Variant report

Variant	nsv831416
Chromosome Location	chr8:105137789-105296965
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1084)
CpG islands
(count:794)
Chromatin interactive
region (count:65)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1084 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:105187628-105188149	GM12878	blood:	n/a	n/a
2	ATF2	chr8:105290522-105291653	GM12878	blood:	n/a	n/a
3	ATF2	chr8:105187576-105188307	GM12878	blood:	n/a	n/a
4	ATF2	chr8:105290398-105291880	GM12878	blood:	n/a	n/a
5	BACH1	chr8:105235242-105235626	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:105293015-105293304	GM12878	blood:	n/a	n/a
7	BATF	chr8:105187698-105188164	GM12878	blood:	n/a	chr8:105187968-105187979
8	BATF	chr8:105290616-105291779	GM12878	blood:	n/a	n/a
9	BATF	chr8:105187644-105188224	GM12878	blood:	n/a	chr8:105187968-105187979
10	BATF	chr8:105257061-105257450	GM12878	blood:	n/a	n/a
11	BATF	chr8:105252782-105253118	GM12878	blood:	n/a	chr8:105252967-105252978
12	BATF	chr8:105257084-105257397	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:105292999-105293357	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:105187686-105188125	GM12878	blood:	n/a	chr8:105187967-105187976 chr8:105187968-105187977
15	BCL11A	chr8:105290588-105291473	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:105187704-105188169	GM12878	blood:	n/a	chr8:105187967-105187976 chr8:105187968-105187977
17	BCL11A	chr8:105290666-105291388	GM12878	blood:	n/a	n/a
18	BCL3	chr8:105290623-105291322	GM12878	blood:	n/a	n/a
19	BCL3	chr8:105187683-105188137	GM12878	blood:	n/a	chr8:105187967-105187976 chr8:105187968-105187977
20	BCLAF1	chr8:105290646-105291612	GM12878	blood:	n/a	n/a
21	BCLAF1	chr8:105290572-105291478	GM12878	blood:	n/a	n/a
22	BCLAF1	chr8:105187709-105188172	GM12878	blood:	n/a	chr8:105187967-105187976 chr8:105187968-105187977
23	BHLHE40	chr8:105290678-105291484	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:105291758-105292036	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:105142582-105142737	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:105187642-105188027	GM12878	blood:	n/a	n/a
27	BRCA1	chr8:105235838-105236141	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr8:105235221-105235500	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:105169737-105169745	K562	blood:	n/a	n/a
30	CEBPB	chr8:105235232-105235543	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:105238181-105238219	HepG2	liver:	n/a	chr8:105238189-105238200 chr8:105238186-105238203
32	CEBPB	chr8:105291094-105291355	GM12878	blood:	n/a	n/a
33	CEBPB	chr8:105169586-105169839	A549	lung:	n/a	chr8:105169762-105169773
34	CEBPB	chr8:105200098-105200302	A549	lung:	n/a	chr8:105200154-105200165
35	CEBPB	chr8:105157369-105157477	H1-hESC	embryonic stem cell:	n/a	chr8:105157378-105157389
36	CEBPB	chr8:105155954-105156248	A549	lung:	n/a	chr8:105156094-105156107
37	CEBPB	chr8:105290525-105291715	GM12878	blood:	n/a	n/a
38	CEBPB	chr8:105157256-105157570	HepG2	liver:	n/a	chr8:105157378-105157389
39	CEBPB	chr8:105218860-105219093	MCF-7	breast:	n/a	n/a
40	CEBPB	chr8:105169580-105169875	HepG2	liver:	n/a	chr8:105169762-105169773
41	CEBPB	chr8:105234414-105234818	A549	lung:	n/a	chr8:105234647-105234660 chr8:105234649-105234660 chr8:105234647-105234660 chr8:105234647-105234660 chr8:105234649-105234660
42	CEBPB	chr8:105267898-105268197	HepG2	liver:	n/a	chr8:105268052-105268063
43	CEBPB	chr8:105200046-105200279	HepG2	liver:	n/a	chr8:105200154-105200165
44	CEBPB	chr8:105155811-105156380	A549	lung:	n/a	chr8:105156094-105156107
45	CEBPB	chr8:105140136-105140210	A549	lung:	n/a	n/a
46	CEBPB	chr8:105213207-105213368	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:105157313-105157494	K562	blood:	n/a	chr8:105157378-105157389
48	CHD1	chr8:105235097-105235911	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr8:105290585-105291370	GM12878	blood:	n/a	n/a
50	CHD2	chr8:105235250-105236397	H1-hESC	embryonic stem cell:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:105264286-105264336	HRCEpiC	kidney:	n/a
2	chr8:105264286-105264336	HRCEpiC	kidney:	n/a
3	chr8:105235606-105235656	HCT-116	colon:	n/a
4	chr8:105275730-105275780	HCT-116	colon:	n/a
5	chr8:105244257-105244307	CMK	blood:	n/a
6	chr8:105235978-105236028	MCF-7	breast:	n/a
7	chr8:105235385-105235435	PFSK-1	brain:	n/a
8	chr8:105235943-105235993	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:105238428-105238478	HEEpiC	esophagus:	n/a
10	chr8:105235943-105235993	GM19239	blood:	n/a
11	chr8:105264286-105264336	U87	brain:	n/a
12	chr8:105238428-105238478	HEK293	kidney:	embryo
13	chr8:105235978-105236028	PANC-1	pancreas:	n/a
14	chr8:105275730-105275780	PFSK-1	brain:	n/a
15	chr8:105238428-105238478	Caco-2	colon:	n/a
16	chr8:105244257-105244307	U87	brain:	n/a
17	chr8:105235943-105235993	U87	brain:	n/a
18	chr8:105235184-105235234	CMK	blood:	n/a
19	chr8:105238428-105238478	HepG2	liver:	n/a
20	chr8:105235606-105235656	HRE	kidney:	n/a
21	chr8:105235606-105235656	LNCaP	prostate:	n/a
22	chr8:105161049-105161099	HCF	heart:	n/a
23	chr8:105244257-105244307	HepG2	liver:	n/a
24	chr8:105235385-105235435	SK-N-MC	brain:	n/a
25	chr8:105257227-105257277	HCPEpiC	choroid plexus:	n/a
26	chr8:105235715-105235765	HCPEpiC	choroid plexus:	n/a
27	chr8:105235978-105236028	LNCaP	prostate:	n/a
28	chr8:105161049-105161099	AG10803	skin:	n/a
29	chr8:105161049-105161099	AG04450	lung:	fetal
30	chr8:105235606-105235656	AG10803	skin:	n/a
31	chr8:105236155-105236205	BJ	skin:	n/a
32	chr8:105235943-105235993	ovcar-3	ovarian:	n/a
33	chr8:105235943-105235993	ECC-1	luminal epithelium:	n/a
34	chr8:105161049-105161099	K562	blood:	n/a
35	chr8:105235943-105235993	AG04449	skin:	fetal
36	chr8:105238428-105238478	NH-A	brain:	n/a
37	chr8:105244257-105244307	HL-60	blood:	n/a
38	chr8:105275730-105275780	SK-N-SH_RA	brain:	n/a
39	chr8:105238428-105238478	HIPEpiC	eye:	n/a
40	chr8:105264286-105264336	T-47D	breast:	n/a
41	chr8:105235184-105235234	HCT-116	colon:	n/a
42	chr8:105235978-105236028	HepG2	liver:	n/a
43	chr8:105161049-105161099	HRPEpiC	eye:	n/a
44	chr8:105235715-105235765	HRCEpiC	kidney:	n/a
45	chr8:105236155-105236205	MCF10A-Er-Src	breast:	n/a
46	chr8:105236155-105236205	SK-N-SH_RA	brain:	n/a
47	chr8:105235184-105235234	MCF10A-Er-Src	breast:	n/a
48	chr8:105235978-105236028	BJ	skin:	n/a
49	chr8:105235385-105235435	A549	lung:	n/a
50	chr8:105235184-105235234	HRE	kidney:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:105153535..105155055-chr8:105174946..105177136,2	MCF-7	breast:
2	chr8:105285336..105288238-chr8:105288266..105292202,3	MCF-7	breast:
3	chr8:105159045..105161974-chr8:105163813..105165825,2	K562	blood:
4	chr8:105259835..105261617-chr8:105265914..105268408,2	MCF-7	breast:
5	chr8:105234081..105236200-chr8:105240839..105243210,2	MCF-7	breast:
6	chr19:35402456..35403352-chr8:105139491..105140129,2	MCF-7	breast:
7	chr8:105241452..105243816-chr8:105245427..105247630,2	K562	blood:
8	chr8:105159045..105161974-chr8:105163813..105165825,2	K562	blood:
9	chr8:105261888..105262834-chr8:105337720..105338325,2	MCF-7	breast:
10	chr8:105259835..105261617-chr8:105265914..105268408,2	MCF-7	breast:
11	chr8:105252275..105253878-chr8:105256264..105258557,2	K562	blood:
12	chr8:105285336..105288238-chr8:105288266..105292202,3	MCF-7	breast:
13	chr8:105242316..105245331-chr8:105245427..105248797,3	K562	blood:
14	chr8:105257993..105258512-chr8:105337979..105338832,2	MCF-7	breast:
15	chr8:105270995..105272876-chr8:105282829..105285136,2	MCF-7	breast:
16	chr8:105285943..105288221-chr8:105290521..105294731,3	MCF-7	breast:
17	chr8:105266002..105266698-chr8:105429985..105430918,2	MCF-7	breast:
18	chr8:105265326..105266631-chr8:105429975..105430855,7	MCF-7	breast:
19	chr8:105241452..105243816-chr8:105245427..105247630,2	K562	blood:
20	chr8:105292474..105294949-chr8:105304192..105307162,2	MCF-7	breast:
21	chr8:105234317..105237730-chr8:105237758..105240241,3	MCF-7	breast:
22	chr8:105273478..105275129-chr8:105275688..105278105,2	MCF-7	breast:
23	chr8:105285943..105288221-chr8:105290521..105294731,3	MCF-7	breast:
24	chr8:104719235..104720149-chr8:105142112..105143028,4	MCF-7	breast:
25	chr8:105270298..105272141-chr8:105273294..105275649,2	MCF-7	breast:
26	chr8:105133539..105135724-chr8:105136660..105138373,2	MCF-7	breast:
27	chr4:162935502..162936005-chr8:105250879..105251379,2	MCF-7	breast:
28	chr8:104776697..104777502-chr8:105142088..105142615,2	K562	blood:
29	chr8:105265353..105266336-chr8:105337969..105339086,6	MCF-7	breast:
30	chr8:105273478..105275129-chr8:105275688..105278105,2	MCF-7	breast:
31	chr8:104718269..104720075-chr8:105140265..105142046,2	MCF-7	breast:
32	chr8:105138025..105140468-chr8:105142058..105143910,2	K562	blood:
33	chr8:105207373..105209743-chr8:105210313..105212333,2	MCF-7	breast:
34	chr8:105156123..105158477-chr8:105160903..105163051,2	MCF-7	breast:
35	chr8:104775882..104776978-chr8:105142360..105143119,4	MCF-7	breast:
36	chr8:105242316..105245331-chr8:105245427..105248797,3	K562	blood:
37	chr8:105153535..105155055-chr8:105174946..105177136,2	MCF-7	breast:
38	chr8:105138025..105140468-chr8:105142058..105143910,2	K562	blood:
39	chr8:105270995..105272876-chr8:105282829..105285136,2	MCF-7	breast:
40	chr8:105242800..105244338-chr8:105249845..105251737,2	MCF-7	breast:
41	chr8:105156123..105158477-chr8:105160903..105163051,2	MCF-7	breast:
42	chr8:104761856..104762718-chr8:105142470..105143058,2	MCF-7	breast:
43	chr8:105270298..105272141-chr8:105273294..105275649,2	MCF-7	breast:
44	chr8:105173950..105176285-chr8:105193428..105195940,2	MCF-7	breast:
45	chr8:105185671..105187346-chr8:105198346..105200773,2	MCF-7	breast:
46	chr8:105252275..105253878-chr8:105256264..105258557,2	K562	blood:
47	chr8:105242800..105244338-chr8:105249845..105251737,2	MCF-7	breast:
48	chr8:105256696..105258713-chr8:105271860..105274203,2	MCF-7	breast:
49	chr8:104808988..104809567-chr8:105142388..105143010,2	MCF-7	breast:
50	chr8:105225180..105227788-chr8:105237415..105240052,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPYS-3	chr8:105285254-105285273	NONHSAT128202
2	lnc-DPYS-3	chr8:105285318-105285422	NONHSAT128203
3	lnc-DPYS-3	chr8:105292603-105292695	NONHSAT128203
4	lnc-DPYS-3	chr8:105283530-105284720	NONHSAT128202
5	lnc-DPYS-3	chr8:105284395-105284720	NONHSAT128203

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RIMS2	hsa-miR-1	chr8:105264369-105264389

Variant related genes	Relation type
RIMS2	TF binding region
RIMS2	CpG island
ENSG00000176406	chromatin interactions

Extended variants
information (count: 5657 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:5657 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115944441	chr8:105137804-105137805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576264497	chr8:105137811-105137812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543625620	chr8:105137875-105137876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182240049	chr8:105137965-105137966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574278219	chr8:105138011-105138012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144118281	chr8:105138046-105138047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11993919	chr8:105138078-105138079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs113265919	chr8:105138085-105138086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73299422	chr8:105138133-105138134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539357471	chr8:105138232-105138233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563386610	chr8:105138295-105138296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530694356	chr8:105138311-105138312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549199413	chr8:105138327-105138328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558882849	chr8:105138332-105138333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567405154	chr8:105138342-105138343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79794162	chr8:105138353-105138354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547474200	chr8:105138376-105138377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566095157	chr8:105138407-105138408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539532961	chr8:105138683-105138684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76629196	chr8:105138698-105138699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557796552	chr8:105138719-105138720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77399315	chr8:105138850-105138851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7832239	chr8:105138902-105138903	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs555937647	chr8:105138954-105138955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574247955	chr8:105138995-105138996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73299424	chr8:105139010-105139011	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552676333	chr8:105139026-105139027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34205139	chr8:105139035-105139036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560908505	chr8:105139072-105139073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577676553	chr8:105139083-105139084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199555022	chr8:105139103-105139104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545041888	chr8:105139110-105139111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563323314	chr8:105139130-105139131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530628977	chr8:105139140-105139141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs16870993	chr8:105139230-105139231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs114403227	chr8:105139261-105139262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369299539	chr8:105139360-105139361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574096258	chr8:105139382-105139383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543664756	chr8:105139435-105139436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7815109	chr8:105139471-105139472	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185423226	chr8:105139492-105139493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190871056	chr8:105139509-105139510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533129747	chr8:105139562-105139563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73299426	chr8:105139611-105139612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376264559	chr8:105139628-105139629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199573807	chr8:105139730-105139731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183924619	chr8:105139736-105139737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77104770	chr8:105139753-105139754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544968641	chr8:105139760-105139761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72685008	chr8:105139794-105139795	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:114)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105115400-105150000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:105138600-105139000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:105138600-105139200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:105139600-105140400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:105140400-105145400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:105142400-105142600	Enhancers	Brain Cingulate Gyrus	brain
7	chr8:105142400-105142800	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr8:105142400-105143000	Enhancers	Brain Hippocampus Middle	brain
9	chr8:105143800-105149200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:105145400-105145800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:105150000-105150200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:105150000-105150600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:105150600-105155600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:105151600-105160800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:105155200-105155800	Enhancers	A549	lung
16	chr8:105155200-105156400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:105155400-105156000	Enhancers	HMEC	breast
18	chr8:105155400-105156400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:105155400-105156800	Enhancers	NHEK	skin
20	chr8:105155600-105156000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:105155600-105156000	Enhancers	Adipose Nuclei	Adipose
22	chr8:105155600-105156400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:105155600-105156400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:105155600-105157000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:105155800-105156200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr8:105155800-105156200	Active TSS	A549	lung
27	chr8:105156000-105161000	Weak transcription	Adipose Nuclei	Adipose
28	chr8:105156200-105156800	Enhancers	A549	lung
29	chr8:105156400-105160800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:105156400-105188400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:105157000-105160800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:105160800-105161000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr8:105160800-105161000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:105160800-105161400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:105160800-105161400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:105160800-105161600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:105160800-105161800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:105160800-105163000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:105161000-105161600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:105161000-105161600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:105161000-105161600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:105161000-105161600	Enhancers	Adipose Nuclei	Adipose
43	chr8:105161200-105161400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr8:105161200-105161600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:105161600-105161800	Enhancers	Fetal Kidney	kidney
46	chr8:105161600-105163800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:105161800-105163200	Weak transcription	Fetal Kidney	kidney
48	chr8:105163000-105166200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:105163800-105165400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:105166200-105167000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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