Variant report

Variant	nsv962147
Chromosome Location	chr16:46704148-46713998
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	ARID3A	chr16:46707412-46707608	HepG2	liver:	n/a	n/a
2	BATF	chr16:46708611-46708840	GM12878	blood:	n/a	n/a
3	BHLHE40	chr16:46707413-46707487	K562	blood:	n/a	n/a
4	BHLHE40	chr16:46707447-46707607	GM12878	blood:	n/a	n/a
5	CHD1	chr16:46707077-46707871	IMR90	lung:	n/a	n/a
6	CTCF	chr16:46707380-46707530	WI-38	lung:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
7	CTCF	chr16:46707400-46707550	GM12875	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
8	CTCF	chr16:46707377-46707588	A549	lung:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
9	CTCF	chr16:46707420-46707570	GM12873	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
10	CTCF	chr16:46707440-46707590	HEK293	kidney:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
11	CTCF	chr16:46707315-46707630	Gliobla	brain:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
12	CTCF	chr16:46707350-46707585	HepG2	liver:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
13	CTCF	chr16:46707440-46707590	NHDF-neo	bronchial:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
14	CTCF	chr16:46707800-46707950	HVMF	connective:	n/a	n/a
15	CTCF	chr16:46707420-46707570	SK-N-SH_RA	brain:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
16	CTCF	chr16:46707420-46707570	AG09309	skin:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
17	CTCF	chr16:46707420-46707570	NHEK	skin:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
18	CTCF	chr16:46707440-46707590	AG04450	lung:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
19	CTCF	chr16:46707340-46707616	LNCaP	prostate:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
20	CTCF	chr16:46707420-46707570	NB4	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
21	CTCF	chr16:46707400-46707550	GM12864	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
22	CTCF	chr16:46707440-46707590	AG10803	skin:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
23	CTCF	chr16:46707420-46707570	GM12801	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
24	CTCF	chr16:46707820-46707970	GM12873	blood:	n/a	n/a
25	CTCF	chr16:46707440-46707590	MCF-7	breast:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
26	CTCF	chr16:46707400-46707550	HMEC	breast:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
27	CTCF	chr16:46707357-46707617	GM13977	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
28	CTCF	chr16:46707420-46707570	HA-sp	spinal cord:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
29	CTCF	chr16:46707400-46707550	GM12874	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
30	CTCF	chr16:46707342-46707589	MCF-7	breast:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
31	CTCF	chr16:46707348-46707580	MCF-7	breast:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
32	CTCF	chr16:46707305-46707615	A549	lung:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
33	CTCF	chr16:46707140-46707290	AG04449	skin:	n/a	n/a
34	CTCF	chr16:46707440-46707590	Caco-2	colon:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
35	CTCF	chr16:46707420-46707570	GM12864	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
36	CTCF	chr16:46707420-46707570	GM12867	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
37	CTCF	chr16:46707420-46707570	HBMEC	blood vessel:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
38	CTCF	chr16:46707420-46707570	GM12868	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
39	CTCF	chr16:46707420-46707570	AoAF	blood vessel:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
40	CTCF	chr16:46707352-46707615	Lung_OC	lung:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
41	CTCF	chr16:46707400-46707550	WERI-Rb-1	eye:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
42	CTCF	chr16:46707362-46707615	LNCaP	prostate:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
43	CTCF	chr16:46707334-46707583	GM12891	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
44	CTCF	chr16:46707420-46707570	HFF-Myc	foreskin:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
45	CTCF	chr16:46707420-46707570	BJ	skin:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
46	CTCF	chr16:46707302-46707606	K562	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
47	CTCF	chr16:46707343-46707611	GM19240	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
48	CTCF	chr16:46707160-46707310	GM12801	blood:	n/a	n/a
49	CTCF	chr16:46707289-46707610	MCF-7	breast:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503
50	CTCF	chr16:46707330-46707608	GM19239	blood:	n/a	chr16:46707486-46707502 chr16:46707487-46707508 chr16:46707490-46707498 chr16:46707485-46707503

No.	Distal block	Cell Line	Cell type
1	chr16:46706996..46707945-chr16:46942502..46943366,7	K562	blood:
2	chr16:46707953..46708653-chr16:46887447..46888372,2	K562	blood:
3	chr16:46704847..46706863-chr16:46794204..46795904,2	MCF-7	breast:
4	chr16:46707389..46708210-chr16:46835449..46836029,2	MCF-7	breast:
5	chr16:46701863..46703903-chr16:46713521..46715933,2	K562	blood:
6	chr16:46711146..46713693-chr16:46721499..46723929,2	K562	blood:
7	chr16:46705954..46707514-chr16:46711367..46713742,2	K562	blood:
8	chr16:46707772..46709754-chr16:46720793..46723011,2	MCF-7	breast:
9	chr16:46707001..46707974-chr16:46963384..46964655,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYLK3-5	chr16:46707358-46707839	NONHSAT142259

Variant related genes	Relation type
VPS35	TF binding region
ENSG00000091651	chromatin interactions
ENSG00000069329	chromatin interactions

Extended variants
information (count: 308 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:308 , 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	rs181820153	chr16:46704157-46704158	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537061971	chr16:46704163-46704164	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151255401	chr16:46704170-46704171	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140874021	chr16:46704217-46704218	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535642842	chr16:46704218-46704219	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185214191	chr16:46704276-46704277	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28375498	chr16:46704320-46704321	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572333391	chr16:46704321-46704322	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28439596	chr16:46704323-46704324	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545891494	chr16:46704379-46704380	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564282843	chr16:46704385-46704386	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150177379	chr16:46704414-46704415	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543802325	chr16:46704415-46704416	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190756074	chr16:46704460-46704461	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529202502	chr16:46704478-46704479	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373366586	chr16:46704496-46704497	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138933318	chr16:46704497-46704498	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533206628	chr16:46704501-46704502	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551457398	chr16:46704502-46704503	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141293466	chr16:46704559-46704560	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530400933	chr16:46704579-46704580	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548981476	chr16:46704586-46704587	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376302736	chr16:46704619-46704620	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560798000	chr16:46704654-46704655	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567184958	chr16:46704668-46704669	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536124485	chr16:46704676-46704677	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530912589	chr16:46704827-46704828	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554092114	chr16:46704896-46704897	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565926031	chr16:46704900-46704901	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539653364	chr16:46704937-46704938	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36309	chr16:46704949-46704950	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs202082366	chr16:46705040-46705041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576503344	chr16:46705138-46705139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543417354	chr16:46705153-46705154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552717173	chr16:46705172-46705173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374860055	chr16:46705223-46705224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181602739	chr16:46705225-46705226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573976492	chr16:46705300-46705301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541328160	chr16:46705327-46705328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201337400	chr16:46705337-46705338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1657194	chr16:46705343-46705344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7500918	chr16:46705368-46705369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74818035	chr16:46705389-46705390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79583197	chr16:46705390-46705391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36310	chr16:46705502-46705503	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs71380965	chr16:46705558-46705559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4966616	chr16:46705576-46705577	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs377510356	chr16:46705579-46705580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563205724	chr16:46705591-46705592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370652451	chr16:46705607-46705608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46689000-46713600	Strong transcription	Fetal Muscle Trunk	muscle
2	chr16:46689200-46715800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:46689800-46705400	Weak transcription	Small Intestine	intestine
4	chr16:46689800-46716200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr16:46690400-46716200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr16:46691000-46705800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr16:46691000-46714800	Strong transcription	Skeletal Muscle Female	skeletal muscle
8	chr16:46691000-46715000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr16:46691000-46715600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr16:46691000-46716200	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr16:46691000-46716800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr16:46691000-46718000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr16:46691200-46705800	Strong transcription	Duodenum Mucosa	Duodenum
14	chr16:46691200-46714800	Strong transcription	Liver	Liver
15	chr16:46691200-46716200	Strong transcription	Adipose Nuclei	Adipose
16	chr16:46691200-46716400	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr16:46691200-46716800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr16:46691200-46717000	Strong transcription	Dnd41	blood
19	chr16:46691200-46717400	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr16:46691600-46707800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr16:46691600-46708800	Strong transcription	Duodenum Smooth Muscle	Duodenum
22	chr16:46692000-46705800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr16:46692000-46706000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr16:46692200-46706600	Strong transcription	Placenta	Placenta
25	chr16:46692400-46716800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr16:46692600-46705800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr16:46692600-46707000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr16:46692600-46716200	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr16:46692600-46717000	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr16:46692800-46706200	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr16:46692800-46717400	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr16:46693000-46706800	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr16:46693000-46713200	Strong transcription	Fetal Intestine Large	intestine
34	chr16:46693000-46715200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr16:46693000-46716800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr16:46693200-46706000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr16:46694000-46716600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr16:46694000-46717600	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr16:46694200-46716600	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr16:46694200-46716800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr16:46694600-46716800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr16:46695000-46716400	Weak transcription	Stomach Mucosa	stomach
43	chr16:46695600-46705000	Strong transcription	Brain Substantia Nigra	brain
44	chr16:46695800-46705800	Strong transcription	Left Ventricle	heart
45	chr16:46696600-46704200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr16:46696600-46705400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr16:46697000-46704200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr16:46697000-46704200	Weak transcription	Gastric	stomach
49	chr16:46697000-46704400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr16:46697000-46711400	Weak transcription	Esophagus	oesophagus

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