Variant report

Variant	nsv871067
Chromosome Location	chr1:103407999-103509323
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	ARID3A	chr1:103502292-103502351	K562	blood:	n/a	n/a
3	BRCA1	chr1:103436155-103436294	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:103463557-103463788	A549	lung:	n/a	chr1:103463691-103463704 chr1:103463691-103463702 chr1:103463691-103463702 chr1:103463712-103463725 chr1:103463691-103463704
5	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
6	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
7	CEBPB	chr1:103420187-103420500	HepG2	liver:	n/a	chr1:103420350-103420361
8	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
9	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
10	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
11	CEBPB	chr1:103420192-103420551	H1-hESC	embryonic stem cell:	n/a	chr1:103420350-103420361
12	CEBPB	chr1:103420192-103420500	IMR90	lung:	n/a	chr1:103420350-103420361
13	CEBPB	chr1:103424437-103424754	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:103420205-103420542	A549	lung:	n/a	chr1:103420350-103420361
15	CTCF	chr1:103436140-103436290	HCFaa	heart:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
16	CTCF	chr1:103436171-103436402	ProgFib	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
17	CTCF	chr1:103436140-103436290	HEEpiC	esophagus:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
18	CTCF	chr1:103436180-103436330	GM12867	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
19	CTCF	chr1:103436140-103436290	SK-N-SH_RA	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
20	CTCF	chr1:103436153-103436432	GM20000	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
21	CTCF	chr1:103436200-103436350	AG09309	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
22	CTCF	chr1:103436200-103436350	HepG2	liver:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
23	CTCF	chr1:103436180-103436330	GM12865	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
24	CTCF	chr1:103436140-103436290	HEK293	kidney:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
25	CTCF	chr1:103436120-103436270	GM12875	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
26	CTCF	chr1:103436089-103436370	MCF-7	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
27	CTCF	chr1:103436183-103436398	Fibrobl	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
28	CTCF	chr1:103436140-103436290	NHLF	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
29	CTCF	chr1:103436189-103436414	GM19238	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
30	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
31	CTCF	chr1:103436277-103436287	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:103436140-103436290	SAEC	small airway:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
33	CTCF	chr1:103436160-103436310	HMEC	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
34	CTCF	chr1:103436236-103436402	GM12891	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255
35	CTCF	chr1:103436160-103436310	HRPEpiC	eye:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
36	CTCF	chr1:103436160-103436310	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
37	CTCF	chr1:103436180-103436330	WERI-Rb-1	eye:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
38	CTCF	chr1:103436136-103436287	Lung_OC	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
39	CTCF	chr1:103436140-103436290	WERI-Rb-1	eye:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
40	CTCF	chr1:103436160-103436310	HA-sp	spinal cord:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
41	CTCF	chr1:103436220-103436370	HBMEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
42	CTCF	chr1:103436140-103436290	GM12874	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
43	CTCF	chr1:103436444-103436548	GM10248	blood:	n/a	n/a
44	CTCF	chr1:103436020-103436170	HAc	cerebellar:	n/a	n/a
45	CTCF	chr1:103436220-103436370	GM12870	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
46	CTCF	chr1:103436200-103436350	GM12866	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
47	CTCF	chr1:103436160-103436310	GM12878	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
48	CTCF	chr1:103436140-103436290	AG09319	gingival:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
49	CTCF	chr1:103436082-103436313	ECC-1	luminal epithelium:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
50	CTCF	chr1:103436140-103436290	HMEC	breast:	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	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
2	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
3	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
4	chr1:103259174..103259873-chr1:103435676..103436665,2	MCF-7	breast:
5	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
6	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:
7	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:

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

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

Extended variants
information (count: 4216 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:4216 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2622865	chr1:103407999-103408000	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370828209	chr1:103408032-103408033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550052102	chr1:103408048-103408049	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567922907	chr1:103408050-103408051	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535444783	chr1:103408086-103408087	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547058793	chr1:103408097-103408098	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201229734	chr1:103408116-103408117	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78930547	chr1:103408119-103408120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565463511	chr1:103408121-103408122	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371658953	chr1:103408143-103408144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75851277	chr1:103408159-103408160	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192281665	chr1:103408163-103408164	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376015690	chr1:103408178-103408179	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576585074	chr1:103408180-103408181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12045404	chr1:103408269-103408270	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs74110511	chr1:103408281-103408282	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs573924325	chr1:103408291-103408292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541465452	chr1:103408293-103408294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559870595	chr1:103408410-103408411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61812682	chr1:103408445-103408446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199996479	chr1:103408490-103408491	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183653480	chr1:103408545-103408546	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546015824	chr1:103408596-103408597	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140317924	chr1:103408644-103408645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376316230	chr1:103408647-103408648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564078929	chr1:103408681-103408682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17127273	chr1:103408688-103408689	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs577669575	chr1:103408731-103408732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549772658	chr1:103408745-103408746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376471518	chr1:103408789-103408790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17127276	chr1:103408866-103408867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557368257	chr1:103408907-103408908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528833917	chr1:103408912-103408913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181460038	chr1:103409008-103409009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200504706	chr1:103409009-103409010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs67904807	chr1:103409028-103409029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376246634	chr1:103409030-103409031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140902443	chr1:103409038-103409039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs67346875	chr1:103409039-103409040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61159892	chr1:103409041-103409042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115549181	chr1:103409079-103409080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12088773	chr1:103409090-103409091	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs12046389	chr1:103409100-103409101	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs570118982	chr1:103409156-103409157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537675860	chr1:103409158-103409159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555763813	chr1:103409208-103409209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189589239	chr1:103409209-103409210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535008835	chr1:103409239-103409240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1463044	chr1:103409295-103409296	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs2616010	chr1:103409317-103409318	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:197 , 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	chr1:103397800-103414200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:103400200-103424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:103400800-103444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:103403600-103412000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr1:103405400-103409600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:103405800-103444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:103407400-103426000	Weak transcription	NH-A	brain
12	chr1:103407400-103426600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:103407600-103408400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr1:103407800-103408200	Enhancers	A549	lung
15	chr1:103407800-103412600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:103408400-103408600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:103409600-103412600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:103412000-103412800	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr1:103412600-103417000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:103412600-103421400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:103412800-103424800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:103414200-103415800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:103417000-103429200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:103421400-103429800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:103422800-103426400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:103423000-103468200	Weak transcription	HSMMtube	muscle
28	chr1:103423800-103476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:103424400-103424600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:103424400-103424600	Enhancers	Fetal Heart	heart
31	chr1:103424400-103435200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:103424600-103432200	Weak transcription	Fetal Heart	heart
33	chr1:103424800-103425000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr1:103424800-103429200	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:103426000-103427400	Strong transcription	NH-A	brain
37	chr1:103426400-103427000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:103426600-103428000	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr1:103427000-103427600	Enhancers	Brain Germinal Matrix	brain
40	chr1:103427000-103451400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:103427400-103452400	Weak transcription	NH-A	brain
42	chr1:103428000-103435000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:103429200-103430200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:103429200-103433200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:103429800-103432200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:103430200-103440600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr1:103432200-103432600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:103432200-103432600	Enhancers	Fetal Heart	heart
49	chr1:103432600-103434600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr1:103432600-103434600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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