Variant report

Variant	nsv871372
Chromosome Location	chr1:103403752-103564540
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	ARID3A	chr1:103424463-103424755	HepG2	liver:	n/a	n/a
3	BRCA1	chr1:103436155-103436294	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
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	chr1:103420192-103420500	IMR90	lung:	n/a	chr1:103420350-103420361
7	CEBPB	chr1:103420187-103420500	HepG2	liver:	n/a	chr1:103420350-103420361
8	CEBPB	chr1:103549640-103549851	HepG2	liver:	n/a	chr1:103549780-103549791
9	CEBPB	chr1:103519688-103519996	A549	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
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	chr1:103519664-103520007	IMR90	lung:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
13	CEBPB	chr1:103549647-103549882	IMR90	lung:	n/a	chr1:103549780-103549791
14	CEBPB	chr1:103522115-103522329	IMR90	lung:	n/a	chr1:103522213-103522224
15	CEBPB	chr1:103522064-103522370	HepG2	liver:	n/a	chr1:103522213-103522224
16	CEBPB	chr1:103420205-103420542	A549	lung:	n/a	chr1:103420350-103420361
17	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
18	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
19	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
20	CEBPB	chr1:103420192-103420551	H1-hESC	embryonic stem cell:	n/a	chr1:103420350-103420361
21	CEBPB	chr1:103519790-103519887	H1-hESC	embryonic stem cell:	n/a	chr1:103519829-103519842 chr1:103519831-103519840 chr1:103519831-103519840 chr1:103519831-103519840
22	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
23	CEBPB	chr1:103424437-103424754	HepG2	liver:	n/a	n/a
24	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
25	CTCF	chr1:103436155-103436356	GM13976	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
26	CTCF	chr1:103436112-103436394	GM10248	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
27	CTCF	chr1:103436140-103436290	HMEC	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
28	CTCF	chr1:103436153-103436432	GM20000	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
29	CTCF	chr1:103436140-103436290	GM06990	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
30	CTCF	chr1:103436140-103436290	SAEC	small airway:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
31	CTCF	chr1:103436417-103436485	GM12892	blood:	n/a	n/a
32	CTCF	chr1:103436180-103436330	NHEK	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
33	CTCF	chr1:103436140-103436290	GM12864	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
34	CTCF	chr1:103436277-103436287	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:103436415-103436416	GM19238	blood:	n/a	n/a
36	CTCF	chr1:103436140-103436290	HPAF	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
37	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
38	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
39	CTCF	chr1:103436236-103436402	GM12891	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255
40	CTCF	chr1:103436142-103436410	Gliobla	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
41	CTCF	chr1:103436146-103436396	H1-hESC	embryonic stem cell:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
42	CTCF	chr1:103436140-103436290	NHLF	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
43	CTCF	chr1:103436140-103436290	HL-60	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
44	CTCF	chr1:103436479-103436542	GM13976	blood:	n/a	n/a
45	CTCF	chr1:103436140-103436290	GM12872	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
46	CTCF	chr1:103436127-103436380	GM13977	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
47	CTCF	chr1:103436123-103436326	T-47D	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
48	CTCF	chr1:103436140-103436290	AG10803	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
49	CTCF	chr1:103435960-103436571	A549	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
50	CTCF	chr1:103436190-103436341	MCF-7	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	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
2	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:
3	chr1:103546900..103548973-chr1:103549511..103551130,2	K562	blood:
4	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:
5	chr1:103303886..103305574-chr1:103404633..103406434,2	MCF-7	breast:
6	chr1:103259174..103259873-chr1:103435676..103436665,2	MCF-7	breast:
7	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
8	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
9	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:

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	chr1:103466993-103467187	NONHSAT004880
5	lnc-AMY1B-5	chr1:103468303-103468347	NONHSAT004880

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

Extended variants
information (count: 6787 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:6787 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1975919	chr1:103403752-103403753	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74110508	chr1:103403760-103403761	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563208647	chr1:103403791-103403792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555238439	chr1:103403792-103403793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188941957	chr1:103403811-103403812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72983794	chr1:103403832-103403833	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs2622882	chr1:103403914-103403915	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs5776665	chr1:103403938-103403939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71575647	chr1:103403943-103403944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1975918	chr1:103403944-103403945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201332852	chr1:103403945-103403946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200440778	chr1:103403946-103403947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112872699	chr1:103403947-103403948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146207328	chr1:103403948-103403949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112329031	chr1:103403949-103403950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78543913	chr1:103403957-103403958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143379816	chr1:103404018-103404019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2252081	chr1:103404047-103404048	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs72683274	chr1:103404053-103404054	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190916431	chr1:103404082-103404083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1975917	chr1:103404107-103404108	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs552795899	chr1:103404150-103404151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182806052	chr1:103404194-103404195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1564142	chr1:103404197-103404198	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76508520	chr1:103404201-103404202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187187243	chr1:103404210-103404211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2376262	chr1:103404219-103404220	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs113459092	chr1:103404224-103404225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114323960	chr1:103404230-103404231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1564141	chr1:103404236-103404237	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs113001469	chr1:103404252-103404253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368424654	chr1:103404260-103404261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs57009972	chr1:103404316-103404317	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1564140	chr1:103404323-103404324	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs191699710	chr1:103404359-103404360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571820832	chr1:103404374-103404375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2126643	chr1:103404384-103404385	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs368417810	chr1:103404388-103404389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569564128	chr1:103404394-103404395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536237729	chr1:103404436-103404437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555972509	chr1:103404498-103404499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554991103	chr1:103404520-103404521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377124424	chr1:103404547-103404548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199519627	chr1:103404569-103404570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369184573	chr1:103404571-103404572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372541879	chr1:103404579-103404580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1131487	chr1:103404604-103404605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141514115	chr1:103404636-103404637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533984546	chr1:103404642-103404643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377436438	chr1:103404683-103404684	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:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103386000-103407000	Weak transcription	NH-A	brain
3	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:103397800-103414200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:103398600-103407200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr1:103399000-103404000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:103399400-103406800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:103399600-103406800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:103400200-103424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:103400800-103405000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:103400800-103444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:103403200-103406800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:103403200-103406800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:103403200-103407000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:103403400-103404600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:103403600-103412000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr1:103404000-103404600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:103404600-103405200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:103404600-103405400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:103405000-103405800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:103405200-103407800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:103405400-103409600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:103405800-103444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr1:103406200-103407200	Enhancers	HMEC	breast
27	chr1:103406800-103407200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:103406800-103407200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:103406800-103407200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr1:103406800-103407200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:103406800-103407200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:103406800-103407400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr1:103406800-103407400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:103406800-103407400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:103406800-103407400	Enhancers	A549	lung
36	chr1:103407000-103407200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr1:103407000-103407400	Enhancers	NH-A	brain
38	chr1:103407000-103407600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr1:103407200-103407400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr1:103407400-103407800	Weak transcription	A549	lung
41	chr1:103407400-103426000	Weak transcription	NH-A	brain
42	chr1:103407400-103426600	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:103407600-103408400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:103407800-103408200	Enhancers	A549	lung
45	chr1:103407800-103412600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:103408400-103408600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr1:103409600-103412600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:103412000-103412800	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:103412600-103417000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:103412600-103421400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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