Variant report

Variant	nsv981910
Chromosome Location	chr8:11185560-11189634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:11189540-11189557	Kidney_OC	kidney:	n/a	n/a
2	CTCF	chr8:11189027-11189105	A549	lung:	n/a	n/a
3	MYC	chr8:11189383-11189438	H1-hESC	embryonic stem cell:	n/a	n/a
4	MYC	chr8:11189450-11189474	MCF-7	breast:	n/a	n/a
5	NR2F2	chr8:11188126-11188419	K562	blood:	n/a	n/a
6	PAX5	chr8:11186639-11187235	GM12878	blood:	n/a	n/a
7	PAX5	chr8:11186866-11187083	GM12892	blood:	n/a	n/a
8	PAX5	chr8:11186849-11187100	GM12878	blood:	n/a	n/a
9	PAX5	chr8:11186795-11187094	GM12878	blood:	n/a	n/a
10	POLR2A	chr8:11188788-11189623	GM12878	blood:	n/a	n/a
11	POLR2A	chr8:11187297-11187517	GM12878	blood:	n/a	n/a
12	POLR2A	chr8:11189464-11189474	MCF-7	breast:	n/a	n/a
13	POLR2A	chr8:11185419-11185599	K562	blood:	n/a	n/a
14	POLR2A	chr8:11188922-11189116	Gliobla	brain:	n/a	n/a
15	POLR2A	chr8:11185820-11186596	K562	blood:	n/a	n/a
16	POLR2A	chr8:11186646-11186647	HepG2	liver:	n/a	n/a
17	POLR2A	chr8:11188944-11189036	ProgFib	skin:	n/a	n/a
18	POLR2A	chr8:11188939-11189114	MCF-7	breast:	n/a	n/a
19	POLR2A	chr8:11188918-11189516	MCF-7	breast:	n/a	n/a
20	POLR2A	chr8:11189009-11189114	Hela-S3	cervix:	n/a	n/a
21	SP1	chr8:11188324-11188660	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11188490-11188540	H1-hESC	embryonic stem cell:	embryo
2	chr8:11188675-11188725	PFSK-1	brain:	n/a
3	chr8:11188675-11188725	HNPCEpiC	eye:	n/a
4	chr8:11188675-11188725	HEK293	kidney:	embryo
5	chr8:11188490-11188540	AG09309	skin:	n/a
6	chr8:11188675-11188725	CMK	blood:	n/a
7	chr8:11188490-11188540	MCF-7	breast:	n/a
8	chr8:11188490-11188540	GM12878	blood:	n/a
9	chr8:11188490-11188540	BE2_C	brain:	n/a
10	chr8:11188490-11188540	U87	brain:	n/a
11	chr8:11188490-11188540	HCT-116	colon:	n/a
12	chr8:11188675-11188725	ProgFib	skin:	n/a
13	chr8:11188490-11188540	NB4	blood:	n/a
14	chr8:11188490-11188540	Hepatocyte	liver:	n/a
15	chr8:11188675-11188725	SKMC	muscle:	n/a
16	chr8:11188490-11188540	PrEC	prostate:	n/a
17	chr8:11188675-11188725	BJ	skin:	n/a
18	chr8:11188675-11188725	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:11188675-11188725	U87	brain:	n/a
20	chr8:11188675-11188725	AG04449	skin:	fetal
21	chr8:11188675-11188725	K562	blood:	n/a
22	chr8:11188490-11188540	AoSMC	blood vessel:	n/a
23	chr8:11188675-11188725	NB4	blood:	n/a
24	chr8:11188675-11188725	HEEpiC	esophagus:	n/a
25	chr8:11188675-11188725	H1-hESC	embryonic stem cell:	embryo
26	chr8:11188675-11188725	HIPEpiC	eye:	n/a
27	chr8:11188675-11188725	AG09319	gingival:	n/a
28	chr8:11188490-11188540	PANC-1	pancreas:	n/a
29	chr8:11188490-11188540	HepG2	liver:	n/a
30	chr8:11188675-11188725	NT2-D1	testis:	n/a
31	chr8:11188490-11188540	GM06990	blood:	n/a
32	chr8:11188490-11188540	Caco-2	colon:	n/a
33	chr8:11188675-11188725	SAEC	small airway:	n/a
34	chr8:11188490-11188540	HIPEpiC	eye:	n/a
35	chr8:11188675-11188725	SK-N-SH_RA	brain:	n/a
36	chr8:11188675-11188725	HCM	heart:	n/a
37	chr8:11188675-11188725	ECC-1	luminal epithelium:	n/a
38	chr8:11188490-11188540	NHDF-neo	bronchial:	n/a
39	chr8:11188490-11188540	HCF	heart:	n/a
40	chr8:11188675-11188725	LNCaP	prostate:	n/a
41	chr8:11188675-11188725	HMEC	breast:	n/a
42	chr8:11188490-11188540	HRE	kidney:	n/a
43	chr8:11188490-11188540	GM12891	blood:	n/a
44	chr8:11188490-11188540	Jurkat	blood:	n/a
45	chr8:11188675-11188725	Hela-S3	cervix:	n/a
46	chr8:11188490-11188540	SK-N-SH	brain:	n/a
47	chr8:11188675-11188725	GM12891	blood:	n/a
48	chr8:11188490-11188540	RPTEC	kidney:	n/a
49	chr8:11188675-11188725	A549	lung:	n/a
50	chr8:11188675-11188725	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11140705..11143665-chr8:11184811..11187065,2	K562	blood:
2	chr8:11170423..11173089-chr8:11183633..11185692,2	K562	blood:

No data

Variant related genes	Relation type
SLC35G5	TF binding region
ENSG00000246477	TF binding region
SLC35G5	CpG island
ENSG00000246477	CpG island
ENSG00000104643	chromatin interactions

Extended variants
information (count: 350 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536069623	chr8:11185562-11185563	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs554715935	chr8:11185611-11185612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115710618	chr8:11185617-11185618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200369268	chr8:11185671-11185672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199585578	chr8:11185672-11185673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200766204	chr8:11185674-11185675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs558558304	chr8:11185756-11185757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576865736	chr8:11185774-11185775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541024128	chr8:11185777-11185778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs58012595	chr8:11185791-11185792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs77463979	chr8:11185793-11185794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370565058	chr8:11185813-11185814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs151066674	chr8:11185853-11185854	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs373254661	chr8:11185854-11185855	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs542071167	chr8:11185869-11185870	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs58045369	chr8:11185881-11185882	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs67935075	chr8:11185882-11185883	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs2736263	chr8:11185908-11185909	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143049208	chr8:11185949-11185950	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552875593	chr8:11185980-11185981	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs573454551	chr8:11185991-11185992	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564768772	chr8:11186074-11186075	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs532151275	chr8:11186097-11186098	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs188006258	chr8:11186100-11186101	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs192912715	chr8:11186105-11186106	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs536318224	chr8:11186121-11186122	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs542478979	chr8:11186129-11186130	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs540475067	chr8:11186131-11186132	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs146167078	chr8:11186151-11186152	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs113660465	chr8:11186163-11186164	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs536842901	chr8:11186171-11186172	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs558468338	chr8:11186175-11186176	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs11782706	chr8:11186215-11186216	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs534705443	chr8:11186228-11186229	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs76300339	chr8:11186238-11186239	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs372811217	chr8:11186267-11186268	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs544144677	chr8:11186294-11186295	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs542335186	chr8:11186342-11186343	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs149869346	chr8:11186403-11186404	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs143883613	chr8:11186414-11186415	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs546035746	chr8:11186424-11186425	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs564782992	chr8:11186436-11186437	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs35418978	chr8:11186453-11186454	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs547439166	chr8:11186469-11186470	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs377708255	chr8:11186471-11186472	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs148632646	chr8:11186503-11186504	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs372018626	chr8:11186505-11186506	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs531450047	chr8:11186526-11186527	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs548308343	chr8:11186538-11186539	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs569647023	chr8:11186540-11186541	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
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
Acute myeloid leukemia	21251322	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
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11171600-11191400	Weak transcription	Psoas Muscle	Psoas
2	chr8:11176000-11185600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:11176000-11187800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:11176000-11189000	Weak transcription	Gastric	stomach
5	chr8:11176600-11187000	Weak transcription	Colonic Mucosa	Colon
6	chr8:11178200-11186000	Weak transcription	Fetal Intestine Small	intestine
7	chr8:11178200-11186400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:11178600-11186800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:11178800-11186200	Weak transcription	Fetal Heart	heart
10	chr8:11179400-11187600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:11179600-11186200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:11179800-11186400	Weak transcription	Brain Germinal Matrix	brain
13	chr8:11179800-11188000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr8:11180600-11185800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr8:11180600-11185800	Weak transcription	Fetal Muscle Leg	muscle
16	chr8:11180600-11186000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:11180600-11187000	Weak transcription	Lung	lung
18	chr8:11180600-11190200	Weak transcription	A549	lung
19	chr8:11181600-11186600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr8:11182200-11186600	Weak transcription	Fetal Brain Female	brain
21	chr8:11182400-11188800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:11182400-11193600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:11182600-11186800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr8:11182600-11188800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr8:11182800-11186600	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr8:11182800-11187600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:11183000-11185600	Weak transcription	Spleen	Spleen
28	chr8:11183000-11186000	Weak transcription	Fetal Thymus	thymus
29	chr8:11183000-11186200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr8:11183000-11186400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:11183000-11186400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr8:11183000-11186400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:11183000-11186600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr8:11183000-11186600	Weak transcription	Fetal Intestine Large	intestine
35	chr8:11183000-11186800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:11183000-11187000	Weak transcription	Thymus	Thymus
37	chr8:11183000-11187400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr8:11183000-11187400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr8:11183000-11188400	Weak transcription	Aorta	Aorta
40	chr8:11183000-11188600	Weak transcription	Ovary	ovary
41	chr8:11183000-11189000	Weak transcription	Brain Anterior Caudate	brain
42	chr8:11183000-11189800	Weak transcription	Primary B cells from cord blood	blood
43	chr8:11183200-11185800	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr8:11183200-11186000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:11183400-11186400	Weak transcription	Primary T cells from cord blood	blood
46	chr8:11183600-11185800	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr8:11183800-11186000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr8:11183800-11186400	Weak transcription	Primary hematopoietic stem cells	blood
49	chr8:11183800-11190200	Weak transcription	Liver	Liver
50	chr8:11184000-11185800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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