Variant report

Variant	nsv1052256
Chromosome Location	chr12:49048506-49065987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:490)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:49053671-49054067	ECC-1	luminal epithelium:	n/a	n/a
2	CEBPB	chr12:49053672-49054042	K562	blood:	n/a	n/a
3	CEBPB	chr12:49053616-49054097	A549	lung:	n/a	n/a
4	CEBPB	chr12:49053691-49054078	A549	lung:	n/a	n/a
5	CEBPB	chr12:49063285-49063408	K562	blood:	n/a	n/a
6	CEBPB	chr12:49053670-49054037	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:49063317-49063347	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:49053677-49054033	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:49053702-49054026	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:49053676-49054038	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:49053678-49054022	A549	lung:	n/a	n/a
12	CEBPB	chr12:49053725-49053965	K562	blood:	n/a	n/a
13	CEBPB	chr12:49053699-49054034	MCF-7	breast:	n/a	n/a
14	CTCF	chr12:49065420-49065570	A549	lung:	n/a	n/a
15	EP300	chr12:49061195-49061245	K562	blood:	n/a	n/a
16	FOS	chr12:49056764-49056874	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr12:49065090-49065588	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr12:49065070-49065546	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:49065198-49065538	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr12:49065116-49065438	MCF10A-Er-Src	breast:	n/a	n/a
21	FOXA2	chr12:49063027-49063160	HepG2	liver:	n/a	n/a
22	HEY1	chr12:49057878-49058111	K562	blood:	n/a	n/a
23	MAFK	chr12:49052166-49052226	HepG2	liver:	n/a	chr12:49052178-49052192 chr12:49052180-49052191
24	POLR2A	chr12:49057902-49058053	HepG2	liver:	n/a	n/a
25	POLR2A	chr12:49058253-49058289	HepG2	liver:	n/a	n/a
26	POLR2A	chr12:49062419-49062666	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr12:49059747-49059963	MCF-7	breast:	n/a	n/a
28	POLR2A	chr12:49064550-49065018	GM12878	blood:	n/a	n/a
29	POLR2A	chr12:49052653-49052880	MCF-7	breast:	n/a	n/a
30	POLR2A	chr12:49054711-49054720	MCF-7	breast:	n/a	n/a
31	POLR2A	chr12:49052277-49052465	HepG2	liver:	n/a	n/a
32	POLR2A	chr12:49064679-49064862	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr12:49060681-49060842	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:49060859-49060902	MCF-7	breast:	n/a	n/a
35	POLR2A	chr12:49054563-49054634	ProgFib	skin:	n/a	n/a
36	POLR2A	chr12:49049205-49049285	MCF-7	breast:	n/a	n/a
37	POLR2A	chr12:49051943-49051960	MCF-7	breast:	n/a	n/a
38	POLR2A	chr12:49059535-49059997	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:49050779-49050991	GM12878	blood:	n/a	n/a
40	POLR2A	chr12:49056685-49056854	MCF-7	breast:	n/a	n/a
41	POLR2A	chr12:49064607-49064764	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr12:49060487-49060704	K562	blood:	n/a	n/a
43	POLR2A	chr12:49050344-49050648	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:49064825-49064843	MCF-7	breast:	n/a	n/a
45	POLR2A	chr12:49065251-49065763	GM12878	blood:	n/a	n/a
46	POLR2A	chr12:49054071-49054389	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr12:49053010-49053031	MCF-7	breast:	n/a	n/a
48	POLR2A	chr12:49062941-49063166	HepG2	liver:	n/a	n/a
49	POLR2A	chr12:49047803-49048518	K562	blood:	n/a	n/a
50	POLR2A	chr12:49051198-49051950	HepG2	liver:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49061475-49061525	HCT-116	colon:	n/a
2	chr12:49050713-49050763	HCPEpiC	choroid plexus:	n/a
3	chr12:49061475-49061525	HCT-116	colon:	n/a
4	chr12:49050713-49050763	HCPEpiC	choroid plexus:	n/a
5	chr12:49051651-49051701	SKMC	muscle:	n/a
6	chr12:49048478-49048528	NH-A	brain:	n/a
7	chr12:49062856-49062906	SK-N-SH	brain:	n/a
8	chr12:49061475-49061525	SK-N-SH	brain:	n/a
9	chr12:49062856-49062906	HCT-116	colon:	n/a
10	chr12:49050713-49050763	HUVEC	blood vessel:	n/a
11	chr12:49051651-49051701	T-47D	breast:	n/a
12	chr12:49051651-49051701	AG09309	skin:	n/a
13	chr12:49048478-49048528	HCM	heart:	n/a
14	chr12:49051651-49051701	HEEpiC	esophagus:	n/a
15	chr12:49050903-49050953	HCPEpiC	choroid plexus:	n/a
16	chr12:49051651-49051701	HepG2	liver:	n/a
17	chr12:49050903-49050953	HAEpiC	amniotic membrane:	n/a
18	chr12:49062438-49062488	HIPEpiC	eye:	n/a
19	chr12:49050460-49050510	HRE	kidney:	n/a
20	chr12:49048478-49048528	NT2-D1	testis:	n/a
21	chr12:49048478-49048528	SK-N-SH_RA	brain:	n/a
22	chr12:49050713-49050763	HCF	heart:	n/a
23	chr12:49062438-49062488	HCPEpiC	choroid plexus:	n/a
24	chr12:49050713-49050763	K562	blood:	n/a
25	chr12:49062856-49062906	AG10803	skin:	n/a
26	chr12:49050713-49050763	AG09319	gingival:	n/a
27	chr12:49050713-49050763	ECC-1	luminal epithelium:	n/a
28	chr12:49048478-49048528	LNCaP	prostate:	n/a
29	chr12:49050713-49050763	AG04449	skin:	fetal
30	chr12:49050460-49050510	NT2-D1	testis:	n/a
31	chr12:49050713-49050763	Jurkat	blood:	n/a
32	chr12:49050460-49050510	HCPEpiC	choroid plexus:	n/a
33	chr12:49062438-49062488	HCT-116	colon:	n/a
34	chr12:49050903-49050953	NB4	blood:	n/a
35	chr12:49050460-49050510	HRPEpiC	eye:	n/a
36	chr12:49050713-49050763	LNCaP	prostate:	n/a
37	chr12:49050460-49050510	AG10803	skin:	n/a
38	chr12:49050460-49050510	GM12891	blood:	n/a
39	chr12:49048478-49048528	IMR90	lung:	fetal
40	chr12:49061475-49061525	NHBE	bronchial:	n/a
41	chr12:49061475-49061525	MCF-7	breast:	n/a
42	chr12:49050903-49050953	PANC-1	pancreas:	n/a
43	chr12:49048478-49048528	NB4	blood:	n/a
44	chr12:49062438-49062488	MCF-7	breast:	n/a
45	chr12:49051651-49051701	SAEC	small airway:	n/a
46	chr12:49050460-49050510	AoSMC	blood vessel:	n/a
47	chr12:49050903-49050953	BE2_C	brain:	n/a
48	chr12:49050713-49050763	MCF-7	breast:	n/a
49	chr12:49050903-49050953	PFSK-1	brain:	n/a
50	chr12:49051651-49051701	LNCaP	prostate:	n/a

(count:20 , 50 per page) page: 1

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

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
ENSG00000221491	chromatin interactions
ENSG00000139620	chromatin interactions
ENSG00000206612	chromatin interactions
ENSG00000129315	chromatin interactions
ENSG00000207313	chromatin interactions

Extended variants
information (count: 725 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17238458	chr12:49048506-49048507	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78989778	chr12:49048533-49048534	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs74693075	chr12:49048534-49048535	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553838883	chr12:49048583-49048584	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139236103	chr12:49048602-49048603	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545853662	chr12:49048653-49048654	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553792341	chr12:49048663-49048664	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572108198	chr12:49048669-49048670	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371113486	chr12:49048702-49048703	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374488532	chr12:49048731-49048732	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs188565949	chr12:49048733-49048734	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs3741628	chr12:49048738-49048739	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs191760160	chr12:49048757-49048758	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184048897	chr12:49048781-49048782	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529908395	chr12:49048841-49048842	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540480648	chr12:49048855-49048856	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374093731	chr12:49048861-49048862	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374159623	chr12:49048866-49048867	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368081073	chr12:49048875-49048876	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532268354	chr12:49048896-49048897	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552003382	chr12:49048939-49048940	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576425547	chr12:49048950-49048951	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200583816	chr12:49048964-49048965	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs6580690	chr12:49048985-49048986	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs531209624	chr12:49049010-49049011	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116615200	chr12:49049013-49049014	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568454710	chr12:49049047-49049048	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561684401	chr12:49049108-49049109	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534121140	chr12:49049117-49049118	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554370591	chr12:49049118-49049119	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs571710332	chr12:49049123-49049124	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs539884457	chr12:49049127-49049128	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542281413	chr12:49049212-49049213	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs59304927	chr12:49049213-49049214	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560671405	chr12:49049214-49049215	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs200332389	chr12:49049351-49049352	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs78886616	chr12:49049353-49049354	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs57078760	chr12:49049365-49049366	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7484753	chr12:49049368-49049369	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs114820475	chr12:49049401-49049402	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187619634	chr12:49049421-49049422	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561087007	chr12:49049428-49049429	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs371230661	chr12:49049432-49049433	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540414619	chr12:49049476-49049477	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190431872	chr12:49049520-49049521	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560259459	chr12:49049537-49049538	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528180108	chr12:49049595-49049596	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs576986040	chr12:49049598-49049599	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs531334251	chr12:49049610-49049611	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs115594702	chr12:49049665-49049666	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 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:462 , 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	chr12:49037800-49056600	Strong transcription	Fetal Muscle Trunk	muscle
3	chr12:49037800-49072400	Strong transcription	Placenta	Placenta
4	chr12:49038200-49070800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr12:49038400-49060600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr12:49038800-49071800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:49039000-49072200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:49039400-49068800	Weak transcription	Right Atrium	heart
9	chr12:49039400-49071800	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:49039800-49071000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:49039800-49071000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr12:49040000-49057000	Strong transcription	Dnd41	blood
13	chr12:49040000-49059400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:49040000-49072600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:49040400-49051800	Strong transcription	HSMM	muscle
16	chr12:49040400-49060600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:49040400-49072800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:49041000-49071800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:49041200-49061200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr12:49041200-49068200	Strong transcription	Stomach Smooth Muscle	stomach
21	chr12:49041600-49065200	Weak transcription	Stomach Mucosa	stomach
22	chr12:49041800-49054400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr12:49041800-49065200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:49041800-49070800	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr12:49041800-49071000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr12:49041800-49072400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr12:49041800-49073800	Strong transcription	Fetal Intestine Large	intestine
28	chr12:49042400-49056800	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr12:49042400-49065200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:49042400-49072800	Strong transcription	Fetal Muscle Leg	muscle
31	chr12:49042600-49064200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr12:49043000-49049400	Strong transcription	Primary hematopoietic stem cells	blood
33	chr12:49043400-49049200	Strong transcription	Brain Cingulate Gyrus	brain
34	chr12:49043600-49054600	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr12:49043800-49057600	Strong transcription	Muscle Satellite Cultured Cells	--
36	chr12:49043800-49068800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:49044000-49055000	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr12:49044000-49068200	Strong transcription	Duodenum Mucosa	Duodenum
39	chr12:49044200-49056600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:49044200-49057000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:49044200-49059800	Strong transcription	A549	lung
42	chr12:49044200-49071000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr12:49044200-49072400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr12:49044200-49072800	Strong transcription	Fetal Thymus	thymus
45	chr12:49044400-49056400	Strong transcription	Primary T cells from cord blood	blood
46	chr12:49044400-49056600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:49044400-49057000	Strong transcription	NHEK	skin
48	chr12:49044400-49065200	Strong transcription	Osteobl	bone
49	chr12:49044400-49071000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:49044400-49071400	Strong transcription	Thymus	Thymus

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