Variant report

Variant	nsv6342
Chromosome Location	chr8:107644092-107688898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:771)
CpG islands
(count:672)
Chromatin interactive
region (count:59)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:107655909-107656088	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:107669496-107670184	K562	blood:	n/a	n/a
3	ATF1	chr8:107672077-107672403	K562	blood:	n/a	n/a
4	ATF2	chr8:107679899-107681267	GM12878	blood:	n/a	n/a
5	ATF2	chr8:107682037-107682595	GM12878	blood:	n/a	n/a
6	ATF2	chr8:107670513-107671278	GM12878	blood:	n/a	n/a
7	ATF2	chr8:107679984-107681167	GM12878	blood:	n/a	n/a
8	ATF2	chr8:107670521-107671235	GM12878	blood:	n/a	n/a
9	BATF	chr8:107670789-107671191	GM12878	blood:	n/a	chr8:107671069-107671078
10	BATF	chr8:107680706-107681133	GM12878	blood:	n/a	n/a
11	BATF	chr8:107670908-107671186	GM12878	blood:	n/a	chr8:107671069-107671078
12	BATF	chr8:107680198-107680577	GM12878	blood:	n/a	n/a
13	BATF	chr8:107682117-107682451	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:107682100-107682488	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:107680119-107680471	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:107682174-107682418	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:107670867-107671123	GM12878	blood:	n/a	chr8:107670996-107671005
18	BCL11A	chr8:107670831-107671237	GM12878	blood:	n/a	chr8:107670850-107670859 chr8:107670996-107671005
19	BCL3	chr8:107669738-107670258	A549	lung:	n/a	n/a
20	BCL3	chr8:107669740-107670301	A549	lung:	n/a	n/a
21	BCLAF1	chr8:107679899-107680383	GM12878	blood:	n/a	n/a
22	BCLAF1	chr8:107682005-107682528	GM12878	blood:	n/a	n/a
23	BCLAF1	chr8:107669493-107669928	GM12878	blood:	n/a	n/a
24	BCLAF1	chr8:107670828-107671286	GM12878	blood:	n/a	chr8:107670850-107670859 chr8:107670996-107671005
25	BCLAF1	chr8:107670701-107671279	GM12878	blood:	n/a	chr8:107670850-107670859 chr8:107670996-107671005
26	BHLHE40	chr8:107669643-107671219	GM12878	blood:	n/a	chr8:107670549-107670565 chr8:107670557-107670573
27	BHLHE40	chr8:107669652-107670233	K562	blood:	n/a	n/a
28	BHLHE40	chr8:107669779-107670156	A549	lung:	n/a	n/a
29	BHLHE40	chr8:107680082-107680725	GM12878	blood:	n/a	n/a
30	BHLHE40	chr8:107669620-107670826	HepG2	liver:	n/a	chr8:107670549-107670565 chr8:107670557-107670573
31	BRCA1	chr8:107669831-107670143	HepG2	liver:	n/a	n/a
32	BRCA1	chr8:107671160-107671169	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr8:107669334-107670094	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr8:107670518-107670948	K562	blood:	n/a	n/a
35	CBX3	chr8:107685992-107686375	K562	blood:	n/a	n/a
36	CBX3	chr8:107685965-107686413	K562	blood:	n/a	n/a
37	CBX3	chr8:107669499-107670421	K562	blood:	n/a	n/a
38	CCNT2	chr8:107669576-107670688	K562	blood:	n/a	n/a
39	CEBPB	chr8:107656316-107656669	IMR90	lung:	n/a	chr8:107656476-107656487 chr8:107656475-107656488 chr8:107656475-107656488
40	CEBPB	chr8:107676837-107676901	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:107645372-107645572	K562	blood:	n/a	chr8:107645514-107645527 chr8:107645516-107645527 chr8:107645514-107645527 chr8:107645514-107645527
42	CEBPB	chr8:107663145-107663362	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:107656321-107656666	A549	lung:	n/a	chr8:107656476-107656487 chr8:107656475-107656488 chr8:107656475-107656488
44	CEBPB	chr8:107655876-107656663	HepG2	liver:	n/a	chr8:107656476-107656487 chr8:107656475-107656488 chr8:107656475-107656488
45	CEBPB	chr8:107656386-107656588	H1-hESC	embryonic stem cell:	n/a	chr8:107656476-107656487 chr8:107656475-107656488 chr8:107656475-107656488
46	CEBPB	chr8:107669542-107670971	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr8:107656308-107656651	K562	blood:	n/a	chr8:107656476-107656487 chr8:107656475-107656488 chr8:107656475-107656488
48	CEBPB	chr8:107679930-107681336	GM12878	blood:	n/a	n/a
49	CEBPD	chr8:107669613-107669865	HepG2	liver:	n/a	n/a
50	CHD1	chr8:107669064-107671535	IMR90	lung:	n/a	chr8:107669794-107669804

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107666942-107666992	HEK293	kidney:	embryo
2	chr8:107666942-107666992	HEK293	kidney:	embryo
3	chr8:107670759-107670809	HL-60	blood:	n/a
4	chr8:107669856-107669906	SK-N-SH_RA	brain:	n/a
5	chr8:107669906-107669956	IMR90	lung:	fetal
6	chr8:107669783-107669833	AG04450	lung:	fetal
7	chr8:107672853-107672903	SK-N-MC	brain:	n/a
8	chr8:107676292-107676342	SAEC	small airway:	n/a
9	chr8:107670759-107670809	AG04450	lung:	fetal
10	chr8:107669778-107669828	Hepatocyte	liver:	n/a
11	chr8:107669787-107669837	AG09319	gingival:	n/a
12	chr8:107670759-107670809	HRPEpiC	eye:	n/a
13	chr8:107666942-107666992	BE2_C	brain:	n/a
14	chr8:107669787-107669837	Hepatocyte	liver:	n/a
15	chr8:107670759-107670809	BE2_C	brain:	n/a
16	chr8:107670161-107670211	SAEC	small airway:	n/a
17	chr8:107669906-107669956	NHBE	bronchial:	n/a
18	chr8:107669783-107669833	T-47D	breast:	n/a
19	chr8:107670161-107670211	HMEC	breast:	n/a
20	chr8:107669856-107669906	PANC-1	pancreas:	n/a
21	chr8:107672853-107672903	AG10803	skin:	n/a
22	chr8:107672853-107672903	HRPEpiC	eye:	n/a
23	chr8:107670759-107670809	HCT-116	colon:	n/a
24	chr8:107670358-107670408	HIPEpiC	eye:	n/a
25	chr8:107669856-107669906	HRPEpiC	eye:	n/a
26	chr8:107670759-107670809	HMEC	breast:	n/a
27	chr8:107669783-107669833	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:107669856-107669906	ECC-1	luminal epithelium:	n/a
29	chr8:107669783-107669833	IMR90	lung:	fetal
30	chr8:107670358-107670408	HCF	heart:	n/a
31	chr8:107672853-107672903	SK-N-SH	brain:	n/a
32	chr8:107670161-107670211	HRE	kidney:	n/a
33	chr8:107670759-107670809	AG09319	gingival:	n/a
34	chr8:107666942-107666992	AG10803	skin:	n/a
35	chr8:107669906-107669956	AG04449	skin:	fetal
36	chr8:107669778-107669828	HCPEpiC	choroid plexus:	n/a
37	chr8:107669856-107669906	AG09309	skin:	n/a
38	chr8:107669856-107669906	PFSK-1	brain:	n/a
39	chr8:107666942-107666992	HL-60	blood:	n/a
40	chr8:107672853-107672903	SK-N-SH_RA	brain:	n/a
41	chr8:107669778-107669828	HEK293	kidney:	embryo
42	chr8:107669906-107669956	PANC-1	pancreas:	n/a
43	chr8:107672853-107672903	HEEpiC	esophagus:	n/a
44	chr8:107670358-107670408	HRCEpiC	kidney:	n/a
45	chr8:107669787-107669837	LNCaP	prostate:	n/a
46	chr8:107670759-107670809	Hela-S3	cervix:	n/a
47	chr8:107670759-107670809	GM06990	blood:	n/a
48	chr8:107669906-107669956	HepG2	liver:	n/a
49	chr8:107669787-107669837	MCF-7	breast:	n/a
50	chr8:107666942-107666992	HRPEpiC	eye:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:107661627..107663921-chr8:107666779..107668430,2	K562	blood:
2	chr8:107646939..107648517-chr8:107654197..107656388,2	K562	blood:
3	chr8:107686163..107688960-chr8:107711945..107714088,2	K562	blood:
4	chr8:107665950..107668451-chr8:107679150..107681504,2	K562	blood:
5	chr8:107652178..107654915-chr8:107656607..107660694,3	MCF-7	breast:
6	chr8:107655517..107658061-chr8:107665588..107668318,2	K562	blood:
7	chr8:107658421..107660854-chr8:107669209..107671356,2	MCF-7	breast:
8	chr8:107661308..107663122-chr8:107664022..107665824,2	MCF-7	breast:
9	chr8:107661322..107665334-chr8:107667515..107672070,5	MCF-7	breast:
10	chr8:107675484..107677313-chr8:107687976..107690913,2	K562	blood:
11	chr8:107645119..107648350-chr8:107651625..107653934,3	MCF-7	breast:
12	chr8:107651808..107653690-chr8:107657768..107660605,2	K562	blood:
13	chr8:107642362..107644036-chr8:107644982..107647021,2	MCF-7	breast:
14	chr8:107635982..107636832-chr8:107655490..107656098,4	MCF-7	breast:
15	chr8:107659254..107661687-chr8:107668405..107671504,3	K562	blood:
16	chr8:107650778..107653806-chr8:107654268..107656995,3	MCF-7	breast:
17	chr8:107665950..107668451-chr8:107679150..107681504,2	K562	blood:
18	chr8:107680913..107683388-chr8:107685068..107687950,2	K562	blood:
19	chr8:107678069..107680134-chr8:107683675..107685585,2	K562	blood:
20	chr8:107669240..107670746-chr8:107683326..107685917,3	MCF-7	breast:
21	chr8:107650778..107653806-chr8:107654268..107656995,3	MCF-7	breast:
22	chr8:107655640..107658655-chr8:107669482..107672339,4	MCF-7	breast:
23	chr8:107670148..107672369-chr8:107708725..107710422,2	MCF-7	breast:
24	chr8:107627292..107630232-chr8:107665410..107668409,2	MCF-7	breast:
25	chr8:107677870..107679876-chr8:107686793..107689768,2	MCF-7	breast:
26	chr8:107655118..107656989-chr8:107657155..107658925,2	MCF-7	breast:
27	chr8:107677870..107679876-chr8:107686793..107689768,2	MCF-7	breast:
28	chr8:107646860..107649484-chr8:107667686..107669336,2	MCF-7	breast:
29	chr8:107652584..107654414-chr8:107662891..107664399,2	MCF-7	breast:
30	chr8:107685113..107687431-chr8:107693590..107695570,2	K562	blood:
31	chr8:107628700..107633249-chr8:107668680..107671616,7	MCF-7	breast:
32	chr8:107646860..107649484-chr8:107667686..107669336,2	MCF-7	breast:
33	chr8:107659105..107661326-chr8:107669258..107671281,2	K562	blood:
34	chr8:107661627..107663921-chr8:107666779..107668430,2	K562	blood:
35	chr8:107678069..107680134-chr8:107683675..107685585,2	K562	blood:
36	chr8:107628207..107632288-chr8:107667853..107671892,6	MCF-7	breast:
37	chr8:107667927..107672716-chr8:107687873..107691651,4	MCF-7	breast:
38	chr8:107655292..107657539-chr8:107669144..107670814,2	K562	blood:
39	chr8:107639670..107643693-chr8:107648577..107651527,3	MCF-7	breast:
40	chr8:107645119..107648350-chr8:107651625..107653934,3	MCF-7	breast:
41	chr8:107652178..107654915-chr8:107656607..107660694,3	MCF-7	breast:
42	chr8:107661308..107663122-chr8:107664022..107665824,2	MCF-7	breast:
43	chr8:107652584..107654414-chr8:107662891..107664399,2	MCF-7	breast:
44	chr8:107682179..107684259-chr8:107690430..107692278,2	MCF-7	breast:
45	chr8:107655517..107658061-chr8:107665588..107668318,2	K562	blood:
46	chr8:107655208..107657686-chr8:107667462..107672091,4	MCF-7	breast:
47	chr7:56119419..56122353-chr8:107669214..107670843,2	MCF-7	breast:
48	chr8:107629734..107630516-chr8:107670589..107671141,2	MCF-7	breast:
49	chr8:107646939..107648517-chr8:107654197..107656388,2	K562	blood:
50	chr8:107655118..107656989-chr8:107657155..107658925,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABRA-1	chr8:107668339-107668593	ENSG00000253582.1
2	lnc-ABRA-1	chr8:107669730-107669776	ENSG00000253582.1

No data

Variant related genes	Relation type
OXR1	TF binding region
ENSG00000253582	TF binding region
OXR1	CpG island
ENSG00000253582	CpG island
ENSG00000253676	chromatin interactions
ENSG00000164830	chromatin interactions
ENSG00000146731	chromatin interactions
ENSG00000253582	chromatin interactions

Extended variants
information (count: 1489 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575014722	chr8:107644109-107644110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541940305	chr8:107644126-107644127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560608425	chr8:107644174-107644175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556067087	chr8:107644186-107644187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527797723	chr8:107644190-107644191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34114521	chr8:107644220-107644221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552110434	chr8:107644338-107644339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564141371	chr8:107644357-107644358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539312939	chr8:107644416-107644417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531495807	chr8:107644433-107644434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114473488	chr8:107644462-107644463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559298294	chr8:107644478-107644479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190330672	chr8:107644498-107644499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572032813	chr8:107644519-107644520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139853517	chr8:107644532-107644533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565734027	chr8:107644550-107644551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539542595	chr8:107644561-107644562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557785519	chr8:107644624-107644625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537877128	chr8:107644654-107644655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143930270	chr8:107644668-107644669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538525178	chr8:107644697-107644698	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556846522	chr8:107644721-107644722	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575055103	chr8:107644734-107644735	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs113425096	chr8:107644753-107644754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376071489	chr8:107644797-107644798	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529053420	chr8:107644837-107644838	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542377701	chr8:107644870-107644871	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554079311	chr8:107644903-107644904	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs57468381	chr8:107644909-107644910	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs572158987	chr8:107644924-107644925	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541020898	chr8:107644927-107644928	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112458196	chr8:107644961-107644962	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545936642	chr8:107644981-107644982	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564127244	chr8:107645000-107645001	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs531629029	chr8:107645044-107645045	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs185265418	chr8:107645068-107645069	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs561987137	chr8:107645081-107645082	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190107002	chr8:107645096-107645097	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs529189025	chr8:107645182-107645183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs181233256	chr8:107645191-107645192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113178761	chr8:107645201-107645202	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370845264	chr8:107645203-107645204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565783976	chr8:107645235-107645236	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533050217	chr8:107645332-107645333	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs111937031	chr8:107645343-107645344	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs569649958	chr8:107645408-107645409	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs577731276	chr8:107645416-107645417	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555086366	chr8:107645420-107645421	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs145639691	chr8:107645438-107645439	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535774432	chr8:107645460-107645461	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Multiple myeloma	17550852	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107601600-107669600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:107620400-107653400	Weak transcription	Aorta	Aorta
3	chr8:107630600-107657200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:107636800-107657400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:107637200-107648400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:107642000-107647400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:107643000-107656600	Weak transcription	Stomach Mucosa	stomach
8	chr8:107643400-107658800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr8:107648200-107649200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:107648400-107648600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:107648400-107648800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:107648400-107649400	Enhancers	Fetal Heart	heart
13	chr8:107648600-107662400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr8:107648800-107649000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr8:107649000-107649200	Enhancers	HSMMtube	muscle
16	chr8:107649000-107649600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:107649000-107650000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr8:107650800-107651000	Enhancers	K562	blood
19	chr8:107653200-107654000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:107653400-107653600	Enhancers	Aorta	Aorta
21	chr8:107653400-107654200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:107654800-107656000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr8:107655800-107656400	Enhancers	HepG2	liver
24	chr8:107655800-107656800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:107656600-107657800	Enhancers	Stomach Mucosa	stomach
26	chr8:107656800-107657400	Enhancers	NHEK	skin
27	chr8:107657000-107658200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr8:107657200-107658000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:107657200-107658200	Enhancers	HMEC	breast
30	chr8:107657200-107658600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:107657400-107657600	Flanking Active TSS	NHEK	skin
32	chr8:107657400-107658200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:107657600-107657800	Enhancers	NHEK	skin
34	chr8:107657800-107658000	Flanking Active TSS	NHEK	skin
35	chr8:107657800-107661200	Weak transcription	Stomach Mucosa	stomach
36	chr8:107658000-107658200	Enhancers	NHEK	skin
37	chr8:107658000-107661200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:107658200-107659200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr8:107658200-107668800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:107658600-107668600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:107658800-107659200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:107658800-107659400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr8:107659200-107660600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr8:107659400-107660600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:107659400-107660600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:107659600-107660000	Enhancers	Primary B cells from cord blood	blood
47	chr8:107659800-107660200	Enhancers	Primary hematopoietic stem cells	blood
48	chr8:107660200-107661000	Enhancers	Liver	Liver
49	chr8:107660600-107666400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:107661000-107661400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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