Variant report

Variant	nsv539551
Chromosome Location	chr8:38993423-39181079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:719)
CpG islands
(count:671)
Chromatin interactive
region (count:18)
LncRNA
region (count:64)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:719 , 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	ARID3A	chr8:39066252-39067029	HepG2	liver:	n/a	n/a
2	ATF1	chr8:39169144-39169211	K562	blood:	n/a	n/a
3	ATF1	chr8:39006915-39007034	K562	blood:	n/a	n/a
4	ATF1	chr8:39090849-39091203	K562	blood:	n/a	n/a
5	ATF2	chr8:39049548-39050082	GM12878	blood:	n/a	n/a
6	ATF2	chr8:39049571-39049957	GM12878	blood:	n/a	n/a
7	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
8	BATF	chr8:39041970-39042150	GM12878	blood:	n/a	chr8:39042066-39042077
9	BATF	chr8:39049634-39049874	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:39049732-39049952	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:39135297-39135321	K562	blood:	n/a	n/a
12	BHLHE40	chr8:39066583-39066692	HepG2	liver:	n/a	n/a
13	BRCA1	chr8:39044344-39044448	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr8:39090639-39091440	HCT-116	colon:	n/a	n/a
15	CBX3	chr8:39099996-39100457	HCT-116	colon:	n/a	n/a
16	CEBPB	chr8:39049617-39050215	GM12878	blood:	n/a	n/a
17	CEBPB	chr8:39081633-39081827	HepG2	liver:	n/a	chr8:39081740-39081751
18	CEBPB	chr8:39144160-39144242	A549	lung:	n/a	n/a
19	CEBPB	chr8:39172450-39172643	K562	blood:	n/a	chr8:39172538-39172549
20	CEBPB	chr8:39122247-39122648	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr8:39081045-39081110	HepG2	liver:	n/a	chr8:39081090-39081101
22	CEBPB	chr8:39172365-39172592	A549	lung:	n/a	chr8:39172538-39172549
23	CEBPB	chr8:39169394-39169417	A549	lung:	n/a	n/a
24	CEBPB	chr8:39006116-39006135	HepG2	liver:	n/a	n/a
25	CEBPZ	chr8:39139103-39139155	HepG2	liver:	n/a	n/a
26	CHD1	chr8:39142862-39142883	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:39001100-39001250	K562	blood:	n/a	n/a
28	CTCF	chr8:39130439-39130732	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:39001106-39001157	GM19239	blood:	n/a	n/a
30	CTCF	chr8:39001260-39001410	GM12870	blood:	n/a	n/a
31	CTCF	chr8:39132460-39132610	AG04449	skin:	n/a	chr8:39132567-39132580 chr8:39132565-39132583 chr8:39132568-39132578
32	CTCF	chr8:39041800-39041950	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr8:39064460-39064610	HepG2	liver:	n/a	n/a
34	CTCF	chr8:39130506-39130726	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:39130359-39130849	SK-N-SH	brain:	n/a	n/a
36	CTCF	chr8:39130480-39130630	GM12869	blood:	n/a	n/a
37	CTCF	chr8:39130510-39130722	Gliobla	brain:	n/a	n/a
38	CTCF	chr8:39130523-39130715	LNCaP	prostate:	n/a	n/a
39	CTCF	chr8:39130540-39130690	GM12871	blood:	n/a	n/a
40	CTCF	chr8:39090955-39091033	GM13976	blood:	n/a	n/a
41	CTCF	chr8:39130520-39130670	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr8:39130520-39130670	AG10803	skin:	n/a	n/a
43	CTCF	chr8:38995899-38995921	GM13976	blood:	n/a	n/a
44	CTCF	chr8:39130540-39130690	Caco-2	colon:	n/a	n/a
45	CTCF	chr8:39130520-39130670	HCFaa	heart:	n/a	n/a
46	CTCF	chr8:39130451-39130721	A549	lung:	n/a	n/a
47	CTCF	chr8:39028220-39028360	K562	blood:	n/a	n/a
48	CTCF	chr8:39073750-39073792	Medullo	brain:	n/a	n/a
49	CTCF	chr8:39026280-39026430	GM06990	blood:	n/a	n/a
50	CTCF	chr8:39130480-39130630	HVMF	connective:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39171866-39171916	PrEC	prostate:	n/a
2	chr8:39172097-39172147	HNPCEpiC	eye:	n/a
3	chr8:39172111-39172161	Caco-2	colon:	n/a
4	chr8:39172120-39172170	AG10803	skin:	n/a
5	chr8:39172022-39172072	A549	lung:	n/a
6	chr8:39172120-39172170	GM06990	blood:	n/a
7	chr8:39172099-39172149	NHBE	bronchial:	n/a
8	chr8:39172111-39172161	PANC-1	pancreas:	n/a
9	chr8:39077124-39077174	SKMC	muscle:	n/a
10	chr8:39171648-39171698	AoSMC	blood vessel:	n/a
11	chr8:39171648-39171698	Hepatocyte	liver:	n/a
12	chr8:39172120-39172170	SKMC	muscle:	n/a
13	chr8:39172120-39172170	AG09319	gingival:	n/a
14	chr8:39172020-39172070	HEEpiC	esophagus:	n/a
15	chr8:39172022-39172072	CMK	blood:	n/a
16	chr8:39172022-39172072	ECC-1	luminal epithelium:	n/a
17	chr8:39077124-39077174	GM12891	blood:	n/a
18	chr8:39077124-39077174	HCM	heart:	n/a
19	chr8:39172097-39172147	AoSMC	blood vessel:	n/a
20	chr8:39172097-39172147	HCT-116	colon:	n/a
21	chr8:39172022-39172072	IMR90	lung:	fetal
22	chr8:39172099-39172149	HNPCEpiC	eye:	n/a
23	chr8:39171620-39171670	MCF-7	breast:	n/a
24	chr8:39172020-39172070	HAEpiC	amniotic membrane:	n/a
25	chr8:39172120-39172170	HepG2	liver:	n/a
26	chr8:39172099-39172149	Caco-2	colon:	n/a
27	chr8:39171620-39171670	AG09319	gingival:	n/a
28	chr8:39171648-39171698	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:39172097-39172147	SK-N-SH	brain:	n/a
30	chr8:39171620-39171670	ovcar-3	ovarian:	n/a
31	chr8:39037993-39038043	BJ	skin:	n/a
32	chr8:39077124-39077174	IMR90	lung:	fetal
33	chr8:39172097-39172147	LNCaP	prostate:	n/a
34	chr8:39172020-39172070	HepG2	liver:	n/a
35	chr8:39172120-39172170	HL-60	blood:	n/a
36	chr8:39171648-39171698	ECC-1	luminal epithelium:	n/a
37	chr8:39037993-39038043	NHBE	bronchial:	n/a
38	chr8:39172099-39172149	HAEpiC	amniotic membrane:	n/a
39	chr8:39172120-39172170	ProgFib	skin:	n/a
40	chr8:39172099-39172149	HCM	heart:	n/a
41	chr8:39171620-39171670	NT2-D1	testis:	n/a
42	chr8:39172020-39172070	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:39077124-39077174	HepG2	liver:	n/a
44	chr8:39171648-39171698	U87	brain:	n/a
45	chr8:39171648-39171698	AG04449	skin:	fetal
46	chr8:39171620-39171670	HepG2	liver:	n/a
47	chr8:39037993-39038043	MCF-7	breast:	n/a
48	chr8:39172097-39172147	NHBE	bronchial:	n/a
49	chr8:39171866-39171916	IMR90	lung:	fetal
50	chr8:39172022-39172072	MCF-7	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39080941..39082777-chr8:39089064..39090963,2	K562	blood:
2	chr8:39079754..39082023-chr8:39086400..39088238,2	MCF-7	breast:
3	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
4	chr8:39079754..39082023-chr8:39086400..39088238,2	MCF-7	breast:
5	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
6	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
7	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
8	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
9	chr15:50661566..50662138-chr8:39161334..39161854,2	MCF-7	breast:
10	chr8:39039766..39041714-chr8:39045737..39047937,2	K562	blood:
11	chr8:39107586..39109155-chr8:39112907..39115245,2	K562	blood:
12	chr8:39039766..39041714-chr8:39045737..39047937,2	K562	blood:
13	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
14	chr8:39080941..39082777-chr8:39089064..39090963,2	K562	blood:
15	chr8:38964712..38965432-chr8:39130166..39131088,2	MCF-7	breast:
16	chr8:38964583..38965453-chr8:39130431..39131111,2	MCF-7	breast:
17	chr8:39170463..39172530-chr8:39174983..39176968,2	MCF-7	breast:
18	chr6:156717380..156718086-chr8:39158912..39159795,2	MCF-7	breast:

(count:64 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM9-1	chr8:39133347-39133385	NONHSAT126144
2	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126155
3	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126148
4	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126151
5	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126151
6	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126152
7	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126156
8	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126148
9	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126151
10	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126154
11	lnc-ADAM9-1	chr8:39128394-39128433	NONHSAT126144
12	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126154
13	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126156
14	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126153
15	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126155
16	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT147628
17	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126157
18	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126150
19	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT147628
20	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126152
21	lnc-ADAM9-1	chr8:39142312-39142428	NONHSAT126143
22	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126155
23	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126151
24	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126150
25	lnc-ADAM9-1	chr8:39142312-39142430	NONHSAT126144
26	lnc-ADAM32-1	chr8:39180489-39181258	NONHSAT126149
27	lnc-ADAM9-1	chr8:39141105-39141143	NONHSAT126143
28	lnc-ADAM9-1	chr8:39131831-39131869	NONHSAT126145
29	lnc-ADAM32-1	chr8:39172110-39172236	NONHSAT126148
30	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126149
31	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126153
32	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126149
33	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126157
34	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT126155
35	lnc-ADAM9-1	chr8:39114706-39114862	NONHSAT126143
36	lnc-TM2D2-6	chr8:39167428-39167962	NONHSAT126147
37	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126155
38	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126153
39	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126152
40	lnc-ADAM32-1	chr8:39172974-39173053	NONHSAT126152
41	lnc-ADAM32-1	chr8:39173006-39173053	NONHSAT126156
42	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT147628
43	lnc-ADAM9-1	chr8:39141105-39141143	NONHSAT126144
44	lnc-ADAM32-1	chr8:39180489-39180565	NONHSAT147628
45	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126156
46	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126149
47	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT147628
48	lnc-ADAM9-1	chr8:39133347-39133816	NONHSAT126145
49	lnc-ADAM9-1	chr8:39131831-39131869	NONHSAT126144
50	lnc-ADAM32-1	chr8:39180080-39180158	NONHSAT126149

No data

Variant related genes	Relation type
ADAM32	TF binding region
ADAM5	TF binding region
ENSG00000253160	TF binding region
RPL3P10	TF binding region
ADAM32	CpG island
ADAM5	CpG island
ENSG00000253160	CpG island
RPL3P10	CpG island
ENSG00000197140	chromatin interactions
ENSG00000196115	chromatin interactions

Extended variants
information (count: 5177 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:5177 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543592733	chr8:38993459-38993460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563830883	chr8:38993464-38993465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532756076	chr8:38993465-38993466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546490820	chr8:38993538-38993539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560074289	chr8:38993582-38993583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6994035	chr8:38993605-38993606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs547367198	chr8:38993615-38993616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560763456	chr8:38993637-38993638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529757837	chr8:38993676-38993677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549616688	chr8:38993734-38993735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142330227	chr8:38993812-38993813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113788081	chr8:38993852-38993853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186763012	chr8:38993890-38993891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74329598	chr8:38993892-38993893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192168960	chr8:38993959-38993960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534655450	chr8:38993984-38993985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370643250	chr8:38994095-38994096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373613021	chr8:38994144-38994145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554935919	chr8:38994182-38994183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201616533	chr8:38994186-38994187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201047294	chr8:38994223-38994224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574750620	chr8:38994256-38994257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80106805	chr8:38994262-38994263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376282411	chr8:38994325-38994326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183448691	chr8:38994328-38994329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543352112	chr8:38994379-38994380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577477202	chr8:38994426-38994427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546398925	chr8:38994446-38994447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560036359	chr8:38994553-38994554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60084248	chr8:38994563-38994564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188034089	chr8:38994602-38994603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373505543	chr8:38994620-38994621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560896218	chr8:38994625-38994626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529681042	chr8:38994638-38994639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549432456	chr8:38994662-38994663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563026981	chr8:38994698-38994699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376137165	chr8:38994710-38994711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146655858	chr8:38994729-38994730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551947547	chr8:38994738-38994739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576297608	chr8:38994793-38994794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537208203	chr8:38994910-38994911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534878252	chr8:38994914-38994915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563544369	chr8:38994919-38994920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548191392	chr8:38994940-38994941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191341392	chr8:38994997-38994998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537064688	chr8:38995004-38995005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557420423	chr8:38995011-38995012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139131889	chr8:38995013-38995014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182479253	chr8:38995017-38995018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561448045	chr8:38995099-38995100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	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
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Lung cancer	21569311	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164919	CNVD
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Squamous cell cancer	19001599	CNVD
Cone-rod dystrophy	22138850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Chordoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20932292	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:38971200-39036400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:38979200-39001000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:39001000-39001600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:39001000-39001600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:39001000-39001800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:39001000-39001800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:39001000-39002200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:39001200-39001600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:39001200-39001800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:39001600-39015000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:39001800-39013800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:39004000-39014800	Weak transcription	Left Ventricle	heart
13	chr8:39004200-39013600	Weak transcription	Aorta	Aorta
14	chr8:39006200-39018000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr8:39006400-39007200	Enhancers	HUVEC	blood vessel
16	chr8:39007800-39015200	Weak transcription	Ovary	ovary
17	chr8:39008400-39018600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr8:39008800-39012400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr8:39009400-39012600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:39012800-39013200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:39013600-39014000	ZNF genes & repeats	Aorta	Aorta
22	chr8:39013600-39015800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:39013800-39014000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:39013800-39018600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:39014000-39015200	Weak transcription	Aorta	Aorta
26	chr8:39015000-39015600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:39015000-39016200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:39015200-39015800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:39015200-39016200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:39015200-39016200	ZNF genes & repeats	Aorta	Aorta
31	chr8:39015200-39016200	ZNF genes & repeats	Ovary	ovary
32	chr8:39015400-39016000	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr8:39015600-39018200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:39015800-39016200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:39015800-39016200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr8:39015800-39018200	Weak transcription	Osteobl	bone
37	chr8:39015800-39018600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:39016200-39017000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:39016200-39018400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:39016200-39025800	Weak transcription	Aorta	Aorta
41	chr8:39016200-39036200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr8:39016200-39036400	Weak transcription	Ovary	ovary
43	chr8:39018000-39019400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr8:39018000-39019400	Enhancers	HUVEC	blood vessel
45	chr8:39018200-39018800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:39018200-39019000	Enhancers	Osteobl	bone
47	chr8:39018200-39019200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr8:39018200-39019400	Enhancers	NH-A	brain
49	chr8:39018600-39018800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:39018600-39018800	Enhancers	Placenta Amnion	Placenta Amnion

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