456214..112456969-chr8:112758072..112758694,3	MCF-7	breast:
7	chr8:112439221..112439930-chr8:112809136..112809948,2	MCF-7	breast:
8	chr8:112455862..112457106-chr8:112809020..112809893,6	MCF-7	breast:
9	chr8:112458264..112460243-chr8:112464717..112466485,2	K562	blood:
10	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
11	chr8:112471086..112471839-chr8:112809518..112810102,2	MCF-7	breast:
12	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
13	chr8:112456153..112457084-chr8:112809101..112810085,7	MCF-7	breast:
14	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
15	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
16	chr8:112437770..112438280-chr8:112809131..112809707,2	MCF-7	breast:
17	chr8:112466504..112469313-chr8:112470334..112472257,2	MCF-7	breast:
18	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
19	chr8:112570236..112571107-chr8:139584283..139585016,2	MCF-7	breast:
20	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
21	chr8:112466504..112469313-chr8:112470334..112472257,2	MCF-7	breast:
22	chr8:112479743..112482044-chr8:112494341..112496246,2	K562	blood:
23	chr8:112458264..112460243-chr8:112464717..112466485,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-4	chr8:112478407-112478529	ENSG00000253434.1
2	lnc-RP11-67H2.1.1-3	chr8:112711744-112711881	XLOC_006902
3	lnc-RP11-422N16.3.1-4	chr8:112399907-112399971	ENSG00000253434.1
4	lnc-RP11-67H2.1.1-3	chr8:112712240-112712497	XLOC_006902
5	lnc-RP11-67H2.1.1-3	chr8:112711743-112711881	NONHSAT128330
6	lnc-CSMD3-4	chr8:112633687-112634026	NONHSAT128329
7	lnc-RP11-422N16.3.1-4	chr8:112525276-112525364	ENSG00000253434.1
8	lnc-RP11-422N16.3.1-4	chr8:112527241-112527565	ENSG00000253434.1
9	lnc-RP11-422N16.3.1-4	chr8:112478407-112478529	ENSG00000253434.1
10	lnc-RP11-422N16.3.1-4	chr8:112428744-112428771	ENSG00000253434.1
11	lnc-RP11-422N16.3.1-4	chr8:112554278-112554452	ENSG00000253434.1
12	lnc-RP11-422N16.3.1-4	chr8:112555148-112555202	ENSG00000253434.1
13	lnc-RP11-422N16.3.1-4	chr8:112482610-112482846	ENSG00000253434.1
14	lnc-RP11-422N16.3.1-4	chr8:112388892-112388939	ENSG00000253434.1
15	lnc-RP11-422N16.3.1-4	chr8:112525276-112525364	ENSG00000253434.1
16	lnc-RP11-67H2.1.1-3	chr8:112712239-112712497	NONHSAT128330
17	lnc-RP11-422N16.3.1-4	chr8:112392832-112393097	NONHSAT128327
18	lnc-RP11-422N16.3.1-4	chr8:112392702-112392921	ENSG00000253434.1
19	lnc-RP11-422N16.3.1-4	chr8:112478407-112478529	ENSG00000253434.1
20	lnc-RP11-422N16.3.1-4	chr8:112388868-112388919	ENSG00000253434.1

Variant related genes	Relation type
ENSG00000253156	TF binding region
ENSG00000253434	TF binding region
ENSG00000255033	TF binding region
ENSG00000253156	CpG island
ENSG00000253434	CpG island
ENSG00000255033	CpG island
ENSG00000253434	chromatin interactions
ACSL1	miRNA target sites
ACPL2	miRNA target sites

Extended variants
information (count: 3961 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3961 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546003996	chr8:112384124-112384125	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184799708	chr8:112384147-112384148	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs75488626	chr8:112384155-112384156	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531670540	chr8:112384187-112384188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs541754341	chr8:112384213-112384214	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561337090	chr8:112384216-112384217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529995930	chr8:112384227-112384228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546705020	chr8:112384261-112384262	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs73341404	chr8:112384310-112384311	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532455682	chr8:112384364-112384365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs189389049	chr8:112384375-112384376	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs180999134	chr8:112384413-112384414	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs569349913	chr8:112384427-112384428	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs185927216	chr8:112384485-112384486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs117524376	chr8:112384531-112384532	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568080824	chr8:112384563-112384564	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552688603	chr8:112384643-112384644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs117470278	chr8:112386018-112386019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187886122	chr8:112386050-112386051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548060995	chr8:112386170-112386171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190854105	chr8:112386191-112386192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564686353	chr8:112387211-112387212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76524349	chr8:112387213-112387214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535769753	chr8:112387217-112387218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544047922	chr8:112387311-112387312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563147646	chr8:112387330-112387331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528825800	chr8:112387344-112387345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184480037	chr8:112387352-112387353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565467649	chr8:112387398-112387399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189625650	chr8:112387427-112387428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551330992	chr8:112387452-112387453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76179372	chr8:112387466-112387467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79935158	chr8:112387475-112387476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557182491	chr8:112387498-112387499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570082362	chr8:112387533-112387534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74654436	chr8:112387617-112387618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376778536	chr8:112387633-112387634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192517339	chr8:112387665-112387666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144389928	chr8:112387681-112387682	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs184504208	chr8:112387689-112387690	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs541534712	chr8:112387706-112387707	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs558071274	chr8:112387713-112387714	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs578092122	chr8:112387715-112387716	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575518783	chr8:112387723-112387724	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369787836	chr8:112387729-112387730	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs35895652	chr8:112387755-112387756	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs189025275	chr8:112387756-112387757	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs140146693	chr8:112387766-112387767	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs143776116	chr8:112387805-112387806	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs542246749	chr8:112387850-112387851	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112386000-112386200	Enhancers	Lung	lung
2	chr8:112387200-112387800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr8:112387200-112387800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr8:112387200-112388000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:112387200-112388800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:112387400-112387600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:112387400-112389000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr8:112387600-112392400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:112387800-112399600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr8:112388000-112388800	Enhancers	Adipose Nuclei	Adipose
11	chr8:112388200-112388800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:112388200-112388800	Enhancers	Ovary	ovary
13	chr8:112388800-112389200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:112388800-112389800	Weak transcription	Ovary	ovary
15	chr8:112388800-112390800	Active TSS	Adipose Nuclei	Adipose
16	chr8:112389000-112389200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr8:112389200-112389800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr8:112389200-112390200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr8:112390000-112390400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:112390200-112390600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr8:112390200-112390800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr8:112390400-112390600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:112390400-112390600	Enhancers	Ovary	ovary
24	chr8:112390600-112390800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
25	chr8:112390800-112392400	Weak transcription	Adipose Nuclei	Adipose
26	chr8:112390800-112392600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr8:112392400-112392600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:112392400-112393000	Enhancers	Adipose Nuclei	Adipose
29	chr8:112392600-112393200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:112397400-112397600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:112397400-112397600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr8:112397400-112397600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
33	chr8:112397400-112397600	ZNF genes & repeats	Esophagus	oesophagus
34	chr8:112397400-112397600	ZNF genes & repeats	Gastric	stomach
35	chr8:112397400-112397600	Flanking Bivalent TSS/Enh	Left Ventricle	heart
36	chr8:112397400-112397600	Enhancers	Lung	lung
37	chr8:112397400-112397600	ZNF genes & repeats	Pancreas	Pancrea
38	chr8:112397400-112397600	Enhancers	Right Atrium	heart
39	chr8:112397600-112399600	Weak transcription	Pancreas	Pancrea
40	chr8:112399200-112399400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:112399400-112399600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:112399600-112399800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:112399600-112399800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr8:112399600-112399800	Enhancers	Pancreas	Pancrea
45	chr8:112409800-112410200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr8:112409800-112410600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:112410000-112410800	Enhancers	Fetal Heart	heart
48	chr8:112410000-112411000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr8:112410200-112410600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr8:112410200-112410600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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