Variant report

Variant	nsv967216
Chromosome Location	chr3:49764885-49776535
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	CEBPB	chr3:49771138-49771325	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr3:49766851-49766931	GM13976	blood:	n/a	n/a
3	CTCF	chr3:49770120-49770270	GM12871	blood:	n/a	n/a
4	CTCF	chr3:49768670-49768700	Lung_OC	lung:	n/a	n/a
5	E2F4	chr3:49776527-49776619	MCF10A-Er-Src	breast:	n/a	n/a
6	ELF1	chr3:49764430-49764893	GM12878	blood:	n/a	n/a
7	FOS	chr3:49771143-49771224	MCF10A-Er-Src	breast:	n/a	n/a
8	FOSL2	chr3:49772309-49772538	HepG2	liver:	n/a	chr3:49772450-49772458 chr3:49772449-49772458 chr3:49772449-49772459 chr3:49772450-49772457 chr3:49772448-49772460
9	GTF2B	chr3:49767799-49768021	K562	blood:	n/a	n/a
10	HNF4A	chr3:49772238-49772414	HepG2	liver:	n/a	chr3:49772376-49772391 chr3:49772376-49772391 chr3:49772376-49772391
11	HNF4A	chr3:49770041-49770290	HepG2	liver:	n/a	chr3:49770174-49770188
12	JUND	chr3:49772312-49772524	HepG2	liver:	n/a	chr3:49772450-49772458 chr3:49772449-49772458 chr3:49772449-49772459 chr3:49772448-49772459 chr3:49772450-49772457 chr3:49772448-49772460
13	MAFF	chr3:49767762-49767766	K562	blood:	n/a	n/a
14	NRF1	chr3:49775925-49775938	H1-hESC	embryonic stem cell:	n/a	n/a
15	PML	chr3:49767762-49768048	K562	blood:	n/a	n/a
16	POLR2A	chr3:49757760-49765712	HepG2	liver:	n/a	n/a
17	POLR2A	chr3:49764443-49764903	GM12892	blood:	n/a	n/a
18	POLR2A	chr3:49767955-49768286	K562	blood:	n/a	n/a
19	POLR2A	chr3:49765473-49765718	MCF-7	breast:	n/a	n/a
20	POLR2A	chr3:49768939-49768963	HepG2	liver:	n/a	n/a
21	POLR2A	chr3:49765269-49765271	A549	lung:	n/a	n/a
22	POLR2A	chr3:49772322-49772334	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr3:49765418-49765622	GM12878	blood:	n/a	n/a
24	POLR2A	chr3:49765243-49765690	H1-neurons	neurons:	n/a	n/a
25	POLR2A	chr3:49765112-49765198	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:49768806-49768876	HepG2	liver:	n/a	n/a
27	POLR2A	chr3:49765265-49765583	HepG2	liver:	n/a	n/a
28	POLR2A	chr3:49765083-49765155	MCF-7	breast:	n/a	n/a
29	POLR2A	chr3:49774932-49775318	HepG2	liver:	n/a	n/a
30	POLR2A	chr3:49765411-49765747	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr3:49765441-49765652	GM12878	blood:	n/a	n/a
32	POLR2A	chr3:49775999-49776034	K562	blood:	n/a	n/a
33	POLR2A	chr3:49768134-49768157	HepG2	liver:	n/a	n/a
34	POLR2A	chr3:49764408-49764946	GM12892	blood:	n/a	n/a
35	POLR2A	chr3:49765528-49765665	K562	blood:	n/a	n/a
36	POLR2A	chr3:49765471-49765480	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr3:49764573-49764919	H1-neurons	neurons:	n/a	n/a
38	POLR2A	chr3:49770239-49770261	MCF-7	breast:	n/a	n/a
39	POLR2A	chr3:49765039-49765796	K562	blood:	n/a	n/a
40	POLR2A	chr3:49770180-49770426	HepG2	liver:	n/a	n/a
41	POLR2A	chr3:49765685-49765775	K562	blood:	n/a	n/a
42	POLR2A	chr3:49772956-49773075	K562	blood:	n/a	n/a
43	POLR2A	chr3:49767461-49767736	HepG2	liver:	n/a	n/a
44	POLR2A	chr3:49768226-49768244	HepG2	liver:	n/a	n/a
45	POLR2A	chr3:49764896-49765047	K562	blood:	n/a	n/a
46	POLR2A	chr3:49768884-49768889	HepG2	liver:	n/a	n/a
47	POLR2A	chr3:49772343-49772382	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr3:49771330-49771333	HepG2	liver:	n/a	n/a
49	POLR2A	chr3:49774716-49774759	HepG2	liver:	n/a	n/a
50	POLR2A	chr3:49768249-49768281	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:49765843..49767368-chr3:49767924..49770492,2	K562	blood:
2	chr3:49763340..49765220-chr3:49771723..49774304,2	MCF-7	breast:
3	chr3:49719733..49721602-chr3:49767313..49769950,2	K562	blood:
4	chr3:49765843..49767368-chr3:49767924..49770492,2	K562	blood:
5	chr3:49763618..49765527-chr3:49766623..49769354,2	K562	blood:
6	chr3:49761055..49763701-chr3:49764283..49769369,4	MCF-7	breast:
7	chr3:49774827..49777820-chr3:49822579..49825134,2	K562	blood:
8	chr3:49763618..49765527-chr3:49766623..49769354,2	K562	blood:
9	chr3:49763340..49765220-chr3:49771723..49774304,2	MCF-7	breast:
10	chr3:49774405..49776029-chr3:49777710..49781166,3	K562	blood:

Variant related genes	Relation type
AMIGO3	TF binding region
GMPPB	TF binding region
IP6K1	TF binding region
ENSG00000176095	chromatin interactions
ENSG00000164062	chromatin interactions
ENSG00000173540	chromatin interactions

Extended variants
information (count: 401 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17657345	chr3:49764900-49764901	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs372277698	chr3:49764906-49764907	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs375322351	chr3:49764910-49764911	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs367884894	chr3:49764935-49764936	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs147499631	chr3:49764956-49764957	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs117326328	chr3:49765009-49765010	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs150703602	chr3:49765013-49765014	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs376477427	chr3:49765017-49765018	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs112349786	chr3:49765041-49765042	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs370210802	chr3:49765068-49765069	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs72936049	chr3:49765100-49765101	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115140901	chr3:49765109-49765110	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs142704958	chr3:49765174-49765175	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs554257626	chr3:49765205-49765206	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs374134120	chr3:49765209-49765210	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs569280911	chr3:49765231-49765232	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs536673162	chr3:49765264-49765265	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs558553817	chr3:49765303-49765304	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs147312277	chr3:49765355-49765356	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534514948	chr3:49765364-49765365	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs553083918	chr3:49765367-49765368	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574555421	chr3:49765388-49765389	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573689427	chr3:49765403-49765404	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs543111122	chr3:49765421-49765422	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs36078435	chr3:49765455-49765456	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs140914398	chr3:49765478-49765479	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs2307021	chr3:49765483-49765484	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs369664452	chr3:49765507-49765508	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs577495317	chr3:49765533-49765534	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs149764153	chr3:49765545-49765546	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs34675186	chr3:49765557-49765558	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs375665750	chr3:49765591-49765592	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs370259789	chr3:49765600-49765601	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs147379936	chr3:49765623-49765624	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs374592396	chr3:49765629-49765630	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs375536774	chr3:49765632-49765633	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs34964130	chr3:49765665-49765666	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs151229839	chr3:49765679-49765680	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs137918392	chr3:49765692-49765693	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs191955742	chr3:49765721-49765722	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs370846796	chr3:49765728-49765729	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs530250719	chr3:49765805-49765806	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547856744	chr3:49765807-49765808	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183029520	chr3:49765816-49765817	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545258760	chr3:49765820-49765821	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563683149	chr3:49765841-49765842	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139078445	chr3:49765892-49765893	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570355435	chr3:49765901-49765902	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534876468	chr3:49765907-49765908	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185811095	chr3:49765912-49765913	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
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	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49762000-49770000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:49762000-49773800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:49762000-49775000	Weak transcription	Psoas Muscle	Psoas
4	chr3:49762000-49778000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:49762200-49765200	Weak transcription	Fetal Kidney	kidney
6	chr3:49762200-49765800	Enhancers	Stomach Mucosa	stomach
7	chr3:49762200-49765800	Strong transcription	NHLF	lung
8	chr3:49762200-49768800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr3:49762200-49769000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr3:49762400-49765000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr3:49762400-49765800	Strong transcription	Brain Hippocampus Middle	brain
12	chr3:49762400-49766000	Strong transcription	Fetal Lung	lung
13	chr3:49762400-49766400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr3:49762400-49768800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr3:49762400-49768800	Weak transcription	HUVEC	blood vessel
16	chr3:49762400-49771000	Strong transcription	Brain Inferior Temporal Lobe	brain
17	chr3:49762400-49772200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr3:49762400-49773000	Weak transcription	Fetal Heart	heart
19	chr3:49762400-49776800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:49762400-49781600	Strong transcription	Fetal Stomach	stomach
21	chr3:49762600-49765400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:49762600-49765800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:49762600-49765800	Strong transcription	Lung	lung
24	chr3:49762600-49765800	Strong transcription	Right Ventricle	heart
25	chr3:49762600-49766000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr3:49762600-49766000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:49762600-49766000	Strong transcription	Brain Angular Gyrus	brain
28	chr3:49762600-49766000	Strong transcription	Thymus	Thymus
29	chr3:49762600-49768400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:49762600-49768400	Weak transcription	Fetal Brain Male	brain
31	chr3:49762600-49770400	Strong transcription	Brain Germinal Matrix	brain
32	chr3:49762600-49774600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:49762600-49776400	Strong transcription	Fetal Brain Female	brain
34	chr3:49762600-49776800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:49762600-49777000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:49762600-49777200	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr3:49762600-49777600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr3:49762600-49781800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr3:49762600-49785200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:49762600-49809000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr3:49762800-49765400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr3:49762800-49765400	Strong transcription	Esophagus	oesophagus
43	chr3:49762800-49765800	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr3:49762800-49765800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr3:49762800-49765800	Genic enhancers	Primary B cells from peripheral blood	blood
46	chr3:49762800-49765800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr3:49762800-49765800	Strong transcription	Adipose Nuclei	Adipose
48	chr3:49762800-49765800	Strong transcription	Brain Anterior Caudate	brain
49	chr3:49762800-49765800	Strong transcription	Stomach Smooth Muscle	stomach
50	chr3:49762800-49765800	Strong transcription	Spleen	Spleen

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