Variant report

Variant	nsv1002604
Chromosome Location	chr3:46809376-46868816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:610)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:46853993-46854163	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
3	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
4	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
5	CBX3	chr3:46862333-46862734	K562	blood:	n/a	n/a
6	CBX3	chr3:46864817-46865093	K562	blood:	n/a	n/a
7	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
8	CBX3	chr3:46862397-46862721	K562	blood:	n/a	n/a
9	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
10	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
12	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
13	CTCF	chr3:46853580-46853730	SAEC	small airway:	n/a	n/a
14	CTCF	chr3:46850120-46850270	GM12873	blood:	n/a	chr3:46850217-46850226
15	CTCF	chr3:46850080-46850230	GM12873	blood:	n/a	chr3:46850217-46850226
16	CTCF	chr3:46854876-46854950	GM20000	blood:	n/a	n/a
17	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
19	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
20	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
22	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
24	CTCF	chr3:46854325-46854386	GM20000	blood:	n/a	n/a
25	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
26	CTCF	chr3:46865442-46865496	Kidney_OC	kidney:	n/a	n/a
27	E2F6	chr3:46853813-46854245	A549	lung:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
28	E2F6	chr3:46853178-46854309	H1-hESC	embryonic stem cell:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
29	E2F6	chr3:46853117-46854270	H1-hESC	embryonic stem cell:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
30	E2F6	chr3:46853742-46854273	K562	blood:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
31	E2F6	chr3:46853875-46854203	K562	blood:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
32	E2F6	chr3:46852724-46853059	H1-hESC	embryonic stem cell:	n/a	n/a
33	E2F6	chr3:46853441-46854290	K562	blood:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
34	E2F6	chr3:46852784-46853010	K562	blood:	n/a	n/a
35	E2F6	chr3:46852676-46853072	H1-hESC	embryonic stem cell:	n/a	n/a
36	E2F6	chr3:46853655-46854327	A549	lung:	n/a	chr3:46854080-46854089 chr3:46854114-46854124
37	EBF1	chr3:46821837-46822068	GM12878	blood:	n/a	chr3:46821936-46821947 chr3:46821916-46821927
38	EGR1	chr3:46853932-46854191	K562	blood:	n/a	chr3:46854075-46854088 chr3:46854080-46854090 chr3:46854075-46854088 chr3:46854074-46854089
39	EGR1	chr3:46853492-46853662	K562	blood:	n/a	chr3:46853569-46853584
40	ELF1	chr3:46853116-46853473	K562	blood:	n/a	chr3:46853305-46853318
41	FAM48A	chr3:46839688-46839827	GM12878	blood:	n/a	n/a
42	FOS	chr3:46838841-46839336	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:46838831-46839342	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:46838787-46838951	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:46839048-46839240	MCF10A-Er-Src	breast:	n/a	n/a
46	FOXA2	chr3:46829923-46830493	A549	lung:	n/a	n/a
47	FOXA2	chr3:46830000-46830297	A549	lung:	n/a	n/a
48	GABPA	chr3:46853075-46853379	K562	blood:	n/a	n/a
49	GTF2F1	chr3:46853507-46853707	H1-hESC	embryonic stem cell:	n/a	n/a
50	HCFC1	chr3:46853986-46854083	K562	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46854297-46854347	HEK293	kidney:	embryo
2	chr3:46854173-46854223	RPTEC	kidney:	n/a
3	chr3:46854311-46854361	T-47D	breast:	n/a
4	chr3:46854311-46854361	NT2-D1	testis:	n/a
5	chr3:46854231-46854281	A549	lung:	n/a
6	chr3:46854311-46854361	BJ	skin:	n/a
7	chr3:46854231-46854281	HMEC	breast:	n/a
8	chr3:46854311-46854361	SAEC	small airway:	n/a
9	chr3:46853986-46854036	GM06990	blood:	n/a
10	chr3:46850588-46850638	LNCaP	prostate:	n/a
11	chr3:46853631-46853681	AG09319	gingival:	n/a
12	chr3:46853850-46853900	MCF-7	breast:	n/a
13	chr3:46853631-46853681	U87	brain:	n/a
14	chr3:46854297-46854347	GM12891	blood:	n/a
15	chr3:46853910-46853960	HRCEpiC	kidney:	n/a
16	chr3:46854231-46854281	Caco-2	colon:	n/a
17	chr3:46856803-46856853	GM12878	blood:	n/a
18	chr3:46853850-46853900	NT2-D1	testis:	n/a
19	chr3:46856803-46856853	NB4	blood:	n/a
20	chr3:46854231-46854281	HEK293	kidney:	embryo
21	chr3:46853850-46853900	H1-hESC	embryonic stem cell:	embryo
22	chr3:46854311-46854361	RPTEC	kidney:	n/a
23	chr3:46856803-46856853	BE2_C	brain:	n/a
24	chr3:46853631-46853681	HEEpiC	esophagus:	n/a
25	chr3:46853631-46853681	PANC-1	pancreas:	n/a
26	chr3:46853631-46853681	T-47D	breast:	n/a
27	chr3:46854311-46854361	HRE	kidney:	n/a
28	chr3:46853850-46853900	T-47D	breast:	n/a
29	chr3:46850588-46850638	GM06990	blood:	n/a
30	chr3:46854297-46854347	AG04450	lung:	fetal
31	chr3:46853850-46853900	HNPCEpiC	eye:	n/a
32	chr3:46850588-46850638	AG09319	gingival:	n/a
33	chr3:46854297-46854347	BE2_C	brain:	n/a
34	chr3:46853850-46853900	HCM	heart:	n/a
35	chr3:46850588-46850638	MCF-7	breast:	n/a
36	chr3:46854311-46854361	U87	brain:	n/a
37	chr3:46853850-46853900	AoSMC	blood vessel:	n/a
38	chr3:46853910-46853960	NT2-D1	testis:	n/a
39	chr3:46853986-46854036	U87	brain:	n/a
40	chr3:46850588-46850638	HCF	heart:	n/a
41	chr3:46853986-46854036	HRE	kidney:	n/a
42	chr3:46853986-46854036	NHDF-neo	bronchial:	n/a
43	chr3:46856803-46856853	HAEpiC	amniotic membrane:	n/a
44	chr3:46853910-46853960	ovcar-3	ovarian:	n/a
45	chr3:46853850-46853900	ovcar-3	ovarian:	n/a
46	chr3:46853986-46854036	SKMC	muscle:	n/a
47	chr3:46854311-46854361	AoSMC	blood vessel:	n/a
48	chr3:46854231-46854281	GM12878	blood:	n/a
49	chr3:46854173-46854223	HRE	kidney:	n/a
50	chr3:46854173-46854223	NB4	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
2	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
3	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
4	chr3:46858188..46860125-chr3:46939783..46942119,2	K562	blood:
5	chr3:46864966..46867284-chr3:46873787..46876389,2	K562	blood:
6	chr3:46853522..46855564-chr3:46864841..46866780,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46853712-46854064	NONHSAT089457
2	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS45	TF binding region
PRSS50	TF binding region
PRSS44	TF binding region
ENSG00000238013	CpG island
PRSS45	CpG island
PRSS50	CpG island
PRSS44	CpG island
ENSG00000188086	chromatin interactions
ENSG00000178055	chromatin interactions
ENSG00000206549	chromatin interactions

Extended variants
information (count: 850 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189891321	chr3:46809607-46809608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs201879098	chr3:46809633-46809634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs75521520	chr3:46809711-46809712	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs566670239	chr3:46809750-46809751	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs56128295	chr3:46809752-46809753	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs200874382	chr3:46809753-46809754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs375538710	chr3:46809794-46809795	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs548916433	chr3:46809854-46809855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs149732333	chr3:46809937-46809938	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs537773545	chr3:46809972-46809973	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs538392229	chr3:46810000-46810001	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs369070546	chr3:46819367-46819368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531855668	chr3:46819448-46819449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182402372	chr3:46819456-46819457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185700703	chr3:46819459-46819460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142963928	chr3:46819532-46819533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551271861	chr3:46819574-46819575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34312097	chr3:46819623-46819624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373511005	chr3:46819624-46819625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550025872	chr3:46819639-46819640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190655361	chr3:46819687-46819688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376146002	chr3:46819696-46819697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566787763	chr3:46819701-46819702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533816842	chr3:46819702-46819703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201486529	chr3:46819706-46819707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4289374	chr3:46819731-46819732	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs182514572	chr3:46819863-46819864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565634255	chr3:46819906-46819907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566880081	chr3:46819920-46819921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537550492	chr3:46819926-46819927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537823460	chr3:46819959-46819960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185583516	chr3:46820000-46820001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4287935	chr3:46820012-46820013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145958671	chr3:46820040-46820041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556342830	chr3:46820062-46820063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4287934	chr3:46820121-46820122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557840869	chr3:46820136-46820137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547318829	chr3:46829956-46829957	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs28775418	chr3:46829960-46829961	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs369030597	chr3:46830012-46830013	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373033212	chr3:46830023-46830024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs28799376	chr3:46830061-46830062	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs28827623	chr3:46830204-46830205	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs568028967	chr3:46830210-46830211	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs28879181	chr3:46830251-46830252	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs547499693	chr3:46830276-46830277	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs569032994	chr3:46830310-46830311	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs539887783	chr3:46830339-46830340	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs9873861	chr3:46830397-46830398	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs576923605	chr3:46830407-46830408	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46809600-46810000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:46819200-46820200	Enhancers	Primary B cells from cord blood	blood
3	chr3:46819600-46820000	Enhancers	Primary B cells from peripheral blood	blood
4	chr3:46829800-46831000	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr3:46830400-46831000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr3:46830800-46831200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:46844000-46844400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:46844000-46844400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:46844400-46847400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr3:46845600-46846400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:46846400-46851400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:46847800-46849600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:46848400-46852800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:46848600-46849200	Enhancers	Fetal Intestine Large	intestine
15	chr3:46849000-46852600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:46849200-46851800	Weak transcription	Fetal Intestine Large	intestine
17	chr3:46849600-46849800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr3:46849800-46850000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:46850000-46850400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr3:46850000-46850600	Enhancers	GM12878-XiMat	blood
21	chr3:46850000-46852600	Weak transcription	Right Ventricle	heart
22	chr3:46850200-46850400	Enhancers	Fetal Thymus	thymus
23	chr3:46850400-46850600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:46850400-46851400	Weak transcription	Fetal Thymus	thymus
25	chr3:46850400-46853200	Weak transcription	Fetal Intestine Small	intestine
26	chr3:46850600-46850800	Enhancers	Lung	lung
27	chr3:46850600-46851800	Weak transcription	GM12878-XiMat	blood
28	chr3:46850600-46852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr3:46851000-46852200	Weak transcription	Lung	lung
30	chr3:46851000-46853600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr3:46851400-46852000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:46851400-46852200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:46851400-46852200	Enhancers	Thymus	Thymus
34	chr3:46851400-46853200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:46851400-46853200	Enhancers	Fetal Thymus	thymus
36	chr3:46851800-46852000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:46851800-46852000	Enhancers	Fetal Intestine Large	intestine
38	chr3:46851800-46852200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:46851800-46852400	Enhancers	GM12878-XiMat	blood
40	chr3:46851800-46853400	Enhancers	K562	blood
41	chr3:46851800-46856800	Enhancers	Fetal Heart	heart
42	chr3:46852000-46853000	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr3:46852000-46853000	Enhancers	Spleen	Spleen
44	chr3:46852000-46853200	Enhancers	Placenta Amnion	Placenta Amnion
45	chr3:46852200-46852400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr3:46852200-46852400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:46852200-46852600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr3:46852200-46852600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr3:46852200-46852600	Active TSS	Thymus	Thymus
50	chr3:46852200-46853400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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