Variant report

Variant	nsv946243
Chromosome Location	chr1:144681312-144710724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:351)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:351 , 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	BCL11A	chr1:144687719-144687979	GM12878	blood:	n/a	n/a
4	BCL11A	chr1:144690657-144691064	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:144690359-144690638	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
7	CEBPD	chr1:144690310-144690706	K562	blood:	n/a	n/a
8	CEBPD	chr1:144706674-144707423	K562	blood:	n/a	n/a
9	CTCF	chr1:144697679-144697749	GM20000	blood:	n/a	n/a
10	CTCF	chr1:144697610-144697821	MCF-7	breast:	n/a	n/a
11	CTCF	chr1:144692660-144692810	GM12866	blood:	n/a	n/a
12	CTCF	chr1:144697620-144697770	GM12873	blood:	n/a	n/a
13	CTCF	chr1:144692700-144692850	A549	lung:	n/a	n/a
14	CTCF	chr1:144697588-144697750	GM19238	blood:	n/a	n/a
15	CTCF	chr1:144697600-144697750	BJ	skin:	n/a	n/a
16	CTCF	chr1:144697580-144697730	HVMF	connective:	n/a	n/a
17	CTCF	chr1:144697558-144697875	GM12878	blood:	n/a	n/a
18	CTCF	chr1:144697620-144697770	AG09309	skin:	n/a	n/a
19	CTCF	chr1:144697620-144697770	BE2_C	brain:	n/a	n/a
20	CTCF	chr1:144692640-144692790	AG10803	skin:	n/a	n/a
21	CTCF	chr1:144697611-144697742	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr1:144692670-144692877	K562	blood:	n/a	n/a
23	CTCF	chr1:144697614-144697713	GM12891	blood:	n/a	n/a
24	CTCF	chr1:144697588-144697802	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr1:144692640-144692790	AG04449	skin:	n/a	n/a
26	CTCF	chr1:144697580-144697730	AG04450	lung:	n/a	n/a
27	CTCF	chr1:144697604-144697816	GM12878	blood:	n/a	n/a
28	CTCF	chr1:144697620-144697770	HCM	heart:	n/a	n/a
29	CTCF	chr1:144697600-144697750	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr1:144697620-144697770	GM12864	blood:	n/a	n/a
31	CTCF	chr1:144697600-144697750	HPF	lung:	n/a	n/a
32	CTCF	chr1:144697640-144697790	NHLF	lung:	n/a	n/a
33	CTCF	chr1:144697580-144697730	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr1:144697645-144697785	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr1:144692721-144692844	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:144692755-144692810	Gliobla	brain:	n/a	n/a
37	CTCF	chr1:144700840-144700990	GM12873	blood:	n/a	n/a
38	CTCF	chr1:144697580-144697730	GM12868	blood:	n/a	n/a
39	CTCF	chr1:144697640-144697790	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:144697600-144697750	HMF	breast:	n/a	n/a
41	CTCF	chr1:144700840-144700990	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr1:144697661-144697798	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr1:144697600-144697750	HRE	kidney:	n/a	n/a
44	CTCF	chr1:144697600-144697750	GM12875	blood:	n/a	n/a
45	CTCF	chr1:144700840-144700990	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr1:144697600-144697750	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr1:144697607-144697798	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr1:144697604-144697805	K562	blood:	n/a	n/a
49	CTCF	chr1:144697633-144697713	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:144692640-144692790	AG09309	skin:	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	SAEC	small airway:	n/a
3	chr1:144692074-144692124	Jurkat	blood:	n/a
4	chr1:144692074-144692124	HEK293	kidney:	embryo
5	chr1:144692074-144692124	AG09319	gingival:	n/a
6	chr1:144692074-144692124	MCF-7	breast:	n/a
7	chr1:144692074-144692124	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:144692074-144692124	GM06990	blood:	n/a
9	chr1:144692074-144692124	HAEpiC	amniotic membrane:	n/a
10	chr1:144692074-144692124	HCM	heart:	n/a
11	chr1:144692074-144692124	K562	blood:	n/a
12	chr1:144692074-144692124	BJ	skin:	n/a
13	chr1:144692074-144692124	HL-60	blood:	n/a
14	chr1:144692074-144692124	MCF10A-Er-Src	breast:	n/a
15	chr1:144692074-144692124	U87	brain:	n/a
16	chr1:144692074-144692124	GM19239	blood:	n/a
17	chr1:144692074-144692124	SK-N-MC	brain:	n/a
18	chr1:144692074-144692124	PFSK-1	brain:	n/a
19	chr1:144692074-144692124	PrEC	prostate:	n/a
20	chr1:144692074-144692124	HRE	kidney:	n/a
21	chr1:144692074-144692124	AoSMC	blood vessel:	n/a
22	chr1:144692074-144692124	HRCEpiC	kidney:	n/a
23	chr1:144692074-144692124	H1-hESC	embryonic stem cell:	embryo
24	chr1:144692074-144692124	ovcar-3	ovarian:	n/a
25	chr1:144692074-144692124	HMEC	breast:	n/a
26	chr1:144692074-144692124	CMK	blood:	n/a
27	chr1:144692074-144692124	HEEpiC	esophagus:	n/a
28	chr1:144692074-144692124	HCPEpiC	choroid plexus:	n/a
29	chr1:144692074-144692124	NHDF-neo	bronchial:	n/a
30	chr1:144692074-144692124	GM12878	blood:	n/a
31	chr1:144692074-144692124	RPTEC	kidney:	n/a
32	chr1:144692074-144692124	NHBE	bronchial:	n/a
33	chr1:144692074-144692124	AG09309	skin:	n/a
34	chr1:144692074-144692124	GM12891	blood:	n/a
35	chr1:144692074-144692124	SKMC	muscle:	n/a
36	chr1:144692074-144692124	Hela-S3	cervix:	n/a
37	chr1:144692074-144692124	HCF	heart:	n/a
38	chr1:144692074-144692124	ECC-1	luminal epithelium:	n/a
39	chr1:144692074-144692124	LNCaP	prostate:	n/a
40	chr1:144692074-144692124	GM12892	blood:	n/a
41	chr1:144692074-144692124	A549	lung:	n/a
42	chr1:144692074-144692124	SK-N-SH_RA	brain:	n/a
43	chr1:144692074-144692124	Hepatocyte	liver:	n/a
44	chr1:144692074-144692124	ProgFib	skin:	n/a
45	chr1:144692074-144692124	AG10803	skin:	n/a
46	chr1:144692074-144692124	SK-N-SH	brain:	n/a
47	chr1:144692074-144692124	T-47D	breast:	n/a
48	chr1:144692074-144692124	NB4	blood:	n/a
49	chr1:144692074-144692124	AG04449	skin:	fetal
50	chr1:144692074-144692124	Caco-2	colon:	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	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
3	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
4	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:
5	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:

No data

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

Extended variants
information (count: 908 )
Associated
traits (count: 164 )

Variant overlapped rSNPs/rCNVs (count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371161127	chr1:144681352-144681353	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs374254607	chr1:144681377-144681378	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199881692	chr1:144681389-144681390	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs587668965	chr1:144681402-144681403	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs587703260	chr1:144681460-144681461	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs587773490	chr1:144681508-144681509	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112805905	chr1:144681513-144681514	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs587656214	chr1:144681528-144681529	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs587725019	chr1:144681568-144681569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs587600288	chr1:144681613-144681614	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs587656375	chr1:144681618-144681619	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs587707725	chr1:144681622-144681623	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs587610907	chr1:144681627-144681628	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs587667209	chr1:144681644-144681645	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs71265228	chr1:144681653-144681654	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs71265227	chr1:144681687-144681688	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs587744931	chr1:144681701-144681702	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs641666	chr1:144681723-144681724	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs587601338	chr1:144681798-144681799	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs67467472	chr1:144681814-144681815	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114098845	chr1:144681820-144681821	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61805401	chr1:144681844-144681845	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs61805402	chr1:144681913-144681914	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587663330	chr1:144681916-144681917	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587743288	chr1:144681919-144681920	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587610237	chr1:144681949-144681950	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587692583	chr1:144681961-144681962	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587723970	chr1:144681988-144681989	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587644019	chr1:144681990-144681991	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587702980	chr1:144682072-144682073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138524629	chr1:144682096-144682097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs67254729	chr1:144682110-144682111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs67728364	chr1:144682113-144682114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148662694	chr1:144682161-144682162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587776032	chr1:144682190-144682191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs587643826	chr1:144682220-144682221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587695480	chr1:144682222-144682223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587757412	chr1:144682228-144682229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587647424	chr1:144682242-144682243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587710810	chr1:144682351-144682352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587767749	chr1:144682366-144682367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs587642729	chr1:144682442-144682443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587708423	chr1:144682455-144682456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587609339	chr1:144682458-144682459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587660879	chr1:144682494-144682495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs71222073	chr1:144682536-144682537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587713734	chr1:144682548-144682549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143734847	chr1:144682709-144682710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146810223	chr1:144682852-144682853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587594486	chr1:144682874-144682875	Weak transcription Enhancers	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:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144672600-144691600	Weak transcription	Left Ventricle	heart
2	chr1:144673400-144681600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:144674000-144685600	Weak transcription	Brain Hippocampus Middle	brain
4	chr1:144674000-144691600	Weak transcription	Fetal Muscle Leg	muscle
5	chr1:144674200-144689600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:144674400-144687600	Weak transcription	Psoas Muscle	Psoas
7	chr1:144674800-144683400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr1:144674800-144690400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr1:144675600-144689400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:144675800-144689600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:144676200-144681600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:144676200-144681600	Weak transcription	Fetal Heart	heart
13	chr1:144676200-144689800	Weak transcription	HSMM	muscle
14	chr1:144676400-144681600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr1:144676400-144685600	Weak transcription	Placenta	Placenta
16	chr1:144676400-144689600	Weak transcription	Brain Anterior Caudate	brain
17	chr1:144676400-144689600	Weak transcription	HSMMtube	muscle
18	chr1:144676600-144689600	Weak transcription	K562	blood
19	chr1:144676800-144697400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr1:144679800-144681600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:144679800-144685000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr1:144679800-144685200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr1:144679800-144685200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:144679800-144685600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr1:144680000-144683400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr1:144680000-144683400	Weak transcription	Osteobl	bone
27	chr1:144680000-144685600	Weak transcription	Brain Angular Gyrus	brain
28	chr1:144680000-144689600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr1:144681600-144681800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr1:144681600-144681800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:144681600-144681800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr1:144681600-144682000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:144681600-144682600	Enhancers	Fetal Heart	heart
34	chr1:144681600-144683600	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr1:144681800-144682000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:144681800-144685600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr1:144681800-144689400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr1:144682000-144683400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:144682000-144684800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:144682600-144683000	Weak transcription	Fetal Heart	heart
41	chr1:144683000-144683800	Enhancers	Fetal Heart	heart
42	chr1:144683400-144683600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:144683400-144683600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr1:144683400-144683600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr1:144683400-144683600	Genic enhancers	Brain Inferior Temporal Lobe	brain
46	chr1:144683400-144683600	Enhancers	Osteobl	bone
47	chr1:144683400-144683800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:144683400-144683800	Enhancers	Brain Cingulate Gyrus	brain
49	chr1:144683400-144695000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:144683600-144685000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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