Variant report

Variant	nsv8627
Chromosome Location	chr10:43324929-43354934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:228)
CpG islands
(count:611)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:228 , 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	ATF1	chr10:43327236-43327383	K562	blood:	n/a	n/a
2	CHD1	chr10:43332780-43332819	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr10:43340397-43340579	MCF-7	breast:	n/a	n/a
4	CTCF	chr10:43332196-43332383	Fibrobl	skin:	n/a	chr10:43332301-43332308
5	CTCF	chr10:43332160-43332310	HPAF	blood vessel:	n/a	chr10:43332301-43332308
6	CTCF	chr10:43340435-43340478	Kidney_OC	kidney:	n/a	n/a
7	CTCF	chr10:43332200-43332350	SK-N-SH_RA	brain:	n/a	chr10:43332301-43332308
8	CTCF	chr10:43340226-43340754	HCT-116	colon:	n/a	n/a
9	CTCF	chr10:43352620-43352770	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr10:43332200-43332350	HBMEC	blood vessel:	n/a	chr10:43332301-43332308
11	CTCF	chr10:43332220-43332370	HCM	heart:	n/a	chr10:43332301-43332308
12	CTCF	chr10:43340399-43340597	MCF-7	breast:	n/a	n/a
13	CTCF	chr10:43340380-43340530	HepG2	liver:	n/a	n/a
14	CTCF	chr10:43332193-43332323	HUVEC	blood vessel:	n/a	chr10:43332301-43332308
15	CTCF	chr10:43332220-43332370	HUVEC	blood vessel:	n/a	chr10:43332301-43332308
16	CTCF	chr10:43332260-43332410	HFF	foreskin:	n/a	chr10:43332395-43332408 chr10:43332395-43332408 chr10:43332301-43332308
17	CTCF	chr10:43340411-43340553	K562	blood:	n/a	n/a
18	CTCF	chr10:43332220-43332370	GM12874	blood:	n/a	chr10:43332301-43332308
19	CTCF	chr10:43336168-43336219	Medullo	brain:	n/a	n/a
20	CTCF	chr10:43352672-43352789	K562	blood:	n/a	n/a
21	CTCF	chr10:43340407-43340675	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:43332177-43332346	SK-N-SH_RA	brain:	n/a	chr10:43332301-43332308
23	CTCF	chr10:43332220-43332370	GM12873	blood:	n/a	chr10:43332301-43332308
24	CTCF	chr10:43352620-43352770	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr10:43340380-43340530	HCT-116	colon:	n/a	n/a
26	CTCF	chr10:43332180-43332330	HPAF	blood vessel:	n/a	chr10:43332301-43332308
27	CTCF	chr10:43340420-43340570	MCF-7	breast:	n/a	n/a
28	CTCF	chr10:43331800-43331950	HPF	lung:	n/a	n/a
29	CTCF	chr10:43354657-43354706	GM13976	blood:	n/a	n/a
30	CTCF	chr10:43332260-43332410	GM12874	blood:	n/a	chr10:43332395-43332408 chr10:43332395-43332408 chr10:43332301-43332308
31	CTCF	chr10:43337032-43337129	LNCaP	prostate:	n/a	n/a
32	CTCF	chr10:43332180-43332330	HRE	kidney:	n/a	chr10:43332301-43332308
33	CTCF	chr10:43332160-43332310	HepG2	liver:	n/a	chr10:43332301-43332308
34	CTCF	chr10:43340380-43340530	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr10:43332177-43332330	HepG2	liver:	n/a	chr10:43332301-43332308
36	CTCF	chr10:43352640-43352790	HMEC	breast:	n/a	n/a
37	CTCF	chr10:43340328-43340649	HepG2	liver:	n/a	n/a
38	CTCF	chr10:43352600-43352750	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr10:43332180-43332330	HRPEpiC	eye:	n/a	chr10:43332301-43332308
40	CTCF	chr10:43331700-43331850	HCM	heart:	n/a	n/a
41	CTCF	chr10:43332164-43332400	NHEK	skin:	n/a	chr10:43332301-43332308
42	CTCF	chr10:43340422-43340578	LNCaP	prostate:	n/a	n/a
43	CTCF	chr10:43332180-43332330	RPTEC	kidney:	n/a	chr10:43332301-43332308
44	CTCF	chr10:43340445-43340555	NHEK	skin:	n/a	n/a
45	CTCF	chr10:43340254-43340729	MCF-7	breast:	n/a	n/a
46	CTCF	chr10:43352600-43352750	HMEC	breast:	n/a	n/a
47	CTCF	chr10:43352735-43352777	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr10:43332200-43332350	HPF	lung:	n/a	chr10:43332301-43332308
49	CTCF	chr10:43340380-43340530	A549	lung:	n/a	n/a
50	CTCF	chr10:43352723-43352831	GM10266	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43335974-43336024	HRPEpiC	eye:	n/a
2	chr10:43335974-43336024	HRPEpiC	eye:	n/a
3	chr10:43335974-43336024	GM12878	blood:	n/a
4	chr10:43332693-43332743	AG04450	lung:	fetal
5	chr10:43354902-43354952	T-47D	breast:	n/a
6	chr10:43332443-43332493	SAEC	small airway:	n/a
7	chr10:43332693-43332743	HUVEC	blood vessel:	n/a
8	chr10:43332329-43332379	HEEpiC	esophagus:	n/a
9	chr10:43332737-43332787	ovcar-3	ovarian:	n/a
10	chr10:43334380-43334430	HCT-116	colon:	n/a
11	chr10:43332329-43332379	PFSK-1	brain:	n/a
12	chr10:43335974-43336024	GM19239	blood:	n/a
13	chr10:43332329-43332379	ovcar-3	ovarian:	n/a
14	chr10:43332443-43332493	Jurkat	blood:	n/a
15	chr10:43332737-43332787	ECC-1	luminal epithelium:	n/a
16	chr10:43334380-43334430	NB4	blood:	n/a
17	chr10:43354873-43354923	NHBE	bronchial:	n/a
18	chr10:43354902-43354952	HCF	heart:	n/a
19	chr10:43332737-43332787	GM06990	blood:	n/a
20	chr10:43332443-43332493	SK-N-MC	brain:	n/a
21	chr10:43335974-43336024	AG04450	lung:	fetal
22	chr10:43332693-43332743	HNPCEpiC	eye:	n/a
23	chr10:43354873-43354923	NH-A	brain:	n/a
24	chr10:43329092-43329142	AG04449	skin:	fetal
25	chr10:43332693-43332743	SAEC	small airway:	n/a
26	chr10:43354873-43354923	NB4	blood:	n/a
27	chr10:43354902-43354952	NB4	blood:	n/a
28	chr10:43354902-43354952	HAEpiC	amniotic membrane:	n/a
29	chr10:43332737-43332787	SAEC	small airway:	n/a
30	chr10:43329092-43329142	NHBE	bronchial:	n/a
31	chr10:43335974-43336024	Hepatocyte	liver:	n/a
32	chr10:43354902-43354952	PFSK-1	brain:	n/a
33	chr10:43332693-43332743	HEEpiC	esophagus:	n/a
34	chr10:43332693-43332743	HCPEpiC	choroid plexus:	n/a
35	chr10:43354873-43354923	Jurkat	blood:	n/a
36	chr10:43332443-43332493	NB4	blood:	n/a
37	chr10:43332693-43332743	HCF	heart:	n/a
38	chr10:43332737-43332787	HEK293	kidney:	embryo
39	chr10:43334380-43334430	BJ	skin:	n/a
40	chr10:43332737-43332787	HRPEpiC	eye:	n/a
41	chr10:43332737-43332787	HNPCEpiC	eye:	n/a
42	chr10:43334380-43334430	GM19239	blood:	n/a
43	chr10:43354873-43354923	HRE	kidney:	n/a
44	chr10:43354902-43354952	RPTEC	kidney:	n/a
45	chr10:43354902-43354952	SK-N-SH	brain:	n/a
46	chr10:43335974-43336024	HPAEpiC	pulmonary alveolar:	n/a
47	chr10:43335974-43336024	HEEpiC	esophagus:	n/a
48	chr10:43354902-43354952	HRE	kidney:	n/a
49	chr10:43329092-43329142	GM12878	blood:	n/a
50	chr10:43334380-43334430	CMK	blood:	n/a

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BMS1	hsa-miR-30a-5p	chr10:43327447-43327468

Variant related genes	Relation type
RNU6-885P	TF binding region
RNU6-885P	CpG island

Extended variants
information (count: 1265 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562697446	chr10:43324973-43324974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184562914	chr10:43325010-43325011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79345941	chr10:43325067-43325068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558216941	chr10:43325099-43325100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573291799	chr10:43325199-43325200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548567092	chr10:43325209-43325210	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567180570	chr10:43325211-43325212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188303087	chr10:43325218-43325219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192889953	chr10:43325222-43325223	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185486489	chr10:43325247-43325248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201137998	chr10:43325286-43325287	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201682970	chr10:43325287-43325288	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538687695	chr10:43325289-43325290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs398075105	chr10:43325293-43325294	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398013298	chr10:43325294-43325295	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557099904	chr10:43325330-43325331	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189247017	chr10:43325384-43325385	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536465812	chr10:43325409-43325410	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554549182	chr10:43325446-43325447	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181996352	chr10:43325475-43325476	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540259640	chr10:43325476-43325477	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558576674	chr10:43325489-43325490	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546044792	chr10:43325512-43325513	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184757212	chr10:43325558-43325559	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188029050	chr10:43325583-43325584	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544260499	chr10:43325586-43325587	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112097011	chr10:43325593-43325594	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10900276	chr10:43325606-43325607	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs542443357	chr10:43325653-43325654	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368570049	chr10:43325658-43325659	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs41295810	chr10:43325664-43325665	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs201739639	chr10:43325682-43325683	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372559744	chr10:43325695-43325696	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369831218	chr10:43325700-43325701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374194864	chr10:43325769-43325770	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377616718	chr10:43325777-43325778	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552907353	chr10:43325792-43325793	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144403555	chr10:43325798-43325799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370668862	chr10:43325825-43325826	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200894282	chr10:43325832-43325833	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201022846	chr10:43325839-43325840	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550664789	chr10:43325840-43325841	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377058786	chr10:43325843-43325844	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568964255	chr10:43325844-43325845	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141528123	chr10:43325847-43325848	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201871271	chr10:43325851-43325852	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199956903	chr10:43325869-43325870	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201582130	chr10:43325881-43325882	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374201960	chr10:43325895-43325896	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368682397	chr10:43325896-43325897	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43279800-43328200	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr10:43293200-43332400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr10:43301800-43325800	Weak transcription	NHLF	lung
4	chr10:43303600-43325800	Weak transcription	Colon Smooth Muscle	Colon
5	chr10:43303600-43332200	Weak transcription	NHDF-Ad	bronchial
6	chr10:43308200-43328200	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr10:43309800-43330000	Weak transcription	Small Intestine	intestine
8	chr10:43310400-43327400	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr10:43311200-43329000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr10:43311400-43329000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr10:43311600-43328200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr10:43312000-43328400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr10:43313400-43325200	Weak transcription	HUVEC	blood vessel
14	chr10:43313400-43325600	Weak transcription	Hela-S3	cervix
15	chr10:43313400-43325800	Weak transcription	Fetal Brain Male	brain
16	chr10:43314400-43325400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr10:43314400-43325600	Weak transcription	Brain Anterior Caudate	brain
18	chr10:43314400-43325800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:43314400-43332200	Weak transcription	Right Atrium	heart
20	chr10:43314600-43325800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr10:43314600-43329800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr10:43315200-43325400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr10:43317800-43328200	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr10:43317800-43328200	Strong transcription	Fetal Intestine Large	intestine
25	chr10:43317800-43328200	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr10:43317800-43328200	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr10:43318200-43327200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr10:43318800-43325800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr10:43318800-43327000	Weak transcription	HSMM	muscle
30	chr10:43319200-43326400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr10:43319400-43325400	Weak transcription	HepG2	liver
32	chr10:43319400-43325400	Weak transcription	NH-A	brain
33	chr10:43319400-43325400	Weak transcription	Osteobl	bone
34	chr10:43320000-43325600	Weak transcription	HSMMtube	muscle
35	chr10:43320000-43329000	Weak transcription	Fetal Heart	heart
36	chr10:43320000-43332600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr10:43320400-43326800	Strong transcription	Fetal Intestine Small	intestine
38	chr10:43320400-43328400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr10:43320800-43325200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr10:43320800-43325400	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr10:43320800-43325400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr10:43320800-43325800	Weak transcription	Fetal Kidney	kidney
43	chr10:43321000-43325400	Weak transcription	Fetal Thymus	thymus
44	chr10:43321000-43325600	Weak transcription	Primary hematopoietic stem cells	blood
45	chr10:43321200-43325400	Weak transcription	A549	lung
46	chr10:43321400-43325600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr10:43321400-43325800	Weak transcription	Fetal Lung	lung
48	chr10:43321400-43332800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr10:43321600-43325600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:43321600-43328200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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