Variant report

Variant	nsv822079
Chromosome Location	chr3:50116177-50126157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:50125919-50126486	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:50126030-50126356	K562	blood:	n/a	n/a
3	ATF2	chr3:50126134-50126573	GM12878	blood:	n/a	n/a
4	BCL3	chr3:50125898-50126550	A549	lung:	n/a	n/a
5	BCLAF1	chr3:50119709-50120135	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:50126147-50126482	K562	blood:	n/a	n/a
7	BHLHE40	chr3:50126009-50126467	GM12878	blood:	n/a	n/a
8	BRCA1	chr3:50126105-50126680	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr3:50125780-50126506	K562	blood:	n/a	n/a
10	CEBPB	chr3:50116423-50116545	K562	blood:	n/a	n/a
11	CEBPB	chr3:50126024-50126507	Hela-S3	cervix:	n/a	n/a
12	CHD1	chr3:50125809-50128121	IMR90	lung:	n/a	n/a
13	CHD1	chr3:50126062-50127612	GM12878	blood:	n/a	n/a
14	CHD2	chr3:50126120-50126989	GM12878	blood:	n/a	n/a
15	CHD2	chr3:50126117-50126998	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr3:50126134-50126785	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr3:50125984-50126631	GM12878	blood:	n/a	n/a
18	CREB1	chr3:50126122-50126540	A549	lung:	n/a	n/a
19	CREB1	chr3:50126090-50126531	H1-hESC	embryonic stem cell:	n/a	n/a
20	CUX1	chr3:50126077-50126419	K562	blood:	n/a	n/a
21	CUX1	chr3:50126088-50126190	GM12878	blood:	n/a	n/a
22	E2F4	chr3:50126071-50126527	MCF10A-Er-Src	breast:	n/a	n/a
23	EBF1	chr3:50126121-50126619	GM12878	blood:	n/a	n/a
24	EBF1	chr3:50120571-50120604	GM12878	blood:	n/a	n/a
25	ELF1	chr3:50126144-50126410	K562	blood:	n/a	chr3:50126375-50126384
26	ELF1	chr3:50126096-50126510	K562	blood:	n/a	chr3:50126375-50126384
27	ELF1	chr3:50126133-50127241	GM12878	blood:	n/a	chr3:50126375-50126384 chr3:50126538-50126547
28	ELK1	chr3:50126032-50126417	GM12878	blood:	n/a	n/a
29	EP300	chr3:50126125-50126363	GM12878	blood:	n/a	n/a
30	EP300	chr3:50126066-50126643	GM12878	blood:	n/a	n/a
31	EP300	chr3:50126157-50126658	GM12878	blood:	n/a	n/a
32	EP300	chr3:50126090-50126499	HepG2	liver:	n/a	n/a
33	ETS1	chr3:50126030-50126494	GM12878	blood:	n/a	chr3:50126327-50126338 chr3:50126253-50126266
34	ETS1	chr3:50126146-50126451	A549	lung:	n/a	chr3:50126327-50126338 chr3:50126253-50126266
35	ETS1	chr3:50125986-50126549	A549	lung:	n/a	chr3:50126327-50126338 chr3:50126253-50126266
36	FOS	chr3:50119910-50120051	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr3:50126130-50126419	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr3:50126061-50126419	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXA1	chr3:50126157-50126347	T-47D	breast:	n/a	n/a
40	FOXM1	chr3:50126032-50126725	GM12878	blood:	n/a	n/a
41	FOXP2	chr3:50126149-50126505	SK-N-MC	brain:	n/a	n/a
42	GATA2	chr3:50125750-50126077	SH-SY5Y	brain:	n/a	n/a
43	GTF2F1	chr3:50126032-50126535	Hela-S3	cervix:	n/a	n/a
44	GTF2F1	chr3:50126124-50126595	K562	blood:	n/a	n/a
45	GTF3C2	chr3:50125744-50126311	Hela-S3	cervix:	n/a	n/a
46	HA-E2F1	chr3:50126025-50126737	MCF-7	breast:	n/a	n/a
47	HCFC1	chr3:50125732-50127483	Hela-S3	cervix:	n/a	n/a
48	HCFC1	chr3:50126021-50126722	K562	blood:	n/a	n/a
49	HEY1	chr3:50126018-50126657	HepG2	liver:	n/a	n/a
50	HEY1	chr3:50126092-50126618	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:50126100-50126150	HRPEpiC	eye:	n/a
2	chr3:50126067-50126117	HMEC	breast:	n/a
3	chr3:50126100-50126150	HAEpiC	amniotic membrane:	n/a
4	chr3:50122624-50122674	U87	brain:	n/a
5	chr3:50126100-50126150	NHDF-neo	bronchial:	n/a
6	chr3:50126100-50126150	HCM	heart:	n/a
7	chr3:50122624-50122674	AG04449	skin:	fetal
8	chr3:50126067-50126117	NHDF-neo	bronchial:	n/a
9	chr3:50126028-50126078	GM12878	blood:	n/a
10	chr3:50126100-50126150	BE2_C	brain:	n/a
11	chr3:50122624-50122674	GM12892	blood:	n/a
12	chr3:50126100-50126150	PFSK-1	brain:	n/a
13	chr3:50126067-50126117	T-47D	breast:	n/a
14	chr3:50126100-50126150	PrEC	prostate:	n/a
15	chr3:50126028-50126078	PrEC	prostate:	n/a
16	chr3:50126028-50126078	GM19239	blood:	n/a
17	chr3:50126067-50126117	GM12891	blood:	n/a
18	chr3:50126028-50126078	SK-N-SH_RA	brain:	n/a
19	chr3:50126028-50126078	GM12891	blood:	n/a
20	chr3:50126067-50126117	HAEpiC	amniotic membrane:	n/a
21	chr3:50126067-50126117	NT2-D1	testis:	n/a
22	chr3:50126067-50126117	AG10803	skin:	n/a
23	chr3:50122624-50122674	ProgFib	skin:	n/a
24	chr3:50126067-50126117	GM19239	blood:	n/a
25	chr3:50126100-50126150	SK-N-MC	brain:	n/a
26	chr3:50126100-50126150	GM12891	blood:	n/a
27	chr3:50126100-50126150	NH-A	brain:	n/a
28	chr3:50126067-50126117	HRCEpiC	kidney:	n/a
29	chr3:50126100-50126150	IMR90	lung:	fetal
30	chr3:50126028-50126078	NB4	blood:	n/a
31	chr3:50126028-50126078	HIPEpiC	eye:	n/a
32	chr3:50126067-50126117	HCM	heart:	n/a
33	chr3:50126100-50126150	SKMC	muscle:	n/a
34	chr3:50122624-50122674	HCM	heart:	n/a
35	chr3:50122624-50122674	AG10803	skin:	n/a
36	chr3:50126028-50126078	AG09319	gingival:	n/a
37	chr3:50126028-50126078	ovcar-3	ovarian:	n/a
38	chr3:50126028-50126078	AoSMC	blood vessel:	n/a
39	chr3:50126028-50126078	SAEC	small airway:	n/a
40	chr3:50126067-50126117	AG09319	gingival:	n/a
41	chr3:50126028-50126078	Hela-S3	cervix:	n/a
42	chr3:50126067-50126117	NHBE	bronchial:	n/a
43	chr3:50126067-50126117	PANC-1	pancreas:	n/a
44	chr3:50126028-50126078	A549	lung:	n/a
45	chr3:50126028-50126078	MCF-7	breast:	n/a
46	chr3:50126100-50126150	U87	brain:	n/a
47	chr3:50126067-50126117	ECC-1	luminal epithelium:	n/a
48	chr3:50126067-50126117	SK-N-MC	brain:	n/a
49	chr3:50126100-50126150	SAEC	small airway:	n/a
50	chr3:50126067-50126117	PFSK-1	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49966762..49969614-chr3:50125142..50129125,3	K562	blood:
2	chr3:49976300..49979550-chr3:50125389..50128777,3	K562	blood:
3	chr3:49966031..49968659-chr3:50125180..50127794,3	K562	blood:
4	chr3:49975788..49978611-chr3:50125447..50127862,2	MCF-7	breast:
5	chr3:50122524..50125290-chr3:50125428..50127425,2	K562	blood:
6	chr3:50126080..50126817-chr3:197025051..197025628,2	Hela-S3	cervix:
7	chr3:50125762..50129022-chr3:50137938..50141076,4	K562	blood:
8	chr3:50125097..50128236-chr3:50128554..50131975,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM5-1	chr3:50124168-50124422	expReg_chr3_4587_+

No data

Variant related genes	Relation type
RBM5	TF binding region
RBM5	CpG island
ENSG00000227375	chromatin interactions
ENSG00000003756	chromatin interactions
ENSG00000004534	chromatin interactions
ENSG00000164077	chromatin interactions
ENSG00000075711	chromatin interactions

Extended variants
information (count: 334 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:334 , 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	rs560437317	chr3:50116183-50116184	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs542698507	chr3:50116209-50116210	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs542863439	chr3:50116212-50116213	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs141857355	chr3:50116336-50116337	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs72299589	chr3:50116339-50116340	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs13324545	chr3:50116342-50116343	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs377723458	chr3:50116358-50116359	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs6787299	chr3:50116468-50116469	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs527695367	chr3:50116473-50116474	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77815052	chr3:50116512-50116513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200320184	chr3:50116513-50116514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199520110	chr3:50116514-50116515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549878013	chr3:50116570-50116571	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564905750	chr3:50116599-50116600	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547241299	chr3:50116691-50116692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532157617	chr3:50116694-50116695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572674114	chr3:50116732-50116733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565551213	chr3:50116762-50116763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565838732	chr3:50116853-50116854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148025175	chr3:50116861-50116862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183977156	chr3:50116872-50116873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543666525	chr3:50116889-50116890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189272210	chr3:50116890-50116891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180822507	chr3:50116897-50116898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556254771	chr3:50116992-50116993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571382206	chr3:50117084-50117085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538654085	chr3:50117152-50117153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550750950	chr3:50117177-50117178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185807796	chr3:50117214-50117215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62263589	chr3:50117240-50117241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs5848908	chr3:50117243-50117244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547177063	chr3:50117244-50117245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200718377	chr3:50117260-50117261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2624816	chr3:50117312-50117313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs536450077	chr3:50117329-50117330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148458768	chr3:50117375-50117376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543299962	chr3:50117393-50117394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62263590	chr3:50117420-50117421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs190716555	chr3:50117445-50117446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543995384	chr3:50117463-50117464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564994184	chr3:50117486-50117487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150845673	chr3:50117519-50117520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2624817	chr3:50117520-50117521	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs559290954	chr3:50117527-50117528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529973018	chr3:50117532-50117533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs118122460	chr3:50117533-50117534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181778521	chr3:50117576-50117577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530640370	chr3:50117618-50117619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577863037	chr3:50117620-50117621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571420545	chr3:50117646-50117647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Cancer	20164919	CNVD
Autism	20531469	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50082400-50116200	Strong transcription	Fetal Thymus	thymus
2	chr3:50082600-50116200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:50084200-50116600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:50089200-50116200	Strong transcription	Duodenum Mucosa	Duodenum
5	chr3:50089200-50116400	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr3:50097200-50116200	Strong transcription	Brain Cingulate Gyrus	brain
7	chr3:50104200-50123400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:50105800-50116200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:50105800-50116200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:50105800-50116400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:50106000-50116200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:50106200-50125800	Weak transcription	Stomach Mucosa	stomach
13	chr3:50108800-50126000	Weak transcription	Fetal Heart	heart
14	chr3:50110200-50126000	Weak transcription	NHLF	lung
15	chr3:50110600-50125800	Weak transcription	Small Intestine	intestine
16	chr3:50111000-50125800	Weak transcription	Colonic Mucosa	Colon
17	chr3:50111000-50126000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr3:50111200-50119000	Weak transcription	Fetal Brain Male	brain
19	chr3:50111200-50119800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr3:50111200-50126200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:50112200-50125800	Weak transcription	K562	blood
22	chr3:50112800-50119600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr3:50113000-50119400	Weak transcription	Esophagus	oesophagus
24	chr3:50113000-50125800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr3:50113000-50125800	Weak transcription	A549	lung
26	chr3:50113000-50126000	Weak transcription	NH-A	brain
27	chr3:50113200-50116200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr3:50113200-50119600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr3:50113200-50119600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:50113200-50119600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr3:50113200-50119600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr3:50113200-50119600	Weak transcription	HUVEC	blood vessel
33	chr3:50113200-50120200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:50113200-50120200	Weak transcription	Spleen	Spleen
35	chr3:50113200-50125600	Weak transcription	HepG2	liver
36	chr3:50113200-50125800	Weak transcription	Colon Smooth Muscle	Colon
37	chr3:50113200-50125800	Weak transcription	Gastric	stomach
38	chr3:50113200-50125800	Weak transcription	Pancreas	Pancrea
39	chr3:50113200-50125800	Weak transcription	Psoas Muscle	Psoas
40	chr3:50113200-50126200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:50113400-50117800	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr3:50113400-50118000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr3:50113400-50118800	Weak transcription	Primary B cells from cord blood	blood
44	chr3:50113400-50118800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr3:50113400-50119600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr3:50113400-50125600	Weak transcription	Dnd41	blood
47	chr3:50113400-50125800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr3:50113400-50125800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr3:50113400-50125800	Weak transcription	Brain Substantia Nigra	brain
50	chr3:50113400-50125800	Weak transcription	Rectal Mucosa Donor 31	rectum

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