Variant report

Variant	nsv1018457
Chromosome Location	chr8:48289643-48321308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48290032-48290503	HepG2	liver:	n/a	n/a
2	CEBPB	chr8:48295944-48296144	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr8:48290834-48291033	HepG2	liver:	n/a	chr8:48290887-48290898
4	CEBPB	chr8:48319234-48319535	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:48290699-48291069	Hela-S3	cervix:	n/a	chr8:48290887-48290898
6	CEBPB	chr8:48319249-48319458	A549	lung:	n/a	n/a
7	CEBPB	chr8:48289986-48290427	HepG2	liver:	n/a	chr8:48290228-48290239
8	CEBPB	chr8:48296821-48297103	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:48296798-48297104	K562	blood:	n/a	n/a
10	CEBPB	chr8:48290155-48290305	HepG2	liver:	n/a	chr8:48290228-48290239
11	CEBPB	chr8:48296774-48297241	IMR90	lung:	n/a	n/a
12	CTCF	chr8:48296240-48296390	MCF-7	breast:	n/a	chr8:48296295-48296303 chr8:48296293-48296306
13	CTCF	chr8:48294260-48294410	SAEC	small airway:	n/a	n/a
14	CTCF	chr8:48292724-48292831	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:48294232-48294417	NHEK	skin:	n/a	n/a
16	CTCF	chr8:48291540-48291690	SAEC	small airway:	n/a	n/a
17	CTCF	chr8:48296240-48296390	NHEK	skin:	n/a	chr8:48296295-48296303 chr8:48296293-48296306
18	CTCF	chr8:48292746-48292805	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:48296260-48296410	HMEC	breast:	n/a	chr8:48296295-48296303 chr8:48296293-48296306
20	CTCF	chr8:48291520-48291670	HAc	cerebellar:	n/a	n/a
21	CTCF	chr8:48292763-48292848	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:48291380-48291530	HMEC	breast:	n/a	n/a
23	CTCF	chr8:48291480-48291630	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr8:48291460-48291610	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:48296320-48296470	SAEC	small airway:	n/a	n/a
26	CTCF	chr8:48292729-48292839	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:48291440-48291590	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr8:48292600-48292890	Caco-2	colon:	n/a	n/a
29	CTCF	chr8:48291440-48291590	HMF	breast:	n/a	n/a
30	CTCF	chr8:48317260-48317410	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr8:48292752-48292813	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:48294240-48294390	HMEC	breast:	n/a	n/a
33	CTCF	chr8:48294200-48294350	HMEC	breast:	n/a	n/a
34	CTCF	chr8:48291500-48291650	NHEK	skin:	n/a	n/a
35	CTCF	chr8:48291540-48291690	NHEK	skin:	n/a	n/a
36	CTCF	chr8:48291480-48291630	HCFaa	heart:	n/a	n/a
37	CTCF	chr8:48307020-48307170	HepG2	liver:	n/a	n/a
38	CUX1	chr8:48307444-48307452	GM12878	blood:	n/a	n/a
39	E2F4	chr8:48294210-48294589	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr8:48297198-48297336	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr8:48299900-48300180	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr8:48290035-48290368	GM12878	blood:	n/a	chr8:48290210-48290221
43	EGR1	chr8:48291642-48292032	ECC-1	luminal epithelium:	n/a	n/a
44	EP300	chr8:48290063-48290441	HepG2	liver:	n/a	n/a
45	EP300	chr8:48295962-48296065	Hela-S3	cervix:	n/a	n/a
46	EP300	chr8:48290098-48290404	HepG2	liver:	n/a	n/a
47	EP300	chr8:48292590-48293005	T-47D	breast:	n/a	n/a
48	EP300	chr8:48290036-48290232	GM12878	blood:	n/a	n/a
49	EP300	chr8:48290059-48290393	HepG2	liver:	n/a	n/a
50	EP300	chr8:48290747-48291027	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48297271-48297321	NT2-D1	testis:	n/a
2	chr8:48297271-48297321	HCF	heart:	n/a
3	chr8:48297271-48297321	NHDF-neo	bronchial:	n/a
4	chr8:48297271-48297321	IMR90	lung:	fetal
5	chr8:48297271-48297321	NB4	blood:	n/a
6	chr8:48297271-48297321	PANC-1	pancreas:	n/a
7	chr8:48297271-48297321	GM12878	blood:	n/a
8	chr8:48297271-48297321	HRPEpiC	eye:	n/a
9	chr8:48297271-48297321	BE2_C	brain:	n/a
10	chr8:48297271-48297321	T-47D	breast:	n/a
11	chr8:48297271-48297321	AG10803	skin:	n/a
12	chr8:48297271-48297321	K562	blood:	n/a
13	chr8:48297271-48297321	GM06990	blood:	n/a
14	chr8:48297271-48297321	RPTEC	kidney:	n/a
15	chr8:48297271-48297321	PFSK-1	brain:	n/a
16	chr8:48297271-48297321	U87	brain:	n/a
17	chr8:48297271-48297321	AoSMC	blood vessel:	n/a
18	chr8:48297271-48297321	NHBE	bronchial:	n/a
19	chr8:48297271-48297321	SK-N-SH	brain:	n/a
20	chr8:48297271-48297321	ECC-1	luminal epithelium:	n/a
21	chr8:48297271-48297321	ovcar-3	ovarian:	n/a
22	chr8:48297271-48297321	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:48297271-48297321	HRCEpiC	kidney:	n/a
24	chr8:48297271-48297321	BJ	skin:	n/a
25	chr8:48297271-48297321	Hepatocyte	liver:	n/a
26	chr8:48297271-48297321	HepG2	liver:	n/a
27	chr8:48297271-48297321	HUVEC	blood vessel:	n/a
28	chr8:48297271-48297321	AG04450	lung:	fetal
29	chr8:48297271-48297321	HIPEpiC	eye:	n/a
30	chr8:48297271-48297321	HCM	heart:	n/a
31	chr8:48297271-48297321	Caco-2	colon:	n/a
32	chr8:48297271-48297321	GM19239	blood:	n/a
33	chr8:48297271-48297321	HNPCEpiC	eye:	n/a
34	chr8:48297271-48297321	NH-A	brain:	n/a
35	chr8:48297271-48297321	MCF-7	breast:	n/a
36	chr8:48297271-48297321	CMK	blood:	n/a
37	chr8:48297271-48297321	H1-hESC	embryonic stem cell:	embryo
38	chr8:48297271-48297321	HCPEpiC	choroid plexus:	n/a
39	chr8:48297271-48297321	SKMC	muscle:	n/a
40	chr8:48297271-48297321	HEEpiC	esophagus:	n/a
41	chr8:48297271-48297321	MCF10A-Er-Src	breast:	n/a
42	chr8:48297271-48297321	HMEC	breast:	n/a
43	chr8:48297271-48297321	AG04449	skin:	fetal
44	chr8:48297271-48297321	Jurkat	blood:	n/a
45	chr8:48297271-48297321	A549	lung:	n/a
46	chr8:48297271-48297321	SAEC	small airway:	n/a
47	chr8:48297271-48297321	Hela-S3	cervix:	n/a
48	chr8:48297271-48297321	ProgFib	skin:	n/a
49	chr8:48297271-48297321	SK-N-MC	brain:	n/a
50	chr8:48297271-48297321	SK-N-SH_RA	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48276921..48279533-chr8:48290586..48293171,2	MCF-7	breast:
2	chr8:48291685..48296788-chr8:48648654..48651770,5	MCF-7	breast:
3	chr8:48288492..48291157-chr8:48291634..48296219,4	MCF-7	breast:
4	chr8:48289062..48291222-chr8:48292317..48294318,2	K562	blood:
5	chr8:48297848..48299871-chr8:48301045..48303414,2	K562	blood:
6	chr8:48286201..48287772-chr8:48290885..48293117,2	MCF-7	breast:
7	chr8:48285193..48287244-chr8:48293396..48296107,2	K562	blood:
8	chr8:48296378..48299348-chr8:48301045..48303894,3	K562	blood:
9	chr8:48296378..48299348-chr8:48301045..48303894,3	K562	blood:
10	chr8:48289062..48291222-chr8:48292317..48294318,2	K562	blood:
11	chr8:48297848..48299871-chr8:48301045..48303414,2	K562	blood:
12	chr8:48300186..48303081-chr8:48648494..48650857,2	MCF-7	breast:
13	chr8:48296590..48299380-chr8:48299721..48303188,4	MCF-7	breast:
14	chr8:48288492..48291157-chr8:48291634..48296219,4	MCF-7	breast:
15	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
16	chr8:48316678..48319260-chr8:48343262..48344870,2	MCF-7	breast:
17	chr8:48305764..48309024-chr8:53624660..53627223,3	K562	blood:
18	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
19	chr8:48287238..48289798-chr8:48645955..48647701,2	MCF-7	breast:
20	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
21	chr8:48296590..48299380-chr8:48299721..48303188,4	MCF-7	breast:
22	chr8:48264421..48266947-chr8:48288790..48290307,2	MCF-7	breast:
23	chr8:48293039..48294618-chr8:48649399..48651169,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-5	chr8:48300905-48301048	NONHSAT126443

No data

Variant related genes	Relation type
SPIDR	TF binding region
SPIDR	CpG island
ENSG00000221869	chromatin interactions
ENSG00000023287	chromatin interactions

Extended variants
information (count: 1140 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1140 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111899582	chr8:48289662-48289663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558903108	chr8:48289663-48289664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577354571	chr8:48289716-48289717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544609150	chr8:48289736-48289737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562839362	chr8:48289853-48289854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138215428	chr8:48289856-48289857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140674085	chr8:48289859-48289860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560503010	chr8:48289906-48289907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556157698	chr8:48289916-48289917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528187429	chr8:48289954-48289955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150091301	chr8:48290025-48290026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571379948	chr8:48290123-48290124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138407964	chr8:48290148-48290149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192990864	chr8:48290175-48290176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569180789	chr8:48290190-48290191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549145565	chr8:48290241-48290242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141205718	chr8:48290295-48290296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146969585	chr8:48290296-48290297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184743368	chr8:48290342-48290343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534070124	chr8:48290343-48290344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138104526	chr8:48290344-48290345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189574399	chr8:48290419-48290420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117749250	chr8:48290498-48290499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7824929	chr8:48290619-48290620	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556299562	chr8:48290676-48290677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7839055	chr8:48290688-48290689	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs143632607	chr8:48290749-48290750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560583278	chr8:48290750-48290751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534788252	chr8:48290852-48290853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557732734	chr8:48290853-48290854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572782425	chr8:48290854-48290855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577576952	chr8:48290893-48290894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367570450	chr8:48290956-48290957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200069368	chr8:48290979-48290980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564981326	chr8:48291020-48291021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191369171	chr8:48291032-48291033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550797003	chr8:48291041-48291042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577745669	chr8:48291048-48291049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539721091	chr8:48291068-48291069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548490451	chr8:48291093-48291094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114726341	chr8:48291127-48291128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534198302	chr8:48291132-48291133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184976382	chr8:48291247-48291248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7464484	chr8:48291265-48291266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570934107	chr8:48291282-48291283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144112934	chr8:48291350-48291351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148277407	chr8:48291360-48291361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574674846	chr8:48291405-48291406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574255810	chr8:48291417-48291418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141380521	chr8:48291433-48291434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Lung cancer	18438408	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
Pancreatic endocrine tumor	17639061	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
low-grade B-cell lymphoma tumor	18367492	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
small cell lung cancer	20016488	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
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD

Chromatin state (count:697 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48248800-48309600	Weak transcription	Thymus	Thymus
2	chr8:48262400-48309600	Weak transcription	Fetal Stomach	stomach
3	chr8:48263200-48297200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:48266600-48297200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:48266800-48290200	Weak transcription	HSMMtube	muscle
6	chr8:48266800-48297000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:48267000-48295400	Weak transcription	HSMM	muscle
8	chr8:48267800-48295000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:48278800-48309000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr8:48279000-48291800	Weak transcription	Esophagus	oesophagus
11	chr8:48279000-48299600	Weak transcription	Spleen	Spleen
12	chr8:48279000-48310200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr8:48279200-48290000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:48280400-48289800	Weak transcription	Small Intestine	intestine
15	chr8:48280600-48311200	Weak transcription	Aorta	Aorta
16	chr8:48281600-48291600	Weak transcription	Fetal Thymus	thymus
17	chr8:48282200-48290000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:48282200-48301200	Weak transcription	Primary B cells from peripheral blood	blood
19	chr8:48282200-48311200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr8:48282200-48312200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr8:48282400-48290000	Weak transcription	NHEK	skin
22	chr8:48282400-48291400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:48282400-48300200	Weak transcription	Primary T cells from cord blood	blood
24	chr8:48282400-48321200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr8:48282600-48290000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:48282800-48289800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr8:48282800-48289800	Weak transcription	GM12878-XiMat	blood
28	chr8:48282800-48290000	Weak transcription	HMEC	breast
29	chr8:48282800-48292800	Weak transcription	Psoas Muscle	Psoas
30	chr8:48282800-48299800	Weak transcription	Dnd41	blood
31	chr8:48283600-48297200	Weak transcription	Right Atrium	heart
32	chr8:48283800-48300200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:48284000-48290200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr8:48284000-48291600	Weak transcription	Lung	lung
35	chr8:48284000-48300400	Weak transcription	Primary hematopoietic stem cells	blood
36	chr8:48284200-48290000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr8:48284200-48300200	Weak transcription	Primary B cells from cord blood	blood
38	chr8:48284200-48301000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr8:48284600-48290000	Weak transcription	Hela-S3	cervix
40	chr8:48284600-48296600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:48284800-48289800	Weak transcription	A549	lung
42	chr8:48288200-48290800	Enhancers	HepG2	liver
43	chr8:48288400-48292600	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr8:48288600-48289800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr8:48288600-48290800	Enhancers	Liver	Liver
46	chr8:48288600-48294400	Enhancers	Fetal Lung	lung
47	chr8:48288600-48296600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr8:48288600-48296800	Enhancers	Stomach Mucosa	stomach
49	chr8:48288800-48290000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr8:48288800-48290400	Enhancers	Duodenum Mucosa	Duodenum

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