Variant report

Variant	nsv1059419
Chromosome Location	chr20:23675365-23750153
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	chr20:23747026-23747352	A549	lung:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747029-23747041 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
2	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
3	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
4	CEBPB	chr20:23747142-23747274	K562	blood:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
5	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
6	CEBPB	chr20:23747045-23747345	HepG2	liver:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
7	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
8	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
9	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
10	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
11	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
12	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
13	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
14	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
15	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
16	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
17	CTCF	chr20:23704860-23705010	HFF	foreskin:	n/a	n/a
18	CTCF	chr20:23729720-23729870	GM12875	blood:	n/a	n/a
19	CTCF	chr20:23704380-23704530	GM12873	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
20	CTCF	chr20:23729640-23729790	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr20:23704340-23704490	GM06990	blood:	n/a	n/a
22	CTCF	chr20:23704340-23704490	GM12878	blood:	n/a	n/a
23	CTCF	chr20:23715700-23715850	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr20:23729447-23729530	GM19239	blood:	n/a	n/a
25	CTCF	chr20:23704191-23704227	GM19240	blood:	n/a	n/a
26	CTCF	chr20:23729713-23729903	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr20:23704403-23704695	Kidney_OC	kidney:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
28	CTCF	chr20:23729821-23729900	GM13977	blood:	n/a	n/a
29	CTCF	chr20:23704735-23704844	GM12878	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
30	CTCF	chr20:23729741-23729801	GM19239	blood:	n/a	n/a
31	CTCF	chr20:23704340-23704490	AG09319	gingival:	n/a	n/a
32	CTCF	chr20:23704346-23704900	HUVEC	blood vessel:	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	chr20:23701861-23701880	LNCaP	prostate:	n/a	n/a
34	CTCF	chr20:23704420-23704570	GM12875	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
35	CTCF	chr20:23704340-23704490	HCFaa	heart:	n/a	n/a
36	CTCF	chr20:23704337-23704656	GM12878	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
37	CTCF	chr20:23704420-23704570	HCPEpiC	choroid plexus:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
38	CTCF	chr20:23704340-23704490	BE2_C	brain:	n/a	n/a
39	CTCF	chr20:23704380-23704530	HRPEpiC	eye:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
40	CTCF	chr20:23677891-23677951	GM20000	blood:	n/a	n/a
41	CTCF	chr20:23704880-23705030	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr20:23729676-23729700	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr20:23704375-23704634	Spleen_OC	spleen:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
44	CTCF	chr20:23704381-23704601	Lung_OC	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
45	CTCF	chr20:23704340-23704490	AG10803	skin:	n/a	n/a
46	CTCF	chr20:23704360-23704510	Hela-S3	cervix:	n/a	chr20:23704496-23704505
47	CTCF	chr20:23704340-23704490	GM12864	blood:	n/a	n/a
48	CTCF	chr20:23704640-23704790	GM12864	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704740-23704758
49	CTCF	chr20:23704657-23704875	H1-hESC	embryonic stem cell:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
50	CTCF	chr20:23704340-23704490	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23728814-23728864	HRE	kidney:	n/a
2	chr20:23728814-23728864	HRE	kidney:	n/a
3	chr20:23732595-23732645	PrEC	prostate:	n/a
4	chr20:23732595-23732645	NHBE	bronchial:	n/a
5	chr20:23732873-23732923	GM06990	blood:	n/a
6	chr20:23731367-23731417	GM12878	blood:	n/a
7	chr20:23728814-23728864	LNCaP	prostate:	n/a
8	chr20:23732595-23732645	RPTEC	kidney:	n/a
9	chr20:23728814-23728864	RPTEC	kidney:	n/a
10	chr20:23728814-23728864	Jurkat	blood:	n/a
11	chr20:23732595-23732645	HRPEpiC	eye:	n/a
12	chr20:23732873-23732923	HCF	heart:	n/a
13	chr20:23732873-23732923	LNCaP	prostate:	n/a
14	chr20:23728814-23728864	U87	brain:	n/a
15	chr20:23728814-23728864	AG10803	skin:	n/a
16	chr20:23728432-23728482	AG10803	skin:	n/a
17	chr20:23728432-23728482	LNCaP	prostate:	n/a
18	chr20:23728432-23728482	SKMC	muscle:	n/a
19	chr20:23731367-23731417	Jurkat	blood:	n/a
20	chr20:23728432-23728482	HRCEpiC	kidney:	n/a
21	chr20:23728814-23728864	HCM	heart:	n/a
22	chr20:23728432-23728482	A549	lung:	n/a
23	chr20:23728432-23728482	HCT-116	colon:	n/a
24	chr20:23732595-23732645	HL-60	blood:	n/a
25	chr20:23731367-23731417	ovcar-3	ovarian:	n/a
26	chr20:23732595-23732645	HEK293	kidney:	embryo
27	chr20:23731367-23731417	HNPCEpiC	eye:	n/a
28	chr20:23728814-23728864	HNPCEpiC	eye:	n/a
29	chr20:23732595-23732645	HCF	heart:	n/a
30	chr20:23728432-23728482	Hepatocyte	liver:	n/a
31	chr20:23732595-23732645	ECC-1	luminal epithelium:	n/a
32	chr20:23731367-23731417	SK-N-SH_RA	brain:	n/a
33	chr20:23728814-23728864	GM12891	blood:	n/a
34	chr20:23728432-23728482	U87	brain:	n/a
35	chr20:23728814-23728864	MCF-7	breast:	n/a
36	chr20:23732873-23732923	AG09319	gingival:	n/a
37	chr20:23732595-23732645	GM12892	blood:	n/a
38	chr20:23728432-23728482	AG09319	gingival:	n/a
39	chr20:23731367-23731417	BJ	skin:	n/a
40	chr20:23732595-23732645	SK-N-MC	brain:	n/a
41	chr20:23731367-23731417	Caco-2	colon:	n/a
42	chr20:23728814-23728864	HEEpiC	esophagus:	n/a
43	chr20:23728814-23728864	Hela-S3	cervix:	n/a
44	chr20:23728814-23728864	NT2-D1	testis:	n/a
45	chr20:23732873-23732923	HL-60	blood:	n/a
46	chr20:23728432-23728482	HIPEpiC	eye:	n/a
47	chr20:23731367-23731417	U87	brain:	n/a
48	chr20:23732595-23732645	NB4	blood:	n/a
49	chr20:23732873-23732923	AG10803	skin:	n/a
50	chr20:23728432-23728482	MCF10A-Er-Src	breast:	n/a

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

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

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

Extended variants
information (count: 2788 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2788 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184690798	chr20:23675421-23675422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188395161	chr20:23675422-23675423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148934359	chr20:23675453-23675454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375083256	chr20:23675464-23675465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180764268	chr20:23675489-23675490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548480307	chr20:23675578-23675579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186484682	chr20:23675586-23675587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534216512	chr20:23675589-23675590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547712715	chr20:23675604-23675605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571012431	chr20:23675636-23675637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202063145	chr20:23675638-23675639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7269105	chr20:23675668-23675669	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556594816	chr20:23675672-23675673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576522381	chr20:23675688-23675689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566628468	chr20:23675704-23675705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373506256	chr20:23675716-23675717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535809050	chr20:23675771-23675772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376744758	chr20:23675799-23675800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574832563	chr20:23675807-23675808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540505893	chr20:23675826-23675827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560116789	chr20:23675843-23675844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576939581	chr20:23675844-23675845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534258977	chr20:23675856-23675857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569154723	chr20:23675880-23675881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114902504	chr20:23675886-23675887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs8121100	chr20:23675898-23675899	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs151072618	chr20:23675946-23675947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577340261	chr20:23675989-23675990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189305948	chr20:23675997-23675998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548049713	chr20:23676035-23676036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570980780	chr20:23676126-23676127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539991036	chr20:23676130-23676131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550017839	chr20:23676175-23676176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570118188	chr20:23676211-23676212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6036485	chr20:23676216-23676217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555838711	chr20:23676218-23676219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187156738	chr20:23676228-23676229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386813386	chr20:23676259-23676260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533865521	chr20:23676298-23676299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553998658	chr20:23676308-23676309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576973441	chr20:23676346-23676347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545934946	chr20:23676358-23676359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538034661	chr20:23676370-23676371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7270964	chr20:23676406-23676407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs6048999	chr20:23676414-23676415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs370462464	chr20:23676433-23676434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200331867	chr20:23676492-23676493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574422190	chr20:23676496-23676497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373961393	chr20:23676572-23676573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367699638	chr20:23676585-23676586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23671400-23676000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr20:23672000-23675800	Enhancers	HUVEC	blood vessel
3	chr20:23672200-23675800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:23673200-23676400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:23673400-23675800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr20:23673400-23676000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr20:23674000-23676400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr20:23674400-23675400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr20:23674400-23675400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr20:23674600-23675600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr20:23674600-23676000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr20:23674800-23675800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr20:23674800-23675800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr20:23675000-23675800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr20:23675000-23675800	Enhancers	HepG2	liver
16	chr20:23675000-23676400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr20:23675200-23675600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr20:23675200-23675800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr20:23675200-23676000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr20:23675200-23676400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr20:23675400-23675800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr20:23675400-23675800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr20:23675600-23675800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr20:23675800-23677800	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr20:23675800-23681600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr20:23676400-23679200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr20:23677800-23678600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr20:23678000-23678200	Enhancers	GM12878-XiMat	blood
29	chr20:23679200-23680600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:23679800-23680000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr20:23680000-23681800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr20:23681200-23681400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr20:23681400-23682800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr20:23681600-23682200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr20:23681800-23683000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr20:23682200-23684800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr20:23682400-23683000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr20:23682800-23684000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr20:23684800-23685000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr20:23694000-23694400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr20:23694200-23694600	Enhancers	HMEC	breast
42	chr20:23695000-23695400	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr20:23697800-23698600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr20:23698600-23698800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr20:23698800-23699400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr20:23700200-23701000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr20:23702200-23702400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr20:23703600-23704000	Enhancers	Left Ventricle	heart
49	chr20:23713600-23714200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr20:23714200-23719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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