Variant report

Variant	nsv890962
Chromosome Location	chr8:63708519-63812686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:229)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:229 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr8:63771581-63771822	GM12878	blood:	n/a	n/a
2	BATF	chr8:63768987-63769287	GM12878	blood:	n/a	chr8:63769159-63769170 chr8:63769160-63769170
3	BATF	chr8:63771525-63771873	GM12878	blood:	n/a	n/a
4	BCL11A	chr8:63800466-63800690	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:63800468-63801027	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:63709354-63709419	GM12878	blood:	n/a	n/a
7	CBX3	chr8:63721432-63721611	K562	blood:	n/a	n/a
8	CBX3	chr8:63721317-63721624	K562	blood:	n/a	n/a
9	CEBPB	chr8:63780063-63780234	HepG2	liver:	n/a	n/a
10	CHD1	chr8:63800431-63800581	GM12878	blood:	n/a	n/a
11	CHD2	chr8:63800514-63800926	GM12878	blood:	n/a	n/a
12	CTCF	chr8:63776640-63776790	AG04449	skin:	n/a	n/a
13	CTCF	chr8:63776700-63776850	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr8:63770432-63770512	GM12878	blood:	n/a	n/a
15	CTCF	chr8:63776680-63776830	AG10803	skin:	n/a	n/a
16	CTCF	chr8:63776680-63776825	GM10266	blood:	n/a	n/a
17	CTCF	chr8:63776640-63776790	GM12871	blood:	n/a	n/a
18	CTCF	chr8:63776709-63776773	GM19238	blood:	n/a	n/a
19	CTCF	chr8:63776702-63776778	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr8:63776660-63776810	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr8:63776680-63776830	HCFaa	heart:	n/a	n/a
22	CTCF	chr8:63776660-63776810	GM12871	blood:	n/a	n/a
23	CTCF	chr8:63776680-63776830	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr8:63776720-63776870	SAEC	small airway:	n/a	n/a
25	CTCF	chr8:63794245-63794278	GM10266	blood:	n/a	n/a
26	CTCF	chr8:63710640-63710790	GM12878	blood:	n/a	n/a
27	CTCF	chr8:63776654-63776833	GM12892	blood:	n/a	n/a
28	CTCF	chr8:63776660-63776810	HVMF	connective:	n/a	n/a
29	CTCF	chr8:63776683-63776807	GM19240	blood:	n/a	n/a
30	CTCF	chr8:63776648-63776831	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr8:63776593-63776880	K562	blood:	n/a	n/a
32	CTCF	chr8:63776620-63776770	HVMF	connective:	n/a	n/a
33	CTCF	chr8:63776716-63776769	K562	blood:	n/a	n/a
34	CTCF	chr8:63729120-63729270	GM12864	blood:	n/a	n/a
35	CTCF	chr8:63776615-63776838	GM12891	blood:	n/a	n/a
36	CTCF	chr8:63776660-63776810	GM12868	blood:	n/a	n/a
37	CTCF	chr8:63721528-63721561	GM13976	blood:	n/a	n/a
38	CTCF	chr8:63776431-63777078	SK-N-SH	brain:	n/a	n/a
39	CTCF	chr8:63776707-63776708	GM19238	blood:	n/a	n/a
40	CTCF	chr8:63776640-63776790	GM12875	blood:	n/a	n/a
41	CUX1	chr8:63801270-63801337	GM12878	blood:	n/a	n/a
42	CUX1	chr8:63800499-63800611	GM12878	blood:	n/a	n/a
43	CUX1	chr8:63806757-63807026	GM12878	blood:	n/a	n/a
44	E2F4	chr8:63722700-63722848	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr8:63811776-63811804	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr8:63806584-63806726	MCF10A-Er-Src	breast:	n/a	chr8:63806675-63806684
47	EBF1	chr8:63810180-63810342	GM12878	blood:	n/a	chr8:63810288-63810299
48	EBF1	chr8:63800430-63801073	GM12878	blood:	n/a	chr8:63800798-63800809
49	EBF1	chr8:63773858-63774050	GM12878	blood:	n/a	chr8:63773942-63773953
50	EBF1	chr8:63753381-63753605	GM12878	blood:	n/a	chr8:63753502-63753515 chr8:63753503-63753513 chr8:63753504-63753513 chr8:63753504-63753513

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63776755-63776805	K562	blood:	n/a
2	chr8:63776508-63776558	AG09319	gingival:	n/a
3	chr8:63776762-63776812	HEEpiC	esophagus:	n/a
4	chr8:63776508-63776558	MCF10A-Er-Src	breast:	n/a
5	chr8:63777430-63777480	MCF-7	breast:	n/a
6	chr8:63776755-63776805	GM19239	blood:	n/a
7	chr8:63777430-63777480	HRCEpiC	kidney:	n/a
8	chr8:63776755-63776805	SKMC	muscle:	n/a
9	chr8:63776642-63776692	HCF	heart:	n/a
10	chr8:63776755-63776805	HRPEpiC	eye:	n/a
11	chr8:63777430-63777480	HepG2	liver:	n/a
12	chr8:63776762-63776812	PrEC	prostate:	n/a
13	chr8:63776762-63776812	SK-N-SH	brain:	n/a
14	chr8:63776642-63776692	HUVEC	blood vessel:	n/a
15	chr8:63776762-63776812	GM06990	blood:	n/a
16	chr8:63776508-63776558	HRPEpiC	eye:	n/a
17	chr8:63776762-63776812	IMR90	lung:	fetal
18	chr8:63776642-63776692	BJ	skin:	n/a
19	chr8:63776508-63776558	MCF-7	breast:	n/a
20	chr8:63776755-63776805	AoSMC	blood vessel:	n/a
21	chr8:63776642-63776692	HCT-116	colon:	n/a
22	chr8:63776755-63776805	ECC-1	luminal epithelium:	n/a
23	chr8:63776642-63776692	RPTEC	kidney:	n/a
24	chr8:63776642-63776692	HNPCEpiC	eye:	n/a
25	chr8:63776642-63776692	HMEC	breast:	n/a
26	chr8:63776762-63776812	HL-60	blood:	n/a
27	chr8:63777430-63777480	Hela-S3	cervix:	n/a
28	chr8:63776508-63776558	HMEC	breast:	n/a
29	chr8:63776762-63776812	AG10803	skin:	n/a
30	chr8:63777430-63777480	HCT-116	colon:	n/a
31	chr8:63776755-63776805	Hela-S3	cervix:	n/a
32	chr8:63777430-63777480	GM19239	blood:	n/a
33	chr8:63776508-63776558	HRE	kidney:	n/a
34	chr8:63776642-63776692	GM12878	blood:	n/a
35	chr8:63776642-63776692	IMR90	lung:	fetal
36	chr8:63776508-63776558	AG09309	skin:	n/a
37	chr8:63776508-63776558	AG04449	skin:	fetal
38	chr8:63776755-63776805	NHDF-neo	bronchial:	n/a
39	chr8:63776508-63776558	U87	brain:	n/a
40	chr8:63776642-63776692	HAEpiC	amniotic membrane:	n/a
41	chr8:63776508-63776558	H1-hESC	embryonic stem cell:	embryo
42	chr8:63776755-63776805	HAEpiC	amniotic membrane:	n/a
43	chr8:63776755-63776805	SAEC	small airway:	n/a
44	chr8:63776762-63776812	MCF-7	breast:	n/a
45	chr8:63777430-63777480	IMR90	lung:	fetal
46	chr8:63776755-63776805	HMEC	breast:	n/a
47	chr8:63776755-63776805	HCM	heart:	n/a
48	chr8:63777430-63777480	AG04450	lung:	fetal
49	chr8:63776508-63776558	GM12892	blood:	n/a
50	chr8:63776508-63776558	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:92008019..92008867-chr8:63749542..63750231,2	MCF-7	breast:
2	chr10:1231043..1232833-chr8:63744046..63746893,2	K562	blood:
3	chr1:28832582..28833084-chr8:63789537..63790057,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGH-2	chr8:63775641-63776740	NONHSAT126908

No data

Variant related genes	Relation type
XRCC6P4	TF binding region
ENSG00000253431	TF binding region
XRCC6P4	CpG island
ENSG00000253431	CpG island
ENSG00000242125	chromatin interactions
ENSG00000185736	chromatin interactions

Extended variants
information (count: 2862 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2862 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182459301	chr8:63708807-63708808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552393638	chr8:63708812-63708813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2170112	chr8:63708858-63708859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs187524397	chr8:63708901-63708902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71255362	chr8:63708971-63708972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540601684	chr8:63708978-63708979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552583209	chr8:63708988-63708989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62512420	chr8:63709003-63709004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs73256942	chr8:63709029-63709030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs116389918	chr8:63709059-63709060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530740002	chr8:63709060-63709061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545743421	chr8:63709072-63709073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75891208	chr8:63709089-63709090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192044935	chr8:63709115-63709116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182734789	chr8:63709163-63709164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189067907	chr8:63709169-63709170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149814266	chr8:63709208-63709209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527616008	chr8:63709218-63709219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145815794	chr8:63709227-63709228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530133968	chr8:63709229-63709230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547690055	chr8:63709234-63709235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148527009	chr8:63709237-63709238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570110928	chr8:63709249-63709250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370245994	chr8:63709337-63709338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144656283	chr8:63709348-63709349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6150611	chr8:63709349-63709350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs398008069	chr8:63709375-63709376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371407422	chr8:63709381-63709382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375728614	chr8:63709385-63709386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537669367	chr8:63709399-63709400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558913181	chr8:63709439-63709440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs16929587	chr8:63709449-63709450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs34583002	chr8:63709484-63709485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535024331	chr8:63709551-63709552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574645206	chr8:63709605-63709606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369270243	chr8:63709618-63709619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193044671	chr8:63709643-63709644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184532167	chr8:63709655-63709656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187543533	chr8:63709681-63709682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545958916	chr8:63709773-63709774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535340954	chr8:63709801-63709802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564310812	chr8:63709819-63709820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10957239	chr8:63709842-63709843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573169043	chr8:63709872-63709873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540580588	chr8:63709891-63709892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373484028	chr8:63709901-63709902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533544390	chr8:63709927-63709928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559738504	chr8:63709967-63709968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376518659	chr8:63709976-63709977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530117771	chr8:63709984-63709985	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Disorders of sex development	21048976	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
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
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
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63708800-63709800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:63709400-63710400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:63709600-63710000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:63710000-63710200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:63711000-63711400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:63712200-63712600	Active TSS	Fetal Heart	heart
7	chr8:63713000-63713600	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr8:63726000-63726800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
9	chr8:63726800-63731400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:63733200-63733600	Enhancers	Brain Germinal Matrix	brain
11	chr8:63737400-63742000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:63738600-63740000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:63739000-63740200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr8:63739600-63739800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:63740000-63741200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:63740200-63741200	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr8:63741200-63741600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:63741200-63741600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:63741200-63741600	Enhancers	Fetal Stomach	stomach
20	chr8:63741400-63741600	Enhancers	Left Ventricle	heart
21	chr8:63741600-63745000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr8:63743400-63744000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:63750000-63750400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:63750600-63751000	Enhancers	Fetal Brain Male	brain
25	chr8:63757400-63759000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:63758000-63758400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:63758000-63758400	Enhancers	Fetal Stomach	stomach
28	chr8:63758000-63758600	Enhancers	Fetal Lung	lung
29	chr8:63759000-63776400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:63767000-63767200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:63767800-63768000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:63768800-63769600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:63773000-63774800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr8:63773600-63775800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr8:63775800-63776200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:63776000-63776400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:63776400-63776800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:63776400-63776800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
39	chr8:63776400-63776800	Active TSS	Gastric	stomach
40	chr8:63776400-63777000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:63776400-63777000	Active TSS	Duodenum Mucosa	Duodenum
42	chr8:63776600-63777000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:63776600-63777000	Active TSS	Thymus	Thymus
44	chr8:63776600-63777200	Active TSS	K562	blood
45	chr8:63776600-63777600	ZNF genes & repeats	Fetal Brain Female	brain
46	chr8:63776800-63777200	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr8:63776800-63777200	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr8:63776800-63777400	Enhancers	Placenta	Placenta
49	chr8:63777200-63777600	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:63777600-63779800	Weak transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links