Variant report

Variant	nsv547962
Chromosome Location	chr1:155158414-155160941
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:155158577-155158581	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr1:155159720-155159870	Caco-2	colon:	n/a	n/a
3	CTCF	chr1:155158300-155158450	GM06990	blood:	n/a	n/a
4	CTCF	chr1:155158792-155158813	Kidney_OC	kidney:	n/a	n/a
5	CTCF	chr1:155158817-155158836	Kidney_OC	kidney:	n/a	n/a
6	EBF1	chr1:155157523-155158492	GM12878	blood:	n/a	n/a
7	EBF1	chr1:155157491-155158699	GM12878	blood:	n/a	n/a
8	EBF1	chr1:155157528-155158545	GM12878	blood:	n/a	n/a
9	ESR1	chr1:155160875-155161905	T-47D	breast:	n/a	chr1:155160982-155160997
10	GABPA	chr1:155158759-155159058	H1-hESC	embryonic stem cell:	n/a	chr1:155158973-155158982
11	MAX	chr1:155158501-155158529	GM12878	blood:	n/a	n/a
12	NR3C1	chr1:155160931-155161824	A549	lung:	n/a	n/a
13	PAX5	chr1:155157822-155158513	GM12878	blood:	n/a	n/a
14	PAX5	chr1:155157676-155158496	GM12878	blood:	n/a	chr1:155157744-155157762
15	POLR2A	chr1:155153389-155161077	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr1:155158758-155158944	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr1:155159623-155159839	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr1:155159940-155159990	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr1:155158062-155158478	SK-N-SH	brain:	n/a	n/a
20	POLR2A	chr1:155153520-155161231	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr1:155156664-155159106	H1-neurons	neurons:	n/a	n/a
22	POLR2A	chr1:155158171-155159363	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr1:155159245-155159348	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr1:155159398-155159454	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr1:155160682-155161162	H1-neurons	neurons:	n/a	n/a
26	POLR2A	chr1:155158864-155159004	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr1:155160779-155161012	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr1:155158562-155158990	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr1:155159183-155160440	H1-neurons	neurons:	n/a	n/a
30	POLR2A	chr1:155157772-155158774	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr1:155160547-155160614	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr1:155160288-155160544	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr1:155158751-155158963	H1-hESC	embryonic stem cell:	n/a	n/a
34	RUNX3	chr1:155157581-155158433	GM12878	blood:	n/a	n/a
35	RUNX3	chr1:155157862-155158416	GM12878	blood:	n/a	n/a
36	RXRA	chr1:155160937-155161927	HepG2	liver:	n/a	n/a
37	SIN3A	chr1:155158746-155158899	H1-hESC	embryonic stem cell:	n/a	n/a
38	SPI1	chr1:155157402-155158495	GM12878	blood:	n/a	chr1:155157762-155157775 chr1:155158098-155158105 chr1:155157833-155157846 chr1:155157763-155157776 chr1:155157553-155157560 chr1:155157764-155157773 chr1:155158009-155158022
39	TCF3	chr1:155160926-155161900	GM12878	blood:	n/a	n/a
40	WRNIP1	chr1:155158595-155158597	GM12878	blood:	n/a	n/a
41	YY1	chr1:155158553-155159018	H1-hESC	embryonic stem cell:	n/a	chr1:155158973-155158982
42	ZNF263	chr1:155158893-155159392	HEK293-T-REx	kidney:	n/a	chr1:155159058-155159067 chr1:155159141-155159150

No.	Distal block	Cell Line	Cell type
1	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
2	chr1:155096309..155104200-chr1:155157595..155166389,23	MCF-7	breast:
3	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
4	chr1:155092552..155095095-chr1:155160179..155163739,4	MCF-7	breast:
5	chr1:155160293..155162117-chr1:155291803..155294447,2	K562	blood:
6	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
7	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
8	chr1:155139118..155143025-chr1:155155964..155158470,4	MCF-7	breast:

Variant related genes	Relation type
MIR92B	TF binding region
MUC1	TF binding region
ENSG00000273088	TF binding region
ENSG00000160766	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000202027	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000225855	chromatin interactions

Extended variants
information (count: 111 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11465210	chr1:155158414-155158415	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs1611773	chr1:155158532-155158533	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139043100	chr1:155158601-155158602	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs369597551	chr1:155158602-155158603	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549073561	chr1:155158604-155158605	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs1611772	chr1:155158605-155158606	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs199968990	chr1:155158634-155158635	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs11465209	chr1:155158650-155158651	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145965712	chr1:155158711-155158712	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs578209866	chr1:155158719-155158720	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374314292	chr1:155158736-155158737	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139881730	chr1:155158843-155158844	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557887684	chr1:155158844-155158845	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184988099	chr1:155158855-155158856	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12566541	chr1:155158912-155158913	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs113989545	chr1:155158944-155158945	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375269773	chr1:155158945-155158946	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs142212980	chr1:155158946-155158947	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs58446580	chr1:155158968-155158969	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543430885	chr1:155159004-155159005	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs561508595	chr1:155159007-155159008	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551247105	chr1:155159036-155159037	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573915720	chr1:155159067-155159068	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187046852	chr1:155159073-155159074	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs566798251	chr1:155159155-155159156	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs28414349	chr1:155159188-155159189	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559170904	chr1:155159250-155159251	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs532965137	chr1:155159264-155159265	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs142159143	chr1:155159293-155159294	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368083573	chr1:155159294-155159295	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs377291958	chr1:155159299-155159300	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs563457321	chr1:155159325-155159326	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs530880538	chr1:155159348-155159349	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370083076	chr1:155159397-155159398	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549386573	chr1:155159469-155159470	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201219557	chr1:155159496-155159497	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs151187351	chr1:155159594-155159595	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs555426932	chr1:155159605-155159606	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201758571	chr1:155159658-155159659	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148332231	chr1:155159708-155159709	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs191544901	chr1:155159717-155159718	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372682991	chr1:155159718-155159719	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs572153326	chr1:155159745-155159746	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200639498	chr1:155159773-155159774	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs557552446	chr1:155159798-155159799	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs1611771	chr1:155159895-155159896	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs367561217	chr1:155159896-155159897	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs371436760	chr1:155159907-155159908	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs374941067	chr1:155159914-155159915	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs369318053	chr1:155159918-155159919	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	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
Retinoblastoma	19183342	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
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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155146600-155163000	Weak transcription	Aorta	Aorta
2	chr1:155149600-155158800	Weak transcription	A549	lung
3	chr1:155149600-155162000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:155149600-155162600	Weak transcription	Small Intestine	intestine
5	chr1:155149600-155162800	Weak transcription	NHDF-Ad	bronchial
6	chr1:155149800-155158800	Strong transcription	Fetal Stomach	stomach
7	chr1:155149800-155162000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:155149800-155162200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:155150000-155162000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr1:155150000-155163000	Weak transcription	Fetal Brain Male	brain
11	chr1:155150200-155162400	Weak transcription	Dnd41	blood
12	chr1:155150400-155161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr1:155150600-155162000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr1:155150800-155161800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr1:155151000-155162000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr1:155151200-155162000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:155152200-155162800	Weak transcription	Osteobl	bone
18	chr1:155152400-155163000	Weak transcription	HUVEC	blood vessel
19	chr1:155152600-155161800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:155152600-155161800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:155152600-155162000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr1:155152600-155162200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:155152600-155162400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:155152600-155162800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr1:155152600-155163000	Weak transcription	Brain Substantia Nigra	brain
26	chr1:155152800-155162000	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr1:155152800-155162200	Weak transcription	Fetal Thymus	thymus
28	chr1:155152800-155162400	Weak transcription	Brain Anterior Caudate	brain
29	chr1:155152800-155163000	Weak transcription	NH-A	brain
30	chr1:155153000-155161800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:155153000-155162400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr1:155154800-155162200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr1:155155000-155162200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:155155000-155162200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:155155000-155162800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:155155200-155161800	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr1:155155200-155162000	Weak transcription	NHLF	lung
38	chr1:155155400-155162200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr1:155155400-155162400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:155155800-155158800	Enhancers	Spleen	Spleen
41	chr1:155156000-155159000	Enhancers	Fetal Muscle Leg	muscle
42	chr1:155156000-155159200	Enhancers	Primary B cells from peripheral blood	blood
43	chr1:155156200-155158600	Genic enhancers	Esophagus	oesophagus
44	chr1:155156200-155158600	Enhancers	Fetal Muscle Trunk	muscle
45	chr1:155156400-155158600	Enhancers	Primary B cells from cord blood	blood
46	chr1:155156400-155159000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr1:155156400-155161000	Enhancers	Pancreas	Pancrea
48	chr1:155156400-155161800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr1:155156600-155159400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr1:155156600-155159400	Genic enhancers	Gastric	stomach

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