Variant report

Variant	esv3381217
Chromosome Location	chr12:56644285-56649383
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:30)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:30 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA1	chr12:56646835-56647369	PBDE	blood:	n/a	chr12:56646990-56646999 chr12:56646991-56647008 chr12:56646990-56646999
2	MYC	chr12:56646023-56646039	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr12:56647158-56647183	MCF-7	breast:	n/a	n/a
4	POLR2A	chr12:56646623-56647055	U87	brain:	n/a	n/a
5	POLR2A	chr12:56645456-56645595	HepG2	liver:	n/a	n/a
6	POLR2A	chr12:56646827-56646939	K562	blood:	n/a	n/a
7	POLR2A	chr12:56647135-56647136	MCF-7	breast:	n/a	n/a
8	POLR2A	chr12:56648896-56648958	K562	blood:	n/a	n/a
9	POLR2A	chr12:56649093-56649226	HepG2	liver:	n/a	n/a
10	POLR2A	chr12:56648306-56648572	K562	blood:	n/a	n/a
11	POLR2A	chr12:56645291-56645318	HepG2	liver:	n/a	n/a
12	POLR2A	chr12:56644260-56644325	HUVEC	blood vessel:	n/a	n/a
13	POLR2A	chr12:56646634-56647337	K562	blood:	n/a	n/a
14	POLR2A	chr12:56646208-56647515	U87	brain:	n/a	n/a
15	POLR2A	chr12:56647984-56648037	HepG2	liver:	n/a	n/a
16	POLR2A	chr12:56647109-56647356	K562	blood:	n/a	n/a
17	POLR2A	chr12:56646558-56646887	GM12878	blood:	n/a	n/a
18	POLR2A	chr12:56647465-56647477	K562	blood:	n/a	n/a
19	POLR2A	chr12:56645717-56645772	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr12:56644764-56644868	GM12878	blood:	n/a	n/a
21	POLR2A	chr12:56647302-56647602	K562	blood:	n/a	n/a
22	POLR2A	chr12:56646544-56646546	MCF-7	breast:	n/a	n/a
23	POLR2A	chr12:56646573-56647099	HepG2	liver:	n/a	n/a
24	POLR2A	chr12:56648559-56648969	PFSK-1	brain:	n/a	n/a
25	POLR2A	chr12:56648044-56648328	HepG2	liver:	n/a	n/a
26	POLR2A	chr12:56646558-56646670	MCF-7	breast:	n/a	n/a
27	POLR2A	chr12:56646696-56646726	MCF-7	breast:	n/a	n/a
28	POLR2A	chr12:56646723-56647509	U87	brain:	n/a	n/a
29	POLR2A	chr12:56646997-56647138	A549	lung:	n/a	n/a
30	WRNIP1	chr12:56646873-56646929	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56649358-56649408	ovcar-3	ovarian:	n/a
2	chr12:56649358-56649408	A549	lung:	n/a
3	chr12:56649358-56649408	HAEpiC	amniotic membrane:	n/a
4	chr12:56649358-56649408	BE2_C	brain:	n/a
5	chr12:56649358-56649408	HIPEpiC	eye:	n/a
6	chr12:56649358-56649408	HMEC	breast:	n/a
7	chr12:56649358-56649408	HL-60	blood:	n/a
8	chr12:56649358-56649408	MCF-7	breast:	n/a
9	chr12:56649358-56649408	ECC-1	luminal epithelium:	n/a
10	chr12:56649358-56649408	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:56649358-56649408	SAEC	small airway:	n/a
12	chr12:56649358-56649408	AG10803	skin:	n/a
13	chr12:56649358-56649408	GM06990	blood:	n/a
14	chr12:56649358-56649408	HCT-116	colon:	n/a
15	chr12:56649358-56649408	HCM	heart:	n/a
16	chr12:56649358-56649408	HUVEC	blood vessel:	n/a
17	chr12:56649358-56649408	RPTEC	kidney:	n/a
18	chr12:56649358-56649408	PANC-1	pancreas:	n/a
19	chr12:56649358-56649408	U87	brain:	n/a
20	chr12:56649358-56649408	AoSMC	blood vessel:	n/a
21	chr12:56649358-56649408	Caco-2	colon:	n/a
22	chr12:56649358-56649408	AG09319	gingival:	n/a
23	chr12:56649358-56649408	AG04450	lung:	fetal
24	chr12:56649358-56649408	GM12892	blood:	n/a
25	chr12:56649358-56649408	NH-A	brain:	n/a
26	chr12:56649358-56649408	Hepatocyte	liver:	n/a
27	chr12:56649358-56649408	HRE	kidney:	n/a
28	chr12:56649358-56649408	NB4	blood:	n/a
29	chr12:56649358-56649408	Hela-S3	cervix:	n/a
30	chr12:56649358-56649408	HCF	heart:	n/a
31	chr12:56649358-56649408	BJ	skin:	n/a
32	chr12:56649358-56649408	HEK293	kidney:	embryo
33	chr12:56649358-56649408	SK-N-SH	brain:	n/a
34	chr12:56649358-56649408	K562	blood:	n/a
35	chr12:56649358-56649408	SKMC	muscle:	n/a
36	chr12:56649358-56649408	HRPEpiC	eye:	n/a
37	chr12:56649358-56649408	T-47D	breast:	n/a
38	chr12:56649358-56649408	AG09309	skin:	n/a
39	chr12:56649358-56649408	HNPCEpiC	eye:	n/a
40	chr12:56649358-56649408	HCPEpiC	choroid plexus:	n/a
41	chr12:56649358-56649408	GM12891	blood:	n/a
42	chr12:56649358-56649408	HEEpiC	esophagus:	n/a
43	chr12:56649358-56649408	SK-N-MC	brain:	n/a
44	chr12:56649358-56649408	PFSK-1	brain:	n/a
45	chr12:56649358-56649408	AG04449	skin:	fetal
46	chr12:56649358-56649408	MCF10A-Er-Src	breast:	n/a
47	chr12:56649358-56649408	HepG2	liver:	n/a
48	chr12:56649358-56649408	LNCaP	prostate:	n/a
49	chr12:56649358-56649408	GM19239	blood:	n/a
50	chr12:56649358-56649408	GM12878	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56510333..56513421-chr12:56649218..56653989,6	MCF-7	breast:
2	chr12:56617137..56618996-chr12:56645914..56648386,2	MCF-7	breast:
3	chr12:56632924..56644144-chr12:56648283..56654213,19	MCF-7	breast:
4	chr12:56614200..56620176-chr12:56644045..56650698,8	K562	blood:
5	chr12:56632067..56634668-chr12:56642933..56645753,2	K562	blood:
6	chr12:56621685..56625461-chr12:56647318..56652615,5	MCF-7	breast:
7	chr12:56636502..56647526-chr12:56648654..56655042,17	K562	blood:
8	chr12:56648518..56655064-chr12:56657769..56662263,7	K562	blood:
9	chr12:56649316..56652198-chr12:56727445..56729500,2	K562	blood:
10	chr12:56613899..56621490-chr12:56648204..56656770,13	K562	blood:
11	chr12:56636502..56647526-chr12:56648654..56655042,17	K562	blood:
12	chr12:56629936..56632374-chr12:56645303..56647914,2	MCF-7	breast:

No data

Variant related genes	Relation type
ANKRD52	TF binding region
ANKRD52	CpG island
ENSG00000135473	chromatin interactions
ENSG00000139540	chromatin interactions
ENSG00000139645	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000181852	chromatin interactions
ENSG00000135469	chromatin interactions
ENSG00000139579	chromatin interactions

Extended variants
information (count: 203 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:203 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564605200	chr12:56644285-56644286	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs528582780	chr12:56644297-56644298	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs189828861	chr12:56644454-56644455	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192913034	chr12:56644512-56644513	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs576152353	chr12:56644519-56644520	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs60547094	chr12:56644533-56644534	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs529583177	chr12:56644544-56644545	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs537798697	chr12:56644561-56644562	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372494069	chr12:56644584-56644585	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs150520320	chr12:56644591-56644592	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs569490372	chr12:56644603-56644604	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs79850577	chr12:56644669-56644670	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs532938272	chr12:56644670-56644671	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs551091908	chr12:56644724-56644725	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536815784	chr12:56644788-56644789	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs556758208	chr12:56644811-56644812	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs1274492	chr12:56644841-56644842	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533663512	chr12:56644844-56644845	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs59822547	chr12:56644886-56644887	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs567097777	chr12:56644909-56644910	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537680968	chr12:56644913-56644914	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs556032441	chr12:56644917-56644918	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577909237	chr12:56644944-56644945	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs184627566	chr12:56645004-56645005	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs557879129	chr12:56645006-56645007	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs573254603	chr12:56645020-56645021	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs575956498	chr12:56645085-56645086	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs12368168	chr12:56645097-56645098	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs368310435	chr12:56645098-56645099	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs558636534	chr12:56645136-56645137	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs562193445	chr12:56645146-56645147	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs529495687	chr12:56645147-56645148	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs544865098	chr12:56645171-56645172	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs180799302	chr12:56645173-56645174	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs563149075	chr12:56645225-56645226	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552034000	chr12:56645253-56645254	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572179771	chr12:56645321-56645322	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs541216948	chr12:56645322-56645323	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs117632237	chr12:56645349-56645350	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs551321568	chr12:56645456-56645457	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs566364237	chr12:56645457-56645458	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs527314237	chr12:56645463-56645464	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs112944721	chr12:56645480-56645481	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs567061526	chr12:56645499-56645500	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs11286294	chr12:56645523-56645524	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs75469688	chr12:56645543-56645544	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs398019707	chr12:56645544-56645545	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs537648345	chr12:56645562-56645563	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs561113547	chr12:56645572-56645573	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs571482190	chr12:56645586-56645587	Weak transcription Strong transcription	Chromatin interactive region	4 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	19115005	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

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56624400-56646000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:56628600-56644600	Strong transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:56628600-56649800	Strong transcription	Fetal Stomach	stomach
4	chr12:56629000-56649400	Strong transcription	Thymus	Thymus
5	chr12:56629000-56650400	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr12:56629200-56649600	Strong transcription	Brain Germinal Matrix	brain
7	chr12:56629200-56650000	Strong transcription	Liver	Liver
8	chr12:56629200-56650200	Strong transcription	Brain Anterior Caudate	brain
9	chr12:56629400-56649600	Strong transcription	Fetal Muscle Leg	muscle
10	chr12:56629600-56649600	Strong transcription	Fetal Brain Female	brain
11	chr12:56629800-56649400	Strong transcription	Skeletal Muscle Male	skeletal muscle
12	chr12:56629800-56649800	Strong transcription	Stomach Smooth Muscle	stomach
13	chr12:56629800-56650000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:56629800-56650200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:56629800-56650200	Strong transcription	Primary T cells from cord blood	blood
16	chr12:56630000-56644600	Strong transcription	Lung	lung
17	chr12:56630000-56648600	Strong transcription	Dnd41	blood
18	chr12:56630000-56649400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr12:56630000-56649600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr12:56630000-56649600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:56630000-56649800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr12:56630000-56650200	Strong transcription	Fetal Muscle Trunk	muscle
23	chr12:56630000-56650600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:56630200-56650000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr12:56630400-56644400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr12:56630400-56650200	Strong transcription	Fetal Thymus	thymus
27	chr12:56630600-56650400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:56631000-56650000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr12:56631800-56649400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr12:56632200-56650200	Strong transcription	Brain Inferior Temporal Lobe	brain
31	chr12:56632400-56650200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr12:56632600-56650200	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:56632600-56650200	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr12:56632800-56649600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr12:56632800-56649600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr12:56632800-56650000	Strong transcription	H9 Cell Line	embryonic stem cell
37	chr12:56632800-56650000	Strong transcription	NHEK	skin
38	chr12:56633000-56650000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:56633000-56650200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:56633000-56650200	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr12:56633000-56650400	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr12:56633000-56650600	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr12:56633200-56649600	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr12:56633200-56650000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr12:56633200-56650600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:56633400-56649600	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr12:56633400-56649800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr12:56633400-56650000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr12:56633400-56650000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr12:56633600-56650600	Strong transcription	Primary monocytes fromperipheralblood	blood

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