Variant report

Variant	nsv912873
Chromosome Location	chr20:40601021-40675704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:491)
CpG islands
(count:488)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr20:40647659-40647822	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr20:40627170-40627384	K562	blood:	n/a	n/a
3	CEBPB	chr20:40647682-40647879	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr20:40627152-40627530	A549	lung:	n/a	n/a
5	CEBPB	chr20:40627131-40627520	MCF-7	breast:	n/a	n/a
6	CEBPB	chr20:40627142-40627502	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr20:40627145-40627545	MCF-7	breast:	n/a	n/a
8	CEBPB	chr20:40627135-40627507	HepG2	liver:	n/a	n/a
9	CEBPB	chr20:40645687-40645913	HepG2	liver:	n/a	chr20:40645799-40645810
10	CEBPB	chr20:40627126-40627511	K562	blood:	n/a	n/a
11	CEBPB	chr20:40627127-40627488	IMR90	lung:	n/a	n/a
12	CEBPB	chr20:40627138-40627498	A549	lung:	n/a	n/a
13	CEBPB	chr20:40627152-40627483	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr20:40668107-40668126	GM12878	blood:	n/a	n/a
15	CHD2	chr20:40647765-40647956	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr20:40647601-40648098	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr20:40653279-40653583	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr20:40647631-40648088	HepG2	liver:	n/a	n/a
19	CREB1	chr20:40647688-40647950	K562	blood:	n/a	n/a
20	CREB1	chr20:40647615-40648080	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr20:40647680-40647830	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr20:40656646-40656792	K562	blood:	n/a	chr20:40656715-40656723 chr20:40656712-40656733
23	CTCF	chr20:40647712-40647894	GM19240	blood:	n/a	n/a
24	CTCF	chr20:40669840-40669990	GM12869	blood:	n/a	n/a
25	CTCF	chr20:40656433-40657033	MCF-7	breast:	n/a	chr20:40656715-40656723 chr20:40656712-40656733
26	CTCF	chr20:40669900-40670050	HepG2	liver:	n/a	chr20:40670020-40670038 chr20:40670023-40670032 chr20:40670020-40670033 chr20:40670018-40670036
27	CTCF	chr20:40647664-40647938	MCF-7	breast:	n/a	n/a
28	CTCF	chr20:40668700-40668850	Caco-2	colon:	n/a	n/a
29	CTCF	chr20:40647720-40647870	GM12873	blood:	n/a	n/a
30	CTCF	chr20:40653800-40653950	MCF-7	breast:	n/a	n/a
31	CTCF	chr20:40669940-40670090	MCF-7	breast:	n/a	chr20:40670020-40670038 chr20:40670023-40670032 chr20:40670020-40670033 chr20:40670018-40670036
32	CTCF	chr20:40647508-40648082	MCF-7	breast:	n/a	n/a
33	CTCF	chr20:40656674-40656803	HepG2	liver:	n/a	chr20:40656715-40656723 chr20:40656712-40656733
34	CTCF	chr20:40669940-40670090	HRE	kidney:	n/a	chr20:40670020-40670038 chr20:40670023-40670032 chr20:40670020-40670033 chr20:40670018-40670036
35	CTCF	chr20:40656515-40656790	H1-hESC	embryonic stem cell:	n/a	chr20:40656715-40656723 chr20:40656712-40656733
36	CTCF	chr20:40647720-40647870	HL-60	blood:	n/a	n/a
37	CTCF	chr20:40656680-40656830	Caco-2	colon:	n/a	chr20:40656715-40656723 chr20:40656712-40656733
38	CTCF	chr20:40647760-40647910	GM06990	blood:	n/a	n/a
39	CTCF	chr20:40647680-40647898	Medullo	brain:	n/a	n/a
40	CTCF	chr20:40647680-40647830	A549	lung:	n/a	n/a
41	CTCF	chr20:40647740-40647890	GM12875	blood:	n/a	n/a
42	CTCF	chr20:40669854-40670168	K562	blood:	n/a	chr20:40670020-40670038 chr20:40670023-40670032 chr20:40670020-40670033 chr20:40670018-40670036
43	CTCF	chr20:40656748-40656750	Lung_OC	lung:	n/a	n/a
44	CTCF	chr20:40668740-40668890	HEK293	kidney:	n/a	n/a
45	CTCF	chr20:40669900-40670050	GM12872	blood:	n/a	chr20:40670020-40670038 chr20:40670023-40670032 chr20:40670020-40670033 chr20:40670018-40670036
46	CTCF	chr20:40647680-40647830	NB4	blood:	n/a	n/a
47	CTCF	chr20:40647720-40647870	GM12864	blood:	n/a	n/a
48	CTCF	chr20:40647700-40647850	GM12864	blood:	n/a	n/a
49	CTCF	chr20:40669940-40670090	Caco-2	colon:	n/a	chr20:40670020-40670038 chr20:40670023-40670032 chr20:40670020-40670033 chr20:40670018-40670036
50	CTCF	chr20:40647760-40647910	GM12872	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:40631638-40631688	HRCEpiC	kidney:	n/a
2	chr20:40627235-40627285	HAEpiC	amniotic membrane:	n/a
3	chr20:40627194-40627244	Jurkat	blood:	n/a
4	chr20:40627977-40628027	GM12878	blood:	n/a
5	chr20:40627194-40627244	AoSMC	blood vessel:	n/a
6	chr20:40631638-40631688	GM19239	blood:	n/a
7	chr20:40628070-40628120	HPAEpiC	pulmonary alveolar:	n/a
8	chr20:40631638-40631688	HNPCEpiC	eye:	n/a
9	chr20:40626459-40626509	HEEpiC	esophagus:	n/a
10	chr20:40631638-40631688	AG09319	gingival:	n/a
11	chr20:40626459-40626509	GM12892	blood:	n/a
12	chr20:40627977-40628027	AoSMC	blood vessel:	n/a
13	chr20:40624642-40624692	PrEC	prostate:	n/a
14	chr20:40627235-40627285	PANC-1	pancreas:	n/a
15	chr20:40627665-40627715	K562	blood:	n/a
16	chr20:40631638-40631688	PANC-1	pancreas:	n/a
17	chr20:40626459-40626509	MCF10A-Er-Src	breast:	n/a
18	chr20:40628070-40628120	HCF	heart:	n/a
19	chr20:40624642-40624692	AG04449	skin:	fetal
20	chr20:40631638-40631688	SK-N-MC	brain:	n/a
21	chr20:40627665-40627715	NH-A	brain:	n/a
22	chr20:40627194-40627244	ovcar-3	ovarian:	n/a
23	chr20:40631638-40631688	SAEC	small airway:	n/a
24	chr20:40627977-40628027	Caco-2	colon:	n/a
25	chr20:40628070-40628120	SK-N-SH	brain:	n/a
26	chr20:40628070-40628120	ProgFib	skin:	n/a
27	chr20:40631638-40631688	HMEC	breast:	n/a
28	chr20:40627665-40627715	HEEpiC	esophagus:	n/a
29	chr20:40624642-40624692	NHDF-neo	bronchial:	n/a
30	chr20:40624642-40624692	GM12892	blood:	n/a
31	chr20:40624642-40624692	HRPEpiC	eye:	n/a
32	chr20:40627977-40628027	ovcar-3	ovarian:	n/a
33	chr20:40626459-40626509	HCF	heart:	n/a
34	chr20:40627665-40627715	AoSMC	blood vessel:	n/a
35	chr20:40627977-40628027	SAEC	small airway:	n/a
36	chr20:40626459-40626509	HRCEpiC	kidney:	n/a
37	chr20:40626459-40626509	HCPEpiC	choroid plexus:	n/a
38	chr20:40627235-40627285	GM12891	blood:	n/a
39	chr20:40627194-40627244	HCT-116	colon:	n/a
40	chr20:40631638-40631688	HL-60	blood:	n/a
41	chr20:40624642-40624692	ECC-1	luminal epithelium:	n/a
42	chr20:40626459-40626509	IMR90	lung:	fetal
43	chr20:40627977-40628027	HCT-116	colon:	n/a
44	chr20:40627235-40627285	HUVEC	blood vessel:	n/a
45	chr20:40627235-40627285	NB4	blood:	n/a
46	chr20:40626459-40626509	BJ	skin:	n/a
47	chr20:40627235-40627285	RPTEC	kidney:	n/a
48	chr20:40627235-40627285	HepG2	liver:	n/a
49	chr20:40624642-40624692	A549	lung:	n/a
50	chr20:40627977-40628027	HRE	kidney:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:40585759..40586528-chr20:40647402..40648048,2	MCF-7	breast:
2	chr20:40597592..40600264-chr20:40602753..40604871,2	MCF-7	breast:
3	chr20:40375062..40375607-chr20:40647290..40648219,3	MCF-7	breast:
4	chr20:40656350..40657204-chr20:40669571..40670470,3	MCF-7	breast:
5	chr20:40584661..40585630-chr20:40647278..40648249,12	MCF-7	breast:
6	chr20:40517658..40518318-chr20:40647636..40648238,2	MCF-7	breast:
7	chr20:40366961..40367845-chr20:40669695..40670564,4	MCF-7	breast:
8	chr20:40585063..40585585-chr20:40647501..40648295,2	MCF-7	breast:
9	chr20:40584635..40586108-chr20:40669291..40670823,9	MCF-7	breast:
10	chr20:40656318..40657155-chr20:41159287..41160221,3	MCF-7	breast:
11	chr20:40654476..40656939-chr20:40661204..40663699,2	MCF-7	breast:
12	chr20:40621776..40623735-chr20:40625539..40627420,2	K562	blood:
13	chr20:40674875..40676426-chr20:40681256..40683922,2	K562	blood:
14	chr20:40362868..40363717-chr20:40647339..40648278,3	MCF-7	breast:
15	chr20:40656308..40657087-chr20:40809458..40810142,2	MCF-7	breast:
16	chr1:241662179..241663106-chr20:40656255..40656903,2	MCF-7	breast:
17	chr20:40650350..40652233-chr20:40653774..40655907,3	K562	blood:
18	chr20:40641988..40644961-chr20:40646504..40648867,2	K562	blood:
19	chr20:40654476..40656939-chr20:40661204..40663699,2	MCF-7	breast:
20	chr20:40596592..40599038-chr20:40600387..40603360,2	K562	blood:
21	chr20:40366989..40367893-chr20:40647466..40648275,6	MCF-7	breast:
22	chr20:40656350..40657204-chr20:40669571..40670470,3	MCF-7	breast:
23	chr20:40597538..40599530-chr20:40601597..40603360,2	K562	blood:
24	chr20:40621776..40623735-chr20:40625539..40627420,2	K562	blood:
25	chr20:40647561..40648111-chr3:943417..944121,2	MCF-7	breast:
26	chr20:40625261..40628055-chr20:40628538..40631191,2	MCF-7	breast:
27	chr20:40650350..40652233-chr20:40653774..40655907,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPIN3-2	chr20:40619780-40619910	ENSG00000225458.1
2	lnc-PTPRT-1	chr20:40643181-40643316	XLOC_013745
3	lnc-PTPRT-1	chr20:40644062-40644118	XLOC_013745
4	lnc-PTPRT-1	chr20:40642674-40642897	XLOC_013745

No data

Variant related genes	Relation type
ENSG00000225458	TF binding region
ENSG00000228959	TF binding region
ENSG00000223651	TF binding region
ENSG00000225458	CpG island
ENSG00000228959	CpG island
ENSG00000223651	CpG island
ENSG00000228959	chromatin interactions
ENSG00000223651	chromatin interactions

Extended variants
information (count: 1606 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1000337	chr20:40601021-40601022	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185747345	chr20:40601064-40601065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533163761	chr20:40601065-40601066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73124713	chr20:40601077-40601078	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575098653	chr20:40601085-40601086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544022561	chr20:40601092-40601093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563822347	chr20:40601097-40601098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373887781	chr20:40601111-40601112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532630684	chr20:40601126-40601127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138627935	chr20:40601132-40601133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8120362	chr20:40601138-40601139	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs8120363	chr20:40601145-40601146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6124404	chr20:40601184-40601185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567181341	chr20:40601185-40601186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143319037	chr20:40601190-40601191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7344021	chr20:40601197-40601198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75917002	chr20:40601213-40601214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569438514	chr20:40601240-40601241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1000336	chr20:40601248-40601249	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs113306911	chr20:40601249-40601250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568056781	chr20:40601265-40601266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149031227	chr20:40601287-40601288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139379282	chr20:40601304-40601305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78445412	chr20:40601338-40601339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529111784	chr20:40601350-40601351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555006092	chr20:40601364-40601365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115493787	chr20:40601371-40601372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2179438	chr20:40601384-40601385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190654693	chr20:40601392-40601393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181755196	chr20:40601393-40601394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546003082	chr20:40601399-40601400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11906728	chr20:40601496-40601497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568675322	chr20:40601506-40601507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185929746	chr20:40601525-40601526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571218608	chr20:40601545-40601546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542196799	chr20:40601558-40601559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76579213	chr20:40601610-40601611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529913823	chr20:40601622-40601623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6093542	chr20:40601663-40601664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549597824	chr20:40601669-40601670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150034641	chr20:40601674-40601675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532304039	chr20:40601682-40601683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557583655	chr20:40601692-40601693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551997707	chr20:40601711-40601712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6093543	chr20:40601721-40601722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570520754	chr20:40601728-40601729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188830856	chr20:40601732-40601733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181283873	chr20:40601737-40601738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144299763	chr20:40601746-40601747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537758412	chr20:40601805-40601806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	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
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian cancer	19193619	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelodysplastic syndrome	17634407	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	22539939	CNVD
Myelofibrosis	22110671	CNVD
Cervical cancer	16585170	CNVD
Ovarian neoplasms	16753589	CNVD
Infertility	21528002	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:40599600-40602600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr20:40600200-40601400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr20:40600200-40601600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr20:40600600-40601200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr20:40600600-40601400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr20:40600600-40601600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr20:40602600-40606000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr20:40603200-40603400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr20:40606200-40607000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr20:40607200-40607800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr20:40607600-40607800	Bivalent Enhancer	HepG2	liver
12	chr20:40618400-40618600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr20:40618600-40618800	Enhancers	HUVEC	blood vessel
14	chr20:40618600-40619000	Enhancers	Fetal Brain Male	brain
15	chr20:40618600-40619200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr20:40618600-40619400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr20:40618600-40619400	Enhancers	Fetal Muscle Leg	muscle
18	chr20:40618600-40619800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr20:40618800-40619200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr20:40618800-40619200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr20:40618800-40619200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr20:40618800-40619200	Flanking Active TSS	HUVEC	blood vessel
23	chr20:40619000-40619200	Bivalent Enhancer	Brain Angular Gyrus	brain
24	chr20:40619200-40620000	Enhancers	HUVEC	blood vessel
25	chr20:40619600-40619800	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr20:40625400-40631800	Weak transcription	Right Atrium	heart
27	chr20:40626200-40626600	Active TSS	Brain Substantia Nigra	brain
28	chr20:40627000-40627800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr20:40627000-40628000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr20:40627400-40627800	ZNF genes & repeats	Spleen	Spleen
31	chr20:40630200-40630400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr20:40633600-40635200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr20:40633600-40635200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr20:40633600-40635200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr20:40633600-40635400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr20:40633800-40634000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr20:40633800-40634600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr20:40633800-40634800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr20:40633800-40635200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr20:40633800-40635200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr20:40633800-40635400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr20:40634000-40634600	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr20:40634600-40635400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr20:40649000-40649400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr20:40656800-40658000	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr20:40658600-40665800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr20:40664800-40666400	Enhancers	Fetal Intestine Large	intestine
48	chr20:40665400-40666000	Enhancers	Fetal Intestine Small	intestine
49	chr20:40665800-40668000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr20:40668000-40668600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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