Variant report

Variant	esv3364328
Chromosome Location	chr8:6423194-6425692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:245)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:6424597-6424648	GM12892	blood:	n/a	n/a
2	CTCF	chr8:6424644-6424787	GM19239	blood:	n/a	n/a
3	CTCF	chr8:6424143-6424201	GM12891	blood:	n/a	n/a
4	CTCF	chr8:6424026-6424131	GM19239	blood:	n/a	n/a
5	CTCF	chr8:6424009-6424086	ProgFib	skin:	n/a	n/a
6	CTCF	chr8:6424203-6424360	GM19239	blood:	n/a	n/a
7	CTCF	chr8:6424019-6424025	GM19239	blood:	n/a	n/a
8	CTCF	chr8:6424331-6424355	GM12878	blood:	n/a	n/a
9	CTCF	chr8:6424377-6424518	GM19239	blood:	n/a	n/a
10	MYC	chr8:6424736-6424848	MCF-7	breast:	n/a	n/a
11	MYC	chr8:6424885-6424899	MCF-7	breast:	n/a	n/a
12	MYC	chr8:6423811-6423952	MCF-7	breast:	n/a	chr8:6423843-6423850
13	MYC	chr8:6424041-6424070	MCF-7	breast:	n/a	n/a
14	MYC	chr8:6424028-6424310	MCF-7	breast:	n/a	n/a
15	MYC	chr8:6423814-6424927	MCF-7	breast:	n/a	chr8:6423843-6423850
16	MYC	chr8:6424173-6424846	MCF-7	breast:	n/a	n/a
17	MYC	chr8:6424076-6424106	MCF-7	breast:	n/a	n/a
18	NR2C2	chr8:6423914-6424901	GM12878	blood:	n/a	n/a
19	POLR2A	chr8:6424515-6424580	Gliobla	brain:	n/a	n/a
20	POLR2A	chr8:6424373-6424483	Gliobla	brain:	n/a	n/a
21	POLR2A	chr8:6423765-6424947	MCF-7	breast:	n/a	n/a
22	POLR2A	chr8:6423289-6423308	K562	blood:	n/a	n/a
23	POLR2A	chr8:6424542-6424786	A549	lung:	n/a	n/a
24	POLR2A	chr8:6423804-6424956	MCF-7	breast:	n/a	n/a
25	REST	chr8:6424472-6424614	PANC-1	pancreas:	n/a	n/a
26	TCF3	chr8:6424197-6424845	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6423908-6423958	IMR90	lung:	fetal
2	chr8:6423908-6423958	IMR90	lung:	fetal
3	chr8:6424726-6424776	AG04450	lung:	fetal
4	chr8:6424269-6424319	PANC-1	pancreas:	n/a
5	chr8:6423908-6423958	PFSK-1	brain:	n/a
6	chr8:6424269-6424319	HMEC	breast:	n/a
7	chr8:6424636-6424686	K562	blood:	n/a
8	chr8:6423908-6423958	Caco-2	colon:	n/a
9	chr8:6424636-6424686	NH-A	brain:	n/a
10	chr8:6424269-6424319	HAEpiC	amniotic membrane:	n/a
11	chr8:6423908-6423958	GM06990	blood:	n/a
12	chr8:6424726-6424776	NB4	blood:	n/a
13	chr8:6424726-6424776	AG04449	skin:	fetal
14	chr8:6424726-6424776	IMR90	lung:	fetal
15	chr8:6424726-6424776	CMK	blood:	n/a
16	chr8:6423908-6423958	PrEC	prostate:	n/a
17	chr8:6424636-6424686	HAEpiC	amniotic membrane:	n/a
18	chr8:6424636-6424686	HRPEpiC	eye:	n/a
19	chr8:6424269-6424319	NH-A	brain:	n/a
20	chr8:6423908-6423958	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:6424636-6424686	Caco-2	colon:	n/a
22	chr8:6424636-6424686	ECC-1	luminal epithelium:	n/a
23	chr8:6424269-6424319	NHBE	bronchial:	n/a
24	chr8:6424269-6424319	MCF-7	breast:	n/a
25	chr8:6424636-6424686	AG10803	skin:	n/a
26	chr8:6424636-6424686	NHDF-neo	bronchial:	n/a
27	chr8:6423908-6423958	HCPEpiC	choroid plexus:	n/a
28	chr8:6424636-6424686	MCF10A-Er-Src	breast:	n/a
29	chr8:6424726-6424776	HAEpiC	amniotic membrane:	n/a
30	chr8:6424726-6424776	BE2_C	brain:	n/a
31	chr8:6424269-6424319	AG04450	lung:	fetal
32	chr8:6424726-6424776	PANC-1	pancreas:	n/a
33	chr8:6423908-6423958	HCM	heart:	n/a
34	chr8:6423908-6423958	AG04450	lung:	fetal
35	chr8:6424726-6424776	HCF	heart:	n/a
36	chr8:6424636-6424686	Jurkat	blood:	n/a
37	chr8:6423908-6423958	Hela-S3	cervix:	n/a
38	chr8:6424269-6424319	HCT-116	colon:	n/a
39	chr8:6423908-6423958	LNCaP	prostate:	n/a
40	chr8:6424636-6424686	AG09309	skin:	n/a
41	chr8:6424726-6424776	HIPEpiC	eye:	n/a
42	chr8:6423908-6423958	HL-60	blood:	n/a
43	chr8:6424269-6424319	SK-N-MC	brain:	n/a
44	chr8:6424269-6424319	HCF	heart:	n/a
45	chr8:6424269-6424319	IMR90	lung:	fetal
46	chr8:6424726-6424776	PFSK-1	brain:	n/a
47	chr8:6424636-6424686	IMR90	lung:	fetal
48	chr8:6424726-6424776	ECC-1	luminal epithelium:	n/a
49	chr8:6424636-6424686	AG04449	skin:	fetal
50	chr8:6424269-6424319	MCF10A-Er-Src	breast:	n/a

No data

Variant related genes	Relation type
ANGPT2	TF binding region
ANGPT2	CpG island

Extended variants
information (count: 195 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:195 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564454082	chr8:6423207-6423208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111698198	chr8:6423227-6423228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185000010	chr8:6423255-6423256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557206883	chr8:6423281-6423282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558368112	chr8:6423283-6423284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563763769	chr8:6423291-6423292	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs531425751	chr8:6423297-6423298	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs548352454	chr8:6423304-6423305	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568014155	chr8:6423367-6423368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141178140	chr8:6423370-6423371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116431373	chr8:6423379-6423380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570748114	chr8:6423415-6423416	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539382328	chr8:6423436-6423437	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370459192	chr8:6423465-6423466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570380246	chr8:6423494-6423495	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs56954299	chr8:6423528-6423529	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7003563	chr8:6423535-6423536	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs138999898	chr8:6423536-6423537	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76054991	chr8:6423583-6423584	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189284695	chr8:6423584-6423585	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541056857	chr8:6423601-6423602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111547586	chr8:6423609-6423610	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564161979	chr8:6423621-6423622	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146430622	chr8:6423623-6423624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117383704	chr8:6423628-6423629	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563859079	chr8:6423631-6423632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529509000	chr8:6423638-6423639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541935867	chr8:6423650-6423651	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561799050	chr8:6423676-6423677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527254504	chr8:6423833-6423834	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs547386268	chr8:6423845-6423846	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs570365906	chr8:6423893-6423894	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs191469219	chr8:6423907-6423908	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs2167072	chr8:6423911-6423912	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs555217414	chr8:6423930-6423931	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs7817089	chr8:6423932-6423933	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs575155065	chr8:6423933-6423934	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs7833871	chr8:6423963-6423964	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs555421552	chr8:6423971-6423972	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs565809318	chr8:6423975-6423976	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs7817104	chr8:6423978-6423979	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs558092244	chr8:6423986-6423987	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs7832816	chr8:6423987-6423988	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2442528	chr8:6423992-6423993	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs371685658	chr8:6423996-6423997	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183947050	chr8:6424000-6424001	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529510827	chr8:6424030-6424031	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543269721	chr8:6424032-6424033	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs560007983	chr8:6424057-6424058	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs527344763	chr8:6424058-6424059	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6364200-6478200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:6407800-6423800	Weak transcription	Spleen	Spleen
3	chr8:6415200-6424000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:6416800-6442400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:6417600-6424000	Weak transcription	NHEK	skin
6	chr8:6417600-6442800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:6419000-6462400	Weak transcription	GM12878-XiMat	blood
8	chr8:6419600-6423400	Weak transcription	Primary T cells from cord blood	blood
9	chr8:6419600-6423800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:6419800-6423600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:6420000-6427400	Weak transcription	Thymus	Thymus
12	chr8:6420600-6423800	Weak transcription	Pancreas	Pancrea
13	chr8:6420800-6423800	Weak transcription	Gastric	stomach
14	chr8:6420800-6424000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr8:6420800-6424200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:6420800-6424400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr8:6420800-6427600	Weak transcription	NHDF-Ad	bronchial
18	chr8:6420800-6429800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:6420800-6433200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:6421000-6423800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:6421000-6423800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:6421000-6423800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:6421000-6423800	Weak transcription	Esophagus	oesophagus
24	chr8:6421000-6423800	Weak transcription	Lung	lung
25	chr8:6421000-6423800	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr8:6421000-6424600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:6421000-6424800	Weak transcription	Fetal Thymus	thymus
28	chr8:6421000-6425200	Weak transcription	Fetal Muscle Leg	muscle
29	chr8:6421000-6425400	Weak transcription	Fetal Stomach	stomach
30	chr8:6421000-6425800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr8:6421000-6426000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr8:6421000-6427400	Weak transcription	Left Ventricle	heart
33	chr8:6421000-6427400	Weak transcription	Ovary	ovary
34	chr8:6421000-6427800	Weak transcription	Aorta	Aorta
35	chr8:6421000-6427800	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr8:6421000-6435400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr8:6421200-6424000	Weak transcription	Adipose Nuclei	Adipose
38	chr8:6421200-6424800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:6421200-6425200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr8:6421200-6425600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:6421200-6436200	Weak transcription	Right Atrium	heart
42	chr8:6421400-6427400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:6421400-6433200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:6421600-6426800	Weak transcription	HUVEC	blood vessel
45	chr8:6421600-6462800	Weak transcription	Primary B cells from cord blood	blood
46	chr8:6421800-6424000	Weak transcription	Duodenum Mucosa	Duodenum
47	chr8:6421800-6427400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr8:6422000-6423800	Enhancers	Dnd41	blood
49	chr8:6422000-6426800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:6422200-6424800	Weak transcription	Primary B cells from peripheral blood	blood

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