Variant report

Variant	nsv525023
Chromosome Location	chr12:67672870-67708669
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:0)
Chromatin interactive
region (count:50)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:204 , 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	chr12:67703123-67703203	K562	blood:	n/a	n/a
2	CEBPB	chr12:67682315-67682640	HepG2	liver:	n/a	n/a
3	CEBPB	chr12:67692962-67693095	K562	blood:	n/a	n/a
4	CEBPZ	chr12:67682798-67682839	HepG2	liver:	n/a	n/a
5	CTCF	chr12:67691680-67691830	AG04450	lung:	n/a	n/a
6	CTCF	chr12:67708580-67708730	RPTEC	kidney:	n/a	n/a
7	CTCF	chr12:67699440-67699590	BE2_C	brain:	n/a	n/a
8	CTCF	chr12:67674660-67674810	GM12865	blood:	n/a	n/a
9	CTCF	chr12:67708600-67708750	HMF	breast:	n/a	n/a
10	CTCF	chr12:67677297-67677337	GM10266	blood:	n/a	n/a
11	CUX1	chr12:67674360-67674535	K562	blood:	n/a	n/a
12	CUX1	chr12:67686532-67686560	K562	blood:	n/a	n/a
13	CUX1	chr12:67702343-67702423	GM12878	blood:	n/a	n/a
14	E2F4	chr12:67696012-67696178	MCF10A-Er-Src	breast:	n/a	n/a
15	EBF1	chr12:67708096-67708219	GM12878	blood:	n/a	n/a
16	EP300	chr12:67681015-67681059	K562	blood:	n/a	n/a
17	EP300	chr12:67690875-67691276	SK-N-SH_RA	brain:	n/a	chr12:67691163-67691177
18	EP300	chr12:67690888-67691239	SK-N-SH_RA	brain:	n/a	chr12:67691163-67691177
19	EP300	chr12:67689870-67690162	SK-N-SH_RA	brain:	n/a	chr12:67690021-67690030
20	EP300	chr12:67689826-67690115	SK-N-SH_RA	brain:	n/a	chr12:67690021-67690030
21	FOS	chr12:67689842-67690151	MCF10A-Er-Src	breast:	n/a	chr12:67690020-67690029 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030
22	FOS	chr12:67689930-67690140	MCF10A-Er-Src	breast:	n/a	chr12:67690020-67690029 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030
23	FOS	chr12:67675307-67675327	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr12:67696017-67696269	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr12:67708591-67708845	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr12:67689856-67690143	MCF10A-Er-Src	breast:	n/a	chr12:67690020-67690029 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030
27	FOS	chr12:67695993-67696270	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr12:67696055-67696289	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr12:67689858-67690144	MCF10A-Er-Src	breast:	n/a	chr12:67690020-67690029 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030 chr12:67690020-67690030
30	FOXA1	chr12:67693430-67693616	HepG2	liver:	n/a	n/a
31	FOXA1	chr12:67693383-67693697	HepG2	liver:	n/a	n/a
32	FOXA1	chr12:67693364-67693749	T-47D	breast:	n/a	n/a
33	FOXA2	chr12:67693289-67693813	A549	lung:	n/a	n/a
34	GATA2	chr12:67693861-67694257	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr12:67690843-67691331	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr12:67696985-67697185	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr12:67708075-67708421	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr12:67701894-67702071	SH-SY5Y	brain:	n/a	chr12:67701950-67701966
39	IRF1	chr12:67698398-67698514	K562	blood:	n/a	n/a
40	IRF1	chr12:67691036-67691341	K562	blood:	n/a	chr12:67691162-67691176 chr12:67691158-67691172
41	JUN	chr12:67689373-67689573	K562	blood:	n/a	n/a
42	JUN	chr12:67692616-67692881	K562	blood:	n/a	n/a
43	KAP1	chr12:67679106-67679468	K562	blood:	n/a	n/a
44	KAP1	chr12:67688314-67688764	K562	blood:	n/a	n/a
45	MAFF	chr12:67684175-67684542	K562	blood:	n/a	chr12:67684345-67684363
46	MAFF	chr12:67681126-67681465	HepG2	liver:	n/a	chr12:67681283-67681301
47	MAFF	chr12:67673899-67674243	HepG2	liver:	n/a	chr12:67674057-67674075
48	MAFF	chr12:67705366-67705381	K562	blood:	n/a	n/a
49	MAFF	chr12:67673887-67674245	K562	blood:	n/a	chr12:67674057-67674075
50	MAFF	chr12:67684145-67684567	HepG2	liver:	n/a	chr12:67684345-67684363

No data

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

No.	Distal block	Cell Line	Cell type
1	chr12:67678774..67680822-chr12:67683989..67686617,2	MCF-7	breast:
2	chr12:67669758..67671716-chr12:67673656..67677648,4	MCF-7	breast:
3	chr12:67674261..67676215-chr12:67685675..67687691,2	MCF-7	breast:
4	chr12:67662594..67666429-chr12:67679888..67683393,4	K562	blood:
5	chr12:67687226..67689484-chr12:67691036..67692664,2	MCF-7	breast:
6	chr12:67672008..67673697-chr12:67685020..67687108,2	K562	blood:
7	chr12:67681823..67684693-chr12:67719727..67722113,2	K562	blood:
8	chr12:67661581..67665640-chr12:67700038..67707681,9	MCF-7	breast:
9	chr12:67662577..67664634-chr12:67685123..67686741,3	MCF-7	breast:
10	chr12:67674261..67676215-chr12:67685675..67687691,2	MCF-7	breast:
11	chr12:67682602..67685085-chr12:67687619..67689287,2	K562	blood:
12	chr12:67668479..67670313-chr12:67704698..67706848,2	K562	blood:
13	chr12:67687173..67689993-chr12:67691527..67694169,2	K562	blood:
14	chr12:67697781..67702337-chr12:67703261..67707738,6	K562	blood:
15	chr12:67674561..67677422-chr12:67679504..67681796,2	MCF-7	breast:
16	chr12:67661368..67664788-chr12:67696254..67698548,3	MCF-7	breast:
17	chr12:67697667..67699390-chr12:67705731..67708067,2	K562	blood:
18	chr12:67699472..67703250-chr12:67704428..67707950,5	K562	blood:
19	chr12:67707079..67709730-chr12:67721053..67723374,2	K562	blood:
20	chr12:67701166..67703768-chr12:67717126..67719527,2	MCF-7	breast:
21	chr12:67678774..67680822-chr12:67683989..67686617,2	MCF-7	breast:
22	chr12:67665523..67668331-chr12:67690936..67692642,2	K562	blood:
23	chr12:67699472..67703250-chr12:67704428..67707950,5	K562	blood:
24	chr12:67674561..67677422-chr12:67679504..67681796,2	MCF-7	breast:
25	chr12:67697781..67702337-chr12:67703261..67707738,6	K562	blood:
26	chr12:67707980..67709583-chr12:67712739..67715234,2	K562	blood:
27	chr12:67708479..67710797-chr12:67718354..67720777,2	MCF-7	breast:
28	chr12:67691505..67693452-chr12:67698059..67700311,2	K562	blood:
29	chr12:67708053..67712275-chr12:67717926..67720355,3	K562	blood:
30	chr12:67680186..67682329-chr12:67685007..67687725,2	MCF-7	breast:
31	chr12:67680186..67682329-chr12:67685007..67687725,2	MCF-7	breast:
32	chr12:67660830..67663060-chr12:67697055..67700742,3	K562	blood:
33	chr12:67673864..67678122-chr12:67685372..67688266,4	K562	blood:
34	chr12:67674548..67676548-chr12:67679088..67681255,2	MCF-7	breast:
35	chr12:67671859..67674650-chr12:67694307..67697083,2	MCF-7	breast:
36	chr12:67673864..67678122-chr12:67685372..67688266,4	K562	blood:
37	chr12:67677931..67680021-chr12:67680762..67682692,2	MCF-7	breast:
38	chr12:67685431..67687281-chr12:67692983..67694546,2	MCF-7	breast:
39	chr12:67701153..67702973-chr12:67706397..67708069,2	MCF-7	breast:
40	chr12:67660883..67663738-chr12:67703241..67705101,2	MCF-7	breast:
41	chr12:67671859..67674650-chr12:67694307..67697083,2	MCF-7	breast:
42	chr12:67685431..67687281-chr12:67692983..67694546,2	MCF-7	breast:
43	chr12:67674548..67676548-chr12:67679088..67681255,2	MCF-7	breast:
44	chr12:67701153..67702973-chr12:67706397..67708069,2	MCF-7	breast:
45	chr12:67677931..67680021-chr12:67680762..67682692,2	MCF-7	breast:
46	chr12:67672008..67673697-chr12:67685020..67687108,2	K562	blood:
47	chr12:67662696..67664703-chr12:67682661..67684692,2	MCF-7	breast:
48	chr12:67697667..67699390-chr12:67705731..67708067,2	K562	blood:
49	chr12:67687173..67689993-chr12:67691527..67694169,2	K562	blood:
50	chr12:67708442..67711026-chr12:67711731..67713764,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DYRK2-3	chr12:67708478-67708952	ENSG00000247008

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CAND1	hsa-miR-186-5p	chr12:67706949-67706970
2	CAND1	hsa-miR-1	chr12:67707549-67707570
3	CAND1	hsa-miR-186-5p	chr12:67707508-67707528
4	CAND1	hsa-miR-1	chr12:67707805-67707827

Variant related genes	Relation type
CAND1	TF binding region
ENSG00000111530	chromatin interactions
SIPA1L2	miRNA target sites

Extended variants
information (count: 1231 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17781645	chr12:67672870-67672871	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs541081070	chr12:67672878-67672879	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7954999	chr12:67672905-67672906	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533460803	chr12:67672908-67672909	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552096520	chr12:67672928-67672929	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563859917	chr12:67672945-67672946	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531161539	chr12:67672951-67672952	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371435615	chr12:67672954-67672955	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79841917	chr12:67672957-67672958	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115187311	chr12:67672972-67672973	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112673564	chr12:67672980-67672981	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372019370	chr12:67673008-67673009	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549877926	chr12:67673099-67673100	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12580790	chr12:67673172-67673173	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs368584792	chr12:67673275-67673276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547090218	chr12:67673297-67673298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185129144	chr12:67673304-67673305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192331189	chr12:67673308-67673309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557671824	chr12:67673317-67673318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56728872	chr12:67673379-67673380	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs183734333	chr12:67673406-67673407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145104634	chr12:67673465-67673466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573805845	chr12:67673474-67673475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558673808	chr12:67673478-67673479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138988152	chr12:67673493-67673494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4264226	chr12:67673519-67673520	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376669052	chr12:67673528-67673529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577998835	chr12:67673591-67673592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141614269	chr12:67673598-67673599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563996885	chr12:67673627-67673628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs775662	chr12:67673652-67673653	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs549615653	chr12:67673840-67673841	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549615388	chr12:67673864-67673865	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs800167	chr12:67673904-67673905	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs187079712	chr12:67673920-67673921	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs775661	chr12:67673929-67673930	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs11176669	chr12:67673980-67673981	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12299042	chr12:67673991-67673992	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs551240418	chr12:67673997-67673998	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113735711	chr12:67674045-67674046	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150754847	chr12:67674089-67674090	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569629468	chr12:67674117-67674118	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542978249	chr12:67674120-67674121	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562760765	chr12:67674126-67674127	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576350775	chr12:67674142-67674143	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536809313	chr12:67674195-67674196	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137991820	chr12:67674211-67674212	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58559744	chr12:67674212-67674213	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534795923	chr12:67674219-67674220	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553463987	chr12:67674278-67674279	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	19115005	CNVD
Lung adenocarcinoma	17982442	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Bone cancer	16732325	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	17850661	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67664600-67684000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr12:67664800-67694400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:67664800-67699600	Weak transcription	Aorta	Aorta
4	chr12:67665200-67673000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr12:67665200-67675400	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr12:67665200-67675800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr12:67665200-67675800	Weak transcription	Placenta	Placenta
8	chr12:67665200-67675800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr12:67665200-67676200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr12:67665200-67678400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:67665200-67684400	Weak transcription	Fetal Muscle Leg	muscle
12	chr12:67665200-67684600	Weak transcription	Thymus	Thymus
13	chr12:67665200-67690200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr12:67665200-67699000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr12:67665400-67687600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr12:67665600-67673800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:67665600-67674600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr12:67666000-67688400	Weak transcription	Fetal Kidney	kidney
19	chr12:67666000-67701000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr12:67666800-67676200	Weak transcription	Fetal Intestine Large	intestine
21	chr12:67667600-67682600	Weak transcription	Lung	lung
22	chr12:67667800-67673200	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr12:67668400-67674400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr12:67668400-67675800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr12:67668400-67678400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr12:67668400-67688200	Weak transcription	HUVEC	blood vessel
27	chr12:67668600-67675800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr12:67668800-67678200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:67669000-67675400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr12:67669000-67675400	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr12:67669200-67673200	Enhancers	Ovary	ovary
32	chr12:67669200-67673400	Weak transcription	Liver	Liver
33	chr12:67669400-67675800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr12:67669400-67683000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:67669600-67673600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr12:67669600-67674000	Weak transcription	Brain Hippocampus Middle	brain
37	chr12:67669600-67675600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:67669800-67673600	Weak transcription	Adipose Nuclei	Adipose
39	chr12:67669800-67675600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr12:67669800-67678000	Weak transcription	NH-A	brain
41	chr12:67670000-67673800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr12:67670000-67674000	Weak transcription	Brain Germinal Matrix	brain
43	chr12:67670000-67675600	Weak transcription	HepG2	liver
44	chr12:67670000-67684200	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr12:67670000-67688800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr12:67670000-67699200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr12:67670200-67698200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:67670400-67675800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr12:67670400-67675800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr12:67670400-67689600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links