Variant report

Variant	nsv972575
Chromosome Location	chr8:124810138-124821383
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	ATF1	chr8:124814572-124814842	K562	blood:	n/a	n/a
2	CEBPB	chr8:124818902-124819212	HepG2	liver:	n/a	n/a
3	CREB1	chr8:124814538-124814863	H1-hESC	embryonic stem cell:	n/a	n/a
4	CREB1	chr8:124814508-124814922	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr8:124815608-124815720	Lung_OC	lung:	n/a	n/a
6	CTCF	chr8:124817120-124817270	MCF-7	breast:	n/a	n/a
7	CTCF	chr8:124811819-124811834	LNCaP	prostate:	n/a	n/a
8	FOXA1	chr8:124818817-124819285	HepG2	liver:	n/a	n/a
9	FOXA2	chr8:124818901-124819208	HepG2	liver:	n/a	n/a
10	GATA3	chr8:124813041-124813242	SH-SY5Y	brain:	n/a	n/a
11	HNF4A	chr8:124818815-124819102	HepG2	liver:	n/a	chr8:124819017-124819030 chr8:124819017-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819030 chr8:124819017-124819029 chr8:124819014-124819032 chr8:124819016-124819030 chr8:124819015-124819030 chr8:124819015-124819030
12	HNF4G	chr8:124818912-124819117	HepG2	liver:	n/a	chr8:124819017-124819030 chr8:124819017-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819029 chr8:124819015-124819030 chr8:124819017-124819030 chr8:124819016-124819030 chr8:124819017-124819029 chr8:124819014-124819032 chr8:124819016-124819030 chr8:124819016-124819031 chr8:124819015-124819030
13	JUND	chr8:124814621-124814724	K562	blood:	n/a	n/a
14	MAFF	chr8:124821154-124821865	HepG2	liver:	n/a	chr8:124821660-124821678
15	MAFF	chr8:124821300-124821860	K562	blood:	n/a	chr8:124821660-124821678
16	MAFK	chr8:124821165-124821877	IMR90	lung:	n/a	chr8:124821662-124821677 chr8:124821303-124821314 chr8:124821304-124821315 chr8:124821661-124821675 chr8:124821663-124821683 chr8:124821304-124821315
17	MAFK	chr8:124821315-124821868	K562	blood:	n/a	chr8:124821662-124821677 chr8:124821661-124821675 chr8:124821663-124821683
18	MAFK	chr8:124821350-124822009	GM12878	blood:	n/a	chr8:124821662-124821677 chr8:124821661-124821675 chr8:124821663-124821683
19	MAFK	chr8:124821183-124821859	HepG2	liver:	n/a	chr8:124821662-124821677 chr8:124821303-124821314 chr8:124821304-124821315 chr8:124821661-124821675 chr8:124821663-124821683 chr8:124821304-124821315
20	MAFK	chr8:124821121-124821871	HepG2	liver:	n/a	chr8:124821662-124821677 chr8:124821303-124821314 chr8:124821304-124821315 chr8:124821661-124821675 chr8:124821663-124821683 chr8:124821304-124821315
21	MYC	chr8:124815613-124815678	MCF-7	breast:	n/a	n/a
22	POLR2A	chr8:124814318-124814334	ProgFib	skin:	n/a	n/a
23	POLR2A	chr8:124813064-124813203	MCF-7	breast:	n/a	n/a
24	POLR2A	chr8:124814624-124814749	GM12878	blood:	n/a	n/a
25	POLR2A	chr8:124815634-124815644	ProgFib	skin:	n/a	n/a
26	POLR2A	chr8:124815592-124815706	MCF-7	breast:	n/a	n/a
27	POLR2A	chr8:124814653-124814898	ProgFib	skin:	n/a	n/a
28	POLR2A	chr8:124818373-124818391	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr8:124814227-124814309	ProgFib	skin:	n/a	n/a
30	POLR2A	chr8:124814708-124814848	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:124792430..124794723-chr8:124811717..124815050,3	MCF-7	breast:
2	chr8:124814412..124816720-chr8:124818333..124820559,2	MCF-7	breast:
3	chr8:124780215..124782108-chr8:124812179..124814853,2	MCF-7	breast:
4	chr8:124817123..124819367-chr8:124820502..124822341,2	K562	blood:
5	chr11:65197972..65198491-chr8:124813387..124814082,2	Hela-S3	cervix:
6	chr8:124818284..124820707-chr8:125487320..125489749,2	K562	blood:
7	chr8:124789924..124791442-chr8:124814631..124817453,2	MCF-7	breast:
8	chr8:124805880..124808291-chr8:124814398..124816910,2	MCF-7	breast:
9	chr8:124794765..124796733-chr8:124809769..124811684,2	MCF-7	breast:
10	chr8:124814571..124816997-chr8:124820753..124822991,2	MCF-7	breast:
11	chr8:124800592..124802803-chr8:124809092..124811067,2	MCF-7	breast:
12	chr8:124779397..124782009-chr8:124814310..124816091,2	K562	blood:
13	chr8:124781412..124783619-chr8:124810704..124812373,2	K562	blood:
14	chr8:124814412..124816720-chr8:124818333..124820559,2	MCF-7	breast:
15	chr8:124807128..124809976-chr8:124813752..124817670,3	K562	blood:
16	chr8:124812507..124814669-chr8:124816701..124818733,2	K562	blood:
17	chr8:124816253..124817960-chr8:124822217..124824038,2	K562	blood:
18	chr8:124812507..124814669-chr8:124816701..124818733,2	K562	blood:

Variant related genes	Relation type
FAM91A1	TF binding region
ENSG00000176853	chromatin interactions

Extended variants
information (count: 370 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546892273	chr8:124810161-124810162	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190309162	chr8:124810189-124810190	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535622994	chr8:124810265-124810266	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367722431	chr8:124810295-124810296	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568168415	chr8:124810310-124810311	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16898872	chr8:124810320-124810321	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs537324128	chr8:124810350-124810351	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377276033	chr8:124810414-124810415	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557267509	chr8:124810427-124810428	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577080634	chr8:124810439-124810440	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531653798	chr8:124810454-124810455	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545945053	chr8:124810577-124810578	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552892929	chr8:124810585-124810586	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572890004	chr8:124810703-124810704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541562489	chr8:124810794-124810795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13265865	chr8:124810817-124810818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182704457	chr8:124810828-124810829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149198909	chr8:124810832-124810833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551413128	chr8:124810885-124810886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187533844	chr8:124810918-124810919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372676269	chr8:124810922-124810923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192785596	chr8:124810928-124810929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116653412	chr8:124810952-124810953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368756680	chr8:124811027-124811028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143332707	chr8:124811033-124811034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529736989	chr8:124811045-124811046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114269094	chr8:124811091-124811092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549529501	chr8:124811111-124811112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138765398	chr8:124811125-124811126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538209827	chr8:124811163-124811164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558194771	chr8:124811210-124811211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116893831	chr8:124811217-124811218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539396521	chr8:124811252-124811253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73337426	chr8:124811284-124811285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185526455	chr8:124811349-124811350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541879442	chr8:124811469-124811470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72715042	chr8:124811489-124811490	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs71516720	chr8:124811498-124811499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187948478	chr8:124811576-124811577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371257981	chr8:124811660-124811661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146944289	chr8:124811685-124811686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376600499	chr8:124811698-124811699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563974631	chr8:124811704-124811705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547804039	chr8:124811709-124811710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148196058	chr8:124811722-124811723	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs369850573	chr8:124811736-124811737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372564179	chr8:124811778-124811779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375848112	chr8:124811786-124811787	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs200455750	chr8:124811788-124811789	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs137915247	chr8:124811801-124811802	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124781800-124811200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:124785400-124815000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:124785600-124815000	Strong transcription	Duodenum Mucosa	Duodenum
4	chr8:124785800-124829000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr8:124786000-124825200	Strong transcription	Fetal Thymus	thymus
6	chr8:124786200-124814400	Strong transcription	HSMM	muscle
7	chr8:124786200-124815200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:124786200-124815400	Strong transcription	Dnd41	blood
9	chr8:124786200-124825200	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr8:124786400-124813800	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr8:124786400-124815000	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr8:124786400-124815200	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr8:124786400-124827200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr8:124786800-124814600	Strong transcription	Placenta	Placenta
15	chr8:124787000-124813800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr8:124787000-124816400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:124787000-124822800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:124787000-124827000	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr8:124787400-124814400	Strong transcription	A549	lung
20	chr8:124787600-124818800	Strong transcription	Liver	Liver
21	chr8:124789200-124824600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr8:124789400-124814800	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr8:124789400-124821600	Weak transcription	Stomach Mucosa	stomach
24	chr8:124789400-124825200	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr8:124789600-124811400	Strong transcription	Fetal Lung	lung
26	chr8:124789800-124827400	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr8:124790000-124827800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:124790200-124828600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:124790600-124814800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:124790800-124813400	Strong transcription	HUVEC	blood vessel
31	chr8:124790800-124814400	Strong transcription	Osteobl	bone
32	chr8:124790800-124815800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr8:124790800-124825200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr8:124791000-124828600	Strong transcription	Primary B cells from cord blood	blood
35	chr8:124791000-124828600	Strong transcription	Primary B cells from peripheral blood	blood
36	chr8:124791200-124814200	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr8:124791200-124815000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:124791200-124815800	Strong transcription	Adipose Nuclei	Adipose
39	chr8:124791200-124828600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:124791200-124828600	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr8:124791200-124829000	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr8:124791200-124829200	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr8:124791400-124814000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr8:124791400-124816000	Strong transcription	Primary T cells from cord blood	blood
45	chr8:124792200-124815600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr8:124793400-124814600	Strong transcription	Fetal Intestine Large	intestine
47	chr8:124793400-124815800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr8:124793600-124814800	Strong transcription	Fetal Muscle Trunk	muscle
49	chr8:124793600-124815800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr8:124793800-124815400	Strong transcription	Left Ventricle	heart

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