Variant report

Variant	nsv429918
Chromosome Location	chr8:55069061-55124075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1044)
CpG islands
(count:427)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:55084292-55084545	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:55078490-55079094	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:55110574-55110575	K562	blood:	n/a	n/a
4	ARID3A	chr8:55078344-55079095	K562	blood:	n/a	n/a
5	ARID3A	chr8:55081786-55082196	K562	blood:	n/a	n/a
6	ARID3A	chr8:55074493-55075038	K562	blood:	n/a	n/a
7	ATF1	chr8:55123572-55123828	K562	blood:	n/a	n/a
8	ATF1	chr8:55074547-55074788	K562	blood:	n/a	n/a
9	ATF3	chr8:55078654-55079059	A549	lung:	n/a	n/a
10	BACH1	chr8:55121907-55122344	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:55121912-55122250	K562	blood:	n/a	n/a
12	BACH1	chr8:55121542-55121581	K562	blood:	n/a	n/a
13	BACH1	chr8:55078432-55079008	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr8:55078182-55078609	GM12878	blood:	n/a	n/a
15	BCL3	chr8:55078654-55079051	A549	lung:	n/a	n/a
16	BCLAF1	chr8:55078325-55079111	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:55081794-55082076	K562	blood:	n/a	n/a
18	BHLHE40	chr8:55121853-55122216	K562	blood:	n/a	n/a
19	BHLHE40	chr8:55104521-55104611	K562	blood:	n/a	n/a
20	BHLHE40	chr8:55081873-55082223	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:55078218-55079045	K562	blood:	n/a	chr8:55078505-55078521
22	BHLHE40	chr8:55078430-55079026	GM12878	blood:	n/a	chr8:55078505-55078521
23	BRCA1	chr8:55121896-55122478	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr8:55078447-55078590	GM12878	blood:	n/a	n/a
25	BRCA1	chr8:55078446-55078986	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr8:55084202-55084761	HCT-116	colon:	n/a	chr8:55084406-55084417 chr8:55084290-55084301 chr8:55084405-55084416 chr8:55084405-55084418
27	CEBPB	chr8:55084230-55084597	A549	lung:	n/a	chr8:55084406-55084417 chr8:55084290-55084301 chr8:55084405-55084416 chr8:55084405-55084418
28	CEBPB	chr8:55081945-55082282	A549	lung:	n/a	chr8:55082125-55082136 chr8:55082126-55082137
29	CEBPB	chr8:55084210-55084630	ECC-1	luminal epithelium:	n/a	chr8:55084406-55084417 chr8:55084290-55084301 chr8:55084405-55084416 chr8:55084405-55084418
30	CEBPB	chr8:55084303-55084568	K562	blood:	n/a	chr8:55084406-55084417 chr8:55084405-55084416 chr8:55084405-55084418
31	CEBPB	chr8:55121809-55122141	K562	blood:	n/a	n/a
32	CEBPB	chr8:55104460-55104796	K562	blood:	n/a	n/a
33	CEBPB	chr8:55121785-55122153	K562	blood:	n/a	n/a
34	CEBPB	chr8:55084215-55084659	MCF-7	breast:	n/a	chr8:55084406-55084417 chr8:55084290-55084301 chr8:55084405-55084416 chr8:55084405-55084418
35	CEBPB	chr8:55071568-55071923	HepG2	liver:	n/a	chr8:55071734-55071745
36	CEBPB	chr8:55069009-55069215	A549	lung:	n/a	n/a
37	CEBPB	chr8:55069601-55069765	K562	blood:	n/a	n/a
38	CEBPB	chr8:55081805-55082348	HCT-116	colon:	n/a	chr8:55082125-55082136 chr8:55082126-55082137
39	CEBPB	chr8:55121793-55122610	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:55084222-55084580	ECC-1	luminal epithelium:	n/a	chr8:55084406-55084417 chr8:55084290-55084301 chr8:55084405-55084416 chr8:55084405-55084418
41	CEBPB	chr8:55071641-55071875	H1-hESC	embryonic stem cell:	n/a	chr8:55071734-55071745
42	CEBPB	chr8:55081834-55082254	A549	lung:	n/a	chr8:55082125-55082136 chr8:55082126-55082137
43	CEBPB	chr8:55071565-55071904	A549	lung:	n/a	chr8:55071734-55071745
44	CEBPB	chr8:55081931-55082293	K562	blood:	n/a	chr8:55082125-55082136 chr8:55082126-55082137
45	CEBPB	chr8:55071525-55071867	MCF-7	breast:	n/a	chr8:55071734-55071745
46	CEBPB	chr8:55121950-55122325	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:55071672-55071800	HepG2	liver:	n/a	chr8:55071734-55071745
48	CEBPB	chr8:55081958-55082249	ECC-1	luminal epithelium:	n/a	chr8:55082125-55082136 chr8:55082126-55082137
49	CEBPB	chr8:55123588-55123854	HepG2	liver:	n/a	chr8:55123698-55123711 chr8:55123698-55123709
50	CEBPB	chr8:55084122-55084673	IMR90	lung:	n/a	chr8:55084406-55084417 chr8:55084290-55084301 chr8:55084405-55084416 chr8:55084405-55084418

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:55088456-55088506	Hepatocyte	liver:	n/a
2	chr8:55091759-55091809	AG04450	lung:	fetal
3	chr8:55087084-55087134	AG04450	lung:	fetal
4	chr8:55087323-55087373	PrEC	prostate:	n/a
5	chr8:55087818-55087868	NHDF-neo	bronchial:	n/a
6	chr8:55091759-55091809	HCT-116	colon:	n/a
7	chr8:55088456-55088506	MCF10A-Er-Src	breast:	n/a
8	chr8:55088456-55088506	HMEC	breast:	n/a
9	chr8:55087400-55087450	GM12891	blood:	n/a
10	chr8:55088456-55088506	U87	brain:	n/a
11	chr8:55087818-55087868	HEEpiC	esophagus:	n/a
12	chr8:55087400-55087450	T-47D	breast:	n/a
13	chr8:55087323-55087373	AG04450	lung:	fetal
14	chr8:55087323-55087373	NT2-D1	testis:	n/a
15	chr8:55088456-55088506	T-47D	breast:	n/a
16	chr8:55087084-55087134	NB4	blood:	n/a
17	chr8:55087323-55087373	A549	lung:	n/a
18	chr8:55087818-55087868	HUVEC	blood vessel:	n/a
19	chr8:55088102-55088152	HUVEC	blood vessel:	n/a
20	chr8:55088456-55088506	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:55088102-55088152	HMEC	breast:	n/a
22	chr8:55088456-55088506	H1-hESC	embryonic stem cell:	embryo
23	chr8:55091759-55091809	GM06990	blood:	n/a
24	chr8:55087818-55087868	AG09309	skin:	n/a
25	chr8:55087400-55087450	ovcar-3	ovarian:	n/a
26	chr8:55088456-55088506	AG04450	lung:	fetal
27	chr8:55087400-55087450	LNCaP	prostate:	n/a
28	chr8:55087323-55087373	NH-A	brain:	n/a
29	chr8:55087323-55087373	GM12891	blood:	n/a
30	chr8:55087400-55087450	MCF10A-Er-Src	breast:	n/a
31	chr8:55088102-55088152	SK-N-MC	brain:	n/a
32	chr8:55087323-55087373	AG04449	skin:	fetal
33	chr8:55088456-55088506	AG09309	skin:	n/a
34	chr8:55087818-55087868	GM06990	blood:	n/a
35	chr8:55087323-55087373	MCF10A-Er-Src	breast:	n/a
36	chr8:55087400-55087450	HCM	heart:	n/a
37	chr8:55087818-55087868	MCF-7	breast:	n/a
38	chr8:55087084-55087134	CMK	blood:	n/a
39	chr8:55091759-55091809	NH-A	brain:	n/a
40	chr8:55087323-55087373	CMK	blood:	n/a
41	chr8:55088456-55088506	HIPEpiC	eye:	n/a
42	chr8:55091759-55091809	BJ	skin:	n/a
43	chr8:55091759-55091809	SAEC	small airway:	n/a
44	chr8:55088102-55088152	HCPEpiC	choroid plexus:	n/a
45	chr8:55091759-55091809	MCF-7	breast:	n/a
46	chr8:55087084-55087134	GM19239	blood:	n/a
47	chr8:55091759-55091809	CMK	blood:	n/a
48	chr8:55088102-55088152	HL-60	blood:	n/a
49	chr8:55087323-55087373	Hepatocyte	liver:	n/a
50	chr8:55087818-55087868	Hepatocyte	liver:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:55116089..55118957-chr8:55122128..55124869,2	K562	blood:
2	chr8:55051494..55052804-chr8:55078053..55079182,7	MCF-7	breast:
3	chr8:55065050..55068391-chr8:55075556..55078164,4	K562	blood:
4	chr8:55121167..55122718-chr8:55130349..55133104,2	K562	blood:
5	chr8:55047476..55049914-chr8:55081634..55083570,2	K562	blood:
6	chr8:55116089..55118957-chr8:55122128..55124869,2	K562	blood:
7	chr8:55081633..55082449-chr8:55390402..55391359,5	MCF-7	breast:
8	chr8:55051550..55052373-chr8:55078712..55079380,2	MCF-7	breast:
9	chr8:55096597..55098362-chr8:55128678..55131200,2	K562	blood:
10	chr8:55009975..55010673-chr8:55078381..55079050,2	MCF-7	breast:
11	chr8:55059169..55061201-chr8:55073934..55076010,2	K562	blood:
12	chr8:55081926..55082576-chr8:55468323..55469121,2	MCF-7	breast:
13	chr2:73460213..73461906-chr8:55093100..55094812,2	MCF-7	breast:
14	chr8:54764122..54764695-chr8:55078382..55079037,2	MCF-7	breast:
15	chr8:55081601..55082159-chr8:55344019..55344673,2	K562	blood:
16	chr8:55047476..55049382-chr8:55079513..55083134,3	K562	blood:
17	chr8:54934858..54936518-chr8:55078242..55080883,2	MCF-7	breast:
18	chr8:54932909..54934927-chr8:55070015..55071943,2	MCF-7	breast:
19	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:
20	chr8:55081573..55082518-chr8:55196033..55196674,3	MCF-7	breast:
21	chr8:55079715..55082663-chr8:55090104..55094116,3	K562	blood:
22	chr8:55079715..55082663-chr8:55090104..55094116,3	K562	blood:
23	chr8:55063976..55066123-chr8:55076521..55079309,2	MCF-7	breast:
24	chr8:54933839..54936004-chr8:55076610..55079390,2	MCF-7	breast:
25	chr8:55065979..55068136-chr8:55068937..55070902,2	K562	blood:
26	chr8:55069882..55072720-chr8:55074795..55076480,2	K562	blood:
27	chr8:55082028..55084437-chr8:55372131..55374437,2	K562	blood:
28	chr8:55081646..55082487-chr8:55464074..55464861,2	MCF-7	breast:
29	chr8:55051516..55052282-chr8:55078096..55078910,2	K562	blood:
30	chr8:55105444..55107201-chr8:55122648..55124928,2	K562	blood:
31	chr8:55064028..55067964-chr8:55074664..55077779,3	K562	blood:
32	chr8:55069882..55072720-chr8:55074795..55076480,2	K562	blood:
33	chr8:55105444..55107201-chr8:55122648..55124928,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYPLA1-3	chr8:55104142-55104595	NONHSAT126629
2	lnc-LYPLA1-4	chr8:55119930-55120066	ucscGeneNc_uc003xrx_2
3	lnc-LYPLA1-4	chr8:55118106-55118331	ucscGeneNc_uc003xrx_2

No data

Variant related genes	Relation type
ENSG00000270980	TF binding region
RNU6ATAC32P	TF binding region
ENSG00000270980	CpG island
RNU6ATAC32P	CpG island
ENSG00000135617	chromatin interactions
ENSG00000147509	chromatin interactions
ENSG00000187735	chromatin interactions
ENSG00000251835	chromatin interactions
ENSG00000135624	chromatin interactions
ENSG00000137547	chromatin interactions

Extended variants
information (count: 1904 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1904 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11991952	chr8:55069061-55069062	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139542536	chr8:55069087-55069088	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534680321	chr8:55069088-55069089	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186072669	chr8:55069118-55069119	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552776447	chr8:55069120-55069121	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546942198	chr8:55069160-55069161	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149694060	chr8:55069213-55069214	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539510815	chr8:55069214-55069215	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs574401248	chr8:55069258-55069259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71517559	chr8:55069287-55069288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566767023	chr8:55069294-55069295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11984645	chr8:55069305-55069306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs34997387	chr8:55069317-55069318	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568912549	chr8:55069342-55069343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11984672	chr8:55069384-55069385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs555072069	chr8:55069416-55069417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565926339	chr8:55069451-55069452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190893541	chr8:55069460-55069461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112857936	chr8:55069515-55069516	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs571074817	chr8:55069517-55069518	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372028024	chr8:55069518-55069519	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs182319163	chr8:55069524-55069525	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs543497571	chr8:55069551-55069552	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs148407692	chr8:55069561-55069562	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs187236965	chr8:55069583-55069584	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs112211970	chr8:55069594-55069595	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs368282866	chr8:55069618-55069619	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs147648848	chr8:55069643-55069644	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs541420718	chr8:55069687-55069688	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs74583935	chr8:55069828-55069829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144453766	chr8:55069829-55069830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531161707	chr8:55069843-55069844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549892189	chr8:55069860-55069861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140194550	chr8:55069871-55069872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77669094	chr8:55069886-55069887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376454299	chr8:55069892-55069893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372004102	chr8:55069898-55069899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200058729	chr8:55069901-55069902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151273070	chr8:55069917-55069918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528989188	chr8:55069925-55069926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191720450	chr8:55069933-55069934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13261058	chr8:55070041-55070042	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183046211	chr8:55070043-55070044	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557667288	chr8:55070082-55070083	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187003539	chr8:55070099-55070100	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs150431548	chr8:55070118-55070119	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138121622	chr8:55070132-55070133	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs34765030	chr8:55070138-55070139	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs141236673	chr8:55070175-55070176	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542769111	chr8:55070184-55070185	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Adenocarcinoma	20824076	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:55061600-55078000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr8:55061600-55078400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:55062200-55078400	Weak transcription	Right Atrium	heart
4	chr8:55063400-55078400	Weak transcription	Ovary	ovary
5	chr8:55063800-55069400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr8:55064000-55078000	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr8:55064200-55070600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr8:55064600-55078400	Weak transcription	Fetal Muscle Leg	muscle
9	chr8:55064800-55078000	Weak transcription	Fetal Intestine Small	intestine
10	chr8:55066400-55071200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:55067000-55071200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr8:55067200-55071000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:55067200-55071000	Weak transcription	Placenta	Placenta
14	chr8:55067200-55071200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:55067200-55071200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:55067200-55071200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr8:55067200-55071400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:55067200-55078000	Weak transcription	NHLF	lung
19	chr8:55067200-55078200	Weak transcription	Primary B cells from cord blood	blood
20	chr8:55067200-55078200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:55067200-55078200	Weak transcription	HSMM	muscle
22	chr8:55067200-55078200	Weak transcription	NHDF-Ad	bronchial
23	chr8:55067200-55078400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:55070600-55070800	Enhancers	Fetal Muscle Trunk	muscle
25	chr8:55070800-55071000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr8:55071000-55071600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr8:55071000-55072000	Enhancers	Placenta	Placenta
28	chr8:55071200-55071800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:55071200-55071800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr8:55071200-55071800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr8:55071200-55072000	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr8:55071200-55072200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:55071400-55071800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr8:55071600-55078200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr8:55071800-55075000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:55071800-55078400	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr8:55072000-55078200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr8:55072200-55078400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:55074800-55076400	Active TSS	K562	blood
40	chr8:55075000-55075200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:55075200-55075600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:55075400-55075600	Enhancers	Primary hematopoietic stem cells	blood
43	chr8:55075600-55075800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:55075600-55078200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr8:55075600-55078200	Weak transcription	Fetal Lung	lung
46	chr8:55075800-55077800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr8:55076400-55078000	Weak transcription	K562	blood
48	chr8:55077000-55078000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr8:55077200-55077400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:55077400-55078400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links