Variant report

Variant	esv1825087
Chromosome Location	chr1:144621683-144709579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:449)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144690796-144691031	GM12878	blood:	n/a	n/a
2	BATF	chr1:144679564-144679880	GM12878	blood:	n/a	n/a
3	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
4	BATF	chr1:144690283-144690581	GM12878	blood:	n/a	chr1:144690289-144690297 chr1:144690402-144690411
5	BATF	chr1:144672666-144672904	GM12878	blood:	n/a	n/a
6	BATF	chr1:144679543-144679819	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:144687719-144687979	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:144690359-144690638	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:144690657-144691064	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:144672707-144672942	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:144621538-144621780	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:144679661-144679667	IMR90	lung:	n/a	n/a
14	CEBPD	chr1:144690310-144690706	K562	blood:	n/a	n/a
15	CEBPD	chr1:144706674-144707423	K562	blood:	n/a	n/a
16	CTCF	chr1:144692660-144692810	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr1:144697620-144697770	RPTEC	kidney:	n/a	n/a
18	CTCF	chr1:144692660-144692810	NHLF	lung:	n/a	n/a
19	CTCF	chr1:144697600-144697750	GM12875	blood:	n/a	n/a
20	CTCF	chr1:144697640-144697790	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr1:144697620-144697770	HCM	heart:	n/a	n/a
22	CTCF	chr1:144697600-144697750	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr1:144692660-144692810	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr1:144621387-144621708	K562	blood:	n/a	n/a
25	CTCF	chr1:144621560-144621710	HCM	heart:	n/a	n/a
26	CTCF	chr1:144699880-144700030	HMEC	breast:	n/a	n/a
27	CTCF	chr1:144697602-144697754	Fibrobl	skin:	n/a	n/a
28	CTCF	chr1:144621403-144621735	A549	lung:	n/a	n/a
29	CTCF	chr1:144697600-144697750	GM12878	blood:	n/a	n/a
30	CTCF	chr1:144697580-144697730	HVMF	connective:	n/a	n/a
31	CTCF	chr1:144697611-144697745	GM19240	blood:	n/a	n/a
32	CTCF	chr1:144700840-144700990	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr1:144697540-144697690	NB4	blood:	n/a	n/a
34	CTCF	chr1:144697535-144697800	HepG2	liver:	n/a	n/a
35	CTCF	chr1:144697620-144697770	HRE	kidney:	n/a	n/a
36	CTCF	chr1:144697620-144697770	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr1:144697640-144697790	HFF	foreskin:	n/a	n/a
38	CTCF	chr1:144697620-144697770	SAEC	small airway:	n/a	n/a
39	CTCF	chr1:144697640-144697790	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:144692721-144692844	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:144696980-144697130	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr1:144697558-144697875	GM12878	blood:	n/a	n/a
43	CTCF	chr1:144621560-144621710	HMEC	breast:	n/a	n/a
44	CTCF	chr1:144697620-144697770	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:144697585-144697776	A549	lung:	n/a	n/a
46	CTCF	chr1:144697620-144697770	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:144697600-144697750	HMF	breast:	n/a	n/a
48	CTCF	chr1:144697640-144697790	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:144696880-144697030	A549	lung:	n/a	n/a
50	CTCF	chr1:144708700-144708850	SAEC	small airway:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144692074-144692124	BE2_C	brain:	n/a
2	chr1:144692074-144692124	H1-hESC	embryonic stem cell:	embryo
3	chr1:144692074-144692124	HEEpiC	esophagus:	n/a
4	chr1:144692074-144692124	SK-N-SH_RA	brain:	n/a
5	chr1:144692074-144692124	IMR90	lung:	fetal
6	chr1:144692074-144692124	A549	lung:	n/a
7	chr1:144692074-144692124	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:144692074-144692124	HNPCEpiC	eye:	n/a
9	chr1:144692074-144692124	NB4	blood:	n/a
10	chr1:144692074-144692124	Jurkat	blood:	n/a
11	chr1:144692074-144692124	NT2-D1	testis:	n/a
12	chr1:144692074-144692124	T-47D	breast:	n/a
13	chr1:144692074-144692124	SK-N-MC	brain:	n/a
14	chr1:144692074-144692124	HMEC	breast:	n/a
15	chr1:144692074-144692124	GM12892	blood:	n/a
16	chr1:144692074-144692124	HAEpiC	amniotic membrane:	n/a
17	chr1:144692074-144692124	AG04449	skin:	fetal
18	chr1:144692074-144692124	PrEC	prostate:	n/a
19	chr1:144692074-144692124	PANC-1	pancreas:	n/a
20	chr1:144692074-144692124	HRPEpiC	eye:	n/a
21	chr1:144692074-144692124	BJ	skin:	n/a
22	chr1:144692074-144692124	HL-60	blood:	n/a
23	chr1:144692074-144692124	ovcar-3	ovarian:	n/a
24	chr1:144692074-144692124	HIPEpiC	eye:	n/a
25	chr1:144692074-144692124	HCT-116	colon:	n/a
26	chr1:144692074-144692124	AG04450	lung:	fetal
27	chr1:144692074-144692124	HCM	heart:	n/a
28	chr1:144692074-144692124	AoSMC	blood vessel:	n/a
29	chr1:144692074-144692124	MCF-7	breast:	n/a
30	chr1:144692074-144692124	HRE	kidney:	n/a
31	chr1:144692074-144692124	HRCEpiC	kidney:	n/a
32	chr1:144692074-144692124	Caco-2	colon:	n/a
33	chr1:144692074-144692124	Hela-S3	cervix:	n/a
34	chr1:144692074-144692124	GM19239	blood:	n/a
35	chr1:144692074-144692124	RPTEC	kidney:	n/a
36	chr1:144692074-144692124	PFSK-1	brain:	n/a
37	chr1:144692074-144692124	GM06990	blood:	n/a
38	chr1:144692074-144692124	SK-N-SH	brain:	n/a
39	chr1:144692074-144692124	HepG2	liver:	n/a
40	chr1:144692074-144692124	NHBE	bronchial:	n/a
41	chr1:144692074-144692124	U87	brain:	n/a
42	chr1:144692074-144692124	AG09319	gingival:	n/a
43	chr1:144692074-144692124	ECC-1	luminal epithelium:	n/a
44	chr1:144692074-144692124	ProgFib	skin:	n/a
45	chr1:144692074-144692124	NHDF-neo	bronchial:	n/a
46	chr1:144692074-144692124	AG09309	skin:	n/a
47	chr1:144692074-144692124	GM12878	blood:	n/a
48	chr1:144692074-144692124	K562	blood:	n/a
49	chr1:144692074-144692124	HCF	heart:	n/a
50	chr1:144692074-144692124	SAEC	small airway:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:
2	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
3	chr1:144687969..144690729-chr1:144930762..144933228,2	MCF-7	breast:
4	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
5	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000215861	TF binding region
ENSG00000215861	CpG island
ENSG00000178104	chromatin interactions

Extended variants
information (count: 1360 )
Associated
traits (count: 165 )

Variant overlapped rSNPs/rCNVs (count:1360 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200577903	chr1:144621705-144621706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587695352	chr1:144621713-144621714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11485970	chr1:144621804-144621805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11488524	chr1:144621817-144621818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11261221	chr1:144621849-144621850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587733321	chr1:144621854-144621855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181153531	chr1:144621859-144621860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587626954	chr1:144621884-144621885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61810916	chr1:144621885-144621886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4990356	chr1:144621942-144621943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587646813	chr1:144621962-144621963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587693972	chr1:144621985-144621986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587751554	chr1:144621995-144621996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587649166	chr1:144622016-144622017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587699596	chr1:144622017-144622018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367641682	chr1:144622041-144622042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186739947	chr1:144622110-144622111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587631193	chr1:144622112-144622113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372375022	chr1:144622127-144622128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28787958	chr1:144622133-144622134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142607672	chr1:144622164-144622165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587684784	chr1:144622166-144622167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587741885	chr1:144622192-144622193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587619051	chr1:144622202-144622203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587676123	chr1:144622207-144622208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587730367	chr1:144622210-144622211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587633895	chr1:144622211-144622212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587661933	chr1:144622212-144622213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587749066	chr1:144622231-144622232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61810918	chr1:144622265-144622266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587693726	chr1:144622284-144622285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201105049	chr1:144622314-144622315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587751900	chr1:144622316-144622317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587620955	chr1:144622342-144622343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587684032	chr1:144622350-144622351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368167029	chr1:144622388-144622389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191491164	chr1:144672446-144672447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183801536	chr1:144672447-144672448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs61810919	chr1:144672527-144672528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587760839	chr1:144672583-144672584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79959259	chr1:144672587-144672588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587640306	chr1:144672588-144672589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587705530	chr1:144672589-144672590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78414287	chr1:144672606-144672607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587775046	chr1:144672634-144672635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112480099	chr1:144672699-144672700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113141305	chr1:144672825-144672826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201588151	chr1:144673060-144673061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199538923	chr1:144673061-144673062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587664256	chr1:144673101-144673102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:165)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144594600-144622000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:144594600-144622000	Weak transcription	Placenta	Placenta
3	chr1:144594800-144621800	Weak transcription	Brain Germinal Matrix	brain
4	chr1:144594800-144621800	Weak transcription	HSMMtube	muscle
5	chr1:144594800-144622000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr1:144594800-144622000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr1:144594800-144623400	Weak transcription	Primary T cells from cord blood	blood
8	chr1:144594800-144623400	Weak transcription	HUVEC	blood vessel
9	chr1:144594800-144624000	Weak transcription	Right Ventricle	heart
10	chr1:144595800-144623200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:144596400-144622000	Weak transcription	NH-A	brain
12	chr1:144598800-144623600	Weak transcription	Hela-S3	cervix
13	chr1:144599400-144621800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr1:144599400-144622000	Weak transcription	Fetal Stomach	stomach
15	chr1:144599400-144623400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:144599800-144623800	Weak transcription	Fetal Intestine Small	intestine
17	chr1:144607800-144622000	Weak transcription	Fetal Intestine Large	intestine
18	chr1:144607800-144622000	Weak transcription	Left Ventricle	heart
19	chr1:144607800-144622000	Weak transcription	Ovary	ovary
20	chr1:144607800-144623600	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr1:144618600-144622000	Weak transcription	Lung	lung
22	chr1:144618600-144623600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:144619600-144623000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr1:144619800-144622000	Weak transcription	Aorta	Aorta
25	chr1:144619800-144622000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr1:144619800-144622200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:144619800-144622200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr1:144619800-144622200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:144619800-144622200	Weak transcription	Stomach Smooth Muscle	stomach
30	chr1:144619800-144623800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:144619800-144623800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:144620000-144623200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:144620400-144622000	Weak transcription	Primary B cells from peripheral blood	blood
34	chr1:144620400-144622000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:144620400-144622000	Weak transcription	Liver	Liver
36	chr1:144620600-144622200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:144620600-144622200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:144620600-144622200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:144620600-144622200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:144620600-144622200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr1:144620600-144622200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:144620600-144622200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr1:144620600-144622200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr1:144620600-144622200	Weak transcription	Spleen	Spleen
45	chr1:144620600-144622200	Weak transcription	Osteobl	bone
46	chr1:144620600-144623200	Weak transcription	Adipose Nuclei	Adipose
47	chr1:144620600-144623600	Weak transcription	Fetal Muscle Leg	muscle
48	chr1:144620600-144623800	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr1:144620600-144623800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:144620600-144623800	Weak transcription	Dnd41	blood

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