Variant report

Variant	nsv882776
Chromosome Location	chr5:118859546-118915408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118860192-118860556	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:118868088-118868866	K562	blood:	n/a	n/a
3	ATF1	chr5:118868403-118868934	K562	blood:	n/a	n/a
4	ATF2	chr5:118873197-118874032	GM12878	blood:	n/a	n/a
5	ATF2	chr5:118914677-118915033	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:118873223-118873968	GM12878	blood:	n/a	n/a
7	BATF	chr5:118873364-118873881	GM12878	blood:	n/a	n/a
8	BATF	chr5:118873272-118873908	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:118873315-118873926	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
10	BCL11A	chr5:118873461-118873945	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
11	BCL3	chr5:118873342-118873895	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
12	BCLAF1	chr5:118873277-118873927	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
13	BCLAF1	chr5:118873198-118873942	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
14	BHLHE40	chr5:118873360-118873825	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:118868487-118868714	K562	blood:	n/a	n/a
16	BRCA1	chr5:118905293-118905295	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr5:118914624-118915116	HCT-116	colon:	n/a	n/a
18	CCNT2	chr5:118868541-118868579	K562	blood:	n/a	n/a
19	CEBPB	chr5:118860187-118860486	HepG2	liver:	n/a	chr5:118860206-118860218
20	CEBPB	chr5:118863620-118863625	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:118873191-118873959	GM12878	blood:	n/a	n/a
22	CEBPB	chr5:118881846-118881850	K562	blood:	n/a	n/a
23	CEBPB	chr5:118881941-118881942	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr5:118873456-118873835	GM12878	blood:	n/a	n/a
25	CTCF	chr5:118914800-118914950	GM12875	blood:	n/a	n/a
26	CTCF	chr5:118873722-118873760	Fibrobl	skin:	n/a	n/a
27	CTCF	chr5:118914760-118914910	GM12871	blood:	n/a	n/a
28	CTCF	chr5:118914705-118914926	A549	lung:	n/a	n/a
29	CTCF	chr5:118914732-118914918	GM12892	blood:	n/a	n/a
30	CTCF	chr5:118914837-118914844	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:118914760-118914910	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr5:118914660-118914810	GM12866	blood:	n/a	n/a
33	CTCF	chr5:118914733-118914838	GM10266	blood:	n/a	n/a
34	CTCF	chr5:118914713-118914918	GM19240	blood:	n/a	n/a
35	CTCF	chr5:118914558-118915085	HCT-116	colon:	n/a	n/a
36	CTCF	chr5:118914720-118914870	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:118914700-118914850	GM12878	blood:	n/a	n/a
38	CTCF	chr5:118914689-118914919	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr5:118914770-118914853	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr5:118914700-118914850	AG10803	skin:	n/a	n/a
41	CTCF	chr5:118904620-118904770	Caco-2	colon:	n/a	n/a
42	CTCF	chr5:118914760-118914910	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr5:118914760-118914910	HAc	cerebellar:	n/a	n/a
44	CTCF	chr5:118914732-118914915	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr5:118914740-118914890	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr5:118914720-118914870	GM12866	blood:	n/a	n/a
47	CTCF	chr5:118914740-118914890	HMEC	breast:	n/a	n/a
48	CTCF	chr5:118914780-118914930	AG09319	gingival:	n/a	n/a
49	CTCF	chr5:118914720-118914870	NHEK	skin:	n/a	n/a
50	CTCF	chr5:118914780-118914930	GM12864	blood:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118894936..118898702-chr5:118910373..118913198,3	K562	blood:
2	chr5:118866950..118868481-chr5:118871752..118873914,2	K562	blood:
3	chr5:118872062..118874467-chr5:118875456..118877548,2	K562	blood:
4	chr5:118868196..118870095-chr5:118875556..118878228,2	K562	blood:
5	chr5:118891974..118894099-chr5:118898157..118900146,2	K562	blood:
6	chr5:118914344..118915154-chr5:119079337..119079948,2	MCF-7	breast:
7	chr5:118872062..118875418-chr5:118875456..118880778,4	K562	blood:
8	chr5:118894367..118897199-chr5:119080311..119081964,2	K562	blood:
9	chr5:118872062..118874467-chr5:118875456..118877548,2	K562	blood:
10	chr5:118866950..118868481-chr5:118871752..118873914,2	K562	blood:
11	chr5:118891974..118894099-chr5:118898157..118900146,2	K562	blood:
12	chr5:118868196..118870095-chr5:118875556..118878228,2	K562	blood:
13	chr5:118828423..118830428-chr5:118858768..118861011,2	K562	blood:
14	chr5:118894936..118898702-chr5:118910373..118913198,3	K562	blood:
15	chr5:118863717..118866521-chr5:118868164..118871056,3	K562	blood:
16	chr5:118872062..118875418-chr5:118875456..118880778,4	K562	blood:
17	chr5:118753614..118755538-chr5:118867454..118869085,2	K562	blood:
18	chr17:59527418..59528358-chr5:118905430..118906391,2	MCF-7	breast:
19	chr5:118863717..118866521-chr5:118868164..118871056,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-11	chr5:118890945-118891353	NONHSAT103440

No data

Variant related genes	Relation type
HSD17B4	TF binding region
FABP5P6	TF binding region
ENSG00000213663	TF binding region
ENSG00000133835	chromatin interactions

Extended variants
information (count: 1916 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1916 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10051019	chr5:118859546-118859547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542754245	chr5:118859559-118859560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528994396	chr5:118859566-118859567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531358126	chr5:118859597-118859598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544885916	chr5:118859598-118859599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2884596	chr5:118859628-118859629	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs491526	chr5:118859658-118859659	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs552173897	chr5:118859669-118859670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs113737623	chr5:118859676-118859677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527614267	chr5:118859678-118859679	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568761491	chr5:118859770-118859771	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111965462	chr5:118859775-118859776	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547349674	chr5:118859805-118859806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567302555	chr5:118859808-118859809	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189998473	chr5:118859832-118859833	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184027763	chr5:118859837-118859838	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569767949	chr5:118859852-118859853	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538395077	chr5:118859877-118859878	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs565999802	chr5:118859886-118859887	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188581288	chr5:118859935-118859936	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs3797368	chr5:118859958-118859959	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs529848561	chr5:118859974-118859975	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs571880551	chr5:118860022-118860023	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534252055	chr5:118860040-118860041	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs200334731	chr5:118860061-118860062	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145159350	chr5:118860138-118860139	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs140733095	chr5:118860155-118860156	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs76693934	chr5:118860165-118860166	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs67990368	chr5:118860169-118860170	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77972558	chr5:118860208-118860209	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs66831568	chr5:118860216-118860217	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556979917	chr5:118860239-118860240	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs572291733	chr5:118860274-118860275	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541005457	chr5:118860290-118860291	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs112918036	chr5:118860318-118860319	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs147899230	chr5:118860323-118860324	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs542483094	chr5:118860337-118860338	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs192325029	chr5:118860340-118860341	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs549808600	chr5:118860355-118860356	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs563337649	chr5:118860386-118860387	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs532129409	chr5:118860399-118860400	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574979292	chr5:118860442-118860443	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551928380	chr5:118860466-118860467	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs375718118	chr5:118860494-118860495	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367603212	chr5:118860498-118860499	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571781386	chr5:118860514-118860515	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369094282	chr5:118860530-118860531	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs534503630	chr5:118860549-118860550	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183295562	chr5:118860560-118860561	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187447839	chr5:118860613-118860614	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118794800-118861200	Weak transcription	HSMM	muscle
2	chr5:118804200-118879600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr5:118832400-118878200	Weak transcription	NH-A	brain
4	chr5:118832600-118868600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr5:118833000-118860200	Weak transcription	Stomach Mucosa	stomach
6	chr5:118838000-118869200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:118840200-118878400	Weak transcription	Psoas Muscle	Psoas
8	chr5:118841000-118880000	Weak transcription	Brain Germinal Matrix	brain
9	chr5:118841200-118880000	Weak transcription	A549	lung
10	chr5:118841400-118873200	Weak transcription	Fetal Brain Male	brain
11	chr5:118842200-118860200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr5:118845800-118868800	Weak transcription	Fetal Heart	heart
13	chr5:118846800-118860200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:118846800-118862800	Weak transcription	Colon Smooth Muscle	Colon
15	chr5:118846800-118878200	Weak transcription	NHLF	lung
16	chr5:118847000-118860000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr5:118847000-118863000	Weak transcription	NHDF-Ad	bronchial
18	chr5:118847000-118868000	Weak transcription	K562	blood
19	chr5:118847200-118873200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:118847200-118877800	Weak transcription	Small Intestine	intestine
21	chr5:118847200-118878200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr5:118847200-118879800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr5:118847400-118861000	Weak transcription	Hela-S3	cervix
24	chr5:118847400-118863000	Weak transcription	HMEC	breast
25	chr5:118847400-118872000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr5:118847400-118873000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr5:118847400-118873200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr5:118847400-118873800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr5:118847400-118875800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr5:118847400-118876000	Weak transcription	Colonic Mucosa	Colon
31	chr5:118847400-118878200	Weak transcription	Rectal Smooth Muscle	rectum
32	chr5:118847400-118879800	Weak transcription	HSMMtube	muscle
33	chr5:118847600-118863400	Weak transcription	Brain Angular Gyrus	brain
34	chr5:118847600-118865000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr5:118847600-118873200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:118847600-118873400	Weak transcription	Fetal Muscle Leg	muscle
37	chr5:118847600-118873600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr5:118847600-118877600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:118847600-118878200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:118847600-118879800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr5:118848000-118863400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr5:118848200-118863200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr5:118848600-118863800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr5:118850000-118865600	Weak transcription	GM12878-XiMat	blood
45	chr5:118851200-118861200	Weak transcription	HUVEC	blood vessel
46	chr5:118851400-118860400	Weak transcription	Primary B cells from cord blood	blood
47	chr5:118851400-118861000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr5:118851600-118862800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:118851800-118876400	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr5:118852000-118861200	Weak transcription	Fetal Thymus	thymus

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