Variant report

Variant	nsv1049296
Chromosome Location	chr12:105518764-105566079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:61)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:105536945-105537002	K562	blood:	n/a	n/a
2	ARID3A	chr12:105563565-105563865	K562	blood:	n/a	n/a
3	ATF1	chr12:105563849-105564049	K562	blood:	n/a	n/a
4	BACH1	chr12:105555203-105555238	K562	blood:	n/a	n/a
5	CEBPB	chr12:105560603-105560787	K562	blood:	n/a	chr12:105560732-105560743 chr12:105560697-105560708
6	CEBPB	chr12:105560565-105560867	HepG2	liver:	n/a	chr12:105560732-105560743 chr12:105560697-105560708
7	CEBPB	chr12:105560586-105560849	Hela-S3	cervix:	n/a	chr12:105560732-105560743 chr12:105560697-105560708
8	CEBPB	chr12:105537517-105537618	HepG2	liver:	n/a	chr12:105537556-105537569 chr12:105537556-105537567
9	CEBPB	chr12:105560550-105560913	A549	lung:	n/a	chr12:105560732-105560743 chr12:105560697-105560708
10	CEBPB	chr12:105560521-105560906	IMR90	lung:	n/a	chr12:105560542-105560553 chr12:105560732-105560743 chr12:105560697-105560708
11	CHD1	chr12:105560355-105560374	GM12878	blood:	n/a	n/a
12	CTCF	chr12:105539896-105539908	K562	blood:	n/a	n/a
13	CTCF	chr12:105522320-105522470	HCT-116	colon:	n/a	n/a
14	CUX1	chr12:105565017-105565184	K562	blood:	n/a	n/a
15	CUX1	chr12:105565609-105565869	K562	blood:	n/a	n/a
16	E2F4	chr12:105538137-105538337	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr12:105519359-105519795	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr12:105555742-105555874	MCF10A-Er-Src	breast:	n/a	n/a
19	EP300	chr12:105563862-105563913	K562	blood:	n/a	n/a
20	EP300	chr12:105536933-105537086	HepG2	liver:	n/a	n/a
21	FAM48A	chr12:105561594-105561625	GM12878	blood:	n/a	n/a
22	FOS	chr12:105560713-105560715	MCF10A-Er-Src	breast:	n/a	n/a
23	FOXA1	chr12:105524510-105524820	HepG2	liver:	n/a	n/a
24	FOXA1	chr12:105524501-105524801	HepG2	liver:	n/a	n/a
25	FOXA1	chr12:105525180-105525411	HepG2	liver:	n/a	n/a
26	FOXA1	chr12:105524397-105524809	HepG2	liver:	n/a	n/a
27	FOXA1	chr12:105524502-105524782	HepG2	liver:	n/a	n/a
28	FOXA2	chr12:105524508-105524763	HepG2	liver:	n/a	n/a
29	GATA1	chr12:105563348-105564178	PBDE	blood:	n/a	chr12:105564034-105564045
30	GATA2	chr12:105535108-105535413	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr12:105559705-105560159	SK-N-SH	brain:	n/a	n/a
32	GATA3	chr12:105551699-105551899	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr12:105535084-105535502	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr12:105550486-105550628	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr12:105558565-105558773	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr12:105552208-105552390	SH-SY5Y	brain:	n/a	n/a
37	IRF1	chr12:105563886-105564259	K562	blood:	n/a	n/a
38	JUND	chr12:105551746-105552036	HepG2	liver:	n/a	chr12:105551854-105551865
39	KAP1	chr12:105554618-105555049	K562	blood:	n/a	n/a
40	MAFF	chr12:105563889-105564564	K562	blood:	n/a	chr12:105564109-105564127 chr12:105564115-105564129
41	MAFF	chr12:105535320-105535674	K562	blood:	n/a	chr12:105535487-105535505 chr12:105535493-105535507
42	MAFF	chr12:105563914-105564498	HepG2	liver:	n/a	chr12:105564109-105564127 chr12:105564115-105564129
43	MAFF	chr12:105550140-105550251	HepG2	liver:	n/a	n/a
44	MAFF	chr12:105528895-105528976	K562	blood:	n/a	n/a
45	MAFF	chr12:105535320-105535677	HepG2	liver:	n/a	chr12:105535487-105535505 chr12:105535493-105535507
46	MAFF	chr12:105550077-105550278	K562	blood:	n/a	n/a
47	MAFK	chr12:105563932-105564523	HepG2	liver:	n/a	chr12:105564111-105564122 chr12:105564226-105564241 chr12:105564417-105564428 chr12:105564111-105564126 chr12:105564415-105564429 chr12:105564115-105564129 chr12:105564417-105564428 chr12:105564412-105564428 chr12:105564112-105564132 chr12:105564114-105564130
48	MAFK	chr12:105550072-105550283	IMR90	lung:	n/a	chr12:105550232-105550243 chr12:105550233-105550244 chr12:105550231-105550245 chr12:105550233-105550244 chr12:105550232-105550243 chr12:105550228-105550244
49	MAFK	chr12:105563914-105564358	K562	blood:	n/a	chr12:105564111-105564122 chr12:105564226-105564241 chr12:105564111-105564126 chr12:105564115-105564129 chr12:105564112-105564132 chr12:105564114-105564130
50	MAFK	chr12:105526121-105526354	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:105531460-105531510	HEEpiC	esophagus:	n/a
2	chr12:105531460-105531510	BE2_C	brain:	n/a
3	chr12:105531460-105531510	HRE	kidney:	n/a
4	chr12:105531460-105531510	HNPCEpiC	eye:	n/a
5	chr12:105531460-105531510	A549	lung:	n/a
6	chr12:105531460-105531510	NHDF-neo	bronchial:	n/a
7	chr12:105531460-105531510	GM12891	blood:	n/a
8	chr12:105531460-105531510	HCF	heart:	n/a
9	chr12:105531460-105531510	H1-hESC	embryonic stem cell:	embryo
10	chr12:105531460-105531510	HRPEpiC	eye:	n/a
11	chr12:105531460-105531510	ProgFib	skin:	n/a
12	chr12:105531460-105531510	AG10803	skin:	n/a
13	chr12:105531460-105531510	HEK293	kidney:	embryo
14	chr12:105531460-105531510	GM06990	blood:	n/a
15	chr12:105531460-105531510	HRCEpiC	kidney:	n/a
16	chr12:105531460-105531510	SK-N-SH_RA	brain:	n/a
17	chr12:105531460-105531510	AG04450	lung:	fetal
18	chr12:105531460-105531510	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:105531460-105531510	SK-N-SH	brain:	n/a
20	chr12:105531460-105531510	CMK	blood:	n/a
21	chr12:105531460-105531510	ECC-1	luminal epithelium:	n/a
22	chr12:105531460-105531510	SK-N-MC	brain:	n/a
23	chr12:105531460-105531510	HMEC	breast:	n/a
24	chr12:105531460-105531510	PFSK-1	brain:	n/a
25	chr12:105531460-105531510	GM12892	blood:	n/a
26	chr12:105531460-105531510	NB4	blood:	n/a
27	chr12:105531460-105531510	PANC-1	pancreas:	n/a
28	chr12:105531460-105531510	Jurkat	blood:	n/a
29	chr12:105531460-105531510	AoSMC	blood vessel:	n/a
30	chr12:105531460-105531510	AG09319	gingival:	n/a
31	chr12:105531460-105531510	IMR90	lung:	fetal
32	chr12:105531460-105531510	AG09309	skin:	n/a
33	chr12:105531460-105531510	U87	brain:	n/a
34	chr12:105531460-105531510	ovcar-3	ovarian:	n/a
35	chr12:105531460-105531510	SAEC	small airway:	n/a
36	chr12:105531460-105531510	NHBE	bronchial:	n/a
37	chr12:105531460-105531510	HAEpiC	amniotic membrane:	n/a
38	chr12:105531460-105531510	MCF-7	breast:	n/a
39	chr12:105531460-105531510	HCT-116	colon:	n/a
40	chr12:105531460-105531510	HCM	heart:	n/a
41	chr12:105531460-105531510	HepG2	liver:	n/a
42	chr12:105531460-105531510	PrEC	prostate:	n/a
43	chr12:105531460-105531510	HUVEC	blood vessel:	n/a
44	chr12:105531460-105531510	NT2-D1	testis:	n/a
45	chr12:105531460-105531510	HL-60	blood:	n/a
46	chr12:105531460-105531510	HIPEpiC	eye:	n/a
47	chr12:105531460-105531510	GM19239	blood:	n/a
48	chr12:105531460-105531510	K562	blood:	n/a
49	chr12:105531460-105531510	NH-A	brain:	n/a
50	chr12:105531460-105531510	RPTEC	kidney:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:105520645..105521436-chr12:105528902..105529458,2	MCF-7	breast:
2	chr12:105500409..105502947-chr12:105543517..105545714,2	MCF-7	breast:
3	chr12:105539501..105541857-chr12:105542488..105545079,2	K562	blood:
4	chr12:105523431..105527512-chr12:105529193..105532336,3	MCF-7	breast:
5	chr12:105561858..105564430-chr12:105566394..105568503,2	MCF-7	breast:
6	chr12:105517574..105520454-chr12:105529893..105532329,2	K562	blood:
7	chr12:105500061..105501858-chr12:105520145..105522733,2	K562	blood:
8	chr12:105559645..105562741-chr12:105564536..105567836,4	K562	blood:
9	chr12:105559645..105562741-chr12:105564536..105567836,4	K562	blood:
10	chr12:105558828..105561885-chr12:105562217..105566116,3	MCF-7	breast:
11	chr12:105520645..105521436-chr12:105528902..105529458,2	MCF-7	breast:
12	chr12:105557729..105562363-chr12:105563109..105566794,6	K562	blood:
13	chr12:105520638..105523143-chr12:105531748..105534535,2	K562	blood:
14	chr12:105557729..105562363-chr12:105563109..105566794,6	K562	blood:
15	chr12:105534493..105537599-chr12:105538790..105541931,3	K562	blood:
16	chr12:105558800..105560574-chr12:105563274..105565679,2	MCF-7	breast:
17	chr12:105500365..105502582-chr12:105544093..105545818,2	K562	blood:
18	chr12:105516186..105519030-chr12:105520787..105522474,2	K562	blood:
19	chr12:105534493..105537599-chr12:105538790..105541931,3	K562	blood:
20	chr12:105546702..105548786-chr12:105550881..105552428,2	K562	blood:
21	chr12:105507638..105509835-chr12:105526539..105528222,2	K562	blood:
22	chr12:105523431..105527512-chr12:105529193..105532336,3	MCF-7	breast:
23	chr12:105529161..105531125-chr12:105630136..105632646,2	K562	blood:
24	chr12:105533571..105536519-chr12:105568593..105570775,2	K562	blood:
25	chr12:105530759..105533680-chr12:105536719..105539215,3	K562	blood:
26	chr12:105532349..105534370-chr12:105534531..105536816,2	K562	blood:
27	chr12:105517574..105520454-chr12:105529893..105532329,2	K562	blood:
28	chr12:105516186..105519030-chr12:105520787..105522474,2	K562	blood:
29	chr12:105562609..105564624-chr12:105567516..105570192,2	K562	blood:
30	chr12:105526996..105528729-chr12:105529355..105531311,2	K562	blood:
31	chr12:105502302..105504240-chr12:105518371..105521182,2	K562	blood:
32	chr12:105542946..105545712-chr12:105628511..105631314,2	MCF-7	breast:
33	chr12:105502740..105505259-chr12:105518776..105521182,3	K562	blood:
34	chr12:105558828..105561885-chr12:105562217..105566116,3	MCF-7	breast:
35	chr12:105532349..105534370-chr12:105534531..105536816,2	K562	blood:
36	chr12:105526996..105528729-chr12:105529355..105531311,2	K562	blood:
37	chr12:105564104..105568210-chr12:105569076..105573485,6	MCF-7	breast:
38	chr12:105558800..105560574-chr12:105563274..105565679,2	MCF-7	breast:
39	chr12:105520638..105523143-chr12:105531748..105534535,2	K562	blood:
40	chr12:105564992..105569001-chr12:105627432..105630831,3	K562	blood:
41	chr12:105546702..105548786-chr12:105550881..105552428,2	K562	blood:
42	chr12:105506299..105509664-chr12:105519012..105521246,3	MCF-7	breast:

No data

Variant related genes	Relation type
KIAA1033	TF binding region
KIAA1033	CpG island
ENSG00000235162	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000136044	chromatin interactions
ENSG00000257999	chromatin interactions

Extended variants
information (count: 1806 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1806 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368356889	chr12:105518830-105518831	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549437890	chr12:105518831-105518832	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559639695	chr12:105518887-105518888	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1196827	chr12:105518896-105518897	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs116639678	chr12:105518923-105518924	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188711829	chr12:105518932-105518933	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537760615	chr12:105518940-105518941	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193281255	chr12:105519067-105519068	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146880435	chr12:105519132-105519133	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139737929	chr12:105519145-105519146	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553028815	chr12:105519149-105519150	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111461021	chr12:105519167-105519168	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369410644	chr12:105519170-105519171	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369555834	chr12:105519172-105519173	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7305712	chr12:105519188-105519189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs368997704	chr12:105519189-105519190	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538200150	chr12:105519221-105519222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558568857	chr12:105519252-105519253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182775358	chr12:105519303-105519304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575163432	chr12:105519441-105519442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544088244	chr12:105519460-105519461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570687696	chr12:105519488-105519489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187424431	chr12:105519515-105519516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144499241	chr12:105519531-105519532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115806480	chr12:105519537-105519538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540097769	chr12:105519553-105519554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537767357	chr12:105519580-105519581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1196826	chr12:105519626-105519627	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570362810	chr12:105519628-105519629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534000566	chr12:105519705-105519706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191508942	chr12:105519711-105519712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200794546	chr12:105519741-105519742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371238473	chr12:105519757-105519758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146437844	chr12:105519767-105519768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530960768	chr12:105519773-105519774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551233397	chr12:105519799-105519800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373847558	chr12:105519807-105519808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184001547	chr12:105519814-105519815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368029316	chr12:105519842-105519843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200763691	chr12:105519861-105519862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35267264	chr12:105519873-105519874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190039477	chr12:105519876-105519877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372217243	chr12:105519878-105519879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376747632	chr12:105519889-105519890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143095626	chr12:105519918-105519919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372430455	chr12:105519971-105519972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76617209	chr12:105519990-105519991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369135061	chr12:105519995-105519996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34434425	chr12:105520069-105520070	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553492952	chr12:105520096-105520097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105502400-105524600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:105503000-105521800	Weak transcription	Stomach Mucosa	stomach
3	chr12:105503800-105525200	Weak transcription	Fetal Heart	heart
4	chr12:105503800-105544200	Weak transcription	Aorta	Aorta
5	chr12:105505200-105530000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:105505200-105531000	Strong transcription	HMEC	breast
7	chr12:105505200-105542600	Strong transcription	Fetal Thymus	thymus
8	chr12:105505200-105559800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:105505200-105564000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr12:105505200-105567400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:105505200-105573000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr12:105505400-105519000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:105505600-105519200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:105505600-105530800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:105505600-105535200	Strong transcription	Muscle Satellite Cultured Cells	--
16	chr12:105505600-105537200	Strong transcription	Osteobl	bone
17	chr12:105505600-105550000	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr12:105505600-105573200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr12:105505800-105571400	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr12:105506000-105529000	Strong transcription	Primary hematopoietic stem cells	blood
21	chr12:105506000-105536800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:105506000-105537200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr12:105506400-105544600	Strong transcription	NHDF-Ad	bronchial
24	chr12:105506400-105573000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:105506600-105549200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr12:105506800-105568800	Strong transcription	Dnd41	blood
27	chr12:105506800-105572400	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr12:105507000-105528400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:105507000-105573200	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr12:105507200-105571400	Strong transcription	Primary B cells from peripheral blood	blood
31	chr12:105507400-105565600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr12:105507600-105527800	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr12:105507600-105571400	Strong transcription	HUVEC	blood vessel
34	chr12:105507600-105572800	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr12:105507800-105563800	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr12:105507800-105573200	Strong transcription	Placenta	Placenta
37	chr12:105508000-105526000	Strong transcription	GM12878-XiMat	blood
38	chr12:105508000-105549200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:105508000-105550400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:105508000-105565400	Strong transcription	Adipose Nuclei	Adipose
41	chr12:105508200-105572800	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr12:105508400-105520000	Strong transcription	Fetal Intestine Large	intestine
43	chr12:105508400-105528000	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr12:105508400-105531800	Strong transcription	Fetal Lung	lung
45	chr12:105508400-105562000	Strong transcription	Primary B cells from cord blood	blood
46	chr12:105508600-105525800	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr12:105508600-105526400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:105508600-105532400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:105508600-105536600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:105508600-105573000	Strong transcription	HUES64 Cell Line	embryonic stem cell

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