Variant report

Variant	nsv946308
Chromosome Location	chr1:147013512-147039086
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:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:147013179..147017190-chr1:147018017..147020849,5	K562	blood:
2	chr1:147031464..147034228-chr1:147042792..147044457,2	K562	blood:
3	chr1:147032900..147033441-chr2:220406181..220407112,2	MCF-7	breast:
4	chr1:147016778..147019851-chr1:147026227..147029377,3	MCF-7	breast:
5	chr1:147030113..147033038-chr1:147036369..147040192,4	MCF-7	breast:
6	chr1:147012761..147015831-chr1:147068894..147072363,4	MCF-7	breast:
7	chr1:147015861..147018726-chr1:147069919..147072296,3	MCF-7	breast:
8	chr1:147011634..147014268-chr1:147023990..147027027,3	MCF-7	breast:
9	chr1:147016778..147019851-chr1:147026227..147029377,3	MCF-7	breast:
10	chr1:147037749..147039764-chr1:147041028..147044624,4	K562	blood:
11	chr1:147016993..147019863-chr1:147022177..147023748,3	MCF-7	breast:
12	chr1:147022754..147025492-chr1:147026294..147028683,2	MCF-7	breast:
13	chr1:147011744..147014234-chr1:147070783..147072314,2	K562	blood:
14	chr1:147010483..147014086-chr1:147140786..147143809,3	MCF-7	breast:
15	chr1:147019962..147021881-chr1:147028732..147030499,2	K562	blood:
16	chr1:147009715..147011902-chr1:147032676..147034909,2	MCF-7	breast:
17	chr1:147018435..147020925-chr1:147022562..147024139,2	K562	blood:
18	chr1:147008733..147014706-chr1:147069097..147075030,9	MCF-7	breast:
19	chr1:147030113..147033038-chr1:147036369..147040192,4	MCF-7	breast:
20	chr1:147011744..147014234-chr1:147070783..147073063,3	K562	blood:
21	chr1:147004459..147006427-chr1:147014371..147016886,2	MCF-7	breast:
22	chr1:147012652..147015179-chr1:147029678..147032847,3	MCF-7	breast:
23	chr1:147019962..147021881-chr1:147028732..147030499,2	K562	blood:
24	chr1:147022754..147025492-chr1:147026294..147028683,2	MCF-7	breast:
25	chr1:147016993..147019863-chr1:147022177..147023748,3	MCF-7	breast:
26	chr1:147018435..147020925-chr1:147022562..147024139,2	K562	blood:
27	chr1:147015520..147016167-chr10:38803805..38804327,2	MCF-7	breast:
28	chr1:147014865..147017655-chr1:147069985..147072469,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000116128	chromatin interactions
ENSG00000162836	chromatin interactions

Extended variants
information (count: 791 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587760278	chr1:147013588-147013589	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs587594965	chr1:147013606-147013607	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587672355	chr1:147013660-147013661	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs35148808	chr1:147013700-147013701	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141781085	chr1:147013713-147013714	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs376680050	chr1:147013714-147013715	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs587634045	chr1:147013733-147013734	Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs587685367	chr1:147013820-147013821	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs587747791	chr1:147013832-147013833	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs594132	chr1:147013836-147013837	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs113473205	chr1:147013861-147013862	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs149091562	chr1:147013912-147013913	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373444424	chr1:147013923-147013924	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs185443838	chr1:147013970-147013971	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367831243	chr1:147013971-147013972	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587655208	chr1:147013996-147013997	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs587694424	chr1:147014015-147014016	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587748347	chr1:147014039-147014040	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587650709	chr1:147014094-147014095	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587703524	chr1:147014164-147014165	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587621416	chr1:147014246-147014247	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs587656202	chr1:147014259-147014260	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587737758	chr1:147014266-147014267	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189705340	chr1:147014311-147014312	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587641563	chr1:147014312-147014313	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112523167	chr1:147014320-147014321	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374941881	chr1:147014322-147014323	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587737150	chr1:147014324-147014325	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183085904	chr1:147014419-147014420	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369330721	chr1:147014462-147014463	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587664717	chr1:147014477-147014478	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs73007950	chr1:147014490-147014491	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587620466	chr1:147014562-147014563	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs191608330	chr1:147014574-147014575	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs74125726	chr1:147014578-147014579	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116592734	chr1:147014581-147014582	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587691455	chr1:147014611-147014612	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs183857333	chr1:147014616-147014617	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs187303421	chr1:147014643-147014644	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377232708	chr1:147014665-147014666	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144755186	chr1:147014743-147014744	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587682020	chr1:147014763-147014764	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587773974	chr1:147014819-147014820	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587658244	chr1:147014988-147014989	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs192647570	chr1:147014995-147014996	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146767095	chr1:147015036-147015037	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs35311986	chr1:147015140-147015141	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112510618	chr1:147015144-147015145	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587656732	chr1:147015173-147015174	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4950460	chr1:147015179-147015180	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:141)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	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
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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	19286668	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
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147012000-147014000	Flanking Active TSS	Dnd41	blood
2	chr1:147012000-147014800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:147012000-147015000	Active TSS	Fetal Kidney	kidney
4	chr1:147012200-147014800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr1:147012400-147014600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:147012400-147014800	Active TSS	Aorta	Aorta
7	chr1:147012400-147014800	Active TSS	Right Atrium	heart
8	chr1:147012400-147015000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:147012400-147015000	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr1:147012400-147015200	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr1:147012400-147015200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:147012400-147015200	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr1:147012600-147014200	Active TSS	H9 Cell Line	embryonic stem cell
14	chr1:147012600-147014200	Active TSS	Brain Substantia Nigra	brain
15	chr1:147012600-147014400	Active TSS	Left Ventricle	heart
16	chr1:147012600-147014400	Active TSS	Lung	lung
17	chr1:147012600-147014400	Active TSS	Psoas Muscle	Psoas
18	chr1:147012600-147014600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr1:147012600-147014600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:147012600-147014600	Active TSS	Right Ventricle	heart
21	chr1:147012600-147014800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:147012600-147015200	Active TSS	Ovary	ovary
23	chr1:147012800-147013600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr1:147012800-147013800	Active TSS	H1 Cell Line	embryonic stem cell
25	chr1:147012800-147013800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:147012800-147013800	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr1:147012800-147013800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr1:147012800-147013800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:147012800-147013800	Active TSS	Fetal Brain Female	brain
30	chr1:147012800-147013800	Active TSS	Pancreas	Pancrea
31	chr1:147012800-147013800	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr1:147012800-147013800	Active TSS	Stomach Mucosa	stomach
33	chr1:147012800-147013800	Active TSS	GM12878-XiMat	blood
34	chr1:147012800-147014000	Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr1:147012800-147014000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:147012800-147014000	Active TSS	Duodenum Mucosa	Duodenum
37	chr1:147012800-147014000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr1:147012800-147014000	Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr1:147012800-147014200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:147012800-147014200	Active TSS	Fetal Heart	heart
41	chr1:147012800-147014400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:147012800-147014400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:147012800-147014600	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr1:147012800-147014600	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr1:147012800-147014600	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr1:147012800-147014600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr1:147012800-147014600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:147012800-147014600	Active TSS	Cortex derived primary cultured neurospheres	brain
49	chr1:147012800-147014600	Active TSS	Brain Angular Gyrus	brain
50	chr1:147012800-147014600	Active TSS	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links