Variant report

Variant	nsv8351
Chromosome Location	chr8:58111632-58138437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:851)
CpG islands
(count:1777)
Chromatin interactive
region (count:25)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58122168-58122783	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58137879-58138528	HepG2	liver:	n/a	n/a
3	ATF1	chr8:58122169-58123010	K562	blood:	n/a	n/a
4	ATF3	chr8:58137924-58138390	A549	lung:	n/a	n/a
5	BACH1	chr8:58122347-58122997	K562	blood:	n/a	n/a
6	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
7	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
8	BHLHE40	chr8:58137964-58138275	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:58118159-58118698	K562	blood:	n/a	n/a
10	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
11	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
12	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
14	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
15	CEBPB	chr8:58135455-58135719	HepG2	liver:	n/a	chr8:58135609-58135620
16	CEBPB	chr8:58138094-58138305	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:58135497-58135726	HepG2	liver:	n/a	chr8:58135609-58135620
18	CEBPB	chr8:58137953-58138466	A549	lung:	n/a	n/a
19	CEBPB	chr8:58135438-58135794	Hela-S3	cervix:	n/a	chr8:58135609-58135620
20	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
21	CEBPB	chr8:58135428-58135788	IMR90	lung:	n/a	chr8:58135609-58135620
22	CEBPB	chr8:58135426-58135823	K562	blood:	n/a	chr8:58135609-58135620
23	CEBPB	chr8:58135407-58135877	A549	lung:	n/a	chr8:58135609-58135620
24	CEBPB	chr8:58138106-58138233	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:58135419-58135810	K562	blood:	n/a	chr8:58135609-58135620
26	CEBPB	chr8:58135416-58135803	HepG2	liver:	n/a	chr8:58135609-58135620
27	CEBPB	chr8:58135434-58135802	A549	lung:	n/a	chr8:58135609-58135620
28	CEBPB	chr8:58137871-58138537	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
30	CEBPB	chr8:58138061-58138288	A549	lung:	n/a	n/a
31	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
32	CEBPB	chr8:58135395-58135845	MCF-7	breast:	n/a	chr8:58135609-58135620
33	CEBPB	chr8:58135367-58135856	MCF-7	breast:	n/a	chr8:58135609-58135620
34	CEBPB	chr8:58135434-58135730	K562	blood:	n/a	chr8:58135609-58135620
35	CEBPD	chr8:58135517-58135669	HepG2	liver:	n/a	n/a
36	CEBPZ	chr8:58118279-58118527	HepG2	liver:	n/a	n/a
37	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
39	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
40	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
41	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
42	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
43	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
44	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
45	CTCF	chr8:58122020-58122443	K562	blood:	n/a	n/a
46	CTCF	chr8:58118300-58118450	GM12869	blood:	n/a	n/a
47	CTCF	chr8:58122160-58122310	A549	lung:	n/a	n/a
48	CTCF	chr8:58122160-58122310	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr8:58122180-58122330	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:58122640-58122790	SK-N-SH_RA	brain:	n/a	n/a

(count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58131602-58131652	RPTEC	kidney:	n/a
2	chr8:58118711-58118761	BJ	skin:	n/a
3	chr8:58130467-58130517	HEEpiC	esophagus:	n/a
4	chr8:58122215-58122265	H1-hESC	embryonic stem cell:	embryo
5	chr8:58128724-58128774	NB4	blood:	n/a
6	chr8:58131602-58131652	Jurkat	blood:	n/a
7	chr8:58128466-58128516	A549	lung:	n/a
8	chr8:58132446-58132496	T-47D	breast:	n/a
9	chr8:58131602-58131652	RPTEC	kidney:	n/a
10	chr8:58118711-58118761	BJ	skin:	n/a
11	chr8:58130467-58130517	HEEpiC	esophagus:	n/a
12	chr8:58122215-58122265	H1-hESC	embryonic stem cell:	embryo
13	chr8:58128724-58128774	NB4	blood:	n/a
14	chr8:58131602-58131652	Jurkat	blood:	n/a
15	chr8:58128466-58128516	A549	lung:	n/a
16	chr8:58132446-58132496	T-47D	breast:	n/a
17	chr8:58120465-58120515	GM19239	blood:	n/a
18	chr8:58117687-58117737	PFSK-1	brain:	n/a
19	chr8:58114950-58115000	SK-N-SH	brain:	n/a
20	chr8:58117794-58117844	AG10803	skin:	n/a
21	chr8:58132446-58132496	HCM	heart:	n/a
22	chr8:58116908-58116958	HEEpiC	esophagus:	n/a
23	chr8:58128724-58128774	AG10803	skin:	n/a
24	chr8:58114950-58115000	HMEC	breast:	n/a
25	chr8:58132229-58132279	GM12878	blood:	n/a
26	chr8:58130467-58130517	PFSK-1	brain:	n/a
27	chr8:58117687-58117737	HNPCEpiC	eye:	n/a
28	chr8:58121215-58121265	HL-60	blood:	n/a
29	chr8:58120465-58120515	HepG2	liver:	n/a
30	chr8:58123513-58123563	MCF-7	breast:	n/a
31	chr8:58124249-58124299	RPTEC	kidney:	n/a
32	chr8:58115012-58115062	GM06990	blood:	n/a
33	chr8:58117125-58117175	SAEC	small airway:	n/a
34	chr8:58119141-58119191	AG10803	skin:	n/a
35	chr8:58130467-58130517	T-47D	breast:	n/a
36	chr8:58129604-58129654	NHDF-neo	bronchial:	n/a
37	chr8:58114915-58114965	PFSK-1	brain:	n/a
38	chr8:58129604-58129654	MCF-7	breast:	n/a
39	chr8:58117794-58117844	NHBE	bronchial:	n/a
40	chr8:58131602-58131652	ovcar-3	ovarian:	n/a
41	chr8:58131602-58131652	AG04450	lung:	fetal
42	chr8:58124249-58124299	HCPEpiC	choroid plexus:	n/a
43	chr8:58138048-58138098	HEEpiC	esophagus:	n/a
44	chr8:58123513-58123563	HRE	kidney:	n/a
45	chr8:58128466-58128516	HIPEpiC	eye:	n/a
46	chr8:58138048-58138098	NHBE	bronchial:	n/a
47	chr8:58132229-58132279	GM12892	blood:	n/a
48	chr8:58129604-58129654	PANC-1	pancreas:	n/a
49	chr8:58131602-58131652	NH-A	brain:	n/a
50	chr8:58115012-58115062	Hela-S3	cervix:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
2	chr8:58129899..58132563-chr8:58137038..58139171,2	K562	blood:
3	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
4	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
5	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
6	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
7	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
8	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
9	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
10	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
11	chr8:58129429..58131931-chr8:58132415..58133992,2	K562	blood:
12	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
13	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
14	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
15	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
16	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
17	chr8:58135656..58136628-chr8:58255573..58256399,7	MCF-7	breast:
18	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
19	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
20	chr8:58137967..58139990-chr8:58271314..58273259,2	MCF-7	breast:
21	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
22	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
23	chr8:58137340..58139312-chr8:58141710..58144515,2	MCF-7	breast:
24	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
25	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58133958-58134166	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58131885-58132182	NONHSAT126742
4	lnc-FAM110B-8	chr8:58133958-58134166	NONHSAT126741
5	lnc-FAM110B-8	chr8:58131162-58131254	ENSG00000253301.1
6	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126742
7	lnc-FAM110B-8	chr8:58130835-58130911	ENSG00000253301.1
8	lnc-FAM110B-8	chr8:58132670-58132795	ENSG00000253301.1
9	lnc-FAM110B-8	chr8:58131648-58131697	ENSG00000253301.1
10	lnc-FAM110B-8	chr8:58136443-58136530	NONHSAT126744
11	lnc-FAM110B-8	chr8:58131969-58132082	ENSG00000253301.1
12	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1
13	lnc-FAM110B-8	chr8:58134728-58134830	ENSG00000253301.1
14	lnc-FAM110B-8	chr8:58131648-58131697	NONHSAT126741
15	lnc-FAM110B-8	chr8:58133148-58133297	ENSG00000253301.1
16	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
17	lnc-FAM110B-8	chr8:58131093-58131254	ENSG00000253301.1
18	lnc-FAM110B-8	chr8:58131969-58132126	ENSG00000253301.1
19	lnc-FAM110B-8	chr8:58131938-58132182	ENSG00000253301.1
20	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
21	lnc-FAM110B-8	chr8:58131969-58132182	ENSG00000253301.1
22	lnc-FAM110B-8	chr8:58131969-58132182	NONHSAT126741
23	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
24	lnc-FAM110B-8	chr8:58131615-58131697	ENSG00000253301.1
25	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126741
26	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126741
27	lnc-FAM110B-8	chr8:58134728-58134830	NONHSAT126741
28	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126742
29	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1

No data

Variant related genes	Relation type
ENSG00000253301	TF binding region
ENSG00000253301	CpG island
ENSG00000253301	chromatin interactions
ENSG00000253871	chromatin interactions

Extended variants
information (count: 1734 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192978099	chr8:58111636-58111637	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs529069181	chr8:58111698-58111699	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575856254	chr8:58111701-58111702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7459925	chr8:58111771-58111772	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs561057776	chr8:58111782-58111783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567199108	chr8:58111785-58111786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566949727	chr8:58111861-58111862	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112846313	chr8:58111862-58111863	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532867748	chr8:58111868-58111869	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185260014	chr8:58111904-58111905	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs202033959	chr8:58111905-58111906	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201631475	chr8:58111908-58111909	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550744291	chr8:58111930-58111931	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534873518	chr8:58111935-58111936	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139279005	chr8:58112025-58112026	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554231853	chr8:58112037-58112038	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181053859	chr8:58112041-58112042	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7463453	chr8:58112053-58112054	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs547406130	chr8:58112061-58112062	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183666101	chr8:58112125-58112126	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539694288	chr8:58112151-58112152	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116517911	chr8:58112188-58112189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539956474	chr8:58112190-58112191	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575792597	chr8:58112210-58112211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535273442	chr8:58112214-58112215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs56383336	chr8:58112247-58112248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574625492	chr8:58112285-58112286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540241395	chr8:58112319-58112320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554107092	chr8:58112326-58112327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577184008	chr8:58112333-58112334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546432854	chr8:58112355-58112356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563175310	chr8:58112358-58112359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531936271	chr8:58112366-58112367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576627027	chr8:58112419-58112420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377616469	chr8:58112438-58112439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs36025411	chr8:58112476-58112477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111262591	chr8:58112527-58112528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527410970	chr8:58112538-58112539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547201007	chr8:58112544-58112545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368638707	chr8:58112553-58112554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62512044	chr8:58112567-58112568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62513461	chr8:58112577-58112578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532799635	chr8:58112578-58112579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549618450	chr8:58112579-58112580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569662906	chr8:58112602-58112603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28787381	chr8:58112648-58112649	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572418656	chr8:58112658-58112659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188033547	chr8:58112679-58112680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28449911	chr8:58112712-58112713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs112971883	chr8:58112720-58112721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:58111800-58112200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
5	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
11	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
12	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
15	chr8:58116600-58117000	Enhancers	Gastric	stomach
16	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
17	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
18	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
21	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:58117000-58118200	Weak transcription	Gastric	stomach
25	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
28	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
30	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
31	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
33	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
34	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
35	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
36	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
38	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
40	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
41	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
43	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:58118200-58118800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
49	chr8:58118200-58118800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
50	chr8:58118200-58118800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

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