Variant report

Variant	esv1820402
Chromosome Location	chr12:58092554-58110211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:58097919-58097933	K562	blood:	n/a	n/a
2	CBX3	chr12:58097706-58098107	K562	blood:	n/a	n/a
3	CBX3	chr12:58097733-58098001	K562	blood:	n/a	n/a
4	CTCF	chr12:58109541-58109729	T-47D	breast:	n/a	n/a
5	CTCF	chr12:58109288-58109375	Spleen_OC	spleen:	n/a	n/a
6	E2F4	chr12:58105714-58106082	MCF10A-Er-Src	breast:	n/a	n/a
7	KAP1	chr12:58105758-58106287	K562	blood:	n/a	n/a
8	KAP1	chr12:58097691-58098068	K562	blood:	n/a	n/a
9	MYC	chr12:58108911-58108962	GM12878	blood:	n/a	n/a
10	POLR2A	chr12:58093883-58094590	GM12892	blood:	n/a	n/a
11	POLR2A	chr12:58094036-58094375	GM12891	blood:	n/a	n/a
12	POLR2A	chr12:58109957-58110054	GM12878	blood:	n/a	n/a
13	POLR2A	chr12:58092271-58092713	K562	blood:	n/a	n/a
14	POLR2A	chr12:58094074-58094428	K562	blood:	n/a	n/a
15	POLR2A	chr12:58093102-58093188	K562	blood:	n/a	n/a
16	POLR2A	chr12:58092185-58092837	GM12878	blood:	n/a	n/a
17	POLR2A	chr12:58093989-58094561	GM12892	blood:	n/a	n/a
18	POLR2A	chr12:58093206-58093266	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr12:58092723-58092775	K562	blood:	n/a	n/a
20	POLR2A	chr12:58093040-58093060	K562	blood:	n/a	n/a
21	POLR2A	chr12:58093078-58093098	K562	blood:	n/a	n/a
22	POLR2A	chr12:58092916-58092919	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr12:58093158-58093184	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr12:58094205-58094370	Gliobla	brain:	n/a	n/a
25	POLR2A	chr12:58094247-58094286	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr12:58094174-58094426	HL-60	blood:	n/a	n/a
27	POLR2A	chr12:58093887-58094466	GM12878	blood:	n/a	n/a
28	POLR2A	chr12:58092202-58092784	GM12892	blood:	n/a	n/a
29	POLR2A	chr12:58108294-58108313	GM12878	blood:	n/a	n/a
30	POLR2A	chr12:58109817-58109870	GM12878	blood:	n/a	n/a
31	POLR2A	chr12:58092317-58092668	GM12891	blood:	n/a	n/a
32	POLR2A	chr12:58110076-58110580	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr12:58094770-58094794	K562	blood:	n/a	n/a
34	POLR2A	chr12:58102306-58102323	K562	blood:	n/a	n/a
35	POLR2A	chr12:58092254-58092759	GM12892	blood:	n/a	n/a
36	POLR2A	chr12:58092803-58093411	GM12892	blood:	n/a	n/a
37	POLR2A	chr12:58093946-58094424	GM12892	blood:	n/a	n/a
38	POLR2A	chr12:58109280-58109499	K562	blood:	n/a	n/a
39	POLR2A	chr12:58092459-58092574	K562	blood:	n/a	n/a
40	POLR2A	chr12:58093908-58094576	K562	blood:	n/a	n/a
41	POLR2A	chr12:58092575-58092718	K562	blood:	n/a	n/a
42	POLR2A	chr12:58092116-58092646	K562	blood:	n/a	n/a
43	POLR2A	chr12:58094176-58094296	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:58091880-58092733	GM12878	blood:	n/a	n/a
45	POLR2A	chr12:58093203-58093263	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr12:58092150-58092837	GM12892	blood:	n/a	n/a
47	POLR2A	chr12:58092383-58092582	MCF10A-Er-Src	breast:	n/a	n/a
48	REST	chr12:58109179-58109359	Hela-S3	cervix:	n/a	n/a
49	RUNX3	chr12:58109159-58109429	GM12878	blood:	n/a	n/a
50	SETDB1	chr12:58097714-58098030	U2OS	brain:	n/a	n/a

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:58090857..58093076-chr12:58101229..58103435,2	K562	blood:
2	chr12:58091939..58093791-chr12:58109661..58112406,2	MCF-7	breast:
3	chr12:58091803..58095471-chr12:58101500..58103505,3	K562	blood:
4	chr12:58095878..58097507-chr12:58102658..58104994,2	K562	blood:
5	chr12:58098435..58100959-chr12:58118325..58121297,2	K562	blood:
6	chr12:58088175..58090012-chr12:58107431..58109845,2	K562	blood:
7	chr12:58095878..58097507-chr12:58102658..58104994,2	K562	blood:
8	chr12:58096280..58099117-chr12:58103405..58105701,2	K562	blood:
9	chr12:58105952..58107601-chr12:58114288..58116400,2	K562	blood:
10	chr12:58102856..58104450-chr12:58105470..58107264,2	MCF-7	breast:
11	chr12:58099859..58102384-chr12:58116011..58117778,2	MCF-7	breast:
12	chr12:58106013..58109009-chr12:58109672..58112534,2	K562	blood:
13	chr12:58089791..58092749-chr12:58117567..58121637,3	MCF-7	breast:
14	chr12:58098671..58101243-chr12:58113313..58115696,2	K562	blood:
15	chr12:58087405..58089121-chr12:58098744..58101715,3	MCF-7	breast:
16	chr12:58098442..58100613-chr12:58118455..58121698,3	MCF-7	breast:
17	chr12:57995985..57998083-chr12:58098335..58100355,2	K562	blood:
18	chr12:58089950..58092612-chr12:58113203..58115184,2	MCF-7	breast:
19	chr12:58096280..58099117-chr12:58103405..58105701,2	K562	blood:
20	chr12:58091539..58093555-chr12:58145620..58147612,2	K562	blood:
21	chr12:58091803..58095471-chr12:58101500..58103505,3	K562	blood:
22	chr12:58090857..58093076-chr12:58101229..58103435,2	K562	blood:
23	chr12:58102856..58104450-chr12:58105470..58107264,2	MCF-7	breast:
24	chr12:58106636..58108328-chr12:58120642..58122227,2	K562	blood:
25	chr12:58108037..58111841-chr12:58122870..58126206,3	K562	blood:
26	chr12:58104338..58106820-chr12:58115614..58118088,2	MCF-7	breast:

No data

Variant related genes	Relation type
OS9	TF binding region
ENSG00000257342	chromatin interactions
ENSG00000257499	chromatin interactions
ENSG00000255737	chromatin interactions
ENSG00000135439	chromatin interactions
ENSG00000135446	chromatin interactions
ENSG00000135506	chromatin interactions

Extended variants
information (count: 593 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7979246	chr12:58092554-58092555	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550744371	chr12:58092571-58092572	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs147279660	chr12:58092624-58092625	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs140695486	chr12:58092661-58092662	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs34657476	chr12:58092806-58092807	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552082801	chr12:58092811-58092812	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192556123	chr12:58092833-58092834	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs534409869	chr12:58092862-58092863	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548940841	chr12:58092885-58092886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555890887	chr12:58092935-58092936	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs116661789	chr12:58092951-58092952	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537945790	chr12:58092981-58092982	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs79256159	chr12:58093080-58093081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184034566	chr12:58093100-58093101	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577194005	chr12:58093124-58093125	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544573713	chr12:58093125-58093126	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs79913618	chr12:58093148-58093149	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571968023	chr12:58093175-58093176	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542460206	chr12:58093176-58093177	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs187775806	chr12:58093177-58093178	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143911866	chr12:58093230-58093231	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529408088	chr12:58093269-58093270	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544678770	chr12:58093292-58093293	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562772027	chr12:58093308-58093309	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533387192	chr12:58093358-58093359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs371159136	chr12:58093414-58093415	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551765718	chr12:58093449-58093450	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567183784	chr12:58093481-58093482	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531294558	chr12:58093498-58093499	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527946039	chr12:58093548-58093549	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs549359847	chr12:58093605-58093606	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567840609	chr12:58093607-58093608	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551207587	chr12:58093614-58093615	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537569538	chr12:58093666-58093667	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10783842	chr12:58093735-58093736	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs534103959	chr12:58093739-58093740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570972153	chr12:58093767-58093768	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538254941	chr12:58093770-58093771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368630734	chr12:58093803-58093804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547340854	chr12:58093809-58093810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151008640	chr12:58093817-58093818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554502165	chr12:58093819-58093820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139595882	chr12:58093820-58093821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543225290	chr12:58093830-58093831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10783843	chr12:58093835-58093836	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs578115314	chr12:58093865-58093866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376559244	chr12:58093890-58093891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545425076	chr12:58093910-58093911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35761230	chr12:58094060-58094061	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76031377	chr12:58094062-58094063	Weak transcription Strong transcription Enhancers	n/a	n/a	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
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
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	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	21390271	CNVD
Cancer	20164919	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
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD

Chromatin state (count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58088800-58093400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:58088800-58097800	Strong transcription	Fetal Muscle Trunk	muscle
3	chr12:58088800-58099400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:58088800-58099400	Weak transcription	Small Intestine	intestine
5	chr12:58089000-58092800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr12:58089000-58092800	Strong transcription	Fetal Lung	lung
7	chr12:58089000-58092800	Strong transcription	Skeletal Muscle Male	skeletal muscle
8	chr12:58089000-58094000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:58089000-58094200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr12:58089000-58095800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr12:58089000-58097000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr12:58089000-58109400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:58089000-58110000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr12:58089200-58094400	Strong transcription	Primary B cells from cord blood	blood
15	chr12:58089200-58094400	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr12:58089200-58094600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr12:58089200-58096800	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr12:58089200-58097200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr12:58089200-58097200	Weak transcription	Stomach Mucosa	stomach
20	chr12:58089200-58097600	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr12:58089200-58097600	Weak transcription	HMEC	breast
22	chr12:58089200-58103400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:58089200-58115400	Weak transcription	Fetal Heart	heart
24	chr12:58089400-58092600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:58089400-58092600	Strong transcription	Brain Angular Gyrus	brain
26	chr12:58089400-58092600	Strong transcription	Lung	lung
27	chr12:58089400-58092800	Strong transcription	Primary B cells from peripheral blood	blood
28	chr12:58089400-58092800	Strong transcription	Primary hematopoietic stem cells	blood
29	chr12:58089400-58093000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:58089400-58093000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr12:58089400-58093000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:58089400-58093000	Strong transcription	Ovary	ovary
33	chr12:58089400-58093200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr12:58089400-58093200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:58089400-58093200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr12:58089400-58093200	Strong transcription	Fetal Thymus	thymus
37	chr12:58089400-58093400	Strong transcription	NHLF	lung
38	chr12:58089400-58093600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:58089400-58093600	Strong transcription	HSMM	muscle
40	chr12:58089400-58094200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:58089400-58094400	Strong transcription	Brain Hippocampus Middle	brain
42	chr12:58089400-58094600	Strong transcription	Fetal Muscle Leg	muscle
43	chr12:58089400-58094600	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr12:58089400-58095000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:58089400-58095000	Strong transcription	Stomach Smooth Muscle	stomach
46	chr12:58089400-58096200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr12:58089400-58096600	Strong transcription	Primary T cells from cord blood	blood
48	chr12:58089400-58096800	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr12:58089600-58092600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr12:58089600-58092600	Strong transcription	Fetal Kidney	kidney

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