Variant report

Variant	nsv519174
Chromosome Location	chr12:48359984-48365265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:48361620-48361770	AG10803	skin:	n/a	n/a
2	CTCF	chr12:48362000-48362150	AG04449	skin:	n/a	n/a
3	GATA3	chr12:48363960-48364148	SH-SY5Y	brain:	n/a	n/a
4	GATA3	chr12:48363157-48363500	SH-SY5Y	brain:	n/a	n/a
5	IRF1	chr12:48363630-48363842	K562	blood:	n/a	chr12:48363780-48363800 chr12:48363788-48363798 chr12:48363788-48363802 chr12:48363785-48363799 chr12:48363784-48363798 chr12:48363655-48363675 chr12:48363789-48363800
6	JUN	chr12:48362711-48362739	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr12:48362536-48363500	SK-N-MC	brain:	n/a	n/a
8	POLR2A	chr12:48364261-48364675	ECC-1	luminal epithelium:	n/a	n/a
9	POLR2A	chr12:48363286-48363311	K562	blood:	n/a	n/a
10	POLR2A	chr12:48364362-48365167	ECC-1	luminal epithelium:	n/a	n/a
11	POLR2A	chr12:48363398-48363506	MCF10A-Er-Src	breast:	n/a	n/a
12	POLR2A	chr12:48364445-48365133	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr12:48363788-48363953	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr12:48360478-48360503	MCF10A-Er-Src	breast:	n/a	n/a
15	POLR2A	chr12:48361634-48361779	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr12:48363681-48363989	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr12:48362796-48363024	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr12:48364862-48364876	HepG2	liver:	n/a	n/a
19	POLR2A	chr12:48363473-48363534	HepG2	liver:	n/a	n/a
20	POLR2A	chr12:48363331-48363457	HepG2	liver:	n/a	n/a
21	POLR2A	chr12:48362733-48362774	K562	blood:	n/a	n/a
22	POLR2A	chr12:48363718-48363931	HUVEC	blood vessel:	n/a	n/a
23	POLR2A	chr12:48364883-48364911	HepG2	liver:	n/a	n/a
24	POLR2A	chr12:48363305-48363323	HepG2	liver:	n/a	n/a
25	POLR2A	chr12:48363057-48363095	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr12:48362743-48363533	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr12:48364120-48364261	GM12878	blood:	n/a	n/a
28	POLR2A	chr12:48363222-48363490	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr12:48362733-48363125	ECC-1	luminal epithelium:	n/a	n/a
30	POLR2A	chr12:48361537-48361721	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr12:48363228-48363451	K562	blood:	n/a	n/a
32	POLR2A	chr12:48362175-48362299	GM12878	blood:	n/a	n/a
33	POLR2A	chr12:48360081-48360199	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:48364804-48364846	MCF-7	breast:	n/a	n/a
35	POLR2A	chr12:48361643-48361703	GM12878	blood:	n/a	n/a
36	POLR2A	chr12:48362763-48362946	K562	blood:	n/a	n/a
37	POLR2A	chr12:48363556-48363655	HepG2	liver:	n/a	n/a
38	POLR2A	chr12:48364686-48364740	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:48362747-48362780	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr12:48359728-48360079	ECC-1	luminal epithelium:	n/a	n/a
41	POLR2A	chr12:48363279-48363394	MCF-7	breast:	n/a	n/a
42	POLR2A	chr12:48364153-48364205	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr12:48364655-48364685	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:48364918-48365169	HepG2	liver:	n/a	n/a
45	POLR2A	chr12:48363181-48363477	ECC-1	luminal epithelium:	n/a	n/a
46	POLR2A	chr12:48361972-48362094	GM12878	blood:	n/a	n/a
47	POLR2A	chr12:48363509-48363513	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr12:48363039-48363054	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr12:48362848-48362877	GM12878	blood:	n/a	n/a
50	SP1	chr12:48361885-48362349	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48359998-48360048	GM06990	blood:	n/a
2	chr12:48359998-48360048	NT2-D1	testis:	n/a
3	chr12:48362039-48362089	LNCaP	prostate:	n/a
4	chr12:48359998-48360048	HepG2	liver:	n/a
5	chr12:48362039-48362089	SK-N-MC	brain:	n/a
6	chr12:48362039-48362089	HRE	kidney:	n/a
7	chr12:48362039-48362089	HCF	heart:	n/a
8	chr12:48362039-48362089	GM12878	blood:	n/a
9	chr12:48359998-48360048	HRCEpiC	kidney:	n/a
10	chr12:48359998-48360048	AG09319	gingival:	n/a
11	chr12:48362039-48362089	AG04450	lung:	fetal
12	chr12:48362039-48362089	IMR90	lung:	fetal
13	chr12:48362039-48362089	AoSMC	blood vessel:	n/a
14	chr12:48362039-48362089	GM12892	blood:	n/a
15	chr12:48359998-48360048	SK-N-MC	brain:	n/a
16	chr12:48359998-48360048	HEK293	kidney:	embryo
17	chr12:48362039-48362089	HepG2	liver:	n/a
18	chr12:48359998-48360048	PANC-1	pancreas:	n/a
19	chr12:48362039-48362089	SKMC	muscle:	n/a
20	chr12:48359998-48360048	HCM	heart:	n/a
21	chr12:48359998-48360048	K562	blood:	n/a
22	chr12:48359998-48360048	NHDF-neo	bronchial:	n/a
23	chr12:48362039-48362089	HAEpiC	amniotic membrane:	n/a
24	chr12:48359998-48360048	HEEpiC	esophagus:	n/a
25	chr12:48362039-48362089	ProgFib	skin:	n/a
26	chr12:48359998-48360048	GM19239	blood:	n/a
27	chr12:48359998-48360048	HIPEpiC	eye:	n/a
28	chr12:48359998-48360048	MCF10A-Er-Src	breast:	n/a
29	chr12:48362039-48362089	NT2-D1	testis:	n/a
30	chr12:48362039-48362089	BJ	skin:	n/a
31	chr12:48359998-48360048	GM12878	blood:	n/a
32	chr12:48362039-48362089	ECC-1	luminal epithelium:	n/a
33	chr12:48362039-48362089	HCM	heart:	n/a
34	chr12:48359998-48360048	Hela-S3	cervix:	n/a
35	chr12:48362039-48362089	HRCEpiC	kidney:	n/a
36	chr12:48359998-48360048	H1-hESC	embryonic stem cell:	embryo
37	chr12:48362039-48362089	H1-hESC	embryonic stem cell:	embryo
38	chr12:48359998-48360048	SK-N-SH_RA	brain:	n/a
39	chr12:48359998-48360048	Caco-2	colon:	n/a
40	chr12:48362039-48362089	T-47D	breast:	n/a
41	chr12:48359998-48360048	PrEC	prostate:	n/a
42	chr12:48359998-48360048	HUVEC	blood vessel:	n/a
43	chr12:48362039-48362089	RPTEC	kidney:	n/a
44	chr12:48362039-48362089	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:48359998-48360048	NHBE	bronchial:	n/a
46	chr12:48362039-48362089	Hela-S3	cervix:	n/a
47	chr12:48362039-48362089	NHDF-neo	bronchial:	n/a
48	chr12:48359998-48360048	U87	brain:	n/a
49	chr12:48362039-48362089	AG04449	skin:	fetal
50	chr12:48362039-48362089	HUVEC	blood vessel:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48362584..48365917-chr12:48368904..48372045,3	K562	blood:
2	chr12:48298891..48301417-chr12:48363482..48365531,2	K562	blood:
3	chr12:48362502..48365466-chr12:48366201..48368271,2	K562	blood:
4	chr12:48360838..48363620-chr12:48364578..48367184,3	K562	blood:
5	chr12:48360838..48363620-chr12:48364578..48367184,3	K562	blood:
6	chr12:48360987..48363483-chr12:48393695..48396604,4	MCF-7	breast:
7	chr12:48296295..48301288-chr12:48356017..48360451,6	MCF-7	breast:
8	chr12:48356653..48359359-chr12:48363444..48365828,3	MCF-7	breast:
9	chr12:48356037..48360072-chr12:48360475..48364952,9	K562	blood:
10	chr12:48365132..48368005-chr12:48368353..48370036,2	K562	blood:
11	chr12:48363983..48366127-chr12:48370745..48372999,2	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM106C	TF binding region
TMEM106C	CpG island
ENSG00000139219	chromatin interactions
ENSG00000111424	chromatin interactions
ENSG00000134291	chromatin interactions

Extended variants
information (count: 219 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:219 , 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	rs2286025	chr12:48359984-48359985	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144276777	chr12:48359998-48359999	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs545983177	chr12:48360092-48360093	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs562776746	chr12:48360150-48360151	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566916249	chr12:48360193-48360194	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531686448	chr12:48360208-48360209	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185214280	chr12:48360269-48360270	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs117976552	chr12:48360284-48360285	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs12721422	chr12:48360389-48360390	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs199816978	chr12:48360441-48360442	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375828528	chr12:48360462-48360463	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34497162	chr12:48360473-48360474	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148733943	chr12:48360477-48360478	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142283364	chr12:48360478-48360479	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539654732	chr12:48360486-48360487	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201729763	chr12:48360490-48360491	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369092568	chr12:48360501-48360502	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371979597	chr12:48360516-48360517	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201972634	chr12:48360522-48360523	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs141659039	chr12:48360536-48360537	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536184775	chr12:48360546-48360547	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs113984159	chr12:48360585-48360586	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2286024	chr12:48360620-48360621	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs150512244	chr12:48360621-48360622	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544864416	chr12:48360641-48360642	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138690964	chr12:48360705-48360706	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115533237	chr12:48360721-48360722	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543934301	chr12:48360745-48360746	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148923967	chr12:48360796-48360797	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562716134	chr12:48360813-48360814	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576142991	chr12:48360827-48360828	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542137635	chr12:48360877-48360878	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561807711	chr12:48360885-48360886	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs202082515	chr12:48360894-48360895	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs117699587	chr12:48360895-48360896	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552717722	chr12:48360947-48360948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373565622	chr12:48360948-48360949	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs80192236	chr12:48360959-48360960	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546949641	chr12:48360961-48360962	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs61917711	chr12:48360962-48360963	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369414742	chr12:48360982-48360983	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200676671	chr12:48360993-48360994	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs199989373	chr12:48360996-48360997	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150814305	chr12:48361002-48361003	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs34111422	chr12:48361003-48361004	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs376852148	chr12:48361018-48361019	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535649901	chr12:48361019-48361020	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370077471	chr12:48361028-48361029	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs549670817	chr12:48361043-48361044	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201552415	chr12:48361047-48361048	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48358200-48360200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr12:48358200-48360800	Weak transcription	Aorta	Aorta
3	chr12:48358200-48363200	Weak transcription	Brain Substantia Nigra	brain
4	chr12:48358200-48364200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr12:48358200-48366200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:48358200-48366200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr12:48358400-48360200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:48358400-48360600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr12:48358400-48360800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:48358400-48360800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr12:48358400-48361000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:48358400-48361000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr12:48358400-48361000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:48358400-48361000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:48358400-48361000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:48358400-48361000	Weak transcription	Liver	Liver
17	chr12:48358400-48361000	Weak transcription	Lung	lung
18	chr12:48358400-48361400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:48358400-48362000	Weak transcription	Esophagus	oesophagus
20	chr12:48358400-48362400	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr12:48358400-48362400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr12:48358400-48362400	Weak transcription	Psoas Muscle	Psoas
23	chr12:48358400-48362800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr12:48358400-48362800	Weak transcription	NH-A	brain
25	chr12:48358400-48364600	Weak transcription	Ovary	ovary
26	chr12:48358400-48365000	Weak transcription	Osteobl	bone
27	chr12:48358400-48365200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr12:48358400-48366400	Weak transcription	Fetal Brain Male	brain
29	chr12:48358400-48367800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:48358400-48367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:48358400-48369800	Weak transcription	Brain Angular Gyrus	brain
32	chr12:48358400-48373000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:48358600-48360000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:48358600-48360000	Strong transcription	Rectal Smooth Muscle	rectum
35	chr12:48358600-48360000	Weak transcription	NHDF-Ad	bronchial
36	chr12:48358600-48360200	Weak transcription	Fetal Brain Female	brain
37	chr12:48358600-48360200	Genic enhancers	Fetal Intestine Large	intestine
38	chr12:48358600-48360800	Weak transcription	Adipose Nuclei	Adipose
39	chr12:48358600-48360800	Weak transcription	Brain Anterior Caudate	brain
40	chr12:48358600-48360800	Strong transcription	Fetal Muscle Trunk	muscle
41	chr12:48358600-48361000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr12:48358600-48361000	Weak transcription	Colon Smooth Muscle	Colon
43	chr12:48358600-48363000	Strong transcription	A549	lung
44	chr12:48358600-48363200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr12:48358600-48363400	Strong transcription	Fetal Thymus	thymus
46	chr12:48358600-48363600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr12:48358600-48363800	Weak transcription	Brain Hippocampus Middle	brain
48	chr12:48358600-48365200	Weak transcription	HSMMtube	muscle
49	chr12:48358600-48366600	Weak transcription	Fetal Lung	lung
50	chr12:48358600-48369400	Weak transcription	Fetal Kidney	kidney

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