Variant report

Variant	nsv1010267
Chromosome Location	chr1:73551169-73628431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:136)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:136 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:73610119-73610138	K562	blood:	n/a	n/a
2	BACH1	chr1:73582602-73582793	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:73593618-73593768	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:73583653-73583671	K562	blood:	n/a	chr1:73583658-73583669
5	CEBPB	chr1:73618648-73618936	A549	lung:	n/a	chr1:73618778-73618789
6	CEBPB	chr1:73598948-73599269	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:73553655-73553743	HepG2	liver:	n/a	chr1:73553724-73553735
8	CEBPB	chr1:73621990-73622190	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:73583491-73583849	HepG2	liver:	n/a	chr1:73583658-73583669
10	CEBPB	chr1:73567817-73568138	HepG2	liver:	n/a	chr1:73567956-73567967
11	CEBPB	chr1:73598943-73599225	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:73621888-73622181	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:73621882-73622201	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:73567904-73567996	H1-hESC	embryonic stem cell:	n/a	chr1:73567956-73567967
15	CEBPB	chr1:73621875-73622188	K562	blood:	n/a	n/a
16	CEBPB	chr1:73621845-73622196	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:73618626-73618958	IMR90	lung:	n/a	chr1:73618778-73618789
18	CEBPB	chr1:73618647-73618856	HepG2	liver:	n/a	chr1:73618778-73618789
19	CEBPB	chr1:73583600-73583804	H1-hESC	embryonic stem cell:	n/a	chr1:73583658-73583669
20	CEBPB	chr1:73618610-73618934	H1-hESC	embryonic stem cell:	n/a	chr1:73618778-73618789
21	CEBPB	chr1:73590167-73590384	HepG2	liver:	n/a	chr1:73590205-73590216 chr1:73590261-73590272
22	CTCF	chr1:73566042-73566215	LNCaP	prostate:	n/a	n/a
23	CTCF	chr1:73566100-73566250	HMEC	breast:	n/a	n/a
24	CTCF	chr1:73571655-73571668	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:73565940-73566090	RPTEC	kidney:	n/a	n/a
26	CTCF	chr1:73556299-73556310	LNCaP	prostate:	n/a	n/a
27	CTCF	chr1:73571600-73571750	HepG2	liver:	n/a	n/a
28	CTCF	chr1:73573409-73573450	GM20000	blood:	n/a	n/a
29	CTCF	chr1:73566092-73566156	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:73565272-73565325	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:73566037-73566202	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr1:73565941-73566244	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:73566060-73566210	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr1:73566040-73566190	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:73565980-73566130	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr1:73566045-73566210	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr1:73571640-73571650	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:73556315-73556324	LNCaP	prostate:	n/a	n/a
39	CTCF	chr1:73565916-73566304	T-47D	breast:	n/a	n/a
40	CTCF	chr1:73566016-73566213	LNCaP	prostate:	n/a	n/a
41	CTCF	chr1:73565980-73566130	HMEC	breast:	n/a	n/a
42	CTCF	chr1:73618997-73619078	Lung_OC	lung:	n/a	n/a
43	CTCF	chr1:73566107-73566180	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr1:73566040-73566190	NHEK	skin:	n/a	n/a
45	CTCF	chr1:73566040-73566190	HL-60	blood:	n/a	n/a
46	CTCF	chr1:73566000-73566150	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr1:73566060-73566210	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr1:73566055-73566226	Medullo	brain:	n/a	n/a
49	CTCF	chr1:73566060-73566210	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:73565973-73566213	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:73583093-73583143	HCM	heart:	n/a
2	chr1:73583093-73583143	HRPEpiC	eye:	n/a
3	chr1:73583093-73583143	HAEpiC	amniotic membrane:	n/a
4	chr1:73583093-73583143	AoSMC	blood vessel:	n/a
5	chr1:73583093-73583143	Hela-S3	cervix:	n/a
6	chr1:73583093-73583143	NB4	blood:	n/a
7	chr1:73583093-73583143	SKMC	muscle:	n/a
8	chr1:73583093-73583143	HRCEpiC	kidney:	n/a
9	chr1:73583093-73583143	GM12892	blood:	n/a
10	chr1:73583093-73583143	NT2-D1	testis:	n/a
11	chr1:73583093-73583143	HRE	kidney:	n/a
12	chr1:73583093-73583143	HEK293	kidney:	embryo
13	chr1:73583093-73583143	HL-60	blood:	n/a
14	chr1:73583093-73583143	MCF10A-Er-Src	breast:	n/a
15	chr1:73583093-73583143	T-47D	breast:	n/a
16	chr1:73583093-73583143	SK-N-SH	brain:	n/a
17	chr1:73583093-73583143	HCT-116	colon:	n/a
18	chr1:73583093-73583143	Hepatocyte	liver:	n/a
19	chr1:73583093-73583143	Jurkat	blood:	n/a
20	chr1:73583093-73583143	U87	brain:	n/a
21	chr1:73583093-73583143	SK-N-MC	brain:	n/a
22	chr1:73583093-73583143	RPTEC	kidney:	n/a
23	chr1:73583093-73583143	HMEC	breast:	n/a
24	chr1:73583093-73583143	MCF-7	breast:	n/a
25	chr1:73583093-73583143	BJ	skin:	n/a
26	chr1:73583093-73583143	GM12891	blood:	n/a
27	chr1:73583093-73583143	ProgFib	skin:	n/a
28	chr1:73583093-73583143	NHBE	bronchial:	n/a
29	chr1:73583093-73583143	GM06990	blood:	n/a
30	chr1:73583093-73583143	AG09319	gingival:	n/a
31	chr1:73583093-73583143	AG10803	skin:	n/a
32	chr1:73583093-73583143	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:73583093-73583143	HUVEC	blood vessel:	n/a
34	chr1:73583093-73583143	HNPCEpiC	eye:	n/a
35	chr1:73583093-73583143	HCF	heart:	n/a
36	chr1:73583093-73583143	BE2_C	brain:	n/a
37	chr1:73583093-73583143	PFSK-1	brain:	n/a
38	chr1:73583093-73583143	A549	lung:	n/a
39	chr1:73583093-73583143	IMR90	lung:	fetal
40	chr1:73583093-73583143	K562	blood:	n/a
41	chr1:73583093-73583143	GM12878	blood:	n/a
42	chr1:73583093-73583143	NHDF-neo	bronchial:	n/a
43	chr1:73583093-73583143	CMK	blood:	n/a
44	chr1:73583093-73583143	Caco-2	colon:	n/a
45	chr1:73583093-73583143	LNCaP	prostate:	n/a
46	chr1:73583093-73583143	AG04449	skin:	fetal
47	chr1:73583093-73583143	AG04450	lung:	fetal
48	chr1:73583093-73583143	ECC-1	luminal epithelium:	n/a
49	chr1:73583093-73583143	SK-N-SH_RA	brain:	n/a
50	chr1:73583093-73583143	HCPEpiC	choroid plexus:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:73578582..73580193-chr1:73580747..73583501,2	K562	blood:
2	chr1:73463171..73465472-chr1:73562170..73563672,2	K562	blood:
3	chr1:73578582..73580193-chr1:73580747..73583501,2	K562	blood:
4	chr1:73623181..73625541-chr16:30564814..30567773,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-9	chr1:73557739-73557932	NONHSAT003931
2	lnc-FPGT-9	chr1:73586405-73586583	NONHSAT003928
3	lnc-FPGT-9	chr1:73573717-73577148	NONHSAT003927
4	lnc-FPGT-9	chr1:73573717-73577147	ucscGeneNc_uc001dfx_2
5	lnc-FPGT-9	chr1:73593344-73593522	NONHSAT003929

No data

Variant related genes	Relation type
KRT8P21	TF binding region
KRT8P21	CpG island

Extended variants
information (count: 1035 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184471096	chr1:73557801-73557802	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs188381391	chr1:73557816-73557817	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs558291290	chr1:73557892-73557893	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs57118574	chr1:73557894-73557895	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs117756481	chr1:73557924-73557925	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs560053341	chr1:73562007-73562008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192306591	chr1:73562139-73562140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542344809	chr1:73562152-73562153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184649537	chr1:73562229-73562230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573547521	chr1:73562235-73562236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557923616	chr1:73562267-73562268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190230323	chr1:73562302-73562303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577868510	chr1:73562308-73562309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181938116	chr1:73562317-73562318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543653046	chr1:73562385-73562386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74091260	chr1:73562396-73562397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142437341	chr1:73562413-73562414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35125509	chr1:73562414-73562415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11800180	chr1:73562423-73562424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533419862	chr1:73562439-73562440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74091261	chr1:73562440-73562441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34206511	chr1:73562451-73562452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34160628	chr1:73562453-73562454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547187050	chr1:73562469-73562470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566981385	chr1:73562497-73562498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544699084	chr1:73562544-73562545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143719616	chr1:73562600-73562601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76116912	chr1:73562616-73562617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555936770	chr1:73562643-73562644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569369025	chr1:73562655-73562656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538244388	chr1:73562686-73562687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185992632	chr1:73562696-73562697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577881842	chr1:73562704-73562705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529268622	chr1:73562741-73562742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189144375	chr1:73562763-73562764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12065149	chr1:73562764-73562765	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12122055	chr1:73562776-73562777	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143814137	chr1:73562794-73562795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74091263	chr1:73562795-73562796	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564827628	chr1:73562797-73562798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74091266	chr1:73562843-73562844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551730292	chr1:73562911-73562912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11800248	chr1:73562912-73562913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564691926	chr1:73562957-73562958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372867482	chr1:73562963-73562964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113880873	chr1:73562967-73562968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72024878	chr1:73562968-73562969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs199846710	chr1:73562969-73562970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562363964	chr1:73562979-73562980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397794599	chr1:73562987-73562988	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73562000-73565400	Enhancers	Fetal Heart	heart
2	chr1:73562200-73564000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr1:73562400-73562800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:73562400-73563800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:73562600-73564000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:73563000-73563600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:73563200-73564200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:73563600-73566200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:73563800-73565000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:73564000-73565200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:73565000-73566000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr1:73565200-73565400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:73565200-73565600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:73565200-73565600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:73565600-73570600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:73566200-73566400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:73570600-73571800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:73570800-73572000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
19	chr1:73572000-73580000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:73580000-73580600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:73580200-73580400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:73580600-73581400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr1:73580600-73581800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr1:73581400-73583400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr1:73581800-73582200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr1:73581800-73582200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:73581800-73582400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr1:73581800-73583200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr1:73581800-73583400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:73582000-73583000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:73582200-73585400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr1:73582400-73582800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr1:73582400-73583000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr1:73609200-73610000	Enhancers	Fetal Heart	heart
35	chr1:73609800-73610200	Enhancers	Primary hematopoietic stem cells	blood
36	chr1:73609800-73610400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:73610000-73610200	Flanking Active TSS	Fetal Heart	heart
38	chr1:73610000-73610400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:73610200-73610400	Enhancers	Fetal Heart	heart
40	chr1:73610400-73610600	Flanking Active TSS	Fetal Heart	heart
41	chr1:73610600-73611000	Enhancers	Fetal Heart	heart
42	chr1:73626400-73626600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:73626600-73627000	Enhancers	Ovary	ovary
44	chr1:73626600-73627800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:73626600-73628600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:73626800-73627400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:73627000-73627400	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr1:73627000-73627400	Weak transcription	Ovary	ovary
49	chr1:73627000-73627600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:73627400-73628400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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