Variant report

Variant	nsv820681
Chromosome Location	chr20:25731048-25780918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:62)
Chromatin interactive
region (count:2)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr20:25734352-25734580	GM12878	blood:	n/a	n/a
2	BCL11A	chr20:25775154-25775349	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:25756665-25756856	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:25737731-25737913	GM12878	blood:	n/a	n/a
5	BHLHE40	chr20:25731988-25732189	K562	blood:	n/a	n/a
6	BRCA1	chr20:25731987-25732070	HepG2	liver:	n/a	n/a
7	CEBPB	chr20:25775210-25775358	K562	blood:	n/a	n/a
8	CEBPB	chr20:25775261-25775345	K562	blood:	n/a	n/a
9	CEBPB	chr20:25741823-25742042	HepG2	liver:	n/a	chr20:25741983-25741994
10	CEBPB	chr20:25741860-25742060	K562	blood:	n/a	chr20:25741983-25741994
11	CEBPB	chr20:25731932-25732389	HepG2	liver:	n/a	n/a
12	CEBPB	chr20:25736429-25736642	HepG2	liver:	n/a	chr20:25736503-25736514 chr20:25736533-25736544
13	CEBPB	chr20:25741990-25742017	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr20:25731486-25732115	HepG2	liver:	n/a	n/a
15	CHD1	chr20:25741744-25742036	IMR90	lung:	n/a	n/a
16	CHD2	chr20:25731489-25731592	HepG2	liver:	n/a	n/a
17	CTCF	chr20:25758100-25758250	A549	lung:	n/a	n/a
18	CTCF	chr20:25735404-25735632	LNCaP	prostate:	n/a	n/a
19	CTCF	chr20:25741780-25741930	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr20:25741900-25742050	HFF	foreskin:	n/a	n/a
21	CTCF	chr20:25741760-25741910	GM12864	blood:	n/a	n/a
22	CTCF	chr20:25776869-25777062	K562	blood:	n/a	n/a
23	CTCF	chr20:25732195-25732293	MCF-7	breast:	n/a	n/a
24	CTCF	chr20:25770966-25771003	Lung_OC	lung:	n/a	n/a
25	CTCF	chr20:25732160-25732310	MCF-7	breast:	n/a	n/a
26	CTCF	chr20:25732220-25732370	MCF-7	breast:	n/a	n/a
27	CTCF	chr20:25776947-25777055	K562	blood:	n/a	n/a
28	CTCF	chr20:25740060-25740210	HepG2	liver:	n/a	n/a
29	CTCF	chr20:25776862-25777134	K562	blood:	n/a	n/a
30	CTCF	chr20:25770956-25770960	Lung_OC	lung:	n/a	n/a
31	CTCF	chr20:25737920-25738070	WI-38	lung:	n/a	n/a
32	CTCF	chr20:25741700-25741850	GM12869	blood:	n/a	n/a
33	CTCF	chr20:25735410-25735655	LNCaP	prostate:	n/a	n/a
34	CTCF	chr20:25741840-25741990	WI-38	lung:	n/a	n/a
35	CTCF	chr20:25732194-25732317	MCF-7	breast:	n/a	n/a
36	CTCF	chr20:25742480-25742630	MCF-7	breast:	n/a	n/a
37	CUX1	chr20:25731567-25731602	K562	blood:	n/a	n/a
38	CUX1	chr20:25741855-25742028	GM12878	blood:	n/a	n/a
39	E2F6	chr20:25731807-25731981	K562	blood:	n/a	n/a
40	EBF1	chr20:25748749-25748970	GM12878	blood:	n/a	n/a
41	EBF1	chr20:25777479-25777661	GM12878	blood:	n/a	n/a
42	EGR1	chr20:25731806-25732260	ECC-1	luminal epithelium:	n/a	chr20:25732030-25732040 chr20:25732103-25732127 chr20:25732030-25732039 chr20:25732030-25732041 chr20:25732030-25732040 chr20:25732029-25732042 chr20:25732030-25732041 chr20:25732028-25732042
43	EGR1	chr20:25731443-25732329	MCF-7	breast:	n/a	chr20:25732030-25732040 chr20:25732103-25732127 chr20:25732030-25732039 chr20:25732030-25732041 chr20:25732030-25732040 chr20:25732029-25732042 chr20:25731749-25731758 chr20:25732030-25732041 chr20:25732028-25732042
44	EGR1	chr20:25731924-25732082	K562	blood:	n/a	chr20:25732030-25732040 chr20:25732030-25732039 chr20:25732030-25732041 chr20:25732030-25732040 chr20:25732029-25732042 chr20:25732030-25732041 chr20:25732028-25732042
45	EP300	chr20:25775090-25775420	GM12878	blood:	n/a	n/a
46	EP300	chr20:25731536-25731557	HepG2	liver:	n/a	n/a
47	EP300	chr20:25775207-25775374	GM12878	blood:	n/a	n/a
48	EP300	chr20:25731967-25732126	HepG2	liver:	n/a	n/a
49	EP300	chr20:25740283-25740289	GM12878	blood:	n/a	n/a
50	EP300	chr20:25765241-25765559	GM12878	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25755634-25755684	HRCEpiC	kidney:	n/a
2	chr20:25755634-25755684	HRCEpiC	kidney:	n/a
3	chr20:25755634-25755684	HCT-116	colon:	n/a
4	chr20:25755634-25755684	Caco-2	colon:	n/a
5	chr20:25755634-25755684	SAEC	small airway:	n/a
6	chr20:25755634-25755684	AG10803	skin:	n/a
7	chr20:25755634-25755684	BJ	skin:	n/a
8	chr20:25755634-25755684	AG09309	skin:	n/a
9	chr20:25755634-25755684	ovcar-3	ovarian:	n/a
10	chr20:25755634-25755684	NHDF-neo	bronchial:	n/a
11	chr20:25755634-25755684	BE2_C	brain:	n/a
12	chr20:25755634-25755684	HEEpiC	esophagus:	n/a
13	chr20:25755634-25755684	HRPEpiC	eye:	n/a
14	chr20:25755634-25755684	NT2-D1	testis:	n/a
15	chr20:25755634-25755684	HIPEpiC	eye:	n/a
16	chr20:25755634-25755684	SKMC	muscle:	n/a
17	chr20:25755634-25755684	AG09319	gingival:	n/a
18	chr20:25755634-25755684	Jurkat	blood:	n/a
19	chr20:25755634-25755684	HNPCEpiC	eye:	n/a
20	chr20:25755634-25755684	LNCaP	prostate:	n/a
21	chr20:25755634-25755684	HAEpiC	amniotic membrane:	n/a
22	chr20:25755634-25755684	HCF	heart:	n/a
23	chr20:25755634-25755684	HCPEpiC	choroid plexus:	n/a
24	chr20:25755634-25755684	HUVEC	blood vessel:	n/a
25	chr20:25755634-25755684	Hepatocyte	liver:	n/a
26	chr20:25755634-25755684	AG04449	skin:	fetal
27	chr20:25755634-25755684	RPTEC	kidney:	n/a
28	chr20:25755634-25755684	K562	blood:	n/a
29	chr20:25755634-25755684	IMR90	lung:	fetal
30	chr20:25755634-25755684	HPAEpiC	pulmonary alveolar:	n/a
31	chr20:25755634-25755684	NHBE	bronchial:	n/a
32	chr20:25755634-25755684	SK-N-SH_RA	brain:	n/a
33	chr20:25755634-25755684	PrEC	prostate:	n/a
34	chr20:25755634-25755684	ProgFib	skin:	n/a
35	chr20:25755634-25755684	SK-N-MC	brain:	n/a
36	chr20:25755634-25755684	NH-A	brain:	n/a
37	chr20:25755634-25755684	SK-N-SH	brain:	n/a
38	chr20:25755634-25755684	U87	brain:	n/a
39	chr20:25755634-25755684	PANC-1	pancreas:	n/a
40	chr20:25755634-25755684	HMEC	breast:	n/a
41	chr20:25755634-25755684	MCF-7	breast:	n/a
42	chr20:25755634-25755684	HepG2	liver:	n/a
43	chr20:25755634-25755684	AoSMC	blood vessel:	n/a
44	chr20:25755634-25755684	HL-60	blood:	n/a
45	chr20:25755634-25755684	ECC-1	luminal epithelium:	n/a
46	chr20:25755634-25755684	NB4	blood:	n/a
47	chr20:25755634-25755684	GM12878	blood:	n/a
48	chr20:25755634-25755684	HRE	kidney:	n/a
49	chr20:25755634-25755684	GM06990	blood:	n/a
50	chr20:25755634-25755684	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:25722229..25725727-chr20:25729009..25731451,3	MCF-7	breast:
2	chr20:25727469..25729069-chr20:25729208..25731767,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GINS1-2	chr20:25731813-25731974	NONHSAT079184
2	lnc-GINS1-2	chr20:25731854-25731974	ENSG00000226465.1
3	lnc-FAM182B-8	chr20:25755746-25755948	NONHSAT079187
4	lnc-FAM182B-8	chr20:25750234-25754795	NONHSAT079187
5	lnc-FAM182B-8	chr20:25755746-25755908	NONHSAT147160
6	lnc-GINS1-2	chr20:25733199-25733422	NONHSAT079184
7	lnc-FAM182B-8	chr20:25754652-25754795	NONHSAT147160
8	lnc-FAM182B-8	chr20:25767381-25767624	NONHSAT079187
9	lnc-GINS1-2	chr20:25731520-25731591	NONHSAT079183
10	lnc-GINS1-2	chr20:25733199-25733397	ENSG00000226465.1
11	lnc-GINS1-2	chr20:25733199-25733422	NONHSAT079183
12	lnc-FAM182B-1	chr20:25730940-25732440	XLOC_013708

No data

Variant related genes	Relation type
FAM182B	TF binding region
ENSG00000226465	TF binding region
FAM182B	CpG island
ENSG00000226465	CpG island
PTPMT1	miRNA target sites

Extended variants
information (count: 1458 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6138652	chr20:25731063-25731064	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs542634457	chr20:25731160-25731161	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs558740817	chr20:25731183-25731184	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs186251946	chr20:25731190-25731191	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs577438728	chr20:25731228-25731229	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs528569084	chr20:25731241-25731242	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs551813670	chr20:25731248-25731249	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs541569603	chr20:25731273-25731274	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs565383633	chr20:25731294-25731295	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs35016365	chr20:25731296-25731297	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs573642289	chr20:25731314-25731315	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs372598712	chr20:25731319-25731320	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs574821662	chr20:25731384-25731385	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs6115276	chr20:25731401-25731402	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs60744587	chr20:25731429-25731430	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6115277	chr20:25731440-25731441	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs6115278	chr20:25731489-25731490	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs567543438	chr20:25731505-25731506	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs541846539	chr20:25731506-25731507	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs141312693	chr20:25731510-25731511	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs57150489	chr20:25731671-25731672	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538257717	chr20:25731694-25731695	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs558201460	chr20:25731712-25731713	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs564016440	chr20:25731729-25731730	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs575010667	chr20:25731742-25731743	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs369409506	chr20:25731767-25731768	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs557160804	chr20:25731819-25731820	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs556492701	chr20:25731832-25731833	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs372050261	chr20:25731846-25731847	Active TSS Bivalent/Poised TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs575484542	chr20:25731869-25731870	Active TSS Bivalent/Poised TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs77584066	chr20:25731875-25731876	Active TSS Bivalent/Poised TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs370846516	chr20:25731938-25731939	Active TSS Bivalent/Poised TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs191824429	chr20:25731955-25731956	Active TSS Bivalent/Poised TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs564307260	chr20:25731990-25731991	Active TSS Bivalent/Poised TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs199906708	chr20:25731996-25731997	Active TSS Bivalent/Poised TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs79601323	chr20:25732026-25732027	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
37	rs200666859	chr20:25732070-25732071	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
38	rs145046246	chr20:25732072-25732073	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
39	rs545443773	chr20:25732150-25732151	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
40	rs565346993	chr20:25732160-25732161	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
41	rs183235737	chr20:25732238-25732239	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
42	rs576040709	chr20:25732243-25732244	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
43	rs76603506	chr20:25732267-25732268	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
44	rs551276382	chr20:25732283-25732284	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
45	rs66983770	chr20:25732343-25732344	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs80216239	chr20:25732385-25732386	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
47	rs529856397	chr20:25732403-25732404	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
48	rs114175690	chr20:25732430-25732431	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	lncRNA	n/a	Overlapped CNVs	n/a
49	rs138984769	chr20:25732443-25732444	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs532098006	chr20:25732461-25732462	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25708000-25731400	Weak transcription	Esophagus	oesophagus
2	chr20:25714400-25731200	Weak transcription	Pancreas	Pancrea
3	chr20:25715600-25731400	Weak transcription	Aorta	Aorta
4	chr20:25724400-25731400	Weak transcription	Brain Angular Gyrus	brain
5	chr20:25726000-25731200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr20:25726000-25731400	Weak transcription	HMEC	breast
7	chr20:25726200-25731200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr20:25726200-25731200	Weak transcription	NHEK	skin
9	chr20:25728600-25731400	Weak transcription	Gastric	stomach
10	chr20:25728800-25731200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr20:25730600-25731400	Enhancers	Colon Smooth Muscle	Colon
12	chr20:25730600-25732400	Active TSS	Rectal Smooth Muscle	rectum
13	chr20:25731000-25731200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr20:25731000-25731200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr20:25731000-25731200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr20:25731000-25731200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr20:25731000-25731200	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr20:25731000-25731200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr20:25731000-25731200	Enhancers	Adipose Nuclei	Adipose
20	chr20:25731000-25731200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr20:25731000-25731200	Enhancers	A549	lung
22	chr20:25731000-25731400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr20:25731000-25731400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr20:25731000-25731400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr20:25731000-25731400	Enhancers	Fetal Thymus	thymus
26	chr20:25731000-25731400	Enhancers	Left Ventricle	heart
27	chr20:25731000-25731400	Enhancers	GM12878-XiMat	blood
28	chr20:25731000-25731400	Flanking Active TSS	HepG2	liver
29	chr20:25731200-25731400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr20:25731200-25731400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr20:25731200-25731400	Enhancers	Primary B cells from peripheral blood	blood
32	chr20:25731200-25731400	Enhancers	Primary hematopoietic stem cells	blood
33	chr20:25731200-25731400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr20:25731200-25731400	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr20:25731200-25731400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr20:25731200-25731400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr20:25731200-25731400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr20:25731200-25731400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr20:25731200-25731400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr20:25731200-25731400	Enhancers	Liver	Liver
41	chr20:25731200-25731400	Enhancers	Fetal Lung	lung
42	chr20:25731200-25731400	Enhancers	Fetal Muscle Trunk	muscle
43	chr20:25731200-25731400	Enhancers	Fetal Muscle Leg	muscle
44	chr20:25731200-25731400	Bivalent Enhancer	Placenta	Placenta
45	chr20:25731200-25731400	Enhancers	Fetal Stomach	stomach
46	chr20:25731200-25731400	Enhancers	Ovary	ovary
47	chr20:25731200-25731400	Enhancers	Pancreas	Pancrea
48	chr20:25731200-25731400	Enhancers	Right Atrium	heart
49	chr20:25731200-25731400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr20:25731200-25731400	Enhancers	Stomach Smooth Muscle	stomach

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