Variant report

Variant	nsv890851
Chromosome Location	chr8:48954143-49031082
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:244)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48954659-48955530	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48986390-48986586	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48987503-48987712	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48989035-48989075	K562	blood:	n/a	n/a
5	ATF1	chr8:48975614-48975808	K562	blood:	n/a	n/a
6	ATF3	chr8:48987856-48987995	K562	blood:	n/a	chr8:48987957-48987966
7	ATF3	chr8:48988882-48989250	K562	blood:	n/a	n/a
8	BACH1	chr8:48988916-48989245	K562	blood:	n/a	n/a
9	BHLHE40	chr8:48954910-48955174	HepG2	liver:	n/a	n/a
10	BHLHE40	chr8:48954919-48955131	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:48954895-48955210	HepG2	liver:	n/a	n/a
12	BHLHE40	chr8:48987771-48988161	HepG2	liver:	n/a	chr8:48987957-48987966 chr8:48987955-48987968 chr8:48987956-48987965 chr8:48987957-48987966 chr8:48987958-48987967 chr8:48987951-48987972
13	BHLHE40	chr8:48987775-48988051	K562	blood:	n/a	chr8:48987957-48987966 chr8:48987955-48987968 chr8:48987956-48987965 chr8:48987957-48987966 chr8:48987958-48987967 chr8:48987951-48987972
14	CBX3	chr8:48993538-48993798	K562	blood:	n/a	n/a
15	CBX3	chr8:48988915-48989393	K562	blood:	n/a	n/a
16	CEBPB	chr8:48988761-48989262	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:48957785-48958040	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:49022674-49022777	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:49018503-49018720	K562	blood:	n/a	n/a
20	CEBPB	chr8:49014054-49014359	K562	blood:	n/a	n/a
21	CEBPB	chr8:48984543-48984581	A549	lung:	n/a	n/a
22	CEBPB	chr8:48988891-48989038	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:48987402-48988232	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:48982549-48982607	A549	lung:	n/a	n/a
25	CEBPB	chr8:48988789-48989066	K562	blood:	n/a	n/a
26	CEBPB	chr8:48986670-48986991	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:49020677-49020863	HepG2	liver:	n/a	chr8:49020750-49020761
28	CEBPB	chr8:49013917-49014635	IMR90	lung:	n/a	chr8:49014432-49014443 chr8:49014432-49014443
29	CEBPB	chr8:48981714-48981906	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:49022405-49022934	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:48979594-48979929	A549	lung:	n/a	n/a
32	CEBPB	chr8:49029261-49029313	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:48987369-48987570	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:48988840-48989134	A549	lung:	n/a	n/a
35	CREB1	chr8:48997106-48997540	K562	blood:	n/a	n/a
36	CTCF	chr8:49018440-49018590	MCF-7	breast:	n/a	chr8:49018459-49018469
37	CTCF	chr8:49018360-49018510	GM12873	blood:	n/a	chr8:49018459-49018469
38	CTCF	chr8:49018500-49018650	Caco-2	colon:	n/a	n/a
39	CTCF	chr8:49018483-49018686	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:49018381-49018761	K562	blood:	n/a	chr8:49018459-49018469
41	CTCF	chr8:49014360-49014510	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr8:49018497-49018686	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:49018341-49018845	MCF-7	breast:	n/a	chr8:49018459-49018469
44	CTCF	chr8:49014458-49014476	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr8:49018549-49018642	K562	blood:	n/a	n/a
46	CTCF	chr8:48984180-48984186	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:48989080-48989230	HMF	breast:	n/a	n/a
48	CTCF	chr8:49018530-49018642	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:49018431-49018752	K562	blood:	n/a	chr8:49018459-49018469
50	CTCF	chr8:49018294-49018904	MCF-7	breast:	n/a	chr8:49018459-49018469

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48986813-48986863	NH-A	brain:	n/a
2	chr8:48986813-48986863	GM12878	blood:	n/a
3	chr8:49021981-49022031	MCF10A-Er-Src	breast:	n/a
4	chr8:48973636-48973686	NHDF-neo	bronchial:	n/a
5	chr8:48973636-48973686	U87	brain:	n/a
6	chr8:49021981-49022031	SKMC	muscle:	n/a
7	chr8:48973636-48973686	SK-N-SH	brain:	n/a
8	chr8:48973636-48973686	SK-N-MC	brain:	n/a
9	chr8:49014558-49014608	HEEpiC	esophagus:	n/a
10	chr8:48986813-48986863	HAEpiC	amniotic membrane:	n/a
11	chr8:49014558-49014608	SK-N-SH_RA	brain:	n/a
12	chr8:49014558-49014608	GM06990	blood:	n/a
13	chr8:48986813-48986863	PrEC	prostate:	n/a
14	chr8:48986813-48986863	ovcar-3	ovarian:	n/a
15	chr8:48986813-48986863	GM06990	blood:	n/a
16	chr8:48986813-48986863	Jurkat	blood:	n/a
17	chr8:48986813-48986863	CMK	blood:	n/a
18	chr8:48986813-48986863	HEEpiC	esophagus:	n/a
19	chr8:49021981-49022031	NT2-D1	testis:	n/a
20	chr8:48986813-48986863	HIPEpiC	eye:	n/a
21	chr8:49014558-49014608	U87	brain:	n/a
22	chr8:49021981-49022031	Jurkat	blood:	n/a
23	chr8:48986813-48986863	SAEC	small airway:	n/a
24	chr8:49014558-49014608	T-47D	breast:	n/a
25	chr8:49014558-49014608	AG09319	gingival:	n/a
26	chr8:49021981-49022031	NHDF-neo	bronchial:	n/a
27	chr8:49014558-49014608	HCM	heart:	n/a
28	chr8:48973636-48973686	HL-60	blood:	n/a
29	chr8:48973636-48973686	SAEC	small airway:	n/a
30	chr8:48973636-48973686	GM06990	blood:	n/a
31	chr8:48986813-48986863	HepG2	liver:	n/a
32	chr8:49014558-49014608	H1-hESC	embryonic stem cell:	embryo
33	chr8:49021981-49022031	U87	brain:	n/a
34	chr8:48986813-48986863	IMR90	lung:	fetal
35	chr8:48973636-48973686	ovcar-3	ovarian:	n/a
36	chr8:49014558-49014608	GM19239	blood:	n/a
37	chr8:48986813-48986863	HMEC	breast:	n/a
38	chr8:49014558-49014608	SKMC	muscle:	n/a
39	chr8:49014558-49014608	RPTEC	kidney:	n/a
40	chr8:48973636-48973686	HCF	heart:	n/a
41	chr8:49021981-49022031	PFSK-1	brain:	n/a
42	chr8:48973636-48973686	CMK	blood:	n/a
43	chr8:48986813-48986863	RPTEC	kidney:	n/a
44	chr8:48973636-48973686	AG04450	lung:	fetal
45	chr8:48973636-48973686	AG04449	skin:	fetal
46	chr8:48986813-48986863	HCT-116	colon:	n/a
47	chr8:48986813-48986863	HEK293	kidney:	embryo
48	chr8:49014558-49014608	GM12878	blood:	n/a
49	chr8:49014558-49014608	SAEC	small airway:	n/a
50	chr8:49021981-49022031	PrEC	prostate:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48982765..48984545-chr8:48987553..48989325,2	K562	blood:
2	chr8:48919706..48922192-chr8:49031082..49033748,2	MCF-7	breast:
3	chr8:48965207..48966957-chr8:48986549..48988912,2	K562	blood:
4	chr8:49023203..49025595-chr8:49035479..49038549,3	K562	blood:
5	chr8:48970388..48974071-chr8:48975063..48978866,4	K562	blood:
6	chr8:48987869..48989634-chr8:48998371..48999991,2	MCF-7	breast:
7	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
8	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
9	chr8:48982765..48984545-chr8:48987553..48989325,2	K562	blood:
10	chr8:48957180..48959047-chr8:48960507..48962710,2	K562	blood:
11	chr8:48949897..48951407-chr8:48952676..48954247,2	MCF-7	breast:
12	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
13	chr8:48984328..48988098-chr8:48992508..48996504,3	K562	blood:
14	chr8:48987869..48989634-chr8:48998371..48999991,2	MCF-7	breast:
15	chr8:48953429..48954984-chr8:48960210..48961992,2	K562	blood:
16	chr8:48919990..48922375-chr8:49014350..49015887,2	MCF-7	breast:
17	chr8:49022447..49025274-chr8:49027665..49030451,2	K562	blood:
18	chr8:48970388..48974071-chr8:48975063..48978866,4	K562	blood:
19	chr8:48871660..48873986-chr8:48986184..48988577,2	MCF-7	breast:
20	chr8:49029286..49030959-chr8:49031763..49033915,2	MCF-7	breast:
21	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
22	chr8:48965207..48966957-chr8:48986549..48988912,2	K562	blood:
23	chr8:48871629..48874079-chr8:48980802..48983659,2	MCF-7	breast:
24	chr8:48955264..48957497-chr8:48959787..48961410,2	K562	blood:
25	chr8:49022447..49025274-chr8:49027665..49030451,2	K562	blood:
26	chr8:48984328..48988098-chr8:48992508..48996504,3	K562	blood:

No data

Variant related genes	Relation type
UBE2V2	TF binding region
UBE2V2	CpG island
ENSG00000104738	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000169139	chromatin interactions

Extended variants
information (count: 2557 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2557 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10958450	chr8:48954143-48954144	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574676730	chr8:48954189-48954190	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs530901761	chr8:48954195-48954196	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549094074	chr8:48954199-48954200	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs144713896	chr8:48954222-48954223	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536908100	chr8:48954251-48954252	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs375680779	chr8:48954263-48954264	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560969674	chr8:48954280-48954281	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs529558458	chr8:48954291-48954292	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs553194534	chr8:48954327-48954328	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571469797	chr8:48954331-48954332	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539159357	chr8:48954372-48954373	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs557803159	chr8:48954444-48954445	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553610108	chr8:48954447-48954448	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs575962145	chr8:48954478-48954479	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369909936	chr8:48954525-48954526	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs573444357	chr8:48954587-48954588	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs45565033	chr8:48954594-48954595	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541322397	chr8:48954600-48954601	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs111268766	chr8:48954601-48954602	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs190057962	chr8:48954625-48954626	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs545188211	chr8:48954853-48954854	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563841242	chr8:48954928-48954929	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530888617	chr8:48955025-48955026	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs181707089	chr8:48955245-48955246	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560939480	chr8:48955250-48955251	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs551991339	chr8:48955252-48955253	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs564966180	chr8:48955271-48955272	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs528772368	chr8:48955272-48955273	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546845701	chr8:48955298-48955299	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs571766987	chr8:48955303-48955304	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs114468124	chr8:48955311-48955312	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs527459891	chr8:48955340-48955341	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550877472	chr8:48955365-48955366	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs74938733	chr8:48955369-48955370	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs536743924	chr8:48955371-48955372	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs555442975	chr8:48955536-48955537	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573639637	chr8:48955537-48955538	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200281870	chr8:48955549-48955550	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185093734	chr8:48955554-48955555	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs116891483	chr8:48955555-48955556	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200746205	chr8:48955652-48955653	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545217661	chr8:48955657-48955658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11557784	chr8:48955672-48955673	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11557776	chr8:48955683-48955684	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563336717	chr8:48955717-48955718	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12680284	chr8:48955783-48955784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575736014	chr8:48955793-48955794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370713340	chr8:48955910-48955911	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568994851	chr8:48955924-48955925	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
22q11 deletion syndrome	20357662	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1206 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48921600-48956000	Weak transcription	Esophagus	oesophagus
2	chr8:48921600-48957400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:48921800-48957400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:48921800-48957400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr8:48921800-48957400	Weak transcription	Stomach Mucosa	stomach
6	chr8:48921800-48960600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr8:48921800-48966800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:48922000-48957600	Weak transcription	Colonic Mucosa	Colon
9	chr8:48922400-48955600	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr8:48922400-48957800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr8:48922400-48958000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:48922400-48975400	Weak transcription	Fetal Brain Male	brain
13	chr8:48922600-48955800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr8:48922600-48956200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr8:48922600-48956200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr8:48922600-48956600	Weak transcription	Brain Anterior Caudate	brain
17	chr8:48922600-48956800	Weak transcription	NHLF	lung
18	chr8:48922600-48957800	Weak transcription	HUVEC	blood vessel
19	chr8:48925000-48957600	Weak transcription	HSMMtube	muscle
20	chr8:48932800-48957200	Weak transcription	Spleen	Spleen
21	chr8:48933000-48956000	Weak transcription	Right Ventricle	heart
22	chr8:48933000-48956600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr8:48933000-48956800	Weak transcription	Gastric	stomach
24	chr8:48933200-48956000	Weak transcription	Fetal Kidney	kidney
25	chr8:48933200-48956200	Weak transcription	Brain Angular Gyrus	brain
26	chr8:48933400-48955800	Weak transcription	HMEC	breast
27	chr8:48933400-48956000	Weak transcription	Stomach Smooth Muscle	stomach
28	chr8:48934600-48956600	Weak transcription	Ovary	ovary
29	chr8:48934800-48955800	Weak transcription	Fetal Brain Female	brain
30	chr8:48934800-48956000	Weak transcription	HSMM	muscle
31	chr8:48935000-48956000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr8:48935000-48956000	Weak transcription	Lung	lung
33	chr8:48935000-48957000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr8:48935000-48957400	Weak transcription	NHEK	skin
35	chr8:48935200-48956000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr8:48935200-48963000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr8:48935400-48955600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr8:48935400-48956000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr8:48935400-48956000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr8:48935400-48956000	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr8:48935400-48956000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr8:48935400-48956800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr8:48935600-48955200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr8:48935600-48955600	Weak transcription	Brain Germinal Matrix	brain
45	chr8:48935600-48956000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:48935600-48956000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr8:48935600-48956200	Weak transcription	NHDF-Ad	bronchial
48	chr8:48935800-48955000	Weak transcription	A549	lung
49	chr8:48936000-48956000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr8:48936000-48956000	Weak transcription	Left Ventricle	heart

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