Variant report

Variant	nsv973997
Chromosome Location	chr12:56992360-56996067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 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	CEBPB	chr12:56996018-56996379	HepG2	liver:	n/a	chr12:56996197-56996208
2	CEBPB	chr12:56996013-56996380	A549	lung:	n/a	chr12:56996197-56996208
3	CEBPB	chr12:56996058-56996342	K562	blood:	n/a	chr12:56996197-56996208
4	CEBPB	chr12:56995954-56996446	A549	lung:	n/a	chr12:56996197-56996208
5	CEBPB	chr12:56996009-56996355	MCF-7	breast:	n/a	chr12:56996197-56996208
6	CEBPB	chr12:56996045-56996432	ECC-1	luminal epithelium:	n/a	chr12:56996197-56996208
7	CEBPB	chr12:56996001-56996392	ECC-1	luminal epithelium:	n/a	chr12:56996197-56996208
8	CEBPB	chr12:56996062-56996322	H1-hESC	embryonic stem cell:	n/a	chr12:56996197-56996208
9	CEBPB	chr12:56996015-56996388	IMR90	lung:	n/a	chr12:56996197-56996208
10	CEBPB	chr12:56996030-56996377	Hela-S3	cervix:	n/a	chr12:56996197-56996208
11	CEBPB	chr12:56996025-56996386	K562	blood:	n/a	chr12:56996197-56996208
12	CTCF	chr12:56995298-56995486	MCF-7	breast:	n/a	n/a
13	CTCF	chr12:56995240-56995390	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr12:56995320-56995470	NHEK	skin:	n/a	n/a
15	CTCF	chr12:56995340-56995490	HAc	cerebellar:	n/a	n/a
16	CTCF	chr12:56995420-56995570	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr12:56995200-56995350	WI-38	lung:	n/a	n/a
18	CTCF	chr12:56995340-56995490	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr12:56995380-56995530	HCT-116	colon:	n/a	n/a
20	CTCF	chr12:56995216-56995559	GM12878	blood:	n/a	n/a
21	CTCF	chr12:56995320-56995470	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr12:56995360-56995510	GM12868	blood:	n/a	n/a
23	CTCF	chr12:56995340-56995490	GM12873	blood:	n/a	n/a
24	CTCF	chr12:56995320-56995470	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:56995320-56995470	HMEC	breast:	n/a	n/a
26	CTCF	chr12:56995179-56995498	K562	blood:	n/a	n/a
27	CTCF	chr12:56995300-56995450	GM12867	blood:	n/a	n/a
28	CTCF	chr12:56995293-56995479	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr12:56995293-56995516	HepG2	liver:	n/a	n/a
30	CTCF	chr12:56995320-56995470	GM12874	blood:	n/a	n/a
31	CTCF	chr12:56995260-56995410	HPF	lung:	n/a	n/a
32	CTCF	chr12:56995335-56995454	ProgFib	skin:	n/a	n/a
33	CTCF	chr12:56995320-56995470	GM12868	blood:	n/a	n/a
34	CTCF	chr12:56995288-56995485	NHEK	skin:	n/a	n/a
35	CTCF	chr12:56995320-56995470	GM12867	blood:	n/a	n/a
36	CTCF	chr12:56995350-56995463	Lung_OC	lung:	n/a	n/a
37	CTCF	chr12:56995340-56995490	NHLF	lung:	n/a	n/a
38	CTCF	chr12:56995280-56995430	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr12:56995280-56995430	HVMF	connective:	n/a	n/a
40	CTCF	chr12:56995320-56995470	GM12873	blood:	n/a	n/a
41	CTCF	chr12:56994540-56994690	K562	blood:	n/a	n/a
42	CTCF	chr12:56995220-56995370	HL-60	blood:	n/a	n/a
43	CTCF	chr12:56995222-56995558	K562	blood:	n/a	n/a
44	CTCF	chr12:56995360-56995510	HEK293	kidney:	n/a	n/a
45	CTCF	chr12:56995420-56995570	GM12869	blood:	n/a	n/a
46	CTCF	chr12:56995340-56995490	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:56995300-56995457	HepG2	liver:	n/a	n/a
48	CTCF	chr12:56995300-56995450	GM12872	blood:	n/a	n/a
49	CTCF	chr12:56995260-56995410	GM12873	blood:	n/a	n/a
50	CTCF	chr12:56995287-56995487	IMR90	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	chr12:56992955-56993005	AG04449	skin:	fetal
2	chr12:56993036-56993086	HepG2	liver:	n/a
3	chr12:56992955-56993005	NT2-D1	testis:	n/a
4	chr12:56993036-56993086	HUVEC	blood vessel:	n/a
5	chr12:56993036-56993086	AG10803	skin:	n/a
6	chr12:56992994-56993044	SK-N-SH	brain:	n/a
7	chr12:56993036-56993086	Jurkat	blood:	n/a
8	chr12:56993036-56993086	PrEC	prostate:	n/a
9	chr12:56992955-56993005	ECC-1	luminal epithelium:	n/a
10	chr12:56992994-56993044	HMEC	breast:	n/a
11	chr12:56993036-56993086	GM06990	blood:	n/a
12	chr12:56993036-56993086	U87	brain:	n/a
13	chr12:56992955-56993005	NHBE	bronchial:	n/a
14	chr12:56992955-56993005	NH-A	brain:	n/a
15	chr12:56993036-56993086	SKMC	muscle:	n/a
16	chr12:56992994-56993044	HCM	heart:	n/a
17	chr12:56993036-56993086	GM19239	blood:	n/a
18	chr12:56992994-56993044	GM19239	blood:	n/a
19	chr12:56992994-56993044	NHBE	bronchial:	n/a
20	chr12:56992994-56993044	BJ	skin:	n/a
21	chr12:56992994-56993044	Jurkat	blood:	n/a
22	chr12:56992994-56993044	HL-60	blood:	n/a
23	chr12:56992955-56993005	MCF10A-Er-Src	breast:	n/a
24	chr12:56992955-56993005	U87	brain:	n/a
25	chr12:56993036-56993086	K562	blood:	n/a
26	chr12:56992955-56993005	LNCaP	prostate:	n/a
27	chr12:56992994-56993044	HUVEC	blood vessel:	n/a
28	chr12:56992955-56993005	Jurkat	blood:	n/a
29	chr12:56993036-56993086	AG09309	skin:	n/a
30	chr12:56992994-56993044	Hela-S3	cervix:	n/a
31	chr12:56993036-56993086	Hela-S3	cervix:	n/a
32	chr12:56993036-56993086	SK-N-SH_RA	brain:	n/a
33	chr12:56992994-56993044	NB4	blood:	n/a
34	chr12:56992994-56993044	Hepatocyte	liver:	n/a
35	chr12:56992955-56993005	SK-N-MC	brain:	n/a
36	chr12:56993036-56993086	SK-N-MC	brain:	n/a
37	chr12:56992955-56993005	SAEC	small airway:	n/a
38	chr12:56992994-56993044	GM12892	blood:	n/a
39	chr12:56992955-56993005	H1-hESC	embryonic stem cell:	embryo
40	chr12:56992955-56993005	GM19239	blood:	n/a
41	chr12:56992955-56993005	GM12892	blood:	n/a
42	chr12:56992955-56993005	Hepatocyte	liver:	n/a
43	chr12:56993036-56993086	ovcar-3	ovarian:	n/a
44	chr12:56992955-56993005	SK-N-SH	brain:	n/a
45	chr12:56993036-56993086	HRCEpiC	kidney:	n/a
46	chr12:56992955-56993005	HRPEpiC	eye:	n/a
47	chr12:56992994-56993044	AG10803	skin:	n/a
48	chr12:56993036-56993086	HCT-116	colon:	n/a
49	chr12:56992994-56993044	IMR90	lung:	fetal
50	chr12:56992955-56993005	HEEpiC	esophagus:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56992973..56997884-chr12:57027374..57031905,8	K562	blood:
2	chr12:56993930..56997262-chr12:57028560..57031023,3	K562	blood:
3	chr12:56987156..56990068-chr12:56991407..56993523,3	MCF-7	breast:
4	chr12:56988887..56992620-chr12:56993590..56996069,4	MCF-7	breast:
5	chr12:56994191..56996366-chr12:57144934..57147543,2	K562	blood:
6	chr12:56991013..56993546-chr12:56999822..57001815,2	K562	blood:
7	chr12:56989810..56992363-chr12:57017983..57019817,2	K562	blood:
8	chr12:56991516..56994347-chr12:57026603..57029452,2	MCF-7	breast:
9	chr12:56995113..56995947-chr12:57030215..57031100,3	MCF-7	breast:
10	chr12:56991513..56993644-chr12:56998882..57001815,3	K562	blood:
11	chr12:56992957..56994766-chr12:56997474..57000200,2	MCF-7	breast:
12	chr12:56990898..56994396-chr12:56995089..56998890,5	K562	blood:
13	chr12:56990818..56993211-chr12:57006081..57007735,2	MCF-7	breast:
14	chr12:56992042..56997013-chr12:57005431..57010145,6	K562	blood:
15	chr12:56995376..56997871-chr12:57023394..57025015,2	K562	blood:
16	chr12:56994821..56997665-chr12:57004443..57006406,2	MCF-7	breast:
17	chr12:56994912..56995832-chr12:57030223..57031358,3	K562	blood:
18	chr12:56995143..56995846-chr12:57030393..57030919,3	MCF-7	breast:
19	chr12:56994056..56995615-chr12:57001455..57004009,2	K562	blood:

No data

Variant related genes	Relation type
BAZ2A	TF binding region
BAZ2A	CpG island
ENSG00000025423	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000198056	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577151039	chr12:56992361-56992362	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541291566	chr12:56992367-56992368	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7970523	chr12:56992377-56992378	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs377757099	chr12:56992390-56992391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370230547	chr12:56992407-56992408	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376866712	chr12:56992412-56992413	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541800501	chr12:56992441-56992442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs59347862	chr12:56992450-56992451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551372747	chr12:56992457-56992458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531488338	chr12:56992465-56992466	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545714962	chr12:56992489-56992490	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151110106	chr12:56992501-56992502	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528419935	chr12:56992543-56992544	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199828506	chr12:56992559-56992560	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370601657	chr12:56992588-56992589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141396501	chr12:56992598-56992599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566085482	chr12:56992626-56992627	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201507665	chr12:56992627-56992628	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2242497	chr12:56992630-56992631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192436067	chr12:56992641-56992642	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143916462	chr12:56992809-56992810	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537536959	chr12:56992815-56992816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146834762	chr12:56992824-56992825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567166976	chr12:56992832-56992833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368741414	chr12:56992834-56992835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200794526	chr12:56992859-56992860	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201646018	chr12:56992870-56992871	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371507859	chr12:56992894-56992895	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375740270	chr12:56992896-56992897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367731696	chr12:56992932-56992933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373086268	chr12:56992939-56992940	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553292948	chr12:56992947-56992948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200742397	chr12:56992955-56992956	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372009622	chr12:56992957-56992958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541491077	chr12:56992994-56992995	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375310491	chr12:56992995-56992996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201934985	chr12:56993018-56993019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369538550	chr12:56993030-56993031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538325571	chr12:56993036-56993037	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374233405	chr12:56993042-56993043	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201074705	chr12:56993053-56993054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200068250	chr12:56993078-56993079	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373446671	chr12:56993087-56993088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376855510	chr12:56993098-56993099	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370265628	chr12:56993124-56993125	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183141027	chr12:56993150-56993151	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373251315	chr12:56993158-56993159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs376597729	chr12:56993189-56993190	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187470087	chr12:56993198-56993199	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548326496	chr12:56993224-56993225	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
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
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
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56954600-56993400	Weak transcription	Fetal Brain Male	brain
2	chr12:56964200-56992600	Weak transcription	Stomach Mucosa	stomach
3	chr12:56977600-57017000	Strong transcription	Placenta	Placenta
4	chr12:56979600-57020400	Strong transcription	Fetal Stomach	stomach
5	chr12:56987600-57012000	Strong transcription	Liver	Liver
6	chr12:56987600-57014800	Strong transcription	Adipose Nuclei	Adipose
7	chr12:56987600-57021000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr12:56988200-57000400	Strong transcription	Hela-S3	cervix
9	chr12:56988200-57001200	Strong transcription	Primary T cells from cord blood	blood
10	chr12:56988200-57010800	Weak transcription	Right Atrium	heart
11	chr12:56988200-57011400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr12:56988200-57011600	Strong transcription	Stomach Smooth Muscle	stomach
13	chr12:56988200-57015600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:56988400-56993600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:56988400-57001000	Strong transcription	NHLF	lung
16	chr12:56988400-57001600	Strong transcription	A549	lung
17	chr12:56988400-57010800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr12:56988400-57011400	Strong transcription	Brain Germinal Matrix	brain
19	chr12:56988400-57016600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:56988400-57017400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:56988400-57018000	Strong transcription	Fetal Intestine Small	intestine
22	chr12:56988400-57018400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr12:56988400-57021600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:56988600-56993600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:56988600-57000400	Strong transcription	HSMM	muscle
26	chr12:56988600-57001200	Strong transcription	NHEK	skin
27	chr12:56988600-57001800	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr12:56988600-57005200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr12:56988600-57010800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:56988600-57010800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr12:56988600-57012000	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr12:56988600-57017200	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr12:56988800-56995200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:56988800-57011400	Strong transcription	Lung	lung
35	chr12:56988800-57011800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:56988800-57012000	Strong transcription	NHDF-Ad	bronchial
37	chr12:56988800-57015200	Strong transcription	Duodenum Mucosa	Duodenum
38	chr12:56988800-57017600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:56988800-57021600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:56989000-56993400	Weak transcription	Fetal Kidney	kidney
41	chr12:56989000-56993600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr12:56989000-56996000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:56989000-56998000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr12:56989000-57001600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr12:56989000-57001600	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr12:56989000-57012200	Strong transcription	Osteobl	bone
47	chr12:56989000-57017600	Strong transcription	Fetal Intestine Large	intestine
48	chr12:56989200-57001600	Strong transcription	Primary B cells from cord blood	blood
49	chr12:56989200-57011600	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr12:56989400-57001400	Strong transcription	Rectal Smooth Muscle	rectum

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