Variant report

Variant	esv1825546
Chromosome Location	chr1:153779296-153821716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:75)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

No data

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:153777336..153779352-chr1:153950102..153952404,2	MCF-7	breast:
2	chr1:153798990..153801978-chr1:153962252..153964582,2	MCF-7	breast:
3	chr1:153793084..153795411-chr1:153931353..153934057,2	MCF-7	breast:
4	chr1:153773297..153774898-chr1:153777098..153779392,2	K562	blood:
5	chr1:153779392..153782114-chr1:153946020..153947637,2	K562	blood:
6	chr1:153775203..153777547-chr1:153784998..153786855,2	MCF-7	breast:
7	chr1:153781038..153783367-chr1:153783420..153785659,2	MCF-7	breast:
8	chr1:153813066..153815919-chr1:153892208..153893963,2	MCF-7	breast:
9	chr1:153814874..153817706-chr1:153820068..153822280,2	K562	blood:
10	chr1:153783970..153785844-chr1:153789077..153791186,2	K562	blood:
11	chr1:153779892..153781769-chr1:153894915..153896486,2	MCF-7	breast:
12	chr1:153781412..153783974-chr1:153933082..153935617,2	MCF-7	breast:
13	chr1:153776789..153780334-chr1:153780412..153785020,5	K562	blood:
14	chr1:153767398..153773135-chr1:153773279..153780360,13	K562	blood:
15	chr1:153811800..153813903-chr1:153896720..153898248,2	MCF-7	breast:
16	chr1:153797679..153802032-chr1:153916832..153919852,5	MCF-7	breast:
17	chr1:153792838..153795369-chr1:153845133..153846957,2	K562	blood:
18	chr1:153791210..153792751-chr1:153952778..153955026,2	K562	blood:
19	chr1:153791791..153793988-chr1:153929348..153931015,2	MCF-7	breast:
20	chr1:153782929..153785587-chr1:153917374..153919279,2	MCF-7	breast:
21	chr1:153793493..153794478-chr1:153958853..153959485,4	K562	blood:
22	chr1:153753381..153755044-chr1:153796141..153797868,2	MCF-7	breast:
23	chr1:153780988..153782911-chr1:153949119..153951026,2	K562	blood:
24	chr1:153791675..153794891-chr1:153798277..153801719,3	MCF-7	breast:
25	chr1:153819949..153821469-chr16:88796842..88798554,3	MCF-7	breast:
26	chr1:153803578..153805707-chr1:153809227..153810744,2	MCF-7	breast:
27	chr1:153777991..153779497-chr1:153782231..153784183,2	K562	blood:
28	chr1:153778414..153782533-chr1:153962253..153965018,3	K562	blood:
29	chr1:153795765..153798553-chr1:153961941..153964653,2	K562	blood:
30	chr1:153783970..153785844-chr1:153789077..153791186,2	K562	blood:
31	chr1:153794811..153797634-chr1:153899769..153901924,2	MCF-7	breast:
32	chr1:153817561..153820058-chr1:153930768..153932279,2	MCF-7	breast:
33	chr1:153748762..153752537-chr1:153776954..153780050,3	K562	blood:
34	chr1:153803578..153805707-chr1:153809227..153810744,2	MCF-7	breast:
35	chr1:153788802..153791182-chr1:153963012..153964796,2	K562	blood:
36	chr1:153784309..153788239-chr1:153961898..153965879,4	K562	blood:
37	chr1:153777991..153779497-chr1:153782231..153784183,2	K562	blood:
38	chr1:153792897..153795866-chr1:153896474..153898654,2	MCF-7	breast:
39	chr1:153783710..153786405-chr1:153913756..153915563,2	MCF-7	breast:
40	chr1:153777962..153780405-chr1:153929432..153931611,2	K562	blood:
41	chr1:153818084..153820618-chr1:153917099..153920025,2	MCF-7	breast:
42	chr1:153779392..153782114-chr1:153944951..153947637,3	K562	blood:
43	chr1:153779706..153782124-chr1:153785202..153786714,2	K562	blood:
44	chr1:153780797..153783971-chr1:153788567..153790595,3	MCF-7	breast:
45	chr1:153791701..153795974-chr1:153918288..153922037,4	MCF-7	breast:
46	chr1:153791929..153794477-chr1:153963416..153966079,2	K562	blood:
47	chr1:153788299..153790098-chr1:153958682..153960325,2	K562	blood:
48	chr1:153791929..153793836-chr1:153962034..153964916,2	K562	blood:
49	chr1:153793861..153794433-chr1:153918747..153919696,3	MCF-7	breast:
50	chr1:153775180..153778108-chr1:153780160..153781973,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DENND4B-4	chr1:153797944-153798260	expReg_chr1_15750_-

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GATAD2B	hsa-miR-590-3p	chr1:153780964-153780985
2	GATAD2B	hsa-miR-32-5p	chr1:153780248-153780268
3	GATAD2B	hsa-miR-590-3p	chr1:153780931-153780951
4	GATAD2B	hsa-miR-32-5p	chr1:153781242-153781236
5	GATAD2B	hsa-miR-590-3p	chr1:153780551-153780570
6	GATAD2B	hsa-miR-32-5p	chr1:153781236-153781256
7	GATAD2B	hsa-miR-186-5p	chr1:153781719-153781740
8	GATAD2B	hsa-miR-590-3p	chr1:153780557-153780550
9	GATAD2B	hsa-miR-32-5p	chr1:153780254-153780247
10	GATAD2B	hsa-miR-590-3p	chr1:153780937-153780930

Variant related genes	Relation type
ENSG00000143545	chromatin interactions
ENSG00000160741	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000231827	chromatin interactions
ENSG00000272654	chromatin interactions
ENSG00000143543	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000198837	chromatin interactions
ENSG00000143614	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000224888	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000273026	chromatin interactions
ENSG00000143554	chromatin interactions

Extended variants
information (count: 1546 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547459190	chr1:153779347-153779348	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs202015857	chr1:153779365-153779366	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs559738108	chr1:153779383-153779384	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs187479995	chr1:153779397-153779398	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs1127091	chr1:153779412-153779413	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs192329538	chr1:153779422-153779423	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs537221129	chr1:153779442-153779443	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs138859599	chr1:153779463-153779464	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs35169408	chr1:153779469-153779470	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs567849088	chr1:153779576-153779577	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs528627248	chr1:153779577-153779578	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs41302127	chr1:153779629-153779630	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs559928274	chr1:153779659-153779660	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs74809494	chr1:153779663-153779664	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs553488206	chr1:153779740-153779741	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs184540759	chr1:153779754-153779755	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs539451577	chr1:153779766-153779767	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs1139619	chr1:153779831-153779832	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576225019	chr1:153779833-153779834	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs573434177	chr1:153779838-153779839	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs368465944	chr1:153779856-153779857	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs545621721	chr1:153780009-153780010	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs207460442	chr1:153780014-153780015	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs565414640	chr1:153780023-153780024	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs142057668	chr1:153780026-153780027	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs531254429	chr1:153780054-153780055	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs529476523	chr1:153780061-153780062	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs561950662	chr1:153780123-153780124	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs551026626	chr1:153780176-153780177	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs541362242	chr1:153780245-153780246	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs9426938	chr1:153780298-153780299	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs145768511	chr1:153780336-153780337	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs545024695	chr1:153780342-153780343	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs115254400	chr1:153780433-153780434	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs187816167	chr1:153780483-153780484	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs549156846	chr1:153780530-153780531	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs567897881	chr1:153780632-153780633	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs528684210	chr1:153780633-153780634	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs547233449	chr1:153780642-153780643	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs571864729	chr1:153780655-153780656	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs539410481	chr1:153780764-153780765	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs557812401	chr1:153780789-153780790	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs368396933	chr1:153780791-153780792	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569750010	chr1:153780882-153780883	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs192942533	chr1:153781050-153781051	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs184195925	chr1:153781106-153781107	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs548657142	chr1:153781271-153781272	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs75480949	chr1:153781274-153781275	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs76230343	chr1:153781275-153781276	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs58886241	chr1:153781295-153781296	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153762600-153779600	Weak transcription	Gastric	stomach
2	chr1:153762600-153779600	Weak transcription	Pancreas	Pancrea
3	chr1:153763600-153780000	Weak transcription	Aorta	Aorta
4	chr1:153763600-153780000	Weak transcription	Ovary	ovary
5	chr1:153763600-153780800	Weak transcription	Colonic Mucosa	Colon
6	chr1:153763800-153779400	Weak transcription	Brain Substantia Nigra	brain
7	chr1:153764000-153779600	Weak transcription	Brain Angular Gyrus	brain
8	chr1:153764400-153779600	Weak transcription	Brain Anterior Caudate	brain
9	chr1:153767000-153779400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr1:153767600-153782600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr1:153767800-153779600	Weak transcription	Fetal Lung	lung
12	chr1:153768000-153779600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr1:153768000-153779600	Weak transcription	Brain Hippocampus Middle	brain
14	chr1:153768000-153781400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:153768200-153779400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:153768200-153779600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:153768200-153779600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr1:153768400-153779800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:153769800-153779400	Weak transcription	Colon Smooth Muscle	Colon
20	chr1:153769800-153781400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr1:153770400-153791400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:153770600-153783600	Weak transcription	Fetal Brain Male	brain
23	chr1:153770800-153792400	Strong transcription	Fetal Stomach	stomach
24	chr1:153771200-153779400	Weak transcription	HepG2	liver
25	chr1:153771800-153791800	Strong transcription	Primary T cells from cord blood	blood
26	chr1:153772000-153792000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr1:153772200-153781200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:153772400-153779600	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:153772600-153781400	Weak transcription	Esophagus	oesophagus
30	chr1:153772600-153791600	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:153773000-153779400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr1:153773600-153791800	Strong transcription	Thymus	Thymus
33	chr1:153774000-153801800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:153774800-153779400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:153775000-153779800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr1:153775000-153798800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:153775600-153779400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:153775600-153779600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr1:153775600-153779600	Weak transcription	Fetal Kidney	kidney
40	chr1:153775800-153779600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr1:153776400-153787800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr1:153776400-153791600	Strong transcription	Fetal Muscle Trunk	muscle
43	chr1:153776600-153779400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:153776800-153779600	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr1:153777000-153779400	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr1:153777000-153779600	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr1:153777000-153780000	Weak transcription	Spleen	Spleen
48	chr1:153777200-153782400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:153777400-153801000	Strong transcription	Fetal Intestine Small	intestine
50	chr1:153777600-153779400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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