Variant report

Variant	nsv823147
Chromosome Location	chr5:96247723-96257836
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	ATF2	chr5:96255265-96255924	GM12878	blood:	n/a	n/a
2	ATF2	chr5:96256765-96257862	GM12878	blood:	n/a	n/a
3	ATF2	chr5:96256477-96257844	GM12878	blood:	n/a	n/a
4	ATF2	chr5:96255290-96255916	GM12878	blood:	n/a	n/a
5	BATF	chr5:96257259-96257681	GM12878	blood:	n/a	n/a
6	BATF	chr5:96255399-96255965	GM12878	blood:	n/a	chr5:96255638-96255649
7	BATF	chr5:96255401-96255848	GM12878	blood:	n/a	chr5:96255638-96255649
8	BCL11A	chr5:96255409-96255847	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:96257303-96257639	GM12878	blood:	n/a	chr5:96257409-96257418
10	BCL3	chr5:96257253-96257642	GM12878	blood:	n/a	chr5:96257409-96257418
11	BCL3	chr5:96257151-96257853	GM12878	blood:	n/a	chr5:96257409-96257418
12	BCL3	chr5:96255373-96255918	GM12878	blood:	n/a	n/a
13	BCLAF1	chr5:96257179-96257720	GM12878	blood:	n/a	chr5:96257409-96257418
14	BCLAF1	chr5:96255351-96255852	GM12878	blood:	n/a	n/a
15	BRCA1	chr5:96250428-96250598	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:96257077-96257860	GM12878	blood:	n/a	n/a
17	CHD2	chr5:96255415-96255883	GM12878	blood:	n/a	n/a
18	CREB1	chr5:96257113-96257808	GM12878	blood:	n/a	n/a
19	CUX1	chr5:96255262-96255785	GM12878	blood:	n/a	n/a
20	CUX1	chr5:96257198-96257708	GM12878	blood:	n/a	n/a
21	E2F4	chr5:96257317-96257523	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr5:96255337-96255818	GM12878	blood:	n/a	n/a
23	EBF1	chr5:96255362-96255846	GM12878	blood:	n/a	n/a
24	EBF1	chr5:96255360-96255876	GM12878	blood:	n/a	n/a
25	EBF1	chr5:96256748-96257763	GM12878	blood:	n/a	n/a
26	EBF1	chr5:96256764-96256987	GM12878	blood:	n/a	n/a
27	EP300	chr5:96255353-96255811	GM12878	blood:	n/a	chr5:96255494-96255508 chr5:96255430-96255444
28	EP300	chr5:96255387-96255739	GM12878	blood:	n/a	chr5:96255494-96255508 chr5:96255430-96255444
29	EP300	chr5:96257289-96257678	GM12878	blood:	n/a	chr5:96257409-96257418
30	FOS	chr5:96257284-96257599	MCF10A-Er-Src	breast:	n/a	chr5:96257409-96257416 chr5:96257408-96257418 chr5:96257409-96257417 chr5:96257407-96257418 chr5:96257409-96257417
31	FOS	chr5:96257304-96257564	MCF10A-Er-Src	breast:	n/a	chr5:96257409-96257416 chr5:96257408-96257418 chr5:96257409-96257417 chr5:96257407-96257418 chr5:96257409-96257417
32	FOS	chr5:96257228-96257599	HUVEC	blood vessel:	n/a	chr5:96257409-96257416 chr5:96257408-96257418 chr5:96257409-96257417 chr5:96257407-96257418 chr5:96257409-96257417
33	FOS	chr5:96257282-96257530	MCF10A-Er-Src	breast:	n/a	chr5:96257409-96257416 chr5:96257408-96257418 chr5:96257409-96257417 chr5:96257407-96257418 chr5:96257409-96257417
34	FOXM1	chr5:96255291-96255895	GM12878	blood:	n/a	n/a
35	FOXM1	chr5:96257185-96257871	GM12878	blood:	n/a	n/a
36	FOXM1	chr5:96257091-96257960	GM12878	blood:	n/a	n/a
37	IKZF1	chr5:96257285-96257675	GM12878	blood:	n/a	n/a
38	IKZF1	chr5:96255506-96255746	GM12878	blood:	n/a	n/a
39	IRF1	chr5:96248193-96248206	K562	blood:	n/a	n/a
40	IRF4	chr5:96255423-96255939	GM12878	blood:	n/a	n/a
41	IRF4	chr5:96255352-96255943	GM12878	blood:	n/a	n/a
42	JUN	chr5:96257232-96257625	HUVEC	blood vessel:	n/a	chr5:96257409-96257416 chr5:96257408-96257418 chr5:96257409-96257417 chr5:96257409-96257417
43	KAP1	chr5:96256990-96257182	K562	blood:	n/a	n/a
44	MAZ	chr5:96256876-96257224	GM12878	blood:	n/a	n/a
45	MEF2A	chr5:96255387-96255901	GM12878	blood:	n/a	n/a
46	MEF2A	chr5:96257273-96257546	K562	blood:	n/a	chr5:96257409-96257417
47	MEF2A	chr5:96257135-96257785	GM12878	blood:	n/a	chr5:96257409-96257417 chr5:96257138-96257159
48	MEF2A	chr5:96257207-96257720	GM12878	blood:	n/a	chr5:96257409-96257417
49	MEF2C	chr5:96257160-96257812	GM12878	blood:	n/a	chr5:96257409-96257417
50	MTA3	chr5:96255369-96255908	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96256918-96256968	HIPEpiC	eye:	n/a
2	chr5:96256918-96256968	GM12892	blood:	n/a
3	chr5:96256918-96256968	HCF	heart:	n/a
4	chr5:96256918-96256968	HCPEpiC	choroid plexus:	n/a
5	chr5:96256918-96256968	A549	lung:	n/a
6	chr5:96256918-96256968	Caco-2	colon:	n/a
7	chr5:96256918-96256968	AoSMC	blood vessel:	n/a
8	chr5:96253798-96253848	BE2_C	brain:	n/a
9	chr5:96256918-96256968	ProgFib	skin:	n/a
10	chr5:96253798-96253848	SAEC	small airway:	n/a
11	chr5:96256918-96256968	MCF10A-Er-Src	breast:	n/a
12	chr5:96256918-96256968	AG10803	skin:	n/a
13	chr5:96256918-96256968	HMEC	breast:	n/a
14	chr5:96256918-96256968	GM12878	blood:	n/a
15	chr5:96256918-96256968	GM12891	blood:	n/a
16	chr5:96253798-96253848	ProgFib	skin:	n/a
17	chr5:96253798-96253848	Caco-2	colon:	n/a
18	chr5:96253798-96253848	NH-A	brain:	n/a
19	chr5:96256918-96256968	GM19239	blood:	n/a
20	chr5:96256918-96256968	ECC-1	luminal epithelium:	n/a
21	chr5:96253798-96253848	MCF10A-Er-Src	breast:	n/a
22	chr5:96253798-96253848	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:96256918-96256968	HCM	heart:	n/a
24	chr5:96253798-96253848	SKMC	muscle:	n/a
25	chr5:96253798-96253848	K562	blood:	n/a
26	chr5:96256918-96256968	SK-N-SH	brain:	n/a
27	chr5:96253798-96253848	HCPEpiC	choroid plexus:	n/a
28	chr5:96253798-96253848	HEK293	kidney:	embryo
29	chr5:96256918-96256968	AG04450	lung:	fetal
30	chr5:96253798-96253848	NB4	blood:	n/a
31	chr5:96253798-96253848	NHBE	bronchial:	n/a
32	chr5:96253798-96253848	AG04449	skin:	fetal
33	chr5:96256918-96256968	Hepatocyte	liver:	n/a
34	chr5:96256918-96256968	U87	brain:	n/a
35	chr5:96253798-96253848	SK-N-MC	brain:	n/a
36	chr5:96253798-96253848	PANC-1	pancreas:	n/a
37	chr5:96253798-96253848	ovcar-3	ovarian:	n/a
38	chr5:96253798-96253848	Jurkat	blood:	n/a
39	chr5:96253798-96253848	AoSMC	blood vessel:	n/a
40	chr5:96253798-96253848	HCF	heart:	n/a
41	chr5:96253798-96253848	Hepatocyte	liver:	n/a
42	chr5:96253798-96253848	HEEpiC	esophagus:	n/a
43	chr5:96253798-96253848	BJ	skin:	n/a
44	chr5:96253798-96253848	HAEpiC	amniotic membrane:	n/a
45	chr5:96256918-96256968	SK-N-SH_RA	brain:	n/a
46	chr5:96253798-96253848	GM12892	blood:	n/a
47	chr5:96256918-96256968	PFSK-1	brain:	n/a
48	chr5:96253798-96253848	MCF-7	breast:	n/a
49	chr5:96256918-96256968	PrEC	prostate:	n/a
50	chr5:96253798-96253848	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:96253236..96255336-chr5:96271138..96273178,2	MCF-7	breast:
2	chr5:96251167..96254648-chr5:96255205..96257867,3	K562	blood:
3	chr5:96251167..96254648-chr5:96255205..96257867,3	K562	blood:
4	chr5:96246528..96248146-chr5:96256371..96258639,2	MCF-7	breast:
5	chr5:96254195..96257346-chr5:96259220..96261586,3	MCF-7	breast:
6	chr5:96246528..96248146-chr5:96256371..96258639,2	MCF-7	breast:
7	chr5:96250090..96254054-chr5:96271244..96274355,3	K562	blood:
8	chr5:96255625..96258387-chr5:96259524..96261476,2	K562	blood:
9	chr5:96196694..96198422-chr5:96257589..96259904,2	K562	blood:
10	chr5:96254910..96258387-chr5:96259473..96261476,3	K562	blood:
11	chr5:96257613..96260808-chr5:96268504..96273197,4	MCF-7	breast:
12	chr5:96239497..96241968-chr5:96254714..96256341,2	K562	blood:

Variant related genes	Relation type
ERAP2	TF binding region
ERAP2	CpG island
ENSG00000113441	chromatin interactions
ENSG00000247121	chromatin interactions

Extended variants
information (count: 384 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10463196	chr5:96247750-96247751	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377674803	chr5:96247767-96247768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370621410	chr5:96247801-96247802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13187896	chr5:96247807-96247808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6873866	chr5:96247810-96247811	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs370566191	chr5:96247816-96247817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536377870	chr5:96247820-96247821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189054421	chr5:96247826-96247827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13163165	chr5:96247827-96247828	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs181832910	chr5:96247852-96247853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187247315	chr5:96247873-96247874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144038026	chr5:96247909-96247910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35943000	chr5:96247913-96247914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114820944	chr5:96247914-96247915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540397957	chr5:96247922-96247923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565191444	chr5:96247962-96247963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548171695	chr5:96247969-96247970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148588652	chr5:96247970-96247971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76870375	chr5:96247978-96247979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2042385	chr5:96247993-96247994	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs76998898	chr5:96247998-96247999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62377803	chr5:96248000-96248001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10463197	chr5:96248045-96248046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530452078	chr5:96248067-96248068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192036251	chr5:96248093-96248094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567042121	chr5:96248098-96248099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142872628	chr5:96248179-96248180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548647885	chr5:96248204-96248205	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs558495151	chr5:96248217-96248218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17487132	chr5:96248254-96248255	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs34454498	chr5:96248271-96248272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182615886	chr5:96248292-96248293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35363714	chr5:96248309-96248310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570819899	chr5:96248312-96248313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150634138	chr5:96248331-96248332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144251459	chr5:96248417-96248418	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148708472	chr5:96248429-96248430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200211238	chr5:96248440-96248441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373000463	chr5:96248461-96248462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575169329	chr5:96248462-96248463	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536000248	chr5:96248475-96248476	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534870563	chr5:96248476-96248477	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374962061	chr5:96248492-96248493	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142362923	chr5:96248496-96248497	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs151262056	chr5:96248499-96248500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537846656	chr5:96248523-96248524	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369880117	chr5:96248529-96248530	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190229753	chr5:96248531-96248532	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554986597	chr5:96248577-96248578	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540434603	chr5:96248631-96248632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96217600-96250000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr5:96218000-96264600	Weak transcription	Right Ventricle	heart
3	chr5:96218600-96259600	Weak transcription	HMEC	breast
4	chr5:96221600-96269200	Weak transcription	Fetal Brain Male	brain
5	chr5:96222000-96268600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:96222400-96258200	Weak transcription	Stomach Mucosa	stomach
7	chr5:96225600-96266400	Weak transcription	Gastric	stomach
8	chr5:96229600-96269600	Weak transcription	Aorta	Aorta
9	chr5:96229800-96256800	Weak transcription	NHEK	skin
10	chr5:96229800-96256800	Weak transcription	Osteobl	bone
11	chr5:96229800-96257000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:96229800-96270000	Weak transcription	Esophagus	oesophagus
13	chr5:96232600-96258400	Weak transcription	Brain Hippocampus Middle	brain
14	chr5:96233000-96255600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr5:96233000-96256200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr5:96233800-96256000	Strong transcription	Primary B cells from peripheral blood	blood
17	chr5:96234200-96255600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr5:96237400-96269200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:96237600-96250600	Weak transcription	Hela-S3	cervix
20	chr5:96237800-96265000	Weak transcription	Fetal Muscle Leg	muscle
21	chr5:96238400-96256800	Weak transcription	NHDF-Ad	bronchial
22	chr5:96239400-96256800	Weak transcription	HSMM	muscle
23	chr5:96239400-96257200	Weak transcription	NHLF	lung
24	chr5:96239600-96252800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:96239800-96268000	Weak transcription	Colonic Mucosa	Colon
26	chr5:96240200-96253600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:96240400-96254200	Strong transcription	GM12878-XiMat	blood
28	chr5:96240600-96256800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:96242000-96259800	Weak transcription	Fetal Stomach	stomach
30	chr5:96242200-96255600	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr5:96242200-96256000	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr5:96242200-96268000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr5:96243400-96257200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr5:96243600-96255000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr5:96243600-96266400	Weak transcription	Brain Angular Gyrus	brain
36	chr5:96243800-96256000	Strong transcription	Fetal Thymus	thymus
37	chr5:96244200-96258600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr5:96244800-96248200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:96245200-96256600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr5:96245400-96258200	Weak transcription	Small Intestine	intestine
41	chr5:96245400-96259600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr5:96245400-96259800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr5:96245600-96248400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr5:96245600-96248400	Weak transcription	Liver	Liver
45	chr5:96245600-96249000	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr5:96245600-96249800	Weak transcription	Primary B cells from cord blood	blood
47	chr5:96245600-96255800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr5:96245800-96249000	Weak transcription	Lung	lung
49	chr5:96245800-96251400	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr5:96245800-96253600	Weak transcription	Placenta	Placenta

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