Variant report

Variant	esv3442808
Chromosome Location	chr20:23683435-23746350
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	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
2	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
3	CEBPB	chr20:23684405-23684588	HepG2	liver:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
4	CEBPB	chr20:23684500-23684595	A549	lung:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
5	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
6	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
7	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
8	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
9	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
10	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
11	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
12	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
13	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
14	CTCF	chr20:23704380-23704530	HMEC	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
15	CTCF	chr20:23704353-23704899	MCF-7	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
16	CTCF	chr20:23704337-23704853	GM19238	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
17	CTCF	chr20:23704640-23704790	HCM	heart:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704740-23704758
18	CTCF	chr20:23704320-23704470	HAc	cerebellar:	n/a	n/a
19	CTCF	chr20:23729640-23729790	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr20:23704356-23704863	Fibrobl	skin:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
21	CTCF	chr20:23704380-23704530	HCM	heart:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
22	CTCF	chr20:23704680-23704830	HRE	kidney:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
23	CTCF	chr20:23704340-23704490	HPF	lung:	n/a	n/a
24	CTCF	chr20:23704460-23704610	GM12866	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
25	CTCF	chr20:23704363-23704834	GM13977	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
26	CTCF	chr20:23704340-23704490	AG04450	lung:	n/a	n/a
27	CTCF	chr20:23704340-23704490	NHEK	skin:	n/a	n/a
28	CTCF	chr20:23704700-23704872	K562	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
29	CTCF	chr20:23704360-23704510	WI-38	lung:	n/a	chr20:23704496-23704505
30	CTCF	chr20:23704960-23705110	RPTEC	kidney:	n/a	n/a
31	CTCF	chr20:23704420-23704570	GM12874	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
32	CTCF	chr20:23704284-23704889	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
33	CTCF	chr20:23704380-23704530	RPTEC	kidney:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
34	CTCF	chr20:23704380-23704530	GM12869	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
35	CTCF	chr20:23704385-23704853	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
36	CTCF	chr20:23704340-23704490	BE2_C	brain:	n/a	n/a
37	CTCF	chr20:23729760-23729910	HEK293	kidney:	n/a	n/a
38	CTCF	chr20:23704940-23705090	HAc	cerebellar:	n/a	n/a
39	CTCF	chr20:23704340-23704490	HMEC	breast:	n/a	n/a
40	CTCF	chr20:23719413-23719451	LNCaP	prostate:	n/a	n/a
41	CTCF	chr20:23704377-23704634	Hela-S3	cervix:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
42	CTCF	chr20:23704420-23704570	HepG2	liver:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
43	CTCF	chr20:23704130-23704247	GM10266	blood:	n/a	n/a
44	CTCF	chr20:23704340-23704490	GM12865	blood:	n/a	n/a
45	CTCF	chr20:23704330-23704621	H1-hESC	embryonic stem cell:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
46	CTCF	chr20:23704740-23704890	Hela-S3	cervix:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
47	CTCF	chr20:23704360-23704510	HEEpiC	esophagus:	n/a	chr20:23704496-23704505
48	CTCF	chr20:23729620-23729770	GM12864	blood:	n/a	n/a
49	CTCF	chr20:23704380-23704530	GM12871	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
50	CTCF	chr20:23704380-23704530	GM12865	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23728432-23728482	A549	lung:	n/a
2	chr20:23728432-23728482	A549	lung:	n/a
3	chr20:23731367-23731417	Hela-S3	cervix:	n/a
4	chr20:23732595-23732645	HIPEpiC	eye:	n/a
5	chr20:23732873-23732923	CMK	blood:	n/a
6	chr20:23732873-23732923	ProgFib	skin:	n/a
7	chr20:23728814-23728864	A549	lung:	n/a
8	chr20:23732595-23732645	ProgFib	skin:	n/a
9	chr20:23732595-23732645	RPTEC	kidney:	n/a
10	chr20:23732873-23732923	PANC-1	pancreas:	n/a
11	chr20:23731367-23731417	ECC-1	luminal epithelium:	n/a
12	chr20:23728814-23728864	MCF-7	breast:	n/a
13	chr20:23728814-23728864	ProgFib	skin:	n/a
14	chr20:23732595-23732645	HRPEpiC	eye:	n/a
15	chr20:23731367-23731417	HPAEpiC	pulmonary alveolar:	n/a
16	chr20:23731367-23731417	ProgFib	skin:	n/a
17	chr20:23732595-23732645	SK-N-SH_RA	brain:	n/a
18	chr20:23728814-23728864	HUVEC	blood vessel:	n/a
19	chr20:23728814-23728864	AoSMC	blood vessel:	n/a
20	chr20:23732873-23732923	Hela-S3	cervix:	n/a
21	chr20:23732595-23732645	GM06990	blood:	n/a
22	chr20:23731367-23731417	GM12891	blood:	n/a
23	chr20:23728432-23728482	AG10803	skin:	n/a
24	chr20:23728814-23728864	HRE	kidney:	n/a
25	chr20:23732595-23732645	AG04449	skin:	fetal
26	chr20:23728432-23728482	ovcar-3	ovarian:	n/a
27	chr20:23728432-23728482	PrEC	prostate:	n/a
28	chr20:23732595-23732645	HL-60	blood:	n/a
29	chr20:23728814-23728864	SK-N-MC	brain:	n/a
30	chr20:23728432-23728482	LNCaP	prostate:	n/a
31	chr20:23731367-23731417	NH-A	brain:	n/a
32	chr20:23728814-23728864	Jurkat	blood:	n/a
33	chr20:23731367-23731417	HCF	heart:	n/a
34	chr20:23732595-23732645	H1-hESC	embryonic stem cell:	embryo
35	chr20:23728432-23728482	HCPEpiC	choroid plexus:	n/a
36	chr20:23731367-23731417	GM06990	blood:	n/a
37	chr20:23731367-23731417	K562	blood:	n/a
38	chr20:23732873-23732923	NH-A	brain:	n/a
39	chr20:23732595-23732645	NHBE	bronchial:	n/a
40	chr20:23732595-23732645	HepG2	liver:	n/a
41	chr20:23731367-23731417	HCM	heart:	n/a
42	chr20:23732595-23732645	AG09309	skin:	n/a
43	chr20:23728432-23728482	HRCEpiC	kidney:	n/a
44	chr20:23732873-23732923	Jurkat	blood:	n/a
45	chr20:23732873-23732923	HUVEC	blood vessel:	n/a
46	chr20:23728432-23728482	ProgFib	skin:	n/a
47	chr20:23732595-23732645	HAEpiC	amniotic membrane:	n/a
48	chr20:23728432-23728482	NT2-D1	testis:	n/a
49	chr20:23732595-23732645	Jurkat	blood:	n/a
50	chr20:23732595-23732645	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
2	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
3	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
4	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
5	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
6	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
7	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
2	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083
3	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083
4	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083

Variant related genes	Relation type
CST1	TF binding region
CST2P1	TF binding region
CST1	CpG island
CST2P1	CpG island

Extended variants
information (count: 2167 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2167 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190240261	chr20:23683447-23683448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529185842	chr20:23683448-23683449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73314070	chr20:23683463-23683464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75983304	chr20:23683483-23683484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79880137	chr20:23683494-23683495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367628203	chr20:23683513-23683514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114532615	chr20:23683515-23683516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150337892	chr20:23683519-23683520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116073552	chr20:23683523-23683524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199609701	chr20:23683534-23683535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181566335	chr20:23683544-23683545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536995569	chr20:23683546-23683547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79476765	chr20:23683551-23683552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386813390	chr20:23683569-23683570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567903271	chr20:23683570-23683571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370679770	chr20:23683584-23683585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374093276	chr20:23683625-23683626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149528234	chr20:23683633-23683634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553320168	chr20:23683637-23683638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536630061	chr20:23683663-23683664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573359071	chr20:23683721-23683722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376603882	chr20:23683739-23683740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386813391	chr20:23683778-23683779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538766476	chr20:23683780-23683781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7274621	chr20:23683809-23683810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs372128308	chr20:23683812-23683813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184509401	chr20:23683834-23683835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2405680	chr20:23683878-23683879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561326785	chr20:23683898-23683899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573888086	chr20:23683900-23683901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542877372	chr20:23683918-23683919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs8120071	chr20:23683933-23683934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528253554	chr20:23683955-23683956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116029924	chr20:23683957-23683958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111594634	chr20:23683963-23683964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141988269	chr20:23683965-23683966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113359083	chr20:23683971-23683972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117850918	chr20:23683978-23683979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188913221	chr20:23684030-23684031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567229588	chr20:23684073-23684074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11320649	chr20:23684101-23684102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111834044	chr20:23684111-23684112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527545722	chr20:23684177-23684178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs118000894	chr20:23684198-23684199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146331354	chr20:23684215-23684216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181315629	chr20:23684223-23684224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566735297	chr20:23684235-23684236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13039215	chr20:23684247-23684248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558723762	chr20:23684327-23684328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369133596	chr20:23684344-23684345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23682200-23684800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:23682800-23684000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr20:23684800-23685000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:23694000-23694400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr20:23694200-23694600	Enhancers	HMEC	breast
6	chr20:23695000-23695400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr20:23697800-23698600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr20:23698600-23698800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr20:23698800-23699400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr20:23700200-23701000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr20:23702200-23702400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr20:23703600-23704000	Enhancers	Left Ventricle	heart
13	chr20:23713600-23714200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:23714200-23719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr20:23715200-23716000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr20:23715400-23716400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr20:23719000-23719400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
20	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr20:23725400-23725800	Enhancers	Osteobl	bone
22	chr20:23725400-23726000	Enhancers	NHLF	lung
23	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
24	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
30	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:23728600-23729200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr20:23728800-23731400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr20:23729200-23730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr20:23730600-23730800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr20:23730600-23731000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr20:23730800-23731000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr20:23731000-23731200	Enhancers	H9 Cell Line	embryonic stem cell
49	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr20:23731200-23731400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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