Variant report

Variant	nsv428454
Chromosome Location	chr1:72504469-72926256
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	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
5	ATF2	chr1:72899205-72899709	GM12878	blood:	n/a	n/a
6	ATF2	chr1:72899199-72899732	GM12878	blood:	n/a	n/a
7	ATF2	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
8	ATF2	chr1:72900663-72901168	GM12878	blood:	n/a	n/a
9	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
10	ATF2	chr1:72898259-72898811	GM12878	blood:	n/a	n/a
11	ATF2	chr1:72900775-72901104	GM12878	blood:	n/a	n/a
12	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
15	BATF	chr1:72898318-72898741	GM12878	blood:	n/a	chr1:72898577-72898588
16	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
17	BATF	chr1:72900806-72901044	GM12878	blood:	n/a	n/a
18	BATF	chr1:72900800-72901152	GM12878	blood:	n/a	n/a
19	BATF	chr1:72899224-72899621	GM12878	blood:	n/a	n/a
20	BATF	chr1:72898304-72898864	GM12878	blood:	n/a	chr1:72898577-72898588
21	BATF	chr1:72899187-72899650	GM12878	blood:	n/a	n/a
22	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:72898316-72898617	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:72900753-72901050	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:72899285-72899619	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:72899283-72899564	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:72898250-72898709	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:72563429-72563467	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:72899271-72899651	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:72898334-72898771	GM12878	blood:	n/a	n/a
31	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr1:72519630-72519642	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
34	CCNT2	chr1:72880174-72880370	K562	blood:	n/a	n/a
35	CEBPB	chr1:72863451-72863893	Hela-S3	cervix:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
36	CEBPB	chr1:72700769-72701072	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:72863538-72863792	H1-hESC	embryonic stem cell:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
38	CEBPB	chr1:72663490-72663831	IMR90	lung:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
39	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr1:72568659-72568859	K562	blood:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
41	CEBPB	chr1:72818201-72818500	HepG2	liver:	n/a	chr1:72818339-72818350
42	CEBPB	chr1:72878983-72879304	IMR90	lung:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
43	CEBPB	chr1:72863488-72863795	ECC-1	luminal epithelium:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
44	CEBPB	chr1:72588279-72588474	HepG2	liver:	n/a	chr1:72588315-72588326 chr1:72588317-72588328 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588317-72588326 chr1:72588315-72588328
45	CEBPB	chr1:72700769-72701168	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:72814338-72814482	A549	lung:	n/a	n/a
47	CEBPB	chr1:72878987-72879223	ECC-1	luminal epithelium:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
48	CEBPB	chr1:72818172-72818482	IMR90	lung:	n/a	chr1:72818339-72818350
49	CEBPB	chr1:72707185-72707435	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:72707137-72707455	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72748124-72748174	AG09309	skin:	n/a
2	chr1:72749581-72749631	AG04449	skin:	fetal
3	chr1:72748607-72748657	GM12892	blood:	n/a
4	chr1:72748124-72748174	AG09309	skin:	n/a
5	chr1:72749581-72749631	AG04449	skin:	fetal
6	chr1:72748607-72748657	GM12892	blood:	n/a
7	chr1:72885079-72885129	SK-N-SH	brain:	n/a
8	chr1:72749880-72749930	NHBE	bronchial:	n/a
9	chr1:72749581-72749631	HCF	heart:	n/a
10	chr1:72750671-72750721	SK-N-SH	brain:	n/a
11	chr1:72749880-72749930	IMR90	lung:	fetal
12	chr1:72749015-72749065	Jurkat	blood:	n/a
13	chr1:72753076-72753126	RPTEC	kidney:	n/a
14	chr1:72748389-72748439	HAEpiC	amniotic membrane:	n/a
15	chr1:72748601-72748651	HMEC	breast:	n/a
16	chr1:72750502-72750552	PrEC	prostate:	n/a
17	chr1:72885180-72885230	Hepatocyte	liver:	n/a
18	chr1:72747802-72747852	AG09319	gingival:	n/a
19	chr1:72749064-72749114	ProgFib	skin:	n/a
20	chr1:72750502-72750552	NB4	blood:	n/a
21	chr1:72749581-72749631	Caco-2	colon:	n/a
22	chr1:72749735-72749785	H1-hESC	embryonic stem cell:	embryo
23	chr1:72884990-72885040	GM06990	blood:	n/a
24	chr1:72749735-72749785	HAEpiC	amniotic membrane:	n/a
25	chr1:72750124-72750174	GM12878	blood:	n/a
26	chr1:72750671-72750721	RPTEC	kidney:	n/a
27	chr1:72748607-72748657	HRE	kidney:	n/a
28	chr1:72749064-72749114	GM12891	blood:	n/a
29	chr1:72749880-72749930	NH-A	brain:	n/a
30	chr1:72749275-72749325	GM06990	blood:	n/a
31	chr1:72749880-72749930	HNPCEpiC	eye:	n/a
32	chr1:72749015-72749065	LNCaP	prostate:	n/a
33	chr1:72750124-72750174	HRCEpiC	kidney:	n/a
34	chr1:72753076-72753126	HEEpiC	esophagus:	n/a
35	chr1:72747802-72747852	SK-N-MC	brain:	n/a
36	chr1:72748139-72748189	K562	blood:	n/a
37	chr1:72750124-72750174	SAEC	small airway:	n/a
38	chr1:72747802-72747852	AG04449	skin:	fetal
39	chr1:72750671-72750721	HCF	heart:	n/a
40	chr1:72885079-72885129	BE2_C	brain:	n/a
41	chr1:72750241-72750291	PANC-1	pancreas:	n/a
42	chr1:72749275-72749325	NH-A	brain:	n/a
43	chr1:72749275-72749325	SK-N-SH_RA	brain:	n/a
44	chr1:72749735-72749785	PrEC	prostate:	n/a
45	chr1:72748389-72748439	PANC-1	pancreas:	n/a
46	chr1:72749581-72749631	GM19239	blood:	n/a
47	chr1:72748607-72748657	T-47D	breast:	n/a
48	chr1:72750671-72750721	GM12892	blood:	n/a
49	chr1:72749064-72749114	Hela-S3	cervix:	n/a
50	chr1:72753076-72753126	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
2	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
3	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:
4	chr1:72863619..72864264-chr11:65396606..65397388,2	MCF-7	breast:
5	chr1:72708937..72709709-chr2:107409969..107410778,2	MCF-7	breast:
6	chr1:72900602..72902220-chr1:72902664..72904300,2	K562	blood:
7	chr1:72752065..72752600-chr8:87527466..87528155,2	MCF-7	breast:
8	chr1:72900602..72902220-chr1:72902664..72904300,2	K562	blood:
9	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
10	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:

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

Extended variants
information (count: 9554 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:9554 , 50 per page) page: 1 2 3 4 5 6 7 ... 192

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17092186	chr1:72504485-72504486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376946167	chr1:72504553-72504554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566056278	chr1:72504619-72504620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552327267	chr1:72504625-72504626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529919049	chr1:72504638-72504639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377224776	chr1:72504643-72504644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556065671	chr1:72504656-72504657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148996592	chr1:72504669-72504670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17580143	chr1:72504700-72504701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548182459	chr1:72504746-72504747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568161044	chr1:72504840-72504841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537441352	chr1:72504853-72504854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143820636	chr1:72504861-72504862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528831372	chr1:72504862-72504863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138502976	chr1:72504873-72504874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553168998	chr1:72504892-72504893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573183475	chr1:72504895-72504896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115076780	chr1:72504946-72504947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141346168	chr1:72504974-72504975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145123230	chr1:72504979-72504980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188617259	chr1:72504989-72504990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2630425	chr1:72505022-72505023	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs556845082	chr1:72505027-72505028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373292947	chr1:72505077-72505078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182146739	chr1:72505102-72505103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs207460192	chr1:72505117-72505118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75146580	chr1:72505246-72505247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11803665	chr1:72505250-72505251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548509989	chr1:72505264-72505265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568718454	chr1:72505274-72505275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560517890	chr1:72505276-72505277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185160732	chr1:72505320-72505321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1486110	chr1:72505345-72505346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542627081	chr1:72505374-72505375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2821282	chr1:72505392-72505393	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs77413021	chr1:72505425-72505426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190061433	chr1:72505434-72505435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141690594	chr1:72505448-72505449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150498830	chr1:72505454-72505455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11806908	chr1:72505465-72505466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs575469018	chr1:72505512-72505513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182178839	chr1:72505527-72505528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187260518	chr1:72505537-72505538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2821281	chr1:72505552-72505553	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539988338	chr1:72505623-72505624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559804449	chr1:72505624-72505625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573132979	chr1:72505632-72505633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138382023	chr1:72505693-72505694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111379566	chr1:72505707-72505708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189823398	chr1:72505708-72505709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
small cell lung cancer	20016488	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
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cancer	21272361	CNVD
Obesity	21131291	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72500600-72512600	Weak transcription	Pancreas	Pancrea
2	chr1:72507800-72508000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:72507800-72508200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:72507800-72508200	Enhancers	Dnd41	blood
5	chr1:72507800-72508200	Enhancers	HUVEC	blood vessel
6	chr1:72507800-72508800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:72508000-72508400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:72508400-72508800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:72508800-72510800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:72510800-72511200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:72512200-72512800	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr1:72512600-72513200	Enhancers	Colon Smooth Muscle	Colon
13	chr1:72512800-72513000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr1:72513000-72513200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr1:72513200-72513800	Weak transcription	Colon Smooth Muscle	Colon
16	chr1:72513200-72518400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr1:72513800-72514400	Enhancers	Colon Smooth Muscle	Colon
18	chr1:72514400-72519800	Weak transcription	Colon Smooth Muscle	Colon
19	chr1:72516000-72517400	Enhancers	HUVEC	blood vessel
20	chr1:72516200-72516600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:72516600-72517400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr1:72516800-72517400	Enhancers	HSMM	muscle
23	chr1:72517200-72517600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:72517200-72517600	Enhancers	NH-A	brain
25	chr1:72517200-72517600	Enhancers	Osteobl	bone
26	chr1:72517400-72517800	Enhancers	HSMMtube	muscle
27	chr1:72519800-72520000	Enhancers	Colon Smooth Muscle	Colon
28	chr1:72520000-72520800	Weak transcription	Colon Smooth Muscle	Colon
29	chr1:72521000-72521400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:72524600-72525000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr1:72524800-72525200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:72524800-72525400	Enhancers	NHEK	skin
33	chr1:72525000-72526000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr1:72525200-72527600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:72525400-72527800	Weak transcription	NHEK	skin
36	chr1:72526000-72526400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:72526000-72526400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:72526000-72526800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr1:72526200-72526800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr1:72526400-72526800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr1:72526400-72526800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:72526400-72526800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:72526400-72527400	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr1:72526800-72527000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:72526800-72527800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr1:72526800-72528000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:72526800-72528200	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr1:72526800-72532400	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr1:72527000-72527800	Enhancers	Brain Substantia Nigra	brain
50	chr1:72527000-72528200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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