Variant report

Variant	nsv539732
Chromosome Location	chr8:117983619-118079816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:736)
CpG islands
(count:122)
Chromatin interactive
region (count:30)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:736 , 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	ATF1	chr8:118022516-118022716	K562	blood:	n/a	n/a
2	ATF1	chr8:118020845-118021044	K562	blood:	n/a	n/a
3	BACH1	chr8:118056998-118057173	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:118069050-118069345	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:118056971-118057168	K562	blood:	n/a	n/a
6	CEBPB	chr8:117987737-117988092	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:118066191-118066303	H1-hESC	embryonic stem cell:	n/a	chr8:118066240-118066251
8	CEBPB	chr8:118066082-118066370	K562	blood:	n/a	chr8:118066240-118066251
9	CEBPB	chr8:118066063-118066386	IMR90	lung:	n/a	chr8:118066240-118066251
10	CEBPB	chr8:117987764-117988129	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr8:118013598-118013930	Hela-S3	cervix:	n/a	chr8:118013765-118013776
12	CEBPB	chr8:118013692-118013912	HepG2	liver:	n/a	chr8:118013765-118013776
13	CEBPB	chr8:118031649-118032296	IMR90	lung:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
14	CEBPB	chr8:118013672-118013901	A549	lung:	n/a	chr8:118013765-118013776
15	CEBPB	chr8:118013646-118013892	IMR90	lung:	n/a	chr8:118013765-118013776
16	CEBPB	chr8:118061644-118061729	A549	lung:	n/a	n/a
17	CEBPB	chr8:117987759-117988074	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:118053547-118053583	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:117987747-117988079	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:118031703-118031883	HepG2	liver:	n/a	chr8:118031801-118031812
21	CEBPB	chr8:117987719-117988131	MCF-7	breast:	n/a	n/a
22	CEBPB	chr8:118031502-118032316	Hela-S3	cervix:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
23	CEBPB	chr8:118045665-118045911	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:117987738-117988116	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:118066068-118066373	A549	lung:	n/a	chr8:118066240-118066251
26	CEBPB	chr8:117987761-117988085	A549	lung:	n/a	n/a
27	CEBPB	chr8:118045572-118046377	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr8:118045623-118045693	A549	lung:	n/a	n/a
29	CEBPB	chr8:118032015-118032280	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:118046948-118047300	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:118031492-118031968	MCF-7	breast:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
32	CEBPB	chr8:117987726-117988118	MCF-7	breast:	n/a	n/a
33	CEBPB	chr8:118031604-118031804	K562	blood:	n/a	chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
34	CEBPB	chr8:117987741-117988084	K562	blood:	n/a	n/a
35	CEBPB	chr8:118066088-118066372	HepG2	liver:	n/a	chr8:118066240-118066251
36	CHD1	chr8:118047103-118047133	GM12878	blood:	n/a	n/a
37	CHD1	chr8:118046933-118047301	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr8:118057079-118057182	HepG2	liver:	n/a	n/a
39	CHD2	chr8:118047102-118047115	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr8:118057003-118057209	A549	lung:	n/a	n/a
41	CTCF	chr8:118057001-118057269	Hela-S3	cervix:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
42	CTCF	chr8:118050240-118050390	RPTEC	kidney:	n/a	chr8:118050294-118050315
43	CTCF	chr8:118050200-118050350	GM12873	blood:	n/a	chr8:118050294-118050315
44	CTCF	chr8:118049956-118050661	SK-N-SH	brain:	n/a	chr8:118050294-118050315
45	CTCF	chr8:118057060-118057210	HUVEC	blood vessel:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
46	CTCF	chr8:118056992-118057269	Pancreas_OC	pancreas:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
47	CTCF	chr8:118031661-118031761	GM12878	blood:	n/a	chr8:118031705-118031721
48	CTCF	chr8:118031520-118031670	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr8:118050240-118050390	AG10803	skin:	n/a	chr8:118050294-118050315
50	CTCF	chr8:118050190-118050423	GM12878	blood:	n/a	chr8:118050294-118050315

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:118075340-118075390	NH-A	brain:	n/a
2	chr8:118075340-118075390	Jurkat	blood:	n/a
3	chr8:118075340-118075390	BJ	skin:	n/a
4	chr8:118075340-118075390	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:118075340-118075390	LNCaP	prostate:	n/a
6	chr8:118075340-118075390	HUVEC	blood vessel:	n/a
7	chr8:118075340-118075390	A549	lung:	n/a
8	chr8:118057038-118057088	K562	blood:	n/a
9	chr8:118057038-118057088	GM06990	blood:	n/a
10	chr8:118075340-118075390	T-47D	breast:	n/a
11	chr8:118075340-118075390	SK-N-SH_RA	brain:	n/a
12	chr8:118057038-118057088	AG09319	gingival:	n/a
13	chr8:118075340-118075390	GM12891	blood:	n/a
14	chr8:118057038-118057088	PANC-1	pancreas:	n/a
15	chr8:118057038-118057088	T-47D	breast:	n/a
16	chr8:118075340-118075390	SK-N-MC	brain:	n/a
17	chr8:118075340-118075390	ovcar-3	ovarian:	n/a
18	chr8:118057038-118057088	HCF	heart:	n/a
19	chr8:118057038-118057088	PFSK-1	brain:	n/a
20	chr8:118075340-118075390	HCPEpiC	choroid plexus:	n/a
21	chr8:118075340-118075390	HAEpiC	amniotic membrane:	n/a
22	chr8:118057038-118057088	A549	lung:	n/a
23	chr8:118075340-118075390	Hela-S3	cervix:	n/a
24	chr8:118075340-118075390	SKMC	muscle:	n/a
25	chr8:118075340-118075390	PrEC	prostate:	n/a
26	chr8:118075340-118075390	GM12892	blood:	n/a
27	chr8:118075340-118075390	U87	brain:	n/a
28	chr8:118057038-118057088	HRPEpiC	eye:	n/a
29	chr8:118075340-118075390	GM12878	blood:	n/a
30	chr8:118057038-118057088	AG10803	skin:	n/a
31	chr8:118057038-118057088	AG09309	skin:	n/a
32	chr8:118075340-118075390	AG04450	lung:	fetal
33	chr8:118075340-118075390	AG09319	gingival:	n/a
34	chr8:118057038-118057088	GM12891	blood:	n/a
35	chr8:118057038-118057088	GM19239	blood:	n/a
36	chr8:118057038-118057088	U87	brain:	n/a
37	chr8:118057038-118057088	NB4	blood:	n/a
38	chr8:118075340-118075390	HIPEpiC	eye:	n/a
39	chr8:118075340-118075390	BE2_C	brain:	n/a
40	chr8:118057038-118057088	AG04449	skin:	fetal
41	chr8:118075340-118075390	HRCEpiC	kidney:	n/a
42	chr8:118057038-118057088	NHBE	bronchial:	n/a
43	chr8:118075340-118075390	HMEC	breast:	n/a
44	chr8:118057038-118057088	AoSMC	blood vessel:	n/a
45	chr8:118057038-118057088	HCM	heart:	n/a
46	chr8:118075340-118075390	AoSMC	blood vessel:	n/a
47	chr8:118075340-118075390	HRPEpiC	eye:	n/a
48	chr8:118057038-118057088	ProgFib	skin:	n/a
49	chr8:118057038-118057088	NHDF-neo	bronchial:	n/a
50	chr8:118075340-118075390	HEEpiC	esophagus:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:117863158..117863821-chr8:118056751..118057499,2	MCF-7	breast:
2	chr8:117965247..117967783-chr8:117993532..117995736,2	MCF-7	breast:
3	chr8:117798759..117799449-chr8:118050248..118050771,2	K562	blood:
4	chr8:117939530..117940032-chr8:118056656..118057269,2	MCF-7	breast:
5	chr8:117939213..117940140-chr8:118049488..118050102,2	MCF-7	breast:
6	chr8:118057127..118057700-chr8:118316063..118316814,2	K562	blood:
7	chr8:118020240..118022931-chr8:118026040..118028339,2	K562	blood:
8	chr8:118042679..118044189-chr9:110363714..110366279,2	MCF-7	breast:
9	chr8:117939006..117940094-chr8:118049813..118050710,7	MCF-7	breast:
10	chr8:118043645..118045454-chr8:118048190..118050683,2	MCF-7	breast:
11	chr8:118056632..118057588-chr8:118316103..118316951,2	MCF-7	breast:
12	chr8:117982304..117985238-chr8:117985646..117987853,2	K562	blood:
13	chr8:117999026..118002004-chr8:118003208..118005639,2	K562	blood:
14	chr8:117862359..117862912-chr8:118049512..118050408,2	MCF-7	breast:
15	chr8:117938653..117939378-chr8:118056475..118057163,2	MCF-7	breast:
16	chr8:117991131..117993472-chr8:117993504..117995886,2	K562	blood:
17	chr8:117965975..117966904-chr8:118049849..118050385,2	MCF-7	breast:
18	chr8:118068187..118070512-chr8:118072749..118074741,2	MCF-7	breast:
19	chr8:117753207..117755356-chr8:118019404..118021027,2	K562	blood:
20	chr8:118020240..118022931-chr8:118026040..118028339,2	K562	blood:
21	chr8:118049690..118050513-chr8:118316119..118316774,2	MCF-7	breast:
22	chr8:117939124..117940068-chr8:118056652..118057163,2	K562	blood:
23	chr8:117899655..117900529-chr8:118049522..118050469,2	MCF-7	breast:
24	chr8:117982304..117985238-chr8:117985646..117987853,2	K562	blood:
25	chr8:117999026..118002004-chr8:118003208..118005639,2	K562	blood:
26	chr8:118043645..118045454-chr8:118048190..118050683,2	MCF-7	breast:
27	chr8:117800389..117801053-chr8:118056632..118057180,2	K562	blood:
28	chr8:118068187..118070512-chr8:118072749..118074741,2	MCF-7	breast:
29	chr8:117978695..117980738-chr8:117985515..117988010,2	MCF-7	breast:
30	chr8:117991131..117993472-chr8:117993504..117995886,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf85-3	chr8:118030185-118030485	NONHSAT128387
2	lnc-C8orf85-4	chr8:118068057-118068384	NONHSAT128388
3	lnc-RAD21-2	chr8:118017080-118019878	ncRnaDb_ncrna_FR361237_1
4	lnc-C8orf85-5	chr8:118019230-118019352	NONHSAT128385

No data

Variant related genes	Relation type
ENSG00000253271	TF binding region
RN7SL228P	TF binding region
ENSG00000253271	CpG island
RN7SL228P	CpG island

Extended variants
information (count: 2800 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:2800 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373233798	chr8:117987423-117987424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529951307	chr8:117987427-117987428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536453888	chr8:117987446-117987447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554665706	chr8:117987518-117987519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181304714	chr8:117987519-117987520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146185408	chr8:117987520-117987521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139058712	chr8:117987534-117987535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576800816	chr8:117987706-117987707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541283929	chr8:117987716-117987717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542397605	chr8:117987731-117987732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs60660242	chr8:117987752-117987753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75666750	chr8:117987759-117987760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530200776	chr8:117987773-117987774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149910625	chr8:117987791-117987792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371110277	chr8:117987796-117987797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548361511	chr8:117987809-117987810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562369623	chr8:117987812-117987813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144962512	chr8:117987834-117987835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552432799	chr8:117987859-117987860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548426722	chr8:117987862-117987863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570785458	chr8:117987866-117987867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545129402	chr8:117987939-117987940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564836853	chr8:117987950-117987951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534711909	chr8:117987970-117987971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186311559	chr8:117988056-117988057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547687071	chr8:117988057-117988058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148634598	chr8:117988066-117988067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376418250	chr8:117988071-117988072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536583749	chr8:117988081-117988082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527236279	chr8:117988230-117988231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554782242	chr8:117988233-117988234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113301209	chr8:117988235-117988236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73312221	chr8:117988322-117988323	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs371425324	chr8:117988347-117988348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537138267	chr8:117988395-117988396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113934510	chr8:117988426-117988427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576723626	chr8:117988430-117988431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375121122	chr8:117988474-117988475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540643795	chr8:117988476-117988477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545086581	chr8:117988480-117988481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199546398	chr8:117988481-117988482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566567868	chr8:117988482-117988483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10112180	chr8:117988483-117988484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78122691	chr8:117988484-117988485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28634108	chr8:117988485-117988486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10112182	chr8:117988489-117988490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78495363	chr8:117988495-117988496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552587097	chr8:117988510-117988511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147823815	chr8:117988515-117988516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190854544	chr8:117988528-117988529	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17268525	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	19204574	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:117987400-117988400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:117987400-117989000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr8:117987600-117988800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr8:117987800-117988400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr8:117987800-117988400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:117988000-117988400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:117998000-117998400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr8:117998000-117998800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:117998000-117999000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:117998000-117999200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:117998200-117998800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:118006800-118008000	Enhancers	Fetal Heart	heart
13	chr8:118007400-118007600	Enhancers	Rectal Smooth Muscle	rectum
14	chr8:118007600-118008800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:118007800-118008000	Weak transcription	Colon Smooth Muscle	Colon
16	chr8:118007800-118008400	Enhancers	Stomach Smooth Muscle	stomach
17	chr8:118008000-118008200	Enhancers	Colon Smooth Muscle	Colon
18	chr8:118008000-118008400	Flanking Active TSS	Fetal Heart	heart
19	chr8:118008200-118011600	Weak transcription	Colon Smooth Muscle	Colon
20	chr8:118008400-118008800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr8:118008400-118010400	Enhancers	Fetal Heart	heart
22	chr8:118008800-118009400	Enhancers	Stomach Smooth Muscle	stomach
23	chr8:118008800-118010600	Enhancers	Rectal Smooth Muscle	rectum
24	chr8:118009200-118009600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr8:118009400-118011400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr8:118009600-118011600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:118009800-118010600	Enhancers	Fetal Stomach	stomach
28	chr8:118010400-118014400	Weak transcription	Fetal Heart	heart
29	chr8:118010600-118011600	Weak transcription	Fetal Stomach	stomach
30	chr8:118010600-118012200	Weak transcription	Rectal Smooth Muscle	rectum
31	chr8:118011400-118012600	Enhancers	Stomach Smooth Muscle	stomach
32	chr8:118011600-118012600	Enhancers	Fetal Stomach	stomach
33	chr8:118011600-118012800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:118011600-118012800	Enhancers	Colon Smooth Muscle	Colon
35	chr8:118012200-118014600	Enhancers	Rectal Smooth Muscle	rectum
36	chr8:118012800-118016600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr8:118014400-118015200	Enhancers	Fetal Heart	heart
38	chr8:118015200-118016400	Weak transcription	Fetal Heart	heart
39	chr8:118016400-118016800	Enhancers	Fetal Heart	heart
40	chr8:118016600-118017600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:118017600-118019800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:118019600-118020000	Enhancers	Fetal Intestine Large	intestine
43	chr8:118019800-118021000	Enhancers	Fetal Intestine Small	intestine
44	chr8:118019800-118021600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:118021600-118022600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:118022400-118023000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:118022400-118023200	Enhancers	Lung	lung
48	chr8:118022600-118023600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr8:118022800-118023000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:118022800-118023200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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