Variant report

Variant	nsv1025685
Chromosome Location	chr8:99706280-99826236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:184)
Chromatin interactive
region (count:60)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99767855-99768102	K562	blood:	n/a	n/a
2	ARID3A	chr8:99737967-99738396	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:99717819-99718081	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:99787627-99788034	K562	blood:	n/a	n/a
5	ARID3A	chr8:99819786-99820263	K562	blood:	n/a	n/a
6	ARID3A	chr8:99780710-99781281	K562	blood:	n/a	n/a
7	ARID3A	chr8:99717786-99718244	K562	blood:	n/a	n/a
8	ARID3A	chr8:99803222-99803452	K562	blood:	n/a	n/a
9	ATF1	chr8:99774162-99774482	K562	blood:	n/a	n/a
10	ATF1	chr8:99780792-99781251	K562	blood:	n/a	n/a
11	ATF1	chr8:99767808-99768061	K562	blood:	n/a	n/a
12	ATF1	chr8:99793198-99793446	K562	blood:	n/a	n/a
13	ATF1	chr8:99787524-99787978	K562	blood:	n/a	n/a
14	ATF1	chr8:99717793-99718078	K562	blood:	n/a	n/a
15	ATF2	chr8:99746079-99746783	GM12878	blood:	n/a	n/a
16	ATF2	chr8:99823227-99823817	GM12878	blood:	n/a	n/a
17	ATF2	chr8:99757361-99757820	GM12878	blood:	n/a	n/a
18	ATF2	chr8:99740507-99741015	GM12878	blood:	n/a	n/a
19	ATF2	chr8:99740370-99741034	GM12878	blood:	n/a	n/a
20	ATF3	chr8:99780903-99781219	K562	blood:	n/a	n/a
21	BACH1	chr8:99766025-99766040	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:99819851-99820147	K562	blood:	n/a	n/a
23	BATF	chr8:99823433-99823722	GM12878	blood:	n/a	chr8:99823605-99823615 chr8:99823604-99823615
24	BATF	chr8:99740524-99740962	GM12878	blood:	n/a	n/a
25	BATF	chr8:99757385-99757743	GM12878	blood:	n/a	n/a
26	BATF	chr8:99740537-99740972	GM12878	blood:	n/a	n/a
27	BATF	chr8:99757427-99757746	GM12878	blood:	n/a	n/a
28	BATF	chr8:99823441-99823754	GM12878	blood:	n/a	chr8:99823605-99823615 chr8:99823604-99823615
29	BCL11A	chr8:99740475-99740948	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:99820251-99820746	GM12878	blood:	n/a	n/a
31	BCLAF1	chr8:99746189-99746729	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:99821604-99821886	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:99780816-99781259	K562	blood:	n/a	n/a
34	BHLHE40	chr8:99774198-99774430	K562	blood:	n/a	n/a
35	BHLHE40	chr8:99740536-99740957	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:99787601-99787865	K562	blood:	n/a	n/a
37	BRCA1	chr8:99768947-99768992	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr8:99780757-99781359	K562	blood:	n/a	n/a
39	CBX3	chr8:99812382-99812780	K562	blood:	n/a	n/a
40	CBX3	chr8:99737870-99738739	HCT-116	colon:	n/a	n/a
41	CCNT2	chr8:99803191-99803452	K562	blood:	n/a	n/a
42	CCNT2	chr8:99787628-99787940	K562	blood:	n/a	n/a
43	CCNT2	chr8:99780904-99781297	K562	blood:	n/a	n/a
44	CCNT2	chr8:99774169-99774441	K562	blood:	n/a	n/a
45	CEBPB	chr8:99712963-99713280	MCF-7	breast:	n/a	n/a
46	CEBPB	chr8:99774033-99774495	K562	blood:	n/a	n/a
47	CEBPB	chr8:99737965-99738511	A549	lung:	n/a	n/a
48	CEBPB	chr8:99738021-99738292	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:99732045-99732311	A549	lung:	n/a	chr8:99732210-99732227 chr8:99732211-99732224 chr8:99732211-99732224 chr8:99732212-99732223 chr8:99732211-99732222
50	CEBPB	chr8:99777458-99777797	K562	blood:	n/a	chr8:99777619-99777632 chr8:99777619-99777632 chr8:99777620-99777631 chr8:99777619-99777630 chr8:99777619-99777632

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99813010-99813060	PrEC	prostate:	n/a
2	chr8:99813010-99813060	PrEC	prostate:	n/a
3	chr8:99812867-99812917	HepG2	liver:	n/a
4	chr8:99812867-99812917	Hela-S3	cervix:	n/a
5	chr8:99813010-99813060	HRE	kidney:	n/a
6	chr8:99812867-99812917	NHDF-neo	bronchial:	n/a
7	chr8:99738789-99738839	AG04449	skin:	fetal
8	chr8:99738789-99738839	SK-N-MC	brain:	n/a
9	chr8:99812867-99812917	GM19239	blood:	n/a
10	chr8:99812867-99812917	U87	brain:	n/a
11	chr8:99812867-99812917	HL-60	blood:	n/a
12	chr8:99813010-99813060	GM12891	blood:	n/a
13	chr8:99812867-99812917	HRPEpiC	eye:	n/a
14	chr8:99813010-99813060	SK-N-SH	brain:	n/a
15	chr8:99738789-99738839	K562	blood:	n/a
16	chr8:99813010-99813060	HAEpiC	amniotic membrane:	n/a
17	chr8:99812867-99812917	HEEpiC	esophagus:	n/a
18	chr8:99738789-99738839	HAEpiC	amniotic membrane:	n/a
19	chr8:99812867-99812917	GM12878	blood:	n/a
20	chr8:99813010-99813060	NHBE	bronchial:	n/a
21	chr8:99812867-99812917	SKMC	muscle:	n/a
22	chr8:99738789-99738839	IMR90	lung:	fetal
23	chr8:99813010-99813060	HIPEpiC	eye:	n/a
24	chr8:99813010-99813060	T-47D	breast:	n/a
25	chr8:99738789-99738839	AoSMC	blood vessel:	n/a
26	chr8:99813010-99813060	NT2-D1	testis:	n/a
27	chr8:99738789-99738839	SK-N-SH	brain:	n/a
28	chr8:99812867-99812917	GM06990	blood:	n/a
29	chr8:99813010-99813060	LNCaP	prostate:	n/a
30	chr8:99738789-99738839	HIPEpiC	eye:	n/a
31	chr8:99738789-99738839	H1-hESC	embryonic stem cell:	embryo
32	chr8:99738789-99738839	NH-A	brain:	n/a
33	chr8:99738789-99738839	U87	brain:	n/a
34	chr8:99813010-99813060	GM19239	blood:	n/a
35	chr8:99813010-99813060	ECC-1	luminal epithelium:	n/a
36	chr8:99813010-99813060	NB4	blood:	n/a
37	chr8:99738789-99738839	SK-N-SH_RA	brain:	n/a
38	chr8:99813010-99813060	BJ	skin:	n/a
39	chr8:99813010-99813060	NHDF-neo	bronchial:	n/a
40	chr8:99813010-99813060	AoSMC	blood vessel:	n/a
41	chr8:99812867-99812917	BJ	skin:	n/a
42	chr8:99812867-99812917	RPTEC	kidney:	n/a
43	chr8:99738789-99738839	SAEC	small airway:	n/a
44	chr8:99813010-99813060	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:99812867-99812917	PANC-1	pancreas:	n/a
46	chr8:99738789-99738839	HPAEpiC	pulmonary alveolar:	n/a
47	chr8:99738789-99738839	GM06990	blood:	n/a
48	chr8:99738789-99738839	Hepatocyte	liver:	n/a
49	chr8:99812867-99812917	NB4	blood:	n/a
50	chr8:99813010-99813060	HepG2	liver:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:99717618..99718408-chr8:100009817..100010611,5	MCF-7	breast:
2	chr8:99778640..99782967-chr8:99784164..99787375,4	MCF-7	breast:
3	chr8:99808268..99810825-chr8:99820563..99822919,2	K562	blood:
4	chr8:99730740..99733168-chr8:99733468..99735673,2	MCF-7	breast:
5	chr8:99766460..99769407-chr8:99772354..99774228,2	K562	blood:
6	chr8:99717940..99718590-chr8:99852903..99853734,2	K562	blood:
7	chr8:99717210..99719465-chr8:99720134..99722023,2	K562	blood:
8	chr8:99823479..99826081-chr8:99837327..99838952,2	MCF-7	breast:
9	chr8:99818410..99822032-chr8:99835031..99838163,3	K562	blood:
10	chr8:99731269..99733203-chr8:99734939..99736957,2	MCF-7	breast:
11	chr8:99717164..99718794-chr8:100022848..100024966,2	K562	blood:
12	chr8:99805802..99807780-chr8:99809302..99811541,2	K562	blood:
13	chr8:99717210..99719507-chr8:99720013..99722023,2	K562	blood:
14	chr8:99714559..99716252-chr8:99834960..99836799,2	MCF-7	breast:
15	chr8:99717210..99719507-chr8:99720013..99722023,2	K562	blood:
16	chr8:99739438..99742023-chr8:99742698..99744611,2	MCF-7	breast:
17	chr8:99738155..99743366-chr8:99746593..99750391,4	MCF-7	breast:
18	chr8:99792612..99794533-chr8:99808664..99811217,2	MCF-7	breast:
19	chr8:99822165..99824664-chr8:99835856..99837909,2	K562	blood:
20	chr8:99808268..99810825-chr8:99820563..99822919,2	K562	blood:
21	chr8:99735526..99738976-chr8:99742014..99743636,3	K562	blood:
22	chr8:99736975..99738718-chr8:99836391..99838419,2	MCF-7	breast:
23	chr8:99738155..99743366-chr8:99746593..99750391,4	MCF-7	breast:
24	chr8:99717523..99718404-chr8:99953348..99953880,2	MCF-7	breast:
25	chr8:99739438..99742023-chr8:99742698..99744611,2	MCF-7	breast:
26	chr8:99713408..99715331-chr8:99956897..99958843,2	MCF-7	breast:
27	chr8:99714532..99716117-chr8:99964323..99966058,2	MCF-7	breast:
28	chr8:99739323..99741904-chr8:99743613..99745750,2	K562	blood:
29	chr8:99717372..99718063-chr8:99877610..99878487,2	MCF-7	breast:
30	chr8:99742630..99744951-chr8:99747576..99749535,2	MCF-7	breast:
31	chr8:99569567..99570631-chr8:99717657..99718318,3	MCF-7	breast:
32	chr8:99766460..99769407-chr8:99772354..99774228,2	K562	blood:
33	chr8:99717696..99718389-chr8:99852834..99853347,2	MCF-7	breast:
34	chr8:99766623..99769438-chr8:99840574..99842500,2	K562	blood:
35	chr8:99774390..99776428-chr8:99778183..99780400,2	K562	blood:
36	chr8:99735526..99738976-chr8:99742014..99743636,3	K562	blood:
37	chr8:99570440..99572311-chr8:99716067..99717678,2	MCF-7	breast:
38	chr8:99748081..99750351-chr8:99836691..99838488,2	MCF-7	breast:
39	chr8:99820768..99823358-chr8:99828939..99831615,2	MCF-7	breast:
40	chr8:99717096..99719428-chr8:99954541..99958044,4	MCF-7	breast:
41	chr8:99739323..99741904-chr8:99743613..99745750,2	K562	blood:
42	chr8:99757864..99758569-chrX:66831854..66832517,2	MCF-7	breast:
43	chr8:99739291..99741165-chr8:99741627..99744092,2	MCF-7	breast:
44	chr8:99778640..99782967-chr8:99784164..99787375,4	MCF-7	breast:
45	chr8:99739198..99741801-chr8:99746895..99749270,2	MCF-7	breast:
46	chr8:99717734..99718483-chr8:100009688..100010929,4	MCF-7	breast:
47	chr8:99782738..99784840-chr8:99792022..99794290,2	MCF-7	breast:
48	chr8:99825787..99827517-chr8:99827594..99829376,2	MCF-7	breast:
49	chr8:99774390..99776428-chr8:99778183..99780400,2	K562	blood:
50	chr8:99730740..99733168-chr8:99733468..99735673,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPL19P14	TF binding region
RPL19P14	CpG island
ENSG00000104375	chromatin interactions
ENSG00000240870	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000164920	chromatin interactions

Extended variants
information (count: 4295 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4295 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573033820	chr8:99706345-99706346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs185859313	chr8:99706387-99706388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188951789	chr8:99706418-99706419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77824885	chr8:99706450-99706451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146340127	chr8:99706461-99706462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564083433	chr8:99706463-99706464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181749088	chr8:99706469-99706470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559966092	chr8:99706494-99706495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546654584	chr8:99706498-99706499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560270198	chr8:99706544-99706545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139587205	chr8:99706582-99706583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370827497	chr8:99706591-99706592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75406403	chr8:99706597-99706598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568566803	chr8:99706630-99706631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187563713	chr8:99706644-99706645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551010406	chr8:99706661-99706662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570789606	chr8:99706669-99706670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539431772	chr8:99706685-99706686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552977983	chr8:99706702-99706703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545121070	chr8:99706732-99706733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144208512	chr8:99706733-99706734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555491429	chr8:99706734-99706735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575372597	chr8:99706741-99706742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544462253	chr8:99706775-99706776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564211885	chr8:99706779-99706780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199815709	chr8:99706783-99706784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560622906	chr8:99706784-99706785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192051165	chr8:99706787-99706788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560234230	chr8:99706797-99706798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528953498	chr8:99706808-99706809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548804491	chr8:99706850-99706851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200463065	chr8:99706865-99706866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182766215	chr8:99706874-99706875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551188733	chr8:99706886-99706887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570786936	chr8:99706887-99706888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539790985	chr8:99706902-99706903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546580212	chr8:99706905-99706906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566531423	chr8:99706938-99706939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535915513	chr8:99706950-99706951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555597025	chr8:99706980-99706981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575728031	chr8:99707014-99707015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537624203	chr8:99707028-99707029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374229018	chr8:99707040-99707041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577993651	chr8:99707041-99707042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540539974	chr8:99707060-99707061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201151410	chr8:99707075-99707076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553752463	chr8:99707130-99707131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186109076	chr8:99707140-99707141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190225458	chr8:99707148-99707149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562426630	chr8:99707153-99707154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
head and neck squamous cell carcinoma	19451471	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
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1436 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99676200-99738200	Weak transcription	Fetal Kidney	kidney
2	chr8:99683400-99712600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:99683600-99712200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr8:99683600-99720400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:99683600-99738000	Weak transcription	NHEK	skin
6	chr8:99684400-99712600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:99695200-99714600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr8:99696000-99712000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:99699800-99712000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:99699800-99712200	Weak transcription	Fetal Stomach	stomach
11	chr8:99699800-99712200	Weak transcription	Ovary	ovary
12	chr8:99699800-99712600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:99699800-99721000	Weak transcription	NHDF-Ad	bronchial
14	chr8:99699800-99721200	Weak transcription	Pancreas	Pancrea
15	chr8:99699800-99721400	Weak transcription	Placenta	Placenta
16	chr8:99699800-99722400	Weak transcription	Lung	lung
17	chr8:99699800-99722600	Weak transcription	Left Ventricle	heart
18	chr8:99700200-99713000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr8:99700400-99710200	Weak transcription	Fetal Heart	heart
20	chr8:99701000-99712400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:99701200-99712600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr8:99701200-99713000	Weak transcription	HSMM	muscle
23	chr8:99701400-99712200	Weak transcription	Fetal Intestine Large	intestine
24	chr8:99702000-99712000	Weak transcription	Fetal Intestine Small	intestine
25	chr8:99702000-99722200	Weak transcription	Fetal Muscle Leg	muscle
26	chr8:99702400-99712800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:99702400-99712800	Weak transcription	Fetal Lung	lung
28	chr8:99702800-99721200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr8:99703400-99712200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:99703400-99712200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr8:99703600-99714600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr8:99703800-99716200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr8:99704400-99722400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr8:99704600-99706400	Weak transcription	Adipose Nuclei	Adipose
35	chr8:99704600-99713000	Weak transcription	Liver	Liver
36	chr8:99704800-99713000	Weak transcription	Gastric	stomach
37	chr8:99705600-99714600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr8:99705800-99706400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr8:99706000-99712800	Weak transcription	GM12878-XiMat	blood
40	chr8:99706000-99722400	Weak transcription	Aorta	Aorta
41	chr8:99706000-99725000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr8:99706200-99712600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:99706400-99722200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr8:99707400-99712400	Weak transcription	Adipose Nuclei	Adipose
45	chr8:99709600-99714200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:99710600-99712200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:99710600-99712800	Weak transcription	Colonic Mucosa	Colon
48	chr8:99711000-99722200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr8:99711400-99713000	Weak transcription	Right Ventricle	heart
50	chr8:99711400-99717600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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