Variant report

Variant	nsv525202
Chromosome Location	chr12:57004668-57013844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:0)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:57007623-57007668	HepG2	liver:	n/a	chr12:57007641-57007652
2	EBF1	chr12:57010163-57010168	GM12878	blood:	n/a	n/a
3	EP300	chr12:57010977-57010983	K562	blood:	n/a	n/a
4	MAFK	chr12:57008829-57008901	HepG2	liver:	n/a	n/a
5	MAFK	chr12:57010857-57010912	K562	blood:	n/a	n/a
6	MYC	chr12:57005926-57005981	GM12878	blood:	n/a	n/a
7	POLR2A	chr12:57005175-57005267	HepG2	liver:	n/a	n/a
8	POLR2A	chr12:57007496-57008058	K562	blood:	n/a	n/a
9	POLR2A	chr12:57009864-57009881	HepG2	liver:	n/a	n/a
10	POLR2A	chr12:57005336-57005592	GM12878	blood:	n/a	n/a
11	POLR2A	chr12:57005564-57005592	MCF-7	breast:	n/a	n/a
12	POLR2A	chr12:57007034-57007271	HepG2	liver:	n/a	n/a
13	POLR2A	chr12:57005290-57005337	GM12878	blood:	n/a	n/a
14	POLR2A	chr12:57007506-57008145	SK-N-MC	brain:	n/a	n/a
15	POLR2A	chr12:57008984-57009190	K562	blood:	n/a	n/a
16	POLR2A	chr12:57005544-57005557	MCF-7	breast:	n/a	n/a
17	POLR2A	chr12:57008831-57008889	GM12878	blood:	n/a	n/a
18	POLR2A	chr12:57009698-57009722	HepG2	liver:	n/a	n/a
19	POLR2A	chr12:57005253-57005303	GM12878	blood:	n/a	n/a
20	POLR2A	chr12:57009742-57009754	HepG2	liver:	n/a	n/a
21	POLR2A	chr12:57008488-57008611	ProgFib	skin:	n/a	n/a
22	POLR2A	chr12:57013754-57013943	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr12:57008037-57008069	HepG2	liver:	n/a	n/a
24	POLR2A	chr12:57010154-57010163	HepG2	liver:	n/a	n/a
25	POLR2A	chr12:57006922-57007080	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr12:57010045-57010056	HepG2	liver:	n/a	n/a
27	POLR2A	chr12:57008051-57008139	GM12878	blood:	n/a	n/a
28	POLR2A	chr12:57005210-57005301	K562	blood:	n/a	n/a
29	POLR2A	chr12:57007717-57008027	MCF-7	breast:	n/a	n/a
30	POLR2A	chr12:57006226-57006462	GM12878	blood:	n/a	n/a
31	POLR2A	chr12:57009235-57009318	K562	blood:	n/a	n/a
32	POLR2A	chr12:57008303-57008341	HepG2	liver:	n/a	n/a
33	POLR2A	chr12:57006291-57006496	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:57012392-57012403	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr12:57005369-57005387	K562	blood:	n/a	n/a
36	POLR2A	chr12:57009639-57009703	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr12:57008682-57009029	PFSK-1	brain:	n/a	n/a
38	POLR2A	chr12:57008261-57009302	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:57007224-57007332	K562	blood:	n/a	n/a
40	POLR2A	chr12:57009609-57009673	HepG2	liver:	n/a	n/a
41	RCOR1	chr12:57010794-57010969	K562	blood:	n/a	n/a
42	STAT3	chr12:57010877-57010916	MCF10A-Er-Src	breast:	n/a	n/a
43	TBL1XR1	chr12:57010856-57010935	K562	blood:	n/a	n/a
44	TCF7L2	chr12:57012032-57012104	HepG2	liver:	n/a	n/a

No data

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57010005..57012841-chr12:57025383..57028519,3	K562	blood:
2	chr12:57008148..57010026-chr12:57012306..57015125,2	MCF-7	breast:
3	chr12:56998330..57000367-chr12:57003607..57006426,2	K562	blood:
4	chr12:57005351..57008593-chr12:57022462..57024744,3	MCF-7	breast:
5	chr12:57006227..57008804-chr12:57012388..57014898,2	MCF-7	breast:
6	chr12:57002618..57004175-chr12:57008066..57010666,2	MCF-7	breast:
7	chr12:57008148..57010026-chr12:57012306..57015125,2	MCF-7	breast:
8	chr12:57007109..57010688-chr12:57028709..57032558,4	K562	blood:
9	chr12:57010005..57012841-chr12:57024813..57028519,3	K562	blood:
10	chr12:56992042..56997013-chr12:57005431..57010145,6	K562	blood:
11	chr12:57007576..57011476-chr12:57012265..57014896,4	K562	blood:
12	chr12:57010896..57011499-chr12:57030149..57030692,2	K562	blood:
13	chr12:56579705..56582945-chr12:57008774..57012343,3	K562	blood:
14	chr12:56994821..56997665-chr12:57004443..57006406,2	MCF-7	breast:
15	chr12:57002806..57005190-chr12:57036695..57039247,2	MCF-7	breast:
16	chr12:57010024..57012085-chr12:57022612..57024595,2	K562	blood:
17	chr12:57011192..57013564-chr12:57014925..57017700,3	K562	blood:
18	chr12:57012523..57015278-chr12:57016203..57018882,3	K562	blood:
19	chr12:57010590..57012820-chr12:57015477..57017795,2	MCF-7	breast:
20	chr12:57009522..57015507-chr12:57021199..57030351,9	MCF-7	breast:
21	chr12:57003620..57005950-chr12:57028617..57030192,2	MCF-7	breast:
22	chr12:57004812..57007762-chr12:57013196..57018019,5	MCF-7	breast:
23	chr12:57006171..57009899-chr12:57021383..57024124,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5B-1	chr12:57009305-57009391	NONHSAT028835
2	lnc-ATP5B-1	chr12:57011179-57011316	NONHSAT028835

No data

Variant related genes	Relation type
BAZ2A	TF binding region
ENSG00000207031	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000110955	chromatin interactions

Extended variants
information (count: 352 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2958139	chr12:57004668-57004669	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527341891	chr12:57004673-57004674	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs7307578	chr12:57004694-57004695	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs193064596	chr12:57004715-57004716	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs375790797	chr12:57004719-57004720	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs549583689	chr12:57004773-57004774	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs150536850	chr12:57004788-57004789	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs565945766	chr12:57004866-57004867	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs185436528	chr12:57004920-57004921	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs560829787	chr12:57004926-57004927	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs565963535	chr12:57004952-57004953	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs189952984	chr12:57004977-57004978	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs191941370	chr12:57004995-57004996	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs370143884	chr12:57005026-57005027	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs567777948	chr12:57005028-57005029	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs139811249	chr12:57005048-57005049	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs556799861	chr12:57005065-57005066	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs578188380	chr12:57005078-57005079	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs141567175	chr12:57005079-57005080	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs554195653	chr12:57005095-57005096	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs184191748	chr12:57005122-57005123	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530441003	chr12:57005267-57005268	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs560517426	chr12:57005302-57005303	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs377351428	chr12:57005320-57005321	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs370348322	chr12:57005375-57005376	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375170579	chr12:57005415-57005416	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529882168	chr12:57005446-57005447	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs370240448	chr12:57005448-57005449	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116827484	chr12:57005498-57005499	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200406851	chr12:57005542-57005543	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200043280	chr12:57005547-57005548	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201862765	chr12:57005548-57005549	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs529970091	chr12:57005556-57005557	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549420706	chr12:57005571-57005572	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370773408	chr12:57005589-57005590	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34043198	chr12:57005661-57005662	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375032854	chr12:57005667-57005668	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2230579	chr12:57005679-57005680	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538352941	chr12:57005680-57005681	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74560967	chr12:57005694-57005695	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372705713	chr12:57005704-57005705	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556736559	chr12:57005724-57005725	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572032902	chr12:57005793-57005794	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546840071	chr12:57005797-57005798	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560419494	chr12:57005798-57005799	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374554603	chr12:57005827-57005828	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188521176	chr12:57005878-57005879	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538895121	chr12:57005899-57005900	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375474120	chr12:57005908-57005909	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs61748825	chr12:57005911-57005912	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
early-passage human iPS cells	21368824	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56977600-57017000	Strong transcription	Placenta	Placenta
2	chr12:56979600-57020400	Strong transcription	Fetal Stomach	stomach
3	chr12:56987600-57012000	Strong transcription	Liver	Liver
4	chr12:56987600-57014800	Strong transcription	Adipose Nuclei	Adipose
5	chr12:56987600-57021000	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr12:56988200-57010800	Weak transcription	Right Atrium	heart
7	chr12:56988200-57011400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:56988200-57011600	Strong transcription	Stomach Smooth Muscle	stomach
9	chr12:56988200-57015600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:56988400-57010800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr12:56988400-57011400	Strong transcription	Brain Germinal Matrix	brain
12	chr12:56988400-57016600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:56988400-57017400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr12:56988400-57018000	Strong transcription	Fetal Intestine Small	intestine
15	chr12:56988400-57018400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr12:56988400-57021600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:56988600-57005200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:56988600-57010800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:56988600-57010800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr12:56988600-57012000	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr12:56988600-57017200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr12:56988800-57011400	Strong transcription	Lung	lung
23	chr12:56988800-57011800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:56988800-57012000	Strong transcription	NHDF-Ad	bronchial
25	chr12:56988800-57015200	Strong transcription	Duodenum Mucosa	Duodenum
26	chr12:56988800-57017600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:56988800-57021600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:56989000-57012200	Strong transcription	Osteobl	bone
29	chr12:56989000-57017600	Strong transcription	Fetal Intestine Large	intestine
30	chr12:56989200-57011600	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr12:56989400-57008800	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr12:56989400-57011400	Strong transcription	Brain Hippocampus Middle	brain
33	chr12:56989400-57019000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr12:56989400-57020000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:56989600-57011400	Strong transcription	H9 Cell Line	embryonic stem cell
36	chr12:56989600-57012800	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr12:56989600-57013200	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr12:56989600-57017400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:56989800-57014800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr12:56990000-57008800	Strong transcription	Right Ventricle	heart
41	chr12:56990000-57012200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr12:56990400-57016600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr12:56990600-57011000	Strong transcription	Brain Cingulate Gyrus	brain
44	chr12:56990600-57011400	Strong transcription	Aorta	Aorta
45	chr12:56990600-57011400	Strong transcription	Colon Smooth Muscle	Colon
46	chr12:56990600-57011400	Strong transcription	Spleen	Spleen
47	chr12:56990600-57011600	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr12:56990600-57016400	Strong transcription	Primary B cells from peripheral blood	blood
49	chr12:56990800-57007600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr12:56990800-57010200	Strong transcription	Skeletal Muscle Female	skeletal muscle

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