Variant report

Variant	nsv946142
Chromosome Location	chr1:113212535-113214320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:62)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:113213019-113213308	T-47D	breast:	n/a	n/a
2	MAFK	chr1:113214069-113214143	HepG2	liver:	n/a	n/a
3	POLR2A	chr1:113214315-113214768	K562	blood:	n/a	n/a
4	POLR2A	chr1:113213257-113213449	K562	blood:	n/a	n/a
5	POLR2A	chr1:113211412-113212741	K562	blood:	n/a	n/a
6	POLR2A	chr1:113212721-113212726	MCF-7	breast:	n/a	n/a
7	POLR2A	chr1:113213217-113213265	MCF-7	breast:	n/a	n/a
8	POLR2A	chr1:113212407-113212548	HepG2	liver:	n/a	n/a
9	POLR2A	chr1:113214019-113219584	K562	blood:	n/a	n/a
10	POLR2A	chr1:113213721-113213916	ProgFib	skin:	n/a	n/a
11	POLR2A	chr1:113213139-113213279	ProgFib	skin:	n/a	n/a
12	POLR2A	chr1:113214234-113217824	GM12892	blood:	n/a	n/a
13	POLR2A	chr1:113212361-113212707	ProgFib	skin:	n/a	n/a
14	POLR2A	chr1:113214290-113214552	GM12891	blood:	n/a	n/a
15	POLR2A	chr1:113212655-113212718	MCF-7	breast:	n/a	n/a
16	POLR2A	chr1:113214313-113214693	GM12892	blood:	n/a	n/a
17	POLR2A	chr1:113212633-113212646	MCF-7	breast:	n/a	n/a
18	POLR2A	chr1:113213396-113213655	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr1:113214194-113214316	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr1:113214306-113214796	K562	blood:	n/a	n/a
21	SP1	chr1:113213963-113214221	H1-hESC	embryonic stem cell:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:113214053-113214103	AG04450	lung:	fetal
2	chr1:113214053-113214103	AG04450	lung:	fetal
3	chr1:113214053-113214103	HepG2	liver:	n/a
4	chr1:113214053-113214103	HL-60	blood:	n/a
5	chr1:113214053-113214103	GM12891	blood:	n/a
6	chr1:113214053-113214103	ECC-1	luminal epithelium:	n/a
7	chr1:113214053-113214103	HCF	heart:	n/a
8	chr1:113214053-113214103	AoSMC	blood vessel:	n/a
9	chr1:113214053-113214103	PANC-1	pancreas:	n/a
10	chr1:113214053-113214103	NHDF-neo	bronchial:	n/a
11	chr1:113214053-113214103	HEK293	kidney:	embryo
12	chr1:113214053-113214103	BJ	skin:	n/a
13	chr1:113214053-113214103	HUVEC	blood vessel:	n/a
14	chr1:113214053-113214103	MCF-7	breast:	n/a
15	chr1:113214053-113214103	RPTEC	kidney:	n/a
16	chr1:113214053-113214103	GM12892	blood:	n/a
17	chr1:113214053-113214103	T-47D	breast:	n/a
18	chr1:113214053-113214103	HCT-116	colon:	n/a
19	chr1:113214053-113214103	HNPCEpiC	eye:	n/a
20	chr1:113214053-113214103	U87	brain:	n/a
21	chr1:113214053-113214103	BE2_C	brain:	n/a
22	chr1:113214053-113214103	Hela-S3	cervix:	n/a
23	chr1:113214053-113214103	K562	blood:	n/a
24	chr1:113214053-113214103	GM12878	blood:	n/a
25	chr1:113214053-113214103	Hepatocyte	liver:	n/a
26	chr1:113214053-113214103	HCM	heart:	n/a
27	chr1:113214053-113214103	NT2-D1	testis:	n/a
28	chr1:113214053-113214103	AG09319	gingival:	n/a
29	chr1:113214053-113214103	ovcar-3	ovarian:	n/a
30	chr1:113214053-113214103	SAEC	small airway:	n/a
31	chr1:113214053-113214103	H1-hESC	embryonic stem cell:	embryo
32	chr1:113214053-113214103	AG09309	skin:	n/a
33	chr1:113214053-113214103	Jurkat	blood:	n/a
34	chr1:113214053-113214103	AG04449	skin:	fetal
35	chr1:113214053-113214103	PrEC	prostate:	n/a
36	chr1:113214053-113214103	HRE	kidney:	n/a
37	chr1:113214053-113214103	SK-N-SH	brain:	n/a
38	chr1:113214053-113214103	HRCEpiC	kidney:	n/a
39	chr1:113214053-113214103	A549	lung:	n/a
40	chr1:113214053-113214103	AG10803	skin:	n/a
41	chr1:113214053-113214103	Caco-2	colon:	n/a
42	chr1:113214053-113214103	NHBE	bronchial:	n/a
43	chr1:113214053-113214103	IMR90	lung:	fetal
44	chr1:113214053-113214103	CMK	blood:	n/a
45	chr1:113214053-113214103	HEEpiC	esophagus:	n/a
46	chr1:113214053-113214103	SKMC	muscle:	n/a
47	chr1:113214053-113214103	GM06990	blood:	n/a
48	chr1:113214053-113214103	MCF10A-Er-Src	breast:	n/a
49	chr1:113214053-113214103	HRPEpiC	eye:	n/a
50	chr1:113214053-113214103	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:113211024..113213434-chr1:113214018..113215567,2	K562	blood:
2	chr1:113214002..113222947-chr1:113236890..113251579,47	MCF-7	breast:
3	chr1:113202139..113204725-chr1:113211463..113213311,2	MCF-7	breast:
4	chr1:113211024..113213434-chr1:113214018..113215567,2	K562	blood:
5	chr1:113199081..113201005-chr1:113210169..113212981,2	K562	blood:
6	chr1:113209056..113210791-chr1:113210932..113214020,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOV10-2	chr1:113213937-113214234	NONHSAT005271

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CAPZA1	hsa-miR-9-5p	chr1:113213664-113213689
2	CAPZA1	hsa-miR-30c-5p	chr1:113213050-113213070
3	CAPZA1	hsa-miR-7-5p	chr1:113213986-113214006
4	CAPZA1	hsa-miR-30c-5p	chr1:113213939-113213946
5	CAPZA1	hsa-miR-7-5p	chr1:113214031-113214054
6	CAPZA1	hsa-miR-30c-5p	chr1:113214105-113214133
7	CAPZA1	hsa-miR-30c-5p	chr1:113213924-113213946
8	CAPZA1	hsa-miR-9-5p	chr1:113213682-113213688

Variant related genes	Relation type
MOV10	TF binding region
MOV10	CpG island
ENSG00000155366	chromatin interactions
ENSG00000225075	chromatin interactions
ENSG00000116489	chromatin interactions
ENSG00000155363	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563996968	chr1:113212557-113212558	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529599201	chr1:113212561-113212562	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570789296	chr1:113212607-113212608	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201851829	chr1:113212649-113212650	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs559987730	chr1:113212655-113212656	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs1060163	chr1:113212673-113212674	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs201104692	chr1:113212689-113212690	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375232761	chr1:113212778-113212779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368445388	chr1:113212779-113212780	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551198154	chr1:113212782-113212783	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs199650232	chr1:113212791-113212792	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200171825	chr1:113212802-113212803	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs371240455	chr1:113212869-113212870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530446657	chr1:113212871-113212872	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185470302	chr1:113212894-113212895	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369766070	chr1:113212909-113212910	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189899505	chr1:113212932-113212933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552801804	chr1:113212965-113212966	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566557789	chr1:113212967-113212968	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538790200	chr1:113212968-113212969	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140993095	chr1:113212976-113212977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370084665	chr1:113212984-113212985	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369976773	chr1:113212985-113212986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs199782772	chr1:113212988-113212989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs72984529	chr1:113212989-113212990	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58051216	chr1:113213003-113213004	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371510141	chr1:113213005-113213006	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs3103452	chr1:113213006-113213007	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557988674	chr1:113213036-113213037	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574588878	chr1:113213042-113213043	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs578027981	chr1:113213089-113213090	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543869587	chr1:113213104-113213105	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs557384181	chr1:113213153-113213154	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs193287417	chr1:113213169-113213170	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138470036	chr1:113213203-113213204	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149626944	chr1:113213223-113213224	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs1060168	chr1:113213248-113213249	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs184963414	chr1:113213257-113213258	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs541959453	chr1:113213264-113213265	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189346901	chr1:113213410-113213411	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs1060171	chr1:113213438-113213439	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375436901	chr1:113213476-113213477	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564859396	chr1:113213486-113213487	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34392165	chr1:113213513-113213514	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs180885116	chr1:113213528-113213529	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550206952	chr1:113213562-113213563	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369709648	chr1:113213641-113213642	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs144340014	chr1:113213647-113213648	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs1802930	chr1:113213649-113213650	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs1802931	chr1:113213695-113213696	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113168800-113215800	Weak transcription	Fetal Heart	heart
2	chr1:113179000-113215600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:113180000-113216000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:113184200-113215600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:113184600-113214800	Strong transcription	Hela-S3	cervix
6	chr1:113185000-113214800	Strong transcription	Dnd41	blood
7	chr1:113185400-113216200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:113186000-113214800	Strong transcription	Fetal Thymus	thymus
9	chr1:113186000-113215000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr1:113186200-113215400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr1:113187000-113213200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:113187000-113215200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:113187200-113215200	Strong transcription	HSMM	muscle
14	chr1:113187400-113215000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:113187800-113216000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:113188400-113215000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:113188800-113213800	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:113189000-113213800	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:113189200-113214600	Strong transcription	NHEK	skin
20	chr1:113189200-113214800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:113189200-113215000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:113189400-113214800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:113189800-113213800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr1:113189800-113215200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:113189800-113215400	Strong transcription	Placenta	Placenta
26	chr1:113189800-113216200	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr1:113190000-113214600	Strong transcription	Liver	Liver
28	chr1:113190000-113215200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:113190000-113215200	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr1:113190000-113215200	Strong transcription	NH-A	brain
31	chr1:113190000-113215400	Strong transcription	Primary B cells from peripheral blood	blood
32	chr1:113190000-113215400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr1:113190200-113214400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr1:113190200-113214600	Strong transcription	Adipose Nuclei	Adipose
35	chr1:113190600-113213000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr1:113190600-113214200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:113190800-113215000	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr1:113191000-113213600	Strong transcription	Primary T cells from cord blood	blood
39	chr1:113191000-113213800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr1:113191000-113215000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr1:113191400-113215200	Strong transcription	Fetal Intestine Large	intestine
42	chr1:113191600-113214800	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr1:113194400-113216000	Weak transcription	Stomach Mucosa	stomach
44	chr1:113195800-113215200	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr1:113196800-113215200	Strong transcription	Duodenum Mucosa	Duodenum
46	chr1:113197000-113213800	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr1:113197000-113214400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:113197000-113214800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr1:113197000-113215000	Strong transcription	Fetal Muscle Trunk	muscle
50	chr1:113197000-113215400	Strong transcription	Osteobl	bone

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