Variant report

Variant	nsv1026755
Chromosome Location	chr8:103676970-103728556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:244)
Chromatin interactive
region (count:124)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:103697962-103697985	HepG2	liver:	n/a	n/a
2	ATF1	chr8:103688489-103688678	K562	blood:	n/a	n/a
3	BACH1	chr8:103714079-103714402	K562	blood:	n/a	n/a
4	BACH1	chr8:103694866-103695097	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:103694858-103694965	K562	blood:	n/a	n/a
6	BHLHE40	chr8:103700615-103700676	K562	blood:	n/a	n/a
7	BHLHE40	chr8:103698218-103698488	K562	blood:	n/a	n/a
8	BRCA1	chr8:103698166-103698499	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr8:103713924-103714813	HCT-116	colon:	n/a	n/a
10	CBX3	chr8:103689287-103689718	K562	blood:	n/a	n/a
11	CBX3	chr8:103689283-103689680	K562	blood:	n/a	n/a
12	CCNT2	chr8:103698181-103698442	K562	blood:	n/a	n/a
13	CEBPB	chr8:103723272-103723471	A549	lung:	n/a	n/a
14	CEBPB	chr8:103689640-103689827	K562	blood:	n/a	n/a
15	CEBPB	chr8:103705406-103705660	A549	lung:	n/a	chr8:103705526-103705539 chr8:103705527-103705538
16	CEBPB	chr8:103684358-103684482	K562	blood:	n/a	chr8:103684433-103684444 chr8:103684433-103684444
17	CEBPB	chr8:103697059-103697201	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:103714598-103715102	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:103678153-103678331	HepG2	liver:	n/a	chr8:103678235-103678246
20	CEBPB	chr8:103714700-103715100	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr8:103689628-103689865	K562	blood:	n/a	n/a
22	CEBPB	chr8:103689676-103689844	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:103697907-103698587	Hela-S3	cervix:	n/a	chr8:103698095-103698107
24	CEBPB	chr8:103697078-103697124	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:103698148-103698427	K562	blood:	n/a	n/a
26	CEBPB	chr8:103704868-103705700	IMR90	lung:	n/a	chr8:103705526-103705539 chr8:103705527-103705538
27	CEBPB	chr8:103705388-103705710	HepG2	liver:	n/a	chr8:103705526-103705539 chr8:103705527-103705538
28	CEBPB	chr8:103696953-103697255	K562	blood:	n/a	n/a
29	CEBPB	chr8:103697048-103697094	HepG2	liver:	n/a	n/a
30	CHD2	chr8:103698063-103698446	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr8:103711128-103711152	K562	blood:	n/a	chr8:103711135-103711144
32	CTCF	chr8:103694920-103695070	RPTEC	kidney:	n/a	n/a
33	CTCF	chr8:103694880-103695030	RPTEC	kidney:	n/a	n/a
34	CTCF	chr8:103693987-103694160	HepG2	liver:	n/a	chr8:103694064-103694085 chr8:103694062-103694080 chr8:103694063-103694079
35	CTCF	chr8:103694740-103694890	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr8:103694880-103695030	NHEK	skin:	n/a	n/a
37	CTCF	chr8:103714245-103714432	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr8:103714158-103714461	GM12878	blood:	n/a	n/a
39	CTCF	chr8:103694860-103695010	GM12864	blood:	n/a	n/a
40	CTCF	chr8:103714280-103714430	GM06990	blood:	n/a	n/a
41	CTCF	chr8:103714260-103714410	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr8:103697760-103697910	NHLF	lung:	n/a	n/a
43	CTCF	chr8:103714153-103714499	IMR90	lung:	n/a	n/a
44	CTCF	chr8:103694860-103695010	GM12873	blood:	n/a	n/a
45	CTCF	chr8:103694880-103695030	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr8:103694880-103695030	GM12867	blood:	n/a	n/a
47	CTCF	chr8:103714249-103714406	Medullo	brain:	n/a	n/a
48	CTCF	chr8:103714200-103714350	HepG2	liver:	n/a	n/a
49	CTCF	chr8:103704080-103704230	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr8:103714320-103714470	HCM	heart:	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	chr8:103714592-103714642	Hepatocyte	liver:	n/a
2	chr8:103705294-103705344	BE2_C	brain:	n/a
3	chr8:103698908-103698958	PFSK-1	brain:	n/a
4	chr8:103714592-103714642	SK-N-SH_RA	brain:	n/a
5	chr8:103679078-103679128	GM12891	blood:	n/a
6	chr8:103714592-103714642	T-47D	breast:	n/a
7	chr8:103714592-103714642	BJ	skin:	n/a
8	chr8:103698908-103698958	RPTEC	kidney:	n/a
9	chr8:103705294-103705344	ProgFib	skin:	n/a
10	chr8:103705294-103705344	NH-A	brain:	n/a
11	chr8:103698908-103698958	HCM	heart:	n/a
12	chr8:103714592-103714642	K562	blood:	n/a
13	chr8:103679078-103679128	HCF	heart:	n/a
14	chr8:103698908-103698958	NT2-D1	testis:	n/a
15	chr8:103679078-103679128	BJ	skin:	n/a
16	chr8:103714592-103714642	HRPEpiC	eye:	n/a
17	chr8:103679078-103679128	H1-hESC	embryonic stem cell:	embryo
18	chr8:103714592-103714642	NB4	blood:	n/a
19	chr8:103705294-103705344	RPTEC	kidney:	n/a
20	chr8:103705294-103705344	NB4	blood:	n/a
21	chr8:103705294-103705344	PrEC	prostate:	n/a
22	chr8:103698908-103698958	LNCaP	prostate:	n/a
23	chr8:103705294-103705344	AG04449	skin:	fetal
24	chr8:103705294-103705344	SAEC	small airway:	n/a
25	chr8:103698908-103698958	HAEpiC	amniotic membrane:	n/a
26	chr8:103698908-103698958	GM19239	blood:	n/a
27	chr8:103705294-103705344	HRCEpiC	kidney:	n/a
28	chr8:103698908-103698958	SK-N-MC	brain:	n/a
29	chr8:103698908-103698958	ProgFib	skin:	n/a
30	chr8:103679078-103679128	NHBE	bronchial:	n/a
31	chr8:103705294-103705344	Jurkat	blood:	n/a
32	chr8:103698908-103698958	HUVEC	blood vessel:	n/a
33	chr8:103705294-103705344	GM12892	blood:	n/a
34	chr8:103698908-103698958	BJ	skin:	n/a
35	chr8:103714592-103714642	RPTEC	kidney:	n/a
36	chr8:103698908-103698958	AG04450	lung:	fetal
37	chr8:103705294-103705344	NHBE	bronchial:	n/a
38	chr8:103705294-103705344	NHDF-neo	bronchial:	n/a
39	chr8:103705294-103705344	GM12891	blood:	n/a
40	chr8:103698908-103698958	PANC-1	pancreas:	n/a
41	chr8:103679078-103679128	HNPCEpiC	eye:	n/a
42	chr8:103705294-103705344	IMR90	lung:	fetal
43	chr8:103714592-103714642	HCT-116	colon:	n/a
44	chr8:103714592-103714642	HIPEpiC	eye:	n/a
45	chr8:103705294-103705344	SKMC	muscle:	n/a
46	chr8:103679078-103679128	CMK	blood:	n/a
47	chr8:103714592-103714642	HUVEC	blood vessel:	n/a
48	chr8:103705294-103705344	HepG2	liver:	n/a
49	chr8:103705294-103705344	GM19239	blood:	n/a
50	chr8:103679078-103679128	LNCaP	prostate:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:103674994..103677007-chr8:103818020..103820756,2	MCF-7	breast:
2	chr8:103722346..103725936-chr8:103727118..103730483,4	MCF-7	breast:
3	chr8:103701636..103704144-chr8:103741047..103743946,2	MCF-7	breast:
4	chr8:102122358..102124025-chr8:103679189..103680764,2	K562	blood:
5	chr8:103725181..103726869-chr8:103817366..103820357,2	MCF-7	breast:
6	chr8:103698102..103699889-chr8:103699942..103703223,3	MCF-7	breast:
7	chr8:103713648..103714314-chr8:103819880..103820381,2	MCF-7	breast:
8	chr8:103676174..103681192-chr8:103681793..103685346,6	K562	blood:
9	chr8:103722346..103725936-chr8:103727118..103730483,4	MCF-7	breast:
10	chr8:103690114..103692545-chr8:103692665..103694981,3	MCF-7	breast:
11	chr8:103669620..103672058-chr8:103696948..103699668,2	K562	blood:
12	chr8:103666427..103669276-chr8:103709893..103712478,4	K562	blood:
13	chr8:103721548..103724506-chr8:103725385..103726893,2	MCF-7	breast:
14	chr8:103701249..103703265-chr8:103716170..103718966,2	K562	blood:
15	chr8:103664622..103666232-chr8:103692078..103693686,2	K562	blood:
16	chr8:103668018..103669942-chr8:103695830..103697855,2	MCF-7	breast:
17	chr8:103683405..103685038-chr8:103689375..103691128,2	MCF-7	breast:
18	chr8:103681131..103683313-chr8:103821848..103824380,2	MCF-7	breast:
19	chr8:103666298..103670296-chr8:103678043..103682174,5	K562	blood:
20	chr8:103714554..103716653-chr8:103768887..103770568,2	MCF-7	breast:
21	chr8:103695038..103697109-chr8:103734957..103736636,2	MCF-7	breast:
22	chr8:103676656..103679236-chr8:103715364..103718387,3	MCF-7	breast:
23	chr8:103709537..103712892-chr8:103713255..103715584,4	K562	blood:
24	chr8:103690697..103697091-chr8:103702860..103706318,8	MCF-7	breast:
25	chr8:103686012..103689687-chr8:103690179..103693773,3	K562	blood:
26	chr8:103724627..103726716-chr8:103817998..103821829,3	MCF-7	breast:
27	chr8:103690697..103697091-chr8:103702860..103706318,8	MCF-7	breast:
28	chr8:103695977..103697957-chr8:103799745..103801613,2	MCF-7	breast:
29	chr8:103693701..103696201-chr8:103709941..103712706,2	MCF-7	breast:
30	chr8:103676656..103679236-chr8:103715364..103718387,3	MCF-7	breast:
31	chr8:103713306..103716801-chr8:103817388..103820104,3	K562	blood:
32	chr8:103683074..103685315-chr8:103686786..103688306,2	K562	blood:
33	chr8:103691078..103693672-chr8:103696647..103699139,2	MCF-7	breast:
34	chr8:103680920..103683026-chr8:103707719..103709439,2	MCF-7	breast:
35	chr8:103713778..103716086-chr8:103819862..103822357,3	MCF-7	breast:
36	chr8:103677991..103679955-chr8:103687094..103689017,2	K562	blood:
37	chr8:103695957..103698904-chr8:103817763..103821166,3	K562	blood:
38	chr17:13131311..13131962-chr8:103714196..103715085,2	MCF-7	breast:
39	chr8:103728137..103730648-chr8:103739686..103741368,2	MCF-7	breast:
40	chr8:103710311..103712892-chr8:103713398..103715584,2	K562	blood:
41	chr8:103676147..103677915-chr8:103792093..103794754,2	K562	blood:
42	chr8:103728412..103729988-chr8:103738738..103740812,2	MCF-7	breast:
43	chr8:103683405..103685038-chr8:103689375..103691128,2	MCF-7	breast:
44	chr8:103705965..103707674-chr8:103821217..103823842,2	K562	blood:
45	chr8:103694162..103696832-chr8:103715442..103717572,2	MCF-7	breast:
46	chr8:103665663..103668046-chr8:103702475..103704422,2	MCF-7	breast:
47	chr8:103669378..103671910-chr8:103714543..103716720,2	MCF-7	breast:
48	chr8:103665593..103668276-chr8:103688725..103691087,4	K562	blood:
49	chr8:103725029..103726872-chr8:103728215..103730220,2	K562	blood:
50	chr8:103708175..103710058-chr8:103712821..103714714,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF10-4	chr8:103700545-103700806	NONHSAT128107
2	lnc-ODF1-3	chr8:103698638-103699234	NONHSAT128106
3	lnc-KLF10-4	chr8:103700968-103701134	NONHSAT128107

No data

Variant related genes	Relation type
ENSG00000250684	TF binding region
ENSG00000250684	CpG island
ENSG00000155090	chromatin interactions
ENSG00000250684	chromatin interactions
ENSG00000253669	chromatin interactions

Extended variants
information (count: 1997 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145877876	chr8:103676973-103676974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552199872	chr8:103676997-103676998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552324580	chr8:103677015-103677016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570839087	chr8:103677119-103677120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538389506	chr8:103677132-103677133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs556685610	chr8:103677196-103677197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569076005	chr8:103677222-103677223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536032166	chr8:103677223-103677224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371083467	chr8:103677227-103677228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573088043	chr8:103677233-103677234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540497696	chr8:103677282-103677283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368838000	chr8:103677284-103677285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192356399	chr8:103677292-103677293	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs183692279	chr8:103677323-103677324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528111918	chr8:103677326-103677327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562200893	chr8:103677382-103677383	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372290327	chr8:103677400-103677401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112193168	chr8:103677453-103677454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542026139	chr8:103677568-103677569	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139835350	chr8:103677643-103677644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530499588	chr8:103677709-103677710	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551200938	chr8:103677711-103677712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35456877	chr8:103677718-103677719	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2436936	chr8:103677723-103677724	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186580254	chr8:103677729-103677730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199908319	chr8:103677736-103677737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377424784	chr8:103677746-103677747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149860920	chr8:103677747-103677748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs71276464	chr8:103677765-103677766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs71574067	chr8:103677823-103677824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs79115279	chr8:103677826-103677827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs71276465	chr8:103677852-103677853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201680295	chr8:103677853-103677854	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372571196	chr8:103677872-103677873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs28869021	chr8:103677882-103677883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568531210	chr8:103677897-103677898	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535927503	chr8:103677898-103677899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548110431	chr8:103677899-103677900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566654162	chr8:103677983-103677984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533879210	chr8:103677994-103677995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558387936	chr8:103678003-103678004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576436346	chr8:103678010-103678011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373742226	chr8:103678026-103678027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537424036	chr8:103678080-103678081	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555858369	chr8:103678081-103678082	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs192980622	chr8:103678102-103678103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184711543	chr8:103678109-103678110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs147681328	chr8:103678120-103678121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs572591585	chr8:103678141-103678142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142482820	chr8:103678209-103678210	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	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
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103670800-103678800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:103671000-103678600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:103671200-103678400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr8:103674600-103679000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:103675400-103677000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:103675400-103678000	Weak transcription	Liver	Liver
7	chr8:103675400-103678400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr8:103675400-103678400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr8:103675400-103678800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr8:103675400-103679000	Weak transcription	Hela-S3	cervix
11	chr8:103675400-103682600	Weak transcription	Right Ventricle	heart
12	chr8:103675400-103698200	Weak transcription	Osteobl	bone
13	chr8:103675600-103677000	Weak transcription	Fetal Intestine Small	intestine
14	chr8:103675600-103678000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr8:103675600-103678200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr8:103675600-103678400	Weak transcription	Placenta	Placenta
17	chr8:103675600-103679800	Weak transcription	K562	blood
18	chr8:103675600-103692800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr8:103675800-103688200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr8:103676000-103678600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:103677000-103679000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr8:103678000-103678800	Enhancers	Duodenum Mucosa	Duodenum
23	chr8:103678200-103678400	Enhancers	Liver	Liver
24	chr8:103678200-103679200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr8:103678200-103679400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:103678400-103678600	Enhancers	Fetal Intestine Large	intestine
27	chr8:103678400-103679200	Enhancers	Placenta	Placenta
28	chr8:103678400-103679800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:103678400-103680000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:103678400-103680000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:103678600-103679400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:103678600-103679400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr8:103678600-103679600	Enhancers	Primary B cells from peripheral blood	blood
34	chr8:103678600-103680000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr8:103678800-103680000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr8:103678800-103680000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:103678800-103680200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:103679000-103679200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr8:103679000-103679800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr8:103679200-103681600	Weak transcription	Placenta	Placenta
41	chr8:103679400-103689400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr8:103679800-103680400	Enhancers	K562	blood
43	chr8:103679800-103706400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:103681600-103681800	Enhancers	Placenta	Placenta
45	chr8:103682600-103683000	Enhancers	Right Ventricle	heart
46	chr8:103682600-103683600	Enhancers	Fetal Muscle Trunk	muscle
47	chr8:103682600-103684000	Enhancers	Fetal Muscle Leg	muscle
48	chr8:103683000-103683600	Enhancers	Adipose Nuclei	Adipose
49	chr8:103686000-103686600	Enhancers	Primary T cells from cord blood	blood
50	chr8:103686000-103687000	Enhancers	Primary T helper cells PMA-I stimulated	--

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