Variant report

Variant	nsv462794
Chromosome Location	chr1:103450196-103539007
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	ARID3A	chr1:103502292-103502351	K562	blood:	n/a	n/a
2	CEBPB	chr1:103519671-103520003	HepG2	liver:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
3	CEBPB	chr1:103522115-103522329	IMR90	lung:	n/a	chr1:103522213-103522224
4	CEBPB	chr1:103519692-103519989	ECC-1	luminal epithelium:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
5	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
6	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
7	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
8	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
9	CEBPB	chr1:103519790-103519887	H1-hESC	embryonic stem cell:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
10	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
11	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
12	CEBPB	chr1:103522064-103522370	HepG2	liver:	n/a	chr1:103522213-103522224
13	CEBPB	chr1:103519664-103520007	IMR90	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
14	CEBPB	chr1:103519688-103519996	A549	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
15	CTCF	chr1:103529460-103529610	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr1:103467700-103467850	BJ	skin:	n/a	chr1:103467740-103467748
17	CTCF	chr1:103467620-103467770	BE2_C	brain:	n/a	chr1:103467740-103467748
18	CTCF	chr1:103489061-103489081	Fibrobl	skin:	n/a	n/a
19	E2F4	chr1:103457989-103458453	MCF10A-Er-Src	breast:	n/a	n/a
20	ELK1	chr1:103474216-103474272	GM12878	blood:	n/a	n/a
21	EP300	chr1:103482033-103482177	K562	blood:	n/a	chr1:103482034-103482043
22	EP300	chr1:103497514-103497813	SK-N-SH_RA	brain:	n/a	chr1:103497580-103497588 chr1:103497645-103497652
23	EP300	chr1:103495066-103495343	SK-N-SH_RA	brain:	n/a	n/a
24	FAM48A	chr1:103481060-103481095	GM12878	blood:	n/a	n/a
25	FOXA2	chr1:103516523-103517022	A549	lung:	n/a	n/a
26	FOXA2	chr1:103534858-103535060	HepG2	liver:	n/a	n/a
27	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
28	GATA3	chr1:103500817-103500879	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr1:103460939-103461128	SH-SY5Y	brain:	n/a	chr1:103461085-103461101
30	GATA3	chr1:103495167-103495348	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr1:103469326-103469402	SH-SY5Y	brain:	n/a	chr1:103469390-103469400
32	JUND	chr1:103498509-103498704	H1-hESC	embryonic stem cell:	n/a	n/a
33	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
34	MAFF	chr1:103500871-103501071	HepG2	liver:	n/a	chr1:103500984-103501002
35	MAFF	chr1:103522922-103522973	HepG2	liver:	n/a	n/a
36	MAFF	chr1:103500931-103500933	K562	blood:	n/a	n/a
37	MAFK	chr1:103535685-103535852	HepG2	liver:	n/a	n/a
38	MAFK	chr1:103500893-103501127	IMR90	lung:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
39	MAFK	chr1:103500873-103501086	HepG2	liver:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
40	MAFK	chr1:103488526-103488726	IMR90	lung:	n/a	n/a
41	MAFK	chr1:103522877-103522988	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAFK	chr1:103522892-103523008	HepG2	liver:	n/a	n/a
43	MAFK	chr1:103488469-103488807	HepG2	liver:	n/a	chr1:103488748-103488768
44	MAFK	chr1:103500869-103501153	HepG2	liver:	n/a	chr1:103500986-103500997 chr1:103500986-103500997 chr1:103500987-103500998 chr1:103500986-103501001 chr1:103500985-103500999 chr1:103500986-103501002
45	MAX	chr1:103498532-103498732	NB4	blood:	n/a	n/a
46	MAZ	chr1:103510189-103510210	Hela-S3	cervix:	n/a	n/a
47	MAZ	chr1:103477655-103477827	HepG2	liver:	n/a	n/a
48	MXI1	chr1:103467282-103467392	GM12878	blood:	n/a	n/a
49	MXI1	chr1:103461574-103461774	GM12878	blood:	n/a	n/a
50	MXI1	chr1:103464776-103464780	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:

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

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

Extended variants
information (count: 3828 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3828 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1463035	chr1:103450196-103450197	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539942688	chr1:103450203-103450204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188769676	chr1:103450229-103450230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12747435	chr1:103450230-103450231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576520840	chr1:103450234-103450235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548974401	chr1:103450272-103450273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544436728	chr1:103450354-103450355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562719372	chr1:103450360-103450361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147091987	chr1:103450405-103450406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548826334	chr1:103450500-103450501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138454665	chr1:103450541-103450542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552176045	chr1:103450576-103450577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527735487	chr1:103450592-103450593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143969024	chr1:103450631-103450632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574035924	chr1:103450655-103450656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181910362	chr1:103450672-103450673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550817190	chr1:103450695-103450696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569000875	chr1:103450696-103450697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536165699	chr1:103450709-103450710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554801955	chr1:103450716-103450717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184592331	chr1:103450791-103450792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533582175	chr1:103450793-103450794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115962455	chr1:103450818-103450819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553173931	chr1:103450871-103450872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12125432	chr1:103450912-103450913	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370896338	chr1:103450952-103450953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556494160	chr1:103451104-103451105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542458054	chr1:103451122-103451123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542159650	chr1:103451166-103451167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112420550	chr1:103451171-103451172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560883981	chr1:103451189-103451190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527977253	chr1:103451248-103451249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189559825	chr1:103451293-103451294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564447101	chr1:103451303-103451304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531859943	chr1:103451349-103451350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565803330	chr1:103451352-103451353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550259132	chr1:103451358-103451359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547101982	chr1:103451383-103451384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570482810	chr1:103451398-103451399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7544130	chr1:103451455-103451456	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs548073813	chr1:103451495-103451496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575167613	chr1:103451499-103451500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77743728	chr1:103451521-103451522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7532572	chr1:103451527-103451528	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs533813095	chr1:103451530-103451531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558150522	chr1:103451564-103451565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570077705	chr1:103451569-103451570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180811326	chr1:103451592-103451593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569535798	chr1:103451619-103451620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186737423	chr1:103451640-103451641	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:171 , 50 per page) page: 1 2 3 4

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	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:103423000-103468200	Weak transcription	HSMMtube	muscle
6	chr1:103423800-103476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:103427000-103451400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:103427400-103452400	Weak transcription	NH-A	brain
10	chr1:103432600-103457400	Weak transcription	Fetal Heart	heart
11	chr1:103435400-103452200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:103442600-103453200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:103444800-103453200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:103445000-103458600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:103445400-103451800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:103446800-103452000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr1:103446800-103497800	Weak transcription	HSMM	muscle
18	chr1:103449200-103545200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:103449600-103450600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:103449800-103450800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:103450600-103457200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:103450800-103470200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:103451400-103454000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:103451800-103457400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:103452000-103455800	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr1:103452200-103453200	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr1:103452400-103453400	Strong transcription	NH-A	brain
28	chr1:103453200-103453800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:103453200-103454000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:103453200-103467400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:103453400-103490000	Weak transcription	NH-A	brain
32	chr1:103454000-103459000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:103454000-103468400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:103455800-103456800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:103456800-103457200	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr1:103457200-103459800	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr1:103457200-103462800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:103457400-103457600	Enhancers	Fetal Heart	heart
39	chr1:103457400-103459200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:103458600-103460800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:103459000-103460200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:103459200-103461800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:103459400-103460600	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr1:103459800-103460800	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:103460200-103461800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:103460200-103516400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:103460800-103465600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:103460800-103466600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:103461800-103466800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:103462800-103463800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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