Variant report

Variant	nsv975473
Chromosome Location	chr12:31895430-31908180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:989)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31899653-31900146	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31901939-31902594	K562	blood:	n/a	n/a
3	ARID3A	chr12:31900208-31900214	K562	blood:	n/a	n/a
4	ARID3A	chr12:31901910-31902691	HepG2	liver:	n/a	n/a
5	ATF1	chr12:31902088-31902581	K562	blood:	n/a	n/a
6	ATF2	chr12:31901708-31902645	GM12878	blood:	n/a	n/a
7	ATF2	chr12:31901758-31902687	GM12878	blood:	n/a	n/a
8	ATF2	chr12:31899661-31900246	GM12878	blood:	n/a	n/a
9	ATF2	chr12:31899563-31900172	GM12878	blood:	n/a	n/a
10	ATF2	chr12:31901982-31902503	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:31902028-31902526	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr12:31901857-31902688	A549	lung:	n/a	n/a
13	ATF3	chr12:31902136-31902441	K562	blood:	n/a	n/a
14	ATF3	chr12:31902095-31902409	HepG2	liver:	n/a	n/a
15	ATF3	chr12:31901886-31902752	A549	lung:	n/a	n/a
16	ATF3	chr12:31899724-31900054	K562	blood:	n/a	n/a
17	ATF3	chr12:31901890-31902594	K562	blood:	n/a	n/a
18	ATF3	chr12:31901829-31902705	HCT-116	colon:	n/a	n/a
19	ATF3	chr12:31901867-31902659	HCT-116	colon:	n/a	n/a
20	BACH1	chr12:31901909-31902527	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:31902009-31902464	K562	blood:	n/a	n/a
22	BATF	chr12:31899705-31900087	GM12878	blood:	n/a	n/a
23	BATF	chr12:31899649-31900068	GM12878	blood:	n/a	n/a
24	BATF	chr12:31901846-31902653	GM12878	blood:	n/a	chr12:31902262-31902273
25	BATF	chr12:31901977-31902530	GM12878	blood:	n/a	chr12:31902262-31902273
26	BCL11A	chr12:31899596-31900120	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:31899736-31899991	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:31902132-31902376	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr12:31901905-31902669	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:31902028-31902625	GM12878	blood:	n/a	n/a
31	BCL3	chr12:31899675-31900041	GM12878	blood:	n/a	n/a
32	BCL3	chr12:31901804-31902807	A549	lung:	n/a	n/a
33	BCL3	chr12:31901863-31902625	GM12878	blood:	n/a	n/a
34	BCL3	chr12:31901887-31902683	A549	lung:	n/a	n/a
35	BCLAF1	chr12:31903328-31904118	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:31899568-31900167	GM12878	blood:	n/a	n/a
37	BCLAF1	chr12:31901863-31902707	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:31901791-31902693	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:31899584-31900095	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:31901988-31902644	K562	blood:	n/a	n/a
41	BHLHE40	chr12:31902006-31902637	A549	lung:	n/a	n/a
42	BHLHE40	chr12:31901833-31902757	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:31902072-31902616	HepG2	liver:	n/a	n/a
44	BHLHE40	chr12:31905586-31905714	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:31902076-31902628	K562	blood:	n/a	n/a
46	BHLHE40	chr12:31899525-31900144	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:31902109-31902535	HepG2	liver:	n/a	n/a
48	BHLHE40	chr12:31903115-31903770	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:31902207-31902543	HepG2	liver:	n/a	n/a
50	BRCA1	chr12:31902088-31902529	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31902503-31902553	HUVEC	blood vessel:	n/a
2	chr12:31902503-31902553	K562	blood:	n/a
3	chr12:31902503-31902553	AoSMC	blood vessel:	n/a
4	chr12:31902503-31902553	BE2_C	brain:	n/a
5	chr12:31902503-31902553	GM12891	blood:	n/a
6	chr12:31902503-31902553	HCM	heart:	n/a
7	chr12:31902503-31902553	HCPEpiC	choroid plexus:	n/a
8	chr12:31902503-31902553	Hela-S3	cervix:	n/a
9	chr12:31902503-31902553	MCF-7	breast:	n/a
10	chr12:31902503-31902553	NHBE	bronchial:	n/a
11	chr12:31902503-31902553	NHDF-neo	bronchial:	n/a
12	chr12:31902503-31902553	HMEC	breast:	n/a
13	chr12:31902503-31902553	HIPEpiC	eye:	n/a
14	chr12:31902503-31902553	SAEC	small airway:	n/a
15	chr12:31902503-31902553	Caco-2	colon:	n/a
16	chr12:31902503-31902553	BJ	skin:	n/a
17	chr12:31902503-31902553	NB4	blood:	n/a
18	chr12:31902503-31902553	GM12878	blood:	n/a
19	chr12:31902503-31902553	AG09319	gingival:	n/a
20	chr12:31902503-31902553	HCF	heart:	n/a
21	chr12:31902503-31902553	SK-N-SH_RA	brain:	n/a
22	chr12:31902503-31902553	ovcar-3	ovarian:	n/a
23	chr12:31902503-31902553	RPTEC	kidney:	n/a
24	chr12:31902503-31902553	GM06990	blood:	n/a
25	chr12:31902503-31902553	NH-A	brain:	n/a
26	chr12:31902503-31902553	HCT-116	colon:	n/a
27	chr12:31902503-31902553	AG09309	skin:	n/a
28	chr12:31902503-31902553	HNPCEpiC	eye:	n/a
29	chr12:31902503-31902553	HEK293	kidney:	embryo
30	chr12:31902503-31902553	Jurkat	blood:	n/a
31	chr12:31902503-31902553	AG04449	skin:	fetal
32	chr12:31902503-31902553	GM12892	blood:	n/a
33	chr12:31902503-31902553	IMR90	lung:	fetal
34	chr12:31902503-31902553	HRE	kidney:	n/a
35	chr12:31902503-31902553	AG10803	skin:	n/a
36	chr12:31902503-31902553	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:31902503-31902553	A549	lung:	n/a
38	chr12:31902503-31902553	T-47D	breast:	n/a
39	chr12:31902503-31902553	H1-hESC	embryonic stem cell:	embryo
40	chr12:31902503-31902553	U87	brain:	n/a
41	chr12:31902503-31902553	HRPEpiC	eye:	n/a
42	chr12:31902503-31902553	PFSK-1	brain:	n/a
43	chr12:31902503-31902553	SK-N-SH	brain:	n/a
44	chr12:31902503-31902553	HRCEpiC	kidney:	n/a
45	chr12:31902503-31902553	AG04450	lung:	fetal
46	chr12:31902503-31902553	HepG2	liver:	n/a
47	chr12:31902503-31902553	GM19239	blood:	n/a
48	chr12:31902503-31902553	HAEpiC	amniotic membrane:	n/a
49	chr12:31902503-31902553	CMK	blood:	n/a
50	chr12:31902503-31902553	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:31867508..31869786-chr12:31900848..31903323,2	K562	blood:
2	chr12:31901665..31904041-chr12:31908599..31911297,2	K562	blood:
3	chr12:31890682..31895418-chr12:31897600..31900050,5	K562	blood:
4	chr12:31884351..31886609-chr12:31902358..31904418,2	MCF-7	breast:
5	chr12:31902284..31904041-chr12:31909797..31911614,2	K562	blood:
6	chr12:31880350..31888706-chr12:31898122..31903847,15	K562	blood:
7	chr12:31902147..31904881-chr12:32110992..32113730,2	MCF-7	breast:
8	chr12:31897495..31899611-chr12:31901750..31904156,2	MCF-7	breast:
9	chr12:31890191..31892449-chr12:31894562..31897405,2	K562	blood:
10	chr12:31889555..31891560-chr12:31894005..31895879,2	MCF-7	breast:
11	chr12:31897495..31899611-chr12:31901750..31904156,2	MCF-7	breast:
12	chr12:31866804..31870237-chr12:31900678..31903673,4	K562	blood:
13	chr12:31883178..31885919-chr12:31902028..31904052,3	K562	blood:
14	chr12:31880235..31884620-chr12:31906466..31910642,5	K562	blood:
15	chr12:31901857..31902801-chr12:31926002..31926958,3	MCF-7	breast:
16	chr12:31900170..31902250-chr12:31904037..31906770,3	MCF-7	breast:
17	chr12:31896972..31898999-chr12:31900743..31902454,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMN1-2	chr12:31900809-31901031	NONHSAT027573
2	lnc-H3F3C-1	chr12:31903114-31904287	XLOC_010043
3	lnc-H3F3C-1	chr12:31906082-31906270	XLOC_010043

No data

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

Extended variants
information (count: 533 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:533 , 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	rs56278950	chr12:31895457-31895458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567105744	chr12:31895497-31895498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536391934	chr12:31895508-31895509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555863917	chr12:31895511-31895512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75195919	chr12:31895519-31895520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575866709	chr12:31895531-31895532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372463988	chr12:31895538-31895539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117958879	chr12:31895546-31895547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189994827	chr12:31895598-31895599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146667079	chr12:31895619-31895620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540925675	chr12:31895658-31895659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561336874	chr12:31895663-31895664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1483729	chr12:31895673-31895674	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs543932877	chr12:31895712-31895713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573470293	chr12:31895722-31895723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371069288	chr12:31895733-31895734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373660299	chr12:31895762-31895763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181575707	chr12:31895855-31895856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs34601520	chr12:31895887-31895888	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs532624319	chr12:31895888-31895889	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552819859	chr12:31895943-31895944	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs559946722	chr12:31895968-31895969	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs7953551	chr12:31896013-31896014	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185838500	chr12:31896047-31896048	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs567292951	chr12:31896061-31896062	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs535854201	chr12:31896088-31896089	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs549875400	chr12:31896233-31896234	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs190162184	chr12:31896260-31896261	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs542833214	chr12:31896293-31896294	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs182574482	chr12:31896334-31896335	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs141676967	chr12:31896343-31896344	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs373511431	chr12:31896356-31896357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs11051554	chr12:31896388-31896389	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534960184	chr12:31896389-31896390	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs148840373	chr12:31896390-31896391	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs574807834	chr12:31896468-31896469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372577250	chr12:31896474-31896475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76966030	chr12:31896487-31896488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563640092	chr12:31896492-31896493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544674233	chr12:31896493-31896494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576435574	chr12:31896496-31896497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186029691	chr12:31896512-31896513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565249030	chr12:31896513-31896514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190884708	chr12:31896535-31896536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377535310	chr12:31896563-31896564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73090402	chr12:31896597-31896598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143520013	chr12:31896632-31896633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531207166	chr12:31896643-31896644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549524615	chr12:31896672-31896673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371122848	chr12:31896717-31896718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31883000-31896000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:31885800-31900200	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr12:31886400-31899400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr12:31887400-31899000	Weak transcription	Lung	lung
5	chr12:31888000-31896800	Enhancers	Fetal Thymus	thymus
6	chr12:31888000-31897400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:31889200-31896600	Enhancers	Thymus	Thymus
8	chr12:31889400-31905800	Enhancers	Primary B cells from peripheral blood	blood
9	chr12:31890000-31897600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:31890000-31899200	Weak transcription	NHDF-Ad	bronchial
11	chr12:31890000-31899400	Weak transcription	NH-A	brain
12	chr12:31890400-31899400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:31891000-31897600	Weak transcription	Hela-S3	cervix
14	chr12:31891200-31895800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr12:31892800-31896000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr12:31893200-31896400	Enhancers	Primary T cells from cord blood	blood
17	chr12:31893200-31896800	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr12:31893400-31896200	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr12:31893400-31896600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr12:31893400-31896800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr12:31893400-31896800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr12:31893400-31900000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr12:31893600-31896000	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr12:31893600-31896400	Enhancers	Primary hematopoietic stem cells	blood
25	chr12:31893600-31905800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:31893800-31895600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:31893800-31895600	Weak transcription	GM12878-XiMat	blood
28	chr12:31893800-31895800	Enhancers	Primary B cells from cord blood	blood
29	chr12:31893800-31896600	Enhancers	Dnd41	blood
30	chr12:31894000-31895800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:31894000-31899000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr12:31894400-31895600	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr12:31894400-31895600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr12:31894400-31896000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:31894400-31897600	Weak transcription	A549	lung
36	chr12:31894400-31897800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:31894400-31899200	Weak transcription	HUVEC	blood vessel
38	chr12:31894400-31903400	Weak transcription	Spleen	Spleen
39	chr12:31894600-31895600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr12:31894600-31899600	Weak transcription	K562	blood
41	chr12:31895200-31895800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr12:31895400-31896600	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr12:31895600-31896400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr12:31895600-31896400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr12:31895600-31896600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:31895600-31896600	Enhancers	GM12878-XiMat	blood
47	chr12:31895600-31896800	Enhancers	Primary T cells fromperipheralblood	blood
48	chr12:31895800-31896000	Weak transcription	Small Intestine	intestine
49	chr12:31895800-31896200	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr12:31895800-31896200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links