Variant report

Variant	nsv461895
Chromosome Location	chr1:72079898-72206799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:72082343-72082505	GM12878	blood:	n/a	chr1:72082460-72082471
2	BHLHE40	chr1:72205203-72205242	GM12878	blood:	n/a	n/a
3	CEBPB	chr1:72128205-72128324	HepG2	liver:	n/a	chr1:72128261-72128272
4	CEBPB	chr1:72132278-72133317	IMR90	lung:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
5	CEBPB	chr1:72103843-72104179	IMR90	lung:	n/a	n/a
6	CEBPB	chr1:72132874-72133198	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
7	CEBPB	chr1:72122476-72122921	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:72132835-72133315	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
9	CEBPB	chr1:72087468-72087896	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:72161508-72161870	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:72093008-72093050	K562	blood:	n/a	chr1:72093010-72093023 chr1:72093010-72093021 chr1:72093010-72093023
12	CEBPB	chr1:72120017-72120305	HepG2	liver:	n/a	chr1:72120144-72120155
13	CEBPB	chr1:72132885-72133214	HepG2	liver:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
14	CEBPB	chr1:72138249-72138465	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:72132850-72133320	Hela-S3	cervix:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
16	CTCF	chr1:72187320-72187470	BE2_C	brain:	n/a	n/a
17	CTCF	chr1:72187278-72187552	GM12878	blood:	n/a	n/a
18	CTCF	chr1:72187211-72187521	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr1:72187280-72187430	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr1:72172142-72172201	NHEK	skin:	n/a	n/a
21	CTCF	chr1:72187200-72187350	RPTEC	kidney:	n/a	n/a
22	CTCF	chr1:72187340-72187490	HEK293	kidney:	n/a	n/a
23	CTCF	chr1:72187440-72187590	NB4	blood:	n/a	n/a
24	CTCF	chr1:72172120-72172270	AG04450	lung:	n/a	n/a
25	CTCF	chr1:72171760-72171910	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr1:72195413-72195513	LNCaP	prostate:	n/a	n/a
27	CTCF	chr1:72187340-72187490	HPF	lung:	n/a	n/a
28	CTCF	chr1:72187409-72187470	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr1:72171780-72171930	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr1:72172100-72172250	BE2_C	brain:	n/a	n/a
31	CTCF	chr1:72172080-72172230	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr1:72187400-72187406	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:72195960-72196110	RPTEC	kidney:	n/a	n/a
34	CTCF	chr1:72187220-72187370	GM12868	blood:	n/a	n/a
35	CTCF	chr1:72171820-72171970	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr1:72187340-72187490	GM12873	blood:	n/a	n/a
37	CTCF	chr1:72172143-72172220	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:72103788-72104037	IMR90	lung:	n/a	n/a
39	CTCF	chr1:72187260-72187410	HMEC	breast:	n/a	n/a
40	CTCF	chr1:72172060-72172210	HepG2	liver:	n/a	n/a
41	CTCF	chr1:72174840-72174893	GM13976	blood:	n/a	n/a
42	CTCF	chr1:72187380-72187530	GM12873	blood:	n/a	n/a
43	CTCF	chr1:72172140-72172290	AG09319	gingival:	n/a	n/a
44	CTCF	chr1:72103877-72104006	NHEK	skin:	n/a	n/a
45	CTCF	chr1:72187340-72187490	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr1:72103891-72103982	GM12878	blood:	n/a	n/a
47	CTCF	chr1:72187340-72187490	NHEK	skin:	n/a	n/a
48	CTCF	chr1:72187380-72187530	BE2_C	brain:	n/a	n/a
49	CTCF	chr1:72187300-72187450	HL-60	blood:	n/a	n/a
50	CTCF	chr1:72171860-72172010	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72190606-72190656	BJ	skin:	n/a
2	chr1:72190606-72190656	Hela-S3	cervix:	n/a
3	chr1:72190606-72190656	MCF-7	breast:	n/a
4	chr1:72190606-72190656	AG10803	skin:	n/a
5	chr1:72190606-72190656	NH-A	brain:	n/a
6	chr1:72190606-72190656	AG09309	skin:	n/a
7	chr1:72190606-72190656	HAEpiC	amniotic membrane:	n/a
8	chr1:72190606-72190656	HMEC	breast:	n/a
9	chr1:72190606-72190656	A549	lung:	n/a
10	chr1:72190606-72190656	HNPCEpiC	eye:	n/a
11	chr1:72190606-72190656	U87	brain:	n/a
12	chr1:72190606-72190656	HepG2	liver:	n/a
13	chr1:72190606-72190656	GM12892	blood:	n/a
14	chr1:72190606-72190656	SK-N-SH_RA	brain:	n/a
15	chr1:72190606-72190656	AG04449	skin:	fetal
16	chr1:72190606-72190656	HEK293	kidney:	embryo
17	chr1:72190606-72190656	HRCEpiC	kidney:	n/a
18	chr1:72190606-72190656	HUVEC	blood vessel:	n/a
19	chr1:72190606-72190656	NHDF-neo	bronchial:	n/a
20	chr1:72190606-72190656	HL-60	blood:	n/a
21	chr1:72190606-72190656	AG09319	gingival:	n/a
22	chr1:72190606-72190656	NHBE	bronchial:	n/a
23	chr1:72190606-72190656	Jurkat	blood:	n/a
24	chr1:72190606-72190656	RPTEC	kidney:	n/a
25	chr1:72190606-72190656	HRPEpiC	eye:	n/a
26	chr1:72190606-72190656	HCF	heart:	n/a
27	chr1:72190606-72190656	GM12878	blood:	n/a
28	chr1:72190606-72190656	ECC-1	luminal epithelium:	n/a
29	chr1:72190606-72190656	PANC-1	pancreas:	n/a
30	chr1:72190606-72190656	H1-hESC	embryonic stem cell:	embryo
31	chr1:72190606-72190656	K562	blood:	n/a
32	chr1:72190606-72190656	SK-N-SH	brain:	n/a
33	chr1:72190606-72190656	SK-N-MC	brain:	n/a
34	chr1:72190606-72190656	HCPEpiC	choroid plexus:	n/a
35	chr1:72190606-72190656	IMR90	lung:	fetal
36	chr1:72190606-72190656	GM12891	blood:	n/a
37	chr1:72190606-72190656	AoSMC	blood vessel:	n/a
38	chr1:72190606-72190656	LNCaP	prostate:	n/a
39	chr1:72190606-72190656	BE2_C	brain:	n/a
40	chr1:72190606-72190656	Hepatocyte	liver:	n/a
41	chr1:72190606-72190656	GM06990	blood:	n/a
42	chr1:72190606-72190656	PrEC	prostate:	n/a
43	chr1:72190606-72190656	MCF10A-Er-Src	breast:	n/a
44	chr1:72190606-72190656	AG04450	lung:	fetal
45	chr1:72190606-72190656	Caco-2	colon:	n/a
46	chr1:72190606-72190656	SAEC	small airway:	n/a
47	chr1:72190606-72190656	GM19239	blood:	n/a
48	chr1:72190606-72190656	ovcar-3	ovarian:	n/a
49	chr1:72190606-72190656	PFSK-1	brain:	n/a
50	chr1:72190606-72190656	HEEpiC	esophagus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
2	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
3	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
4	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
5	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
6	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
7	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
8	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
9	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
10	chr1:71915989..71918426-chr1:72103464..72106010,2	K562	blood:
11	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:

No data

Variant related genes	Relation type
NEGR1	TF binding region
ENSG00000271618	TF binding region
NEGR1	CpG island
ENSG00000271618	CpG island

Extended variants
information (count: 3471 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3471 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10493486	chr1:72079898-72079899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544326683	chr1:72079904-72079905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537753094	chr1:72079923-72079924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558079855	chr1:72079934-72079935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537792046	chr1:72079940-72079941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577558220	chr1:72079977-72079978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533819758	chr1:72080022-72080023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553557580	chr1:72080037-72080038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573794319	chr1:72080040-72080041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183734276	chr1:72080112-72080113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144902161	chr1:72080114-72080115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369960751	chr1:72080157-72080158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77024947	chr1:72080165-72080166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544566133	chr1:72080207-72080208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186925839	chr1:72080217-72080218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368937765	chr1:72080289-72080290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564834638	chr1:72080356-72080357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191341687	chr1:72080384-72080385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546995464	chr1:72080422-72080423	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs560180772	chr1:72080430-72080431	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs184338981	chr1:72080438-72080439	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs12032545	chr1:72080441-72080442	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs568708781	chr1:72080530-72080531	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs187127867	chr1:72080556-72080557	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs147148060	chr1:72080559-72080560	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571539467	chr1:72080581-72080582	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533519112	chr1:72080582-72080583	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs140283107	chr1:72080592-72080593	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs142135704	chr1:72080593-72080594	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs1762732	chr1:72080604-72080605	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs556330986	chr1:72080607-72080608	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs192566768	chr1:72080627-72080628	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs373120997	chr1:72080664-72080665	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs185306396	chr1:72080667-72080668	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs555925988	chr1:72080697-72080698	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs564598282	chr1:72080702-72080703	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs578210259	chr1:72080703-72080704	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs545698626	chr1:72080747-72080748	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs560119523	chr1:72080756-72080757	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs529295395	chr1:72080767-72080768	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs542702990	chr1:72080820-72080821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562678449	chr1:72080839-72080840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531385103	chr1:72080925-72080926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11432692	chr1:72080971-72080972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs397779999	chr1:72080981-72080982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575718621	chr1:72081012-72081013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546070383	chr1:72081027-72081028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189890253	chr1:72081028-72081029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571409939	chr1:72081060-72081061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527586937	chr1:72081061-72081062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72072200-72085200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:72076000-72081800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:72076400-72081600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:72080200-72080400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr1:72080400-72080800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr1:72080800-72081000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr1:72081000-72087000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr1:72081600-72083200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:72081800-72082200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:72083400-72084000	Enhancers	Fetal Stomach	stomach
11	chr1:72083600-72084000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:72083600-72084200	Enhancers	Pancreas	Pancrea
13	chr1:72084000-72084400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:72084400-72087400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:72085200-72085600	Enhancers	Colon Smooth Muscle	Colon
16	chr1:72085600-72093600	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:72087000-72087200	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr1:72087000-72087400	Enhancers	HSMM	muscle
19	chr1:72087000-72088000	Enhancers	NHEK	skin
20	chr1:72087200-72087800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr1:72087200-72088200	Enhancers	Muscle Satellite Cultured Cells	--
22	chr1:72087400-72087800	Weak transcription	HSMM	muscle
23	chr1:72087400-72088000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:72087400-72088000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:72087400-72088000	Enhancers	NHDF-Ad	bronchial
26	chr1:72087600-72088000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:72087600-72088000	Enhancers	NH-A	brain
28	chr1:72087800-72088200	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr1:72087800-72088600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:72087800-72088600	Enhancers	HSMM	muscle
31	chr1:72099200-72099600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:72099200-72100000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:72104000-72104400	Enhancers	NHDF-Ad	bronchial
34	chr1:72104000-72104600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:72104000-72104600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:72104000-72105600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:72104000-72105800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:72104200-72104400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:72104200-72104600	Enhancers	HSMM	muscle
40	chr1:72104200-72104800	Enhancers	Osteobl	bone
41	chr1:72104400-72105400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:72104600-72105800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:72104600-72105800	Weak transcription	HSMM	muscle
44	chr1:72104800-72105200	Enhancers	Thymus	Thymus
45	chr1:72105200-72107200	Weak transcription	Thymus	Thymus
46	chr1:72105400-72106200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr1:72105400-72106800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:72105600-72106200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr1:72105600-72106200	Enhancers	Adipose Nuclei	Adipose
50	chr1:72105600-72106400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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