Variant report

Variant	nsv1043220
Chromosome Location	chr12:49045458-49065987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:279)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr12:49045353-49045942	K562	blood:	n/a	n/a
2	CEBPB	chr12:49053678-49054022	A549	lung:	n/a	n/a
3	CEBPB	chr12:49053699-49054034	MCF-7	breast:	n/a	n/a
4	CEBPB	chr12:49053725-49053965	K562	blood:	n/a	n/a
5	CEBPB	chr12:49053670-49054037	IMR90	lung:	n/a	n/a
6	CEBPB	chr12:49053616-49054097	A549	lung:	n/a	n/a
7	CEBPB	chr12:49053676-49054038	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:49053671-49054067	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr12:49053677-49054033	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:49053672-49054042	K562	blood:	n/a	n/a
11	CEBPB	chr12:49053691-49054078	A549	lung:	n/a	n/a
12	CEBPB	chr12:49063317-49063347	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:49063285-49063408	K562	blood:	n/a	n/a
14	CEBPB	chr12:49053702-49054026	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr12:49065420-49065570	A549	lung:	n/a	n/a
16	EP300	chr12:49061195-49061245	K562	blood:	n/a	n/a
17	FOS	chr12:49065198-49065538	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr12:49065070-49065546	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:49065090-49065588	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr12:49056764-49056874	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr12:49065116-49065438	MCF10A-Er-Src	breast:	n/a	n/a
22	FOSL2	chr12:49045133-49045465	HepG2	liver:	n/a	n/a
23	FOXA2	chr12:49063027-49063160	HepG2	liver:	n/a	n/a
24	GTF2F1	chr12:49045463-49045660	Hela-S3	cervix:	n/a	n/a
25	HEY1	chr12:49057878-49058111	K562	blood:	n/a	n/a
26	MAFF	chr12:49045522-49045838	HepG2	liver:	n/a	chr12:49045580-49045594 chr12:49045655-49045673
27	MAFK	chr12:49045588-49045830	HepG2	liver:	n/a	chr12:49045658-49045669 chr12:49045656-49045670 chr12:49045657-49045668 chr12:49045657-49045672 chr12:49045657-49045668 chr12:49045658-49045669
28	MAFK	chr12:49045553-49045759	Hela-S3	cervix:	n/a	chr12:49045658-49045669 chr12:49045656-49045670 chr12:49045657-49045668 chr12:49045657-49045672 chr12:49045657-49045668 chr12:49045580-49045594 chr12:49045658-49045669 chr12:49045579-49045595
29	MAFK	chr12:49045491-49045837	HepG2	liver:	n/a	chr12:49045658-49045669 chr12:49045656-49045670 chr12:49045657-49045668 chr12:49045657-49045672 chr12:49045657-49045668 chr12:49045580-49045594 chr12:49045658-49045669 chr12:49045579-49045595
30	MAFK	chr12:49052166-49052226	HepG2	liver:	n/a	chr12:49052178-49052192 chr12:49052180-49052191
31	MTA3	chr12:49045189-49045771	GM12878	blood:	n/a	n/a
32	NFATC1	chr12:49044969-49045586	GM12878	blood:	n/a	n/a
33	PML	chr12:49046344-49046766	K562	blood:	n/a	n/a
34	PML	chr12:49045392-49045945	GM12878	blood:	n/a	n/a
35	POLR2A	chr12:49062800-49062999	MCF-7	breast:	n/a	n/a
36	POLR2A	chr12:49063571-49063801	K562	blood:	n/a	n/a
37	POLR2A	chr12:49056323-49057495	HepG2	liver:	n/a	n/a
38	POLR2A	chr12:49055512-49055693	HepG2	liver:	n/a	n/a
39	POLR2A	chr12:49048083-49048399	GM12892	blood:	n/a	n/a
40	POLR2A	chr12:49046171-49046273	GM12878	blood:	n/a	n/a
41	POLR2A	chr12:49051612-49051625	MCF-7	breast:	n/a	n/a
42	POLR2A	chr12:49055406-49055842	GM12892	blood:	n/a	n/a
43	POLR2A	chr12:49065428-49065449	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr12:49056101-49056542	PFSK-1	brain:	n/a	n/a
45	POLR2A	chr12:49056826-49056834	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr12:49045052-49045625	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr12:49046771-49046881	GM12878	blood:	n/a	n/a
48	POLR2A	chr12:49047245-49047659	K562	blood:	n/a	n/a
49	POLR2A	chr12:49044772-49045689	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr12:49045424-49045544	HepG2	liver:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49048323-49048373	AoSMC	blood vessel:	n/a
2	chr12:49051651-49051701	HCF	heart:	n/a
3	chr12:49051651-49051701	NH-A	brain:	n/a
4	chr12:49062438-49062488	HEK293	kidney:	embryo
5	chr12:49050903-49050953	LNCaP	prostate:	n/a
6	chr12:49048478-49048528	HCT-116	colon:	n/a
7	chr12:49050460-49050510	HRCEpiC	kidney:	n/a
8	chr12:49048478-49048528	HAEpiC	amniotic membrane:	n/a
9	chr12:49050713-49050763	Caco-2	colon:	n/a
10	chr12:49048323-49048373	HUVEC	blood vessel:	n/a
11	chr12:49048323-49048373	BE2_C	brain:	n/a
12	chr12:49062438-49062488	GM12891	blood:	n/a
13	chr12:49062438-49062488	RPTEC	kidney:	n/a
14	chr12:49048323-49048373	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:49048478-49048528	T-47D	breast:	n/a
16	chr12:49051651-49051701	ProgFib	skin:	n/a
17	chr12:49062438-49062488	BE2_C	brain:	n/a
18	chr12:49048478-49048528	IMR90	lung:	fetal
19	chr12:49048478-49048528	NHDF-neo	bronchial:	n/a
20	chr12:49048478-49048528	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:49062438-49062488	HRPEpiC	eye:	n/a
22	chr12:49050713-49050763	MCF-7	breast:	n/a
23	chr12:49062856-49062906	SK-N-MC	brain:	n/a
24	chr12:49061475-49061525	GM06990	blood:	n/a
25	chr12:49050460-49050510	Caco-2	colon:	n/a
26	chr12:49050713-49050763	GM19239	blood:	n/a
27	chr12:49051651-49051701	CMK	blood:	n/a
28	chr12:49050903-49050953	Caco-2	colon:	n/a
29	chr12:49062438-49062488	BJ	skin:	n/a
30	chr12:49050460-49050510	HUVEC	blood vessel:	n/a
31	chr12:49051651-49051701	HepG2	liver:	n/a
32	chr12:49050903-49050953	HCF	heart:	n/a
33	chr12:49062438-49062488	Jurkat	blood:	n/a
34	chr12:49050903-49050953	ECC-1	luminal epithelium:	n/a
35	chr12:49051651-49051701	SK-N-SH	brain:	n/a
36	chr12:49050460-49050510	NH-A	brain:	n/a
37	chr12:49061475-49061525	PFSK-1	brain:	n/a
38	chr12:49062438-49062488	HUVEC	blood vessel:	n/a
39	chr12:49050460-49050510	NT2-D1	testis:	n/a
40	chr12:49062438-49062488	PANC-1	pancreas:	n/a
41	chr12:49050903-49050953	HRCEpiC	kidney:	n/a
42	chr12:49062438-49062488	HMEC	breast:	n/a
43	chr12:49051651-49051701	NHDF-neo	bronchial:	n/a
44	chr12:49050903-49050953	GM19239	blood:	n/a
45	chr12:49050713-49050763	HMEC	breast:	n/a
46	chr12:49062438-49062488	Caco-2	colon:	n/a
47	chr12:49051651-49051701	GM12878	blood:	n/a
48	chr12:49048478-49048528	AG09309	skin:	n/a
49	chr12:49061475-49061525	Hepatocyte	liver:	n/a
50	chr12:49048323-49048373	PrEC	prostate:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:49049545..49052092-chr12:49054304..49056885,2	K562	blood:
2	chr12:49065590..49067167-chr12:49068340..49070785,2	K562	blood:
3	chr12:49048440..49050280-chr12:49074964..49076966,2	MCF-7	breast:
4	chr12:49049545..49052092-chr12:49054304..49056885,2	K562	blood:
5	chr12:49055891..49058972-chr12:49060822..49063197,4	K562	blood:
6	chr12:49054189..49057394-chr12:49060673..49063657,4	K562	blood:
7	chr12:49055791..49059056-chr12:49060422..49062626,3	MCF-7	breast:
8	chr12:49063053..49065841-chr12:49108552..49110701,2	K562	blood:
9	chr12:49055891..49058972-chr12:49060822..49063197,4	K562	blood:
10	chr12:49041453..49045537-chr12:49046563..49050434,5	MCF-7	breast:
11	chr12:49059501..49061624-chr12:49071853..49074328,2	K562	blood:
12	chr12:49028821..49031213-chr12:49054853..49056356,2	MCF-7	breast:
13	chr12:49046239..49048123-chr12:49073904..49075607,2	MCF-7	breast:
14	chr12:49044206..49046725-chr12:49074611..49077605,2	K562	blood:
15	chr12:49046686..49049905-chr12:49054030..49058402,3	K562	blood:
16	chr12:49043504..49045672-chr12:49045695..49048721,3	MCF-7	breast:
17	chr12:49046686..49049905-chr12:49054030..49058402,3	K562	blood:
18	chr12:49054189..49057394-chr12:49060673..49063657,4	K562	blood:
19	chr12:49052650..49057544-chr12:49071692..49076123,6	K562	blood:
20	chr12:49052583..49059422-chr12:49071692..49076510,9	K562	blood:
21	chr12:49057472..49060439-chr12:49061478..49064555,3	K562	blood:
22	chr12:49055791..49059056-chr12:49060422..49062626,3	MCF-7	breast:
23	chr12:49049997..49051694-chr12:49071950..49074374,2	K562	blood:
24	chr12:49057922..49061014-chr12:49074365..49076510,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNT1-3	chr12:49047221-49047641	NONHSAT028010

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1291	chr12:49048277-49048300	MIMAT0005881

No data

Variant related genes	Relation type
SNORA2A	TF binding region
SNORA34	TF binding region
SNORA2B	TF binding region
KANSL2	TF binding region
SNORA2A	CpG island
SNORA34	CpG island
SNORA2B	CpG island
KANSL2	CpG island
ENSG00000129315	chromatin interactions
ENSG00000207313	chromatin interactions
ENSG00000206612	chromatin interactions
ENSG00000139620	chromatin interactions
ENSG00000221491	chromatin interactions

Extended variants
information (count: 836 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145115480	chr12:49045458-49045459	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs186927762	chr12:49045462-49045463	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372295600	chr12:49045494-49045495	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560091017	chr12:49045495-49045496	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531512495	chr12:49045577-49045578	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528654353	chr12:49045609-49045610	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113046367	chr12:49045655-49045656	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562813871	chr12:49045658-49045659	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs200764189	chr12:49045685-49045686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545315563	chr12:49045710-49045711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs577535845	chr12:49045774-49045775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549842032	chr12:49045781-49045782	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544965229	chr12:49045782-49045783	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147573759	chr12:49045785-49045786	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559925858	chr12:49045793-49045794	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140296251	chr12:49045800-49045801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs142223477	chr12:49045805-49045806	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567295931	chr12:49045826-49045827	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs6580689	chr12:49045831-49045832	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs548825354	chr12:49045838-49045839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs151212414	chr12:49045850-49045851	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534506619	chr12:49045852-49045853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557696594	chr12:49045862-49045863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116840563	chr12:49045873-49045874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536711665	chr12:49045894-49045895	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557040823	chr12:49045934-49045935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs71439456	chr12:49046029-49046030	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573631545	chr12:49046044-49046045	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190218272	chr12:49046065-49046066	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529149016	chr12:49046170-49046171	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553690992	chr12:49046197-49046198	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150356612	chr12:49046270-49046271	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545571142	chr12:49046272-49046273	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34491897	chr12:49046304-49046305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs398019457	chr12:49046323-49046324	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs529461825	chr12:49046348-49046349	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs77473644	chr12:49046485-49046486	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373416010	chr12:49046505-49046506	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs11838121	chr12:49046526-49046527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182226693	chr12:49046648-49046649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112951176	chr12:49046676-49046677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546637504	chr12:49046737-49046738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11835040	chr12:49046768-49046769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs528410519	chr12:49046806-49046807	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11837337	chr12:49046815-49046816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs571324270	chr12:49046844-49046845	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537251781	chr12:49046852-49046853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146481152	chr12:49046853-49046854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567407990	chr12:49046858-49046859	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78628665	chr12:49046894-49046895	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49027600-49046600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:49030000-49047200	Weak transcription	Esophagus	oesophagus
3	chr12:49034600-49045800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:49035000-49045600	Weak transcription	K562	blood
5	chr12:49035200-49046800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:49035400-49046200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:49035400-49047000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr12:49035400-49047000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:49035800-49046800	Weak transcription	Gastric	stomach
10	chr12:49035800-49046800	Weak transcription	Ovary	ovary
11	chr12:49036000-49045600	Weak transcription	Right Ventricle	heart
12	chr12:49036800-49072000	Strong transcription	Liver	Liver
13	chr12:49037000-49046600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:49037000-49046800	Weak transcription	NHLF	lung
15	chr12:49037200-49045600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr12:49037200-49045800	Weak transcription	Fetal Kidney	kidney
17	chr12:49037200-49046400	Weak transcription	HUVEC	blood vessel
18	chr12:49037400-49045600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr12:49037400-49045600	Weak transcription	Fetal Lung	lung
20	chr12:49037400-49046400	Weak transcription	Brain Germinal Matrix	brain
21	chr12:49037400-49046800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr12:49037400-49047400	Weak transcription	Fetal Brain Male	brain
23	chr12:49037800-49056600	Strong transcription	Fetal Muscle Trunk	muscle
24	chr12:49037800-49072400	Strong transcription	Placenta	Placenta
25	chr12:49038200-49070800	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr12:49038400-49045600	Weak transcription	HSMMtube	muscle
27	chr12:49038400-49060600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr12:49038800-49071800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:49039000-49072200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:49039200-49046400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:49039200-49047600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr12:49039400-49068800	Weak transcription	Right Atrium	heart
33	chr12:49039400-49071800	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:49039800-49071000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:49039800-49071000	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr12:49040000-49057000	Strong transcription	Dnd41	blood
37	chr12:49040000-49059400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr12:49040000-49072600	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:49040200-49047800	Weak transcription	Pancreas	Pancrea
40	chr12:49040400-49047400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr12:49040400-49051800	Strong transcription	HSMM	muscle
42	chr12:49040400-49060600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:49040400-49072800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:49041000-49046400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr12:49041000-49046400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr12:49041000-49046400	Weak transcription	Hela-S3	cervix
47	chr12:49041000-49047400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:49041000-49071800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:49041200-49061200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr12:49041200-49068200	Strong transcription	Stomach Smooth Muscle	stomach

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