Variant report

Variant	nsv946238
Chromosome Location	chr1:144538473-144565792
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:1)
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	chr1:144538364..144541386-chr2:5768666..5771588,4	MCF-7	breast:
2	chr1:144538892..144541763-chr2:5768578..5771170,6	MCF-7	breast:
3	chr1:144546200..144546869-chr2:5776993..5777579,2	MCF-7	breast:
4	chr1:144532687..144536786-chr1:144548928..144552960,5	K562	blood:
5	chr1:144542148..144544769-chr1:144547258..144549034,2	K562	blood:
6	chr1:144547858..144551257-chr2:5777928..5781561,5	MCF-7	breast:
7	chr1:144537374..144538908-chr1:149223109..149225532,2	K562	blood:
8	chr1:144545538..144548159-chr1:144550246..144552786,2	MCF-7	breast:
9	chr1:144545202..144547010-chr2:5773815..5775742,3	K562	blood:
10	chr1:144538349..144541013-chr1:144548761..144550305,2	K562	blood:
11	chr1:144545538..144548159-chr1:144550246..144552786,2	MCF-7	breast:
12	chr1:144545457..144547047-chr2:5776987..5778593,2	MCF-7	breast:
13	chr1:144526732..144539178-chr1:149221186..149225476,28	MCF-7	breast:
14	chr1:144545736..144548196-chr2:5778523..5781420,2	K562	blood:
15	chr1:144542148..144544769-chr1:144547258..144549034,2	K562	blood:
16	chr1:144541146..144543284-chr1:144543970..144546879,2	K562	blood:
17	chr1:144543935..144546145-chr1:149223071..149224950,2	K562	blood:
18	chr1:144538349..144541013-chr1:144548761..144550305,2	K562	blood:
19	chr1:144542791..144546909-chr2:5773043..5778423,6	MCF-7	breast:
20	chr1:144541146..144543284-chr1:144543970..144546879,2	K562	blood:
21	chr1:17231777..17233966-chr1:144546760..144549035,2	K562	blood:
22	chr1:144547084..144549074-chr2:5776610..5778586,4	K562	blood:
23	chr1:144545436..144547669-chr1:149222363..149225506,3	K562	blood:
24	chr1:144538903..144539892-chr2:5769586..5770994,3	MCF-7	breast:
25	chr1:144542997..144547075-chr2:5772380..5776386,6	MCF-7	breast:
26	chr1:144539250..144543417-chr1:149221777..149225328,4	MCF-7	breast:
27	chr1:144532670..144534981-chr1:144549798..144552960,4	K562	blood:
28	chr1:144547515..144550528-chr2:5777632..5780972,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-2	chr1:144544950-144545289	NONHSAT005812

No data

Variant related genes	Relation type
ENSG00000201699	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 164 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs744041	chr1:144538557-144538558	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs744042	chr1:144538651-144538652	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587623825	chr1:144538728-144538729	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs2660543	chr1:144538748-144538749	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145338964	chr1:144538792-144538793	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28600815	chr1:144538818-144538819	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587693496	chr1:144538819-144538820	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs937687	chr1:144538857-144538858	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs28631577	chr1:144538963-144538964	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149508420	chr1:144538970-144538971	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148788595	chr1:144538972-144538973	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142410558	chr1:144538983-144538984	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs587755106	chr1:144538987-144538988	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs508610	chr1:144538990-144538991	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112615867	chr1:144539007-144539008	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs202224529	chr1:144539027-144539028	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587625125	chr1:144539031-144539032	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587688258	chr1:144539048-144539049	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587774558	chr1:144539052-144539053	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145798799	chr1:144539053-144539054	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs509542	chr1:144539088-144539089	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs199827697	chr1:144539115-144539116	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138600206	chr1:144539116-144539117	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145391055	chr1:144539206-144539207	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587658351	chr1:144539228-144539229	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587741788	chr1:144539343-144539344	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75737735	chr1:144539353-144539354	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587771816	chr1:144539354-144539355	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs75147172	chr1:144539361-144539362	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576887	chr1:144539381-144539382	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs79235161	chr1:144539383-144539384	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587699351	chr1:144539388-144539389	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587606197	chr1:144539393-144539394	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77103264	chr1:144539414-144539415	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs55651504	chr1:144539416-144539417	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75218414	chr1:144539435-144539436	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs75250775	chr1:144539456-144539457	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs587653523	chr1:144539535-144539536	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587714358	chr1:144539549-144539550	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587611221	chr1:144539579-144539580	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs937058	chr1:144539591-144539592	Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs199942353	chr1:144539620-144539621	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587669429	chr1:144539635-144539636	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2020341	chr1:144539639-144539640	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs142797415	chr1:144539640-144539641	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587613082	chr1:144539651-144539652	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs587674171	chr1:144539676-144539677	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587728394	chr1:144539686-144539687	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587631955	chr1:144539709-144539710	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587705197	chr1:144539711-144539712	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	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
Cancer	17440070	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144534400-144539400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:144534400-144539400	Weak transcription	Right Ventricle	heart
3	chr1:144534400-144540400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:144534600-144539200	Weak transcription	Brain Angular Gyrus	brain
5	chr1:144534600-144539600	Enhancers	NHEK	skin
6	chr1:144535000-144540000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:144535000-144540200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:144535200-144539000	Enhancers	Adipose Nuclei	Adipose
9	chr1:144535200-144539600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:144535400-144539800	Enhancers	Osteobl	bone
11	chr1:144536000-144539400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:144536400-144538600	Weak transcription	Brain Anterior Caudate	brain
13	chr1:144536400-144538800	Weak transcription	Right Atrium	heart
14	chr1:144536800-144538800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:144537000-144538800	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr1:144537000-144539400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:144537000-144539400	Enhancers	Fetal Muscle Leg	muscle
18	chr1:144537000-144539600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:144537000-144540000	Enhancers	Fetal Thymus	thymus
20	chr1:144537000-144540200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:144537200-144538800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:144537200-144539400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr1:144537200-144540200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:144537200-144540200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr1:144537600-144539000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr1:144537600-144540200	Enhancers	Fetal Heart	heart
27	chr1:144537800-144538600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr1:144537800-144538600	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr1:144537800-144538800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:144537800-144538800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr1:144537800-144538800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:144537800-144538800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr1:144537800-144538800	Weak transcription	Pancreas	Pancrea
34	chr1:144537800-144538800	Weak transcription	Spleen	Spleen
35	chr1:144537800-144538800	Weak transcription	Dnd41	blood
36	chr1:144537800-144539000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:144537800-144539000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:144537800-144539000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr1:144537800-144539400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr1:144537800-144539400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:144537800-144539400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:144537800-144539400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr1:144537800-144539400	Enhancers	Fetal Lung	lung
44	chr1:144537800-144542600	Weak transcription	Aorta	Aorta
45	chr1:144538000-144538600	Active TSS	Primary T cells from cord blood	blood
46	chr1:144538000-144538600	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr1:144538000-144538600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr1:144538000-144538600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr1:144538000-144538800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:144538000-144538800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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