Variant report

Variant	nsv534997
Chromosome Location	chr1:72642420-72823477
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	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
5	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
6	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
7	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
10	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
11	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:72707111-72707491	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:72707157-72707388	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
17	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
20	CEBPB	chr1:72823103-72823425	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
22	CEBPB	chr1:72707099-72707502	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:72818201-72818500	HepG2	liver:	n/a	chr1:72818339-72818350
24	CEBPB	chr1:72731625-72731886	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:72812157-72812489	Hela-S3	cervix:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
26	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
27	CEBPB	chr1:72823109-72823461	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:72707117-72707455	A549	lung:	n/a	n/a
30	CEBPB	chr1:72663464-72663828	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
31	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:72656927-72657197	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
34	CEBPB	chr1:72814314-72814570	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:72700804-72701056	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:72707115-72707480	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:72707115-72707489	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:72818172-72818482	IMR90	lung:	n/a	chr1:72818339-72818350
39	CEBPB	chr1:72812174-72812494	HepG2	liver:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
40	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
41	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
42	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr1:72731623-72731775	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:72811065-72811328	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
50	CEBPB	chr1:72812222-72812489	A549	lung:	n/a	chr1:72812301-72812312 chr1:72812343-72812354

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72747802-72747852	SK-N-SH_RA	brain:	n/a
2	chr1:72750502-72750552	BE2_C	brain:	n/a
3	chr1:72753076-72753126	Hela-S3	cervix:	n/a
4	chr1:72747802-72747852	SK-N-SH_RA	brain:	n/a
5	chr1:72750502-72750552	BE2_C	brain:	n/a
6	chr1:72753076-72753126	Hela-S3	cervix:	n/a
7	chr1:72750502-72750552	LNCaP	prostate:	n/a
8	chr1:72753076-72753126	Hepatocyte	liver:	n/a
9	chr1:72750241-72750291	PrEC	prostate:	n/a
10	chr1:72747802-72747852	AG10803	skin:	n/a
11	chr1:72753076-72753126	A549	lung:	n/a
12	chr1:72749735-72749785	U87	brain:	n/a
13	chr1:72753076-72753126	K562	blood:	n/a
14	chr1:72750671-72750721	AG09309	skin:	n/a
15	chr1:72749735-72749785	PrEC	prostate:	n/a
16	chr1:72750241-72750291	RPTEC	kidney:	n/a
17	chr1:72750671-72750721	HRE	kidney:	n/a
18	chr1:72749581-72749631	PANC-1	pancreas:	n/a
19	chr1:72750502-72750552	NHBE	bronchial:	n/a
20	chr1:72747802-72747852	U87	brain:	n/a
21	chr1:72748389-72748439	HL-60	blood:	n/a
22	chr1:72748124-72748174	HIPEpiC	eye:	n/a
23	chr1:72749735-72749785	AG04449	skin:	fetal
24	chr1:72750671-72750721	SAEC	small airway:	n/a
25	chr1:72749064-72749114	ECC-1	luminal epithelium:	n/a
26	chr1:72753076-72753126	GM12878	blood:	n/a
27	chr1:72749064-72749114	HRPEpiC	eye:	n/a
28	chr1:72748607-72748657	HL-60	blood:	n/a
29	chr1:72749880-72749930	BJ	skin:	n/a
30	chr1:72749880-72749930	AG04450	lung:	fetal
31	chr1:72748601-72748651	SKMC	muscle:	n/a
32	chr1:72749015-72749065	NT2-D1	testis:	n/a
33	chr1:72748607-72748657	HCPEpiC	choroid plexus:	n/a
34	chr1:72750241-72750291	IMR90	lung:	fetal
35	chr1:72753076-72753126	HNPCEpiC	eye:	n/a
36	chr1:72749880-72749930	Hela-S3	cervix:	n/a
37	chr1:72750124-72750174	HCF	heart:	n/a
38	chr1:72749275-72749325	HCT-116	colon:	n/a
39	chr1:72748607-72748657	HAEpiC	amniotic membrane:	n/a
40	chr1:72749015-72749065	SKMC	muscle:	n/a
41	chr1:72749275-72749325	HRE	kidney:	n/a
42	chr1:72747802-72747852	MCF-7	breast:	n/a
43	chr1:72749735-72749785	SKMC	muscle:	n/a
44	chr1:72749015-72749065	BE2_C	brain:	n/a
45	chr1:72748607-72748657	HMEC	breast:	n/a
46	chr1:72749015-72749065	RPTEC	kidney:	n/a
47	chr1:72750502-72750552	NHDF-neo	bronchial:	n/a
48	chr1:72748601-72748651	H1-hESC	embryonic stem cell:	embryo
49	chr1:72749581-72749631	H1-hESC	embryonic stem cell:	embryo
50	chr1:72749275-72749325	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72752065..72752600-chr8:87527466..87528155,2	MCF-7	breast:
2	chr1:72708937..72709709-chr2:107409969..107410778,2	MCF-7	breast:
3	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:
4	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:

Variant related genes	Relation type
RPL31P12	TF binding region
NEGR1	TF binding region
GDI2P2	TF binding region
RPL31P12	CpG island
NEGR1	CpG island
GDI2P2	CpG island
ENSG00000139684	chromatin interactions

Extended variants
information (count: 3983 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3983 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74667481	chr1:72642850-72642851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532910091	chr1:72642864-72642865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11209932	chr1:72642877-72642878	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs540670884	chr1:72642903-72642904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560278695	chr1:72642906-72642907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570176983	chr1:72642921-72642922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192389736	chr1:72642938-72642939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181524536	chr1:72642943-72642944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369887717	chr1:72642950-72642951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12098164	chr1:72643035-72643036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562355567	chr1:72643046-72643047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531434679	chr1:72643114-72643115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551137540	chr1:72643116-72643117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149776712	chr1:72643134-72643135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145853153	chr1:72643168-72643169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574277738	chr1:72643202-72643203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549132353	chr1:72643224-72643225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149008352	chr1:72643247-72643248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567103870	chr1:72643266-72643267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12067627	chr1:72643294-72643295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142903428	chr1:72643303-72643304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556261094	chr1:72643339-72643340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112395520	chr1:72643401-72643402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376842053	chr1:72643454-72643455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs80138605	chr1:72643465-72643466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs397860902	chr1:72643466-72643467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189582395	chr1:72643468-72643469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200139133	chr1:72643470-72643471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114464410	chr1:72643473-72643474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs61765616	chr1:72643496-72643497	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs117164529	chr1:72643565-72643566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77418231	chr1:72643628-72643629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578226921	chr1:72643658-72643659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540531333	chr1:72643670-72643671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554143514	chr1:72643799-72643800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573926458	chr1:72643816-72643817	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555888178	chr1:72643825-72643826	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150455305	chr1:72643826-72643827	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566551023	chr1:72643866-72643867	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542594409	chr1:72643898-72643899	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116296724	chr1:72643903-72643904	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531688581	chr1:72643960-72643961	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544841685	chr1:72644008-72644009	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564888174	chr1:72644024-72644025	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146348778	chr1:72644057-72644058	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377072244	chr1:72644060-72644061	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186126079	chr1:72644093-72644094	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12036585	chr1:72644116-72644117	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567270177	chr1:72644122-72644123	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10889943	chr1:72644212-72644213	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72642800-72643800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:72643400-72644200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:72643400-72644200	Enhancers	NHDF-Ad	bronchial
4	chr1:72643400-72644400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr1:72643400-72644400	Enhancers	Osteobl	bone
6	chr1:72643400-72644800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr1:72643600-72643800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:72643600-72644200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:72643600-72644200	Enhancers	HSMM	muscle
10	chr1:72643600-72644200	Enhancers	HSMMtube	muscle
11	chr1:72643600-72644400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:72643600-72644600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:72643600-72644600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:72643600-72645200	Enhancers	Rectal Smooth Muscle	rectum
15	chr1:72643800-72644200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:72643800-72644400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:72643800-72644400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:72643800-72644400	Enhancers	Colon Smooth Muscle	Colon
19	chr1:72644000-72644400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:72644200-72644600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:72644400-72644600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:72644400-72648800	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:72644400-72649000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:72644400-72649000	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr1:72644400-72649200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:72644400-72649200	Weak transcription	Osteobl	bone
27	chr1:72644400-72668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:72644600-72648000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:72644600-72649200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:72644600-72649600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:72644600-72649800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:72644600-72649800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:72644800-72648800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr1:72645200-72649200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr1:72646400-72647000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:72647000-72647200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:72647200-72648800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:72647800-72648000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:72648000-72648200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:72648000-72648200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:72648200-72648600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:72648200-72649000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:72648600-72652000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:72648800-72649000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:72648800-72649600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:72648800-72651200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr1:72648800-72651200	Enhancers	Colon Smooth Muscle	Colon
48	chr1:72649000-72649800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr1:72649000-72649800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr1:72649000-72651000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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