Variant report

Variant	nsv516655
Chromosome Location	chr12:57763520-57811414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:245 , 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	ARID3A	chr12:57783692-57783784	K562	blood:	n/a	n/a
2	ATF1	chr12:57770961-57771291	K562	blood:	n/a	n/a
3	ATF3	chr12:57766015-57766463	A549	lung:	n/a	n/a
4	ATF3	chr12:57765972-57766553	A549	lung:	n/a	n/a
5	BATF	chr12:57798807-57799061	GM12878	blood:	n/a	n/a
6	BCL3	chr12:57765952-57766681	A549	lung:	n/a	chr12:57766187-57766196
7	BRCA1	chr12:57783001-57783040	HepG2	liver:	n/a	n/a
8	CBX3	chr12:57770864-57771335	K562	blood:	n/a	n/a
9	CBX3	chr12:57810033-57810549	HCT-116	colon:	n/a	n/a
10	CCNT2	chr12:57770928-57771144	K562	blood:	n/a	n/a
11	CEBPB	chr12:57774187-57774389	A549	lung:	n/a	n/a
12	CEBPB	chr12:57770885-57771251	K562	blood:	n/a	n/a
13	CEBPB	chr12:57766054-57766466	IMR90	lung:	n/a	chr12:57766342-57766353
14	CEBPB	chr12:57782844-57783196	IMR90	lung:	n/a	n/a
15	CEBPB	chr12:57766017-57766484	A549	lung:	n/a	chr12:57766342-57766353
16	CEBPB	chr12:57804207-57804375	A549	lung:	n/a	chr12:57804289-57804306
17	CEBPB	chr12:57771004-57771238	K562	blood:	n/a	n/a
18	CEBPB	chr12:57765877-57766827	A549	lung:	n/a	chr12:57766342-57766353
19	CEBPB	chr12:57782716-57783480	A549	lung:	n/a	n/a
20	CEBPB	chr12:57782873-57783176	A549	lung:	n/a	n/a
21	CEBPB	chr12:57765986-57766620	A549	lung:	n/a	chr12:57766342-57766353
22	CEBPB	chr12:57771925-57772072	K562	blood:	n/a	n/a
23	CEBPB	chr12:57764495-57764868	IMR90	lung:	n/a	n/a
24	CEBPB	chr12:57804186-57804351	K562	blood:	n/a	chr12:57804289-57804306
25	CEBPD	chr12:57770914-57771369	K562	blood:	n/a	n/a
26	CEBPD	chr12:57770917-57771282	K562	blood:	n/a	n/a
27	CTCF	chr12:57791340-57791490	HVMF	connective:	n/a	n/a
28	CTCF	chr12:57791320-57791470	BE2_C	brain:	n/a	n/a
29	CTCF	chr12:57791280-57791430	A549	lung:	n/a	n/a
30	CTCF	chr12:57791386-57791424	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:57764158-57764203	GM10248	blood:	n/a	n/a
32	CTCF	chr12:57789180-57789330	GM12864	blood:	n/a	n/a
33	CTCF	chr12:57791280-57791430	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr12:57784216-57784291	GM20000	blood:	n/a	n/a
35	CTCF	chr12:57791300-57791450	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr12:57791360-57791430	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:57791320-57791470	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:57810974-57811047	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr12:57791280-57791430	GM12866	blood:	n/a	n/a
40	CTCF	chr12:57791360-57791510	BJ	skin:	n/a	n/a
41	CTCF	chr12:57791340-57791490	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:57791340-57791490	GM12873	blood:	n/a	n/a
43	CTCF	chr12:57791320-57791470	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr12:57791340-57791490	HRE	kidney:	n/a	n/a
45	CTCF	chr12:57791300-57791450	RPTEC	kidney:	n/a	n/a
46	CTCF	chr12:57791320-57791470	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:57789242-57789331	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr12:57801774-57801817	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr12:57791300-57791450	HCFaa	heart:	n/a	n/a
50	CTCF	chr12:57791360-57791510	GM12873	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57783795-57783845	HUVEC	blood vessel:	n/a
2	chr12:57780204-57780254	MCF10A-Er-Src	breast:	n/a
3	chr12:57783795-57783845	HL-60	blood:	n/a
4	chr12:57780179-57780229	HEK293	kidney:	embryo
5	chr12:57780179-57780229	Caco-2	colon:	n/a
6	chr12:57780204-57780254	HepG2	liver:	n/a
7	chr12:57780104-57780154	CMK	blood:	n/a
8	chr12:57780204-57780254	PrEC	prostate:	n/a
9	chr12:57780104-57780154	LNCaP	prostate:	n/a
10	chr12:57780204-57780254	H1-hESC	embryonic stem cell:	embryo
11	chr12:57780179-57780229	AG10803	skin:	n/a
12	chr12:57780179-57780229	NT2-D1	testis:	n/a
13	chr12:57780104-57780154	PFSK-1	brain:	n/a
14	chr12:57780179-57780229	HCPEpiC	choroid plexus:	n/a
15	chr12:57780204-57780254	HCF	heart:	n/a
16	chr12:57783795-57783845	HCT-116	colon:	n/a
17	chr12:57780204-57780254	K562	blood:	n/a
18	chr12:57780179-57780229	AG09319	gingival:	n/a
19	chr12:57780179-57780229	HCM	heart:	n/a
20	chr12:57780204-57780254	GM06990	blood:	n/a
21	chr12:57780179-57780229	HEEpiC	esophagus:	n/a
22	chr12:57780104-57780154	HCF	heart:	n/a
23	chr12:57780179-57780229	CMK	blood:	n/a
24	chr12:57783795-57783845	HRE	kidney:	n/a
25	chr12:57783795-57783845	SK-N-SH	brain:	n/a
26	chr12:57780204-57780254	MCF-7	breast:	n/a
27	chr12:57780204-57780254	HUVEC	blood vessel:	n/a
28	chr12:57783795-57783845	LNCaP	prostate:	n/a
29	chr12:57783795-57783845	NT2-D1	testis:	n/a
30	chr12:57780179-57780229	GM12892	blood:	n/a
31	chr12:57780104-57780154	AG09319	gingival:	n/a
32	chr12:57780179-57780229	AoSMC	blood vessel:	n/a
33	chr12:57780204-57780254	Caco-2	colon:	n/a
34	chr12:57780104-57780154	GM12878	blood:	n/a
35	chr12:57783795-57783845	SAEC	small airway:	n/a
36	chr12:57780179-57780229	BE2_C	brain:	n/a
37	chr12:57780104-57780154	MCF-7	breast:	n/a
38	chr12:57780179-57780229	Hepatocyte	liver:	n/a
39	chr12:57780204-57780254	HEEpiC	esophagus:	n/a
40	chr12:57780179-57780229	GM12878	blood:	n/a
41	chr12:57780104-57780154	PANC-1	pancreas:	n/a
42	chr12:57783795-57783845	GM12878	blood:	n/a
43	chr12:57780104-57780154	NT2-D1	testis:	n/a
44	chr12:57780104-57780154	HRPEpiC	eye:	n/a
45	chr12:57783795-57783845	U87	brain:	n/a
46	chr12:57783795-57783845	ProgFib	skin:	n/a
47	chr12:57780179-57780229	NHDF-neo	bronchial:	n/a
48	chr12:57783795-57783845	PFSK-1	brain:	n/a
49	chr12:57780204-57780254	HNPCEpiC	eye:	n/a
50	chr12:57783795-57783845	HIPEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57762333..57763849-chr12:57764785..57767656,2	K562	blood:
2	chr12:57794748..57796963-chr12:57845333..57847203,2	K562	blood:
3	chr12:57793676..57796142-chr12:57824894..57826820,2	K562	blood:
4	chr12:57781288..57782817-chr12:57789392..57792172,2	K562	blood:
5	chr12:57768640..57770985-chr12:57824479..57826520,2	K562	blood:
6	chr12:57712669..57714928-chr12:57772261..57773947,2	K562	blood:
7	chr12:57806981..57808654-chr12:57810095..57812146,2	K562	blood:
8	chr12:57781288..57782817-chr12:57789392..57792172,2	K562	blood:
9	chr12:57785867..57788077-chr12:57824277..57826744,2	MCF-7	breast:
10	chr12:57763659..57766790-chr12:57770165..57773896,3	K562	blood:
11	chr12:57799547..57802810-chr12:57823046..57826344,4	MCF-7	breast:
12	chr12:57770948..57772819-chr12:57845977..57848344,2	K562	blood:
13	chr12:57808026..57810781-chr12:57822669..57824932,3	MCF-7	breast:
14	chr12:57802362..57803948-chr12:57823721..57826421,2	K562	blood:
15	chr12:57795305..57796807-chr12:57813980..57816529,2	MCF-7	breast:
16	chr12:57810781..57813385-chr12:57826870..57828597,2	K562	blood:
17	chr12:57763659..57766790-chr12:57770165..57773896,3	K562	blood:
18	chr12:57762333..57763849-chr12:57764785..57767656,2	K562	blood:
19	chr12:57811377..57813186-chr12:57823163..57825515,2	MCF-7	breast:
20	chr12:57802999..57804883-chr12:57882930..57884726,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-879P	TF binding region
ENSG00000268367	TF binding region
RNU6-879P	CpG island
ENSG00000268367	CpG island
ENSG00000175189	chromatin interactions
ENSG00000166986	chromatin interactions
ENSG00000179912	chromatin interactions
ENSG00000268367	chromatin interactions
ENSG00000258001	chromatin interactions
ENSG00000139269	chromatin interactions

Extended variants
information (count: 1620 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11172184	chr12:57763520-57763521	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150141681	chr12:57763549-57763550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76606898	chr12:57763562-57763563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184216100	chr12:57763572-57763573	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554935350	chr12:57763581-57763582	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567408510	chr12:57763626-57763627	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189018064	chr12:57763657-57763658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564547653	chr12:57763663-57763664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537229546	chr12:57763732-57763733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138707413	chr12:57763784-57763785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577007369	chr12:57763805-57763806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541088390	chr12:57763866-57763867	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181926875	chr12:57763960-57763961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142760401	chr12:57764036-57764037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147346492	chr12:57764105-57764106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375395714	chr12:57764170-57764171	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112702069	chr12:57764182-57764183	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11172185	chr12:57764183-57764184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530874911	chr12:57764185-57764186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552085289	chr12:57764186-57764187	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563892986	chr12:57764188-57764189	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377478640	chr12:57764189-57764190	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11172186	chr12:57764191-57764192	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
24	rs11172187	chr12:57764193-57764194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547450172	chr12:57764213-57764214	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187428066	chr12:57764221-57764222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536227608	chr12:57764288-57764289	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548594823	chr12:57764312-57764313	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551112392	chr12:57764380-57764381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190539537	chr12:57764411-57764412	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537792864	chr12:57764420-57764421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs180870417	chr12:57764449-57764450	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533537660	chr12:57764655-57764656	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577481009	chr12:57764669-57764670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76599305	chr12:57764747-57764748	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11172188	chr12:57764752-57764753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553085269	chr12:57764769-57764770	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574619891	chr12:57764850-57764851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530577	chr12:57764863-57764864	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150871473	chr12:57764865-57764866	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190556817	chr12:57764866-57764867	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71084748	chr12:57764896-57764897	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530387	chr12:57764923-57764924	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185418429	chr12:57764968-57764969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137954930	chr12:57764974-57764975	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149637620	chr12:57764989-57764990	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564053601	chr12:57764998-57764999	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144368296	chr12:57765004-57765005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540065564	chr12:57765046-57765047	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573775660	chr12:57765107-57765108	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21364760	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57694000-57780000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:57695200-57794600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:57704400-57789200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr12:57722000-57765200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr12:57722800-57771200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr12:57722800-57786200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:57727200-57764400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr12:57728000-57766600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:57731400-57789800	Weak transcription	Small Intestine	intestine
10	chr12:57731600-57796000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr12:57732800-57771800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr12:57734200-57779400	Weak transcription	Spleen	Spleen
13	chr12:57735200-57764400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr12:57736400-57765600	Weak transcription	Ovary	ovary
15	chr12:57736400-57784200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:57736400-57795000	Weak transcription	Right Ventricle	heart
17	chr12:57736600-57782000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr12:57736600-57782400	Weak transcription	HSMM	muscle
19	chr12:57736600-57782800	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr12:57736800-57764400	Weak transcription	HSMMtube	muscle
21	chr12:57736800-57766000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr12:57740400-57784000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr12:57741200-57765000	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr12:57741200-57782800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:57742400-57785800	Weak transcription	Fetal Brain Female	brain
26	chr12:57745000-57787800	Weak transcription	Placenta	Placenta
27	chr12:57745200-57765600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:57745400-57772200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:57749400-57765400	Weak transcription	Brain Angular Gyrus	brain
30	chr12:57749800-57765400	Weak transcription	Brain Hippocampus Middle	brain
31	chr12:57753200-57823800	Weak transcription	Esophagus	oesophagus
32	chr12:57753600-57764600	Weak transcription	Colon Smooth Muscle	Colon
33	chr12:57755800-57770000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr12:57756600-57771000	Weak transcription	K562	blood
35	chr12:57758800-57764600	Weak transcription	Osteobl	bone
36	chr12:57760200-57769800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:57760200-57769800	Weak transcription	Fetal Stomach	stomach
38	chr12:57760400-57764400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:57760400-57764400	Weak transcription	NHDF-Ad	bronchial
40	chr12:57760400-57769000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr12:57760400-57769800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr12:57760400-57775600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:57760600-57764200	Enhancers	Fetal Intestine Large	intestine
44	chr12:57760800-57763600	Enhancers	Fetal Intestine Small	intestine
45	chr12:57761000-57764600	Weak transcription	Primary B cells from peripheral blood	blood
46	chr12:57761000-57766800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr12:57761000-57775800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:57761200-57765600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr12:57761200-57779400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:57761200-57787400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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