Variant report

Variant	nsv899497
Chromosome Location	chr12:105155291-105247010
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1056)
CpG islands
(count:183)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:105217730-105217941	K562	blood:	n/a	n/a
2	ARID3A	chr12:105182686-105182758	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:105179645-105180072	K562	blood:	n/a	n/a
4	ATF1	chr12:105157014-105157341	K562	blood:	n/a	n/a
5	ATF1	chr12:105179655-105180040	K562	blood:	n/a	n/a
6	ATF1	chr12:105217774-105217989	K562	blood:	n/a	n/a
7	ATF1	chr12:105186450-105186578	K562	blood:	n/a	n/a
8	ATF1	chr12:105180755-105181095	K562	blood:	n/a	n/a
9	ATF2	chr12:105221410-105221738	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr12:105179707-105180007	K562	blood:	n/a	n/a
11	BACH1	chr12:105184192-105184703	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:105184395-105184569	K562	blood:	n/a	n/a
13	BACH1	chr12:105221061-105221101	K562	blood:	n/a	n/a
14	BATF	chr12:105157007-105157254	GM12878	blood:	n/a	chr12:105157144-105157155
15	BATF	chr12:105156932-105157316	GM12878	blood:	n/a	chr12:105157144-105157155
16	BATF	chr12:105176141-105176405	GM12878	blood:	n/a	chr12:105176307-105176318
17	BHLHE40	chr12:105179694-105179889	K562	blood:	n/a	n/a
18	BHLHE40	chr12:105186483-105186588	K562	blood:	n/a	n/a
19	BHLHE40	chr12:105184311-105184785	K562	blood:	n/a	n/a
20	CBX3	chr12:105174424-105174780	K562	blood:	n/a	n/a
21	CBX3	chr12:105217718-105218421	K562	blood:	n/a	n/a
22	CBX3	chr12:105219163-105219540	K562	blood:	n/a	n/a
23	CEBPB	chr12:105158238-105158506	K562	blood:	n/a	chr12:105158354-105158365 chr12:105158352-105158363 chr12:105158352-105158365
24	CEBPB	chr12:105195988-105196355	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:105243201-105243461	HepG2	liver:	n/a	chr12:105243302-105243313
26	CEBPB	chr12:105186786-105187049	K562	blood:	n/a	n/a
27	CEBPB	chr12:105163102-105163264	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:105228852-105228907	K562	blood:	n/a	n/a
29	CEBPB	chr12:105158272-105158546	A549	lung:	n/a	chr12:105158354-105158365 chr12:105158352-105158363 chr12:105158352-105158365
30	CEBPB	chr12:105216371-105216646	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:105156959-105157271	IMR90	lung:	n/a	n/a
32	CEBPB	chr12:105159250-105159427	K562	blood:	n/a	n/a
33	CEBPB	chr12:105158206-105158509	HepG2	liver:	n/a	chr12:105158354-105158365 chr12:105158352-105158363 chr12:105158352-105158365
34	CEBPB	chr12:105245129-105245277	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr12:105157032-105157212	K562	blood:	n/a	n/a
36	CEBPB	chr12:105158209-105158468	IMR90	lung:	n/a	chr12:105158354-105158365 chr12:105158352-105158363 chr12:105158352-105158365
37	CEBPB	chr12:105156988-105157250	K562	blood:	n/a	n/a
38	CEBPB	chr12:105158230-105158393	K562	blood:	n/a	chr12:105158354-105158365 chr12:105158352-105158363 chr12:105158352-105158365
39	CEBPB	chr12:105170281-105170457	HepG2	liver:	n/a	chr12:105170416-105170427
40	CEBPB	chr12:105245133-105245247	K562	blood:	n/a	n/a
41	CEBPB	chr12:105158152-105158506	K562	blood:	n/a	chr12:105158354-105158365 chr12:105158352-105158363 chr12:105158352-105158365
42	CEBPB	chr12:105156980-105157278	K562	blood:	n/a	n/a
43	CEBPD	chr12:105179588-105180134	K562	blood:	n/a	n/a
44	CHD2	chr12:105160184-105160250	K562	blood:	n/a	n/a
45	CHD2	chr12:105186919-105186924	K562	blood:	n/a	n/a
46	CREB1	chr12:105184333-105184618	A549	lung:	n/a	n/a
47	CTCF	chr12:105219280-105219430	HMEC	breast:	n/a	n/a
48	CTCF	chr12:105219320-105219470	GM12874	blood:	n/a	n/a
49	CTCF	chr12:105184440-105184590	AG09319	gingival:	n/a	n/a
50	CTCF	chr12:105219332-105219462	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:105239832-105239882	GM12878	blood:	n/a
2	chr12:105239832-105239882	Caco-2	colon:	n/a
3	chr12:105184006-105184056	Hepatocyte	liver:	n/a
4	chr12:105162318-105162368	HCT-116	colon:	n/a
5	chr12:105239832-105239882	K562	blood:	n/a
6	chr12:105239832-105239882	Hela-S3	cervix:	n/a
7	chr12:105162318-105162368	CMK	blood:	n/a
8	chr12:105184006-105184056	T-47D	breast:	n/a
9	chr12:105184006-105184056	HIPEpiC	eye:	n/a
10	chr12:105239832-105239882	HL-60	blood:	n/a
11	chr12:105162318-105162368	SK-N-SH	brain:	n/a
12	chr12:105239832-105239882	T-47D	breast:	n/a
13	chr12:105184006-105184056	HepG2	liver:	n/a
14	chr12:105162318-105162368	HRCEpiC	kidney:	n/a
15	chr12:105162318-105162368	H1-hESC	embryonic stem cell:	embryo
16	chr12:105184006-105184056	NH-A	brain:	n/a
17	chr12:105184006-105184056	K562	blood:	n/a
18	chr12:105162318-105162368	PFSK-1	brain:	n/a
19	chr12:105239832-105239882	RPTEC	kidney:	n/a
20	chr12:105184006-105184056	RPTEC	kidney:	n/a
21	chr12:105239832-105239882	HMEC	breast:	n/a
22	chr12:105184006-105184056	H1-hESC	embryonic stem cell:	embryo
23	chr12:105184006-105184056	HNPCEpiC	eye:	n/a
24	chr12:105184006-105184056	AG09319	gingival:	n/a
25	chr12:105162318-105162368	NHBE	bronchial:	n/a
26	chr12:105184006-105184056	NB4	blood:	n/a
27	chr12:105239832-105239882	A549	lung:	n/a
28	chr12:105184006-105184056	GM19239	blood:	n/a
29	chr12:105239832-105239882	GM12892	blood:	n/a
30	chr12:105239832-105239882	AG10803	skin:	n/a
31	chr12:105239832-105239882	SK-N-MC	brain:	n/a
32	chr12:105184006-105184056	AG09309	skin:	n/a
33	chr12:105162318-105162368	GM12891	blood:	n/a
34	chr12:105162318-105162368	HNPCEpiC	eye:	n/a
35	chr12:105162318-105162368	HRPEpiC	eye:	n/a
36	chr12:105239832-105239882	GM12891	blood:	n/a
37	chr12:105184006-105184056	GM12891	blood:	n/a
38	chr12:105162318-105162368	T-47D	breast:	n/a
39	chr12:105184006-105184056	MCF-7	breast:	n/a
40	chr12:105239832-105239882	Jurkat	blood:	n/a
41	chr12:105239832-105239882	HCT-116	colon:	n/a
42	chr12:105184006-105184056	ovcar-3	ovarian:	n/a
43	chr12:105239832-105239882	SAEC	small airway:	n/a
44	chr12:105162318-105162368	NB4	blood:	n/a
45	chr12:105184006-105184056	HL-60	blood:	n/a
46	chr12:105184006-105184056	Caco-2	colon:	n/a
47	chr12:105162318-105162368	NHDF-neo	bronchial:	n/a
48	chr12:105162318-105162368	K562	blood:	n/a
49	chr12:105184006-105184056	HCT-116	colon:	n/a
50	chr12:105239832-105239882	PANC-1	pancreas:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:105187897..105189481-chr12:105191929..105194027,2	K562	blood:
2	chr12:105180077..105182540-chr12:105221823..105224422,2	K562	blood:
3	chr12:105156899..105157460-chr12:105169554..105170172,2	MCF-7	breast:
4	chr12:105156899..105157460-chr12:105169554..105170172,2	MCF-7	breast:
5	chr12:105154675..105157648-chr12:105161416..105163979,2	K562	blood:
6	chr12:105173249..105175093-chr12:105175948..105178622,2	MCF-7	breast:
7	chr12:105184083..105184965-chr12:105220814..105221546,2	K562	blood:
8	chr12:105166605..105169124-chr12:105175430..105176938,2	MCF-7	breast:
9	chr12:105065660..105066217-chr12:105169545..105170241,2	MCF-7	breast:
10	chr12:105166605..105169124-chr12:105175430..105176938,2	MCF-7	breast:
11	chr12:105226942..105228628-chr12:105231680..105234238,2	K562	blood:
12	chr12:105167548..105170068-chr12:105170304..105172425,2	MCF-7	breast:
13	chr12:105187897..105189481-chr12:105191929..105194027,2	K562	blood:
14	chr12:105073759..105074369-chr12:105221012..105221706,2	MCF-7	breast:
15	chr12:105224461..105226185-chr12:105230145..105232486,2	K562	blood:
16	chr12:105231509..105233737-chr12:105240660..105243241,2	MCF-7	breast:
17	chr12:105146747..105148409-chr12:105161769..105164567,2	K562	blood:
18	chr12:104849993..104852556-chr12:105225356..105227215,2	MCF-7	breast:
19	chr12:104595107..104595677-chr12:105221074..105221593,2	K562	blood:
20	chr12:105172416..105175180-chr12:105175349..105177504,2	K562	blood:
21	chr12:105173249..105175093-chr12:105175948..105178622,2	MCF-7	breast:
22	chr12:105224461..105226185-chr12:105230145..105232486,2	K562	blood:
23	chr12:105212787..105215531-chr12:105216343..105219007,2	K562	blood:
24	chr12:104775369..104776163-chr12:105218864..105219841,3	K562	blood:
25	chr12:105184083..105184965-chr12:105220814..105221546,2	K562	blood:
26	chr12:105154675..105157648-chr12:105161416..105163979,2	K562	blood:
27	chr12:105228136..105230854-chr12:105501668..105503168,2	MCF-7	breast:
28	chr12:105212787..105215531-chr12:105216343..105219007,2	K562	blood:
29	chr12:105231509..105233737-chr12:105240660..105243241,2	MCF-7	breast:
30	chr12:105172416..105175180-chr12:105175349..105177504,2	K562	blood:
31	chr12:105128010..105128991-chr12:105218995..105219838,4	MCF-7	breast:
32	chr12:105184845..105186362-chr12:105189504..105191210,2	K562	blood:
33	chr12:105180077..105182540-chr12:105221823..105224422,2	K562	blood:
34	chr12:105167548..105170068-chr12:105170304..105172425,2	MCF-7	breast:
35	chr12:104775264..104776293-chr12:105218866..105219841,5	MCF-7	breast:
36	chr12:105184845..105186362-chr12:105189504..105191210,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHST11-2	chr12:105167648-105167686	l_719_chr12:105166325-105170689_thyroid
2	lnc-CHST11-2	chr12:105166326-105166656	l_719_chr12:105166325-105170689_thyroid
3	lnc-C12orf45-3	chr12:105151948-105155783	NONHSAT030431
4	lnc-CHST11-2	chr12:105170038-105170689	l_719_chr12:105166325-105170689_thyroid

No data

Variant related genes	Relation type
SLC41A2	TF binding region
ENSG00000222579	TF binding region
SLC41A2	CpG island
ENSG00000222579	CpG island
ENSG00000136052	chromatin interactions
ENSG00000171310	chromatin interactions

Extended variants
information (count: 2930 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2930 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7972699	chr12:105155291-105155292	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529509910	chr12:105155307-105155308	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs375146184	chr12:105155348-105155349	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560074430	chr12:105155398-105155399	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs34003701	chr12:105155400-105155401	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs528122227	chr12:105155432-105155433	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs551378825	chr12:105155453-105155454	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs190991065	chr12:105155488-105155489	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs537160349	chr12:105155558-105155559	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs10179	chr12:105155598-105155599	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs550357346	chr12:105155599-105155600	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs7847	chr12:105155605-105155606	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs536028627	chr12:105155607-105155608	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs544001818	chr12:105155608-105155609	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs1048662	chr12:105155627-105155628	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146122182	chr12:105155643-105155644	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs538516055	chr12:105155663-105155664	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs558145403	chr12:105155758-105155759	Weak transcription Enhancers Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs7488439	chr12:105155815-105155816	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs371380799	chr12:105155824-105155825	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543945303	chr12:105155841-105155842	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574290115	chr12:105155877-105155878	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563622959	chr12:105155878-105155879	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139037340	chr12:105155886-105155887	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183205903	chr12:105155917-105155918	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12307007	chr12:105155923-105155924	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs114832591	chr12:105155927-105155928	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560412826	chr12:105155946-105155947	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188264435	chr12:105155955-105155956	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564899466	chr12:105155975-105155976	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36001868	chr12:105156005-105156006	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530420653	chr12:105156011-105156012	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550690413	chr12:105156041-105156042	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113366878	chr12:105156063-105156064	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567005865	chr12:105156072-105156073	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536068944	chr12:105156123-105156124	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75944730	chr12:105156190-105156191	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566294570	chr12:105156197-105156198	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538553387	chr12:105156201-105156202	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558575383	chr12:105156297-105156298	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs55905284	chr12:105156298-105156299	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554315828	chr12:105156323-105156324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11307984	chr12:105156324-105156325	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79505328	chr12:105156341-105156342	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76801834	chr12:105156345-105156346	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537037843	chr12:105156348-105156349	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557458549	chr12:105156372-105156373	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574204958	chr12:105156373-105156374	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528018012	chr12:105156395-105156396	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12320918	chr12:105156452-105156453	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105137200-105157000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr12:105141600-105155400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr12:105142400-105160800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:105142600-105158000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr12:105142800-105158200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:105143800-105156800	Weak transcription	NHLF	lung
7	chr12:105143800-105160800	Weak transcription	Fetal Muscle Leg	muscle
8	chr12:105144000-105158200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr12:105144200-105156800	Weak transcription	NHDF-Ad	bronchial
10	chr12:105144200-105157000	Weak transcription	NH-A	brain
11	chr12:105144200-105158000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr12:105145200-105155600	Strong transcription	Dnd41	blood
13	chr12:105145200-105158200	Weak transcription	Adipose Nuclei	Adipose
14	chr12:105145400-105161200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:105145600-105162800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:105145800-105161200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:105145800-105161200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr12:105145800-105161400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr12:105146000-105161400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr12:105146800-105156000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr12:105146800-105161200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr12:105148400-105156000	Weak transcription	Pancreas	Pancrea
23	chr12:105149600-105157000	Weak transcription	HMEC	breast
24	chr12:105150000-105156000	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr12:105151400-105156600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:105151400-105156800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:105151400-105158400	Weak transcription	Duodenum Mucosa	Duodenum
28	chr12:105151400-105161200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr12:105151600-105156000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr12:105151600-105156800	Weak transcription	GM12878-XiMat	blood
31	chr12:105151600-105157000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:105151600-105157000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:105151600-105157000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:105151600-105157000	Weak transcription	A549	lung
35	chr12:105151600-105157400	Weak transcription	HSMMtube	muscle
36	chr12:105151600-105158400	Weak transcription	Ovary	ovary
37	chr12:105151600-105160800	Weak transcription	Esophagus	oesophagus
38	chr12:105151600-105161800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:105151600-105162800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:105151800-105157000	Weak transcription	Osteobl	bone
41	chr12:105152200-105158000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr12:105152400-105162600	Weak transcription	Brain Anterior Caudate	brain
43	chr12:105152600-105158000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr12:105152600-105158400	Weak transcription	Placenta	Placenta
45	chr12:105152800-105157000	Weak transcription	Spleen	Spleen
46	chr12:105153000-105156200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr12:105153000-105156400	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr12:105153000-105156800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:105153000-105157000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr12:105153000-105157000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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