Variant report

Variant	nsv967596
Chromosome Location	chr8:62489340-62494513
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr8:62492748-62493019	K562	blood:	n/a	n/a
2	CBX3	chr8:62492713-62493083	K562	blood:	n/a	n/a
3	CEBPB	chr8:62493728-62494030	IMR90	lung:	n/a	chr8:62493838-62493849
4	CEBPB	chr8:62493710-62493994	HepG2	liver:	n/a	chr8:62493838-62493849
5	CTCF	chr8:62490320-62490470	RPTEC	kidney:	n/a	n/a
6	CTCF	chr8:62490279-62490445	K562	blood:	n/a	n/a
7	CTCF	chr8:62490320-62490470	HEK293	kidney:	n/a	n/a
8	CTCF	chr8:62490315-62490367	GM10266	blood:	n/a	n/a
9	CTCF	chr8:62490299-62490425	HUVEC	blood vessel:	n/a	n/a
10	CTCF	chr8:62490305-62490402	LNCaP	prostate:	n/a	n/a
11	CTCF	chr8:62490327-62490419	MCF-7	breast:	n/a	n/a
12	CTCF	chr8:62490300-62490450	HMEC	breast:	n/a	n/a
13	CTCF	chr8:62491857-62492114	A549	lung:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62492022-62492031 chr8:62491939-62491957
14	CTCF	chr8:62491723-62492113	A549	lung:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62492022-62492031 chr8:62491939-62491957
15	CTCF	chr8:62491860-62492010	HEK293	kidney:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62491939-62491957
16	CTCF	chr8:62490260-62490410	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr8:62490280-62490430	HMEC	breast:	n/a	n/a
18	CTCF	chr8:62490304-62490440	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:62491760-62492149	K562	blood:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62492022-62492031 chr8:62491939-62491957
20	CTCF	chr8:62490340-62490490	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:62492275-62492313	Medullo	brain:	n/a	n/a
22	CTCF	chr8:62490260-62490410	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr8:62491711-62492065	A549	lung:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62492022-62492031 chr8:62491939-62491957
24	CTCF	chr8:62490300-62490450	HAc	cerebellar:	n/a	n/a
25	CTCF	chr8:62490300-62490450	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr8:62490325-62490413	Gliobla	brain:	n/a	n/a
27	CTCF	chr8:62490334-62490405	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:62490355-62490414	NHEK	skin:	n/a	n/a
29	CTCF	chr8:62490240-62490390	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr8:62490272-62490478	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:62490324-62490455	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:62490240-62490390	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr8:62490204-62490559	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:62490267-62490460	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:62490263-62490511	T-47D	breast:	n/a	n/a
36	CTCF	chr8:62490300-62490450	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:62490321-62490433	HepG2	liver:	n/a	n/a
38	CTCF	chr8:62490348-62490421	K562	blood:	n/a	n/a
39	CTCF	chr8:62491836-62492088	K562	blood:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62492022-62492031 chr8:62491939-62491957
40	CTCF	chr8:62490240-62490390	HepG2	liver:	n/a	n/a
41	CTCF	chr8:62491860-62492010	NHEK	skin:	n/a	chr8:62491940-62491956 chr8:62491934-62491955 chr8:62491939-62491957
42	FOS	chr8:62494497-62494867	HUVEC	blood vessel:	n/a	chr8:62494671-62494679 chr8:62494669-62494680
43	FOSL2	chr8:62491784-62492400	HepG2	liver:	n/a	n/a
44	FOSL2	chr8:62491362-62491621	HepG2	liver:	n/a	n/a
45	FOSL2	chr8:62490631-62490942	HepG2	liver:	n/a	n/a
46	HEY1	chr8:62490589-62490876	HepG2	liver:	n/a	n/a
47	HEY1	chr8:62490637-62490902	K562	blood:	n/a	n/a
48	HEY1	chr8:62490619-62490915	HepG2	liver:	n/a	n/a
49	HEY1	chr8:62490496-62490888	K562	blood:	n/a	n/a
50	HEY1	chr8:62491402-62491690	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:62494502-62494552	HRCEpiC	kidney:	n/a
2	chr8:62494502-62494552	RPTEC	kidney:	n/a
3	chr8:62494502-62494552	NT2-D1	testis:	n/a
4	chr8:62494502-62494552	MCF10A-Er-Src	breast:	n/a
5	chr8:62494502-62494552	U87	brain:	n/a
6	chr8:62494502-62494552	Hela-S3	cervix:	n/a
7	chr8:62494502-62494552	GM12892	blood:	n/a
8	chr8:62494502-62494552	AG09309	skin:	n/a
9	chr8:62494502-62494552	PrEC	prostate:	n/a
10	chr8:62494502-62494552	MCF-7	breast:	n/a
11	chr8:62494502-62494552	NH-A	brain:	n/a
12	chr8:62494502-62494552	HEK293	kidney:	embryo
13	chr8:62494502-62494552	GM12891	blood:	n/a
14	chr8:62494502-62494552	Caco-2	colon:	n/a
15	chr8:62494502-62494552	SAEC	small airway:	n/a
16	chr8:62494502-62494552	LNCaP	prostate:	n/a
17	chr8:62494502-62494552	SK-N-SH_RA	brain:	n/a
18	chr8:62494502-62494552	HUVEC	blood vessel:	n/a
19	chr8:62494502-62494552	SK-N-MC	brain:	n/a
20	chr8:62494502-62494552	HEEpiC	esophagus:	n/a
21	chr8:62494502-62494552	SKMC	muscle:	n/a
22	chr8:62494502-62494552	BJ	skin:	n/a
23	chr8:62494502-62494552	HCM	heart:	n/a
24	chr8:62494502-62494552	GM06990	blood:	n/a
25	chr8:62494502-62494552	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:62494502-62494552	HCF	heart:	n/a
27	chr8:62494502-62494552	ovcar-3	ovarian:	n/a
28	chr8:62494502-62494552	HCPEpiC	choroid plexus:	n/a
29	chr8:62494502-62494552	HNPCEpiC	eye:	n/a
30	chr8:62494502-62494552	Hepatocyte	liver:	n/a
31	chr8:62494502-62494552	HepG2	liver:	n/a
32	chr8:62494502-62494552	AG09319	gingival:	n/a
33	chr8:62494502-62494552	HAEpiC	amniotic membrane:	n/a
34	chr8:62494502-62494552	AG04449	skin:	fetal
35	chr8:62494502-62494552	HRE	kidney:	n/a
36	chr8:62494502-62494552	NHBE	bronchial:	n/a
37	chr8:62494502-62494552	BE2_C	brain:	n/a
38	chr8:62494502-62494552	HMEC	breast:	n/a
39	chr8:62494502-62494552	SK-N-SH	brain:	n/a
40	chr8:62494502-62494552	IMR90	lung:	fetal
41	chr8:62494502-62494552	HCT-116	colon:	n/a
42	chr8:62494502-62494552	HL-60	blood:	n/a
43	chr8:62494502-62494552	AoSMC	blood vessel:	n/a
44	chr8:62494502-62494552	T-47D	breast:	n/a
45	chr8:62494502-62494552	NHDF-neo	bronchial:	n/a
46	chr8:62494502-62494552	H1-hESC	embryonic stem cell:	embryo
47	chr8:62494502-62494552	HRPEpiC	eye:	n/a
48	chr8:62494502-62494552	AG04450	lung:	fetal
49	chr8:62494502-62494552	GM12878	blood:	n/a
50	chr8:62494502-62494552	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:62488403..62489962-chr8:62494279..62497109,2	MCF-7	breast:
2	chr8:62488403..62489962-chr8:62494279..62497109,2	MCF-7	breast:

Variant related genes	Relation type
KRT8P3	TF binding region
KRT8P3	CpG island

Extended variants
information (count: 285 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139441811	chr8:62489375-62489376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548801422	chr8:62489414-62489415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375490820	chr8:62489457-62489458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570221529	chr8:62489479-62489480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537764424	chr8:62489481-62489482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570499771	chr8:62489536-62489537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7826255	chr8:62489538-62489539	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188000572	chr8:62489540-62489541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535152547	chr8:62489541-62489542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534595239	chr8:62489546-62489547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553091179	chr8:62489584-62489585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555410355	chr8:62489607-62489608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58670418	chr8:62489663-62489664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574881154	chr8:62489669-62489670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28537937	chr8:62489677-62489678	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs574950913	chr8:62489686-62489687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs59795635	chr8:62489693-62489694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554361773	chr8:62489705-62489706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575801137	chr8:62489706-62489707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111361265	chr8:62489709-62489710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180819714	chr8:62489724-62489725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377679548	chr8:62489734-62489735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540761345	chr8:62489741-62489742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560364272	chr8:62489773-62489774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565216726	chr8:62489790-62489791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185573739	chr8:62489798-62489799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541067997	chr8:62489799-62489800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559038996	chr8:62489814-62489815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529806548	chr8:62489828-62489829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12677880	chr8:62489887-62489888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370957490	chr8:62489910-62489911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373887546	chr8:62489913-62489914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13271440	chr8:62489920-62489921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200222932	chr8:62489921-62489922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11435804	chr8:62489931-62489932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370446705	chr8:62489932-62489933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375088460	chr8:62489937-62489938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191110230	chr8:62489968-62489969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183727339	chr8:62489972-62489973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113361818	chr8:62489980-62489981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10634345	chr8:62489982-62489983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372262495	chr8:62490072-62490073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115478993	chr8:62490084-62490085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541766493	chr8:62490123-62490124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372050425	chr8:62490133-62490134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186633417	chr8:62490167-62490168	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571171097	chr8:62490170-62490171	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs35893761	chr8:62490181-62490182	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs534961435	chr8:62490187-62490188	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs114522179	chr8:62490190-62490191	Weak transcription Strong transcription	TF binding region	1 gene(s)	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
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
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
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
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
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62411000-62505800	Weak transcription	Brain Angular Gyrus	brain
2	chr8:62411200-62493800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:62414800-62503400	Weak transcription	Fetal Heart	heart
4	chr8:62442600-62493200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr8:62449800-62503600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr8:62456000-62491600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:62456600-62492800	Weak transcription	Small Intestine	intestine
8	chr8:62456600-62503800	Weak transcription	Stomach Mucosa	stomach
9	chr8:62457000-62496600	Weak transcription	Brain Hippocampus Middle	brain
10	chr8:62457000-62503000	Weak transcription	HSMMtube	muscle
11	chr8:62458000-62497000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:62458800-62491000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:62460200-62495800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr8:62464000-62492400	Weak transcription	Fetal Muscle Leg	muscle
15	chr8:62464000-62492600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr8:62464000-62494000	Weak transcription	HUVEC	blood vessel
17	chr8:62464400-62492600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr8:62466600-62490200	Weak transcription	K562	blood
19	chr8:62466800-62508600	Weak transcription	Pancreas	Pancrea
20	chr8:62467600-62492600	Weak transcription	Spleen	Spleen
21	chr8:62468600-62549000	Weak transcription	Right Ventricle	heart
22	chr8:62470800-62491600	Weak transcription	Fetal Brain Female	brain
23	chr8:62473000-62490600	Weak transcription	Fetal Intestine Large	intestine
24	chr8:62474800-62493400	Weak transcription	HMEC	breast
25	chr8:62474800-62496600	Weak transcription	Placenta	Placenta
26	chr8:62476200-62492200	Weak transcription	Brain Germinal Matrix	brain
27	chr8:62479800-62489600	Weak transcription	Thymus	Thymus
28	chr8:62480000-62492600	Weak transcription	Brain Cingulate Gyrus	brain
29	chr8:62480000-62503600	Weak transcription	NHEK	skin
30	chr8:62480600-62490600	Weak transcription	Psoas Muscle	Psoas
31	chr8:62480800-62493200	Weak transcription	Primary T cells from cord blood	blood
32	chr8:62481000-62494000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr8:62481600-62492600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr8:62481600-62493000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr8:62481600-62493400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr8:62481800-62493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:62484200-62503600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr8:62485200-62490800	Weak transcription	Gastric	stomach
39	chr8:62485400-62492600	Weak transcription	Esophagus	oesophagus
40	chr8:62487000-62489800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:62487000-62491000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr8:62487000-62493800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:62487000-62494800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr8:62487400-62489400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:62487400-62489400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:62487400-62489400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr8:62487400-62489400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr8:62487400-62489400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:62487400-62489400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:62487400-62489400	Strong transcription	Liver	Liver

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