Variant report

Variant	esv3357747
Chromosome Location	chr12:121405281-121427388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:770)
CpG islands
(count:1161)
Chromatin interactive
region (count:27)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121415630-121415655	K562	blood:	n/a	n/a
2	ARID3A	chr12:121418090-121418322	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121416006-121416515	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:121410742-121410940	HepG2	liver:	n/a	n/a
5	ATF1	chr12:121409535-121409969	K562	blood:	n/a	n/a
6	ATF3	chr12:121419340-121419824	A549	lung:	n/a	n/a
7	BCL3	chr12:121418508-121419849	A549	lung:	n/a	chr12:121418966-121418975 chr12:121418656-121418665
8	BCL3	chr12:121417821-121418430	A549	lung:	n/a	chr12:121417844-121417852 chr12:121418147-121418156
9	BCL3	chr12:121418529-121419864	A549	lung:	n/a	chr12:121418966-121418975 chr12:121418656-121418665
10	BCL3	chr12:121415555-121416577	A549	lung:	n/a	n/a
11	BHLHE40	chr12:121415985-121416573	HepG2	liver:	n/a	chr12:121416029-121416045
12	BHLHE40	chr12:121419413-121419434	A549	lung:	n/a	n/a
13	BHLHE40	chr12:121409642-121409879	K562	blood:	n/a	n/a
14	BRCA1	chr12:121415950-121416465	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:121419352-121419665	A549	lung:	n/a	chr12:121419482-121419493
16	CEBPB	chr12:121409690-121410015	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:121419178-121419837	A549	lung:	n/a	chr12:121419482-121419493
18	CEBPB	chr12:121419398-121419601	HepG2	liver:	n/a	chr12:121419482-121419493
19	CEBPB	chr12:121422336-121422574	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:121419268-121419789	A549	lung:	n/a	chr12:121419482-121419493
21	CEBPB	chr12:121409753-121409953	K562	blood:	n/a	n/a
22	CEBPB	chr12:121409634-121410014	K562	blood:	n/a	n/a
23	CEBPB	chr12:121419402-121419568	HepG2	liver:	n/a	chr12:121419482-121419493
24	CEBPD	chr12:121418459-121419167	HepG2	liver:	n/a	n/a
25	CEBPD	chr12:121417895-121418448	HepG2	liver:	n/a	n/a
26	CEBPD	chr12:121415992-121416783	HepG2	liver:	n/a	n/a
27	CHD2	chr12:121419462-121419466	HepG2	liver:	n/a	n/a
28	CHD2	chr12:121417012-121417099	HepG2	liver:	n/a	n/a
29	CHD2	chr12:121422162-121422608	HepG2	liver:	n/a	n/a
30	CHD2	chr12:121416074-121416626	HepG2	liver:	n/a	n/a
31	CHD2	chr12:121410736-121410805	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr12:121417988-121418495	HepG2	liver:	n/a	n/a
33	CHD2	chr12:121418064-121418270	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr12:121418125-121418345	A549	lung:	n/a	n/a
35	CREB1	chr12:121419580-121419878	A549	lung:	n/a	n/a
36	CREB1	chr12:121419238-121419540	A549	lung:	n/a	n/a
37	CREB1	chr12:121416104-121416545	A549	lung:	n/a	n/a
38	CTCF	chr12:121409620-121409770	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr12:121409640-121409790	AG09319	gingival:	n/a	n/a
40	CTCF	chr12:121409600-121409750	HEK293	kidney:	n/a	n/a
41	CTCF	chr12:121409593-121409845	HepG2	liver:	n/a	n/a
42	CTCF	chr12:121409660-121409810	AG04449	skin:	n/a	n/a
43	CTCF	chr12:121409680-121409830	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr12:121410300-121410450	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr12:121409184-121410152	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr12:121409591-121409890	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr12:121409660-121409810	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr12:121409620-121409770	NHLF	lung:	n/a	n/a
49	CTCF	chr12:121409578-121409913	GM12878	blood:	n/a	n/a
50	CTCF	chr12:121410680-121410830	HCPEpiC	choroid plexus:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121409957-121410007	SK-N-SH_RA	brain:	n/a
2	chr12:121410996-121411046	NT2-D1	testis:	n/a
3	chr12:121409957-121410007	SK-N-SH_RA	brain:	n/a
4	chr12:121410996-121411046	NT2-D1	testis:	n/a
5	chr12:121427010-121427060	AG09319	gingival:	n/a
6	chr12:121409673-121409723	BJ	skin:	n/a
7	chr12:121409957-121410007	MCF-7	breast:	n/a
8	chr12:121410996-121411046	GM19239	blood:	n/a
9	chr12:121411269-121411319	HEEpiC	esophagus:	n/a
10	chr12:121416390-121416440	AG04449	skin:	fetal
11	chr12:121416566-121416616	A549	lung:	n/a
12	chr12:121420721-121420771	MCF-7	breast:	n/a
13	chr12:121409957-121410007	NHBE	bronchial:	n/a
14	chr12:121411269-121411319	AG04450	lung:	fetal
15	chr12:121415506-121415556	HAEpiC	amniotic membrane:	n/a
16	chr12:121416566-121416616	HCF	heart:	n/a
17	chr12:121416512-121416562	AG04450	lung:	fetal
18	chr12:121416510-121416560	HIPEpiC	eye:	n/a
19	chr12:121416547-121416597	GM12878	blood:	n/a
20	chr12:121416510-121416560	ovcar-3	ovarian:	n/a
21	chr12:121416612-121416662	GM12891	blood:	n/a
22	chr12:121427010-121427060	PFSK-1	brain:	n/a
23	chr12:121416501-121416551	MCF-7	breast:	n/a
24	chr12:121416566-121416616	HCT-116	colon:	n/a
25	chr12:121409957-121410007	PFSK-1	brain:	n/a
26	chr12:121416796-121416846	HAEpiC	amniotic membrane:	n/a
27	chr12:121416566-121416616	SK-N-MC	brain:	n/a
28	chr12:121415506-121415556	NT2-D1	testis:	n/a
29	chr12:121409673-121409723	PrEC	prostate:	n/a
30	chr12:121417986-121418036	HEK293	kidney:	embryo
31	chr12:121416501-121416551	NHDF-neo	bronchial:	n/a
32	chr12:121410855-121410905	AoSMC	blood vessel:	n/a
33	chr12:121409673-121409723	ECC-1	luminal epithelium:	n/a
34	chr12:121416612-121416662	Jurkat	blood:	n/a
35	chr12:121416510-121416560	HCM	heart:	n/a
36	chr12:121416501-121416551	Caco-2	colon:	n/a
37	chr12:121416390-121416440	Hepatocyte	liver:	n/a
38	chr12:121410855-121410905	NH-A	brain:	n/a
39	chr12:121417986-121418036	Jurkat	blood:	n/a
40	chr12:121416512-121416562	HRPEpiC	eye:	n/a
41	chr12:121415506-121415556	SK-N-SH	brain:	n/a
42	chr12:121416566-121416616	HCM	heart:	n/a
43	chr12:121415506-121415556	PANC-1	pancreas:	n/a
44	chr12:121411269-121411319	HRPEpiC	eye:	n/a
45	chr12:121416547-121416597	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:121416315-121416365	HNPCEpiC	eye:	n/a
47	chr12:121420721-121420771	AG04450	lung:	fetal
48	chr12:121416510-121416560	H1-hESC	embryonic stem cell:	embryo
49	chr12:121410996-121411046	MCF10A-Er-Src	breast:	n/a
50	chr12:121416796-121416846	Hepatocyte	liver:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:121410040..121412493-chr12:121417620..121420402,3	MCF-7	breast:
2	chr12:120803152..120806050-chr12:121419474..121422270,2	K562	blood:
3	chr12:121388985..121390758-chr12:121403541..121406125,2	K562	blood:
4	chr12:121419295..121421296-chr12:121428164..121430442,2	MCF-7	breast:
5	chr12:121416581..121418752-chr12:121419164..121421756,2	K562	blood:
6	chr12:121410040..121412493-chr12:121417620..121420402,3	MCF-7	breast:
7	chr12:121175837..121176393-chr12:121409274..121410074,2	MCF-7	breast:
8	chr12:121426408..121429065-chr12:121429959..121431966,2	MCF-7	breast:
9	chr12:121077883..121078713-chr12:121409304..121410103,2	MCF-7	breast:
10	chr12:121403725..121406245-chr12:121406756..121408586,2	MCF-7	breast:
11	chr12:121403725..121406245-chr12:121406756..121408586,2	MCF-7	breast:
12	chr12:121421859..121423940-chr12:121426161..121428350,2	K562	blood:
13	chr12:121084889..121085528-chr12:121409309..121409932,2	K562	blood:
14	chr12:121159870..121162504-chr12:121416031..121417915,2	K562	blood:
15	chr12:121020899..121021841-chr12:121409286..121409915,3	K562	blood:
16	chr12:121401463..121403474-chr12:121406949..121408762,2	K562	blood:
17	chr12:121417392..121420035-chr12:121422545..121425552,3	K562	blood:
18	chr12:121197842..121198350-chr12:121409283..121409799,2	MCF-7	breast:
19	chr12:121412159..121414001-chr12:121420552..121422609,2	MCF-7	breast:
20	chr12:121174261..121175937-chr12:121403993..121406712,2	MCF-7	breast:
21	chr12:121419406..121422092-chr12:121422475..121425429,2	K562	blood:
22	chr12:121409514..121410021-chr12:121548070..121548945,2	K562	blood:
23	chr12:121427353..121429838-chr12:121441548..121443367,3	K562	blood:
24	chr12:121412159..121414001-chr12:121420552..121422609,2	MCF-7	breast:
25	chr12:121419406..121422092-chr12:121422475..121425429,2	K562	blood:
26	chr12:121421859..121423940-chr12:121426161..121428350,2	K562	blood:
27	chr12:121398625..121400416-chr12:121405425..121406992,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf43-1	chr12:121412188-121412401	ENSG00000241388.2
2	lnc-C12orf43-1	chr12:121407641-121410095	ENSG00000241388.2
3	lnc-C12orf43-1	chr12:121418447-121418709	ENSG00000241388.2
4	lnc-C12orf43-1	chr12:121418447-121418768	ENSG00000241388.2
5	lnc-C12orf43-1	chr12:121410457-121412502	NONHSAT031257
6	lnc-C12orf43-1	chr12:121406416-121406811	ENSG00000241388.2
7	lnc-C12orf43-1	chr12:121417417-121417550	ENSG00000241388.2
8	lnc-C12orf43-1	chr12:121414602-121414724	ENSG00000241388.2
9	lnc-C12orf43-1	chr12:121412288-121412401	ENSG00000241388.2
10	lnc-C12orf43-1	chr12:121408046-121410443	NONHSAT031257
11	lnc-C12orf43-1	chr12:121407933-121408173	ENSG00000241388.2
12	lnc-C12orf43-1	chr12:121405937-121406811	NONHSAT031257

No data

Variant related genes	Relation type
HNF1A-AS1	TF binding region
ENSG00000272214	TF binding region
HNF1A	TF binding region
HNF1A-AS1	CpG island
ENSG00000272214	CpG island
HNF1A	CpG island
ENSG00000157782	chromatin interactions
ENSG00000272214	chromatin interactions
ENSG00000241388	chromatin interactions
ENSG00000256008	chromatin interactions
ENSG00000135097	chromatin interactions
ENSG00000256569	chromatin interactions
ENSG00000265455	chromatin interactions

Extended variants
information (count: 928 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:928 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55913575	chr12:121405288-121405289	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34376030	chr12:121405327-121405328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs398056004	chr12:121405331-121405332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200187150	chr12:121405338-121405339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2251556	chr12:121405424-121405425	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs12049937	chr12:121405436-121405437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573096866	chr12:121405466-121405467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185792295	chr12:121405473-121405474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34409899	chr12:121405511-121405512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530829029	chr12:121405564-121405565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550936099	chr12:121405566-121405567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190066741	chr12:121405591-121405592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564009736	chr12:121405626-121405627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7961178	chr12:121405644-121405645	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs146022831	chr12:121405657-121405658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182613808	chr12:121405706-121405707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186047603	chr12:121405722-121405723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555520523	chr12:121405780-121405781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575398025	chr12:121405781-121405782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537473398	chr12:121405811-121405812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557735314	chr12:121405837-121405838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577509760	chr12:121405840-121405841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546485925	chr12:121405859-121405860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560013094	chr12:121405862-121405863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192127960	chr12:121405874-121405875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2251573	chr12:121405876-121405877	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138568672	chr12:121405916-121405917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368369012	chr12:121405972-121405973	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs541986041	chr12:121405978-121405979	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs561881028	chr12:121406025-121406026	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs530889182	chr12:121406026-121406027	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs199712266	chr12:121406071-121406072	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs183974313	chr12:121406072-121406073	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs533133168	chr12:121406078-121406079	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs546873255	chr12:121406096-121406097	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs566742572	chr12:121406108-121406109	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs372475913	chr12:121406122-121406123	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs554647338	chr12:121406132-121406133	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs533169432	chr12:121406161-121406162	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs142778047	chr12:121406163-121406164	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs543838893	chr12:121406167-121406168	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs143474756	chr12:121406187-121406188	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs563613011	chr12:121406198-121406199	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs537939873	chr12:121406203-121406204	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs112817163	chr12:121406239-121406240	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs571225828	chr12:121406261-121406262	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs533527214	chr12:121406292-121406293	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs2393792	chr12:121406293-121406294	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187601895	chr12:121406346-121406347	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs12311294	chr12:121406363-121406364	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	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
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121394600-121408200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:121395800-121408200	Weak transcription	Fetal Kidney	kidney
3	chr12:121397600-121406800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr12:121397800-121405400	Weak transcription	Pancreas	Pancrea
5	chr12:121400000-121405400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:121400000-121406600	Weak transcription	Gastric	stomach
7	chr12:121400600-121416000	Weak transcription	Small Intestine	intestine
8	chr12:121400800-121406600	Weak transcription	A549	lung
9	chr12:121400800-121406600	Weak transcription	HepG2	liver
10	chr12:121401600-121406600	Weak transcription	Liver	Liver
11	chr12:121403200-121409400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr12:121403800-121411000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr12:121404000-121406600	Weak transcription	Colonic Mucosa	Colon
14	chr12:121404000-121406600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr12:121404000-121406800	Weak transcription	Stomach Mucosa	stomach
16	chr12:121404200-121405400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr12:121404400-121408200	Weak transcription	Esophagus	oesophagus
18	chr12:121404600-121408000	Strong transcription	Fetal Intestine Small	intestine
19	chr12:121404800-121409000	Strong transcription	Fetal Intestine Large	intestine
20	chr12:121404800-121409800	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr12:121405200-121415400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr12:121405400-121407000	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr12:121405400-121409000	Strong transcription	Pancreas	Pancrea
24	chr12:121405400-121409200	Strong transcription	Duodenum Mucosa	Duodenum
25	chr12:121405600-121406400	Weak transcription	Fetal Stomach	stomach
26	chr12:121406400-121407400	Strong transcription	Fetal Stomach	stomach
27	chr12:121406600-121407200	Strong transcription	HepG2	liver
28	chr12:121406600-121407400	Strong transcription	A549	lung
29	chr12:121406600-121408400	Strong transcription	Colonic Mucosa	Colon
30	chr12:121406600-121409000	Strong transcription	Gastric	stomach
31	chr12:121406600-121410800	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr12:121406600-121412400	Genic enhancers	Liver	Liver
33	chr12:121406800-121407000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:121406800-121407000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:121406800-121407000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:121406800-121407200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:121406800-121408400	Strong transcription	Stomach Mucosa	stomach
38	chr12:121407000-121407200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:121407000-121407400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:121407000-121408200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr12:121407000-121409400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:121407200-121407800	Weak transcription	HepG2	liver
43	chr12:121407200-121409400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:121407200-121409800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr12:121407400-121409400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:121407400-121409400	Weak transcription	A549	lung
47	chr12:121407400-121410800	Weak transcription	Fetal Stomach	stomach
48	chr12:121407800-121409200	Strong transcription	HepG2	liver
49	chr12:121408000-121408200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr12:121408000-121414200	Genic enhancers	Fetal Intestine Small	intestine

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