Variant report

Variant	esv3501751
Chromosome Location	chr3:46829898-46852196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
2	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
3	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
4	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
6	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
7	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr3:46850120-46850270	GM12873	blood:	n/a	chr3:46850217-46850226
10	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
12	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
13	CTCF	chr3:46850080-46850230	GM12873	blood:	n/a	chr3:46850217-46850226
14	FAM48A	chr3:46839688-46839827	GM12878	blood:	n/a	n/a
15	FOS	chr3:46839048-46839240	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr3:46838831-46839342	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr3:46838787-46838951	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr3:46838841-46839336	MCF10A-Er-Src	breast:	n/a	n/a
19	FOXA2	chr3:46830000-46830297	A549	lung:	n/a	n/a
20	FOXA2	chr3:46829923-46830493	A549	lung:	n/a	n/a
21	IRF4	chr3:46834873-46835151	GM12878	blood:	n/a	n/a
22	MAFF	chr3:46850465-46850559	K562	blood:	n/a	n/a
23	MAFK	chr3:46840585-46840667	HepG2	liver:	n/a	chr3:46840634-46840649
24	MAFK	chr3:46840601-46840707	HepG2	liver:	n/a	chr3:46840634-46840649
25	MYC	chr3:46839031-46839271	MCF10A-Er-Src	breast:	n/a	n/a
26	MYC	chr3:46850782-46850895	GM12878	blood:	n/a	n/a
27	MYC	chr3:46839013-46839306	MCF10A-Er-Src	breast:	n/a	n/a
28	NFIC	chr3:46834813-46835290	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:46845885-46846085	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr3:46830328-46830486	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr3:46843879-46843920	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr3:46839087-46839319	MCF10A-Er-Src	breast:	n/a	n/a
33	SPI1	chr3:46834840-46835118	GM12878	blood:	n/a	n/a
34	SPI1	chr3:46834811-46835225	GM12891	blood:	n/a	n/a
35	SPI1	chr3:46834905-46835050	GM12878	blood:	n/a	n/a
36	SPI1	chr3:46834747-46835372	GM12878	blood:	n/a	n/a
37	SPI1	chr3:46834870-46835129	GM12891	blood:	n/a	n/a
38	STAT3	chr3:46845912-46846033	MCF10A-Er-Src	breast:	n/a	n/a
39	STAT3	chr3:46845664-46845864	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr3:46839144-46839153	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr3:46848487-46848687	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr3:46843900-46844086	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr3:46839064-46839281	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr3:46840590-46840790	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr3:46839029-46839301	MCF10A-Er-Src	breast:	n/a	n/a
46	TCF12	chr3:46850561-46850799	GM12878	blood:	n/a	n/a
47	TCF12	chr3:46850236-46850499	GM12878	blood:	n/a	chr3:46850424-46850431
48	TCF12	chr3:46834841-46835080	GM12878	blood:	n/a	n/a
49	TCF3	chr3:46850192-46850527	GM12878	blood:	n/a	n/a
50	YY1	chr3:46830531-46830748	H1-hESC	embryonic stem cell:	n/a	chr3:46830605-46830617

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46850588-46850638	SAEC	small airway:	n/a
2	chr3:46850588-46850638	AG09309	skin:	n/a
3	chr3:46850588-46850638	RPTEC	kidney:	n/a
4	chr3:46850588-46850638	HUVEC	blood vessel:	n/a
5	chr3:46850588-46850638	HEK293	kidney:	embryo
6	chr3:46850588-46850638	HRPEpiC	eye:	n/a
7	chr3:46850588-46850638	GM12878	blood:	n/a
8	chr3:46850588-46850638	HIPEpiC	eye:	n/a
9	chr3:46850588-46850638	PANC-1	pancreas:	n/a
10	chr3:46850588-46850638	ECC-1	luminal epithelium:	n/a
11	chr3:46850588-46850638	NH-A	brain:	n/a
12	chr3:46850588-46850638	NHDF-neo	bronchial:	n/a
13	chr3:46850588-46850638	MCF10A-Er-Src	breast:	n/a
14	chr3:46850588-46850638	ProgFib	skin:	n/a
15	chr3:46850588-46850638	GM12891	blood:	n/a
16	chr3:46850588-46850638	HMEC	breast:	n/a
17	chr3:46850588-46850638	HNPCEpiC	eye:	n/a
18	chr3:46850588-46850638	BJ	skin:	n/a
19	chr3:46850588-46850638	A549	lung:	n/a
20	chr3:46850588-46850638	IMR90	lung:	fetal
21	chr3:46850588-46850638	NHBE	bronchial:	n/a
22	chr3:46850588-46850638	Caco-2	colon:	n/a
23	chr3:46850588-46850638	GM19239	blood:	n/a
24	chr3:46850588-46850638	ovcar-3	ovarian:	n/a
25	chr3:46850588-46850638	T-47D	breast:	n/a
26	chr3:46850588-46850638	Hepatocyte	liver:	n/a
27	chr3:46850588-46850638	AG04450	lung:	fetal
28	chr3:46850588-46850638	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:46850588-46850638	SK-N-MC	brain:	n/a
30	chr3:46850588-46850638	LNCaP	prostate:	n/a
31	chr3:46850588-46850638	SKMC	muscle:	n/a
32	chr3:46850588-46850638	SK-N-SH	brain:	n/a
33	chr3:46850588-46850638	HCT-116	colon:	n/a
34	chr3:46850588-46850638	NT2-D1	testis:	n/a
35	chr3:46850588-46850638	NB4	blood:	n/a
36	chr3:46850588-46850638	GM12892	blood:	n/a
37	chr3:46850588-46850638	Hela-S3	cervix:	n/a
38	chr3:46850588-46850638	HL-60	blood:	n/a
39	chr3:46850588-46850638	AG10803	skin:	n/a
40	chr3:46850588-46850638	AG09319	gingival:	n/a
41	chr3:46850588-46850638	H1-hESC	embryonic stem cell:	embryo
42	chr3:46850588-46850638	HRCEpiC	kidney:	n/a
43	chr3:46850588-46850638	PrEC	prostate:	n/a
44	chr3:46850588-46850638	CMK	blood:	n/a
45	chr3:46850588-46850638	AG04449	skin:	fetal
46	chr3:46850588-46850638	HRE	kidney:	n/a
47	chr3:46850588-46850638	HEEpiC	esophagus:	n/a
48	chr3:46850588-46850638	BE2_C	brain:	n/a
49	chr3:46850588-46850638	U87	brain:	n/a
50	chr3:46850588-46850638	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
ENSG00000238013	CpG island

Extended variants
information (count: 307 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:307 , 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	rs547318829	chr3:46829956-46829957	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs28775418	chr3:46829960-46829961	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs369030597	chr3:46830012-46830013	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs373033212	chr3:46830023-46830024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs28799376	chr3:46830061-46830062	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs28827623	chr3:46830204-46830205	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs568028967	chr3:46830210-46830211	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs28879181	chr3:46830251-46830252	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs547499693	chr3:46830276-46830277	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs569032994	chr3:46830310-46830311	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs539887783	chr3:46830339-46830340	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs9873861	chr3:46830397-46830398	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs576923605	chr3:46830407-46830408	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs28835597	chr3:46830416-46830417	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372732992	chr3:46830420-46830421	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs540063967	chr3:46830437-46830438	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553271844	chr3:46830457-46830458	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs574768272	chr3:46830524-46830525	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs541874520	chr3:46830569-46830570	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs563243681	chr3:46830590-46830591	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs183291572	chr3:46830591-46830592	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs545841041	chr3:46830603-46830604	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs6764426	chr3:46830629-46830630	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs576329174	chr3:46830675-46830676	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs528726169	chr3:46830694-46830695	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs6764523	chr3:46830734-46830735	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376287684	chr3:46830735-46830736	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs533971127	chr3:46830796-46830797	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs185798995	chr3:46830943-46830944	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550577486	chr3:46830998-46830999	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568870961	chr3:46831001-46831002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539554633	chr3:46831063-46831064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141008474	chr3:46831065-46831066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573731003	chr3:46831131-46831132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76254953	chr3:46831191-46831192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372162784	chr3:46834796-46834797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs376771917	chr3:46834851-46834852	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs543068216	chr3:46834881-46834882	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs550625350	chr3:46834886-46834887	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs576336238	chr3:46834936-46834937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs6442034	chr3:46835016-46835017	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs150746644	chr3:46835072-46835073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs190282658	chr3:46835076-46835077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565377039	chr3:46835079-46835080	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs533020209	chr3:46835082-46835083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs181250794	chr3:46835106-46835107	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs138997573	chr3:46835144-46835145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs527552896	chr3:46835234-46835235	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs186760162	chr3:46835245-46835246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs7429588	chr3:46835250-46835251	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46829800-46831000	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr3:46830400-46831000	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr3:46830800-46831200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:46844000-46844400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:46844000-46844400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr3:46844400-46847400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:46845600-46846400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:46846400-46851400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:46847800-46849600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:46848400-46852800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:46848600-46849200	Enhancers	Fetal Intestine Large	intestine
12	chr3:46849000-46852600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr3:46849200-46851800	Weak transcription	Fetal Intestine Large	intestine
14	chr3:46849600-46849800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:46849800-46850000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr3:46850000-46850400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr3:46850000-46850600	Enhancers	GM12878-XiMat	blood
18	chr3:46850000-46852600	Weak transcription	Right Ventricle	heart
19	chr3:46850200-46850400	Enhancers	Fetal Thymus	thymus
20	chr3:46850400-46850600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr3:46850400-46851400	Weak transcription	Fetal Thymus	thymus
22	chr3:46850400-46853200	Weak transcription	Fetal Intestine Small	intestine
23	chr3:46850600-46850800	Enhancers	Lung	lung
24	chr3:46850600-46851800	Weak transcription	GM12878-XiMat	blood
25	chr3:46850600-46852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr3:46851000-46852200	Weak transcription	Lung	lung
27	chr3:46851000-46853600	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr3:46851400-46852000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:46851400-46852200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr3:46851400-46852200	Enhancers	Thymus	Thymus
31	chr3:46851400-46853200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:46851400-46853200	Enhancers	Fetal Thymus	thymus
33	chr3:46851800-46852000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr3:46851800-46852000	Enhancers	Fetal Intestine Large	intestine
35	chr3:46851800-46852200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:46851800-46852400	Enhancers	GM12878-XiMat	blood
37	chr3:46851800-46853400	Enhancers	K562	blood
38	chr3:46851800-46856800	Enhancers	Fetal Heart	heart
39	chr3:46852000-46853000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr3:46852000-46853000	Enhancers	Spleen	Spleen
41	chr3:46852000-46853200	Enhancers	Placenta Amnion	Placenta Amnion

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