Variant report

Variant	nsv1042090
Chromosome Location	chr12:10646985-10695398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:239)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:239 , 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	chr12:10653777-10653877	K562	blood:	n/a	n/a
2	ATF2	chr12:10693081-10694102	GM12878	blood:	n/a	n/a
3	ATF2	chr12:10693152-10694036	GM12878	blood:	n/a	n/a
4	BATF	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
5	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
6	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
7	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
9	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
10	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
12	BCLAF1	chr12:10693241-10693808	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:10693305-10693679	GM12878	blood:	n/a	n/a
14	BRCA1	chr12:10676248-10676302	GM12878	blood:	n/a	n/a
15	CEBPB	chr12:10675342-10675509	A549	lung:	n/a	chr12:10675436-10675447
16	CEBPB	chr12:10693180-10693997	GM12878	blood:	n/a	n/a
17	CEBPB	chr12:10675319-10675536	HepG2	liver:	n/a	chr12:10675436-10675447
18	CREB1	chr12:10693203-10694090	GM12878	blood:	n/a	n/a
19	CREB1	chr12:10693316-10693819	GM12878	blood:	n/a	n/a
20	CREB1	chr12:10674190-10674624	GM12878	blood:	n/a	n/a
21	CTCF	chr12:10653780-10653930	GM12878	blood:	n/a	n/a
22	CTCF	chr12:10653780-10653930	GM12874	blood:	n/a	n/a
23	CTCF	chr12:10690080-10690230	GM12872	blood:	n/a	n/a
24	CTCF	chr12:10653770-10653897	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:10653800-10653950	HVMF	connective:	n/a	n/a
26	CTCF	chr12:10653818-10653864	Gliobla	brain:	n/a	n/a
27	CTCF	chr12:10653740-10653890	GM12866	blood:	n/a	n/a
28	CTCF	chr12:10653760-10653910	HMEC	breast:	n/a	n/a
29	CTCF	chr12:10653634-10653989	GM12878	blood:	n/a	n/a
30	CTCF	chr12:10653700-10653850	AG09309	skin:	n/a	n/a
31	CTCF	chr12:10653713-10653872	HepG2	liver:	n/a	n/a
32	CTCF	chr12:10653780-10653930	GM12867	blood:	n/a	n/a
33	CTCF	chr12:10653780-10653930	HepG2	liver:	n/a	n/a
34	CTCF	chr12:10653699-10653953	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:10653740-10653890	BJ	skin:	n/a	n/a
36	CTCF	chr12:10653780-10653930	HCFaa	heart:	n/a	n/a
37	CTCF	chr12:10653695-10653910	A549	lung:	n/a	n/a
38	CTCF	chr12:10653760-10653910	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr12:10653800-10653950	HCM	heart:	n/a	n/a
40	CTCF	chr12:10684484-10684570	GM20000	blood:	n/a	n/a
41	CTCF	chr12:10653780-10653930	GM12872	blood:	n/a	n/a
42	CTCF	chr12:10653660-10653810	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr12:10653660-10653810	NHEK	skin:	n/a	n/a
44	CTCF	chr12:10653820-10653970	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr12:10653740-10653890	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:10653700-10653850	HMF	breast:	n/a	n/a
47	CTCF	chr12:10653720-10653870	GM12865	blood:	n/a	n/a
48	CTCF	chr12:10653840-10653990	HRE	kidney:	n/a	n/a
49	CTCF	chr12:10653680-10653830	AG04450	lung:	n/a	n/a
50	CTCF	chr12:10653820-10653970	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10658539-10658589	K562	blood:	n/a
2	chr12:10658281-10658331	ProgFib	skin:	n/a
3	chr12:10658539-10658589	GM12878	blood:	n/a
4	chr12:10658539-10658589	PrEC	prostate:	n/a
5	chr12:10658539-10658589	SK-N-SH	brain:	n/a
6	chr12:10658425-10658475	SAEC	small airway:	n/a
7	chr12:10658281-10658331	NHDF-neo	bronchial:	n/a
8	chr12:10658281-10658331	PFSK-1	brain:	n/a
9	chr12:10658425-10658475	PANC-1	pancreas:	n/a
10	chr12:10658281-10658331	Hela-S3	cervix:	n/a
11	chr12:10658425-10658475	HCPEpiC	choroid plexus:	n/a
12	chr12:10658281-10658331	SKMC	muscle:	n/a
13	chr12:10658539-10658589	HepG2	liver:	n/a
14	chr12:10658539-10658589	HRCEpiC	kidney:	n/a
15	chr12:10658281-10658331	HCPEpiC	choroid plexus:	n/a
16	chr12:10658281-10658331	HUVEC	blood vessel:	n/a
17	chr12:10658539-10658589	Hepatocyte	liver:	n/a
18	chr12:10658425-10658475	HL-60	blood:	n/a
19	chr12:10658539-10658589	ECC-1	luminal epithelium:	n/a
20	chr12:10658539-10658589	PANC-1	pancreas:	n/a
21	chr12:10658539-10658589	SAEC	small airway:	n/a
22	chr12:10658281-10658331	AoSMC	blood vessel:	n/a
23	chr12:10658425-10658475	NB4	blood:	n/a
24	chr12:10658425-10658475	NHBE	bronchial:	n/a
25	chr12:10658281-10658331	H1-hESC	embryonic stem cell:	embryo
26	chr12:10658281-10658331	HCT-116	colon:	n/a
27	chr12:10658539-10658589	GM12891	blood:	n/a
28	chr12:10658425-10658475	HMEC	breast:	n/a
29	chr12:10658281-10658331	MCF10A-Er-Src	breast:	n/a
30	chr12:10658425-10658475	ovcar-3	ovarian:	n/a
31	chr12:10658281-10658331	HEK293	kidney:	embryo
32	chr12:10658539-10658589	GM19239	blood:	n/a
33	chr12:10658425-10658475	Hepatocyte	liver:	n/a
34	chr12:10658281-10658331	NHBE	bronchial:	n/a
35	chr12:10658425-10658475	BJ	skin:	n/a
36	chr12:10658539-10658589	AG04450	lung:	fetal
37	chr12:10658425-10658475	HUVEC	blood vessel:	n/a
38	chr12:10658539-10658589	NT2-D1	testis:	n/a
39	chr12:10658539-10658589	HUVEC	blood vessel:	n/a
40	chr12:10658425-10658475	HepG2	liver:	n/a
41	chr12:10658539-10658589	HRPEpiC	eye:	n/a
42	chr12:10658539-10658589	Hela-S3	cervix:	n/a
43	chr12:10658281-10658331	CMK	blood:	n/a
44	chr12:10658425-10658475	SK-N-SH_RA	brain:	n/a
45	chr12:10658425-10658475	U87	brain:	n/a
46	chr12:10658281-10658331	ECC-1	luminal epithelium:	n/a
47	chr12:10658281-10658331	HIPEpiC	eye:	n/a
48	chr12:10658539-10658589	HCT-116	colon:	n/a
49	chr12:10658539-10658589	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:10658425-10658475	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10388252..10388816-chr12:10653557..10654233,2	MCF-7	breast:
2	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
3	chr12:10693047..10695502-chr12:10698886..10701191,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000180574	TF binding region
ENSG00000180574	CpG island

Extended variants
information (count: 891 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:891 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559662516	chr12:10649806-10649807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533309922	chr12:10649826-10649827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565267268	chr12:10649867-10649868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78366513	chr12:10649871-10649872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs398097990	chr12:10649872-10649873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79179941	chr12:10649880-10649881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573245558	chr12:10649886-10649887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17741552	chr12:10649953-10649954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35358925	chr12:10649975-10649976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549536303	chr12:10649986-10649987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35744486	chr12:10650119-10650120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs532257726	chr12:10650196-10650197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367670357	chr12:10650311-10650312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs202021150	chr12:10650340-10650341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551780397	chr12:10650341-10650342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565664873	chr12:10650344-10650345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138977255	chr12:10650429-10650430	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs554660858	chr12:10650433-10650434	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs75605964	chr12:10650445-10650446	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs77623142	chr12:10650452-10650453	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs530974045	chr12:10650460-10650461	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs34211590	chr12:10650481-10650482	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs79073821	chr12:10650494-10650495	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs576842951	chr12:10650577-10650578	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs545695184	chr12:10650609-10650610	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs558729589	chr12:10650650-10650651	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs572395727	chr12:10650744-10650745	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs116299112	chr12:10650754-10650755	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs17206822	chr12:10650755-10650756	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs4763543	chr12:10650806-10650807	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189421486	chr12:10650818-10650819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181980770	chr12:10650827-10650828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4763544	chr12:10650862-10650863	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs74863769	chr12:10650883-10650884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73060470	chr12:10650890-10650891	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11838020	chr12:10650917-10650918	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77352905	chr12:10650924-10650925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11837508	chr12:10650940-10650941	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185496593	chr12:10650978-10650979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560488102	chr12:10651027-10651028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550426028	chr12:10651034-10651035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10743901	chr12:10651051-10651052	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs539381582	chr12:10651071-10651072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540559526	chr12:10651072-10651073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149347097	chr12:10651084-10651085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559102689	chr12:10651095-10651096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148033499	chr12:10651096-10651097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535032618	chr12:10651097-10651098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554650873	chr12:10651114-10651115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574619660	chr12:10651118-10651119	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10649800-10651600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr12:10650200-10650400	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr12:10650200-10651800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:10650400-10650800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:10650400-10651000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr12:10650600-10652000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr12:10651000-10651800	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr12:10651600-10652000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr12:10651600-10652200	Enhancers	GM12878-XiMat	blood
10	chr12:10651800-10652000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:10652000-10652200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:10652000-10652400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:10652000-10652400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
14	chr12:10652400-10656800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr12:10652800-10654200	Enhancers	Hela-S3	cervix
16	chr12:10653800-10654200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:10653800-10654200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:10655600-10656000	Enhancers	Brain Hippocampus Middle	brain
19	chr12:10656000-10656400	Flanking Active TSS	Brain Hippocampus Middle	brain
20	chr12:10663200-10663400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr12:10663600-10665200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:10664400-10664800	Active TSS	Brain Hippocampus Middle	brain
23	chr12:10664600-10665000	Active TSS	Brain Anterior Caudate	brain
24	chr12:10664600-10665200	Enhancers	Brain Substantia Nigra	brain
25	chr12:10664800-10665000	Flanking Active TSS	Brain Hippocampus Middle	brain
26	chr12:10665000-10666200	Enhancers	Brain Hippocampus Middle	brain
27	chr12:10665200-10665600	Enhancers	Hela-S3	cervix
28	chr12:10674000-10674600	Enhancers	GM12878-XiMat	blood
29	chr12:10678000-10680800	Weak transcription	Fetal Intestine Small	intestine
30	chr12:10680200-10681000	Enhancers	Fetal Intestine Large	intestine
31	chr12:10680600-10680800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr12:10680800-10681200	Active TSS	Duodenum Mucosa	Duodenum
33	chr12:10680800-10681200	Enhancers	Fetal Intestine Small	intestine
34	chr12:10680800-10681200	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr12:10680800-10681200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr12:10680800-10681200	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr12:10681000-10681800	Weak transcription	Fetal Intestine Large	intestine
38	chr12:10681200-10681400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr12:10681200-10681400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr12:10681200-10682200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr12:10681400-10681800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr12:10681400-10682000	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr12:10681800-10682600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr12:10681800-10682800	Enhancers	Fetal Intestine Large	intestine
45	chr12:10682000-10682200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr12:10682000-10682400	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr12:10682400-10682600	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr12:10682400-10682800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr12:10682400-10683600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr12:10683600-10684000	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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