Variant report

Variant	nsv871286
Chromosome Location	chr1:103455217-103528128
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	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
3	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
4	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
5	CEBPB	chr1:103522064-103522370	HepG2	liver:	n/a	chr1:103522213-103522224
6	CEBPB	chr1:103519790-103519887	H1-hESC	embryonic stem cell:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
7	CEBPB	chr1:103519688-103519996	A549	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
8	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
9	CEBPB	chr1:103522115-103522329	IMR90	lung:	n/a	chr1:103522213-103522224
10	CEBPB	chr1:103519671-103520003	HepG2	liver:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
11	CEBPB	chr1:103519692-103519989	ECC-1	luminal epithelium:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
12	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
13	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
14	CEBPB	chr1:103519664-103520007	IMR90	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
15	CTCF	chr1:103467700-103467850	BJ	skin:	n/a	chr1:103467740-103467748
16	CTCF	chr1:103467620-103467770	BE2_C	brain:	n/a	chr1:103467740-103467748
17	CTCF	chr1:103489061-103489081	Fibrobl	skin:	n/a	n/a
18	E2F4	chr1:103457989-103458453	MCF10A-Er-Src	breast:	n/a	n/a
19	ELK1	chr1:103474216-103474272	GM12878	blood:	n/a	n/a
20	EP300	chr1:103497514-103497813	SK-N-SH_RA	brain:	n/a	chr1:103497580-103497588 chr1:103497645-103497652
21	EP300	chr1:103495066-103495343	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr1:103482033-103482177	K562	blood:	n/a	chr1:103482034-103482043
23	FAM48A	chr1:103481060-103481095	GM12878	blood:	n/a	n/a
24	FOXA2	chr1:103516523-103517022	A549	lung:	n/a	n/a
25	GATA3	chr1:103500817-103500879	SH-SY5Y	brain:	n/a	n/a
26	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
27	GATA3	chr1:103495167-103495348	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr1:103460939-103461128	SH-SY5Y	brain:	n/a	chr1:103461085-103461101
29	GATA3	chr1:103469326-103469402	SH-SY5Y	brain:	n/a	chr1:103469390-103469400
30	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
31	JUND	chr1:103498509-103498704	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAFF	chr1:103500931-103500933	K562	blood:	n/a	n/a
33	MAFF	chr1:103500871-103501071	HepG2	liver:	n/a	chr1:103500984-103501002
34	MAFF	chr1:103522922-103522973	HepG2	liver:	n/a	n/a
35	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
36	MAFK	chr1:103522877-103522988	H1-hESC	embryonic stem cell:	n/a	n/a
37	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
38	MAFK	chr1:103488469-103488807	HepG2	liver:	n/a	chr1:103488748-103488768
39	MAFK	chr1:103522892-103523008	HepG2	liver:	n/a	n/a
40	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
41	MAFK	chr1:103488526-103488726	IMR90	lung:	n/a	n/a
42	MAX	chr1:103498532-103498732	NB4	blood:	n/a	n/a
43	MAZ	chr1:103477655-103477827	HepG2	liver:	n/a	n/a
44	MAZ	chr1:103510189-103510210	Hela-S3	cervix:	n/a	n/a
45	MXI1	chr1:103461574-103461774	GM12878	blood:	n/a	n/a
46	MXI1	chr1:103467282-103467392	GM12878	blood:	n/a	n/a
47	MXI1	chr1:103476805-103476816	K562	blood:	n/a	n/a
48	MXI1	chr1:103464776-103464780	GM12878	blood:	n/a	n/a
49	NFYA	chr1:103491625-103491853	GM12878	blood:	n/a	n/a
50	NR3C1	chr1:103522056-103522268	ECC-1	luminal epithelium:	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	chr1:103467481-103467525	NONHSAT004880
2	lnc-AMY1B-5	chr1:103470000-103470037	NONHSAT004880
3	lnc-AMY1B-5	chr1:103467984-103468037	NONHSAT004880
4	lnc-AMY1B-5	chr1:103468303-103468347	NONHSAT004880
5	lnc-AMY1B-5	chr1:103466993-103467187	NONHSAT004880

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

Extended variants
information (count: 3121 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3121 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1463034	chr1:103455217-103455218	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542538384	chr1:103455272-103455273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189185621	chr1:103455297-103455298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560721449	chr1:103455306-103455307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138712421	chr1:103455318-103455319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181558627	chr1:103455328-103455329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569197400	chr1:103455344-103455345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528103421	chr1:103455400-103455401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142576727	chr1:103455437-103455438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111334875	chr1:103455485-103455486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187661310	chr1:103455513-103455514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546541226	chr1:103455516-103455517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191974313	chr1:103455542-103455543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114365404	chr1:103455555-103455556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564857410	chr1:103455559-103455560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538894642	chr1:103455574-103455575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186007149	chr1:103455600-103455601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575132687	chr1:103455618-103455619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71664951	chr1:103455655-103455656	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190911294	chr1:103455680-103455681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572588616	chr1:103455700-103455701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114652354	chr1:103455715-103455716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34855255	chr1:103455742-103455743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565109269	chr1:103455752-103455753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79646678	chr1:103455769-103455770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551213294	chr1:103455838-103455839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562742335	chr1:103455843-103455844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568706868	chr1:103455880-103455881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199916439	chr1:103455890-103455891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3102056	chr1:103455891-103455892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34757169	chr1:103455900-103455901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397725669	chr1:103455903-103455904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373823042	chr1:103455904-103455905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567001705	chr1:103455905-103455906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527761991	chr1:103455915-103455916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375819312	chr1:103455938-103455939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114866563	chr1:103455964-103455965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138944938	chr1:103455989-103455990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538560936	chr1:103455999-103456000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557272589	chr1:103456038-103456039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548087236	chr1:103456081-103456082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149422061	chr1:103456099-103456100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144691482	chr1:103456162-103456163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115808790	chr1:103456176-103456177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202150545	chr1:103456182-103456183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539908577	chr1:103456203-103456204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34413966	chr1:103456262-103456263	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559560492	chr1:103456263-103456264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577319668	chr1:103456314-103456315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544476062	chr1:103456324-103456325	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:149 , 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	chr1:103400200-103462000	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	chr1:103432600-103457400	Weak transcription	Fetal Heart	heart
9	chr1:103445000-103458600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:103446800-103497800	Weak transcription	HSMM	muscle
11	chr1:103449200-103545200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:103450600-103457200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:103450800-103470200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:103451800-103457400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:103452000-103455800	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr1:103453200-103467400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr1:103453400-103490000	Weak transcription	NH-A	brain
18	chr1:103454000-103459000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:103454000-103468400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:103455800-103456800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:103456800-103457200	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:103457200-103459800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr1:103457200-103462800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:103457400-103457600	Enhancers	Fetal Heart	heart
25	chr1:103457400-103459200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:103458600-103460800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:103459000-103460200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:103459200-103461800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:103459400-103460600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:103459800-103460800	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:103460200-103461800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:103460200-103516400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:103460800-103465600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:103460800-103466600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:103461800-103466800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:103462800-103463800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:103463800-103466600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:103466600-103467000	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr1:103466600-103471200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:103466800-103469400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:103467000-103469400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr1:103467400-103468400	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:103468400-103471400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:103468400-103478600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr1:103469400-103469800	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr1:103469400-103471400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:103469800-103486600	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr1:103470200-103471400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr1:103471200-103475000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:103471400-103471800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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