Variant report

Variant	esv12895
Chromosome Location	chr5:79945853-79948255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:123)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:79948130-79948314	K562	blood:	n/a	n/a
2	BATF	chr5:79945796-79948270	GM12878	blood:	n/a	n/a
3	BATF	chr5:79946204-79948185	GM12878	blood:	n/a	n/a
4	BATF	chr5:79945798-79946130	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:79945745-79947892	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:79946239-79948230	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:79945773-79946175	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:79947896-79948213	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:79945741-79948232	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:79947196-79947508	K562	blood:	n/a	n/a
11	CEBPB	chr5:79947229-79947520	GM12878	blood:	n/a	n/a
12	CEBPD	chr5:79946239-79948298	K562	blood:	n/a	n/a
13	CEBPD	chr5:79945670-79946160	K562	blood:	n/a	n/a
14	CTCF	chr5:79946852-79947113	K562	blood:	n/a	n/a
15	CTCF	chr5:79946487-79946793	K562	blood:	n/a	n/a
16	CTCF	chr5:79946193-79947744	K562	blood:	n/a	n/a
17	CTCF	chr5:79945797-79946109	K562	blood:	n/a	n/a
18	CTCF	chr5:79948080-79948230	Caco-2	colon:	n/a	n/a
19	CTCF	chr5:79945839-79946035	K562	blood:	n/a	n/a
20	CTCF	chr5:79947189-79947853	K562	blood:	n/a	n/a
21	E2F4	chr5:79947816-79948010	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr5:79946246-79948218	GM12878	blood:	n/a	n/a
23	EBF1	chr5:79945748-79946151	GM12878	blood:	n/a	n/a
24	EBF1	chr5:79945803-79948110	GM12878	blood:	n/a	n/a
25	EP300	chr5:79946176-79947830	GM12878	blood:	n/a	n/a
26	EP300	chr5:79947904-79948199	GM12878	blood:	n/a	n/a
27	EP300	chr5:79945694-79948218	GM12878	blood:	n/a	n/a
28	EP300	chr5:79945810-79946103	GM12878	blood:	n/a	n/a
29	FOS	chr5:79947649-79947956	MCF10A-Er-Src	breast:	n/a	chr5:79947812-79947821 chr5:79947810-79947822 chr5:79947813-79947824 chr5:79947811-79947821 chr5:79947811-79947820
30	FOS	chr5:79947668-79947899	MCF10A-Er-Src	breast:	n/a	chr5:79947812-79947821 chr5:79947810-79947822 chr5:79947813-79947824 chr5:79947811-79947821 chr5:79947811-79947820
31	FOS	chr5:79947644-79948006	MCF10A-Er-Src	breast:	n/a	chr5:79947812-79947821 chr5:79947810-79947822 chr5:79947813-79947824 chr5:79947811-79947821 chr5:79947811-79947820
32	FOS	chr5:79947645-79948005	MCF10A-Er-Src	breast:	n/a	chr5:79947812-79947821 chr5:79947810-79947822 chr5:79947813-79947824 chr5:79947811-79947821 chr5:79947811-79947820
33	FOSL2	chr5:79945790-79946144	HepG2	liver:	n/a	n/a
34	FOSL2	chr5:79946232-79948222	HepG2	liver:	n/a	chr5:79947812-79947821 chr5:79947810-79947822 chr5:79947813-79947824 chr5:79947811-79947821 chr5:79947811-79947820
35	FOSL2	chr5:79945717-79948224	HepG2	liver:	n/a	chr5:79947812-79947821 chr5:79947810-79947822 chr5:79947813-79947824 chr5:79947811-79947821 chr5:79947811-79947820
36	FOXA1	chr5:79945655-79947959	HepG2	liver:	n/a	n/a
37	FOXM1	chr5:79945605-79948472	GM12878	blood:	n/a	n/a
38	FOXP2	chr5:79946845-79947546	SK-N-MC	brain:	n/a	n/a
39	FOXP2	chr5:79945801-79946132	PFSK-1	brain:	n/a	n/a
40	FOXP2	chr5:79946426-79946712	PFSK-1	brain:	n/a	n/a
41	FOXP2	chr5:79946716-79948183	PFSK-1	brain:	n/a	n/a
42	FOXP2	chr5:79945802-79946142	SK-N-MC	brain:	n/a	n/a
43	FOXP2	chr5:79946430-79946817	SK-N-MC	brain:	n/a	n/a
44	FOXP2	chr5:79947613-79947974	SK-N-MC	brain:	n/a	n/a
45	GABPA	chr5:79945775-79948219	Hela-S3	cervix:	n/a	n/a
46	GABPA	chr5:79947911-79948010	Hela-S3	cervix:	n/a	n/a
47	GABPA	chr5:79947530-79947830	Hela-S3	cervix:	n/a	n/a
48	GABPA	chr5:79946278-79947143	Hela-S3	cervix:	n/a	n/a
49	GABPA	chr5:79945820-79946056	Hela-S3	cervix:	n/a	n/a
50	GABPA	chr5:79947168-79947513	Hela-S3	cervix:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79946787-79946837	HMEC	breast:	n/a
2	chr5:79946787-79946837	HMEC	breast:	n/a
3	chr5:79946787-79946837	GM12878	blood:	n/a
4	chr5:79947234-79947284	SK-N-MC	brain:	n/a
5	chr5:79946787-79946837	RPTEC	kidney:	n/a
6	chr5:79946787-79946837	BE2_C	brain:	n/a
7	chr5:79947234-79947284	HMEC	breast:	n/a
8	chr5:79947234-79947284	HCPEpiC	choroid plexus:	n/a
9	chr5:79946787-79946837	HCM	heart:	n/a
10	chr5:79946787-79946837	AoSMC	blood vessel:	n/a
11	chr5:79946787-79946837	HEK293	kidney:	embryo
12	chr5:79946787-79946837	BJ	skin:	n/a
13	chr5:79947234-79947284	AG04449	skin:	fetal
14	chr5:79947234-79947284	A549	lung:	n/a
15	chr5:79946787-79946837	HRCEpiC	kidney:	n/a
16	chr5:79946787-79946837	HRE	kidney:	n/a
17	chr5:79947234-79947284	NHBE	bronchial:	n/a
18	chr5:79947234-79947284	GM12878	blood:	n/a
19	chr5:79946787-79946837	GM19239	blood:	n/a
20	chr5:79947234-79947284	K562	blood:	n/a
21	chr5:79946787-79946837	HIPEpiC	eye:	n/a
22	chr5:79946787-79946837	T-47D	breast:	n/a
23	chr5:79947234-79947284	AG09319	gingival:	n/a
24	chr5:79947234-79947284	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:79947234-79947284	AG04450	lung:	fetal
26	chr5:79947234-79947284	SKMC	muscle:	n/a
27	chr5:79947234-79947284	ProgFib	skin:	n/a
28	chr5:79947234-79947284	AG09309	skin:	n/a
29	chr5:79947234-79947284	HEK293	kidney:	embryo
30	chr5:79946787-79946837	SK-N-SH_RA	brain:	n/a
31	chr5:79946787-79946837	IMR90	lung:	fetal
32	chr5:79946787-79946837	HCF	heart:	n/a
33	chr5:79947234-79947284	AG10803	skin:	n/a
34	chr5:79946787-79946837	NHBE	bronchial:	n/a
35	chr5:79947234-79947284	GM12892	blood:	n/a
36	chr5:79946787-79946837	PrEC	prostate:	n/a
37	chr5:79947234-79947284	NT2-D1	testis:	n/a
38	chr5:79947234-79947284	MCF-7	breast:	n/a
39	chr5:79947234-79947284	BJ	skin:	n/a
40	chr5:79946787-79946837	NB4	blood:	n/a
41	chr5:79946787-79946837	U87	brain:	n/a
42	chr5:79946787-79946837	SAEC	small airway:	n/a
43	chr5:79946787-79946837	HCT-116	colon:	n/a
44	chr5:79947234-79947284	HepG2	liver:	n/a
45	chr5:79946787-79946837	NH-A	brain:	n/a
46	chr5:79947234-79947284	Hela-S3	cervix:	n/a
47	chr5:79947234-79947284	GM19239	blood:	n/a
48	chr5:79947234-79947284	IMR90	lung:	fetal
49	chr5:79947234-79947284	U87	brain:	n/a
50	chr5:79946787-79946837	NHDF-neo	bronchial:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:79934758..79936666-chr5:79944561..79946409,2	K562	blood:
2	chr5:79702114..79706204-chr5:79947823..79953616,8	MCF-7	breast:
3	chr5:79939684..79942536-chr5:79944291..79945964,2	MCF-7	breast:
4	chr5:79940209..79946671-chr5:79947972..79952044,13	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD34B-4	chr5:79947242-79947865	NONHSAT102416
2	lnc-ANKRD34B-4	chr5:79946861-79947776	NONHSAT102415
3	lnc-MSH3-2	chr5:79946322-79946361	NONHSAT102414
4	lnc-MSH3-2	chr5:79946605-79946796	NONHSAT102414

No data

Variant related genes	Relation type
MTRNR2L2	TF binding region
MSH3	TF binding region
MTRNR2L2	CpG island
MSH3	CpG island
ENSG00000228716	chromatin interactions
ENSG00000113318	chromatin interactions
ENSG00000039319	chromatin interactions

Extended variants
information (count: 227 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:227 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10942928	chr5:79945871-79945872	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs199844766	chr5:79945875-79945876	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551689879	chr5:79945895-79945896	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs74561694	chr5:79945913-79945914	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs571826098	chr5:79945934-79945935	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs537498428	chr5:79945967-79945968	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs557069457	chr5:79945970-79945971	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs573937678	chr5:79945973-79945974	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs376734277	chr5:79945979-79945980	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs111598346	chr5:79945981-79945982	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs80109921	chr5:79945988-79945989	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201935861	chr5:79945995-79945996	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs374065833	chr5:79945997-79945998	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs78893240	chr5:79946012-79946013	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs75397552	chr5:79946014-79946015	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs536766880	chr5:79946027-79946028	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs74951646	chr5:79946045-79946046	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs140302260	chr5:79946084-79946085	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs75343240	chr5:79946092-79946093	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs77014309	chr5:79946095-79946096	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs113450641	chr5:79946114-79946115	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs111932208	chr5:79946121-79946122	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs112272160	chr5:79946133-79946134	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs76238308	chr5:79946145-79946146	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs75547725	chr5:79946157-79946158	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs376430849	chr5:79946216-79946217	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs374101661	chr5:79946234-79946235	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs189503794	chr5:79946238-79946239	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs78251416	chr5:79946253-79946254	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs78753613	chr5:79946257-79946258	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs545202425	chr5:79946263-79946264	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs113593438	chr5:79946277-79946278	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs79058473	chr5:79946279-79946280	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs80182947	chr5:79946280-79946281	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs181367266	chr5:79946286-79946287	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs78845016	chr5:79946292-79946293	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs368038075	chr5:79946310-79946311	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs371859646	chr5:79946311-79946312	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs375212866	chr5:79946313-79946314	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs369735282	chr5:79946315-79946316	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs372335365	chr5:79946316-79946317	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs77008859	chr5:79946318-79946319	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs544457992	chr5:79946327-79946328	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs560727756	chr5:79946334-79946335	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs548625287	chr5:79946373-79946374	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs79627144	chr5:79946375-79946376	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs836820	chr5:79946380-79946381	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs74464984	chr5:79946394-79946395	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs558205606	chr5:79946401-79946402	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559798398	chr5:79946426-79946427	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	17409424	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79906600-79949200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:79912200-79948000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr5:79913200-79949000	Weak transcription	Spleen	Spleen
4	chr5:79913600-79949400	Weak transcription	Esophagus	oesophagus
5	chr5:79914200-79949400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:79915400-79949200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr5:79916600-79949400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:79919600-79949200	Weak transcription	Colonic Mucosa	Colon
9	chr5:79919600-79949800	Weak transcription	Pancreas	Pancrea
10	chr5:79919800-79949000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr5:79920200-79949000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr5:79920200-79949000	Weak transcription	Stomach Mucosa	stomach
13	chr5:79923600-79949800	Weak transcription	Brain Hippocampus Middle	brain
14	chr5:79924200-79949200	Weak transcription	Colon Smooth Muscle	Colon
15	chr5:79924200-79949400	Weak transcription	Right Ventricle	heart
16	chr5:79924200-79949800	Weak transcription	Left Ventricle	heart
17	chr5:79924400-79949200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:79925000-79946200	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr5:79925200-79948400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:79925200-79948600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:79925600-79949600	Weak transcription	HSMMtube	muscle
22	chr5:79928600-79949200	Weak transcription	NH-A	brain
23	chr5:79929000-79949800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr5:79929200-79949200	Weak transcription	Fetal Brain Male	brain
25	chr5:79929400-79949400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr5:79931400-79949200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr5:79932400-79946400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:79934200-79949600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr5:79935600-79948800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr5:79935600-79949400	Weak transcription	Brain Angular Gyrus	brain
31	chr5:79936400-79949000	Weak transcription	Fetal Kidney	kidney
32	chr5:79936800-79949200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr5:79937000-79949400	Weak transcription	Small Intestine	intestine
34	chr5:79937000-79950000	Weak transcription	Ovary	ovary
35	chr5:79937200-79949000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:79937200-79949000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:79937200-79949400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr5:79937400-79949200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:79937600-79947600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:79937600-79949000	Weak transcription	NHLF	lung
41	chr5:79937600-79949400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr5:79937800-79949800	Weak transcription	Lung	lung
43	chr5:79937800-79949800	Weak transcription	Psoas Muscle	Psoas
44	chr5:79938200-79947400	Strong transcription	Primary hematopoietic stem cells	blood
45	chr5:79938200-79949000	Weak transcription	HepG2	liver
46	chr5:79938600-79949200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr5:79940400-79947600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr5:79940400-79949200	Weak transcription	Fetal Lung	lung
49	chr5:79940600-79949200	Weak transcription	Primary B cells from peripheral blood	blood
50	chr5:79940800-79948600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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