Variant report

Variant	nsv1011358
Chromosome Location	chr1:144887881-144901738
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:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144891174..144892693-chr1:144930887..144933429,2	MCF-7	breast:
2	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
3	chr1:144891477..144893654-chr1:144895299..144897580,2	K562	blood:
4	chr1:144877869..144879998-chr1:144892579..144894748,2	MCF-7	breast:
5	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
6	chr1:144895702..144897735-chr1:144904870..144906981,2	MCF-7	breast:
7	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
8	chr1:144890884..144894068-chr1:146500995..146504405,3	K562	blood:
9	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
10	chr1:17045982..17048017-chr1:144885102..144888081,2	K562	blood:
11	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
12	chr1:144891477..144893654-chr1:144895299..144897580,2	K562	blood:
13	chr1:144892599..144896749-chr1:144930798..144933879,5	MCF-7	breast:
14	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
15	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
16	chr1:144893909..144894771-chr8:51229590..51230343,2	MCF-7	breast:
17	chr1:17046027..17047625-chr1:144886603..144888109,2	MCF-7	breast:
18	chr1:144888141..144890870-chr1:145070504..145072082,2	K562	blood:
19	chr1:144889740..144892703-chr1:146500075..146502138,3	MCF-7	breast:
20	chr1:144892597..144895392-chr11:118795022..118797131,2	MCF-7	breast:
21	chr1:144891445..144893339-chr1:146502271..146504240,2	MCF-7	breast:
22	chr1:144881667..144883836-chr1:144885018..144890367,4	K562	blood:
23	chr1:144893446..144895237-chr1:144930953..144933183,2	MCF-7	breast:
24	chr1:144894819..144897241-chr1:144898698..144901682,2	K562	blood:
25	chr1:144886541..144889030-chr1:144932018..144933743,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000268869	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000110375	chromatin interactions
ENSG00000186174	chromatin interactions

Extended variants
information (count: 444 )
Associated
traits (count: 166 )

Variant overlapped rSNPs/rCNVs (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201231737	chr1:144887882-144887883	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181699896	chr1:144887889-144887890	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199515471	chr1:144887890-144887891	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587739498	chr1:144887924-144887925	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs111927889	chr1:144887947-144887948	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs587692509	chr1:144887950-144887951	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs587748080	chr1:144887954-144887955	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs1698630	chr1:144888003-144888004	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11458074	chr1:144888047-144888048	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs587649960	chr1:144888051-144888052	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs113076933	chr1:144888060-144888061	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs587707046	chr1:144888061-144888062	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs587774524	chr1:144888081-144888082	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs587638440	chr1:144888093-144888094	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1698631	chr1:144888111-144888112	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112384961	chr1:144888160-144888161	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375031836	chr1:144888177-144888178	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587755148	chr1:144888209-144888210	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587645548	chr1:144888292-144888293	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587714673	chr1:144888340-144888341	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587612614	chr1:144888366-144888367	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1698632	chr1:144888371-144888372	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186149228	chr1:144888451-144888452	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190911984	chr1:144888477-144888478	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587606583	chr1:144888505-144888506	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587660547	chr1:144888512-144888513	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs587709990	chr1:144888518-144888519	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377437412	chr1:144888534-144888535	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587594065	chr1:144888550-144888551	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587667907	chr1:144888554-144888555	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587752089	chr1:144888563-144888564	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587748053	chr1:144888577-144888578	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182404299	chr1:144888641-144888642	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs1699828	chr1:144888766-144888767	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587647981	chr1:144888791-144888792	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs587682459	chr1:144888857-144888858	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587766670	chr1:144888865-144888866	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs587614497	chr1:144888883-144888884	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76344197	chr1:144888888-144888889	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185787359	chr1:144888892-144888893	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587750625	chr1:144888900-144888901	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587634228	chr1:144888906-144888907	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587692028	chr1:144888913-144888914	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587770239	chr1:144888965-144888966	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587645033	chr1:144888966-144888967	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2653684	chr1:144888968-144888969	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201095941	chr1:144889007-144889008	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587628949	chr1:144889012-144889013	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587715015	chr1:144889060-144889061	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587597621	chr1:144889092-144889093	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:166)

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
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	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
Breast cancer	17142309	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
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD

Chromatin state (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144850000-144894000	Strong transcription	Stomach Smooth Muscle	stomach
2	chr1:144850400-144894200	Strong transcription	Brain Germinal Matrix	brain
3	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
4	chr1:144860200-144888400	Strong transcription	Fetal Muscle Leg	muscle
5	chr1:144866800-144888000	Strong transcription	Fetal Muscle Trunk	muscle
6	chr1:144868600-144892400	Weak transcription	Fetal Thymus	thymus
7	chr1:144869400-144905000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr1:144874600-144901600	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:144874800-144906600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:144875000-144891400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:144875000-144893600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:144875000-144911000	Weak transcription	Thymus	Thymus
13	chr1:144876800-144892400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:144877000-144890200	Weak transcription	Small Intestine	intestine
15	chr1:144877400-144902200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:144881000-144891800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:144881200-144890800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:144881400-144890600	Weak transcription	Fetal Lung	lung
19	chr1:144881400-144891000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:144881400-144904800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr1:144882000-144892600	Weak transcription	HepG2	liver
22	chr1:144882600-144891800	Weak transcription	Pancreas	Pancrea
23	chr1:144883000-144890000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr1:144883000-144890200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:144883000-144890200	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr1:144883000-144890400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr1:144883000-144891800	Weak transcription	Spleen	Spleen
28	chr1:144883000-144892400	Weak transcription	Esophagus	oesophagus
29	chr1:144883000-144893200	Weak transcription	Fetal Intestine Small	intestine
30	chr1:144883000-144902600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr1:144883000-144902800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:144883000-144911600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:144883200-144889400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:144883200-144890000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:144883200-144890200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:144883200-144890200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:144883200-144890800	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr1:144883200-144891000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr1:144883200-144891800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr1:144883200-144902600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr1:144883600-144890400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:144883600-144892200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr1:144883600-144893200	Weak transcription	Fetal Kidney	kidney
44	chr1:144883800-144889200	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr1:144884200-144892200	Weak transcription	Ovary	ovary
46	chr1:144885200-144888000	Strong transcription	Fetal Brain Female	brain
47	chr1:144885200-144889000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr1:144885400-144888200	Genic enhancers	Left Ventricle	heart
49	chr1:144885400-144890400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr1:144885600-144888000	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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