Variant report

Variant	nsv611458
Chromosome Location	chr8:67986890-68016482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:78)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:78 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:68009478-68009999	K562	blood:	n/a	n/a
2	BACH1	chr8:67998010-67998079	K562	blood:	n/a	n/a
3	BACH1	chr8:68013863-68013960	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:68007657-68007868	HepG2	liver:	n/a	chr8:68007705-68007716
5	CEBPB	chr8:68007700-68007715	K562	blood:	n/a	n/a
6	CEBPB	chr8:67996446-67996798	IMR90	lung:	n/a	n/a
7	CEBPB	chr8:68003361-68003523	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:68007624-68007824	A549	lung:	n/a	chr8:68007705-68007716
9	CTCF	chr8:68000542-68000640	Lung_OC	lung:	n/a	n/a
10	CTCF	chr8:67987860-67988010	NHEK	skin:	n/a	n/a
11	CUX1	chr8:68014271-68014273	K562	blood:	n/a	n/a
12	E2F4	chr8:67991769-67991800	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr8:68014335-68014520	MCF10A-Er-Src	breast:	n/a	n/a
14	GATA3	chr8:67988632-67988958	T-47D	breast:	n/a	n/a
15	GATA3	chr8:67988339-67988997	MCF-7	breast:	n/a	n/a
16	GATA3	chr8:67988605-67988942	T-47D	breast:	n/a	n/a
17	IRF1	chr8:68015267-68015434	K562	blood:	n/a	n/a
18	IRF1	chr8:68009538-68009576	K562	blood:	n/a	n/a
19	IRF1	chr8:68007339-68007358	K562	blood:	n/a	n/a
20	IRF1	chr8:67993017-67993078	K562	blood:	n/a	n/a
21	MAFF	chr8:68013754-68013934	K562	blood:	n/a	n/a
22	MAFF	chr8:68009704-68009867	HepG2	liver:	n/a	n/a
23	MAFK	chr8:68016162-68016163	HepG2	liver:	n/a	n/a
24	MAFK	chr8:68009659-68009864	HepG2	liver:	n/a	n/a
25	MAFK	chr8:68009676-68009831	HepG2	liver:	n/a	n/a
26	MAX	chr8:67993123-67993323	H1-hESC	embryonic stem cell:	n/a	chr8:67993265-67993275 chr8:67993236-67993246
27	MAX	chr8:67993206-67993331	NB4	blood:	n/a	chr8:67993265-67993275 chr8:67993236-67993246
28	MAZ	chr8:68008211-68008322	GM12878	blood:	n/a	n/a
29	MXI1	chr8:68009671-68009808	GM12878	blood:	n/a	n/a
30	MYC	chr8:67989714-67989724	MCF-7	breast:	n/a	n/a
31	MYC	chr8:67989680-67989686	MCF-7	breast:	n/a	n/a
32	MYC	chr8:68004712-68004769	MCF-7	breast:	n/a	n/a
33	MYC	chr8:67989727-67989877	MCF-7	breast:	n/a	n/a
34	MYC	chr8:67989618-67989677	MCF-7	breast:	n/a	n/a
35	NFYA	chr8:68010281-68010403	GM12878	blood:	n/a	n/a
36	PBX3	chr8:67996421-67996807	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr8:67996891-67998932	K562	blood:	n/a	n/a
38	POLR2A	chr8:67993604-67996666	K562	blood:	n/a	n/a
39	POLR2A	chr8:67989609-67989701	MCF-7	breast:	n/a	n/a
40	POLR2A	chr8:67996813-67996966	MCF-7	breast:	n/a	n/a
41	POLR2A	chr8:68005165-68005199	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr8:67999218-68000476	K562	blood:	n/a	n/a
43	POLR2A	chr8:68007826-68007913	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr8:67992070-67992197	ProgFib	skin:	n/a	n/a
45	POLR2A	chr8:68002301-68002470	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr8:67996820-67996926	MCF-7	breast:	n/a	n/a
47	POLR2A	chr8:67990906-67990944	MCF-7	breast:	n/a	n/a
48	POLR2A	chr8:67996907-67996951	ProgFib	skin:	n/a	n/a
49	POLR2A	chr8:67992880-67993279	K562	blood:	n/a	n/a
50	POLR2A	chr8:67989809-67989846	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67996256-67996306	MCF-7	breast:	n/a
2	chr8:67996256-67996306	ovcar-3	ovarian:	n/a
3	chr8:67996256-67996306	Jurkat	blood:	n/a
4	chr8:67996256-67996306	HCPEpiC	choroid plexus:	n/a
5	chr8:67996256-67996306	AG04449	skin:	fetal
6	chr8:67996256-67996306	HL-60	blood:	n/a
7	chr8:67996256-67996306	PrEC	prostate:	n/a
8	chr8:67996256-67996306	SK-N-MC	brain:	n/a
9	chr8:67996256-67996306	CMK	blood:	n/a
10	chr8:67996256-67996306	BJ	skin:	n/a
11	chr8:67996256-67996306	NH-A	brain:	n/a
12	chr8:67996256-67996306	PFSK-1	brain:	n/a
13	chr8:67996256-67996306	GM06990	blood:	n/a
14	chr8:67996256-67996306	GM19239	blood:	n/a
15	chr8:67996256-67996306	GM12892	blood:	n/a
16	chr8:67996256-67996306	T-47D	breast:	n/a
17	chr8:67996256-67996306	HRPEpiC	eye:	n/a
18	chr8:67996256-67996306	ECC-1	luminal epithelium:	n/a
19	chr8:67996256-67996306	HUVEC	blood vessel:	n/a
20	chr8:67996256-67996306	ProgFib	skin:	n/a
21	chr8:67996256-67996306	NHBE	bronchial:	n/a
22	chr8:67996256-67996306	RPTEC	kidney:	n/a
23	chr8:67996256-67996306	K562	blood:	n/a
24	chr8:67996256-67996306	U87	brain:	n/a
25	chr8:67996256-67996306	HRE	kidney:	n/a
26	chr8:67996256-67996306	HNPCEpiC	eye:	n/a
27	chr8:67996256-67996306	Caco-2	colon:	n/a
28	chr8:67996256-67996306	SK-N-SH	brain:	n/a
29	chr8:67996256-67996306	AG09319	gingival:	n/a
30	chr8:67996256-67996306	A549	lung:	n/a
31	chr8:67996256-67996306	AG04450	lung:	fetal
32	chr8:67996256-67996306	IMR90	lung:	fetal
33	chr8:67996256-67996306	HCM	heart:	n/a
34	chr8:67996256-67996306	HCF	heart:	n/a
35	chr8:67996256-67996306	SAEC	small airway:	n/a
36	chr8:67996256-67996306	HepG2	liver:	n/a
37	chr8:67996256-67996306	PANC-1	pancreas:	n/a
38	chr8:67996256-67996306	NB4	blood:	n/a
39	chr8:67996256-67996306	LNCaP	prostate:	n/a
40	chr8:67996256-67996306	MCF10A-Er-Src	breast:	n/a
41	chr8:67996256-67996306	AG10803	skin:	n/a
42	chr8:67996256-67996306	HMEC	breast:	n/a
43	chr8:67996256-67996306	HRCEpiC	kidney:	n/a
44	chr8:67996256-67996306	Hela-S3	cervix:	n/a
45	chr8:67996256-67996306	AG09309	skin:	n/a
46	chr8:67996256-67996306	GM12891	blood:	n/a
47	chr8:67996256-67996306	HEK293	kidney:	embryo
48	chr8:67996256-67996306	GM12878	blood:	n/a
49	chr8:67996256-67996306	SK-N-SH_RA	brain:	n/a
50	chr8:67996256-67996306	HEEpiC	esophagus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67975625..67978171-chr8:68007327..68009716,2	MCF-7	breast:
2	chr8:67974200..67976487-chr8:67991987..67993603,2	K562	blood:
3	chr8:67990677..67996100-chr8:67997550..68001970,5	K562	blood:
4	chr8:67981584..67984987-chr8:67987255..67990503,3	MCF-7	breast:
5	chr8:67977500..67979616-chr8:68012864..68015307,2	MCF-7	breast:
6	chr8:67831270..67834163-chr8:68004872..68007019,2	K562	blood:
7	chr8:67996527..67998674-chr8:68001336..68003420,2	K562	blood:
8	chr8:67831901..67834274-chr8:68007659..68009308,2	K562	blood:
9	chr8:67990308..67993966-chr8:67998315..68001185,4	K562	blood:
10	chr8:67996527..67998674-chr8:68001336..68003420,2	K562	blood:
11	chr8:67976406..67978604-chr8:68001660..68003649,2	K562	blood:
12	chr8:67981900..67985386-chr8:67987036..67990372,4	K562	blood:
13	chr8:67976148..67978802-chr8:68002770..68006546,3	K562	blood:
14	chr8:67978540..67980056-chr8:67997064..67998672,2	K562	blood:
15	chr8:67985384..67988219-chr8:68025028..68027428,3	K562	blood:
16	chr8:67990308..67993966-chr8:67998315..68001185,4	K562	blood:
17	chr8:67981623..67983543-chr8:67991584..67993705,2	K562	blood:
18	chr8:67997747..68001730-chr8:68001894..68004625,4	K562	blood:
19	chr8:67983356..67985019-chr8:67992324..67994930,2	MCF-7	breast:
20	chr8:68006861..68009461-chr8:68010974..68012762,2	K562	blood:
21	chr8:67973320..67975625-chr8:67995468..67997290,2	K562	blood:
22	chr8:67997747..68001730-chr8:68001894..68004625,4	K562	blood:
23	chr8:67830248..67833464-chr8:68001607..68004691,3	K562	blood:
24	chr8:67977046..67978803-chr8:67992749..67996349,3	K562	blood:
25	chr8:67973427..67978093-chr8:68011189..68018690,8	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COPS5-1	chr8:67997226-67997654	expReg_chr8_3344_-

No data

Variant related genes	Relation type
RNA5SP268	TF binding region
CSPP1	TF binding region
COPS5	TF binding region
RNA5SP268	CpG island
CSPP1	CpG island
COPS5	CpG island
ENSG00000121022	chromatin interactions
ENSG00000252637	chromatin interactions
ENSG00000104218	chromatin interactions

Extended variants
information (count: 956 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:956 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6983995	chr8:67986890-67986891	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188578960	chr8:67986897-67986898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568345821	chr8:67986914-67986915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540557482	chr8:67986938-67986939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529389513	chr8:67986946-67986947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397945936	chr8:67987033-67987034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75192553	chr8:67987034-67987035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549222742	chr8:67987065-67987066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569202060	chr8:67987101-67987102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537852966	chr8:67987130-67987131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552008215	chr8:67987164-67987165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150266718	chr8:67987211-67987212	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145827499	chr8:67987265-67987266	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571600498	chr8:67987266-67987267	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193198052	chr8:67987334-67987335	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553928020	chr8:67987348-67987349	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373709401	chr8:67987359-67987360	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573933231	chr8:67987385-67987386	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77170583	chr8:67987417-67987418	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555192789	chr8:67987462-67987463	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575132344	chr8:67987507-67987508	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185117900	chr8:67987562-67987563	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150820435	chr8:67987578-67987579	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376492797	chr8:67987588-67987589	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs57407566	chr8:67987591-67987592	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546964965	chr8:67987617-67987618	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141745669	chr8:67987705-67987706	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189963357	chr8:67987729-67987730	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560354071	chr8:67987827-67987828	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529121401	chr8:67987861-67987862	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549407477	chr8:67987924-67987925	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562849223	chr8:67987936-67987937	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114413573	chr8:67988094-67988095	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551484349	chr8:67988103-67988104	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72654939	chr8:67988196-67988197	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs62513082	chr8:67988269-67988270	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112352274	chr8:67988275-67988276	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147072077	chr8:67988289-67988290	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567491603	chr8:67988330-67988331	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536450902	chr8:67988332-67988333	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555401599	chr8:67988347-67988348	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575244592	chr8:67988356-67988357	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34439328	chr8:67988399-67988400	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537972525	chr8:67988463-67988464	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184035462	chr8:67988476-67988477	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73693106	chr8:67988567-67988568	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs577728199	chr8:67988612-67988613	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377404960	chr8:67988617-67988618	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540503019	chr8:67988627-67988628	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560465648	chr8:67988648-67988649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
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
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Multiple myeloma	16461302	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
Cancer	16751803	CNVD
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	17142309	CNVD
Glioblastoma multiforme	19115005	CNVD
Breast cancer	22522925	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD

Chromatin state (count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67977600-67989400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:67977600-67989600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:67977600-67998200	Weak transcription	Gastric	stomach
4	chr8:67977800-67987200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:67977800-67987400	Weak transcription	Primary B cells from cord blood	blood
6	chr8:67977800-67987400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr8:67977800-68009200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr8:67977800-68010000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr8:67977800-68013800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:67977800-68021800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:67977800-68044000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr8:67978000-67987000	Weak transcription	Fetal Stomach	stomach
13	chr8:67978000-67987200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr8:67978000-67987200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr8:67978000-67987400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr8:67978000-67987600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr8:67978000-67989400	Weak transcription	Small Intestine	intestine
18	chr8:67978000-67995400	Weak transcription	Colonic Mucosa	Colon
19	chr8:67978000-67996800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr8:67978000-68012200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:67978200-67987000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr8:67978200-67987000	Weak transcription	Left Ventricle	heart
23	chr8:67978200-67987200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr8:67978200-67987200	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr8:67978200-67987200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr8:67978200-67987200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr8:67978200-67987200	Weak transcription	Liver	Liver
28	chr8:67978200-67987200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr8:67978200-67987400	Weak transcription	Adipose Nuclei	Adipose
30	chr8:67978200-67987400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr8:67978200-67987400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr8:67978200-67987800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr8:67978200-67987800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr8:67978200-67987800	Weak transcription	Lung	lung
35	chr8:67978200-67989000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:67978200-67990600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:67978200-67992000	Weak transcription	Aorta	Aorta
38	chr8:67978200-67992600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:67978200-68006000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr8:67978200-68012600	Weak transcription	HUVEC	blood vessel
41	chr8:67978200-68074400	Weak transcription	Esophagus	oesophagus
42	chr8:67978400-67987200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr8:67978400-67987400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr8:67978400-67987400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr8:67978400-67987400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:67978400-67987400	Weak transcription	Fetal Brain Male	brain
47	chr8:67978400-67987400	Weak transcription	Fetal Kidney	kidney
48	chr8:67978400-67987400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr8:67978400-67989400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:67978400-67989800	Weak transcription	Stomach Smooth Muscle	stomach

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