Variant report

Variant	nsv891253
Chromosome Location	chr8:105994885-106251476
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1498)
CpG islands
(count:122)
Chromatin interactive
region (count:113)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:106220707-106221154	K562	blood:	n/a	n/a
2	ARID3A	chr8:106104585-106104933	K562	blood:	n/a	n/a
3	ARID3A	chr8:106002548-106002659	K562	blood:	n/a	n/a
4	ARID3A	chr8:106136243-106136505	K562	blood:	n/a	n/a
5	ARID3A	chr8:106243313-106244156	K562	blood:	n/a	chr8:106243316-106243332
6	ARID3A	chr8:106113101-106113326	K562	blood:	n/a	n/a
7	ARID3A	chr8:106110265-106110589	K562	blood:	n/a	n/a
8	ARID3A	chr8:106214260-106214501	K562	blood:	n/a	n/a
9	ATF1	chr8:105997863-105997972	K562	blood:	n/a	n/a
10	ATF1	chr8:106214244-106214490	K562	blood:	n/a	n/a
11	ATF1	chr8:106113059-106113259	K562	blood:	n/a	n/a
12	ATF1	chr8:106240244-106240400	K562	blood:	n/a	n/a
13	ATF1	chr8:106110238-106110657	K562	blood:	n/a	n/a
14	ATF1	chr8:106220981-106220982	K562	blood:	n/a	n/a
15	ATF1	chr8:106190453-106190599	K562	blood:	n/a	n/a
16	ATF1	chr8:106243200-106243395	K562	blood:	n/a	n/a
17	ATF3	chr8:106104600-106104925	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr8:106131917-106132151	K562	blood:	n/a	n/a
19	ATF3	chr8:106104625-106104863	K562	blood:	n/a	n/a
20	BACH1	chr8:106223875-106223923	K562	blood:	n/a	n/a
21	BATF	chr8:106110262-106110621	GM12878	blood:	n/a	n/a
22	BATF	chr8:106012935-106013138	GM12878	blood:	n/a	n/a
23	BCL3	chr8:106146358-106146559	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:106104689-106104910	K562	blood:	n/a	n/a
25	BHLHE40	chr8:106110252-106110554	K562	blood:	n/a	n/a
26	BHLHE40	chr8:106157194-106157286	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:106034536-106034696	K562	blood:	n/a	n/a
28	BRCA1	chr8:106081962-106082383	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr8:106228530-106228773	K562	blood:	n/a	n/a
30	CBX3	chr8:106228497-106228865	K562	blood:	n/a	n/a
31	CBX3	chr8:106210730-106210956	K562	blood:	n/a	n/a
32	CBX3	chr8:106210582-106211052	K562	blood:	n/a	n/a
33	CBX3	chr8:106056189-106056567	K562	blood:	n/a	n/a
34	CBX3	chr8:106025954-106026212	K562	blood:	n/a	n/a
35	CBX3	chr8:106131863-106132252	K562	blood:	n/a	n/a
36	CBX3	chr8:106110192-106110722	K562	blood:	n/a	n/a
37	CBX3	chr8:106056254-106056495	K562	blood:	n/a	n/a
38	CCNT2	chr8:106214286-106214435	K562	blood:	n/a	n/a
39	CCNT2	chr8:106110247-106110598	K562	blood:	n/a	n/a
40	CCNT2	chr8:106104643-106104836	K562	blood:	n/a	n/a
41	CCNT2	chr8:106081681-106081766	K562	blood:	n/a	n/a
42	CCNT2	chr8:106220802-106221008	K562	blood:	n/a	n/a
43	CEBPB	chr8:106101617-106101992	Hela-S3	cervix:	n/a	chr8:106101677-106101690
44	CEBPB	chr8:106242207-106242546	IMR90	lung:	n/a	chr8:106242377-106242388
45	CEBPB	chr8:106242187-106242572	K562	blood:	n/a	chr8:106242377-106242388
46	CEBPB	chr8:106152057-106152064	K562	blood:	n/a	n/a
47	CEBPB	chr8:106038045-106038146	K562	blood:	n/a	chr8:106038094-106038105
48	CEBPB	chr8:106105026-106105089	A549	lung:	n/a	chr8:106105032-106105045 chr8:106105032-106105043 chr8:106105032-106105043 chr8:106105032-106105045
49	CEBPB	chr8:106200245-106200607	K562	blood:	n/a	chr8:106200421-106200432
50	CEBPB	chr8:106250717-106250995	IMR90	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:106185570-106185620	SAEC	small airway:	n/a
2	chr8:106185570-106185620	HMEC	breast:	n/a
3	chr8:106185570-106185620	HEK293	kidney:	embryo
4	chr8:105995203-105995253	Caco-2	colon:	n/a
5	chr8:105995203-105995253	NT2-D1	testis:	n/a
6	chr8:105995203-105995253	K562	blood:	n/a
7	chr8:106185570-106185620	HL-60	blood:	n/a
8	chr8:106185570-106185620	HAEpiC	amniotic membrane:	n/a
9	chr8:105995203-105995253	Hela-S3	cervix:	n/a
10	chr8:106185570-106185620	PFSK-1	brain:	n/a
11	chr8:105995203-105995253	GM12891	blood:	n/a
12	chr8:106185570-106185620	BE2_C	brain:	n/a
13	chr8:106185570-106185620	K562	blood:	n/a
14	chr8:106185570-106185620	HCM	heart:	n/a
15	chr8:105995203-105995253	GM06990	blood:	n/a
16	chr8:105995203-105995253	AG04450	lung:	fetal
17	chr8:106185570-106185620	ECC-1	luminal epithelium:	n/a
18	chr8:105995203-105995253	A549	lung:	n/a
19	chr8:105995203-105995253	H1-hESC	embryonic stem cell:	embryo
20	chr8:105995203-105995253	HAEpiC	amniotic membrane:	n/a
21	chr8:106185570-106185620	HUVEC	blood vessel:	n/a
22	chr8:106185570-106185620	PANC-1	pancreas:	n/a
23	chr8:106185570-106185620	Jurkat	blood:	n/a
24	chr8:106185570-106185620	T-47D	breast:	n/a
25	chr8:105995203-105995253	AG09319	gingival:	n/a
26	chr8:106185570-106185620	GM12892	blood:	n/a
27	chr8:105995203-105995253	Jurkat	blood:	n/a
28	chr8:106185570-106185620	Caco-2	colon:	n/a
29	chr8:105995203-105995253	SK-N-MC	brain:	n/a
30	chr8:105995203-105995253	HCPEpiC	choroid plexus:	n/a
31	chr8:106185570-106185620	HNPCEpiC	eye:	n/a
32	chr8:106185570-106185620	HRPEpiC	eye:	n/a
33	chr8:106185570-106185620	GM06990	blood:	n/a
34	chr8:105995203-105995253	Hepatocyte	liver:	n/a
35	chr8:106185570-106185620	MCF-7	breast:	n/a
36	chr8:105995203-105995253	HepG2	liver:	n/a
37	chr8:106185570-106185620	HEEpiC	esophagus:	n/a
38	chr8:106185570-106185620	AG04449	skin:	fetal
39	chr8:106185570-106185620	NH-A	brain:	n/a
40	chr8:105995203-105995253	NHBE	bronchial:	n/a
41	chr8:105995203-105995253	NH-A	brain:	n/a
42	chr8:106185570-106185620	SK-N-SH	brain:	n/a
43	chr8:105995203-105995253	HRE	kidney:	n/a
44	chr8:106185570-106185620	HIPEpiC	eye:	n/a
45	chr8:105995203-105995253	HUVEC	blood vessel:	n/a
46	chr8:105995203-105995253	HEK293	kidney:	embryo
47	chr8:106185570-106185620	PrEC	prostate:	n/a
48	chr8:106185570-106185620	GM19239	blood:	n/a
49	chr8:105995203-105995253	U87	brain:	n/a
50	chr8:105995203-105995253	ProgFib	skin:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:106162215..106165061-chr8:106166589..106168874,3	K562	blood:
2	chr8:106104293..106104911-chr8:106785023..106785634,3	MCF-7	breast:
3	chr8:106101009..106105530-chr8:106328930..106333222,5	K562	blood:
4	chr8:106104219..106105278-chr8:106672513..106673764,5	MCF-7	breast:
5	chr8:106152151..106154623-chr8:106161739..106164454,2	K562	blood:
6	chr8:106250267..106253166-chr8:106253943..106256912,3	K562	blood:
7	chr8:106065191..106067685-chr8:106074185..106076444,2	K562	blood:
8	chr8:106224560..106226478-chr8:106234242..106236875,2	K562	blood:
9	chr8:106034177..106035101-chr8:106784875..106785931,5	K562	blood:
10	chr8:106098062..106099625-chr8:106102482..106104994,2	MCF-7	breast:
11	chr8:106021613..106024219-chr8:106053554..106055959,2	MCF-7	breast:
12	chr8:106075494..106077166-chr8:106081357..106083896,2	MCF-7	breast:
13	chr8:106185670..106187920-chr8:106191413..106194105,2	K562	blood:
14	chr8:106094210..106096629-chr8:106098616..106100274,3	K562	blood:
15	chr8:106092097..106094824-chr8:106100318..106102369,2	K562	blood:
16	chr8:106136690..106139159-chr8:106144055..106146884,2	MCF-7	breast:
17	chr8:106108103..106110619-chr8:106122748..106124588,2	MCF-7	breast:
18	chr8:106246345..106248515-chr8:106256082..106257588,2	K562	blood:
19	chr8:106241879..106244262-chr8:106249327..106252289,2	K562	blood:
20	chr8:106057531..106060306-chr8:106071260..106074898,3	K562	blood:
21	chr8:106170292..106173280-chr8:106175111..106177873,2	K562	blood:
22	chr8:106182772..106185490-chr8:106187301..106189319,2	K562	blood:
23	chr8:106003697..106006144-chr8:106007178..106008786,2	K562	blood:
24	chr8:106112581..106114529-chr8:106145312..106148061,2	K562	blood:
25	chr8:106082783..106085372-chr8:106087525..106090132,2	K562	blood:
26	chr8:106110955..106112913-chr8:106113488..106116192,2	K562	blood:
27	chr8:106136690..106139159-chr8:106144055..106146884,2	MCF-7	breast:
28	chr8:106104770..106105296-chr8:106154309..106154928,2	MCF-7	breast:
29	chr8:106082783..106085372-chr8:106087525..106090132,2	K562	blood:
30	chr8:106102491..106104440-chr8:106106753..106108347,2	MCF-7	breast:
31	chr8:106082822..106084651-chr8:106097372..106099591,2	K562	blood:
32	chr8:106145928..106149549-chr8:106151108..106155039,3	K562	blood:
33	chr8:106152151..106154623-chr8:106161739..106164454,2	K562	blood:
34	chr8:106087603..106090110-chr8:106101395..106103199,2	K562	blood:
35	chr8:106235711..106237778-chr8:106248922..106250882,2	K562	blood:
36	chr8:106128119..106129741-chr8:106131952..106134022,2	K562	blood:
37	chr8:106237183..106239904-chr8:106240633..106243092,3	K562	blood:
38	chr8:106110267..106112599-chr8:106425928..106428860,2	K562	blood:
39	chr8:106098062..106099625-chr8:106102482..106104994,2	MCF-7	breast:
40	chr8:106224825..106226678-chr8:106784530..106787162,2	K562	blood:
41	chr8:106075494..106077166-chr8:106081357..106083896,2	MCF-7	breast:
42	chr8:106098685..106100875-chr8:106101996..106103590,2	K562	blood:
43	chr8:106112581..106114529-chr8:106145312..106148061,2	K562	blood:
44	chr8:106124290..106126979-chr8:106301850..106304617,2	K562	blood:
45	chr8:106163120..106165061-chr8:106166603..106168874,2	K562	blood:
46	chr8:106138231..106139133-chr8:106146754..106147617,2	MCF-7	breast:
47	chr8:106087603..106090110-chr8:106101395..106103199,2	K562	blood:
48	chr8:106165403..106167393-chr8:106167637..106170274,2	K562	blood:
49	chr8:106104770..106105296-chr8:106154309..106154928,2	MCF-7	breast:
50	chr8:106034373..106035272-chr8:106784809..106785871,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRP12-1	chr8:106179646-106179717	ENSG00000254041.1
2	lnc-LRP12-1	chr8:106200764-106200834	ENSG00000254041.1
3	lnc-LRP12-1	chr8:106155088-106155975	ENSG00000254041.1
4	lnc-LRP12-7	chr8:106031525-106031845	uc_244_-
5	lnc-LRP12-6	chr8:106002536-106002920	NONHSAT128223
6	lnc-ZFPM2-5	chr8:106023335-106023796	NONHSAT128224
7	lnc-ZFPM2-4	chr8:106031525-106031845	uc_244_+

No data

Variant related genes	Relation type
ENSG00000254041	TF binding region
ENSG00000240271	TF binding region
ENSG00000243939	TF binding region
TMCC1P1	TF binding region
ENSG00000253997	TF binding region
ENSG00000254041	CpG island
ENSG00000240271	CpG island
ENSG00000243939	CpG island
TMCC1P1	CpG island
ENSG00000253997	CpG island
ENSG00000148356	chromatin interactions
ENSG00000240271	chromatin interactions
ENSG00000169946	chromatin interactions
ENSG00000197958	chromatin interactions

Extended variants
information (count: 4825 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4825 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4734838	chr8:105994885-105994886	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549304687	chr8:105995004-105995005	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561567869	chr8:105995094-105995095	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563615700	chr8:105995194-105995195	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs74449010	chr8:105995225-105995226	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs79065804	chr8:105995226-105995227	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs80107100	chr8:105995235-105995236	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs546649558	chr8:105995247-105995248	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs140818642	chr8:105995305-105995306	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs552341351	chr8:105995318-105995319	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550624119	chr8:105995363-105995364	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs569172513	chr8:105995378-105995379	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs536590194	chr8:105995410-105995411	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs554577919	chr8:105995484-105995485	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566613814	chr8:105995489-105995490	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186127734	chr8:105995507-105995508	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558803273	chr8:105995550-105995551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186711194	chr8:105995671-105995672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189415801	chr8:105995676-105995677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577747530	chr8:105995677-105995678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs968611	chr8:105995698-105995699	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs17273716	chr8:105995746-105995747	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs181738839	chr8:105995850-105995851	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs575518549	chr8:105995915-105995916	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs543262463	chr8:105995938-105995939	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs561447882	chr8:105995948-105995949	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs143046522	chr8:105995966-105995967	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs148188615	chr8:105995997-105995998	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs141230831	chr8:105996001-105996002	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371276539	chr8:105996064-105996065	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs368305311	chr8:105996102-105996103	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs568398779	chr8:105996103-105996104	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs150733682	chr8:105996127-105996128	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537423119	chr8:105996143-105996144	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186919789	chr8:105996145-105996146	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs372126513	chr8:105996214-105996215	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556546773	chr8:105996258-105996259	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs529660784	chr8:105996270-105996271	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs548436821	chr8:105996281-105996282	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs376727072	chr8:105996291-105996292	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs191394339	chr8:105996293-105996294	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs80069565	chr8:105996367-105996368	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs571402246	chr8:105996382-105996383	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs202136672	chr8:105996393-105996394	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374867423	chr8:105996394-105996395	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs369986683	chr8:105996436-105996437	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs557042125	chr8:105996460-105996461	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs575568966	chr8:105996468-105996469	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs569958110	chr8:105996474-105996475	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs542675079	chr8:105996503-105996504	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105993800-105997000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:105994000-105996400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr8:105994400-105996000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:105994600-105995000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr8:105994600-105995400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr8:105994600-105996200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:105994600-105996200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:105994600-105997200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr8:105994600-105997400	Enhancers	HUVEC	blood vessel
10	chr8:105994800-105995000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:105994800-105995200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:105994800-105995400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:105994800-105995600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr8:105994800-105996000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr8:105994800-105996200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr8:105995000-105995400	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr8:105995000-105995600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:105995000-105995600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr8:105995000-105995800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:105995400-105996600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr8:105995400-106003400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr8:105995600-105996600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr8:105995800-105996000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:105996000-105996200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:105996000-105996800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:105996400-105997000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr8:105996600-105997400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr8:105996800-105997000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:106002600-106003000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:106002800-106004000	Enhancers	Brain Hippocampus Middle	brain
31	chr8:106003000-106004200	Enhancers	Aorta	Aorta
32	chr8:106003200-106003400	Enhancers	Brain Anterior Caudate	brain
33	chr8:106003400-106003600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:106003400-106003600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr8:106003400-106003600	Enhancers	Adipose Nuclei	Adipose
36	chr8:106003400-106003600	Flanking Active TSS	Brain Anterior Caudate	brain
37	chr8:106003400-106003600	Enhancers	Fetal Lung	lung
38	chr8:106003400-106003600	Enhancers	HUVEC	blood vessel
39	chr8:106003400-106004000	Enhancers	Brain Cingulate Gyrus	brain
40	chr8:106003600-106003800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:106003600-106003800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr8:106003600-106003800	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr8:106003600-106003800	Enhancers	Brain Substantia Nigra	brain
44	chr8:106003600-106003800	Flanking Active TSS	Fetal Lung	lung
45	chr8:106003600-106003800	Enhancers	Ovary	ovary
46	chr8:106003600-106004000	Active TSS	Brain Anterior Caudate	brain
47	chr8:106003600-106004000	Active TSS	Fetal Brain Male	brain
48	chr8:106003600-106004200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr8:106003600-106004200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:106003600-106004200	Enhancers	Brain Inferior Temporal Lobe	brain

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