Variant report

Variant	nsv984334
Chromosome Location	chr16:46674416-46704148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:259)
CpG islands
(count:245)
Chromatin interactive
region (count:11)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:46683497-46683728	K562	blood:	n/a	n/a
2	ATF2	chr16:46692684-46693241	GM12878	blood:	n/a	n/a
3	BATF	chr16:46692805-46693089	GM12878	blood:	n/a	n/a
4	BCL11A	chr16:46692944-46693214	GM12878	blood:	n/a	n/a
5	BCL3	chr16:46692761-46693193	GM12878	blood:	n/a	n/a
6	BCLAF1	chr16:46692673-46693262	GM12878	blood:	n/a	n/a
7	BCLAF1	chr16:46692614-46693388	GM12878	blood:	n/a	n/a
8	BHLHE40	chr16:46683487-46683811	K562	blood:	n/a	n/a
9	CEBPB	chr16:46684260-46684454	IMR90	lung:	n/a	n/a
10	CEBPB	chr16:46692819-46693362	GM12878	blood:	n/a	n/a
11	CREB1	chr16:46683394-46683792	K562	blood:	n/a	n/a
12	CTCF	chr16:46682620-46682770	GM12864	blood:	n/a	n/a
13	CTCF	chr16:46702059-46702099	ProgFib	skin:	n/a	n/a
14	CTCF	chr16:46682740-46682890	HPAF	blood vessel:	n/a	n/a
15	CTCF	chr16:46682720-46682870	K562	blood:	n/a	n/a
16	CTCF	chr16:46692900-46693050	GM12875	blood:	n/a	n/a
17	CTCF	chr16:46682700-46682850	AG04450	lung:	n/a	n/a
18	CTCF	chr16:46692880-46693030	GM12873	blood:	n/a	n/a
19	CTCF	chr16:46682676-46682846	K562	blood:	n/a	n/a
20	CTCF	chr16:46692820-46692970	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr16:46682660-46682810	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr16:46682700-46682850	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr16:46692900-46693050	GM12873	blood:	n/a	n/a
24	CTCF	chr16:46682680-46682830	HMF	breast:	n/a	n/a
25	CTCF	chr16:46692840-46692990	GM12869	blood:	n/a	n/a
26	CTCF	chr16:46682720-46682870	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr16:46682640-46682790	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr16:46682660-46682810	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr16:46692840-46692990	GM12873	blood:	n/a	n/a
30	CTCF	chr16:46682700-46682850	HMF	breast:	n/a	n/a
31	CTCF	chr16:46692880-46693030	GM12865	blood:	n/a	n/a
32	CTCF	chr16:46692840-46692990	GM06990	blood:	n/a	n/a
33	CTCF	chr16:46682640-46682790	NB4	blood:	n/a	n/a
34	CTCF	chr16:46692896-46693028	GM19240	blood:	n/a	n/a
35	CTCF	chr16:46682660-46682810	HVMF	connective:	n/a	n/a
36	CTCF	chr16:46682678-46682874	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr16:46682680-46682830	HAc	cerebellar:	n/a	n/a
38	CTCF	chr16:46682680-46682830	K562	blood:	n/a	n/a
39	CTCF	chr16:46682680-46682830	BJ	skin:	n/a	n/a
40	CTCF	chr16:46692870-46693024	GM12878	blood:	n/a	n/a
41	CTCF	chr16:46692908-46692928	K562	blood:	n/a	n/a
42	CTCF	chr16:46692924-46693003	GM10266	blood:	n/a	n/a
43	CTCF	chr16:46682700-46682850	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr16:46692740-46692890	GM12872	blood:	n/a	n/a
45	CTCF	chr16:46682640-46682790	GM12872	blood:	n/a	n/a
46	CTCF	chr16:46682740-46682890	BE2_C	brain:	n/a	n/a
47	CTCF	chr16:46692867-46693012	GM19239	blood:	n/a	n/a
48	CTCF	chr16:46692762-46693102	GM12878	blood:	n/a	n/a
49	CTCF	chr16:46692898-46693021	GM19238	blood:	n/a	n/a
50	CTCF	chr16:46692880-46693030	GM12871	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	chr16:46683727-46683777	SK-N-SH_RA	brain:	n/a
2	chr16:46683727-46683777	SK-N-SH_RA	brain:	n/a
3	chr16:46683644-46683694	HRE	kidney:	n/a
4	chr16:46683727-46683777	HCM	heart:	n/a
5	chr16:46683727-46683777	NHDF-neo	bronchial:	n/a
6	chr16:46694236-46694286	BJ	skin:	n/a
7	chr16:46687332-46687382	RPTEC	kidney:	n/a
8	chr16:46683644-46683694	NT2-D1	testis:	n/a
9	chr16:46683727-46683777	H1-hESC	embryonic stem cell:	embryo
10	chr16:46683727-46683777	Hela-S3	cervix:	n/a
11	chr16:46694236-46694286	HRPEpiC	eye:	n/a
12	chr16:46687332-46687382	Jurkat	blood:	n/a
13	chr16:46683644-46683694	A549	lung:	n/a
14	chr16:46687332-46687382	SK-N-SH	brain:	n/a
15	chr16:46687332-46687382	NH-A	brain:	n/a
16	chr16:46683644-46683694	GM12892	blood:	n/a
17	chr16:46687332-46687382	BJ	skin:	n/a
18	chr16:46683644-46683694	AG10803	skin:	n/a
19	chr16:46694236-46694286	NHDF-neo	bronchial:	n/a
20	chr16:46683644-46683694	MCF-7	breast:	n/a
21	chr16:46687332-46687382	AG09319	gingival:	n/a
22	chr16:46683644-46683694	NH-A	brain:	n/a
23	chr16:46687332-46687382	Hepatocyte	liver:	n/a
24	chr16:46694236-46694286	HL-60	blood:	n/a
25	chr16:46694236-46694286	H1-hESC	embryonic stem cell:	embryo
26	chr16:46683644-46683694	PANC-1	pancreas:	n/a
27	chr16:46683644-46683694	HMEC	breast:	n/a
28	chr16:46683644-46683694	SK-N-MC	brain:	n/a
29	chr16:46694236-46694286	AG10803	skin:	n/a
30	chr16:46683644-46683694	SKMC	muscle:	n/a
31	chr16:46683727-46683777	HPAEpiC	pulmonary alveolar:	n/a
32	chr16:46683644-46683694	T-47D	breast:	n/a
33	chr16:46694236-46694286	HepG2	liver:	n/a
34	chr16:46683727-46683777	AoSMC	blood vessel:	n/a
35	chr16:46683727-46683777	BJ	skin:	n/a
36	chr16:46694236-46694286	IMR90	lung:	fetal
37	chr16:46694236-46694286	HRE	kidney:	n/a
38	chr16:46694236-46694286	T-47D	breast:	n/a
39	chr16:46694236-46694286	A549	lung:	n/a
40	chr16:46694236-46694286	GM12891	blood:	n/a
41	chr16:46694236-46694286	BE2_C	brain:	n/a
42	chr16:46683727-46683777	Caco-2	colon:	n/a
43	chr16:46683727-46683777	U87	brain:	n/a
44	chr16:46683644-46683694	GM12878	blood:	n/a
45	chr16:46687332-46687382	PANC-1	pancreas:	n/a
46	chr16:46683644-46683694	GM06990	blood:	n/a
47	chr16:46694236-46694286	Hepatocyte	liver:	n/a
48	chr16:46683727-46683777	RPTEC	kidney:	n/a
49	chr16:46687332-46687382	A549	lung:	n/a
50	chr16:46683644-46683694	AG04449	skin:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:46682731..46685856-chr16:46692484..46695135,3	K562	blood:
2	chr16:46701863..46703903-chr16:46713521..46715933,2	K562	blood:
3	chr16:46689494..46691834-chr16:46696786..46698368,2	K562	blood:
4	chr16:46688552..46690949-chr16:46691270..46693508,2	K562	blood:
5	chr16:46688552..46690949-chr16:46691270..46693508,2	K562	blood:
6	chr16:46668809..46671156-chr16:46672508..46674689,2	K562	blood:
7	chr16:46690502..46692806-chr16:46719055..46720847,2	MCF-7	breast:
8	chr16:46689494..46691834-chr16:46696786..46698368,2	K562	blood:
9	chr16:46690889..46693240-chr16:46695095..46696661,2	K562	blood:
10	chr16:46663477..46665810-chr16:46674721..46676333,2	K562	blood:
11	chr16:46681844..46684169-chr16:46721518..46723822,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHCBP1-2	chr16:46694608-46694865	ENSG00000261131.1
2	lnc-ORC6-1	chr16:46683038-46683255	NONHSAT142257
3	lnc-SHCBP1-2	chr16:46695441-46695503	ENSG00000261131.1
4	lnc-ORC6-1	chr16:46683582-46683761	NONHSAT142257

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	VPS35	hsa-miR-590-3p	chr16:46694554-46694575
2	VPS35	hsa-miR-24-3p	chr16:46694780-46694801
3	VPS35	hsa-miR-590-3p	chr16:46694205-46694222
4	VPS35	hsa-miR-27a-3p	chr16:46694129-46694151
5	VPS35	hsa-miR-590-3p	chr16:46695671-46695691
6	VPS35	hsa-miR-590-3p	chr16:46694136-46694156
7	VPS35	hsa-miR-590-3p	chr16:46695074-46695094

Variant related genes	Relation type
ENSG00000261131	TF binding region
VPS35	TF binding region
ENSG00000260909	TF binding region
ENSG00000261131	CpG island
VPS35	CpG island
ENSG00000260909	CpG island
ENSG00000260909	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000261131	chromatin interactions
ENSG00000091651	chromatin interactions

Extended variants
information (count: 956 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:956 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577949619	chr16:46674524-46674525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545160894	chr16:46674566-46674567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557292339	chr16:46674639-46674640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575648716	chr16:46674724-46674725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542767170	chr16:46674728-46674729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186246691	chr16:46674738-46674739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367865495	chr16:46674740-46674741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113698840	chr16:46674767-46674768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs700578	chr16:46674790-46674791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs7350845	chr16:46674848-46674849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565163670	chr16:46674959-46674960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532465431	chr16:46675005-46675006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550702614	chr16:46675041-46675042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568966551	chr16:46675044-46675045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4966606	chr16:46675045-46675046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs547976115	chr16:46675065-46675066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140210773	chr16:46675094-46675095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190731777	chr16:46675136-46675137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143452037	chr16:46675141-46675142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571579027	chr16:46675145-46675146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538952059	chr16:46675157-46675158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556616274	chr16:46675170-46675171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575743418	chr16:46675237-46675238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528346356	chr16:46675252-46675253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543256190	chr16:46675323-46675324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554744973	chr16:46675324-46675325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573409480	chr16:46675345-46675346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372770530	chr16:46675417-46675418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540598698	chr16:46675422-46675423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565303732	chr16:46675452-46675453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180904185	chr16:46675472-46675473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544169222	chr16:46675485-46675486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185966709	chr16:46675501-46675502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191293428	chr16:46675506-46675507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548396110	chr16:46675539-46675540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183199064	chr16:46675595-46675596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527405394	chr16:46675596-46675597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551707854	chr16:46675635-46675636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570123915	chr16:46675651-46675652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537890565	chr16:46675716-46675717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574791778	chr16:46675782-46675783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550991751	chr16:46675790-46675791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148158307	chr16:46675815-46675816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141110411	chr16:46675823-46675824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555218210	chr16:46675829-46675830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573347721	chr16:46675839-46675840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534295897	chr16:46675856-46675857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559132764	chr16:46675868-46675869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577306343	chr16:46675950-46675951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544621800	chr16:46675980-46675981	Weak 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:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46655600-46694200	Weak transcription	Right Ventricle	heart
2	chr16:46664000-46682800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr16:46664200-46683000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr16:46667400-46675800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr16:46667400-46683000	Weak transcription	Fetal Muscle Leg	muscle
6	chr16:46670000-46677800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr16:46672200-46674800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr16:46672600-46691200	Weak transcription	Gastric	stomach
9	chr16:46673000-46683000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr16:46674200-46692800	Weak transcription	Ovary	ovary
11	chr16:46674400-46684000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr16:46675800-46676000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr16:46679800-46689800	Weak transcription	Primary B cells from cord blood	blood
14	chr16:46681200-46691000	Weak transcription	Primary T cells from cord blood	blood
15	chr16:46681200-46692600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr16:46681400-46683000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr16:46681400-46683400	Weak transcription	Adipose Nuclei	Adipose
18	chr16:46681400-46692800	Weak transcription	Brain Angular Gyrus	brain
19	chr16:46681400-46693000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr16:46681600-46683200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr16:46681800-46692000	Weak transcription	Brain Hippocampus Middle	brain
22	chr16:46682000-46686600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:46682000-46691000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr16:46682200-46691000	Weak transcription	Left Ventricle	heart
25	chr16:46682200-46692800	Weak transcription	Spleen	Spleen
26	chr16:46682400-46683200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr16:46682800-46683000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr16:46682800-46683000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr16:46682800-46683000	Weak transcription	Aorta	Aorta
30	chr16:46682800-46683000	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr16:46682800-46683000	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr16:46682800-46683000	Enhancers	HSMM	muscle
33	chr16:46682800-46683000	Enhancers	HSMMtube	muscle
34	chr16:46682800-46683200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr16:46682800-46683200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr16:46682800-46683200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr16:46682800-46683200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr16:46682800-46683200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr16:46682800-46683200	Strong transcription	Stomach Smooth Muscle	stomach
40	chr16:46682800-46683200	Enhancers	NHLF	lung
41	chr16:46682800-46684400	Enhancers	Placenta	Placenta
42	chr16:46683000-46683200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr16:46683000-46683200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr16:46683000-46683200	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr16:46683000-46683200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr16:46683000-46683400	Genic enhancers	Fetal Muscle Leg	muscle
47	chr16:46683000-46683400	Enhancers	HMEC	breast
48	chr16:46683000-46683600	Enhancers	Fetal Stomach	stomach
49	chr16:46683000-46683600	Flanking Active TSS	HSMM	muscle
50	chr16:46683000-46683600	Flanking Active TSS	HSMMtube	muscle

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