Variant report

Variant	nsv1000873
Chromosome Location	chr3:77797610-77960031
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	BACH1	chr3:77844137-77844450	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr3:77832062-77832279	K562	blood:	n/a	n/a
3	CEBPB	chr3:77950492-77950745	HepG2	liver:	n/a	chr3:77950663-77950674 chr3:77950623-77950634
4	CEBPB	chr3:77936514-77936705	HepG2	liver:	n/a	chr3:77936644-77936655
5	CEBPB	chr3:77829649-77830020	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:77874416-77874835	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:77846780-77847076	A549	lung:	n/a	chr3:77846905-77846916
8	CEBPB	chr3:77924011-77924215	A549	lung:	n/a	n/a
9	CEBPB	chr3:77910195-77910414	HepG2	liver:	n/a	chr3:77910285-77910296
10	CEBPB	chr3:77805037-77805459	Hela-S3	cervix:	n/a	chr3:77805311-77805324 chr3:77805311-77805322 chr3:77805311-77805324
11	CEBPB	chr3:77829660-77830002	A549	lung:	n/a	n/a
12	CEBPB	chr3:77950514-77950820	A549	lung:	n/a	chr3:77950663-77950674 chr3:77950623-77950634
13	CEBPB	chr3:77805146-77805478	HepG2	liver:	n/a	chr3:77805311-77805324 chr3:77805311-77805322 chr3:77805311-77805324
14	CEBPB	chr3:77846769-77847079	HepG2	liver:	n/a	chr3:77846905-77846916
15	CEBPB	chr3:77829659-77830022	K562	blood:	n/a	n/a
16	CEBPB	chr3:77848661-77848710	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr3:77874392-77874422	GM12878	blood:	n/a	n/a
18	CHD2	chr3:77844157-77844538	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr3:77874408-77874777	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr3:77864637-77864989	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr3:77864840-77864990	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr3:77874797-77874887	MCF-7	breast:	n/a	n/a
23	CTCF	chr3:77864760-77864910	HEEpiC	esophagus:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
24	CTCF	chr3:77864699-77864969	ProgFib	skin:	n/a	chr3:77864818-77864839 chr3:77864823-77864841
25	CTCF	chr3:77864760-77864910	HMEC	breast:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
26	CTCF	chr3:77864800-77864950	Caco-2	colon:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
27	CTCF	chr3:77864800-77864950	HMF	breast:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
28	CTCF	chr3:77864840-77864990	GM12875	blood:	n/a	n/a
29	CTCF	chr3:77864760-77864910	GM12874	blood:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
30	CTCF	chr3:77864711-77864955	NHEK	skin:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
31	CTCF	chr3:77864700-77864850	A549	lung:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
32	CTCF	chr3:77864740-77864890	WERI-Rb-1	eye:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
33	CTCF	chr3:77864780-77864930	GM12872	blood:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
34	CTCF	chr3:77864723-77864919	HepG2	liver:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
35	CTCF	chr3:77864620-77864770	HAc	cerebellar:	n/a	n/a
36	CTCF	chr3:77864734-77864919	Medullo	brain:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
37	CTCF	chr3:77874220-77874370	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr3:77874240-77874390	HMEC	breast:	n/a	n/a
39	CTCF	chr3:77864740-77864890	HCPEpiC	choroid plexus:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
40	CTCF	chr3:77864800-77864950	NHDF-neo	bronchial:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
41	CTCF	chr3:77864740-77864890	HRE	kidney:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
42	CTCF	chr3:77864750-77864921	HepG2	liver:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
43	CTCF	chr3:77864680-77864830	NHEK	skin:	n/a	n/a
44	CTCF	chr3:77864743-77864920	GM12878	blood:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
45	CTCF	chr3:77864840-77864990	HFF	foreskin:	n/a	n/a
46	CTCF	chr3:77874220-77874370	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr3:77864780-77864930	HPF	lung:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
48	CTCF	chr3:77874760-77874910	HMEC	breast:	n/a	n/a
49	CTCF	chr3:77864780-77864930	HVMF	connective:	n/a	chr3:77864823-77864841 chr3:77864818-77864839
50	CTCF	chr3:77864780-77864930	RPTEC	kidney:	n/a	chr3:77864823-77864841 chr3:77864818-77864839

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:77843317-77843367	HMEC	breast:	n/a
2	chr3:77843317-77843367	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:77843317-77843367	ECC-1	luminal epithelium:	n/a
4	chr3:77843317-77843367	SK-N-SH_RA	brain:	n/a
5	chr3:77843317-77843367	AG09319	gingival:	n/a
6	chr3:77843317-77843367	HAEpiC	amniotic membrane:	n/a
7	chr3:77843317-77843367	MCF-7	breast:	n/a
8	chr3:77843317-77843367	NT2-D1	testis:	n/a
9	chr3:77843317-77843367	Jurkat	blood:	n/a
10	chr3:77843317-77843367	H1-hESC	embryonic stem cell:	embryo
11	chr3:77843317-77843367	HRPEpiC	eye:	n/a
12	chr3:77843317-77843367	HRE	kidney:	n/a
13	chr3:77843317-77843367	PrEC	prostate:	n/a
14	chr3:77843317-77843367	GM12892	blood:	n/a
15	chr3:77843317-77843367	SKMC	muscle:	n/a
16	chr3:77843317-77843367	Caco-2	colon:	n/a
17	chr3:77843317-77843367	BE2_C	brain:	n/a
18	chr3:77843317-77843367	A549	lung:	n/a
19	chr3:77843317-77843367	SK-N-SH	brain:	n/a
20	chr3:77843317-77843367	GM12891	blood:	n/a
21	chr3:77843317-77843367	NHBE	bronchial:	n/a
22	chr3:77843317-77843367	BJ	skin:	n/a
23	chr3:77843317-77843367	HCM	heart:	n/a
24	chr3:77843317-77843367	HIPEpiC	eye:	n/a
25	chr3:77843317-77843367	SK-N-MC	brain:	n/a
26	chr3:77843317-77843367	PANC-1	pancreas:	n/a
27	chr3:77843317-77843367	PFSK-1	brain:	n/a
28	chr3:77843317-77843367	LNCaP	prostate:	n/a
29	chr3:77843317-77843367	U87	brain:	n/a
30	chr3:77843317-77843367	RPTEC	kidney:	n/a
31	chr3:77843317-77843367	HEEpiC	esophagus:	n/a
32	chr3:77843317-77843367	HCPEpiC	choroid plexus:	n/a
33	chr3:77843317-77843367	IMR90	lung:	fetal
34	chr3:77843317-77843367	NB4	blood:	n/a
35	chr3:77843317-77843367	SAEC	small airway:	n/a
36	chr3:77843317-77843367	GM06990	blood:	n/a
37	chr3:77843317-77843367	AG09309	skin:	n/a
38	chr3:77843317-77843367	NHDF-neo	bronchial:	n/a
39	chr3:77843317-77843367	AG10803	skin:	n/a
40	chr3:77843317-77843367	NH-A	brain:	n/a
41	chr3:77843317-77843367	HepG2	liver:	n/a
42	chr3:77843317-77843367	AG04450	lung:	fetal
43	chr3:77843317-77843367	HCF	heart:	n/a
44	chr3:77843317-77843367	AG04449	skin:	fetal
45	chr3:77843317-77843367	Hepatocyte	liver:	n/a
46	chr3:77843317-77843367	HCT-116	colon:	n/a
47	chr3:77843317-77843367	CMK	blood:	n/a
48	chr3:77843317-77843367	MCF10A-Er-Src	breast:	n/a
49	chr3:77843317-77843367	ProgFib	skin:	n/a
50	chr3:77843317-77843367	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr3:77864350..77865332-chr3:78253776..78254517,3	MCF-7	breast:
2	chr3:77832530..77834277-chr3:77845042..77847268,2	K562	blood:
3	chr3:77872762..77874698-chr3:77899434..77901272,2	MCF-7	breast:
4	chr3:77872762..77874698-chr3:77899434..77901272,2	MCF-7	breast:
5	chr3:77397316..77398033-chr3:77864577..77865232,2	MCF-7	breast:
6	chr3:77832530..77834277-chr3:77845042..77847268,2	K562	blood:

Variant related genes	Relation type
RNU6-217P	TF binding region
RNU6-217P	CpG island

Extended variants
information (count: 2581 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2581 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531910913	chr3:77804411-77804412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182019569	chr3:77804482-77804483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6795283	chr3:77804495-77804496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546472325	chr3:77804524-77804525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566014640	chr3:77804532-77804533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532992548	chr3:77804557-77804558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185713103	chr3:77804569-77804570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566426346	chr3:77804576-77804577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562489790	chr3:77804598-77804599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528960814	chr3:77804652-77804653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369132067	chr3:77804677-77804678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568727146	chr3:77804752-77804753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537635804	chr3:77804759-77804760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531297845	chr3:77804778-77804779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190522204	chr3:77804796-77804797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576743463	chr3:77805015-77805016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs72583423	chr3:77805064-77805065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200764350	chr3:77805065-77805066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202026943	chr3:77805066-77805067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199986640	chr3:77805068-77805069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74819197	chr3:77805069-77805070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200562941	chr3:77805070-77805071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10627390	chr3:77805078-77805079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10629878	chr3:77805081-77805082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201926223	chr3:77805082-77805083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182406594	chr3:77805099-77805100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150448993	chr3:77805108-77805109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140252509	chr3:77805132-77805133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527989154	chr3:77805187-77805188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570170654	chr3:77805198-77805199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559739504	chr3:77805205-77805206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528825498	chr3:77805306-77805307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145362728	chr3:77805324-77805325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187911280	chr3:77805349-77805350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555870190	chr3:77818809-77818810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545661436	chr3:77818813-77818814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370563301	chr3:77818831-77818832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533975434	chr3:77818849-77818850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116215242	chr3:77818856-77818857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185159673	chr3:77818862-77818863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144140475	chr3:77818872-77818873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115038682	chr3:77818900-77818901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34275822	chr3:77818915-77818916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560768037	chr3:77818921-77818922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528135657	chr3:77818981-77818982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2701072	chr3:77823222-77823223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548908037	chr3:77823276-77823277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2599519	chr3:77823278-77823279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187427291	chr3:77823322-77823323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375021173	chr3:77823329-77823330	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:77804400-77804800	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr3:77805000-77805400	Enhancers	Hela-S3	cervix
3	chr3:77818800-77819000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr3:77823200-77823800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:77823400-77823600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:77823600-77823800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:77823800-77824600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:77828000-77828200	Enhancers	Brain Germinal Matrix	brain
9	chr3:77828200-77828800	Weak transcription	Brain Germinal Matrix	brain
10	chr3:77828800-77829000	Enhancers	Brain Germinal Matrix	brain
11	chr3:77829000-77829400	Weak transcription	Brain Germinal Matrix	brain
12	chr3:77829200-77829800	Enhancers	Fetal Brain Male	brain
13	chr3:77829400-77829800	Active TSS	Brain Germinal Matrix	brain
14	chr3:77829400-77831000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr3:77829600-77829800	Enhancers	Fetal Kidney	kidney
16	chr3:77829600-77830200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr3:77829600-77830200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:77829600-77830200	Enhancers	Fetal Brain Female	brain
19	chr3:77829600-77831200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:77829600-77831600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:77829800-77830200	Flanking Active TSS	Brain Germinal Matrix	brain
22	chr3:77830000-77830400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr3:77830200-77830800	Enhancers	Brain Germinal Matrix	brain
24	chr3:77830600-77831000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr3:77830800-77833000	Weak transcription	Brain Germinal Matrix	brain
26	chr3:77833000-77834200	Enhancers	Brain Germinal Matrix	brain
27	chr3:77839000-77843000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:77843000-77843200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:77843000-77843400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:77843000-77843600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:77843000-77843600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:77843000-77843600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr3:77843000-77844000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:77843000-77844200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr3:77843000-77844400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr3:77843000-77844600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:77843000-77844600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr3:77843000-77844800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr3:77843000-77844800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:77843200-77843600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr3:77843200-77843600	Enhancers	Gastric	stomach
42	chr3:77843200-77844400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr3:77843200-77847800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:77843400-77843600	Enhancers	Brain Germinal Matrix	brain
45	chr3:77843600-77844000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:77843600-77844000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr3:77843600-77844000	Weak transcription	Gastric	stomach
48	chr3:77843600-77848400	Weak transcription	Brain Germinal Matrix	brain
49	chr3:77844000-77844600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr3:77844000-77844600	Enhancers	HUES6 Cell Line	embryonic stem cell

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