Variant report

Variant	esv3325259
Chromosome Location	chr12:51744741-51746212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 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	chr12:51745791-51746000	HepG2	liver:	n/a	n/a
2	BACH1	chr12:51745733-51745990	K562	blood:	n/a	n/a
3	BRCA1	chr12:51745710-51746045	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr12:51745779-51746017	K562	blood:	n/a	n/a
5	CEBPB	chr12:51745675-51746000	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr12:51745510-51746018	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr12:51745732-51746094	A549	lung:	n/a	n/a
8	CTCF	chr12:51745798-51745999	HepG2	liver:	n/a	n/a
9	CTCF	chr12:51745827-51745966	GM13976	blood:	n/a	n/a
10	CTCF	chr12:51745780-51745930	GM12867	blood:	n/a	n/a
11	CTCF	chr12:51745820-51745970	AG09319	gingival:	n/a	n/a
12	CTCF	chr12:51745840-51745990	HCT-116	colon:	n/a	n/a
13	CTCF	chr12:51745860-51746010	A549	lung:	n/a	n/a
14	CTCF	chr12:51745660-51745810	HFF-Myc	foreskin:	n/a	n/a
15	CTCF	chr12:51745781-51745999	LNCaP	prostate:	n/a	n/a
16	CTCF	chr12:51745756-51746010	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr12:51745800-51745950	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr12:51745767-51746011	GM19240	blood:	n/a	n/a
19	CTCF	chr12:51745840-51745990	SAEC	small airway:	n/a	n/a
20	CTCF	chr12:51745800-51745950	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr12:51745764-51745993	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr12:51745780-51745930	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr12:51745800-51745950	AG04449	skin:	n/a	n/a
24	CTCF	chr12:51745840-51745990	HCM	heart:	n/a	n/a
25	CTCF	chr12:51745860-51746010	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr12:51745840-51745990	HVMF	connective:	n/a	n/a
27	CTCF	chr12:51745840-51745990	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr12:51745738-51746043	K562	blood:	n/a	n/a
29	CTCF	chr12:51745748-51746027	Gliobla	brain:	n/a	n/a
30	CTCF	chr12:51745796-51745921	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr12:51745820-51745970	HRE	kidney:	n/a	n/a
32	CTCF	chr12:51745840-51745990	BJ	skin:	n/a	n/a
33	CTCF	chr12:51745800-51745950	BJ	skin:	n/a	n/a
34	CTCF	chr12:51745601-51746180	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:51745820-51745970	GM12865	blood:	n/a	n/a
36	CTCF	chr12:51745769-51746062	A549	lung:	n/a	n/a
37	CTCF	chr12:51745757-51746006	Fibrobl	skin:	n/a	n/a
38	CTCF	chr12:51745800-51745950	K562	blood:	n/a	n/a
39	CTCF	chr12:51745820-51745970	GM12869	blood:	n/a	n/a
40	CTCF	chr12:51745681-51746074	GM12878	blood:	n/a	n/a
41	CTCF	chr12:51745820-51745970	GM12864	blood:	n/a	n/a
42	CTCF	chr12:51745641-51746068	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr12:51745860-51746010	HCM	heart:	n/a	n/a
44	CTCF	chr12:51745820-51745970	HPF	lung:	n/a	n/a
45	CTCF	chr12:51745820-51745970	HepG2	liver:	n/a	n/a
46	CTCF	chr12:51745800-51745950	HMF	breast:	n/a	n/a
47	CTCF	chr12:51745810-51745974	GM20000	blood:	n/a	n/a
48	CTCF	chr12:51745806-51745992	GM10248	blood:	n/a	n/a
49	CTCF	chr12:51745800-51745950	HPF	lung:	n/a	n/a
50	CTCF	chr12:51745688-51746071	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:51745952-51746002	HRCEpiC	kidney:	n/a
2	chr12:51745952-51746002	AG04450	lung:	fetal
3	chr12:51745952-51746002	SAEC	small airway:	n/a
4	chr12:51745952-51746002	GM19239	blood:	n/a
5	chr12:51745952-51746002	BE2_C	brain:	n/a
6	chr12:51745952-51746002	GM12891	blood:	n/a
7	chr12:51745952-51746002	PANC-1	pancreas:	n/a
8	chr12:51745952-51746002	SK-N-MC	brain:	n/a
9	chr12:51745952-51746002	HL-60	blood:	n/a
10	chr12:51745952-51746002	Hepatocyte	liver:	n/a
11	chr12:51745952-51746002	CMK	blood:	n/a
12	chr12:51745952-51746002	AG09319	gingival:	n/a
13	chr12:51745952-51746002	Caco-2	colon:	n/a
14	chr12:51745952-51746002	AoSMC	blood vessel:	n/a
15	chr12:51745952-51746002	SK-N-SH	brain:	n/a
16	chr12:51745952-51746002	HRE	kidney:	n/a
17	chr12:51745952-51746002	HCT-116	colon:	n/a
18	chr12:51745952-51746002	H1-hESC	embryonic stem cell:	embryo
19	chr12:51745952-51746002	HCPEpiC	choroid plexus:	n/a
20	chr12:51745952-51746002	HMEC	breast:	n/a
21	chr12:51745952-51746002	HUVEC	blood vessel:	n/a
22	chr12:51745952-51746002	BJ	skin:	n/a
23	chr12:51745952-51746002	ovcar-3	ovarian:	n/a
24	chr12:51745952-51746002	HCF	heart:	n/a
25	chr12:51745952-51746002	AG09309	skin:	n/a
26	chr12:51745952-51746002	HCM	heart:	n/a
27	chr12:51745952-51746002	AG04449	skin:	fetal
28	chr12:51745952-51746002	T-47D	breast:	n/a
29	chr12:51745952-51746002	AG10803	skin:	n/a
30	chr12:51745952-51746002	RPTEC	kidney:	n/a
31	chr12:51745952-51746002	NH-A	brain:	n/a
32	chr12:51745952-51746002	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:51745952-51746002	A549	lung:	n/a
34	chr12:51745952-51746002	GM12878	blood:	n/a
35	chr12:51745952-51746002	HNPCEpiC	eye:	n/a
36	chr12:51745952-51746002	SK-N-SH_RA	brain:	n/a
37	chr12:51745952-51746002	HAEpiC	amniotic membrane:	n/a
38	chr12:51745952-51746002	NHBE	bronchial:	n/a
39	chr12:51745952-51746002	ECC-1	luminal epithelium:	n/a
40	chr12:51745952-51746002	HEK293	kidney:	embryo
41	chr12:51745952-51746002	NT2-D1	testis:	n/a
42	chr12:51745952-51746002	GM12892	blood:	n/a
43	chr12:51745952-51746002	K562	blood:	n/a
44	chr12:51745952-51746002	HepG2	liver:	n/a
45	chr12:51745952-51746002	SKMC	muscle:	n/a
46	chr12:51745952-51746002	U87	brain:	n/a
47	chr12:51745952-51746002	MCF10A-Er-Src	breast:	n/a
48	chr12:51745952-51746002	NB4	blood:	n/a
49	chr12:51745952-51746002	HRPEpiC	eye:	n/a
50	chr12:51745952-51746002	NHDF-neo	bronchial:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:50468698..50469628-chr12:51745397..51745900,2	K562	blood:
2	chr12:51631532..51634032-chr12:51744589..51747276,3	MCF-7	breast:
3	chr12:51157742..51160263-chr12:51742704..51744822,2	K562	blood:
4	chr12:51441102..51443608-chr12:51745304..51746823,2	K562	blood:
5	chr12:51663386..51664046-chr12:51745481..51746352,2	K562	blood:
6	chr12:51737875..51739498-chr12:51745613..51748065,2	K562	blood:
7	chr12:51734941..51739498-chr12:51744423..51748065,5	K562	blood:
8	chr12:51744372..51748268-chr12:51756905..51759729,4	K562	blood:
9	chr12:51745450..51746290-chr12:51814696..51815264,2	MCF-7	breast:
10	chr12:51441280..51444117-chr12:51744506..51748458,5	MCF-7	breast:
11	chr12:51662264..51665283-chr12:51745297..51747465,3	K562	blood:
12	chr12:51714696..51717509-chr12:51745471..51747033,2	MCF-7	breast:
13	chr12:51159003..51159746-chr12:51745461..51746336,2	K562	blood:
14	chr12:51745453..51745976-chr5:73263142..73263663,3	MCF-7	breast:

No data

Variant related genes	Relation type
CELA1	TF binding region
CELA1	CpG island
ENSG00000050426	chromatin interactions
ENSG00000183283	chromatin interactions
ENSG00000170545	chromatin interactions
ENSG00000123268	chromatin interactions

Extended variants
information (count: 70 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386376520	chr12:51744742-51744743	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs11273416	chr12:51744754-51744755	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs149076307	chr12:51744755-51744756	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs75562681	chr12:51744756-51744757	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs138907967	chr12:51744758-51744759	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs149731416	chr12:51744759-51744760	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs375810374	chr12:51744791-51744792	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569664509	chr12:51744826-51744827	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs187208834	chr12:51744849-51744850	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs74694160	chr12:51744862-51744863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs3858624	chr12:51744867-51744868	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs12322422	chr12:51744885-51744886	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144136291	chr12:51744916-51744917	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533139433	chr12:51745041-51745042	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs191924092	chr12:51745058-51745059	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs569760184	chr12:51745059-51745060	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs535693258	chr12:51745134-51745135	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs549053056	chr12:51745152-51745153	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376307365	chr12:51745164-51745165	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs565660460	chr12:51745169-51745170	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs369554954	chr12:51745207-51745208	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs546435755	chr12:51745267-51745268	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs564531480	chr12:51745283-51745284	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs117392395	chr12:51745307-51745308	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs184176564	chr12:51745313-51745314	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs566067960	chr12:51745367-51745368	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs148703634	chr12:51745374-51745375	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs536763345	chr12:51745379-51745380	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs556678992	chr12:51745420-51745421	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs114911725	chr12:51745447-51745448	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs372802787	chr12:51745450-51745451	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs542508559	chr12:51745473-51745474	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs3858627	chr12:51745478-51745479	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs572456064	chr12:51745480-51745481	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs541467211	chr12:51745481-51745482	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs562145519	chr12:51745488-51745489	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs564494885	chr12:51745512-51745513	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs554105649	chr12:51745549-51745550	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543555571	chr12:51745592-51745593	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs116165275	chr12:51745598-51745599	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs142673669	chr12:51745606-51745607	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs549243665	chr12:51745643-51745644	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565663657	chr12:51745648-51745649	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs528389943	chr12:51745651-51745652	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs2519	chr12:51745690-51745691	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs147355512	chr12:51745724-51745725	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs536704242	chr12:51745730-51745731	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369058228	chr12:51745749-51745750	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570223868	chr12:51745788-51745789	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs3889974	chr12:51745795-51745796	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	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
Urothelial carcinoma	21177765	CNVD
Breast cancer	21509527	CNVD
Breast cancer	20409316	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51731800-51750600	Weak transcription	Spleen	Spleen
2	chr12:51735400-51745400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr12:51735400-51745400	Weak transcription	Brain Substantia Nigra	brain
4	chr12:51735400-51745800	Weak transcription	Fetal Intestine Small	intestine
5	chr12:51735400-51746800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr12:51735400-51747400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:51735400-51747400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:51735400-51747400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr12:51735400-51747600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr12:51735400-51747800	Weak transcription	NHLF	lung
11	chr12:51735400-51750200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr12:51735400-51750600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:51735400-51750600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:51735400-51756000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:51735600-51746800	Weak transcription	Primary T cells from cord blood	blood
16	chr12:51735600-51750600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:51735600-51761400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr12:51735800-51747400	Weak transcription	Dnd41	blood
19	chr12:51736400-51765400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:51739400-51748400	Weak transcription	Gastric	stomach
21	chr12:51739400-51754200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr12:51739600-51744800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:51739600-51750600	Weak transcription	GM12878-XiMat	blood
24	chr12:51740000-51747400	Weak transcription	NHEK	skin
25	chr12:51740200-51745800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:51740200-51746800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:51740400-51747400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:51740400-51747400	Weak transcription	Thymus	Thymus
29	chr12:51740400-51747800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr12:51740600-51747600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr12:51740600-51751000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr12:51740800-51745200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr12:51740800-51753200	Weak transcription	NHDF-Ad	bronchial
34	chr12:51741000-51745400	Weak transcription	Pancreas	Pancrea
35	chr12:51741000-51745600	Weak transcription	Fetal Thymus	thymus
36	chr12:51741000-51747800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr12:51742200-51745800	Weak transcription	K562	blood
38	chr12:51742400-51746000	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr12:51742400-51749600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr12:51743200-51745000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr12:51743200-51750600	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr12:51743400-51745400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr12:51743400-51745600	Weak transcription	Osteobl	bone
44	chr12:51743400-51746200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:51743400-51746800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:51743400-51751600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr12:51744000-51746400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:51744000-51748000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr12:51744200-51745400	Weak transcription	Placenta	Placenta
50	chr12:51744200-51761400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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