Variant report

Variant	nsv871198
Chromosome Location	chr1:103432687-103498029
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	BRCA1	chr1:103436155-103436294	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr1:103457286-103457644	H1-hESC	embryonic stem cell:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
3	CEBPB	chr1:103489916-103490117	HepG2	liver:	n/a	chr1:103489991-103490002 chr1:103489991-103490000
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	chr1:103468048-103468248	HepG2	liver:	n/a	chr1:103468160-103468173 chr1:103468074-103468085 chr1:103468076-103468085
6	CEBPB	chr1:103457305-103457616	HepG2	liver:	n/a	chr1:103457464-103457475 chr1:103457465-103457476
7	CEBPB	chr1:103462260-103462460	HepG2	liver:	n/a	chr1:103462355-103462366 chr1:103462357-103462368
8	CTCF	chr1:103436240-103436390	HEK293	kidney:	n/a	chr1:103436240-103436253 chr1:103436243-103436251
9	CTCF	chr1:103436160-103436310	NB4	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
10	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
11	CTCF	chr1:103436153-103436432	GM20000	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
12	CTCF	chr1:103436220-103436370	AoAF	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
13	CTCF	chr1:103436400-103436550	GM12878	blood:	n/a	n/a
14	CTCF	chr1:103436037-103436432	IMR90	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
15	CTCF	chr1:103436540-103436690	BJ	skin:	n/a	n/a
16	CTCF	chr1:103436428-103436540	Fibrobl	skin:	n/a	n/a
17	CTCF	chr1:103436220-103436370	HBMEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
18	CTCF	chr1:103436080-103436230	HVMF	connective:	n/a	n/a
19	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
20	CTCF	chr1:103436180-103436330	GM12870	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
21	CTCF	chr1:103435977-103436375	HCT-116	colon:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
22	CTCF	chr1:103436160-103436310	AG04450	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
23	CTCF	chr1:103436160-103436310	HCM	heart:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
24	CTCF	chr1:103436140-103436290	BJ	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
25	CTCF	chr1:103436480-103436630	AG09309	skin:	n/a	n/a
26	CTCF	chr1:103436080-103436427	K562	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
27	CTCF	chr1:103436444-103436548	GM10248	blood:	n/a	n/a
28	CTCF	chr1:103436260-103436410	HAc	cerebellar:	n/a	n/a
29	CTCF	chr1:103436140-103436290	NHLF	lung:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
30	CTCF	chr1:103436140-103436290	GM12878	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
31	CTCF	chr1:103436160-103436310	HMEC	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
32	CTCF	chr1:103467700-103467850	BJ	skin:	n/a	chr1:103467740-103467748
33	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
34	CTCF	chr1:103436180-103436330	GM12871	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
35	CTCF	chr1:103436112-103436368	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
36	CTCF	chr1:103436236-103436402	GM12891	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255
37	CTCF	chr1:103436200-103436350	HepG2	liver:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
38	CTCF	chr1:103436120-103436270	Caco-2	colon:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
39	CTCF	chr1:103436180-103436330	RPTEC	kidney:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
40	CTCF	chr1:103436140-103436290	Hela-S3	cervix:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
41	CTCF	chr1:103436020-103436444	MCF-7	breast:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
42	CTCF	chr1:103436160-103436310	HUVEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
43	CTCF	chr1:103467620-103467770	BE2_C	brain:	n/a	chr1:103467740-103467748
44	CTCF	chr1:103436140-103436290	HA-sp	spinal cord:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
45	CTCF	chr1:103436152-103436306	SK-N-SH_RA	brain:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
46	CTCF	chr1:103436600-103436750	AG04450	lung:	n/a	n/a
47	CTCF	chr1:103436126-103436488	GM10266	blood:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
48	CTCF	chr1:103436183-103436398	Fibrobl	skin:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
49	CTCF	chr1:103436160-103436310	HBMEC	blood vessel:	n/a	chr1:103436238-103436256 chr1:103436240-103436253 chr1:103436243-103436251 chr1:103436239-103436255 chr1:103436233-103436254
50	CTCF	chr1:103436188-103436416	GM12892	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	chr1:103016225..103017019-chr1:103436153..103436688,2	MCF-7	breast:
2	chr1:103471408..103474127-chr1:103476869..103478860,2	MCF-7	breast:
3	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
4	chr1:103435891..103438484-chr1:103439465..103441994,2	K562	blood:
5	chr1:103259174..103259873-chr1:103435676..103436665,2	MCF-7	breast:
6	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:

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

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

Extended variants
information (count: 2715 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2715 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11164647	chr1:103432687-103432688	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377210177	chr1:103432723-103432724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187658947	chr1:103432765-103432766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369052277	chr1:103432781-103432782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35303945	chr1:103432783-103432784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12738207	chr1:103432784-103432785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552053849	chr1:103432848-103432849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535340297	chr1:103432851-103432852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553681851	chr1:103432860-103432861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571696072	chr1:103432863-103432864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373059200	chr1:103432865-103432866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192626731	chr1:103432898-103432899	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs570683696	chr1:103432901-103432902	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537867092	chr1:103432922-103432923	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576015738	chr1:103432941-103432942	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs6662599	chr1:103432942-103432943	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs550402169	chr1:103432945-103432946	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs188205954	chr1:103432946-103432947	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs192986293	chr1:103432947-103432948	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573622129	chr1:103432963-103432964	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560131858	chr1:103432965-103432966	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs533668594	chr1:103432998-103432999	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs551445493	chr1:103433022-103433023	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs111471563	chr1:103433038-103433039	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs530880543	chr1:103433039-103433040	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12123005	chr1:103433042-103433043	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs567896552	chr1:103433086-103433087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554452898	chr1:103433105-103433106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369579204	chr1:103433137-103433138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547284982	chr1:103433251-103433252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565592812	chr1:103433253-103433254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539360277	chr1:103433275-103433276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557437466	chr1:103433281-103433282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188757383	chr1:103433305-103433306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536726196	chr1:103433319-103433320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555474592	chr1:103433338-103433339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557763754	chr1:103433343-103433344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574276548	chr1:103433368-103433369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145979260	chr1:103433377-103433378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs67395246	chr1:103433405-103433406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559995897	chr1:103433429-103433430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576646860	chr1:103433439-103433440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543890880	chr1:103433453-103433454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs578241151	chr1:103433477-103433478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545705938	chr1:103433498-103433499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563511513	chr1:103433522-103433523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116229918	chr1:103433596-103433597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181916367	chr1:103433695-103433696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184597586	chr1:103433723-103433724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372820683	chr1:103433726-103433727	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:156 , 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	chr1:103400200-103444200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:103400200-103462000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:103400800-103444200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:103405800-103444200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:103415800-103485200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:103423000-103468200	Weak transcription	HSMMtube	muscle
9	chr1:103423800-103476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:103424400-103435200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:103425000-103478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr1:103427000-103451400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:103427400-103452400	Weak transcription	NH-A	brain
14	chr1:103428000-103435000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:103429200-103433200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr1:103430200-103440600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:103432600-103434600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:103432600-103434600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:103432600-103457400	Weak transcription	Fetal Heart	heart
20	chr1:103433200-103433800	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:103433800-103442800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:103434600-103435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr1:103434600-103435400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr1:103434600-103440800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:103434800-103435400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr1:103435000-103435400	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr1:103435200-103442400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:103435400-103452200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr1:103435800-103446200	Weak transcription	HSMM	muscle
30	chr1:103440600-103444200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:103440800-103443000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:103442400-103445000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:103442600-103453200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:103442800-103446800	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:103443000-103445400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:103444200-103444600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:103444200-103445000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:103444200-103445000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr1:103444200-103446800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:103444600-103444800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:103444800-103453200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:103445000-103448600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:103445000-103448800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:103445000-103458600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:103445400-103451800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:103446200-103446800	Strong transcription	HSMM	muscle
47	chr1:103446800-103448200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:103446800-103452000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:103446800-103497800	Weak transcription	HSMM	muscle
50	chr1:103448200-103449800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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