Variant report

Variant	nsv872467
Chromosome Location	chr1:155345641-155377171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:105)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:105 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155359836-155359982	K562	blood:	n/a	n/a
2	BHLHE40	chr1:155366935-155367210	K562	blood:	n/a	n/a
3	CBX3	chr1:155355636-155355917	K562	blood:	n/a	n/a
4	CEBPB	chr1:155369547-155370031	A549	lung:	n/a	chr1:155369778-155369789
5	CEBPB	chr1:155369589-155369955	K562	blood:	n/a	chr1:155369778-155369789
6	CEBPB	chr1:155369587-155369955	A549	lung:	n/a	chr1:155369778-155369789
7	CEBPB	chr1:155369599-155369957	IMR90	lung:	n/a	chr1:155369778-155369789
8	CEBPB	chr1:155353269-155353462	A549	lung:	n/a	n/a
9	CEBPB	chr1:155369520-155369898	MCF-7	breast:	n/a	chr1:155369778-155369789
10	CEBPB	chr1:155369607-155369903	A549	lung:	n/a	chr1:155369778-155369789
11	CEBPB	chr1:155369552-155369889	K562	blood:	n/a	chr1:155369778-155369789
12	CEBPB	chr1:155369593-155369957	Hela-S3	cervix:	n/a	chr1:155369778-155369789
13	CEBPB	chr1:155369605-155369939	HepG2	liver:	n/a	chr1:155369778-155369789
14	E2F4	chr1:155368157-155368236	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr1:155348017-155348032	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr1:155349493-155349695	GM12878	blood:	n/a	n/a
17	EP300	chr1:155366992-155367181	K562	blood:	n/a	n/a
18	ESR1	chr1:155349389-155349914	ECC-1	luminal epithelium:	n/a	n/a
19	ESR1	chr1:155349351-155349920	ECC-1	luminal epithelium:	n/a	n/a
20	FOS	chr1:155359669-155359962	MCF10A-Er-Src	breast:	n/a	chr1:155359781-155359792
21	FOS	chr1:155359637-155359974	HUVEC	blood vessel:	n/a	chr1:155359781-155359792
22	FOS	chr1:155369603-155369912	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr1:155359653-155360005	MCF10A-Er-Src	breast:	n/a	chr1:155359781-155359792
24	FOS	chr1:155369654-155369845	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:155369611-155369886	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:155368309-155368468	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:155359681-155359972	MCF10A-Er-Src	breast:	n/a	chr1:155359781-155359792
28	FOS	chr1:155369581-155369854	MCF10A-Er-Src	breast:	n/a	n/a
29	GABPA	chr1:155366952-155367243	K562	blood:	n/a	n/a
30	GATA1	chr1:155366771-155367332	PBDE	blood:	n/a	n/a
31	GATA2	chr1:155366891-155367317	K562	blood:	n/a	n/a
32	GATA2	chr1:155359722-155360036	HUVEC	blood vessel:	n/a	n/a
33	GATA3	chr1:155368368-155368421	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr1:155372054-155372073	SH-SY5Y	brain:	n/a	n/a
35	GTF2F1	chr1:155349722-155349728	H1-hESC	embryonic stem cell:	n/a	n/a
36	HDAC2	chr1:155366889-155367173	K562	blood:	n/a	n/a
37	HDAC2	chr1:155366808-155367246	K562	blood:	n/a	n/a
38	JUND	chr1:155368460-155368462	HepG2	liver:	n/a	n/a
39	KAP1	chr1:155357225-155357611	K562	blood:	n/a	n/a
40	MAFF	chr1:155370542-155370641	HepG2	liver:	n/a	n/a
41	MAFF	chr1:155359705-155359942	K562	blood:	n/a	n/a
42	MAFK	chr1:155359694-155359984	K562	blood:	n/a	n/a
43	MAFK	chr1:155370489-155370685	IMR90	lung:	n/a	n/a
44	MAFK	chr1:155359642-155360046	IMR90	lung:	n/a	n/a
45	MAFK	chr1:155370456-155370726	HepG2	liver:	n/a	n/a
46	MAFK	chr1:155354199-155354241	H1-hESC	embryonic stem cell:	n/a	n/a
47	MXI1	chr1:155349510-155349633	K562	blood:	n/a	n/a
48	MXI1	chr1:155361968-155361988	K562	blood:	n/a	n/a
49	MYC	chr1:155369654-155369822	MCF10A-Er-Src	breast:	n/a	n/a
50	NR2F2	chr1:155366782-155367344	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155348145-155348195	PrEC	prostate:	n/a
2	chr1:155348145-155348195	K562	blood:	n/a
3	chr1:155348145-155348195	HEEpiC	esophagus:	n/a
4	chr1:155348145-155348195	NHDF-neo	bronchial:	n/a
5	chr1:155348145-155348195	SAEC	small airway:	n/a
6	chr1:155348145-155348195	HCF	heart:	n/a
7	chr1:155348145-155348195	HCPEpiC	choroid plexus:	n/a
8	chr1:155348145-155348195	A549	lung:	n/a
9	chr1:155348145-155348195	HMEC	breast:	n/a
10	chr1:155348145-155348195	SK-N-SH_RA	brain:	n/a
11	chr1:155348145-155348195	AG04449	skin:	fetal
12	chr1:155348145-155348195	MCF-7	breast:	n/a
13	chr1:155348145-155348195	HNPCEpiC	eye:	n/a
14	chr1:155348145-155348195	PFSK-1	brain:	n/a
15	chr1:155348145-155348195	IMR90	lung:	fetal
16	chr1:155348145-155348195	HRE	kidney:	n/a
17	chr1:155348145-155348195	NB4	blood:	n/a
18	chr1:155348145-155348195	HCT-116	colon:	n/a
19	chr1:155348145-155348195	NH-A	brain:	n/a
20	chr1:155348145-155348195	Caco-2	colon:	n/a
21	chr1:155348145-155348195	T-47D	breast:	n/a
22	chr1:155348145-155348195	ovcar-3	ovarian:	n/a
23	chr1:155348145-155348195	NT2-D1	testis:	n/a
24	chr1:155348145-155348195	GM12878	blood:	n/a
25	chr1:155348145-155348195	HIPEpiC	eye:	n/a
26	chr1:155348145-155348195	LNCaP	prostate:	n/a
27	chr1:155348145-155348195	SK-N-MC	brain:	n/a
28	chr1:155348145-155348195	ECC-1	luminal epithelium:	n/a
29	chr1:155348145-155348195	AG10803	skin:	n/a
30	chr1:155348145-155348195	SK-N-SH	brain:	n/a
31	chr1:155348145-155348195	Jurkat	blood:	n/a
32	chr1:155348145-155348195	HRPEpiC	eye:	n/a
33	chr1:155348145-155348195	GM06990	blood:	n/a
34	chr1:155348145-155348195	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:155348145-155348195	HepG2	liver:	n/a
36	chr1:155348145-155348195	AG09319	gingival:	n/a
37	chr1:155348145-155348195	RPTEC	kidney:	n/a
38	chr1:155348145-155348195	AG09309	skin:	n/a
39	chr1:155348145-155348195	SKMC	muscle:	n/a
40	chr1:155348145-155348195	HEK293	kidney:	embryo
41	chr1:155348145-155348195	GM12891	blood:	n/a
42	chr1:155348145-155348195	HAEpiC	amniotic membrane:	n/a
43	chr1:155348145-155348195	BE2_C	brain:	n/a
44	chr1:155348145-155348195	H1-hESC	embryonic stem cell:	embryo
45	chr1:155348145-155348195	ProgFib	skin:	n/a
46	chr1:155348145-155348195	PANC-1	pancreas:	n/a
47	chr1:155348145-155348195	BJ	skin:	n/a
48	chr1:155348145-155348195	MCF10A-Er-Src	breast:	n/a
49	chr1:155348145-155348195	Hepatocyte	liver:	n/a
50	chr1:155348145-155348195	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155362443..155363274-chr8:38832331..38832952,2	Hela-S3	cervix:
2	chr1:155373048..155375865-chr1:155376338..155379086,2	MCF-7	breast:
3	chr1:155347311..155349082-chr1:155531939..155533502,2	K562	blood:
4	chr1:155349409..155351647-chr1:155355555..155357785,2	MCF-7	breast:
5	chr1:155373048..155375865-chr1:155376338..155379086,2	MCF-7	breast:
6	chr1:155339400..155342003-chr1:155343573..155345841,2	K562	blood:
7	chr1:155365472..155367310-chr1:155376011..155377571,2	K562	blood:
8	chr1:155349409..155351647-chr1:155355555..155357785,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PKLR-5	chr1:155358957-155359511	expReg_chr1_16538_-
2	lnc-PKLR-2	chr1:155365801-155366193	ENSG00000227773.1
3	lnc-PKLR-4	chr1:155358178-155358389	expReg_chr1_16535_-
4	lnc-PKLR-7	chr1:155360786-155361172	expReg_chr1_16541_-
5	lnc-PKLR-2	chr1:155366715-155366769	ENSG00000227773.1
6	lnc-PKLR-6	chr1:155359921-155360669	expReg_chr1_16540_-

No data

Variant related genes	Relation type
ASH1L-IT1	TF binding region
ASH1L	TF binding region
ASH1L-IT1	CpG island
ASH1L	CpG island
ENSG00000116539	chromatin interactions
ENSG00000227773	chromatin interactions

Extended variants
information (count: 1086 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12035771	chr1:155345641-155345642	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548431808	chr1:155345643-155345644	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566825933	chr1:155345645-155345646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528367878	chr1:155345651-155345652	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187512578	chr1:155345694-155345695	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528271638	chr1:155345704-155345705	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372837372	chr1:155345759-155345760	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531862384	chr1:155345766-155345767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552555287	chr1:155345808-155345809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35455134	chr1:155345819-155345820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570788500	chr1:155345824-155345825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs538313488	chr1:155345834-155345835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556738765	chr1:155345852-155345853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569034727	chr1:155345991-155345992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193268019	chr1:155345999-155346000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554878628	chr1:155346074-155346075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573110101	chr1:155346096-155346097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183668396	chr1:155346108-155346109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558503263	chr1:155346165-155346166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370317016	chr1:155346170-155346171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138045074	chr1:155346185-155346186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149100213	chr1:155346221-155346222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536533974	chr1:155346236-155346237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201967391	chr1:155346239-155346240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370206441	chr1:155346301-155346302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562251263	chr1:155346432-155346433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530185598	chr1:155346456-155346457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372813894	chr1:155346463-155346464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565162158	chr1:155346481-155346482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187523656	chr1:155346500-155346501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560586829	chr1:155346554-155346555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28438500	chr1:155346571-155346572	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113442378	chr1:155346581-155346582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567766094	chr1:155346600-155346601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561497651	chr1:155346654-155346655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12078402	chr1:155346689-155346690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73008961	chr1:155346709-155346710	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs71517782	chr1:155346742-155346743	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs550253157	chr1:155346746-155346747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184306999	chr1:155346753-155346754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188608544	chr1:155346756-155346757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548389563	chr1:155346760-155346761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551323219	chr1:155346780-155346781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534091750	chr1:155346859-155346860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111267304	chr1:155346940-155346941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374370217	chr1:155347041-155347042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192424421	chr1:155347077-155347078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552611039	chr1:155347092-155347093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55727820	chr1:155347123-155347124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116323375	chr1:155347191-155347192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155296200-155349400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:155296600-155348200	Strong transcription	Fetal Stomach	stomach
3	chr1:155297800-155357400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:155299600-155353600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:155303000-155352800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:155306000-155348200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr1:155306200-155375400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr1:155310000-155347800	Strong transcription	Fetal Intestine Small	intestine
9	chr1:155312400-155407400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr1:155313000-155348400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:155323800-155349400	Strong transcription	Fetal Thymus	thymus
12	chr1:155327800-155347200	Weak transcription	Psoas Muscle	Psoas
13	chr1:155330000-155349000	Weak transcription	Aorta	Aorta
14	chr1:155330200-155362400	Weak transcription	Stomach Mucosa	stomach
15	chr1:155333000-155351200	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr1:155333200-155348800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:155334000-155349600	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr1:155334800-155349600	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr1:155335200-155349200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:155336000-155348200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr1:155337400-155348200	Strong transcription	Fetal Muscle Leg	muscle
22	chr1:155337600-155347600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:155337600-155350000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr1:155337800-155348200	Strong transcription	Primary T cells from cord blood	blood
25	chr1:155337800-155348200	Strong transcription	Fetal Muscle Trunk	muscle
26	chr1:155337800-155348600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr1:155337800-155350000	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr1:155337800-155351600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:155338000-155348000	Strong transcription	Thymus	Thymus
30	chr1:155338600-155349600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:155339600-155346400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
32	chr1:155339600-155348000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:155339800-155347600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr1:155340600-155347800	Weak transcription	HMEC	breast
35	chr1:155340600-155361200	Weak transcription	Fetal Heart	heart
36	chr1:155340600-155362600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:155340600-155364200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr1:155340800-155345800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr1:155340800-155345800	Weak transcription	Spleen	Spleen
40	chr1:155340800-155346800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr1:155340800-155346800	Weak transcription	Colon Smooth Muscle	Colon
42	chr1:155340800-155349600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr1:155340800-155355600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr1:155340800-155357600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:155340800-155361800	Weak transcription	Right Ventricle	heart
46	chr1:155340800-155364800	Weak transcription	Small Intestine	intestine
47	chr1:155341200-155347200	Weak transcription	HSMM	muscle
48	chr1:155341600-155349800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:155341600-155351000	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr1:155341800-155348200	Strong transcription	Brain Germinal Matrix	brain

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