Variant report

Variant	nsv871567
Chromosome Location	chr1:103416690-103499049
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	chr1:103424463-103424755	HepG2	liver:	n/a	n/a
2	BRCA1	chr1:103436155-103436294	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:103420187-103420500	HepG2	liver:	n/a	chr1:103420350-103420361
4	CEBPB	chr1:103420205-103420542	A549	lung:	n/a	chr1:103420350-103420361
5	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
6	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
7	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
8	CEBPB	chr1:103420192-103420500	IMR90	lung:	n/a	chr1:103420350-103420361
9	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
10	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
11	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
12	CEBPB	chr1:103424437-103424754	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:103420192-103420551	H1-hESC	embryonic stem cell:	n/a	chr1:103420350-103420361
14	CTCF	chr1:103436140-103436290	HMEC	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
15	CTCF	chr1:103436160-103436310	GM12878	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
16	CTCF	chr1:103436180-103436330	GM12864	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
17	CTCF	chr1:103436194-103436392	A549	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
18	CTCF	chr1:103436277-103436287	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:103436020-103436170	HAc	cerebellar:	n/a	n/a
20	CTCF	chr1:103436180-103436330	NHEK	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
21	CTCF	chr1:103436140-103436290	BJ	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
22	CTCF	chr1:103436489-103436518	GM12892	blood:	n/a	n/a
23	CTCF	chr1:103436160-103436310	HBMEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
24	CTCF	chr1:103436094-103436352	A549	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
25	CTCF	chr1:103467700-103467850	BJ	skin:	n/a	chr1:103467740-103467748
26	CTCF	chr1:103436140-103436290	GM12875	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
27	CTCF	chr1:103436240-103436390	GM12872	blood:	n/a	chr1:103436240-103436253 chr1:103436243-103436251
28	CTCF	chr1:103436200-103436350	SK-N-SH_RA	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
29	CTCF	chr1:103436155-103436372	HepG2	liver:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
30	CTCF	chr1:103436160-103436310	AG04450	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
31	CTCF	chr1:103436080-103436427	K562	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
32	CTCF	chr1:103436112-103436368	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
33	CTCF	chr1:103436160-103436310	HFF-Myc	foreskin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
34	CTCF	chr1:103436140-103436290	HEK293	kidney:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
35	CTCF	chr1:103436160-103436310	HMEC	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
36	CTCF	chr1:103436415-103436416	GM19238	blood:	n/a	n/a
37	CTCF	chr1:103436140-103436290	GM12868	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
38	CTCF	chr1:103436140-103436290	AG09309	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
39	CTCF	chr1:103436140-103436290	GM12872	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
40	CTCF	chr1:103436120-103436270	HVMF	connective:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
41	CTCF	chr1:103435994-103436641	SK-N-SH	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
42	CTCF	chr1:103436236-103436402	GM12891	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255
43	CTCF	chr1:103436600-103436750	AG04450	lung:	n/a	n/a
44	CTCF	chr1:103436140-103436290	HMF	breast:	n/a	chr1:103436238-103436256 chr1:103436233-103436254 chr1:103436240-103436253 chr1:103436239-103436255 chr1:103436243-103436251
45	CTCF	chr1:103436160-103436310	NB4	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
46	CTCF	chr1:103436220-103436370	HBMEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
47	CTCF	chr1:103436138-103436362	LNCaP	prostate:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
48	CTCF	chr1:103436171-103436402	ProgFib	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
49	CTCF	chr1:103436037-103436432	IMR90	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
50	CTCF	chr1:103436220-103436370	GM12870	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254

No.	Distal block	Cell Line	Cell type
1	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
2	chr1:103259174..103259873-chr1:103435676..103436665,2	MCF-7	breast:
3	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:
4	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
5	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
6	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
7	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:

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

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

Extended variants
information (count: 3421 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3421 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6691075	chr1:103416690-103416691	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554510352	chr1:103416707-103416708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568915234	chr1:103416751-103416752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115229340	chr1:103416812-103416813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548293221	chr1:103416855-103416856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531407432	chr1:103416869-103416870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187923003	chr1:103416890-103416891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534545939	chr1:103416945-103416946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112509811	chr1:103416962-103416963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147601452	chr1:103416967-103416968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539983820	chr1:103416971-103416972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556947054	chr1:103416980-103416981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72683280	chr1:103416986-103416987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149047464	chr1:103416992-103416993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555776312	chr1:103417020-103417021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377672822	chr1:103417069-103417070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573452314	chr1:103417120-103417121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540502795	chr1:103417152-103417153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192205664	chr1:103417170-103417171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61812695	chr1:103417173-103417174	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs12751686	chr1:103417177-103417178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544899625	chr1:103417188-103417189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2061708	chr1:103417203-103417204	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs530059263	chr1:103417204-103417205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111354772	chr1:103417223-103417224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566660998	chr1:103417224-103417225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528282200	chr1:103417253-103417254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115514007	chr1:103417259-103417260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571420964	chr1:103417260-103417261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75546123	chr1:103417290-103417291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557306436	chr1:103417292-103417293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140090643	chr1:103417301-103417302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571816236	chr1:103417314-103417315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568839740	chr1:103417353-103417354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536280606	chr1:103417354-103417355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72985732	chr1:103417364-103417365	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs572892739	chr1:103417390-103417391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141110304	chr1:103417412-103417413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558844701	chr1:103417424-103417425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577384785	chr1:103417430-103417431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551763436	chr1:103417448-103417449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184988543	chr1:103417452-103417453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562871290	chr1:103417455-103417456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187907679	chr1:103417538-103417539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56412519	chr1:103417540-103417541	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs3102051	chr1:103417593-103417594	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs72683281	chr1:103417602-103417603	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs552646689	chr1:103417661-103417662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114806195	chr1:103417667-103417668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34837300	chr1:103417688-103417689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:178 , 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	chr1:103400200-103424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:103400800-103444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:103405800-103444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:103407400-103426000	Weak transcription	NH-A	brain
9	chr1:103407400-103426600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:103412600-103417000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:103412600-103421400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:103412800-103424800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:103417000-103429200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:103421400-103429800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:103422800-103426400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:103423000-103468200	Weak transcription	HSMMtube	muscle
18	chr1:103423800-103476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:103424400-103424600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:103424400-103424600	Enhancers	Fetal Heart	heart
21	chr1:103424400-103435200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:103424600-103432200	Weak transcription	Fetal Heart	heart
23	chr1:103424800-103425000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr1:103424800-103429200	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:103426000-103427400	Strong transcription	NH-A	brain
27	chr1:103426400-103427000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:103426600-103428000	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr1:103427000-103427600	Enhancers	Brain Germinal Matrix	brain
30	chr1:103427000-103451400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:103427400-103452400	Weak transcription	NH-A	brain
32	chr1:103428000-103435000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:103429200-103430200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:103429200-103433200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:103429800-103432200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:103430200-103440600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:103432200-103432600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:103432200-103432600	Enhancers	Fetal Heart	heart
39	chr1:103432600-103434600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:103432600-103434600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:103432600-103457400	Weak transcription	Fetal Heart	heart
42	chr1:103433200-103433800	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr1:103433800-103442800	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr1:103434600-103435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:103434600-103435400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr1:103434600-103440800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:103434800-103435400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:103435000-103435400	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:103435200-103442400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:103435400-103452200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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