Variant report

Variant	esv2762068
Chromosome Location	chr20:24908860-24974986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1363)
CpG islands
(count:1162)
Chromatin interactive
region (count:51)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:24967944-24968352	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:24973296-24974567	HepG2	liver:	n/a	n/a
3	ATF1	chr20:24973246-24973765	K562	blood:	n/a	n/a
4	ATF1	chr20:24929614-24929792	K562	blood:	n/a	n/a
5	ATF2	chr20:24973181-24973726	GM12878	blood:	n/a	n/a
6	ATF3	chr20:24973308-24973589	K562	blood:	n/a	n/a
7	BACH1	chr20:24973119-24973730	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr20:24911107-24911328	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr20:24910908-24911117	GM12878	blood:	n/a	n/a
10	BCL3	chr20:24967861-24968253	GM12878	blood:	n/a	n/a
11	BCL3	chr20:24973091-24974085	A549	lung:	n/a	chr20:24973526-24973535
12	BCL3	chr20:24960955-24961618	GM12878	blood:	n/a	n/a
13	BCL3	chr20:24972617-24973771	A549	lung:	n/a	chr20:24973526-24973535
14	BCL3	chr20:24960904-24961578	GM12878	blood:	n/a	n/a
15	BCLAF1	chr20:24973139-24973792	GM12878	blood:	n/a	chr20:24973526-24973535
16	BCLAF1	chr20:24972912-24973862	GM12878	blood:	n/a	chr20:24973526-24973535
17	BHLHE40	chr20:24973004-24973916	GM12878	blood:	n/a	n/a
18	BHLHE40	chr20:24941606-24941880	GM12878	blood:	n/a	n/a
19	BHLHE40	chr20:24935541-24936134	GM12878	blood:	n/a	n/a
20	BHLHE40	chr20:24972706-24973888	HepG2	liver:	n/a	n/a
21	BHLHE40	chr20:24930500-24930689	K562	blood:	n/a	n/a
22	BHLHE40	chr20:24972688-24973890	K562	blood:	n/a	n/a
23	BRCA1	chr20:24972738-24972796	HepG2	liver:	n/a	n/a
24	BRCA1	chr20:24943336-24943356	HepG2	liver:	n/a	n/a
25	BRCA1	chr20:24972660-24972852	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr20:24973183-24973856	HepG2	liver:	n/a	n/a
27	BRCA1	chr20:24973260-24973676	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr20:24973338-24973434	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr20:24973023-24973383	GM12878	blood:	n/a	n/a
30	CBX3	chr20:24973220-24973878	K562	blood:	n/a	n/a
31	CCNT2	chr20:24972881-24973726	K562	blood:	n/a	chr20:24973450-24973459
32	CEBPB	chr20:24973173-24973941	GM12878	blood:	n/a	n/a
33	CEBPB	chr20:24969813-24970157	HepG2	liver:	n/a	chr20:24969988-24969999 chr20:24970032-24970043
34	CEBPB	chr20:24967984-24968332	A549	lung:	n/a	n/a
35	CEBPB	chr20:24967935-24968346	IMR90	lung:	n/a	n/a
36	CEBPB	chr20:24966043-24966247	HepG2	liver:	n/a	chr20:24966165-24966176
37	CEBPB	chr20:24932722-24932922	HepG2	liver:	n/a	n/a
38	CEBPB	chr20:24967950-24968350	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr20:24911058-24911415	MCF-7	breast:	n/a	n/a
40	CEBPB	chr20:24973435-24973644	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr20:24967888-24968349	HepG2	liver:	n/a	n/a
42	CEBPB	chr20:24911036-24911479	MCF-7	breast:	n/a	n/a
43	CEBPB	chr20:24967962-24968270	K562	blood:	n/a	n/a
44	CEBPB	chr20:24911081-24911323	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr20:24968794-24969303	HepG2	liver:	n/a	chr20:24968929-24968941
46	CEBPB	chr20:24967890-24968308	MCF-7	breast:	n/a	n/a
47	CEBPB	chr20:24967894-24968259	HepG2	liver:	n/a	n/a
48	CEBPB	chr20:24967975-24968259	HepG2	liver:	n/a	n/a
49	CEBPB	chr20:24967916-24968391	HepG2	liver:	n/a	n/a
50	CEBPB	chr20:24973286-24973630	HepG2	liver:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:24974362-24974412	HRCEpiC	kidney:	n/a
2	chr20:24933798-24933848	ECC-1	luminal epithelium:	n/a
3	chr20:24972666-24972716	U87	brain:	n/a
4	chr20:24974362-24974412	HRCEpiC	kidney:	n/a
5	chr20:24933798-24933848	ECC-1	luminal epithelium:	n/a
6	chr20:24972666-24972716	U87	brain:	n/a
7	chr20:24929695-24929745	HCT-116	colon:	n/a
8	chr20:24929716-24929766	HCPEpiC	choroid plexus:	n/a
9	chr20:24973756-24973806	GM19239	blood:	n/a
10	chr20:24930041-24930091	MCF-7	breast:	n/a
11	chr20:24929687-24929737	HEK293	kidney:	embryo
12	chr20:24929822-24929872	GM12892	blood:	n/a
13	chr20:24933798-24933848	Caco-2	colon:	n/a
14	chr20:24973309-24973359	HCT-116	colon:	n/a
15	chr20:24930099-24930149	SKMC	muscle:	n/a
16	chr20:24930041-24930091	HEK293	kidney:	embryo
17	chr20:24969842-24969892	A549	lung:	n/a
18	chr20:24929716-24929766	HMEC	breast:	n/a
19	chr20:24973309-24973359	SAEC	small airway:	n/a
20	chr20:24940490-24940540	HCF	heart:	n/a
21	chr20:24973309-24973359	IMR90	lung:	fetal
22	chr20:24973309-24973359	Hela-S3	cervix:	n/a
23	chr20:24929822-24929872	HCM	heart:	n/a
24	chr20:24933798-24933848	HAEpiC	amniotic membrane:	n/a
25	chr20:24929695-24929745	Hepatocyte	liver:	n/a
26	chr20:24929695-24929745	ECC-1	luminal epithelium:	n/a
27	chr20:24973756-24973806	NH-A	brain:	n/a
28	chr20:24929716-24929766	HCM	heart:	n/a
29	chr20:24929607-24929657	H1-hESC	embryonic stem cell:	embryo
30	chr20:24929607-24929657	GM12892	blood:	n/a
31	chr20:24940490-24940540	NH-A	brain:	n/a
32	chr20:24973333-24973383	AG10803	skin:	n/a
33	chr20:24974362-24974412	NHBE	bronchial:	n/a
34	chr20:24929716-24929766	Jurkat	blood:	n/a
35	chr20:24974362-24974412	AG04450	lung:	fetal
36	chr20:24973699-24973749	SK-N-SH_RA	brain:	n/a
37	chr20:24974362-24974412	HCF	heart:	n/a
38	chr20:24930041-24930091	HAEpiC	amniotic membrane:	n/a
39	chr20:24973333-24973383	GM19239	blood:	n/a
40	chr20:24972666-24972716	HRE	kidney:	n/a
41	chr20:24973309-24973359	PFSK-1	brain:	n/a
42	chr20:24944010-24944060	PFSK-1	brain:	n/a
43	chr20:24973756-24973806	ECC-1	luminal epithelium:	n/a
44	chr20:24929695-24929745	RPTEC	kidney:	n/a
45	chr20:24929822-24929872	Hela-S3	cervix:	n/a
46	chr20:24929607-24929657	Hepatocyte	liver:	n/a
47	chr20:24972666-24972716	HIPEpiC	eye:	n/a
48	chr20:24973613-24973663	H1-hESC	embryonic stem cell:	embryo
49	chr20:24973309-24973359	BE2_C	brain:	n/a
50	chr20:24929607-24929657	GM12891	blood:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:24959468..24961705-chr20:24961994..24965467,4	K562	blood:
2	chr20:24909343..24912693-chr20:24913170..24916017,4	MCF-7	breast:
3	chr20:24974985..24976149-chr20:25046073..25047055,8	K562	blood:
4	chr1:151227020..151227760-chr20:24972743..24973473,2	Hela-S3	cervix:
5	chr20:24972059..24974449-chr20:25176101..25177683,2	MCF-7	breast:
6	chr20:24964453..24967113-chr20:24967610..24970437,2	MCF-7	breast:
7	chr20:24932720..24935500-chr20:24938353..24940512,2	MCF-7	breast:
8	chr20:24959468..24961705-chr20:24961994..24965467,4	K562	blood:
9	chr20:24909343..24912693-chr20:24913170..24916017,4	MCF-7	breast:
10	chr20:24962499..24965944-chr20:24971624..24973670,3	MCF-7	breast:
11	chr20:24959138..24961345-chr20:25043562..25046337,2	MCF-7	breast:
12	chr20:24970831..24976063-chr20:25037253..25040567,5	MCF-7	breast:
13	chr20:24932720..24935500-chr20:24938353..24940512,2	MCF-7	breast:
14	chr20:24914439..24915971-chr20:24971852..24973942,2	MCF-7	breast:
15	chr20:24971946..24973582-chr20:25227704..25229248,2	MCF-7	breast:
16	chr20:24974024..24975149-chr20:25046038..25047090,7	MCF-7	breast:
17	chr20:24972184..24974531-chr20:25057258..25059368,3	MCF-7	breast:
18	chr20:24973762..24975336-chr20:25378149..25379762,2	MCF-7	breast:
19	chr20:24962863..24965787-chr20:24971009..24974027,3	K562	blood:
20	chr20:24963189..24966768-chr20:24970100..24973416,3	MCF-7	breast:
21	chr20:24974984..24975902-chr20:25119798..25120321,2	MCF-7	breast:
22	chr20:24973677..24976371-chr20:25035249..25037062,2	MCF-7	breast:
23	chr20:24940462..24942946-chr20:24945395..24947544,2	MCF-7	breast:
24	chr20:24949924..24953271-chr20:24955139..24959186,4	K562	blood:
25	chr20:24949924..24953271-chr20:24955139..24959186,4	K562	blood:
26	chr20:24974051..24974784-chr20:25159865..25160396,2	MCF-7	breast:
27	chr20:24968082..24971017-chr20:24971333..24974516,3	MCF-7	breast:
28	chr20:24934127..24936359-chr20:24972026..24973630,2	MCF-7	breast:
29	chr20:24959038..24961782-chr20:24965978..24967936,3	MCF-7	breast:
30	chr20:24964453..24967113-chr20:24967610..24970437,2	MCF-7	breast:
31	chr20:24971936..24974944-chr20:25175039..25178381,3	MCF-7	breast:
32	chr20:24971839..24974533-chr20:25228512..25230139,2	MCF-7	breast:
33	chr20:24974829..24976836-chr20:24997683..25000384,2	MCF-7	breast:
34	chr20:24974463..24977428-chr20:25038810..25041777,2	MCF-7	breast:
35	chr12:30948297..30949147-chr20:24972886..24973794,2	Hela-S3	cervix:
36	chr20:24944898..24946529-chr20:24971755..24973854,2	MCF-7	breast:
37	chr20:24959038..24961782-chr20:24965978..24967936,3	MCF-7	breast:
38	chr20:24912941..24914562-chr20:24924394..24926104,2	MCF-7	breast:
39	chr20:24974184..24976552-chr20:25044724..25047326,32	MCF-7	breast:
40	chr20:24764889..24765421-chr20:24919390..24920112,2	MCF-7	breast:
41	chr20:24914670..24916704-chr20:24919775..24921335,2	MCF-7	breast:
42	chr20:24963187..24967390-chr20:24970058..24973702,4	K562	blood:
43	chr20:24972188..24974753-chr20:24992355..24994002,2	K562	blood:
44	chr20:24914670..24916704-chr20:24919775..24921335,2	MCF-7	breast:
45	chr20:24972575..24975462-chr20:25603621..25605250,2	K562	blood:
46	chr20:24912941..24914562-chr20:24924394..24926104,2	MCF-7	breast:
47	chr20:24940462..24942946-chr20:24945395..24947544,2	MCF-7	breast:
48	chr20:24910467..24912747-chr20:24972358..24974415,2	MCF-7	breast:
49	chr20:24953664..24955815-chr20:24961799..24963768,2	MCF-7	breast:
50	chr20:24974373..24975913-chr20:24978993..24980704,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf3-1	chr20:24911284-24912866	ENSG00000250527
2	lnc-C20orf3-1	chr20:24913047-24913619	ENSG00000250527

No data

Variant related genes	Relation type
APMAP	TF binding region
RNU6-1257P	TF binding region
CST7	TF binding region
APMAP	CpG island
RNU6-1257P	CpG island
CST7	CpG island
ENSG00000207355	chromatin interactions
ENSG00000197586	chromatin interactions
ENSG00000101474	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000154930	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000100987	chromatin interactions
ENSG00000235884	chromatin interactions
YOD1	miRNA target sites
ZNF148	miRNA target sites

Extended variants
information (count: 3150 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3150 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548930707	chr20:24908863-24908864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149510879	chr20:24908874-24908875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184321993	chr20:24908878-24908879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530023185	chr20:24908942-24908943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6050152	chr20:24908947-24908948	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs227617	chr20:24908964-24908965	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs2150647	chr20:24908965-24908966	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs193061681	chr20:24908980-24908981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185579788	chr20:24908994-24908995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2150648	chr20:24909021-24909022	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs576452649	chr20:24909042-24909043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541973140	chr20:24909099-24909100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377559448	chr20:24909106-24909107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146310551	chr20:24909126-24909127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62216716	chr20:24909127-24909128	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541320949	chr20:24909135-24909136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190053510	chr20:24909148-24909149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533464983	chr20:24909164-24909165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543947103	chr20:24909190-24909191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537723307	chr20:24909209-24909210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141724643	chr20:24909210-24909211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563747552	chr20:24909236-24909237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144188771	chr20:24909287-24909288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549129942	chr20:24909288-24909289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565679400	chr20:24909289-24909290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528133832	chr20:24909331-24909332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551406200	chr20:24909346-24909347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151064828	chr20:24909409-24909410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571474143	chr20:24909417-24909418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs227618	chr20:24909472-24909473	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181397619	chr20:24909481-24909482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567382503	chr20:24909484-24909485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535921539	chr20:24909499-24909500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183996035	chr20:24909521-24909522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs227619	chr20:24909577-24909578	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs534743042	chr20:24909650-24909651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557731118	chr20:24909651-24909652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149836048	chr20:24909656-24909657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543797929	chr20:24909677-24909678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553241899	chr20:24909683-24909684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374745400	chr20:24909688-24909689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570360770	chr20:24909692-24909693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6138413	chr20:24909718-24909719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563886043	chr20:24909733-24909734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529512432	chr20:24909736-24909737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542737277	chr20:24909753-24909754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559450516	chr20:24909765-24909766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528197321	chr20:24909767-24909768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188508354	chr20:24909775-24909776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77734042	chr20:24909831-24909832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24901400-24915200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:24907600-24911000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:24908600-24911400	Enhancers	Placenta	Placenta
4	chr20:24908600-24912400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr20:24908800-24909400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr20:24908800-24910400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr20:24908800-24911200	Weak transcription	HSMMtube	muscle
8	chr20:24909400-24909600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr20:24909400-24911400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr20:24909400-24912000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr20:24909600-24910600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr20:24909600-24913400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr20:24910400-24910800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr20:24910400-24911000	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr20:24910400-24911000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr20:24910400-24911000	Enhancers	HMEC	breast
17	chr20:24910400-24911000	Enhancers	NHEK	skin
18	chr20:24910400-24911200	Enhancers	Pancreas	Pancrea
19	chr20:24910400-24911200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr20:24910400-24913200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr20:24910600-24910800	Enhancers	Fetal Kidney	kidney
22	chr20:24910600-24910800	Bivalent Enhancer	HepG2	liver
23	chr20:24910600-24911000	Enhancers	Liver	Liver
24	chr20:24910600-24911000	Enhancers	Duodenum Mucosa	Duodenum
25	chr20:24910600-24911000	Enhancers	Esophagus	oesophagus
26	chr20:24910600-24911000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr20:24910600-24911000	Enhancers	Stomach Mucosa	stomach
28	chr20:24910600-24911200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr20:24910600-24911200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr20:24910600-24911200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr20:24910600-24911200	Enhancers	Fetal Intestine Small	intestine
32	chr20:24910600-24911600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr20:24910600-24911800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr20:24910600-24911800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr20:24910600-24911800	Enhancers	Fetal Intestine Large	intestine
36	chr20:24910600-24912200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr20:24910600-24913000	Enhancers	Fetal Thymus	thymus
38	chr20:24910800-24911800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr20:24910800-24912000	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr20:24910800-24912400	Enhancers	Adipose Nuclei	Adipose
41	chr20:24911000-24911200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr20:24911000-24911200	Enhancers	Colonic Mucosa	Colon
43	chr20:24911000-24911200	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr20:24911000-24911200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
45	chr20:24911000-24911400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr20:24911000-24911600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr20:24911000-24911600	Enhancers	Primary hematopoietic stem cells	blood
48	chr20:24911000-24911600	Flanking Active TSS	Liver	Liver
49	chr20:24911000-24911800	Active TSS	Rectal Smooth Muscle	rectum
50	chr20:24911000-24911800	Flanking Active TSS	HMEC	breast

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