Variant report

Variant	nsv971685
Chromosome Location	chr8:95903266-95905138
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	BATF	chr8:95903425-95903626	GM12878	blood:	n/a	n/a
2	BATF	chr8:95903394-95903658	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:95903383-95903626	GM12878	blood:	n/a	n/a
4	CEBPB	chr8:95902981-95903289	A549	lung:	n/a	chr8:95903136-95903149 chr8:95903138-95903147 chr8:95903137-95903148 chr8:95903136-95903147 chr8:95903136-95903147 chr8:95903136-95903149 chr8:95903138-95903147 chr8:95903138-95903147 chr8:95903138-95903147 chr8:95903136-95903149
5	CEBPB	chr8:95903031-95903266	IMR90	lung:	n/a	chr8:95903136-95903149 chr8:95903138-95903147 chr8:95903137-95903148 chr8:95903136-95903147 chr8:95903136-95903147 chr8:95903136-95903149 chr8:95903138-95903147 chr8:95903138-95903147 chr8:95903138-95903147 chr8:95903136-95903149
6	CEBPB	chr8:95902986-95903315	HepG2	liver:	n/a	chr8:95903136-95903149 chr8:95903138-95903147 chr8:95903137-95903148 chr8:95903136-95903147 chr8:95903136-95903147 chr8:95903136-95903149 chr8:95903138-95903147 chr8:95903138-95903147 chr8:95903138-95903147 chr8:95903136-95903149
7	EBF1	chr8:95903338-95903684	GM12878	blood:	n/a	n/a
8	EP300	chr8:95903383-95903651	GM12878	blood:	n/a	n/a
9	IKZF1	chr8:95903395-95903466	GM12878	blood:	n/a	n/a
10	MEF2A	chr8:95903275-95903566	GM12878	blood:	n/a	n/a
11	NFIC	chr8:95903238-95903745	GM12878	blood:	n/a	n/a
12	PAX5	chr8:95903324-95903713	GM12878	blood:	n/a	n/a
13	PAX5	chr8:95903443-95903603	GM12878	blood:	n/a	n/a
14	POU2F2	chr8:95903450-95903602	GM12878	blood:	n/a	chr8:95903578-95903591
15	POU2F2	chr8:95903311-95903749	GM12891	blood:	n/a	chr8:95903578-95903591
16	POU2F2	chr8:95903258-95903750	GM12878	blood:	n/a	chr8:95903578-95903591 chr8:95903286-95903298
17	POU2F2	chr8:95903367-95903740	GM12878	blood:	n/a	chr8:95903578-95903591
18	POU2F2	chr8:95903396-95903733	GM12891	blood:	n/a	chr8:95903578-95903591
19	RCOR1	chr8:95903400-95903625	GM12878	blood:	n/a	n/a
20	RELA	chr8:95903249-95903683	GM12878	blood:	n/a	n/a
21	RELA	chr8:95903350-95903690	GM19099	blood:	n/a	n/a
22	RUNX3	chr8:95903282-95903746	GM12878	blood:	n/a	n/a
23	RUNX3	chr8:95903244-95903746	GM12878	blood:	n/a	n/a
24	TBL1XR1	chr8:95903414-95903623	GM12878	blood:	n/a	n/a
25	TBP	chr8:95903384-95903616	GM12878	blood:	n/a	n/a
26	TCF12	chr8:95903402-95903663	GM12878	blood:	n/a	n/a
27	WRNIP1	chr8:95903581-95903611	GM12878	blood:	n/a	n/a
28	ZNF384	chr8:95903350-95903535	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95904183-95904233	AG04449	skin:	fetal
2	chr8:95904183-95904233	PrEC	prostate:	n/a
3	chr8:95904183-95904233	HUVEC	blood vessel:	n/a
4	chr8:95904183-95904233	HNPCEpiC	eye:	n/a
5	chr8:95904183-95904233	ovcar-3	ovarian:	n/a
6	chr8:95904183-95904233	HEEpiC	esophagus:	n/a
7	chr8:95904183-95904233	HepG2	liver:	n/a
8	chr8:95904183-95904233	H1-hESC	embryonic stem cell:	embryo
9	chr8:95904183-95904233	AoSMC	blood vessel:	n/a
10	chr8:95904183-95904233	GM19239	blood:	n/a
11	chr8:95904183-95904233	GM12892	blood:	n/a
12	chr8:95904183-95904233	HCF	heart:	n/a
13	chr8:95904183-95904233	ECC-1	luminal epithelium:	n/a
14	chr8:95904183-95904233	HCT-116	colon:	n/a
15	chr8:95904183-95904233	MCF10A-Er-Src	breast:	n/a
16	chr8:95904183-95904233	GM12891	blood:	n/a
17	chr8:95904183-95904233	SKMC	muscle:	n/a
18	chr8:95904183-95904233	SK-N-SH_RA	brain:	n/a
19	chr8:95904183-95904233	AG09309	skin:	n/a
20	chr8:95904183-95904233	ProgFib	skin:	n/a
21	chr8:95904183-95904233	PANC-1	pancreas:	n/a
22	chr8:95904183-95904233	T-47D	breast:	n/a
23	chr8:95904183-95904233	SK-N-SH	brain:	n/a
24	chr8:95904183-95904233	HMEC	breast:	n/a
25	chr8:95904183-95904233	HIPEpiC	eye:	n/a
26	chr8:95904183-95904233	SAEC	small airway:	n/a
27	chr8:95904183-95904233	HRE	kidney:	n/a
28	chr8:95904183-95904233	MCF-7	breast:	n/a
29	chr8:95904183-95904233	GM12878	blood:	n/a
30	chr8:95904183-95904233	AG09319	gingival:	n/a
31	chr8:95904183-95904233	SK-N-MC	brain:	n/a
32	chr8:95904183-95904233	U87	brain:	n/a
33	chr8:95904183-95904233	BJ	skin:	n/a
34	chr8:95904183-95904233	NHBE	bronchial:	n/a
35	chr8:95904183-95904233	HL-60	blood:	n/a
36	chr8:95904183-95904233	Hela-S3	cervix:	n/a
37	chr8:95904183-95904233	HAEpiC	amniotic membrane:	n/a
38	chr8:95904183-95904233	AG10803	skin:	n/a
39	chr8:95904183-95904233	HPAEpiC	pulmonary alveolar:	n/a
40	chr8:95904183-95904233	HEK293	kidney:	embryo
41	chr8:95904183-95904233	NHDF-neo	bronchial:	n/a
42	chr8:95904183-95904233	HCPEpiC	choroid plexus:	n/a
43	chr8:95904183-95904233	NH-A	brain:	n/a
44	chr8:95904183-95904233	NB4	blood:	n/a
45	chr8:95904183-95904233	Jurkat	blood:	n/a
46	chr8:95904183-95904233	HCM	heart:	n/a
47	chr8:95904183-95904233	GM06990	blood:	n/a
48	chr8:95904183-95904233	K562	blood:	n/a
49	chr8:95904183-95904233	NT2-D1	testis:	n/a
50	chr8:95904183-95904233	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:95905055..95911257-chr8:96032486..96039313,18	MCF-7	breast:
2	chr8:95905045..95910108-chr8:95959761..95963234,8	MCF-7	breast:

Variant related genes	Relation type
NDUFAF6	TF binding region
CCNE2	TF binding region
ENSG00000243979	TF binding region
NDUFAF6	CpG island
CCNE2	CpG island
ENSG00000243979	CpG island
ENSG00000156170	chromatin interactions
ENSG00000253878	chromatin interactions
ENSG00000164938	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539775794	chr8:95903284-95903285	Weak transcription Strong transcription Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
2	rs553653653	chr8:95903332-95903333	Weak transcription Strong transcription Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs556269131	chr8:95903337-95903338	Weak transcription Strong transcription Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs576114863	chr8:95903390-95903391	Weak transcription Strong transcription Genic enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs113616310	chr8:95903496-95903497	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs138117506	chr8:95903506-95903507	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs142474623	chr8:95903551-95903552	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs574634057	chr8:95903563-95903564	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs543532453	chr8:95903582-95903583	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs28399562	chr8:95903610-95903611	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs538864288	chr8:95903629-95903630	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs75662692	chr8:95903681-95903682	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs75786496	chr8:95903684-95903685	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs532122744	chr8:95903688-95903689	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs75013955	chr8:95903709-95903710	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs75192149	chr8:95903715-95903716	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs545453666	chr8:95903721-95903722	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs559611375	chr8:95903723-95903724	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs528331981	chr8:95903754-95903755	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116963277	chr8:95903761-95903762	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561540429	chr8:95903793-95903794	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192411897	chr8:95903800-95903801	Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550640927	chr8:95903835-95903836	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570586587	chr8:95903879-95903880	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75283931	chr8:95903886-95903887	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34021439	chr8:95903887-95903888	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78334619	chr8:95903890-95903891	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539839395	chr8:95903900-95903901	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546636834	chr8:95903902-95903903	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79531125	chr8:95903905-95903906	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75047158	chr8:95903908-95903909	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376945646	chr8:95903946-95903947	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535772126	chr8:95903983-95903984	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556038849	chr8:95903986-95903987	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28399561	chr8:95904006-95904007	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs139270033	chr8:95904069-95904070	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs71273430	chr8:95904130-95904131	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs71273431	chr8:95904140-95904141	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs116473344	chr8:95904162-95904163	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs576827301	chr8:95904170-95904171	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs545790022	chr8:95904185-95904186	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	CpG island	2 gene(s)	Overlapped CNVs	n/a
42	rs184825178	chr8:95904190-95904191	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	CpG island	2 gene(s)	Overlapped CNVs	n/a
43	rs11783941	chr8:95904195-95904196	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs11776830	chr8:95904198-95904199	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs143194042	chr8:95904219-95904220	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs530642374	chr8:95904240-95904241	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28399560	chr8:95904243-95904244	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs188907205	chr8:95904275-95904276	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373555748	chr8:95904308-95904309	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192292606	chr8:95904314-95904315	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
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
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
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95837000-95905600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:95838200-95905600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:95839400-95904400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:95870200-95905200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:95870600-95905600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr8:95874400-95904600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:95875600-95904400	Strong transcription	Fetal Thymus	thymus
8	chr8:95876200-95906600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr8:95879200-95906600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:95881200-95905800	Weak transcription	Spleen	Spleen
11	chr8:95882200-95906600	Weak transcription	Gastric	stomach
12	chr8:95883400-95905600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:95883600-95905600	Weak transcription	Small Intestine	intestine
14	chr8:95886000-95905600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:95886000-95906400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:95887200-95904600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr8:95887600-95906200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:95888200-95906600	Weak transcription	Ovary	ovary
19	chr8:95890000-95906200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr8:95890200-95906600	Weak transcription	Lung	lung
21	chr8:95890600-95906800	Weak transcription	Aorta	Aorta
22	chr8:95890800-95905800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr8:95890800-95905800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr8:95890800-95905800	Weak transcription	Psoas Muscle	Psoas
25	chr8:95891000-95906600	Weak transcription	Left Ventricle	heart
26	chr8:95891400-95905400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr8:95891400-95905600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr8:95891600-95904800	Weak transcription	Fetal Heart	heart
29	chr8:95891800-95905800	Weak transcription	Esophagus	oesophagus
30	chr8:95891800-95906000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr8:95892400-95906400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr8:95893600-95905800	Weak transcription	HepG2	liver
33	chr8:95893800-95906000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr8:95894000-95905200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:95894000-95905600	Weak transcription	Primary T cells from cord blood	blood
36	chr8:95894000-95905600	Weak transcription	NHLF	lung
37	chr8:95894000-95905800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr8:95894000-95905800	Weak transcription	Stomach Smooth Muscle	stomach
39	chr8:95894000-95906200	Weak transcription	Fetal Kidney	kidney
40	chr8:95894400-95905600	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr8:95894600-95905600	Weak transcription	Placenta	Placenta
42	chr8:95894800-95905400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr8:95894800-95905600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr8:95894800-95905600	Weak transcription	Duodenum Mucosa	Duodenum
45	chr8:95894800-95905800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr8:95894800-95905800	Weak transcription	Colon Smooth Muscle	Colon
47	chr8:95894800-95905800	Weak transcription	Rectal Smooth Muscle	rectum
48	chr8:95894800-95906000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr8:95894800-95906400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:95895000-95905600	Weak transcription	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links