Variant report

Variant	nsv461884
Chromosome Location	chr1:72077549-72238691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

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	chr1:72230483-72230683	Hela-S3	cervix:	n/a	chr1:72230589-72230600
4	CEBPB	chr1:72122476-72122921	IMR90	lung:	n/a	n/a
5	CEBPB	chr1:72120017-72120305	HepG2	liver:	n/a	chr1:72120144-72120155
6	CEBPB	chr1:72103843-72104179	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:72230419-72230782	HepG2	liver:	n/a	chr1:72230589-72230600
8	CEBPB	chr1:72132874-72133198	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
9	CEBPB	chr1:72132835-72133315	ECC-1	luminal epithelium:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
10	CEBPB	chr1:72230408-72230785	IMR90	lung:	n/a	chr1:72230589-72230600
11	CEBPB	chr1:72132885-72133214	HepG2	liver:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
12	CEBPB	chr1:72161508-72161870	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:72132850-72133320	Hela-S3	cervix:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
14	CEBPB	chr1:72230467-72230667	H1-hESC	embryonic stem cell:	n/a	chr1:72230589-72230600
15	CEBPB	chr1:72138249-72138465	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:72132278-72133317	IMR90	lung:	n/a	chr1:72133033-72133044 chr1:72133032-72133045 chr1:72133032-72133045 chr1:72133121-72133134
17	CEBPB	chr1:72128205-72128324	HepG2	liver:	n/a	chr1:72128261-72128272
18	CEBPB	chr1:72214678-72215002	IMR90	lung:	n/a	chr1:72214832-72214845
19	CEBPB	chr1:72087468-72087896	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:72093008-72093050	K562	blood:	n/a	chr1:72093010-72093023 chr1:72093010-72093021 chr1:72093010-72093023
21	CEBPB	chr1:72230432-72230774	A549	lung:	n/a	chr1:72230589-72230600
22	CTCF	chr1:72171840-72171990	AG04450	lung:	n/a	n/a
23	CTCF	chr1:72187280-72187430	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr1:72172143-72172220	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:72187340-72187490	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr1:72187200-72187350	RPTEC	kidney:	n/a	n/a
27	CTCF	chr1:72187320-72187470	BE2_C	brain:	n/a	n/a
28	CTCF	chr1:72187220-72187370	GM12868	blood:	n/a	n/a
29	CTCF	chr1:72187380-72187530	GM12873	blood:	n/a	n/a
30	CTCF	chr1:72187380-72187530	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr1:72187360-72187510	HPF	lung:	n/a	n/a
32	CTCF	chr1:72187340-72187490	NHEK	skin:	n/a	n/a
33	CTCF	chr1:72187340-72187490	HEK293	kidney:	n/a	n/a
34	CTCF	chr1:72172060-72172210	HepG2	liver:	n/a	n/a
35	CTCF	chr1:72172080-72172230	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr1:72219856-72219911	Fibrobl	skin:	n/a	n/a
37	CTCF	chr1:72195413-72195513	LNCaP	prostate:	n/a	n/a
38	CTCF	chr1:72187440-72187590	NB4	blood:	n/a	n/a
39	CTCF	chr1:72187360-72187510	HRE	kidney:	n/a	n/a
40	CTCF	chr1:72172120-72172270	AG04450	lung:	n/a	n/a
41	CTCF	chr1:72171760-72171910	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr1:72172140-72172290	AG09319	gingival:	n/a	n/a
43	CTCF	chr1:72171840-72171990	AG10803	skin:	n/a	n/a
44	CTCF	chr1:72171820-72171970	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:72171860-72172010	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:72187211-72187521	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr1:72219500-72219650	WI-38	lung:	n/a	n/a
48	CTCF	chr1:72187340-72187490	HPF	lung:	n/a	n/a
49	CTCF	chr1:72172020-72172170	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr1:72172142-72172201	NHEK	skin:	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	NH-A	brain:	n/a
2	chr1:72190606-72190656	HIPEpiC	eye:	n/a
3	chr1:72190606-72190656	HEEpiC	esophagus:	n/a
4	chr1:72190606-72190656	AG09309	skin:	n/a
5	chr1:72190606-72190656	AG10803	skin:	n/a
6	chr1:72190606-72190656	RPTEC	kidney:	n/a
7	chr1:72190606-72190656	BJ	skin:	n/a
8	chr1:72190606-72190656	Hela-S3	cervix:	n/a
9	chr1:72190606-72190656	T-47D	breast:	n/a
10	chr1:72190606-72190656	PFSK-1	brain:	n/a
11	chr1:72190606-72190656	Caco-2	colon:	n/a
12	chr1:72190606-72190656	LNCaP	prostate:	n/a
13	chr1:72190606-72190656	HNPCEpiC	eye:	n/a
14	chr1:72190606-72190656	GM12878	blood:	n/a
15	chr1:72190606-72190656	H1-hESC	embryonic stem cell:	embryo
16	chr1:72190606-72190656	HUVEC	blood vessel:	n/a
17	chr1:72190606-72190656	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:72190606-72190656	HEK293	kidney:	embryo
19	chr1:72190606-72190656	SK-N-SH_RA	brain:	n/a
20	chr1:72190606-72190656	Jurkat	blood:	n/a
21	chr1:72190606-72190656	CMK	blood:	n/a
22	chr1:72190606-72190656	GM12891	blood:	n/a
23	chr1:72190606-72190656	Hepatocyte	liver:	n/a
24	chr1:72190606-72190656	NHBE	bronchial:	n/a
25	chr1:72190606-72190656	HRCEpiC	kidney:	n/a
26	chr1:72190606-72190656	NHDF-neo	bronchial:	n/a
27	chr1:72190606-72190656	HCT-116	colon:	n/a
28	chr1:72190606-72190656	MCF10A-Er-Src	breast:	n/a
29	chr1:72190606-72190656	AoSMC	blood vessel:	n/a
30	chr1:72190606-72190656	AG09319	gingival:	n/a
31	chr1:72190606-72190656	IMR90	lung:	fetal
32	chr1:72190606-72190656	A549	lung:	n/a
33	chr1:72190606-72190656	K562	blood:	n/a
34	chr1:72190606-72190656	NB4	blood:	n/a
35	chr1:72190606-72190656	BE2_C	brain:	n/a
36	chr1:72190606-72190656	HRPEpiC	eye:	n/a
37	chr1:72190606-72190656	HMEC	breast:	n/a
38	chr1:72190606-72190656	HCF	heart:	n/a
39	chr1:72190606-72190656	U87	brain:	n/a
40	chr1:72190606-72190656	NT2-D1	testis:	n/a
41	chr1:72190606-72190656	ProgFib	skin:	n/a
42	chr1:72190606-72190656	PANC-1	pancreas:	n/a
43	chr1:72190606-72190656	HCPEpiC	choroid plexus:	n/a
44	chr1:72190606-72190656	GM06990	blood:	n/a
45	chr1:72190606-72190656	AG04450	lung:	fetal
46	chr1:72190606-72190656	PrEC	prostate:	n/a
47	chr1:72190606-72190656	AG04449	skin:	fetal
48	chr1:72190606-72190656	GM12892	blood:	n/a
49	chr1:72190606-72190656	HepG2	liver:	n/a
50	chr1:72190606-72190656	GM19239	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:72187008..72189556-chr1:72189903..72192438,2	MCF-7	breast:
2	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
3	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
4	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
5	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
6	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
7	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
8	chr1:72129396..72131726-chr1:72132350..72134861,2	K562	blood:
9	chr1:72142368..72144115-chr1:72151008..72153823,2	K562	blood:
10	chr1:72161617..72164423-chr1:72171650..72174212,2	MCF-7	breast:
11	chr1:72166413..72168725-chr1:72192259..72193957,2	K562	blood:
12	chr1:71915989..71918426-chr1:72103464..72106010,2	K562	blood:
13	chr1:72187008..72189556-chr1:72189903..72192438,2	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: 4462 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:4462 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs928615	chr1:72077549-72077550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139934480	chr1:72077595-72077596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577035884	chr1:72077616-72077617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1213508	chr1:72077631-72077632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs528065438	chr1:72077643-72077644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547802917	chr1:72077644-72077645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561410447	chr1:72077650-72077651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530528264	chr1:72077670-72077671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530311191	chr1:72077676-72077677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534762443	chr1:72077687-72077688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540184390	chr1:72077706-72077707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547250887	chr1:72077762-72077763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12089388	chr1:72077765-72077766	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs35354398	chr1:72077789-72077790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188099188	chr1:72077828-72077829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566273847	chr1:72077862-72077863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369905363	chr1:72077921-72077922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191837230	chr1:72077932-72077933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147553934	chr1:72077935-72077936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560021587	chr1:72077987-72077988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537545794	chr1:72078025-72078026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184105966	chr1:72078035-72078036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142090521	chr1:72078039-72078040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35481917	chr1:72078082-72078083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375255146	chr1:72078102-72078103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189187612	chr1:72078107-72078108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144285566	chr1:72078134-72078135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145583587	chr1:72078142-72078143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148874608	chr1:72078163-72078164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539311088	chr1:72078170-72078171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75933417	chr1:72078177-72078178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551102227	chr1:72078205-72078206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563700753	chr1:72078233-72078234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370861964	chr1:72078270-72078271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571185531	chr1:72078312-72078313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143627863	chr1:72078335-72078336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181594320	chr1:72078340-72078341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79184273	chr1:72078362-72078363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552521295	chr1:72078414-72078415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187389029	chr1:72078425-72078426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376377802	chr1:72078459-72078460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368640080	chr1:72078494-72078495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548558730	chr1:72078505-72078506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78467000	chr1:72078546-72078547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148061438	chr1:72078548-72078549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs915218	chr1:72078549-72078550	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs526710	chr1:72078584-72078585	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs367798066	chr1:72078636-72078637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375577507	chr1:72078662-72078663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs598323	chr1:72078698-72078699	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:110)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr1:72076600-72078200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr1:72078400-72079000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:72078600-72079200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:72080200-72080400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr1:72080400-72080800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr1:72080800-72081000	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr1:72081000-72087000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr1:72081600-72083200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:72081800-72082200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:72083400-72084000	Enhancers	Fetal Stomach	stomach
14	chr1:72083600-72084000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:72083600-72084200	Enhancers	Pancreas	Pancrea
16	chr1:72084000-72084400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:72084400-72087400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:72085200-72085600	Enhancers	Colon Smooth Muscle	Colon
19	chr1:72085600-72093600	Weak transcription	Colon Smooth Muscle	Colon
20	chr1:72087000-72087200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr1:72087000-72087400	Enhancers	HSMM	muscle
22	chr1:72087000-72088000	Enhancers	NHEK	skin
23	chr1:72087200-72087800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr1:72087200-72088200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:72087400-72087800	Weak transcription	HSMM	muscle
26	chr1:72087400-72088000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:72087400-72088000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:72087400-72088000	Enhancers	NHDF-Ad	bronchial
29	chr1:72087600-72088000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:72087600-72088000	Enhancers	NH-A	brain
31	chr1:72087800-72088200	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr1:72087800-72088600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:72087800-72088600	Enhancers	HSMM	muscle
34	chr1:72099200-72099600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:72099200-72100000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:72104000-72104400	Enhancers	NHDF-Ad	bronchial
37	chr1:72104000-72104600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:72104000-72104600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr1:72104000-72105600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:72104000-72105800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:72104200-72104400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:72104200-72104600	Enhancers	HSMM	muscle
43	chr1:72104200-72104800	Enhancers	Osteobl	bone
44	chr1:72104400-72105400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:72104600-72105800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:72104600-72105800	Weak transcription	HSMM	muscle
47	chr1:72104800-72105200	Enhancers	Thymus	Thymus
48	chr1:72105200-72107200	Weak transcription	Thymus	Thymus
49	chr1:72105400-72106200	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:72105400-72106800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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