Variant report

Variant	esv1792589
Chromosome Location	chr8:69066748-69085741
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	chr8:69071955-69072222	K562	blood:	n/a	n/a
2	CBX3	chr8:69071899-69072226	K562	blood:	n/a	n/a
3	CEBPB	chr8:69066911-69067138	IMR90	lung:	n/a	n/a
4	CEBPB	chr8:69077628-69077931	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:69066895-69067163	K562	blood:	n/a	n/a
6	CEBPB	chr8:69066955-69067203	HepG2	liver:	n/a	n/a
7	CTCF	chr8:69067439-69067461	K562	blood:	n/a	n/a
8	CTCF	chr8:69079624-69079657	Pancreas_OC	pancreas:	n/a	n/a
9	E2F4	chr8:69069178-69069503	MCF10A-Er-Src	breast:	n/a	n/a
10	E2F4	chr8:69068573-69068655	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr8:69077765-69077927	GM12878	blood:	n/a	n/a
12	EBF1	chr8:69066715-69066850	GM12878	blood:	n/a	chr8:69066769-69066780
13	EP300	chr8:69067375-69067457	K562	blood:	n/a	n/a
14	EP300	chr8:69080380-69080580	K562	blood:	n/a	n/a
15	FAM48A	chr8:69082214-69082343	GM12878	blood:	n/a	n/a
16	FOXA1	chr8:69084529-69084694	T-47D	breast:	n/a	n/a
17	IRF1	chr8:69069477-69069614	K562	blood:	n/a	n/a
18	IRF1	chr8:69067291-69067790	K562	blood:	n/a	chr8:69067540-69067554 chr8:69067748-69067762 chr8:69067539-69067552 chr8:69067748-69067761 chr8:69067540-69067550
19	IRF1	chr8:69068116-69068144	K562	blood:	n/a	n/a
20	IRF1	chr8:69067062-69067172	K562	blood:	n/a	n/a
21	JUN	chr8:69072059-69072326	K562	blood:	n/a	n/a
22	KAP1	chr8:69071548-69072712	K562	blood:	n/a	n/a
23	MAFF	chr8:69067311-69067528	HepG2	liver:	n/a	chr8:69067397-69067415
24	MAFF	chr8:69067221-69067556	K562	blood:	n/a	chr8:69067397-69067415
25	MAFK	chr8:69067274-69067556	K562	blood:	n/a	chr8:69067399-69067414
26	MAFK	chr8:69067297-69067523	H1-hESC	embryonic stem cell:	n/a	chr8:69067399-69067414
27	MAFK	chr8:69067270-69067474	HepG2	liver:	n/a	chr8:69067399-69067414
28	MAFK	chr8:69077296-69077537	H1-hESC	embryonic stem cell:	n/a	chr8:69077394-69077410 chr8:69077395-69077409 chr8:69077392-69077412
29	MAFK	chr8:69067276-69067540	HepG2	liver:	n/a	chr8:69067399-69067414
30	MAFK	chr8:69067278-69067567	IMR90	lung:	n/a	chr8:69067399-69067414
31	MXI1	chr8:69067891-69067905	K562	blood:	n/a	n/a
32	MYC	chr8:69084571-69084745	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr8:69066588-69066902	H1-neurons	neurons:	n/a	n/a
34	REST	chr8:69084520-69084697	U87	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
35	REST	chr8:69084288-69084993	H1-hESC	embryonic stem cell:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
36	REST	chr8:69084410-69084825	HepG2	liver:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
37	REST	chr8:69084340-69084930	PFSK-1	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
38	REST	chr8:69084574-69084679	PANC-1	pancreas:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
39	REST	chr8:69084445-69084760	HepG2	liver:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
40	REST	chr8:69084534-69084731	SK-N-SH	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
41	REST	chr8:69084491-69084886	PANC-1	pancreas:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
42	REST	chr8:69084504-69084694	PFSK-1	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
43	REST	chr8:69084514-69084807	SK-N-SH	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
44	REST	chr8:69084523-69084817	HCT-116	colon:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
45	REST	chr8:69084527-69084706	GM12878	blood:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
46	REST	chr8:69084513-69084716	GM12878	blood:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
47	REST	chr8:69084422-69084864	HL-60	blood:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
48	REST	chr8:69084181-69085148	HL-60	blood:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
49	REST	chr8:69084379-69084755	PFSK-1	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639
50	REST	chr8:69084443-69084806	U87	brain:	n/a	chr8:69084625-69084634 chr8:69084630-69084639 chr8:69084619-69084639 chr8:69084619-69084639 chr8:69084619-69084639

No.	Distal block	Cell Line	Cell type
1	chr8:68988620..68991285-chr8:69064188..69067097,2	K562	blood:
2	chr6:91347083..91349227-chr8:69066919..69069417,2	MCF-7	breast:
3	chr8:69084432..69086381-chr8:69131521..69133145,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254051	TF binding region
PREX2	TF binding region

Extended variants
information (count: 685 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:685 , 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	rs1434781	chr8:69066793-69066794	Weak transcription Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369516584	chr8:69066805-69066806	Weak transcription Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143191125	chr8:69066924-69066925	Weak transcription Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112400786	chr8:69066967-69066968	Weak transcription Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs570362134	chr8:69067033-69067034	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs539347243	chr8:69067057-69067058	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs552273531	chr8:69067090-69067091	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566033593	chr8:69067092-69067093	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs546709576	chr8:69067097-69067098	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs191997731	chr8:69067112-69067113	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs565022846	chr8:69067120-69067121	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183141893	chr8:69067211-69067212	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574604962	chr8:69067217-69067218	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554932108	chr8:69067240-69067241	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs187472089	chr8:69067245-69067246	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs192027030	chr8:69067261-69067262	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs139986427	chr8:69067271-69067272	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs113130556	chr8:69067316-69067317	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs576238473	chr8:69067334-69067335	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs4582543	chr8:69067352-69067353	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs151157666	chr8:69067394-69067395	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372850425	chr8:69067396-69067397	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs571960272	chr8:69067406-69067407	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs150091537	chr8:69067435-69067436	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs140209378	chr8:69067446-69067447	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs150335092	chr8:69067449-69067450	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs529863416	chr8:69067511-69067512	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138031541	chr8:69067536-69067537	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563906888	chr8:69067572-69067573	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs184131156	chr8:69067597-69067598	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs187958685	chr8:69067607-69067608	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs566248936	chr8:69067617-69067618	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs577701556	chr8:69067632-69067633	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192815418	chr8:69067733-69067734	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs142194738	chr8:69067767-69067768	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs537181835	chr8:69067774-69067775	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs377004083	chr8:69067870-69067871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557048182	chr8:69067893-69067894	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs73263332	chr8:69067895-69067896	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184380442	chr8:69067952-69067953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558775799	chr8:69067976-69067977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572289452	chr8:69068018-69068019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541024999	chr8:69068032-69068033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554635262	chr8:69068046-69068047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542817066	chr8:69068050-69068051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543509267	chr8:69068098-69068099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563263909	chr8:69068105-69068106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34916909	chr8:69068124-69068125	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs562689900	chr8:69068150-69068151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532696276	chr8:69068179-69068180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69020000-69082600	Weak transcription	Fetal Stomach	stomach
2	chr8:69021000-69067600	Weak transcription	Right Ventricle	heart
3	chr8:69033200-69066800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:69041000-69068400	Weak transcription	Lung	lung
5	chr8:69043600-69107000	Weak transcription	Brain Substantia Nigra	brain
6	chr8:69045400-69066800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr8:69046600-69083200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:69046800-69070800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr8:69047000-69070000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr8:69052600-69104600	Weak transcription	Brain Hippocampus Middle	brain
11	chr8:69055800-69070800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr8:69061800-69074000	Weak transcription	Adipose Nuclei	Adipose
13	chr8:69063800-69068200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:69064800-69067200	Strong transcription	HUVEC	blood vessel
15	chr8:69065200-69067600	Enhancers	K562	blood
16	chr8:69065200-69070000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:69065200-69074000	Weak transcription	Left Ventricle	heart
18	chr8:69065600-69070600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:69066200-69066800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:69066200-69067000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr8:69066200-69067200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:69066200-69067400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr8:69066200-69067400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr8:69066200-69067400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:69066600-69067600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:69066800-69067200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr8:69066800-69067200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr8:69066800-69067400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr8:69067000-69067400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr8:69067000-69082600	Weak transcription	Brain Anterior Caudate	brain
31	chr8:69067200-69070600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr8:69067200-69070600	Weak transcription	HUVEC	blood vessel
33	chr8:69067200-69074800	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr8:69067400-69067800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:69067400-69068400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr8:69067400-69068800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr8:69067400-69068800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:69067400-69070400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr8:69067600-69067800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:69067800-69068000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:69067800-69069800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr8:69068000-69068200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:69068200-69068800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:69068200-69076400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:69068400-69068600	ZNF genes & repeats	Lung	lung
46	chr8:69068400-69069800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr8:69068600-69087200	Weak transcription	Lung	lung
48	chr8:69068800-69069200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:69068800-69075000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr8:69068800-69075600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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