Variant report

Variant	esv3384611
Chromosome Location	chr8:61461615-61480346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:61474082-61474230	HepG2	liver:	n/a	n/a
2	ATF2	chr8:61469014-61469546	GM12878	blood:	n/a	n/a
3	BATF	chr8:61469172-61469396	GM12878	blood:	n/a	n/a
4	BATF	chr8:61469131-61469410	GM12878	blood:	n/a	n/a
5	BCL3	chr8:61469223-61469504	GM12878	blood:	n/a	n/a
6	BCLAF1	chr8:61471526-61472082	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:61476050-61476114	GM12878	blood:	n/a	n/a
8	CEBPB	chr8:61466757-61467139	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:61466726-61467140	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:61466809-61467093	A549	lung:	n/a	n/a
11	CEBPB	chr8:61465847-61466066	K562	blood:	n/a	n/a
12	CEBPB	chr8:61466806-61467081	HepG2	liver:	n/a	n/a
13	CTCF	chr8:61473000-61473150	BJ	skin:	n/a	n/a
14	CTCF	chr8:61470060-61470210	SK-N-SH_RA	brain:	n/a	n/a
15	CUX1	chr8:61469227-61469475	GM12878	blood:	n/a	n/a
16	E2F4	chr8:61475014-61475430	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr8:61466939-61467139	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr8:61471737-61471961	GM12878	blood:	n/a	n/a
19	EP300	chr8:61469229-61469363	GM12878	blood:	n/a	n/a
20	EP300	chr8:61469189-61469418	GM12878	blood:	n/a	chr8:61469219-61469233
21	FOS	chr8:61466736-61467138	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr8:61472924-61473090	MCF10A-Er-Src	breast:	n/a	chr8:61473027-61473035 chr8:61473026-61473036 chr8:61473027-61473034
23	FOS	chr8:61466671-61467088	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr8:61466471-61467143	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:61473059-61473062	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:61472951-61473151	MCF10A-Er-Src	breast:	n/a	chr8:61473027-61473035 chr8:61473026-61473036 chr8:61473027-61473034
27	FOS	chr8:61466730-61467088	MCF10A-Er-Src	breast:	n/a	n/a
28	FOXA1	chr8:61473975-61474397	HepG2	liver:	n/a	n/a
29	FOXA2	chr8:61474062-61474317	HepG2	liver:	n/a	n/a
30	GATA3	chr8:61467995-61468403	SK-N-SH	brain:	n/a	n/a
31	JUND	chr8:61473018-61473147	HepG2	liver:	n/a	chr8:61473027-61473035 chr8:61473026-61473036 chr8:61473027-61473034
32	MAFF	chr8:61465280-61465481	HepG2	liver:	n/a	n/a
33	MAFF	chr8:61472255-61472455	HepG2	liver:	n/a	n/a
34	MAFF	chr8:61472297-61472503	K562	blood:	n/a	n/a
35	MAFK	chr8:61475968-61475993	HepG2	liver:	n/a	n/a
36	MAFK	chr8:61465245-61465464	HepG2	liver:	n/a	chr8:61465373-61465387
37	MAFK	chr8:61462446-61462789	IMR90	lung:	n/a	n/a
38	MAFK	chr8:61472313-61472500	HepG2	liver:	n/a	chr8:61472364-61472379
39	MAFK	chr8:61465185-61465495	HepG2	liver:	n/a	chr8:61465373-61465387
40	MAFK	chr8:61472254-61472483	HepG2	liver:	n/a	chr8:61472364-61472379
41	MAZ	chr8:61476141-61476155	GM12878	blood:	n/a	n/a
42	MEF2A	chr8:61468933-61469514	GM12878	blood:	n/a	chr8:61469322-61469339
43	MXI1	chr8:61471621-61472114	GM12878	blood:	n/a	n/a
44	MXI1	chr8:61469218-61469642	GM12878	blood:	n/a	n/a
45	MYC	chr8:61466796-61467138	MCF10A-Er-Src	breast:	n/a	n/a
46	NFE2	chr8:61471913-61471944	GM12878	blood:	n/a	n/a
47	NFIC	chr8:61469046-61469589	GM12878	blood:	n/a	n/a
48	NFIC	chr8:61469043-61469637	GM12878	blood:	n/a	n/a
49	POLR2A	chr8:61471797-61471875	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr8:61466133-61467222	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61474558-61474608	CMK	blood:	n/a
2	chr8:61474558-61474608	AoSMC	blood vessel:	n/a
3	chr8:61474558-61474608	HEK293	kidney:	embryo
4	chr8:61474558-61474608	SAEC	small airway:	n/a
5	chr8:61474558-61474608	PFSK-1	brain:	n/a
6	chr8:61474558-61474608	HCPEpiC	choroid plexus:	n/a
7	chr8:61474558-61474608	AG09309	skin:	n/a
8	chr8:61474558-61474608	BJ	skin:	n/a
9	chr8:61474558-61474608	Caco-2	colon:	n/a
10	chr8:61474558-61474608	A549	lung:	n/a
11	chr8:61474558-61474608	AG04450	lung:	fetal
12	chr8:61474558-61474608	ProgFib	skin:	n/a
13	chr8:61474558-61474608	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:61474558-61474608	GM19239	blood:	n/a
15	chr8:61474558-61474608	LNCaP	prostate:	n/a
16	chr8:61474558-61474608	HepG2	liver:	n/a
17	chr8:61474558-61474608	MCF10A-Er-Src	breast:	n/a
18	chr8:61474558-61474608	ECC-1	luminal epithelium:	n/a
19	chr8:61474558-61474608	Jurkat	blood:	n/a
20	chr8:61474558-61474608	SKMC	muscle:	n/a
21	chr8:61474558-61474608	HRPEpiC	eye:	n/a
22	chr8:61474558-61474608	HL-60	blood:	n/a
23	chr8:61474558-61474608	HCM	heart:	n/a
24	chr8:61474558-61474608	RPTEC	kidney:	n/a
25	chr8:61474558-61474608	AG09319	gingival:	n/a
26	chr8:61474558-61474608	PrEC	prostate:	n/a
27	chr8:61474558-61474608	AG10803	skin:	n/a
28	chr8:61474558-61474608	Hepatocyte	liver:	n/a
29	chr8:61474558-61474608	PANC-1	pancreas:	n/a
30	chr8:61474558-61474608	GM12892	blood:	n/a
31	chr8:61474558-61474608	K562	blood:	n/a
32	chr8:61474558-61474608	BE2_C	brain:	n/a
33	chr8:61474558-61474608	HCT-116	colon:	n/a
34	chr8:61474558-61474608	GM06990	blood:	n/a
35	chr8:61474558-61474608	H1-hESC	embryonic stem cell:	embryo
36	chr8:61474558-61474608	T-47D	breast:	n/a
37	chr8:61474558-61474608	U87	brain:	n/a
38	chr8:61474558-61474608	NB4	blood:	n/a
39	chr8:61474558-61474608	Hela-S3	cervix:	n/a
40	chr8:61474558-61474608	HNPCEpiC	eye:	n/a
41	chr8:61474558-61474608	IMR90	lung:	fetal
42	chr8:61474558-61474608	HAEpiC	amniotic membrane:	n/a
43	chr8:61474558-61474608	MCF-7	breast:	n/a
44	chr8:61474558-61474608	HRE	kidney:	n/a
45	chr8:61474558-61474608	GM12878	blood:	n/a
46	chr8:61474558-61474608	NHDF-neo	bronchial:	n/a
47	chr8:61474558-61474608	HCF	heart:	n/a
48	chr8:61474558-61474608	HUVEC	blood vessel:	n/a
49	chr8:61474558-61474608	HRCEpiC	kidney:	n/a
50	chr8:61474558-61474608	HIPEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:61428999..61430549-chr8:61472398..61474659,2	MCF-7	breast:
2	chr8:61427882..61431077-chr8:61476306..61480801,4	MCF-7	breast:
3	chr8:61462263..61464328-chr8:61464426..61466572,2	K562	blood:
4	chr8:61427866..61430946-chr8:61475959..61479177,3	MCF-7	breast:
5	chr8:61471508..61475092-chr8:61475799..61479657,3	K562	blood:
6	chr8:61479050..61481877-chr8:61482344..61485938,5	K562	blood:
7	chr8:61427715..61429441-chr8:61463246..61465194,2	K562	blood:
8	chr8:61456960..61460406-chr8:61461099..61464995,4	K562	blood:
9	chr8:61479439..61481118-chr8:61492027..61494400,2	K562	blood:
10	chr8:61466223..61468183-chr8:61469041..61471139,3	K562	blood:
11	chr8:61471508..61475092-chr8:61475799..61479657,3	K562	blood:
12	chr8:61462867..61465242-chr8:61590817..61592724,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA8-4	chr8:61464928-61465595	ENSG00000255321.1
2	lnc-CA8-11	chr8:61478325-61480362	ucscGeneNc_uc003xuc_1
3	lnc-CHD7-4	chr8:61471411-61471838	NONHSAT126835
4	lnc-CA8-4	chr8:61464516-61464536	ENSG00000255321.1

No data

Variant related genes	Relation type
ENSG00000255321	TF binding region
RAB2A	TF binding region
ENSG00000255321	CpG island
RAB2A	CpG island
ENSG00000104388	chromatin interactions
ENSG00000171316	chromatin interactions
ENSG00000251396	chromatin interactions
ENSG00000255321	chromatin interactions

Extended variants
information (count: 681 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540103177	chr8:61461648-61461649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs202124331	chr8:61461687-61461688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566710894	chr8:61461691-61461692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7819215	chr8:61461760-61461761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555541444	chr8:61461768-61461769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113972960	chr8:61461771-61461772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567774410	chr8:61461774-61461775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200269946	chr8:61461799-61461800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556891090	chr8:61461822-61461823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575162578	chr8:61461835-61461836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546065525	chr8:61461883-61461884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557807761	chr8:61461888-61461889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552849025	chr8:61461935-61461936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71525414	chr8:61461947-61461948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561875615	chr8:61461955-61461956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529377120	chr8:61461972-61461973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544406176	chr8:61461980-61461981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562884761	chr8:61461981-61461982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533211242	chr8:61461984-61461985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552045034	chr8:61461986-61461987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2737444	chr8:61461992-61461993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566774543	chr8:61462018-61462019	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527985948	chr8:61462026-61462027	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568222281	chr8:61462028-61462029	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34956255	chr8:61462039-61462040	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs57783701	chr8:61462055-61462056	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189561646	chr8:61462073-61462074	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567543266	chr8:61462111-61462112	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141426852	chr8:61462118-61462119	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556816669	chr8:61462131-61462132	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568826174	chr8:61462140-61462141	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35959880	chr8:61462147-61462148	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs72648594	chr8:61462172-61462173	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs369427326	chr8:61462194-61462195	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143589329	chr8:61462209-61462210	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11778115	chr8:61462223-61462224	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs573787255	chr8:61462254-61462255	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13257359	chr8:61462295-61462296	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs562885292	chr8:61462301-61462302	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73259438	chr8:61462396-61462397	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545031601	chr8:61462403-61462404	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560127667	chr8:61462440-61462441	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536982031	chr8:61462451-61462452	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527952433	chr8:61462462-61462463	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549296035	chr8:61462522-61462523	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs11778888	chr8:61462541-61462542	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs531855171	chr8:61462618-61462619	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs113551153	chr8:61462630-61462631	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566268342	chr8:61462654-61462655	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs73259441	chr8:61462695-61462696	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Pancreatic cancer	21811587	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
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
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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	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
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61433800-61472600	Weak transcription	HUVEC	blood vessel
2	chr8:61434600-61467600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr8:61434600-61472600	Weak transcription	Placenta	Placenta
4	chr8:61434800-61480600	Weak transcription	HMEC	breast
5	chr8:61435400-61470800	Weak transcription	NHEK	skin
6	chr8:61435400-61471800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr8:61437200-61462600	Weak transcription	NH-A	brain
8	chr8:61437400-61463200	Weak transcription	HSMM	muscle
9	chr8:61438000-61488600	Weak transcription	Fetal Brain Female	brain
10	chr8:61438400-61469600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr8:61439400-61494600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:61440800-61480000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr8:61443800-61472800	Weak transcription	Thymus	Thymus
14	chr8:61444000-61462800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr8:61446000-61462400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:61447400-61463600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:61447400-61466800	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr8:61447600-61462800	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr8:61447600-61465400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr8:61447600-61469200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr8:61447600-61472600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr8:61447800-61466600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:61447800-61466800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:61448600-61465200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr8:61448600-61465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:61448600-61505400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr8:61448800-61462200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:61449000-61473800	Weak transcription	HSMMtube	muscle
29	chr8:61449400-61472800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr8:61449600-61462000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr8:61449600-61466200	Weak transcription	Fetal Lung	lung
32	chr8:61449800-61462400	Weak transcription	Osteobl	bone
33	chr8:61450600-61464400	Weak transcription	Fetal Muscle Leg	muscle
34	chr8:61451200-61468400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr8:61451200-61469600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr8:61451400-61463000	Weak transcription	Esophagus	oesophagus
37	chr8:61451400-61469800	Weak transcription	Lung	lung
38	chr8:61451400-61472400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:61451400-61472400	Weak transcription	Ovary	ovary
40	chr8:61451400-61472600	Weak transcription	Fetal Stomach	stomach
41	chr8:61451400-61472600	Weak transcription	Spleen	Spleen
42	chr8:61451400-61482200	Weak transcription	Right Ventricle	heart
43	chr8:61451800-61465400	Weak transcription	Stomach Mucosa	stomach
44	chr8:61451800-61475800	Weak transcription	Fetal Heart	heart
45	chr8:61452400-61472400	Weak transcription	Liver	Liver
46	chr8:61453400-61472600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:61453800-61463800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr8:61453800-61465400	Weak transcription	Brain Anterior Caudate	brain
49	chr8:61453800-61470600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:61454400-61462000	Weak transcription	Brain Angular Gyrus	brain

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