Variant report

Variant	nsv482697
Chromosome Location	chr1:78786028-78935333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:702)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:78837896-78837928	HepG2	liver:	n/a	n/a
2	BATF	chr1:78843105-78843329	GM12878	blood:	n/a	chr1:78843215-78843225 chr1:78843214-78843225
3	BHLHE40	chr1:78799389-78799413	K562	blood:	n/a	n/a
4	BHLHE40	chr1:78799187-78799342	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:78917853-78917854	GM12878	blood:	n/a	n/a
6	BRCA1	chr1:78890922-78890931	GM12878	blood:	n/a	n/a
7	CBX3	chr1:78799051-78799452	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:78799190-78799489	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr1:78849603-78849953	HepG2	liver:	n/a	chr1:78849767-78849780 chr1:78849768-78849779
10	CEBPB	chr1:78799112-78799421	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:78799082-78799447	A549	lung:	n/a	n/a
12	CEBPB	chr1:78849685-78849950	A549	lung:	n/a	chr1:78849767-78849780 chr1:78849768-78849779
13	CEBPB	chr1:78843100-78843380	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:78851167-78851444	IMR90	lung:	n/a	chr1:78851358-78851371 chr1:78851231-78851242 chr1:78851308-78851319
15	CEBPB	chr1:78930370-78930599	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:78907559-78907963	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:78799167-78799427	MCF-7	breast:	n/a	n/a
18	CEBPB	chr1:78888820-78889033	HepG2	liver:	n/a	chr1:78888887-78888898
19	CEBPB	chr1:78799074-78799506	MCF-7	breast:	n/a	n/a
20	CEBPB	chr1:78849627-78849938	Hela-S3	cervix:	n/a	chr1:78849767-78849780 chr1:78849768-78849779
21	CEBPB	chr1:78851186-78851422	HepG2	liver:	n/a	chr1:78851358-78851371 chr1:78851231-78851242 chr1:78851308-78851319
22	CEBPB	chr1:78835332-78835529	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:78799134-78799410	A549	lung:	n/a	n/a
24	CEBPB	chr1:78798955-78799578	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:78805741-78805988	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:78799110-78799421	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:78805716-78806058	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:78843186-78843361	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:78927369-78927451	A549	lung:	n/a	n/a
30	CEBPB	chr1:78799117-78799398	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:78835287-78835568	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:78849600-78849921	IMR90	lung:	n/a	chr1:78849767-78849780 chr1:78849768-78849779
33	CEBPB	chr1:78789070-78789354	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr1:78903200-78903350	AG10803	skin:	n/a	chr1:78903285-78903303
35	CTCF	chr1:78799180-78799330	AG09319	gingival:	n/a	chr1:78799281-78799290
36	CTCF	chr1:78852660-78852810	HPF	lung:	n/a	n/a
37	CTCF	chr1:78879420-78879570	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr1:78811340-78811490	HCFaa	heart:	n/a	n/a
39	CTCF	chr1:78799200-78799350	BE2_C	brain:	n/a	chr1:78799281-78799290
40	CTCF	chr1:78799178-78799391	SK-N-SH_RA	brain:	n/a	chr1:78799281-78799290
41	CTCF	chr1:78799200-78799350	GM12869	blood:	n/a	chr1:78799281-78799290
42	CTCF	chr1:78879822-78879852	Lung_OC	lung:	n/a	n/a
43	CTCF	chr1:78791124-78791224	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:78799139-78799503	MCF-7	breast:	n/a	chr1:78799281-78799290
45	CTCF	chr1:78799226-78799371	MCF-7	breast:	n/a	chr1:78799281-78799290
46	CTCF	chr1:78903180-78903330	AG10803	skin:	n/a	chr1:78903285-78903303
47	CTCF	chr1:78799120-78799270	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:78903200-78903350	HCPEpiC	choroid plexus:	n/a	chr1:78903285-78903303
49	CTCF	chr1:78903140-78903290	AG04450	lung:	n/a	n/a
50	CTCF	chr1:78843130-78843248	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78892408-78892458	RPTEC	kidney:	n/a
2	chr1:78805320-78805370	Jurkat	blood:	n/a
3	chr1:78892408-78892458	SKMC	muscle:	n/a
4	chr1:78892408-78892458	ProgFib	skin:	n/a
5	chr1:78805320-78805370	HEK293	kidney:	embryo
6	chr1:78805320-78805370	HEEpiC	esophagus:	n/a
7	chr1:78805320-78805370	AG09319	gingival:	n/a
8	chr1:78892408-78892458	NH-A	brain:	n/a
9	chr1:78805320-78805370	HMEC	breast:	n/a
10	chr1:78892408-78892458	CMK	blood:	n/a
11	chr1:78892408-78892458	AG04450	lung:	fetal
12	chr1:78892408-78892458	HEK293	kidney:	embryo
13	chr1:78892408-78892458	PrEC	prostate:	n/a
14	chr1:78892408-78892458	GM12892	blood:	n/a
15	chr1:78805320-78805370	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:78892408-78892458	SK-N-SH	brain:	n/a
17	chr1:78892408-78892458	U87	brain:	n/a
18	chr1:78892408-78892458	PFSK-1	brain:	n/a
19	chr1:78892408-78892458	HepG2	liver:	n/a
20	chr1:78805320-78805370	MCF10A-Er-Src	breast:	n/a
21	chr1:78805320-78805370	IMR90	lung:	fetal
22	chr1:78892408-78892458	K562	blood:	n/a
23	chr1:78805320-78805370	SK-N-MC	brain:	n/a
24	chr1:78892408-78892458	IMR90	lung:	fetal
25	chr1:78805320-78805370	A549	lung:	n/a
26	chr1:78805320-78805370	NHDF-neo	bronchial:	n/a
27	chr1:78805320-78805370	AG09309	skin:	n/a
28	chr1:78805320-78805370	RPTEC	kidney:	n/a
29	chr1:78805320-78805370	HRE	kidney:	n/a
30	chr1:78892408-78892458	H1-hESC	embryonic stem cell:	embryo
31	chr1:78805320-78805370	H1-hESC	embryonic stem cell:	embryo
32	chr1:78892408-78892458	GM12878	blood:	n/a
33	chr1:78892408-78892458	NT2-D1	testis:	n/a
34	chr1:78805320-78805370	NT2-D1	testis:	n/a
35	chr1:78805320-78805370	HL-60	blood:	n/a
36	chr1:78805320-78805370	PANC-1	pancreas:	n/a
37	chr1:78805320-78805370	HepG2	liver:	n/a
38	chr1:78892408-78892458	ovcar-3	ovarian:	n/a
39	chr1:78805320-78805370	GM12892	blood:	n/a
40	chr1:78892408-78892458	LNCaP	prostate:	n/a
41	chr1:78892408-78892458	HCPEpiC	choroid plexus:	n/a
42	chr1:78892408-78892458	BE2_C	brain:	n/a
43	chr1:78805320-78805370	HRCEpiC	kidney:	n/a
44	chr1:78805320-78805370	AG10803	skin:	n/a
45	chr1:78892408-78892458	HEEpiC	esophagus:	n/a
46	chr1:78805320-78805370	T-47D	breast:	n/a
47	chr1:78805320-78805370	PrEC	prostate:	n/a
48	chr1:78892408-78892458	GM12891	blood:	n/a
49	chr1:78892408-78892458	ECC-1	luminal epithelium:	n/a
50	chr1:78805320-78805370	NB4	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:78466521..78469448-chr1:78786020..78788848,2	K562	blood:
2	chr1:78913260..78915491-chr1:78917336..78919213,2	K562	blood:
3	chr1:78913260..78915491-chr1:78917336..78919213,2	K562	blood:
4	chr1:78800150..78802250-chr1:78803313..78804839,2	K562	blood:
5	chr1:78800150..78802250-chr1:78803313..78804839,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTGFR-1	chr1:78834222-78834412	NONHSAT004072
2	lnc-PTGFR-1	chr1:78834968-78835147	NONHSAT004072
3	lnc-PTGFR-1	chr1:78808210-78808324	NONHSAT004072
4	lnc-PTGFR-1	chr1:78834222-78834412	ENSG00000237413.1
5	lnc-PTGFR-1	chr1:78808210-78808324	ENSG00000237413.1
6	lnc-PTGFR-1	chr1:78834968-78835149	ENSG00000237413.1

No data

Variant related genes	Relation type
ENSG00000227556	TF binding region
RNA5SP23	TF binding region
ENSG00000227556	CpG island
RNA5SP23	CpG island

Extended variants
information (count: 4686 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4686 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574330447	chr1:78786041-78786042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568846950	chr1:78786076-78786077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554767426	chr1:78786102-78786103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75795994	chr1:78786126-78786127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566595126	chr1:78786139-78786140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535198255	chr1:78786140-78786141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369111459	chr1:78786191-78786192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7521129	chr1:78786208-78786209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs34864597	chr1:78786220-78786221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577290028	chr1:78786231-78786232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182858524	chr1:78786312-78786313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187415791	chr1:78786322-78786323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35495495	chr1:78786359-78786360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563167033	chr1:78786403-78786404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148750972	chr1:78786421-78786422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548717381	chr1:78786423-78786424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560000759	chr1:78786468-78786469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192314105	chr1:78786471-78786472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551962990	chr1:78786542-78786543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570146774	chr1:78786556-78786557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537437825	chr1:78786623-78786624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185647297	chr1:78786636-78786637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149612686	chr1:78786647-78786648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376039604	chr1:78786683-78786684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142614563	chr1:78786690-78786691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534039920	chr1:78786705-78786706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1412845	chr1:78786758-78786759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12068173	chr1:78786779-78786780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12021616	chr1:78786791-78786792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573280380	chr1:78786812-78786813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558370027	chr1:78786838-78786839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113793960	chr1:78786888-78786889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189328543	chr1:78786895-78786896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544616042	chr1:78786900-78786901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556900051	chr1:78786954-78786955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575037376	chr1:78786986-78786987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192264113	chr1:78786988-78786989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560765287	chr1:78787002-78787003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11162465	chr1:78787005-78787006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184604979	chr1:78787031-78787032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188629425	chr1:78787042-78787043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545524054	chr1:78787043-78787044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12125026	chr1:78787069-78787070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs140567965	chr1:78787074-78787075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568027605	chr1:78787087-78787088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144540033	chr1:78787113-78787114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181299652	chr1:78787128-78787129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565903893	chr1:78787185-78787186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185900370	chr1:78787266-78787267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12029753	chr1:78787274-78787275	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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
Ewing''s sarcoma	17952124	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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78784800-78788400	Weak transcription	NHLF	lung
2	chr1:78784800-78788800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr1:78788400-78789200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:78788400-78789200	Enhancers	NHLF	lung
5	chr1:78788400-78789800	Enhancers	Hela-S3	cervix
6	chr1:78788800-78789600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:78791200-78791600	Enhancers	Liver	Liver
8	chr1:78794600-78795600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:78795000-78795400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr1:78799200-78799800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:78799400-78800000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr1:78799400-78800800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:78799400-78800800	Enhancers	NHLF	lung
14	chr1:78799600-78801400	Enhancers	NHDF-Ad	bronchial
15	chr1:78799800-78804200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:78800000-78800400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:78800000-78801400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:78800400-78801400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr1:78800800-78801200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:78800800-78804600	Weak transcription	NHLF	lung
21	chr1:78801200-78801600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:78801400-78804200	Weak transcription	NHDF-Ad	bronchial
23	chr1:78801400-78804800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr1:78801400-78805000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:78801600-78804600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:78804200-78804800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:78804200-78805000	Enhancers	NHDF-Ad	bronchial
28	chr1:78804600-78805000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:78804600-78805000	Enhancers	NHLF	lung
30	chr1:78804600-78805000	Enhancers	Osteobl	bone
31	chr1:78804600-78805600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:78804600-78806400	Enhancers	HMEC	breast
33	chr1:78804600-78806800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:78804600-78807000	Enhancers	Hela-S3	cervix
35	chr1:78804600-78808400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:78804800-78805000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:78804800-78805000	ZNF genes & repeats	Pancreas	Pancrea
38	chr1:78804800-78805200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:78804800-78806000	Enhancers	NH-A	brain
40	chr1:78804800-78806600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr1:78804800-78806800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:78804800-78806800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:78804800-78807000	Enhancers	HUVEC	blood vessel
44	chr1:78805000-78805200	Flanking Active TSS	NHDF-Ad	bronchial
45	chr1:78805000-78805200	Flanking Active TSS	NHLF	lung
46	chr1:78805000-78805400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:78805000-78805600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:78805000-78805600	Enhancers	A549	lung
49	chr1:78805000-78805600	Flanking Active TSS	Osteobl	bone
50	chr1:78805000-78805800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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