Variant report

Variant	esv3502154
Chromosome Location	chr12:9243906-9317851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1036)
CpG islands
(count:673)
Chromatin interactive
region (count:17)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9275966-9276528	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:9274241-9275270	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:9287888-9289159	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:9268152-9269004	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:9284068-9285425	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:9275901-9275983	K562	blood:	n/a	n/a
7	ATF1	chr12:9270894-9271140	K562	blood:	n/a	n/a
8	BATF	chr12:9258708-9258921	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:9274748-9275094	HepG2	liver:	n/a	n/a
10	BHLHE40	chr12:9284768-9285070	HepG2	liver:	n/a	n/a
11	BHLHE40	chr12:9270815-9270818	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:9266596-9266862	HepG2	liver:	n/a	n/a
13	BHLHE40	chr12:9274743-9275213	HepG2	liver:	n/a	n/a
14	BRCA1	chr12:9297247-9297916	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr12:9300416-9300530	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr12:9292484-9293424	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr12:9261110-9261445	HepG2	liver:	n/a	n/a
18	BRCA1	chr12:9275010-9275210	HepG2	liver:	n/a	n/a
19	CBX3	chr12:9287860-9288204	HCT-116	colon:	n/a	n/a
20	CEBPB	chr12:9251581-9251858	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:9284517-9285192	HepG2	liver:	n/a	chr12:9284799-9284810
22	CEBPB	chr12:9249163-9249549	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:9284466-9285279	HepG2	liver:	n/a	chr12:9284799-9284810 chr12:9284483-9284491
24	CEBPB	chr12:9255965-9256138	K562	blood:	n/a	n/a
25	CEBPB	chr12:9284618-9285214	MCF-7	breast:	n/a	chr12:9284799-9284810
26	CEBPB	chr12:9256004-9256238	A549	lung:	n/a	n/a
27	CEBPB	chr12:9292444-9293414	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:9284599-9285123	HepG2	liver:	n/a	chr12:9284799-9284810
29	CEBPB	chr12:9274654-9275169	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:9271566-9271586	A549	lung:	n/a	n/a
31	CEBPB	chr12:9284555-9285223	HepG2	liver:	n/a	chr12:9284799-9284810
32	CEBPB	chr12:9284560-9285227	MCF-7	breast:	n/a	chr12:9284799-9284810
33	CEBPB	chr12:9274709-9275022	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:9279010-9279015	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr12:9267531-9267921	Hela-S3	cervix:	n/a	chr12:9267699-9267710
36	CEBPB	chr12:9275982-9276655	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:9249173-9249541	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:9268271-9268738	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:9266548-9266784	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:9284594-9285211	Hela-S3	cervix:	n/a	chr12:9284799-9284810
41	CEBPB	chr12:9296984-9297730	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:9284670-9285036	A549	lung:	n/a	chr12:9284799-9284810
43	CEBPB	chr12:9285768-9286913	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr12:9268350-9269035	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:9266533-9266891	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:9249211-9249510	A549	lung:	n/a	n/a
47	CEBPB	chr12:9266522-9266892	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:9267543-9267894	HepG2	liver:	n/a	chr12:9267699-9267710
49	CEBPB	chr12:9274742-9275093	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:9274732-9275174	HepG2	liver:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9269178-9269228	MCF10A-Er-Src	breast:	n/a
2	chr12:9265053-9265103	PFSK-1	brain:	n/a
3	chr12:9269178-9269228	MCF10A-Er-Src	breast:	n/a
4	chr12:9265053-9265103	PFSK-1	brain:	n/a
5	chr12:9280420-9280470	AoSMC	blood vessel:	n/a
6	chr12:9265030-9265080	Hepatocyte	liver:	n/a
7	chr12:9280567-9280617	SAEC	small airway:	n/a
8	chr12:9269671-9269721	PFSK-1	brain:	n/a
9	chr12:9277178-9277228	HRPEpiC	eye:	n/a
10	chr12:9269178-9269228	SK-N-MC	brain:	n/a
11	chr12:9277178-9277228	HCM	heart:	n/a
12	chr12:9287358-9287408	LNCaP	prostate:	n/a
13	chr12:9268379-9268429	NHBE	bronchial:	n/a
14	chr12:9287358-9287408	SAEC	small airway:	n/a
15	chr12:9280923-9280973	IMR90	lung:	fetal
16	chr12:9277178-9277228	PFSK-1	brain:	n/a
17	chr12:9268379-9268429	ProgFib	skin:	n/a
18	chr12:9268379-9268429	K562	blood:	n/a
19	chr12:9269671-9269721	BE2_C	brain:	n/a
20	chr12:9277178-9277228	RPTEC	kidney:	n/a
21	chr12:9269671-9269721	NB4	blood:	n/a
22	chr12:9287358-9287408	T-47D	breast:	n/a
23	chr12:9280567-9280617	AoSMC	blood vessel:	n/a
24	chr12:9280420-9280470	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:9280420-9280470	HNPCEpiC	eye:	n/a
26	chr12:9280567-9280617	SK-N-SH	brain:	n/a
27	chr12:9269178-9269228	BE2_C	brain:	n/a
28	chr12:9269178-9269228	HNPCEpiC	eye:	n/a
29	chr12:9265053-9265103	BJ	skin:	n/a
30	chr12:9265030-9265080	HepG2	liver:	n/a
31	chr12:9277178-9277228	AG10803	skin:	n/a
32	chr12:9265989-9266039	CMK	blood:	n/a
33	chr12:9269178-9269228	NHDF-neo	bronchial:	n/a
34	chr12:9280923-9280973	HNPCEpiC	eye:	n/a
35	chr12:9280420-9280470	BJ	skin:	n/a
36	chr12:9280567-9280617	GM19239	blood:	n/a
37	chr12:9280567-9280617	Jurkat	blood:	n/a
38	chr12:9280567-9280617	HIPEpiC	eye:	n/a
39	chr12:9280923-9280973	HMEC	breast:	n/a
40	chr12:9269178-9269228	AG04450	lung:	fetal
41	chr12:9265030-9265080	AG09309	skin:	n/a
42	chr12:9268379-9268429	GM19239	blood:	n/a
43	chr12:9265053-9265103	ProgFib	skin:	n/a
44	chr12:9265053-9265103	MCF10A-Er-Src	breast:	n/a
45	chr12:9269671-9269721	NT2-D1	testis:	n/a
46	chr12:9265053-9265103	NH-A	brain:	n/a
47	chr12:9269178-9269228	SK-N-SH	brain:	n/a
48	chr12:9268379-9268429	IMR90	lung:	fetal
49	chr12:9265030-9265080	HRCEpiC	kidney:	n/a
50	chr12:9268379-9268429	LNCaP	prostate:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9216885..9219408-chr12:9300483..9302545,2	MCF-7	breast:
2	chr12:9286914..9287420-chr12:92539193..92539798,2	Hela-S3	cervix:
3	chr12:9216174..9218577-chr12:9277293..9280144,3	MCF-7	breast:
4	chr12:9284631..9285460-chr12:9432685..9433670,3	MCF-7	breast:
5	chr12:9289234..9291527-chr12:9295649..9297561,2	K562	blood:
6	chr12:9215493..9217658-chr12:9271346..9273980,2	MCF-7	breast:
7	chr12:9236127..9237912-chr12:9246166..9247720,2	MCF-7	breast:
8	chr12:9256413..9259113-chr12:9259461..9261361,2	K562	blood:
9	chr12:9216566..9218445-chr12:9283863..9285445,2	MCF-7	breast:
10	chr12:9265907..9267822-chr12:9274659..9276392,2	MCF-7	breast:
11	chr12:9248855..9251571-chr12:9264323..9266629,2	MCF-7	breast:
12	chr12:9248855..9251571-chr12:9264323..9266629,2	MCF-7	breast:
13	chr12:9284806..9285460-chr12:9433144..9433670,2	MCF-7	breast:
14	chr12:9312713..9314692-chr12:9319396..9321179,2	MCF-7	breast:
15	chr12:9265907..9267822-chr12:9274659..9276392,2	MCF-7	breast:
16	chr12:9289234..9291527-chr12:9295649..9297561,2	K562	blood:
17	chr12:9265762..9267378-chr12:9267657..9270590,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PZP-6	chr12:9268360-9268657	NONHSAT026387
2	lnc-PZP-6	chr12:9268360-9268613	NONHSAT026388
3	lnc-PZP-6	chr12:9265956-9266139	NONHSAT026387
4	lnc-A2M-2	chr12:9308477-9308968	NONHSAT026391
5	lnc-KLRG1-5	chr12:9287680-9288187	NONHSAT026390
6	lnc-PZP-6	chr12:9265235-9265285	NONHSAT026387
7	lnc-PZP-6	chr12:9267754-9268032	NONHSAT026388

No data

Variant related genes	Relation type
A2M	TF binding region
ENSG00000211542	TF binding region
ENSG00000256937	TF binding region
ENSG00000256720	TF binding region
TPT1P12	TF binding region
A2M	CpG island
ENSG00000211542	CpG island
ENSG00000256937	CpG island
ENSG00000256720	CpG island
TPT1P12	CpG island
ENSG00000126838	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000175899	chromatin interactions
ENSG00000245105	chromatin interactions
ENSG00000214851	chromatin interactions

Extended variants
information (count: 1781 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144752316	chr12:9243930-9243931	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs375590271	chr12:9243974-9243975	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs369403894	chr12:9243980-9243981	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs202109195	chr12:9243984-9243985	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs113336172	chr12:9244000-9244001	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs11831793	chr12:9244053-9244054	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11833893	chr12:9244102-9244103	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567420533	chr12:9244125-9244126	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs75577698	chr12:9244202-9244203	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs189181970	chr12:9244213-9244214	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370486633	chr12:9244262-9244263	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs113973	chr12:9244267-9244268	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs377631518	chr12:9244283-9244284	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs193224243	chr12:9244309-9244310	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs185614809	chr12:9244344-9244345	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs117834356	chr12:9244367-9244368	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs190176108	chr12:9244370-9244371	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs566891839	chr12:9244419-9244420	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs375975796	chr12:9244451-9244452	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs181843508	chr12:9244517-9244518	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs56016864	chr12:9244582-9244583	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs185691585	chr12:9244589-9244590	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188842631	chr12:9244630-9244631	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs226410	chr12:9244643-9244644	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs569578186	chr12:9244729-9244730	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs226409	chr12:9245005-9245006	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538155737	chr12:9245035-9245036	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs181310504	chr12:9245088-9245089	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs185135459	chr12:9245131-9245132	Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs226408	chr12:9245201-9245202	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs190874780	chr12:9245269-9245270	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183930314	chr12:9245322-9245323	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs35291816	chr12:9245345-9245346	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs572069623	chr12:9245354-9245355	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs142156322	chr12:9245421-9245422	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs146832219	chr12:9245452-9245453	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs114641862	chr12:9245469-9245470	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs7971254	chr12:9245471-9245472	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs140606617	chr12:9245486-9245487	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs73244216	chr12:9245542-9245543	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs144208457	chr12:9245734-9245735	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs226407	chr12:9245779-9245780	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113813656	chr12:9245845-9245846	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs373682803	chr12:9245954-9245955	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs187364339	chr12:9245968-9245969	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs371612562	chr12:9246033-9246034	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs73244220	chr12:9246037-9246038	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs200524075	chr12:9246041-9246042	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545926870	chr12:9246077-9246078	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs367601457	chr12:9246110-9246111	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9218200-9266200	Weak transcription	Fetal Kidney	kidney
2	chr12:9219200-9266000	Weak transcription	Esophagus	oesophagus
3	chr12:9232200-9264600	Weak transcription	Brain Hippocampus Middle	brain
4	chr12:9232400-9244600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr12:9235000-9253600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr12:9235200-9265800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr12:9236600-9258800	Weak transcription	Fetal Heart	heart
8	chr12:9237200-9252200	Weak transcription	Psoas Muscle	Psoas
9	chr12:9237200-9261200	Strong transcription	Liver	Liver
10	chr12:9237200-9265200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:9237400-9264200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:9237600-9246000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr12:9237800-9258400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:9238600-9246800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:9238600-9265800	Strong transcription	Skeletal Muscle Female	skeletal muscle
16	chr12:9238800-9246600	Strong transcription	Stomach Smooth Muscle	stomach
17	chr12:9239400-9262800	Strong transcription	Duodenum Smooth Muscle	Duodenum
18	chr12:9239400-9264000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr12:9239600-9265000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr12:9240800-9267600	Weak transcription	Fetal Intestine Large	intestine
21	chr12:9241000-9244000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr12:9241000-9246600	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr12:9241200-9246000	Strong transcription	Left Ventricle	heart
24	chr12:9241200-9247000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr12:9241200-9262800	Strong transcription	Adipose Nuclei	Adipose
26	chr12:9241600-9264000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:9242400-9246800	Strong transcription	Aorta	Aorta
28	chr12:9242400-9247000	Strong transcription	Ovary	ovary
29	chr12:9242600-9245400	Strong transcription	Rectal Smooth Muscle	rectum
30	chr12:9242600-9246200	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr12:9242800-9245200	Strong transcription	Gastric	stomach
32	chr12:9242800-9245600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr12:9242800-9246000	Strong transcription	Placenta	Placenta
34	chr12:9242800-9246800	Strong transcription	Fetal Stomach	stomach
35	chr12:9242800-9246800	Strong transcription	Spleen	Spleen
36	chr12:9243000-9246800	Strong transcription	Lung	lung
37	chr12:9243000-9251400	Weak transcription	Primary T cells from cord blood	blood
38	chr12:9243000-9274800	Weak transcription	Small Intestine	intestine
39	chr12:9243400-9244600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr12:9243400-9245400	Strong transcription	Colon Smooth Muscle	Colon
41	chr12:9243400-9245600	Weak transcription	Fetal Brain Male	brain
42	chr12:9243400-9265400	Weak transcription	Fetal Muscle Leg	muscle
43	chr12:9243600-9244200	Weak transcription	Right Ventricle	heart
44	chr12:9243600-9245200	Strong transcription	Colonic Mucosa	Colon
45	chr12:9243600-9247000	Strong transcription	Fetal Lung	lung
46	chr12:9243800-9244400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr12:9243800-9245600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:9243800-9252000	Strong transcription	HepG2	liver
49	chr12:9244000-9244800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:9244200-9244600	Strong transcription	Right Ventricle	heart

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