Variant report

Variant	esv1792957
Chromosome Location	chr1:144674799-144709579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr1:144690283-144690581	GM12878	blood:	n/a	chr1:144690289-144690297 chr1:144690402-144690411
3	BATF	chr1:144679543-144679819	GM12878	blood:	n/a	n/a
4	BATF	chr1:144679564-144679880	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:144690657-144691064	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:144687719-144687979	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:144690359-144690638	GM12878	blood:	n/a	n/a
9	CEBPB	chr1:144679661-144679667	IMR90	lung:	n/a	n/a
10	CEBPD	chr1:144690310-144690706	K562	blood:	n/a	n/a
11	CEBPD	chr1:144706674-144707423	K562	blood:	n/a	n/a
12	CTCF	chr1:144697605-144697784	HepG2	liver:	n/a	n/a
13	CTCF	chr1:144697640-144697790	GM12867	blood:	n/a	n/a
14	CTCF	chr1:144697620-144697770	SAEC	small airway:	n/a	n/a
15	CTCF	chr1:144697580-144697730	HCT-116	colon:	n/a	n/a
16	CTCF	chr1:144692640-144692790	AG09309	skin:	n/a	n/a
17	CTCF	chr1:144692700-144692850	A549	lung:	n/a	n/a
18	CTCF	chr1:144692680-144692830	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:144697614-144697713	GM12891	blood:	n/a	n/a
20	CTCF	chr1:144697620-144697770	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr1:144697600-144697750	SAEC	small airway:	n/a	n/a
22	CTCF	chr1:144697627-144697727	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr1:144697100-144697250	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr1:144697579-144697823	Gliobla	brain:	n/a	n/a
25	CTCF	chr1:144697580-144697730	AG04450	lung:	n/a	n/a
26	CTCF	chr1:144692680-144692830	HCT-116	colon:	n/a	n/a
27	CTCF	chr1:144697649-144697796	GM13976	blood:	n/a	n/a
28	CTCF	chr1:144697560-144697710	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr1:144692660-144692810	RPTEC	kidney:	n/a	n/a
30	CTCF	chr1:144697580-144697730	GM12864	blood:	n/a	n/a
31	CTCF	chr1:144697640-144697790	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr1:144697553-144697759	GM12892	blood:	n/a	n/a
33	CTCF	chr1:144697432-144697916	A549	lung:	n/a	n/a
34	CTCF	chr1:144692640-144692790	NHEK	skin:	n/a	n/a
35	CTCF	chr1:144697607-144697798	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr1:144697620-144697770	AG09309	skin:	n/a	n/a
37	CTCF	chr1:144697620-144697770	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:144697580-144697730	BJ	skin:	n/a	n/a
39	CTCF	chr1:144697620-144697770	GM12874	blood:	n/a	n/a
40	CTCF	chr1:144692670-144692877	K562	blood:	n/a	n/a
41	CTCF	chr1:144692669-144692973	K562	blood:	n/a	n/a
42	CTCF	chr1:144696980-144697130	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr1:144692706-144692842	ProgFib	skin:	n/a	n/a
44	CTCF	chr1:144697668-144697791	Medullo	brain:	n/a	n/a
45	CTCF	chr1:144697620-144697770	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr1:144692660-144692810	HVMF	connective:	n/a	n/a
47	CTCF	chr1:144692714-144692833	Fibrobl	skin:	n/a	n/a
48	CTCF	chr1:144697620-144697770	GM12873	blood:	n/a	n/a
49	CTCF	chr1:144692640-144692790	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:144697600-144697750	HUVEC	blood vessel:	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	HCF	heart:	n/a
2	chr1:144692074-144692124	SK-N-SH_RA	brain:	n/a
3	chr1:144692074-144692124	LNCaP	prostate:	n/a
4	chr1:144692074-144692124	H1-hESC	embryonic stem cell:	embryo
5	chr1:144692074-144692124	NHDF-neo	bronchial:	n/a
6	chr1:144692074-144692124	GM19239	blood:	n/a
7	chr1:144692074-144692124	AG10803	skin:	n/a
8	chr1:144692074-144692124	PFSK-1	brain:	n/a
9	chr1:144692074-144692124	PANC-1	pancreas:	n/a
10	chr1:144692074-144692124	K562	blood:	n/a
11	chr1:144692074-144692124	HepG2	liver:	n/a
12	chr1:144692074-144692124	HCT-116	colon:	n/a
13	chr1:144692074-144692124	SKMC	muscle:	n/a
14	chr1:144692074-144692124	MCF10A-Er-Src	breast:	n/a
15	chr1:144692074-144692124	NT2-D1	testis:	n/a
16	chr1:144692074-144692124	HUVEC	blood vessel:	n/a
17	chr1:144692074-144692124	GM12892	blood:	n/a
18	chr1:144692074-144692124	BJ	skin:	n/a
19	chr1:144692074-144692124	U87	brain:	n/a
20	chr1:144692074-144692124	AG09309	skin:	n/a
21	chr1:144692074-144692124	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:144692074-144692124	T-47D	breast:	n/a
23	chr1:144692074-144692124	ovcar-3	ovarian:	n/a
24	chr1:144692074-144692124	HNPCEpiC	eye:	n/a
25	chr1:144692074-144692124	HRPEpiC	eye:	n/a
26	chr1:144692074-144692124	HL-60	blood:	n/a
27	chr1:144692074-144692124	AG04450	lung:	fetal
28	chr1:144692074-144692124	SK-N-MC	brain:	n/a
29	chr1:144692074-144692124	SAEC	small airway:	n/a
30	chr1:144692074-144692124	Hepatocyte	liver:	n/a
31	chr1:144692074-144692124	CMK	blood:	n/a
32	chr1:144692074-144692124	AoSMC	blood vessel:	n/a
33	chr1:144692074-144692124	GM06990	blood:	n/a
34	chr1:144692074-144692124	HRCEpiC	kidney:	n/a
35	chr1:144692074-144692124	HEK293	kidney:	embryo
36	chr1:144692074-144692124	HCPEpiC	choroid plexus:	n/a
37	chr1:144692074-144692124	ProgFib	skin:	n/a
38	chr1:144692074-144692124	SK-N-SH	brain:	n/a
39	chr1:144692074-144692124	AG04449	skin:	fetal
40	chr1:144692074-144692124	RPTEC	kidney:	n/a
41	chr1:144692074-144692124	Caco-2	colon:	n/a
42	chr1:144692074-144692124	GM12878	blood:	n/a
43	chr1:144692074-144692124	IMR90	lung:	fetal
44	chr1:144692074-144692124	MCF-7	breast:	n/a
45	chr1:144692074-144692124	HIPEpiC	eye:	n/a
46	chr1:144692074-144692124	HCM	heart:	n/a
47	chr1:144692074-144692124	ECC-1	luminal epithelium:	n/a
48	chr1:144692074-144692124	NB4	blood:	n/a
49	chr1:144692074-144692124	HMEC	breast:	n/a
50	chr1:144692074-144692124	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:144687969..144690729-chr1:144930762..144933228,2	MCF-7	breast:
2	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
3	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
4	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:
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: 1211 )
Associated
traits (count: 164 )

Variant overlapped rSNPs/rCNVs (count:1211 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111555074	chr1:144674818-144674819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs66921165	chr1:144674819-144674820	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587721151	chr1:144674869-144674870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538192	chr1:144674892-144674893	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72701814	chr1:144674900-144674901	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373149468	chr1:144674915-144674916	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587654795	chr1:144674920-144674921	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199984330	chr1:144674924-144674925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367938438	chr1:144674925-144674926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61810933	chr1:144674926-144674927	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111534436	chr1:144674927-144674928	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111449106	chr1:144674928-144674929	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371178957	chr1:144674930-144674931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375089391	chr1:144674932-144674933	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587631438	chr1:144674991-144674992	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587688849	chr1:144675009-144675010	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587747853	chr1:144675051-144675052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199930076	chr1:144675100-144675101	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587594621	chr1:144675173-144675174	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs635094	chr1:144675179-144675180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587690946	chr1:144675183-144675184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587727286	chr1:144675297-144675298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587620629	chr1:144675306-144675307	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587662517	chr1:144675309-144675310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587736316	chr1:144675381-144675382	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587618119	chr1:144675392-144675393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147973685	chr1:144675428-144675429	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1663974	chr1:144675445-144675446	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587698015	chr1:144675461-144675462	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587767770	chr1:144675472-144675473	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200376774	chr1:144675477-144675478	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587620169	chr1:144675487-144675488	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587693539	chr1:144675492-144675493	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149566295	chr1:144675501-144675502	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587649292	chr1:144675512-144675513	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587712774	chr1:144675535-144675536	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587776061	chr1:144675557-144675558	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200762578	chr1:144675560-144675561	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587666411	chr1:144675562-144675563	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587735872	chr1:144675580-144675581	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587594769	chr1:144675594-144675595	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587670622	chr1:144675611-144675612	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587701357	chr1:144675612-144675613	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587607335	chr1:144675620-144675621	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587655738	chr1:144675642-144675643	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587743283	chr1:144675676-144675677	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587630586	chr1:144675688-144675689	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587665382	chr1:144675696-144675697	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201695002	chr1:144675730-144675731	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587746882	chr1:144675737-144675738	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:164)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144672600-144676200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr1:144672600-144691600	Weak transcription	Left Ventricle	heart
3	chr1:144673200-144675400	Weak transcription	Placenta	Placenta
4	chr1:144673200-144679400	Weak transcription	Liver	Liver
5	chr1:144673200-144679600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:144673400-144681600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr1:144673600-144675400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:144673600-144675400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:144673800-144676400	Strong transcription	HSMMtube	muscle
10	chr1:144673800-144677200	Weak transcription	Brain Germinal Matrix	brain
11	chr1:144674000-144675600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr1:144674000-144676400	Strong transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:144674000-144676800	Strong transcription	Skeletal Muscle Male	skeletal muscle
14	chr1:144674000-144685600	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:144674000-144691600	Weak transcription	Fetal Muscle Leg	muscle
16	chr1:144674200-144689600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:144674400-144674800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:144674400-144675600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:144674400-144676200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:144674400-144676600	Strong transcription	K562	blood
21	chr1:144674400-144679400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:144674400-144687600	Weak transcription	Psoas Muscle	Psoas
23	chr1:144674600-144674800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:144674600-144674800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr1:144674600-144674800	Enhancers	Brain Angular Gyrus	brain
26	chr1:144674600-144674800	Genic enhancers	Brain Anterior Caudate	brain
27	chr1:144674600-144674800	Enhancers	Brain Cingulate Gyrus	brain
28	chr1:144674600-144674800	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr1:144674600-144674800	Enhancers	Fetal Heart	heart
30	chr1:144674600-144674800	Enhancers	Rectal Smooth Muscle	rectum
31	chr1:144674600-144674800	Enhancers	Right Ventricle	heart
32	chr1:144674600-144674800	Enhancers	Stomach Smooth Muscle	stomach
33	chr1:144674600-144674800	Enhancers	HSMM	muscle
34	chr1:144674600-144674800	Enhancers	NHDF-Ad	bronchial
35	chr1:144674600-144674800	Enhancers	Osteobl	bone
36	chr1:144674600-144675000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:144674600-144676200	Enhancers	Colon Smooth Muscle	Colon
38	chr1:144674600-144676800	Weak transcription	Fetal Brain Female	brain
39	chr1:144674600-144679600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr1:144674800-144675200	Weak transcription	Brain Anterior Caudate	brain
41	chr1:144674800-144675400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr1:144674800-144675400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:144674800-144675400	Weak transcription	Fetal Heart	heart
44	chr1:144674800-144675400	Weak transcription	HSMM	muscle
45	chr1:144674800-144675400	Weak transcription	Osteobl	bone
46	chr1:144674800-144677400	Weak transcription	Right Ventricle	heart
47	chr1:144674800-144678400	Weak transcription	NHDF-Ad	bronchial
48	chr1:144674800-144679200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:144674800-144679600	Weak transcription	Brain Angular Gyrus	brain
50	chr1:144674800-144683400	Weak transcription	Brain Cingulate Gyrus	brain

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