Variant report

Variant	nsv891278
Chromosome Location	chr8:110251998-110308776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:244)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110289281-110289645	HepG2	liver:	n/a	n/a
2	ATF2	chr8:110274349-110274803	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:110307193-110307196	HepG2	liver:	n/a	n/a
4	BRCA1	chr8:110294420-110294571	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr8:110283781-110284300	HCT-116	colon:	n/a	n/a
6	CBX3	chr8:110295193-110295518	K562	blood:	n/a	n/a
7	CBX3	chr8:110304602-110305153	HCT-116	colon:	n/a	n/a
8	CBX3	chr8:110283791-110284340	HCT-116	colon:	n/a	n/a
9	CBX3	chr8:110283892-110284221	K562	blood:	n/a	n/a
10	CBX3	chr8:110283811-110284240	K562	blood:	n/a	n/a
11	CEBPB	chr8:110265928-110266293	K562	blood:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
12	CEBPB	chr8:110265987-110266274	H1-hESC	embryonic stem cell:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
13	CEBPB	chr8:110289230-110289603	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:110304659-110305178	A549	lung:	n/a	chr8:110304939-110304952
15	CEBPB	chr8:110289326-110289508	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:110304600-110305096	IMR90	lung:	n/a	chr8:110304939-110304952
17	CEBPB	chr8:110304424-110305358	HCT-116	colon:	n/a	chr8:110304939-110304952
18	CEBPB	chr8:110278818-110278920	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:110258108-110258384	A549	lung:	n/a	chr8:110258218-110258229
20	CEBPB	chr8:110258117-110258334	HepG2	liver:	n/a	chr8:110258218-110258229
21	CEBPB	chr8:110258049-110258387	IMR90	lung:	n/a	chr8:110258218-110258229
22	CEBPB	chr8:110266003-110266249	A549	lung:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
23	CEBPB	chr8:110304601-110305135	Hela-S3	cervix:	n/a	chr8:110304939-110304952
24	CEBPB	chr8:110304827-110305100	A549	lung:	n/a	chr8:110304939-110304952
25	CEBPB	chr8:110280529-110280673	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:110294414-110294618	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:110265971-110266273	IMR90	lung:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
28	CEBPB	chr8:110278803-110278974	K562	blood:	n/a	n/a
29	CEBPB	chr8:110265965-110266292	HepG2	liver:	n/a	chr8:110266104-110266117 chr8:110266104-110266115
30	CEBPB	chr8:110294169-110294703	MCF-7	breast:	n/a	n/a
31	CEBPB	chr8:110278754-110278970	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:110304560-110305134	HCT-116	colon:	n/a	chr8:110304939-110304952
33	CHD1	chr8:110274336-110274349	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr8:110294401-110294667	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr8:110274460-110274867	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr8:110274399-110274809	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr8:110274349-110274916	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr8:110274432-110274941	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:110294500-110294650	GM12874	blood:	n/a	n/a
40	CTCF	chr8:110294384-110294737	GM12878	blood:	n/a	n/a
41	CTCF	chr8:110294520-110294670	AG09319	gingival:	n/a	n/a
42	CTCF	chr8:110294460-110294610	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr8:110294500-110294650	HMEC	breast:	n/a	n/a
44	CTCF	chr8:110294480-110294630	K562	blood:	n/a	n/a
45	CTCF	chr8:110294500-110294650	GM12873	blood:	n/a	n/a
46	CTCF	chr8:110294500-110294650	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr8:110294391-110294706	IMR90	lung:	n/a	n/a
48	CTCF	chr8:110294220-110294370	NHEK	skin:	n/a	n/a
49	CTCF	chr8:110294496-110294608	A549	lung:	n/a	n/a
50	CTCF	chr8:110274380-110274530	HAc	cerebellar:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110280928-110280978	T-47D	breast:	n/a
2	chr8:110274914-110274964	SKMC	muscle:	n/a
3	chr8:110274914-110274964	HCT-116	colon:	n/a
4	chr8:110272720-110272770	HCT-116	colon:	n/a
5	chr8:110280928-110280978	SK-N-SH_RA	brain:	n/a
6	chr8:110274914-110274964	AG09309	skin:	n/a
7	chr8:110253782-110253832	IMR90	lung:	fetal
8	chr8:110272720-110272770	HAEpiC	amniotic membrane:	n/a
9	chr8:110274914-110274964	HEK293	kidney:	embryo
10	chr8:110253782-110253832	NH-A	brain:	n/a
11	chr8:110274914-110274964	HAEpiC	amniotic membrane:	n/a
12	chr8:110253782-110253832	PrEC	prostate:	n/a
13	chr8:110274914-110274964	BJ	skin:	n/a
14	chr8:110272720-110272770	HRCEpiC	kidney:	n/a
15	chr8:110274914-110274964	HL-60	blood:	n/a
16	chr8:110274914-110274964	NT2-D1	testis:	n/a
17	chr8:110253782-110253832	NT2-D1	testis:	n/a
18	chr8:110272720-110272770	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:110280928-110280978	HUVEC	blood vessel:	n/a
20	chr8:110274914-110274964	ovcar-3	ovarian:	n/a
21	chr8:110272720-110272770	HL-60	blood:	n/a
22	chr8:110253782-110253832	HRPEpiC	eye:	n/a
23	chr8:110253782-110253832	NB4	blood:	n/a
24	chr8:110280928-110280978	ECC-1	luminal epithelium:	n/a
25	chr8:110274914-110274964	RPTEC	kidney:	n/a
26	chr8:110253782-110253832	SK-N-MC	brain:	n/a
27	chr8:110253782-110253832	PANC-1	pancreas:	n/a
28	chr8:110280928-110280978	PrEC	prostate:	n/a
29	chr8:110272720-110272770	HCPEpiC	choroid plexus:	n/a
30	chr8:110280928-110280978	Jurkat	blood:	n/a
31	chr8:110253782-110253832	NHDF-neo	bronchial:	n/a
32	chr8:110280928-110280978	BJ	skin:	n/a
33	chr8:110274914-110274964	LNCaP	prostate:	n/a
34	chr8:110274914-110274964	AoSMC	blood vessel:	n/a
35	chr8:110253782-110253832	GM19239	blood:	n/a
36	chr8:110280928-110280978	SK-N-MC	brain:	n/a
37	chr8:110274914-110274964	HRCEpiC	kidney:	n/a
38	chr8:110274914-110274964	HRE	kidney:	n/a
39	chr8:110274914-110274964	K562	blood:	n/a
40	chr8:110274914-110274964	SAEC	small airway:	n/a
41	chr8:110253782-110253832	HCT-116	colon:	n/a
42	chr8:110280928-110280978	HNPCEpiC	eye:	n/a
43	chr8:110280928-110280978	NHDF-neo	bronchial:	n/a
44	chr8:110274914-110274964	SK-N-SH	brain:	n/a
45	chr8:110253782-110253832	HIPEpiC	eye:	n/a
46	chr8:110272720-110272770	SAEC	small airway:	n/a
47	chr8:110280928-110280978	AG09309	skin:	n/a
48	chr8:110274914-110274964	AG10803	skin:	n/a
49	chr8:110280928-110280978	MCF-7	breast:	n/a
50	chr8:110274914-110274964	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:110237132..110238315-chr8:110294080..110295100,5	MCF-7	breast:
2	chr8:110284682..110286826-chr8:110289156..110291459,2	MCF-7	breast:
3	chr8:110252631..110254624-chr8:110265466..110267437,3	MCF-7	breast:
4	chr8:110282798..110284490-chr8:110290384..110293883,3	K562	blood:
5	chr8:110266910..110269823-chr8:110274098..110276440,2	MCF-7	breast:
6	chr8:110284180..110285865-chr8:110286825..110289616,2	K562	blood:
7	chr8:110302918..110306043-chr8:110308192..110310489,3	MCF-7	breast:
8	chr8:110267160..110271575-chr8:110275719..110280785,4	MCF-7	breast:
9	chr8:110298680..110300639-chr8:110303623..110306620,2	K562	blood:
10	chr8:110293728..110295786-chr8:110296881..110298730,2	MCF-7	breast:
11	chr8:110284939..110287374-chr8:110293583..110295372,2	MCF-7	breast:
12	chr8:110284180..110285865-chr8:110286825..110289616,2	K562	blood:
13	chr8:110305748..110308660-chr8:110346435..110347987,2	K562	blood:
14	chr8:110293214..110295684-chr8:110300331..110302859,2	MCF-7	breast:
15	chr8:110293728..110295786-chr8:110296881..110298730,2	MCF-7	breast:
16	chr8:110251256..110254212-chr8:110254485..110256380,2	K562	blood:
17	chr8:110274950..110277941-chr8:110345336..110348153,2	MCF-7	breast:
18	chr8:110284939..110287374-chr8:110293583..110295372,2	MCF-7	breast:
19	chr8:109930431..109931332-chr8:110293724..110294960,8	MCF-7	breast:
20	chr8:110265183..110267675-chr8:110271618..110273789,2	K562	blood:
21	chr8:110296774..110299286-chr8:110348162..110350315,2	K562	blood:
22	chr8:110276401..110278429-chr8:110280186..110282933,2	MCF-7	breast:
23	chr8:110284682..110286826-chr8:110289156..110291459,2	MCF-7	breast:
24	chr8:110274391..110276446-chr8:110278687..110281148,2	MCF-7	breast:
25	chr8:110302918..110306043-chr8:110308192..110310489,3	MCF-7	breast:
26	chr8:110273357..110276985-chr8:110278828..110281749,3	K562	blood:
27	chr8:110251271..110254204-chr8:110279241..110281441,2	K562	blood:
28	chr8:110265183..110267675-chr8:110271618..110273789,2	K562	blood:
29	chr8:110282798..110284490-chr8:110290384..110293883,3	K562	blood:
30	chr8:110266910..110269823-chr8:110274098..110276440,2	MCF-7	breast:
31	chr8:110279580..110281414-chr8:110552685..110555457,2	MCF-7	breast:
32	chr8:110273357..110276985-chr8:110278828..110281749,3	K562	blood:
33	chr8:110252631..110254624-chr8:110265466..110267437,3	MCF-7	breast:
34	chr8:109914966..109916782-chr8:110304946..110307932,2	MCF-7	breast:
35	chr8:110251271..110254204-chr8:110279241..110281441,2	K562	blood:
36	chr8:110271725..110274616-chr8:110342573..110345047,2	K562	blood:
37	chr8:110249700..110252178-chr8:110258243..110259912,2	K562	blood:
38	chr8:110267160..110271575-chr8:110275719..110280785,4	MCF-7	breast:
39	chr8:110238617..110240882-chr8:110264919..110266571,2	MCF-7	breast:
40	chr8:110274484..110277076-chr8:110350109..110352539,2	K562	blood:
41	chr8:110293214..110295684-chr8:110300331..110302859,2	MCF-7	breast:
42	chr8:110300725..110303179-chr8:110304720..110306354,2	MCF-7	breast:
43	chr8:110130537..110131463-chr8:110294292..110294801,2	MCF-7	breast:
44	chr8:110251256..110254212-chr8:110254485..110256380,2	K562	blood:
45	chr8:110300725..110303179-chr8:110304720..110306354,2	MCF-7	breast:
46	chr8:110252748..110254805-chr8:110344261..110345885,2	K562	blood:
47	chr8:110249700..110252178-chr8:110258243..110259912,2	K562	blood:
48	chr8:110276401..110278429-chr8:110280186..110282933,2	MCF-7	breast:
49	chr8:110298680..110300639-chr8:110303623..110306620,2	K562	blood:
50	chr8:110274391..110276446-chr8:110278687..110281148,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000250267	TF binding region
ENSG00000250267	CpG island
ENSG00000120533	chromatin interactions
ENSG00000147654	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000253796	chromatin interactions

Extended variants
information (count: 2110 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2110 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2926214	chr8:110251998-110251999	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79212596	chr8:110252018-110252019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551587679	chr8:110252043-110252044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149521245	chr8:110252113-110252114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375456462	chr8:110252116-110252117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182735061	chr8:110252181-110252182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186455436	chr8:110252204-110252205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539868313	chr8:110252277-110252278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79157555	chr8:110252302-110252303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191303338	chr8:110252366-110252367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141169442	chr8:110252390-110252391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35137345	chr8:110252416-110252417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73303256	chr8:110252470-110252471	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs376522296	chr8:110252482-110252483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144996068	chr8:110252540-110252541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148698607	chr8:110252567-110252568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531980399	chr8:110252601-110252602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548591725	chr8:110252612-110252613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568771144	chr8:110252638-110252639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527666038	chr8:110252703-110252704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547777548	chr8:110252724-110252725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76179693	chr8:110252736-110252737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374439266	chr8:110252770-110252771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556664395	chr8:110252771-110252772	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573575363	chr8:110252817-110252818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547594142	chr8:110252827-110252828	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568946280	chr8:110252842-110252843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79208352	chr8:110252868-110252869	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554543448	chr8:110252871-110252872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138093495	chr8:110252925-110252926	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62512061	chr8:110252943-110252944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574360020	chr8:110252968-110252969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79451500	chr8:110253065-110253066	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536341106	chr8:110253073-110253074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182760495	chr8:110253146-110253147	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76754364	chr8:110253241-110253242	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141798255	chr8:110253302-110253303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150134278	chr8:110253396-110253397	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562645043	chr8:110253408-110253409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548548589	chr8:110253410-110253411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538281994	chr8:110253433-110253434	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558785921	chr8:110253458-110253459	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77961444	chr8:110253498-110253499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs60584579	chr8:110253558-110253559	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs187408085	chr8:110253571-110253572	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527948206	chr8:110253598-110253599	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs80116547	chr8:110253617-110253618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564469154	chr8:110253703-110253704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533405439	chr8:110253748-110253749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549989209	chr8:110253755-110253756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
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
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110211200-110311600	Weak transcription	Right Ventricle	heart
2	chr8:110234800-110264200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr8:110235400-110271400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:110235400-110275000	Weak transcription	Fetal Brain Male	brain
5	chr8:110235800-110252600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:110236000-110264200	Weak transcription	Spleen	Spleen
7	chr8:110236000-110265400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr8:110236200-110264200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr8:110236200-110308800	Weak transcription	Thymus	Thymus
10	chr8:110236200-110309200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr8:110236400-110257400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:110236600-110264200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr8:110236600-110344200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr8:110237000-110283800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr8:110237200-110271400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:110237600-110259200	Weak transcription	Brain Anterior Caudate	brain
17	chr8:110237800-110254200	Weak transcription	Fetal Thymus	thymus
18	chr8:110237800-110254200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr8:110237800-110254800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr8:110237800-110264200	Weak transcription	Fetal Lung	lung
21	chr8:110237800-110271400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:110238000-110311600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr8:110238200-110254200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr8:110238200-110264200	Weak transcription	Fetal Muscle Leg	muscle
25	chr8:110238200-110286600	Weak transcription	Ovary	ovary
26	chr8:110239200-110257600	Weak transcription	Lung	lung
27	chr8:110239600-110255200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr8:110239600-110274400	Weak transcription	Pancreas	Pancrea
29	chr8:110239800-110254200	Weak transcription	Liver	Liver
30	chr8:110240400-110274800	Weak transcription	Small Intestine	intestine
31	chr8:110241400-110253800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr8:110241800-110256200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr8:110241800-110295600	Weak transcription	Psoas Muscle	Psoas
34	chr8:110242000-110252800	Weak transcription	HSMM	muscle
35	chr8:110242000-110274400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:110242000-110274600	Weak transcription	HSMMtube	muscle
37	chr8:110242000-110283600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr8:110242200-110252000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr8:110242200-110254200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:110242200-110255800	Weak transcription	Hela-S3	cervix
41	chr8:110242200-110266200	Weak transcription	Fetal Intestine Small	intestine
42	chr8:110242200-110274400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:110242200-110289800	Weak transcription	Colonic Mucosa	Colon
44	chr8:110242400-110252800	Weak transcription	HUVEC	blood vessel
45	chr8:110242400-110255000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr8:110242400-110274200	Weak transcription	NH-A	brain
47	chr8:110242400-110274400	Weak transcription	Gastric	stomach
48	chr8:110242400-110282800	Weak transcription	A549	lung
49	chr8:110242400-110305000	Weak transcription	NHLF	lung
50	chr8:110242600-110291200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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