Variant report

Variant	nsv546936
Chromosome Location	chr1:103438795-103499896
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	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
2	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
3	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
4	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
5	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
6	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
7	CTCF	chr1:103467620-103467770	BE2_C	brain:	n/a	chr1:103467740-103467748
8	CTCF	chr1:103467700-103467850	BJ	skin:	n/a	chr1:103467740-103467748
9	CTCF	chr1:103489061-103489081	Fibrobl	skin:	n/a	n/a
10	E2F4	chr1:103457989-103458453	MCF10A-Er-Src	breast:	n/a	n/a
11	ELK1	chr1:103446015-103446030	GM12878	blood:	n/a	n/a
12	ELK1	chr1:103474216-103474272	GM12878	blood:	n/a	n/a
13	EP300	chr1:103482033-103482177	K562	blood:	n/a	chr1:103482034-103482043
14	EP300	chr1:103497514-103497813	SK-N-SH_RA	brain:	n/a	chr1:103497580-103497588 chr1:103497645-103497652
15	EP300	chr1:103495066-103495343	SK-N-SH_RA	brain:	n/a	n/a
16	FAM48A	chr1:103481060-103481095	GM12878	blood:	n/a	n/a
17	FOS	chr1:103442142-103442382	MCF10A-Er-Src	breast:	n/a	chr1:103442214-103442221 chr1:103442215-103442226 chr1:103442213-103442223 chr1:103442214-103442222 chr1:103442213-103442223 chr1:103442213-103442223 chr1:103442214-103442222
18	GATA3	chr1:103483910-103484121	SH-SY5Y	brain:	n/a	chr1:103483910-103483926 chr1:103484011-103484019 chr1:103484008-103484021 chr1:103483984-103483991 chr1:103483911-103483921 chr1:103484010-103484019 chr1:103483957-103483973 chr1:103483959-103483971 chr1:103484012-103484019
19	GATA3	chr1:103495167-103495348	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr1:103469326-103469402	SH-SY5Y	brain:	n/a	chr1:103469390-103469400
21	GATA3	chr1:103460939-103461128	SH-SY5Y	brain:	n/a	chr1:103461085-103461101
22	JUND	chr1:103467623-103468040	H1-hESC	embryonic stem cell:	n/a	chr1:103467779-103467791 chr1:103467781-103467790 chr1:103467782-103467789 chr1:103467780-103467790 chr1:103467781-103467789
23	JUND	chr1:103498509-103498704	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAFF	chr1:103439965-103440198	HepG2	liver:	n/a	n/a
25	MAFF	chr1:103442880-103443227	K562	blood:	n/a	chr1:103443040-103443054 chr1:103443041-103443059
26	MAFF	chr1:103442863-103443228	HepG2	liver:	n/a	chr1:103443040-103443054 chr1:103443041-103443059
27	MAFK	chr1:103442868-103443222	HepG2	liver:	n/a	chr1:103443039-103443055 chr1:103443042-103443057 chr1:103443037-103443057 chr1:103443040-103443054
28	MAFK	chr1:103442926-103443142	H1-hESC	embryonic stem cell:	n/a	chr1:103443039-103443055 chr1:103443042-103443057 chr1:103443037-103443057 chr1:103443040-103443054
29	MAFK	chr1:103442870-103443217	HepG2	liver:	n/a	chr1:103443039-103443055 chr1:103443042-103443057 chr1:103443037-103443057 chr1:103443040-103443054
30	MAFK	chr1:103488469-103488807	HepG2	liver:	n/a	chr1:103488748-103488768
31	MAFK	chr1:103488526-103488726	IMR90	lung:	n/a	n/a
32	MAFK	chr1:103442858-103443224	IMR90	lung:	n/a	chr1:103443039-103443055 chr1:103443042-103443057 chr1:103443037-103443057 chr1:103443040-103443054
33	MAFK	chr1:103442900-103443129	Hela-S3	cervix:	n/a	chr1:103443039-103443055 chr1:103443042-103443057 chr1:103443037-103443057 chr1:103443040-103443054
34	MAFK	chr1:103439964-103440231	HepG2	liver:	n/a	chr1:103440095-103440109
35	MAFK	chr1:103439971-103440226	HepG2	liver:	n/a	chr1:103440095-103440109
36	MAFK	chr1:103442873-103443191	K562	blood:	n/a	chr1:103443039-103443055 chr1:103443042-103443057 chr1:103443037-103443057 chr1:103443040-103443054
37	MAX	chr1:103498532-103498732	NB4	blood:	n/a	n/a
38	MAZ	chr1:103477655-103477827	HepG2	liver:	n/a	n/a
39	MXI1	chr1:103461574-103461774	GM12878	blood:	n/a	n/a
40	MXI1	chr1:103476805-103476816	K562	blood:	n/a	n/a
41	MXI1	chr1:103467282-103467392	GM12878	blood:	n/a	n/a
42	MXI1	chr1:103464776-103464780	GM12878	blood:	n/a	n/a
43	MYC	chr1:103442400-103442516	H1-hESC	embryonic stem cell:	n/a	n/a
44	NFYA	chr1:103491625-103491853	GM12878	blood:	n/a	n/a
45	POLR2A	chr1:103467208-103467320	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:103498773-103498930	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr1:103489703-103489763	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr1:103439216-103439332	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr1:103497360-103497385	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr1:103468500-103468715	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:
2	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-5	chr1:103467984-103468037	NONHSAT004880
2	lnc-AMY1B-5	chr1:103468303-103468347	NONHSAT004880
3	lnc-AMY1B-5	chr1:103466993-103467187	NONHSAT004880
4	lnc-AMY1B-5	chr1:103467481-103467525	NONHSAT004880
5	lnc-AMY1B-5	chr1:103470000-103470037	NONHSAT004880

Variant related genes	Relation type
COL11A1	TF binding region
ENSG00000060718	chromatin interactions
MBD4	miRNA target sites
TMPO	miRNA target sites
FOXO1	miRNA target sites
NHLRC3	miRNA target sites

Extended variants
information (count: 2566 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2566 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12118365	chr1:103438795-103438796	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574090020	chr1:103438813-103438814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535034562	chr1:103438876-103438877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553360405	chr1:103438879-103438880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572011318	chr1:103438880-103438881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143616442	chr1:103438885-103438886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187449519	chr1:103438897-103438898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191998697	chr1:103438941-103438942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373387981	chr1:103438954-103438955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1841835	chr1:103439030-103439031	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs80054610	chr1:103439052-103439053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529616792	chr1:103439246-103439247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138113043	chr1:103439269-103439270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142393735	chr1:103439273-103439274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145924969	chr1:103439308-103439309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551881484	chr1:103439443-103439444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138599565	chr1:103439522-103439523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78922235	chr1:103439528-103439529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370877379	chr1:103439569-103439570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549565307	chr1:103439599-103439600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190594447	chr1:103439635-103439636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142086527	chr1:103439735-103439736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142463397	chr1:103439736-103439737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145922710	chr1:103439743-103439744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4013868	chr1:103439750-103439751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79870729	chr1:103439751-103439752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113503416	chr1:103439752-103439753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76163572	chr1:103439753-103439754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192502673	chr1:103439781-103439782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553323482	chr1:103439798-103439799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2622878	chr1:103439819-103439820	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs539142972	chr1:103439880-103439881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141187150	chr1:103439881-103439882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150673416	chr1:103439940-103439941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543987428	chr1:103439959-103439960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533713178	chr1:103439973-103439974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184482241	chr1:103440044-103440045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574356277	chr1:103440052-103440053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188999624	chr1:103440057-103440058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559468248	chr1:103440062-103440063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533399864	chr1:103440079-103440080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545166115	chr1:103440084-103440085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181336436	chr1:103440087-103440088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185605551	chr1:103440128-103440129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368420835	chr1:103440182-103440183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543217039	chr1:103440218-103440219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560757419	chr1:103440249-103440250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189189126	chr1:103440275-103440276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181551026	chr1:103440314-103440315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368422725	chr1:103440390-103440391	Weak transcription Strong transcription	n/a	n/a	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	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:103400800-103444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:103405800-103444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:103423000-103468200	Weak transcription	HSMMtube	muscle
9	chr1:103423800-103476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr1:103427000-103451400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:103427400-103452400	Weak transcription	NH-A	brain
13	chr1:103430200-103440600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:103432600-103457400	Weak transcription	Fetal Heart	heart
15	chr1:103433800-103442800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr1:103434600-103440800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:103435200-103442400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:103435400-103452200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:103435800-103446200	Weak transcription	HSMM	muscle
20	chr1:103440600-103444200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:103440800-103443000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:103442400-103445000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:103442600-103453200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:103442800-103446800	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:103443000-103445400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:103444200-103444600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:103444200-103445000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:103444200-103445000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr1:103444200-103446800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:103444600-103444800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:103444800-103453200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:103445000-103448600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:103445000-103448800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:103445000-103458600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:103445400-103451800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:103446200-103446800	Strong transcription	HSMM	muscle
37	chr1:103446800-103448200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:103446800-103452000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr1:103446800-103497800	Weak transcription	HSMM	muscle
40	chr1:103448200-103449800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:103448600-103449600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:103448800-103449200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:103449200-103545200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:103449600-103450600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:103449800-103450800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:103450600-103457200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:103450800-103470200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:103451400-103454000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:103451800-103457400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:103452000-103455800	Strong transcription	Cortex derived primary cultured neurospheres	brain

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