Variant report

Variant	nsv916496
Chromosome Location	chr8:107813722-108338822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3104)
CpG islands
(count:1039)
Chromatin interactive
region (count:169)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3104 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:107847369-107847671	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:108128388-108129306	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:108299697-108300171	K562	blood:	n/a	n/a
4	ARID3A	chr8:108322085-108323462	K562	blood:	n/a	chr8:108322161-108322177
5	ARID3A	chr8:108333818-108334046	K562	blood:	n/a	n/a
6	ARID3A	chr8:107839351-107839525	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:108337533-108337702	K562	blood:	n/a	n/a
8	ARID3A	chr8:108307010-108307086	K562	blood:	n/a	n/a
9	ARID3A	chr8:108327268-108328057	K562	blood:	n/a	n/a
10	ARID3A	chr8:108335073-108335222	K562	blood:	n/a	n/a
11	ARID3A	chr8:108317027-108317777	K562	blood:	n/a	n/a
12	ATF1	chr8:108317326-108317759	K562	blood:	n/a	n/a
13	ATF1	chr8:108220761-108220901	K562	blood:	n/a	n/a
14	ATF1	chr8:107991251-107991436	K562	blood:	n/a	n/a
15	ATF1	chr8:108318725-108318911	K562	blood:	n/a	n/a
16	ATF1	chr8:108184522-108184787	K562	blood:	n/a	n/a
17	ATF1	chr8:108227519-108227917	K562	blood:	n/a	n/a
18	ATF1	chr8:108294452-108294537	K562	blood:	n/a	n/a
19	ATF1	chr8:108155224-108155260	K562	blood:	n/a	n/a
20	ATF1	chr8:108130183-108130443	K562	blood:	n/a	n/a
21	ATF1	chr8:107944698-107944731	K562	blood:	n/a	n/a
22	ATF1	chr8:108299729-108300273	K562	blood:	n/a	n/a
23	ATF1	chr8:108203175-108203176	K562	blood:	n/a	n/a
24	ATF1	chr8:107970799-107971055	K562	blood:	n/a	n/a
25	ATF1	chr8:108080937-108081234	K562	blood:	n/a	n/a
26	ATF1	chr8:108335129-108335332	K562	blood:	n/a	n/a
27	ATF1	chr8:108327332-108327831	K562	blood:	n/a	n/a
28	ATF1	chr8:108160223-108160605	K562	blood:	n/a	n/a
29	ATF1	chr8:108190858-108190862	K562	blood:	n/a	n/a
30	ATF1	chr8:108300549-108300640	K562	blood:	n/a	n/a
31	ATF1	chr8:108322486-108323333	K562	blood:	n/a	n/a
32	ATF1	chr8:108319459-108319785	K562	blood:	n/a	n/a
33	ATF1	chr8:108336368-108336835	K562	blood:	n/a	n/a
34	ATF2	chr8:107869938-107870367	GM12878	blood:	n/a	n/a
35	ATF3	chr8:107869846-107870396	A549	lung:	n/a	chr8:107870180-107870190 chr8:107870177-107870190 chr8:107870180-107870190 chr8:107870177-107870187 chr8:107870178-107870191 chr8:107870180-107870188 chr8:107870180-107870187 chr8:107870179-107870187 chr8:107870178-107870189 chr8:107870176-107870191 chr8:107870178-107870189
36	ATF3	chr8:108128397-108129326	A549	lung:	n/a	n/a
37	ATF3	chr8:107869820-107870425	A549	lung:	n/a	chr8:107870180-107870190 chr8:107870177-107870190 chr8:107870180-107870190 chr8:107870177-107870187 chr8:107870178-107870191 chr8:107870180-107870188 chr8:107870180-107870187 chr8:107870179-107870187 chr8:107870178-107870189 chr8:107870176-107870191 chr8:107870178-107870189
38	ATF3	chr8:107875874-107876817	A549	lung:	n/a	n/a
39	ATF3	chr8:107875898-107876687	A549	lung:	n/a	n/a
40	ATF3	chr8:108152827-108153465	A549	lung:	n/a	n/a
41	ATF3	chr8:108322410-108322926	K562	blood:	n/a	n/a
42	ATF3	chr8:108128510-108129327	A549	lung:	n/a	n/a
43	BACH1	chr8:108299333-108299369	K562	blood:	n/a	n/a
44	BACH1	chr8:107891138-107891321	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:108184808-108184812	K562	blood:	n/a	n/a
46	BACH1	chr8:108117123-108117620	K562	blood:	n/a	n/a
47	BACH1	chr8:108117140-108117585	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr8:107870106-107870388	GM12878	blood:	n/a	n/a
49	BATF	chr8:107870077-107870410	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:108183442-108183607	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:108253163-108253213	Caco-2	colon:	n/a
2	chr8:108080760-108080810	T-47D	breast:	n/a
3	chr8:108253163-108253213	Caco-2	colon:	n/a
4	chr8:108080760-108080810	T-47D	breast:	n/a
5	chr8:108253163-108253213	GM12878	blood:	n/a
6	chr8:108080760-108080810	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:107876626-107876676	HCM	heart:	n/a
8	chr8:108263868-108263918	GM12891	blood:	n/a
9	chr8:108298379-108298429	AG09309	skin:	n/a
10	chr8:107870405-107870455	Jurkat	blood:	n/a
11	chr8:108238734-108238784	SK-N-SH	brain:	n/a
12	chr8:108163998-108164048	NH-A	brain:	n/a
13	chr8:108144638-108144688	HepG2	liver:	n/a
14	chr8:108263868-108263918	IMR90	lung:	fetal
15	chr8:108178488-108178538	H1-hESC	embryonic stem cell:	embryo
16	chr8:108298379-108298429	HNPCEpiC	eye:	n/a
17	chr8:107994813-107994863	HEEpiC	esophagus:	n/a
18	chr8:108163998-108164048	AG04450	lung:	fetal
19	chr8:107994813-107994863	HRCEpiC	kidney:	n/a
20	chr8:108238734-108238784	HepG2	liver:	n/a
21	chr8:107890251-107890301	AG04449	skin:	fetal
22	chr8:108298379-108298429	Jurkat	blood:	n/a
23	chr8:108238734-108238784	GM12892	blood:	n/a
24	chr8:108163998-108164048	HUVEC	blood vessel:	n/a
25	chr8:108253163-108253213	AoSMC	blood vessel:	n/a
26	chr8:107937633-107937683	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:108080760-108080810	HEK293	kidney:	embryo
28	chr8:108208344-108208394	RPTEC	kidney:	n/a
29	chr8:107994813-107994863	A549	lung:	n/a
30	chr8:108263868-108263918	GM12878	blood:	n/a
31	chr8:108239870-108239920	AG04450	lung:	fetal
32	chr8:108314948-108314998	HAEpiC	amniotic membrane:	n/a
33	chr8:108178448-108178498	AG04450	lung:	fetal
34	chr8:108163998-108164048	SKMC	muscle:	n/a
35	chr8:108298379-108298429	U87	brain:	n/a
36	chr8:108239870-108239920	HNPCEpiC	eye:	n/a
37	chr8:107994813-107994863	PANC-1	pancreas:	n/a
38	chr8:108208344-108208394	HAEpiC	amniotic membrane:	n/a
39	chr8:107937633-107937683	A549	lung:	n/a
40	chr8:108263868-108263918	SK-N-SH_RA	brain:	n/a
41	chr8:108314948-108314998	PFSK-1	brain:	n/a
42	chr8:108144638-108144688	HCT-116	colon:	n/a
43	chr8:108239870-108239920	SAEC	small airway:	n/a
44	chr8:107890251-107890301	HCM	heart:	n/a
45	chr8:108238734-108238784	GM19239	blood:	n/a
46	chr8:108238734-108238784	HAEpiC	amniotic membrane:	n/a
47	chr8:107937633-107937683	SKMC	muscle:	n/a
48	chr8:108263868-108263918	HepG2	liver:	n/a
49	chr8:107937633-107937683	GM12892	blood:	n/a
50	chr8:108238734-108238784	RPTEC	kidney:	n/a

(count:169 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:108324753..108329300-chr8:108347441..108349729,6	K562	blood:
2	chr8:107776853..107777682-chr8:107843674..107844419,2	MCF-7	breast:
3	chr8:107717038..107717971-chr8:107868547..107869164,2	MCF-7	breast:
4	chr8:108296299..108298566-chr8:108418407..108420457,2	K562	blood:
5	chr8:108092379..108094443-chr8:108095250..108098096,2	K562	blood:
6	chr8:108046046..108048588-chr8:108049288..108050905,2	K562	blood:
7	chr8:108080564..108081493-chr8:108508119..108508723,3	MCF-7	breast:
8	chr8:108302915..108304989-chr8:108320621..108322739,2	K562	blood:
9	chr8:107963274..107965164-chr8:107984156..107985885,2	K562	blood:
10	chr8:108323023..108324851-chr8:108334237..108336849,2	K562	blood:
11	chr8:107823015..107825825-chr8:107828969..107830508,2	MCF-7	breast:
12	chr8:107868665..107869314-chr8:108544200..108544991,2	MCF-7	breast:
13	chr8:108080620..108081304-chr8:108767705..108768455,2	K562	blood:
14	chr8:107775413..107775971-chr8:107868475..107869338,2	MCF-7	breast:
15	chr8:108318722..108321630-chr8:108322464..108324818,2	MCF-7	breast:
16	chr8:107777185..107778453-chr8:107844735..107846577,8	MCF-7	breast:
17	chr8:108154566..108158695-chr8:108159110..108161002,3	MCF-7	breast:
18	chr8:107844267..107847790-chr8:107864374..107867207,3	MCF-7	breast:
19	chr8:108080615..108081581-chr8:108544165..108544964,3	K562	blood:
20	chr8:107716434..107716966-chr8:107858248..107858913,2	MCF-7	breast:
21	chr8:108238270..108239984-chr8:108244378..108246016,2	MCF-7	breast:
22	chr8:108259977..108262546-chr8:108268516..108270127,2	K562	blood:
23	chr8:108237961..108240814-chr8:108249385..108251392,2	K562	blood:
24	chr8:108230563..108232066-chr8:108238210..108240412,2	K562	blood:
25	chr8:108102909..108105054-chr8:108106250..108108382,2	K562	blood:
26	chr8:108304086..108305949-chr8:108321318..108324299,2	K562	blood:
27	chr8:108305763..108307455-chr8:108312597..108314682,2	K562	blood:
28	chr8:108267217..108269846-chr9:87536986..87539408,2	MCF-7	breast:
29	chr8:108268822..108271577-chr8:108272819..108274650,2	K562	blood:
30	chr8:108000485..108003336-chr8:108004872..108006735,2	MCF-7	breast:
31	chr8:108220971..108223579-chr8:108224873..108228653,3	K562	blood:
32	chr8:108000485..108003336-chr8:108004872..108006735,2	MCF-7	breast:
33	chr8:108316746..108319440-chr8:108325367..108326969,2	K562	blood:
34	chr8:108300911..108303354-chr8:108304518..108307945,3	K562	blood:
35	chr8:107881925..107884632-chr8:107886674..107888381,2	MCF-7	breast:
36	chr8:108312705..108315142-chr8:108317270..108319695,2	MCF-7	breast:
37	chr8:54467456..54468959-chr8:108144854..108147714,2	MCF-7	breast:
38	chr8:108297727..108300004-chr8:108306380..108308421,2	K562	blood:
39	chr8:108080826..108081683-chr8:108793557..108794150,2	MCF-7	breast:
40	chr8:108325638..108328700-chr8:108330925..108333725,3	K562	blood:
41	chr8:106952193..106952705-chr8:107868814..107869363,2	MCF-7	breast:
42	chr8:107858278..107858789-chr8:108024820..108025365,2	MCF-7	breast:
43	chr8:108230563..108232066-chr8:108238210..108240412,2	K562	blood:
44	chr8:108237961..108240814-chr8:108249385..108251392,2	K562	blood:
45	chr8:108304841..108306771-chr8:108325164..108328030,2	K562	blood:
46	chr8:107996657..107998949-chr8:108007798..108009962,2	MCF-7	breast:
47	chr8:107776572..107779204-chr8:107860586..107863485,2	K562	blood:
48	chr8:107858278..107858789-chr8:108024820..108025365,2	MCF-7	breast:
49	chr8:108304882..108307212-chr8:108347757..108349335,2	K562	blood:
50	chr8:108316746..108319440-chr8:108325367..108326969,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT1-1	chr8:108184556-108184583	NONHSAT128258
2	lnc-ANGPT1-1	chr8:108178377-108178524	NONHSAT128258
3	lnc-ANGPT1-1	chr8:108178104-108178267	NONHSAT128258

No data

Variant related genes	Relation type
HMGB1P46	TF binding region
ENSG00000211995	TF binding region
ANGPT1	TF binding region
HMGB1P46	CpG island
ENSG00000211995	CpG island
ANGPT1	CpG island
ENSG00000154188	chromatin interactions
ENSG00000104408	chromatin interactions
ENSG00000183520	chromatin interactions
ENSG00000211995	chromatin interactions

Extended variants
information (count: 17055 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:17055 , 50 per page) page: 1 2 3 4 5 6 7 ... 342

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34338619	chr8:107813799-107813800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571529812	chr8:107813841-107813842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561312291	chr8:107813853-107813854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534232647	chr8:107813854-107813855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546488477	chr8:107813873-107813874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113954330	chr8:107813936-107813937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79519086	chr8:107813985-107813986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79984624	chr8:107814031-107814032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550329676	chr8:107814038-107814039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75744361	chr8:107814039-107814040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536324524	chr8:107814067-107814068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139086623	chr8:107814089-107814090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545155347	chr8:107814091-107814092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572786484	chr8:107814099-107814100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184807883	chr8:107814116-107814117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11987857	chr8:107814129-107814130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs578239672	chr8:107814131-107814132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545728133	chr8:107814143-107814144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144070381	chr8:107814199-107814200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575774444	chr8:107814235-107814236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186771184	chr8:107814237-107814238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561273641	chr8:107814240-107814241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191336876	chr8:107814312-107814313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183525198	chr8:107814316-107814317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540196153	chr8:107814337-107814338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189333828	chr8:107814369-107814370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117870160	chr8:107814371-107814372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182220046	chr8:107814436-107814437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28733507	chr8:107814469-107814470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556810269	chr8:107814472-107814473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550491734	chr8:107814487-107814488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569019611	chr8:107814511-107814512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2930486	chr8:107814554-107814555	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs548262964	chr8:107814555-107814556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562255699	chr8:107814565-107814566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73702421	chr8:107814596-107814597	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533880129	chr8:107814620-107814621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558550203	chr8:107814668-107814669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185318094	chr8:107814687-107814688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539316961	chr8:107814756-107814757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557402781	chr8:107814758-107814759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575783463	chr8:107814780-107814781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373475769	chr8:107814784-107814785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs386728591	chr8:107814788-107814789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550559021	chr8:107814809-107814810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11415326	chr8:107814827-107814828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs397795668	chr8:107814838-107814839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146455371	chr8:107814910-107814911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140757350	chr8:107814918-107814919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373694321	chr8:107814936-107814937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	21645411	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:2160 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107807600-107814400	Weak transcription	Aorta	Aorta
2	chr8:107809600-107821000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:107812800-107815400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:107813000-107813800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:107813400-107814200	Enhancers	Psoas Muscle	Psoas
6	chr8:107813600-107813800	Enhancers	A549	lung
7	chr8:107814000-107814800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr8:107814200-107815200	Weak transcription	Psoas Muscle	Psoas
9	chr8:107814400-107814800	Enhancers	Aorta	Aorta
10	chr8:107814400-107814800	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr8:107814800-107820400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:107814800-107823400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr8:107815200-107815400	Enhancers	Psoas Muscle	Psoas
14	chr8:107815400-107820200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr8:107818800-107819200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:107818800-107819200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:107820000-107821600	Enhancers	Adipose Nuclei	Adipose
18	chr8:107820200-107820400	Enhancers	HSMMtube	muscle
19	chr8:107820200-107821200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr8:107820400-107821200	Enhancers	Fetal Heart	heart
21	chr8:107820400-107821200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr8:107820600-107821200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:107821000-107821200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:107821200-107822800	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:107821200-107825400	Weak transcription	Fetal Heart	heart
26	chr8:107821600-107822800	Weak transcription	Adipose Nuclei	Adipose
27	chr8:107822800-107823400	Enhancers	Adipose Nuclei	Adipose
28	chr8:107822800-107826000	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr8:107823400-107823800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr8:107823800-107824000	Enhancers	Spleen	Spleen
31	chr8:107823800-107824800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr8:107824800-107825000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr8:107825000-107825400	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr8:107825400-107825800	Enhancers	Fetal Heart	heart
35	chr8:107825400-107825800	Enhancers	Fetal Muscle Leg	muscle
36	chr8:107825400-107826400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr8:107828600-107832600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:107829400-107829800	Enhancers	Fetal Muscle Leg	muscle
39	chr8:107834000-107837200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:107834600-107837200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:107835000-107835400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:107835000-107835400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr8:107835000-107835600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr8:107835400-107835600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:107835400-107836600	Enhancers	Primary hematopoietic stem cells	blood
46	chr8:107835600-107836400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:107836000-107836600	Enhancers	HepG2	liver
48	chr8:107836000-107836600	Enhancers	K562	blood
49	chr8:107836000-107836800	Enhancers	Fetal Heart	heart
50	chr8:107836400-107836600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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