Variant report

Variant	nsv1014214
Chromosome Location	chr1:72740734-72808756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:671)
CpG islands
(count:1099)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
2	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
3	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
6	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
10	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
11	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
14	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
15	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
16	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:72746375-72746718	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
21	CHD1	chr1:72748366-72748381	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr1:72748624-72750228	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:72748543-72748846	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:72749095-72750447	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr1:72748405-72750930	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr1:72750306-72750765	GM12878	blood:	n/a	n/a
27	CREB1	chr1:72748399-72748786	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr1:72748477-72748773	A549	lung:	n/a	n/a
29	CTBP2	chr1:72747565-72750445	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:72748380-72748530	HCM	heart:	n/a	n/a
31	CTCF	chr1:72750128-72750223	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr1:72748300-72748450	NHLF	lung:	n/a	n/a
33	CTCF	chr1:72746500-72746650	HMF	breast:	n/a	n/a
34	CTCF	chr1:72750087-72750252	Medullo	brain:	n/a	n/a
35	CTCF	chr1:72748380-72748530	HVMF	connective:	n/a	n/a
36	CTCF	chr1:72750000-72750150	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr1:72750100-72750250	Caco-2	colon:	n/a	n/a
38	CTCF	chr1:72748340-72748490	GM06990	blood:	n/a	n/a
39	CTCF	chr1:72748440-72748590	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr1:72748119-72748224	ProgFib	skin:	n/a	n/a
41	CTCF	chr1:72788380-72788530	RPTEC	kidney:	n/a	n/a
42	CTCF	chr1:72750180-72750330	WI-38	lung:	n/a	n/a
43	CTCF	chr1:72748100-72748250	AG04450	lung:	n/a	chr1:72748229-72748238 chr1:72748226-72748236
44	CTCF	chr1:72748420-72748570	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:72788380-72788530	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr1:72748100-72748250	AG04449	skin:	n/a	chr1:72748229-72748238 chr1:72748226-72748236
47	CTCF	chr1:72750060-72750210	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr1:72750020-72750170	HCM	heart:	n/a	n/a
49	CTCF	chr1:72750040-72750190	AG04450	lung:	n/a	n/a
50	CTCF	chr1:72748480-72748630	AG09319	gingival:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72748389-72748439	AG09319	gingival:	n/a
2	chr1:72748389-72748439	AG09319	gingival:	n/a
3	chr1:72749735-72749785	Caco-2	colon:	n/a
4	chr1:72749581-72749631	Hela-S3	cervix:	n/a
5	chr1:72749275-72749325	GM12878	blood:	n/a
6	chr1:72748139-72748189	HCPEpiC	choroid plexus:	n/a
7	chr1:72750124-72750174	PrEC	prostate:	n/a
8	chr1:72748389-72748439	GM12878	blood:	n/a
9	chr1:72747802-72747852	HIPEpiC	eye:	n/a
10	chr1:72747802-72747852	ProgFib	skin:	n/a
11	chr1:72749275-72749325	HepG2	liver:	n/a
12	chr1:72750241-72750291	NH-A	brain:	n/a
13	chr1:72748610-72748660	NHDF-neo	bronchial:	n/a
14	chr1:72750241-72750291	Hela-S3	cervix:	n/a
15	chr1:72749880-72749930	CMK	blood:	n/a
16	chr1:72750671-72750721	PFSK-1	brain:	n/a
17	chr1:72750241-72750291	PFSK-1	brain:	n/a
18	chr1:72750241-72750291	AG04450	lung:	fetal
19	chr1:72750124-72750174	CMK	blood:	n/a
20	chr1:72750671-72750721	SAEC	small airway:	n/a
21	chr1:72748607-72748657	ECC-1	luminal epithelium:	n/a
22	chr1:72747802-72747852	HEEpiC	esophagus:	n/a
23	chr1:72750124-72750174	ProgFib	skin:	n/a
24	chr1:72748607-72748657	A549	lung:	n/a
25	chr1:72748139-72748189	HepG2	liver:	n/a
26	chr1:72749581-72749631	BE2_C	brain:	n/a
27	chr1:72748601-72748651	SK-N-SH_RA	brain:	n/a
28	chr1:72749275-72749325	LNCaP	prostate:	n/a
29	chr1:72749064-72749114	H1-hESC	embryonic stem cell:	embryo
30	chr1:72749581-72749631	Jurkat	blood:	n/a
31	chr1:72748607-72748657	ovcar-3	ovarian:	n/a
32	chr1:72749275-72749325	NHDF-neo	bronchial:	n/a
33	chr1:72750241-72750291	NHDF-neo	bronchial:	n/a
34	chr1:72748124-72748174	A549	lung:	n/a
35	chr1:72749064-72749114	HMEC	breast:	n/a
36	chr1:72750124-72750174	AG09309	skin:	n/a
37	chr1:72749275-72749325	HMEC	breast:	n/a
38	chr1:72749275-72749325	Hela-S3	cervix:	n/a
39	chr1:72748607-72748657	AoSMC	blood vessel:	n/a
40	chr1:72749064-72749114	PrEC	prostate:	n/a
41	chr1:72749015-72749065	SK-N-MC	brain:	n/a
42	chr1:72750502-72750552	BE2_C	brain:	n/a
43	chr1:72750124-72750174	HEK293	kidney:	embryo
44	chr1:72750241-72750291	MCF10A-Er-Src	breast:	n/a
45	chr1:72749064-72749114	HEK293	kidney:	embryo
46	chr1:72748607-72748657	NHBE	bronchial:	n/a
47	chr1:72748389-72748439	HCM	heart:	n/a
48	chr1:72749064-72749114	HEEpiC	esophagus:	n/a
49	chr1:72750124-72750174	AG10803	skin:	n/a
50	chr1:72748601-72748651	RPTEC	kidney:	n/a

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

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

No data

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

Extended variants
information (count: 691 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9326098	chr1:72740734-72740735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371118036	chr1:72740743-72740744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562378746	chr1:72740744-72740745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181616118	chr1:72740749-72740750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550909597	chr1:72740770-72740771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570959015	chr1:72740814-72740815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533464499	chr1:72740818-72740819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138804883	chr1:72740821-72740822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566658586	chr1:72740822-72740823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141972890	chr1:72740826-72740827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555396716	chr1:72740847-72740848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569099162	chr1:72740889-72740890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146386120	chr1:72740927-72740928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114114906	chr1:72740959-72740960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577358196	chr1:72741011-72741012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533626829	chr1:72741115-72741116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553178372	chr1:72741125-72741126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573379569	chr1:72741212-72741213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542371868	chr1:72741227-72741228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116396183	chr1:72741242-72741243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575845453	chr1:72741254-72741255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544662972	chr1:72741255-72741256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567265420	chr1:72741311-72741312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564465496	chr1:72741332-72741333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186752840	chr1:72741340-72741341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547097265	chr1:72741351-72741352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560545136	chr1:72741376-72741377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371199038	chr1:72741381-72741382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11584542	chr1:72741382-72741383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs138482888	chr1:72741409-72741410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368047049	chr1:72741419-72741420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192056552	chr1:72741452-72741453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557669222	chr1:72741465-72741466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538140838	chr1:72741466-72741467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550994523	chr1:72741481-72741482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570887996	chr1:72741491-72741492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533516584	chr1:72741500-72741501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375212416	chr1:72741534-72741535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553466478	chr1:72741558-72741559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182939494	chr1:72741613-72741614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535672906	chr1:72741666-72741667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575857827	chr1:72741683-72741684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185820218	chr1:72741711-72741712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72942940	chr1:72741737-72741738	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544907051	chr1:72741744-72741745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189727901	chr1:72741746-72741747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552865908	chr1:72741765-72741766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182340163	chr1:72741775-72741776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531300318	chr1:72741782-72741783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187717449	chr1:72741807-72741808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72737600-72744200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72738000-72744200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr1:72738000-72745800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:72739000-72744400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:72739200-72741600	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:72741600-72741800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:72741600-72741800	Enhancers	Brain Angular Gyrus	brain
8	chr1:72741600-72741800	Enhancers	Colon Smooth Muscle	Colon
9	chr1:72741800-72742000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:72741800-72742200	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:72741800-72742800	Weak transcription	Brain Angular Gyrus	brain
12	chr1:72742200-72744000	Enhancers	Colon Smooth Muscle	Colon
13	chr1:72742400-72742600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:72742600-72742800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr1:72742600-72742800	Enhancers	Brain Substantia Nigra	brain
16	chr1:72742600-72743000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr1:72742800-72743000	Enhancers	Brain Angular Gyrus	brain
18	chr1:72742800-72743000	Enhancers	Brain Cingulate Gyrus	brain
19	chr1:72742800-72743200	Enhancers	Dnd41	blood
20	chr1:72742800-72744000	Weak transcription	Brain Substantia Nigra	brain
21	chr1:72742800-72745800	Weak transcription	Brain Anterior Caudate	brain
22	chr1:72743000-72745000	Weak transcription	Brain Angular Gyrus	brain
23	chr1:72743000-72745000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:72743000-72745800	Weak transcription	Brain Cingulate Gyrus	brain
25	chr1:72743200-72743600	Weak transcription	Dnd41	blood
26	chr1:72743600-72745800	Enhancers	Dnd41	blood
27	chr1:72743800-72744200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:72743800-72751600	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr1:72744000-72744200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:72744000-72745000	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:72744000-72745200	Enhancers	Brain Substantia Nigra	brain
32	chr1:72744200-72744400	Enhancers	NHDF-Ad	bronchial
33	chr1:72744200-72744600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr1:72744200-72744800	Active TSS	Stomach Smooth Muscle	stomach
35	chr1:72744200-72744800	Enhancers	HUVEC	blood vessel
36	chr1:72744200-72745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:72744200-72745800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:72744200-72746000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:72744400-72744600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:72744400-72745000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:72744400-72745800	Weak transcription	NHDF-Ad	bronchial
42	chr1:72744400-72746400	Enhancers	Rectal Smooth Muscle	rectum
43	chr1:72744600-72744800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:72744600-72745200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:72744600-72745600	Enhancers	Osteobl	bone
46	chr1:72744600-72745800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr1:72744800-72745000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:72744800-72745000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:72744800-72745000	Flanking Active TSS	Stomach Smooth Muscle	stomach
50	chr1:72744800-72745000	Enhancers	NHLF	lung

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