Variant report

Variant	esv11695
Chromosome Location	chr12:31904381-31911808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:212)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:212 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31909974-31910231	HepG2	liver:	n/a	n/a
2	ATF1	chr12:31910164-31910364	K562	blood:	n/a	n/a
3	ATF3	chr12:31909916-31910330	K562	blood:	n/a	n/a
4	BATF	chr12:31911249-31911568	GM12878	blood:	n/a	chr12:31911426-31911437 chr12:31911370-31911381
5	BHLHE40	chr12:31909902-31910373	K562	blood:	n/a	n/a
6	BHLHE40	chr12:31910013-31910250	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:31905586-31905714	GM12878	blood:	n/a	n/a
8	BRCA1	chr12:31905289-31905411	GM12878	blood:	n/a	n/a
9	CBX3	chr12:31911178-31911673	HCT-116	colon:	n/a	n/a
10	CBX3	chr12:31909939-31910274	K562	blood:	n/a	n/a
11	CCNT2	chr12:31909897-31910312	K562	blood:	n/a	n/a
12	CEBPB	chr12:31910003-31910337	K562	blood:	n/a	n/a
13	CEBPB	chr12:31909759-31910308	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr12:31909882-31910292	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr12:31909944-31910464	K562	blood:	n/a	n/a
16	CEBPD	chr12:31909935-31910418	K562	blood:	n/a	n/a
17	CHD1	chr12:31904911-31905466	GM12878	blood:	n/a	n/a
18	CHD1	chr12:31909867-31909939	GM12878	blood:	n/a	n/a
19	CHD1	chr12:31908725-31908765	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr12:31903052-31904416	GM12878	blood:	n/a	n/a
21	CHD2	chr12:31905006-31905711	GM12878	blood:	n/a	n/a
22	CHD2	chr12:31909894-31910240	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr12:31909937-31910197	GM12878	blood:	n/a	n/a
24	CUX1	chr12:31905302-31905839	GM12878	blood:	n/a	n/a
25	E2F4	chr12:31911350-31911662	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr12:31904754-31904919	GM12878	blood:	n/a	n/a
27	EBF1	chr12:31905259-31905832	GM12878	blood:	n/a	n/a
28	EBF1	chr12:31909871-31910215	GM12878	blood:	n/a	n/a
29	ELK1	chr12:31906093-31906094	GM12878	blood:	n/a	n/a
30	EP300	chr12:31910040-31910050	GM12878	blood:	n/a	n/a
31	EP300	chr12:31909947-31910259	Hela-S3	cervix:	n/a	n/a
32	EP300	chr12:31903812-31904819	ECC-1	luminal epithelium:	n/a	n/a
33	EP300	chr12:31909876-31910350	K562	blood:	n/a	n/a
34	EP300	chr12:31905474-31905761	K562	blood:	n/a	n/a
35	EP300	chr12:31904936-31905120	K562	blood:	n/a	n/a
36	EP300	chr12:31904853-31905276	GM12878	blood:	n/a	n/a
37	EP300	chr12:31909938-31910378	HepG2	liver:	n/a	n/a
38	EP300	chr12:31905520-31905835	GM12878	blood:	n/a	n/a
39	EP300	chr12:31904954-31905407	GM12878	blood:	n/a	n/a
40	EP300	chr12:31909621-31910599	ECC-1	luminal epithelium:	n/a	n/a
41	EP300	chr12:31909764-31910397	ECC-1	luminal epithelium:	n/a	n/a
42	ESRRA	chr12:31902945-31906220	GM12878	blood:	n/a	chr12:31905114-31905124 chr12:31905112-31905124 chr12:31905112-31905125 chr12:31905114-31905124
43	FOS	chr12:31911230-31911624	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr12:31911229-31911640	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr12:31911225-31911580	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr12:31904492-31904659	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr12:31909933-31910230	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr12:31911207-31911650	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr12:31909931-31910254	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr12:31909932-31910232	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31906089..31908319-chr12:31910376..31912978,2	K562	blood:
2	chr12:31902147..31904881-chr12:32110992..32113730,2	MCF-7	breast:
3	chr12:31902284..31904041-chr12:31909797..31911614,2	K562	blood:
4	chr12:31880235..31884620-chr12:31906466..31910642,5	K562	blood:
5	chr12:31900170..31902250-chr12:31904037..31906770,3	MCF-7	breast:
6	chr12:31901665..31904041-chr12:31908599..31911297,2	K562	blood:
7	chr12:31884351..31886609-chr12:31902358..31904418,2	MCF-7	breast:
8	chr12:31880356..31882113-chr12:31908651..31911633,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-H3F3C-1	chr12:31906082-31906270	XLOC_010043

No data

Variant related genes	Relation type
ENSG00000223722	TF binding region
ENSG00000256843	TF binding region
ENSG00000151743	chromatin interactions
ENSG00000223722	chromatin interactions
ENSG00000256843	chromatin interactions
ENSG00000174718	chromatin interactions
MEOX2	miRNA target sites

Extended variants
information (count: 291 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563412746	chr12:31904467-31904468	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs7954275	chr12:31904510-31904511	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7954354	chr12:31904528-31904529	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs191514643	chr12:31904531-31904532	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs140901883	chr12:31904537-31904538	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs11051560	chr12:31904556-31904557	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11833397	chr12:31904558-31904559	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561902244	chr12:31904597-31904598	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs142384214	chr12:31904632-31904633	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs544544518	chr12:31904651-31904652	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs564426293	chr12:31904668-31904669	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs78960882	chr12:31904686-31904687	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs182830676	chr12:31904687-31904688	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs11051561	chr12:31904695-31904696	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs151301607	chr12:31904717-31904718	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs117358315	chr12:31904774-31904775	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs11051562	chr12:31904794-31904795	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186833355	chr12:31904805-31904806	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs372364343	chr12:31904813-31904814	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs568134148	chr12:31904816-31904817	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs571919507	chr12:31904823-31904824	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs191252391	chr12:31904831-31904832	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs564637955	chr12:31904832-31904833	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs183568565	chr12:31904870-31904871	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs200941809	chr12:31904879-31904880	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs551703461	chr12:31904881-31904882	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs117674180	chr12:31904961-31904962	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs370343150	chr12:31904990-31904991	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555478046	chr12:31905005-31905006	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs11051564	chr12:31905053-31905054	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544434077	chr12:31905055-31905056	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187866784	chr12:31905068-31905069	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533259891	chr12:31905073-31905074	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540153278	chr12:31905095-31905096	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560570342	chr12:31905106-31905107	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs140583551	chr12:31905130-31905131	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548939963	chr12:31905162-31905163	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562659781	chr12:31905189-31905190	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77614737	chr12:31905190-31905191	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150494594	chr12:31905343-31905344	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571748438	chr12:31905359-31905360	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112717441	chr12:31905390-31905391	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534528465	chr12:31905416-31905417	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556120607	chr12:31905417-31905418	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566498356	chr12:31905427-31905428	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs535462718	chr12:31905428-31905429	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs114066063	chr12:31905441-31905442	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs116433179	chr12:31905463-31905464	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs34831980	chr12:31905572-31905573	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112306317	chr12:31905643-31905644	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31889400-31905800	Enhancers	Primary B cells from peripheral blood	blood
2	chr12:31893600-31905800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:31899600-31905200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:31900000-31905200	Weak transcription	Primary T cells from cord blood	blood
5	chr12:31900000-31905800	Enhancers	Primary B cells from cord blood	blood
6	chr12:31900000-31906400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:31901000-31909800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:31901400-31904400	Enhancers	HepG2	liver
9	chr12:31901800-31905600	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr12:31901800-31905800	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr12:31902000-31904600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr12:31902400-31905400	Weak transcription	Adipose Nuclei	Adipose
13	chr12:31902600-31904400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr12:31902600-31904400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr12:31902600-31904400	Enhancers	K562	blood
16	chr12:31902600-31904800	Enhancers	HUVEC	blood vessel
17	chr12:31902600-31905200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr12:31902600-31905200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr12:31902600-31905200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:31902600-31905200	Weak transcription	HSMMtube	muscle
21	chr12:31902600-31905400	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr12:31902600-31906400	Enhancers	Primary T cells fromperipheralblood	blood
23	chr12:31902600-31908600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr12:31902600-31908600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr12:31902600-31912800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr12:31902800-31904400	Enhancers	A549	lung
27	chr12:31903000-31904400	Flanking Active TSS	GM12878-XiMat	blood
28	chr12:31903000-31904800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr12:31903000-31904800	Enhancers	Dnd41	blood
30	chr12:31903200-31904600	Enhancers	NHEK	skin
31	chr12:31903200-31905600	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr12:31903200-31905600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr12:31903400-31904800	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr12:31903400-31905600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
35	chr12:31903400-31905600	Enhancers	Spleen	Spleen
36	chr12:31903600-31904800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:31903600-31905400	Enhancers	Placenta	Placenta
38	chr12:31903600-31912800	Weak transcription	Gastric	stomach
39	chr12:31903800-31904600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr12:31903800-31905000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr12:31903800-31905000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr12:31903800-31905200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr12:31903800-31905800	Weak transcription	Right Atrium	heart
44	chr12:31903800-31909800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:31904000-31904400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:31904000-31904800	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr12:31904000-31905000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr12:31904000-31905400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr12:31904000-31905600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr12:31904000-31909600	Weak transcription	HMEC	breast

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