Variant report

Variant	nsv1055248
Chromosome Location	chr20:23677900-23740341
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	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
2	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
3	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
4	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
5	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
6	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
7	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
8	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
9	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
10	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
11	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
12	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
13	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
14	CTCF	chr20:23704350-23704892	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
15	CTCF	chr20:23704340-23704490	GM12872	blood:	n/a	n/a
16	CTCF	chr20:23732332-23732473	K562	blood:	n/a	n/a
17	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
18	CTCF	chr20:23704080-23704230	GM12873	blood:	n/a	n/a
19	CTCF	chr20:23704300-23704674	IMR90	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
20	CTCF	chr20:23703638-23703722	MCF-7	breast:	n/a	n/a
21	CTCF	chr20:23704620-23704770	HMF	breast:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704740-23704758
22	CTCF	chr20:23688540-23688690	HepG2	liver:	n/a	n/a
23	CTCF	chr20:23729687-23729765	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr20:23704420-23704570	GM12872	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
25	CTCF	chr20:23704355-23704882	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
26	CTCF	chr20:23704360-23704510	AG04449	skin:	n/a	chr20:23704496-23704505
27	CTCF	chr20:23729767-23729821	MCF-7	breast:	n/a	n/a
28	CTCF	chr20:23704420-23704570	GM12874	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
29	CTCF	chr20:23736125-23736162	MCF-7	breast:	n/a	chr20:23736138-23736151
30	CTCF	chr20:23704380-23704530	GM12866	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
31	CTCF	chr20:23729640-23729790	HepG2	liver:	n/a	n/a
32	CTCF	chr20:23704380-23704530	HVMF	connective:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
33	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
34	CTCF	chr20:23729760-23729910	K562	blood:	n/a	n/a
35	CTCF	chr20:23704380-23704530	GM12864	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
36	CTCF	chr20:23704735-23704844	GM12878	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
37	CTCF	chr20:23704384-23704589	GM20000	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
38	CTCF	chr20:23704420-23704570	WERI-Rb-1	eye:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
39	CTCF	chr20:23729640-23729790	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr20:23704700-23704872	K562	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
41	CTCF	chr20:23704673-23704843	ProgFib	skin:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
42	CTCF	chr20:23704356-23704848	GM10266	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
43	CTCF	chr20:23704669-23704828	GM19240	blood:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
44	CTCF	chr20:23704360-23704510	HBMEC	blood vessel:	n/a	chr20:23704496-23704505
45	CTCF	chr20:23704920-23705070	HVMF	connective:	n/a	n/a
46	CTCF	chr20:23704380-23704530	NB4	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
47	CTCF	chr20:23729720-23729870	GM12875	blood:	n/a	n/a
48	CTCF	chr20:23704380-23704530	GM12867	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
49	CTCF	chr20:23704380-23704530	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
50	CTCF	chr20:23715700-23715850	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23728814-23728864	HIPEpiC	eye:	n/a
2	chr20:23728432-23728482	Jurkat	blood:	n/a
3	chr20:23731367-23731417	HCM	heart:	n/a
4	chr20:23731367-23731417	PrEC	prostate:	n/a
5	chr20:23731367-23731417	H1-hESC	embryonic stem cell:	embryo
6	chr20:23728432-23728482	AG10803	skin:	n/a
7	chr20:23732873-23732923	HNPCEpiC	eye:	n/a
8	chr20:23728814-23728864	GM12892	blood:	n/a
9	chr20:23728814-23728864	GM06990	blood:	n/a
10	chr20:23731367-23731417	SKMC	muscle:	n/a
11	chr20:23732595-23732645	HEEpiC	esophagus:	n/a
12	chr20:23731367-23731417	NHBE	bronchial:	n/a
13	chr20:23728432-23728482	HRPEpiC	eye:	n/a
14	chr20:23732873-23732923	GM19239	blood:	n/a
15	chr20:23728814-23728864	Jurkat	blood:	n/a
16	chr20:23728814-23728864	K562	blood:	n/a
17	chr20:23728814-23728864	HCT-116	colon:	n/a
18	chr20:23728814-23728864	NT2-D1	testis:	n/a
19	chr20:23732873-23732923	T-47D	breast:	n/a
20	chr20:23728432-23728482	GM12892	blood:	n/a
21	chr20:23732873-23732923	SK-N-SH_RA	brain:	n/a
22	chr20:23731367-23731417	SK-N-MC	brain:	n/a
23	chr20:23728814-23728864	HEK293	kidney:	embryo
24	chr20:23728432-23728482	Hela-S3	cervix:	n/a
25	chr20:23728814-23728864	AG10803	skin:	n/a
26	chr20:23732873-23732923	AG10803	skin:	n/a
27	chr20:23732873-23732923	HUVEC	blood vessel:	n/a
28	chr20:23728814-23728864	HNPCEpiC	eye:	n/a
29	chr20:23732595-23732645	AG09309	skin:	n/a
30	chr20:23732595-23732645	SK-N-SH_RA	brain:	n/a
31	chr20:23731367-23731417	AoSMC	blood vessel:	n/a
32	chr20:23732595-23732645	SK-N-SH	brain:	n/a
33	chr20:23728814-23728864	IMR90	lung:	fetal
34	chr20:23732595-23732645	HL-60	blood:	n/a
35	chr20:23732595-23732645	PFSK-1	brain:	n/a
36	chr20:23731367-23731417	NHDF-neo	bronchial:	n/a
37	chr20:23728432-23728482	ovcar-3	ovarian:	n/a
38	chr20:23728432-23728482	HNPCEpiC	eye:	n/a
39	chr20:23731367-23731417	AG04450	lung:	fetal
40	chr20:23728432-23728482	HIPEpiC	eye:	n/a
41	chr20:23732873-23732923	AG09309	skin:	n/a
42	chr20:23728814-23728864	HRPEpiC	eye:	n/a
43	chr20:23728432-23728482	U87	brain:	n/a
44	chr20:23728814-23728864	AG04450	lung:	fetal
45	chr20:23732873-23732923	HAEpiC	amniotic membrane:	n/a
46	chr20:23728432-23728482	HUVEC	blood vessel:	n/a
47	chr20:23731367-23731417	BJ	skin:	n/a
48	chr20:23728432-23728482	HCF	heart:	n/a
49	chr20:23732873-23732923	SKMC	muscle:	n/a
50	chr20:23731367-23731417	AG10803	skin:	n/a

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

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

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

Extended variants
information (count: 2114 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2114 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139245693	chr20:23677930-23677931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543326648	chr20:23677957-23677958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs8118801	chr20:23677979-23677980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs34438831	chr20:23678037-23678038	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs545501786	chr20:23678051-23678052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565196644	chr20:23678055-23678056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530819479	chr20:23678056-23678057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563721961	chr20:23678063-23678064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550610114	chr20:23678073-23678074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560939334	chr20:23678101-23678102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192510083	chr20:23678102-23678103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548985973	chr20:23678120-23678121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371065771	chr20:23678122-23678123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183839423	chr20:23678132-23678133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149994201	chr20:23678136-23678137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551458333	chr20:23678140-23678141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374381099	chr20:23678182-23678183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571413756	chr20:23678252-23678253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73902134	chr20:23678305-23678306	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs188797848	chr20:23678357-23678358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6076116	chr20:23678358-23678359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146576011	chr20:23678364-23678365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371848072	chr20:23678369-23678370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553359224	chr20:23678400-23678401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192860199	chr20:23678401-23678402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111593977	chr20:23678412-23678413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575374450	chr20:23678421-23678422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs397864452	chr20:23678452-23678453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1538908	chr20:23678464-23678465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1538909	chr20:23678467-23678468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4602282	chr20:23678500-23678501	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542917809	chr20:23678521-23678522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1538910	chr20:23678551-23678552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs561586980	chr20:23678568-23678569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551326951	chr20:23678587-23678588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571449350	chr20:23678608-23678609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184261492	chr20:23678645-23678646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139722613	chr20:23678654-23678655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34009670	chr20:23678659-23678660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550664783	chr20:23678675-23678676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550704588	chr20:23678687-23678688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143708659	chr20:23678692-23678693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146837674	chr20:23678706-23678707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567099695	chr20:23678745-23678746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539312361	chr20:23678765-23678766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558762431	chr20:23678807-23678808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187046471	chr20:23678832-23678833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562664390	chr20:23678862-23678863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs118105956	chr20:23678889-23678890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs947010	chr20:23678890-23678891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23675800-23681600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:23676400-23679200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr20:23677800-23678600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr20:23678000-23678200	Enhancers	GM12878-XiMat	blood
5	chr20:23679200-23680600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:23679800-23680000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr20:23680000-23681800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr20:23681200-23681400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr20:23681400-23682800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr20:23681600-23682200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr20:23681800-23683000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr20:23682200-23684800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr20:23682400-23683000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr20:23682800-23684000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr20:23684800-23685000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr20:23694000-23694400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr20:23694200-23694600	Enhancers	HMEC	breast
18	chr20:23695000-23695400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr20:23697800-23698600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr20:23698600-23698800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr20:23698800-23699400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr20:23700200-23701000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr20:23702200-23702400	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr20:23703600-23704000	Enhancers	Left Ventricle	heart
25	chr20:23713600-23714200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr20:23714200-23719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr20:23715200-23716000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr20:23715400-23716400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr20:23719000-23719400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
32	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr20:23725400-23725800	Enhancers	Osteobl	bone
34	chr20:23725400-23726000	Enhancers	NHLF	lung
35	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
36	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
42	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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