Variant report

Variant	nsv438209
Chromosome Location	chr12:49058814-49071245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:49069482-49069483	K562	blood:	n/a	n/a
2	CEBPB	chr12:49063285-49063408	K562	blood:	n/a	n/a
3	CEBPB	chr12:49063317-49063347	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr12:49067607-49067690	A549	lung:	n/a	n/a
5	CTCF	chr12:49067646-49067698	MCF-7	breast:	n/a	n/a
6	CTCF	chr12:49067663-49067680	MCF-7	breast:	n/a	n/a
7	CTCF	chr12:49065420-49065570	A549	lung:	n/a	n/a
8	EP300	chr12:49061195-49061245	K562	blood:	n/a	n/a
9	FOS	chr12:49065116-49065438	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr12:49065070-49065546	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr12:49065090-49065588	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr12:49065198-49065538	MCF10A-Er-Src	breast:	n/a	n/a
13	FOXA2	chr12:49063027-49063160	HepG2	liver:	n/a	n/a
14	GABPA	chr12:49066249-49066350	GM12878	blood:	n/a	n/a
15	JUN	chr12:49070885-49071074	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr12:49060681-49060842	HepG2	liver:	n/a	n/a
17	POLR2A	chr12:49062655-49062692	MCF-7	breast:	n/a	n/a
18	POLR2A	chr12:49060836-49060845	MCF-7	breast:	n/a	n/a
19	POLR2A	chr12:49060847-49060945	MCF-7	breast:	n/a	n/a
20	POLR2A	chr12:49071208-49071335	K562	blood:	n/a	n/a
21	POLR2A	chr12:49062941-49063166	HepG2	liver:	n/a	n/a
22	POLR2A	chr12:49065251-49065763	GM12878	blood:	n/a	n/a
23	POLR2A	chr12:49069940-49070145	MCF-7	breast:	n/a	n/a
24	POLR2A	chr12:49065428-49065449	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr12:49069039-49069175	GM12878	blood:	n/a	n/a
26	POLR2A	chr12:49065166-49065712	GM12878	blood:	n/a	n/a
27	POLR2A	chr12:49063571-49063801	K562	blood:	n/a	n/a
28	POLR2A	chr12:49059781-49059830	HepG2	liver:	n/a	n/a
29	POLR2A	chr12:49064679-49064862	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr12:49062257-49062440	HepG2	liver:	n/a	n/a
31	POLR2A	chr12:49059712-49059746	MCF-7	breast:	n/a	n/a
32	POLR2A	chr12:49065233-49065516	GM12891	blood:	n/a	n/a
33	POLR2A	chr12:49062187-49062190	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:49067543-49067705	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr12:49062627-49062660	HepG2	liver:	n/a	n/a
36	POLR2A	chr12:49059819-49059961	GM12878	blood:	n/a	n/a
37	POLR2A	chr12:49061948-49062288	GM12878	blood:	n/a	n/a
38	POLR2A	chr12:49064475-49064919	GM12892	blood:	n/a	n/a
39	POLR2A	chr12:49064136-49064283	K562	blood:	n/a	n/a
40	POLR2A	chr12:49061221-49061393	HepG2	liver:	n/a	n/a
41	POLR2A	chr12:49064086-49064351	K562	blood:	n/a	n/a
42	POLR2A	chr12:49059535-49059997	GM12878	blood:	n/a	n/a
43	POLR2A	chr12:49062897-49062981	K562	blood:	n/a	n/a
44	POLR2A	chr12:49064081-49064399	GM12878	blood:	n/a	n/a
45	POLR2A	chr12:49060487-49060704	K562	blood:	n/a	n/a
46	POLR2A	chr12:49065283-49065515	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr12:49063481-49063848	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr12:49062800-49062999	MCF-7	breast:	n/a	n/a
49	POLR2A	chr12:49063548-49063770	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:49062170-49062246	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	chr12:49061475-49061525	SKMC	muscle:	n/a
2	chr12:49062438-49062488	HepG2	liver:	n/a
3	chr12:49061475-49061525	PANC-1	pancreas:	n/a
4	chr12:49062438-49062488	BE2_C	brain:	n/a
5	chr12:49061475-49061525	GM06990	blood:	n/a
6	chr12:49062856-49062906	GM12878	blood:	n/a
7	chr12:49062438-49062488	NHDF-neo	bronchial:	n/a
8	chr12:49061475-49061525	HCT-116	colon:	n/a
9	chr12:49061475-49061525	HEEpiC	esophagus:	n/a
10	chr12:49062856-49062906	AG04450	lung:	fetal
11	chr12:49061475-49061525	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:49062438-49062488	HUVEC	blood vessel:	n/a
13	chr12:49062856-49062906	IMR90	lung:	fetal
14	chr12:49061475-49061525	HepG2	liver:	n/a
15	chr12:49061475-49061525	BE2_C	brain:	n/a
16	chr12:49062856-49062906	ProgFib	skin:	n/a
17	chr12:49061475-49061525	IMR90	lung:	fetal
18	chr12:49062438-49062488	NHBE	bronchial:	n/a
19	chr12:49062856-49062906	HCT-116	colon:	n/a
20	chr12:49062856-49062906	NHDF-neo	bronchial:	n/a
21	chr12:49062856-49062906	NT2-D1	testis:	n/a
22	chr12:49062856-49062906	NH-A	brain:	n/a
23	chr12:49062438-49062488	BJ	skin:	n/a
24	chr12:49062856-49062906	K562	blood:	n/a
25	chr12:49062856-49062906	ECC-1	luminal epithelium:	n/a
26	chr12:49061475-49061525	K562	blood:	n/a
27	chr12:49062856-49062906	H1-hESC	embryonic stem cell:	embryo
28	chr12:49062856-49062906	PFSK-1	brain:	n/a
29	chr12:49062856-49062906	BE2_C	brain:	n/a
30	chr12:49061475-49061525	Hepatocyte	liver:	n/a
31	chr12:49061475-49061525	MCF-7	breast:	n/a
32	chr12:49062438-49062488	Jurkat	blood:	n/a
33	chr12:49061475-49061525	GM12891	blood:	n/a
34	chr12:49061475-49061525	ECC-1	luminal epithelium:	n/a
35	chr12:49062856-49062906	AG04449	skin:	fetal
36	chr12:49062856-49062906	HRCEpiC	kidney:	n/a
37	chr12:49062438-49062488	T-47D	breast:	n/a
38	chr12:49062856-49062906	PANC-1	pancreas:	n/a
39	chr12:49061475-49061525	AG04449	skin:	fetal
40	chr12:49062438-49062488	NH-A	brain:	n/a
41	chr12:49062856-49062906	BJ	skin:	n/a
42	chr12:49062438-49062488	HRE	kidney:	n/a
43	chr12:49062856-49062906	MCF10A-Er-Src	breast:	n/a
44	chr12:49061475-49061525	HEK293	kidney:	embryo
45	chr12:49062856-49062906	SAEC	small airway:	n/a
46	chr12:49062438-49062488	SK-N-MC	brain:	n/a
47	chr12:49062438-49062488	GM12891	blood:	n/a
48	chr12:49061475-49061525	HCM	heart:	n/a
49	chr12:49062856-49062906	HL-60	blood:	n/a
50	chr12:49062438-49062488	ovcar-3	ovarian:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:49065590..49067167-chr12:49068340..49070785,2	K562	blood:
2	chr12:49065590..49067167-chr12:49068340..49070785,2	K562	blood:
3	chr12:49063053..49065841-chr12:49108552..49110701,2	K562	blood:
4	chr12:49052583..49059422-chr12:49071692..49076510,9	K562	blood:
5	chr12:49059501..49061624-chr12:49071853..49074328,2	K562	blood:
6	chr12:49057472..49060439-chr12:49061478..49064555,3	K562	blood:
7	chr12:49055791..49059056-chr12:49060422..49062626,3	MCF-7	breast:
8	chr12:49055891..49058972-chr12:49060822..49063197,4	K562	blood:
9	chr12:49071141..49073350-chr12:49108510..49110706,2	K562	blood:
10	chr12:49066447..49069366-chr12:49075089..49076869,2	MCF-7	breast:
11	chr12:49069459..49071260-chr12:49074212..49076184,2	MCF-7	breast:
12	chr12:49054189..49057394-chr12:49060673..49063657,4	K562	blood:
13	chr12:49057922..49061014-chr12:49074365..49076510,4	K562	blood:
14	chr12:49055791..49059056-chr12:49060422..49062626,3	MCF-7	breast:
15	chr12:49055891..49058972-chr12:49060822..49063197,4	K562	blood:
16	chr12:48933826..48935713-chr12:49066983..49069233,2	MCF-7	breast:

No data

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

Extended variants
information (count: 505 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4500528	chr12:49058814-49058815	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140975002	chr12:49058820-49058821	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs112164415	chr12:49058822-49058823	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536428551	chr12:49058829-49058830	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs536666564	chr12:49058863-49058864	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs553496808	chr12:49058880-49058881	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573377836	chr12:49058886-49058887	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545051177	chr12:49058910-49058911	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558667721	chr12:49058914-49058915	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558549057	chr12:49058978-49058979	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544227389	chr12:49059069-49059070	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371901213	chr12:49059073-49059074	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553404634	chr12:49059074-49059075	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182615559	chr12:49059080-49059081	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188014596	chr12:49059226-49059227	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78888641	chr12:49059329-49059330	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs75586368	chr12:49059332-49059333	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76259769	chr12:49059333-49059334	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75369053	chr12:49059338-49059339	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534748650	chr12:49059385-49059386	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542580344	chr12:49059393-49059394	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559454780	chr12:49059396-49059397	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370537515	chr12:49059428-49059429	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554403536	chr12:49059475-49059476	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs375644693	chr12:49059503-49059504	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs116884389	chr12:49059553-49059554	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192993841	chr12:49059567-49059568	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs56034061	chr12:49059641-49059642	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368600066	chr12:49059691-49059692	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs141835477	chr12:49059692-49059693	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542744334	chr12:49059753-49059754	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs550585027	chr12:49059794-49059795	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs146255165	chr12:49059813-49059814	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577644876	chr12:49059911-49059912	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560665122	chr12:49059912-49059913	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543302367	chr12:49059932-49059933	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs111720759	chr12:49059983-49059984	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182669801	chr12:49060003-49060004	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs558606020	chr12:49060019-49060020	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150011150	chr12:49060021-49060022	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs561583400	chr12:49060078-49060079	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537967482	chr12:49060090-49060091	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs111725923	chr12:49060103-49060104	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs538633698	chr12:49060106-49060107	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs574746675	chr12:49060114-49060115	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs77388107	chr12:49060161-49060162	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs77538349	chr12:49060164-49060165	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs374409034	chr12:49060177-49060178	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs148721887	chr12:49060182-49060183	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564954651	chr12:49060184-49060185	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49036800-49072000	Strong transcription	Liver	Liver
2	chr12:49037800-49072400	Strong transcription	Placenta	Placenta
3	chr12:49038200-49070800	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr12:49038400-49060600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr12:49038800-49071800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:49039000-49072200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:49039400-49068800	Weak transcription	Right Atrium	heart
8	chr12:49039400-49071800	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:49039800-49071000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:49039800-49071000	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr12:49040000-49059400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:49040000-49072600	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr12:49040400-49060600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:49040400-49072800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:49041000-49071800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:49041200-49061200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr12:49041200-49068200	Strong transcription	Stomach Smooth Muscle	stomach
18	chr12:49041600-49065200	Weak transcription	Stomach Mucosa	stomach
19	chr12:49041800-49065200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:49041800-49070800	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr12:49041800-49071000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr12:49041800-49072400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr12:49041800-49073800	Strong transcription	Fetal Intestine Large	intestine
24	chr12:49042400-49065200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr12:49042400-49072800	Strong transcription	Fetal Muscle Leg	muscle
26	chr12:49042600-49064200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:49043800-49068800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:49044000-49068200	Strong transcription	Duodenum Mucosa	Duodenum
29	chr12:49044200-49059800	Strong transcription	A549	lung
30	chr12:49044200-49071000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr12:49044200-49072400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:49044200-49072800	Strong transcription	Fetal Thymus	thymus
33	chr12:49044400-49065200	Strong transcription	Osteobl	bone
34	chr12:49044400-49071000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:49044400-49071400	Strong transcription	Thymus	Thymus
36	chr12:49044400-49072400	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:49044600-49072400	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr12:49044800-49068000	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr12:49044800-49071200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr12:49045000-49067600	Strong transcription	Left Ventricle	heart
41	chr12:49045000-49071600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:49045200-49068200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:49045200-49069400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr12:49045200-49070400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr12:49045400-49072600	Strong transcription	Primary B cells from peripheral blood	blood
46	chr12:49045600-49071800	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr12:49045600-49072400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:49045600-49073400	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr12:49046200-49067400	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr12:49046200-49072600	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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