Variant report

Variant	nsv560055
Chromosome Location	chr12:106634722-106641710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:366)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:106641123-106641230	GM12878	blood:	n/a	n/a
2	BHLHE40	chr12:106641682-106641768	K562	blood:	n/a	chr12:106641740-106641756
3	BHLHE40	chr12:106641655-106641899	HepG2	liver:	n/a	chr12:106641740-106641756
4	BHLHE40	chr12:106641572-106641918	GM12878	blood:	n/a	chr12:106641740-106641756
5	CCNT2	chr12:106641692-106641893	K562	blood:	n/a	n/a
6	CEBPB	chr12:106639646-106640005	Hela-S3	cervix:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
7	CEBPB	chr12:106639807-106639998	H1-hESC	embryonic stem cell:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
8	CEBPB	chr12:106639649-106640022	A549	lung:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
9	CEBPB	chr12:106639695-106639963	HepG2	liver:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
10	CEBPB	chr12:106639683-106640014	IMR90	lung:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
11	CEBPB	chr12:106639596-106640084	A549	lung:	n/a	chr12:106639828-106639839 chr12:106639827-106639840
12	CHD1	chr12:106639633-106643296	IMR90	lung:	n/a	chr12:106641025-106641035
13	CHD2	chr12:106639604-106640069	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr12:106641149-106641203	GM12878	blood:	n/a	n/a
15	CHD2	chr12:106640657-106641082	Hela-S3	cervix:	n/a	chr12:106641025-106641035
16	CREB1	chr12:106641338-106642036	A549	lung:	n/a	n/a
17	CTCF	chr12:106640780-106640930	AG04449	skin:	n/a	n/a
18	CTCF	chr12:106641180-106641330	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr12:106641188-106641345	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr12:106641020-106641170	NHEK	skin:	n/a	chr12:106641027-106641040
21	CTCF	chr12:106641160-106641310	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr12:106641180-106641330	GM12865	blood:	n/a	n/a
23	CTCF	chr12:106641151-106641404	IMR90	lung:	n/a	n/a
24	CTCF	chr12:106641080-106641230	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr12:106641180-106641330	AG04450	lung:	n/a	n/a
26	CTCF	chr12:106641160-106641310	HAc	cerebellar:	n/a	n/a
27	CTCF	chr12:106641200-106641350	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr12:106641240-106641390	HFF	foreskin:	n/a	n/a
29	CTCF	chr12:106641200-106641350	GM12866	blood:	n/a	n/a
30	CTCF	chr12:106641020-106641170	BJ	skin:	n/a	chr12:106641027-106641040
31	CTCF	chr12:106641140-106641290	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr12:106641200-106641350	GM12864	blood:	n/a	n/a
33	CTCF	chr12:106641200-106641350	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr12:106641200-106641350	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr12:106641160-106641310	RPTEC	kidney:	n/a	n/a
36	CTCF	chr12:106641160-106641310	AG04449	skin:	n/a	n/a
37	CTCF	chr12:106641180-106641330	HMF	breast:	n/a	n/a
38	CTCF	chr12:106641200-106641350	GM12869	blood:	n/a	n/a
39	CTCF	chr12:106641200-106641350	GM12871	blood:	n/a	n/a
40	CTCF	chr12:106641225-106641303	GM12878	blood:	n/a	n/a
41	CTCF	chr12:106641140-106641290	AG09309	skin:	n/a	n/a
42	CTCF	chr12:106641140-106641290	GM12874	blood:	n/a	n/a
43	CTCF	chr12:106640960-106641110	AG04450	lung:	n/a	chr12:106641027-106641040
44	CTCF	chr12:106641248-106641265	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:106641200-106641350	GM12873	blood:	n/a	n/a
46	CTCF	chr12:106641225-106641338	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr12:106641100-106641250	HVMF	connective:	n/a	n/a
48	CTCF	chr12:106641120-106641270	AG09319	gingival:	n/a	n/a
49	CTCF	chr12:106641140-106641290	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr12:106640935-106641008	GM13976	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:106636634-106636684	PrEC	prostate:	n/a
2	chr12:106639919-106639969	HEK293	kidney:	embryo
3	chr12:106636634-106636684	HRE	kidney:	n/a
4	chr12:106638076-106638126	AG09319	gingival:	n/a
5	chr12:106636634-106636684	HNPCEpiC	eye:	n/a
6	chr12:106641008-106641058	AG10803	skin:	n/a
7	chr12:106641486-106641536	HMEC	breast:	n/a
8	chr12:106641486-106641536	HRE	kidney:	n/a
9	chr12:106639919-106639969	T-47D	breast:	n/a
10	chr12:106641008-106641058	AoSMC	blood vessel:	n/a
11	chr12:106641486-106641536	NB4	blood:	n/a
12	chr12:106641486-106641536	PFSK-1	brain:	n/a
13	chr12:106641486-106641536	HepG2	liver:	n/a
14	chr12:106641486-106641536	HUVEC	blood vessel:	n/a
15	chr12:106641134-106641184	BE2_C	brain:	n/a
16	chr12:106636634-106636684	HRPEpiC	eye:	n/a
17	chr12:106641134-106641184	NT2-D1	testis:	n/a
18	chr12:106641008-106641058	PFSK-1	brain:	n/a
19	chr12:106641134-106641184	Hepatocyte	liver:	n/a
20	chr12:106641486-106641536	ProgFib	skin:	n/a
21	chr12:106639919-106639969	AG04450	lung:	fetal
22	chr12:106639919-106639969	LNCaP	prostate:	n/a
23	chr12:106639919-106639969	AG09319	gingival:	n/a
24	chr12:106641486-106641536	ECC-1	luminal epithelium:	n/a
25	chr12:106641134-106641184	SK-N-SH_RA	brain:	n/a
26	chr12:106641008-106641058	HAEpiC	amniotic membrane:	n/a
27	chr12:106638076-106638126	GM12892	blood:	n/a
28	chr12:106641134-106641184	GM12892	blood:	n/a
29	chr12:106638076-106638126	Hepatocyte	liver:	n/a
30	chr12:106641134-106641184	NB4	blood:	n/a
31	chr12:106641008-106641058	NH-A	brain:	n/a
32	chr12:106638076-106638126	GM12878	blood:	n/a
33	chr12:106636634-106636684	ProgFib	skin:	n/a
34	chr12:106639919-106639969	BE2_C	brain:	n/a
35	chr12:106636634-106636684	HEK293	kidney:	embryo
36	chr12:106636634-106636684	BJ	skin:	n/a
37	chr12:106638076-106638126	ovcar-3	ovarian:	n/a
38	chr12:106636634-106636684	A549	lung:	n/a
39	chr12:106638076-106638126	Jurkat	blood:	n/a
40	chr12:106641134-106641184	HNPCEpiC	eye:	n/a
41	chr12:106641486-106641536	ovcar-3	ovarian:	n/a
42	chr12:106636634-106636684	NH-A	brain:	n/a
43	chr12:106641486-106641536	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:106641134-106641184	HepG2	liver:	n/a
45	chr12:106636634-106636684	HUVEC	blood vessel:	n/a
46	chr12:106636634-106636684	U87	brain:	n/a
47	chr12:106641486-106641536	HEEpiC	esophagus:	n/a
48	chr12:106641134-106641184	AG04449	skin:	fetal
49	chr12:106641008-106641058	HepG2	liver:	n/a
50	chr12:106638076-106638126	GM12891	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:106633129..106634918-chr12:106751021..106753631,2	MCF-7	breast:
2	chr12:106637683..106639757-chr12:106691523..106693781,3	MCF-7	breast:
3	chr12:106640559..106643459-chr12:107485293..107487296,2	K562	blood:
4	chr12:106622589..106625717-chr12:106638331..106640361,3	MCF-7	breast:
5	chr12:106640021..106643402-chr12:106749618..106753030,5	MCF-7	breast:
6	chr12:106627619..106631130-chr12:106633186..106636182,4	MCF-7	breast:
7	chr12:106636406..106639904-chr12:106695865..106698141,3	MCF-7	breast:
8	chr12:106639346..106644112-chr12:106694122..106698214,13	MCF-7	breast:
9	chr12:106639693..106641308-chr12:106715072..106718036,2	MCF-7	breast:
10	chr12:106640063..106644049-chr12:106694395..106698756,11	MCF-7	breast:
11	chr12:106640861..106643735-chr12:106674267..106678317,3	MCF-7	breast:
12	chr12:106634944..106646449-chr12:106667585..106679535,27	MCF-7	breast:
13	chr12:106630484..106633329-chr12:106636143..106637779,2	K562	blood:
14	chr12:106531582..106534564-chr12:106638638..106642825,4	MCF-7	breast:
15	chr12:105500524..105503114-chr12:106640734..106642263,2	MCF-7	breast:
16	chr12:106639673..106643649-chr12:106748400..106753718,9	MCF-7	breast:
17	chr12:106641570..106642137-chr12:106697112..106697741,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUAK1-2	chr12:106640493-106640734	ENSG00000258355.1
2	lnc-NUAK1-2	chr12:106639391-106639460	ENSG00000258355.1

No data

Variant related genes	Relation type
ENSG00000258355	TF binding region
ENSG00000258355	CpG island
ENSG00000166046	chromatin interactions
ENSG00000238609	chromatin interactions
ENSG00000136026	chromatin interactions
ENSG00000008405	chromatin interactions
ENSG00000013503	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000257548	chromatin interactions
ENSG00000074590	chromatin interactions
ENSG00000136051	chromatin interactions

Extended variants
information (count: 221 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:221 , 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	rs1215740	chr12:106634722-106634723	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs56234907	chr12:106634733-106634734	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs141430315	chr12:106634800-106634801	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559793319	chr12:106634806-106634807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534035465	chr12:106634816-106634817	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553995647	chr12:106634823-106634824	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1215741	chr12:106634872-106634873	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184779277	chr12:106634923-106634924	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562483716	chr12:106634937-106634938	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187071426	chr12:106634941-106634942	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7980268	chr12:106635049-106635050	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191121171	chr12:106635058-106635059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551737673	chr12:106635075-106635076	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371199850	chr12:106635109-106635110	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs67670636	chr12:106635110-106635111	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374330749	chr12:106635134-106635135	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569880268	chr12:106635179-106635180	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372558374	chr12:106635211-106635212	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564510043	chr12:106635235-106635236	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375832701	chr12:106635255-106635256	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183626027	chr12:106635321-106635322	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546823348	chr12:106635336-106635337	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs560291554	chr12:106635358-106635359	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532685604	chr12:106635390-106635391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552416861	chr12:106635425-106635426	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569165197	chr12:106635477-106635478	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs61942132	chr12:106635551-106635552	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs11112913	chr12:106635568-106635569	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548283058	chr12:106635612-106635613	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189303112	chr12:106635630-106635631	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534266016	chr12:106635694-106635695	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554034265	chr12:106635793-106635794	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577077599	chr12:106635828-106635829	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553368536	chr12:106635885-106635886	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548833373	chr12:106635903-106635904	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539753996	chr12:106635918-106635919	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs193291025	chr12:106636006-106636007	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142033154	chr12:106636064-106636065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144812738	chr12:106636065-106636066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12426351	chr12:106636097-106636098	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs561510794	chr12:106636120-106636121	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534466655	chr12:106636160-106636161	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557296367	chr12:106636170-106636171	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572133425	chr12:106636172-106636173	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533360671	chr12:106636176-106636177	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs60738914	chr12:106636224-106636225	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs3782702	chr12:106636245-106636246	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs185097494	chr12:106636246-106636247	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1215807	chr12:106636457-106636458	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552452423	chr12:106636459-106636460	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:756 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106621400-106638200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr12:106622200-106639000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr12:106622200-106639600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr12:106625200-106636800	Weak transcription	Right Atrium	heart
5	chr12:106625200-106640800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:106628600-106638600	Weak transcription	Fetal Brain Male	brain
7	chr12:106628800-106637000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:106629000-106638400	Strong transcription	Fetal Muscle Trunk	muscle
9	chr12:106629200-106636200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:106629200-106636600	Strong transcription	Osteobl	bone
11	chr12:106629200-106636800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:106629200-106637600	Strong transcription	Fetal Stomach	stomach
13	chr12:106629400-106637000	Strong transcription	NHDF-Ad	bronchial
14	chr12:106629400-106639000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:106629800-106635800	Weak transcription	Fetal Kidney	kidney
16	chr12:106630000-106636800	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:106630200-106635200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:106630200-106638600	Weak transcription	Hela-S3	cervix
19	chr12:106630200-106638600	Strong transcription	NHLF	lung
20	chr12:106630400-106636400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:106630400-106637200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr12:106630400-106637200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:106630400-106637400	Strong transcription	NHEK	skin
24	chr12:106630400-106638200	Strong transcription	HSMM	muscle
25	chr12:106630600-106634800	Strong transcription	HSMMtube	muscle
26	chr12:106630600-106638600	Weak transcription	Small Intestine	intestine
27	chr12:106630800-106636600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:106631200-106636800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:106631400-106634800	Strong transcription	Adipose Nuclei	Adipose
30	chr12:106631400-106634800	Weak transcription	Thymus	Thymus
31	chr12:106631400-106638400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:106631400-106638600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:106631600-106638400	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr12:106631800-106634800	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr12:106631800-106637000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr12:106631800-106637200	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr12:106631800-106638400	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr12:106632000-106635000	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:106632000-106637200	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr12:106632200-106636400	Strong transcription	Placenta	Placenta
41	chr12:106632200-106638200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:106632600-106634800	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr12:106632600-106634800	Strong transcription	Colonic Mucosa	Colon
44	chr12:106632800-106635000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:106632800-106639000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:106633000-106637800	Strong transcription	NH-A	brain
47	chr12:106633200-106634800	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr12:106633200-106638400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr12:106633400-106636200	Weak transcription	Fetal Heart	heart
50	chr12:106633400-106638800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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