Variant report

Variant	nsv912685
Chromosome Location	chr20:13134768-13234124
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:804)
CpG islands
(count:2442)
Chromatin interactive
region (count:15)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:13224184-13225291	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:13225796-13226403	HepG2	liver:	n/a	n/a
3	ATF2	chr20:13227864-13228573	GM12878	blood:	n/a	n/a
4	ATF3	chr20:13224327-13224907	A549	lung:	n/a	n/a
5	BACH1	chr20:13200843-13201401	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr20:13181780-13181787	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr20:13163606-13164033	GM12878	blood:	n/a	n/a
8	BATF	chr20:13193400-13193707	GM12878	blood:	n/a	chr20:13193566-13193577
9	BATF	chr20:13227971-13228436	GM12878	blood:	n/a	chr20:13228049-13228062 chr20:13228309-13228318
10	BATF	chr20:13163682-13164044	GM12878	blood:	n/a	n/a
11	BCL11A	chr20:13228024-13228227	GM12878	blood:	n/a	n/a
12	BCL11A	chr20:13163630-13164022	GM12878	blood:	n/a	n/a
13	BCL11A	chr20:13163681-13163961	GM12878	blood:	n/a	n/a
14	BCL11A	chr20:13227920-13228337	GM12878	blood:	n/a	n/a
15	BCL3	chr20:13224249-13224988	A549	lung:	n/a	n/a
16	BCLAF1	chr20:13227948-13228349	GM12878	blood:	n/a	n/a
17	BCLAF1	chr20:13202292-13202561	GM12878	blood:	n/a	chr20:13202323-13202336 chr20:13202322-13202335
18	BCLAF1	chr20:13227848-13228366	GM12878	blood:	n/a	n/a
19	BHLHE40	chr20:13202406-13202798	GM12878	blood:	n/a	chr20:13202735-13202744 chr20:13202736-13202745 chr20:13202734-13202743 chr20:13202735-13202744
20	BHLHE40	chr20:13202575-13202811	A549	lung:	n/a	chr20:13202735-13202744 chr20:13202736-13202745 chr20:13202734-13202743 chr20:13202735-13202744
21	BHLHE40	chr20:13225966-13226376	HepG2	liver:	n/a	n/a
22	BHLHE40	chr20:13155225-13155231	GM12878	blood:	n/a	n/a
23	BHLHE40	chr20:13202299-13202958	HepG2	liver:	n/a	chr20:13202735-13202744 chr20:13202736-13202745 chr20:13202734-13202743 chr20:13202735-13202744
24	BHLHE40	chr20:13228283-13228432	HepG2	liver:	n/a	n/a
25	BHLHE40	chr20:13224471-13225052	HepG2	liver:	n/a	n/a
26	BRCA1	chr20:13226049-13226099	HepG2	liver:	n/a	n/a
27	CEBPB	chr20:13153925-13154285	MCF-7	breast:	n/a	n/a
28	CEBPB	chr20:13224155-13225034	A549	lung:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
29	CEBPB	chr20:13215558-13215966	HepG2	liver:	n/a	chr20:13215696-13215707
30	CEBPB	chr20:13197205-13197572	HepG2	liver:	n/a	chr20:13197352-13197363
31	CEBPB	chr20:13224389-13225013	HepG2	liver:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
32	CEBPB	chr20:13162914-13163118	HepG2	liver:	n/a	chr20:13163039-13163052 chr20:13163039-13163050
33	CEBPB	chr20:13202439-13202467	HepG2	liver:	n/a	n/a
34	CEBPB	chr20:13226009-13226301	MCF-7	breast:	n/a	chr20:13226151-13226162
35	CEBPB	chr20:13224364-13224858	A549	lung:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
36	CEBPB	chr20:13153915-13154162	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr20:13210960-13211143	HepG2	liver:	n/a	chr20:13211020-13211031
38	CEBPB	chr20:13153879-13154237	HepG2	liver:	n/a	n/a
39	CEBPB	chr20:13187664-13187887	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:13232220-13232400	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:13169732-13169897	HepG2	liver:	n/a	chr20:13169781-13169792
42	CEBPB	chr20:13224206-13224843	A549	lung:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
43	CEBPB	chr20:13224425-13224784	HepG2	liver:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
44	CEBPB	chr20:13216563-13216696	HepG2	liver:	n/a	chr20:13216627-13216638
45	CEBPB	chr20:13173190-13173200	HepG2	liver:	n/a	n/a
46	CEBPB	chr20:13226062-13226309	A549	lung:	n/a	chr20:13226151-13226162
47	CEBPB	chr20:13224375-13224834	MCF-7	breast:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
48	CEBPB	chr20:13169738-13169788	A549	lung:	n/a	n/a
49	CEBPB	chr20:13224365-13224817	MCF-7	breast:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
50	CEBPB	chr20:13162951-13163056	Hela-S3	cervix:	n/a	chr20:13163039-13163052 chr20:13163039-13163050

(count:2442 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:13200980-13201030	MCF10A-Er-Src	breast:	n/a
2	chr20:13200973-13201023	HCM	heart:	n/a
3	chr20:13200980-13201030	MCF10A-Er-Src	breast:	n/a
4	chr20:13200973-13201023	HCM	heart:	n/a
5	chr20:13201328-13201378	HRE	kidney:	n/a
6	chr20:13201844-13201894	GM12891	blood:	n/a
7	chr20:13201342-13201392	MCF10A-Er-Src	breast:	n/a
8	chr20:13200944-13200994	IMR90	lung:	fetal
9	chr20:13202222-13202272	RPTEC	kidney:	n/a
10	chr20:13201456-13201506	HCPEpiC	choroid plexus:	n/a
11	chr20:13202702-13202752	NHDF-neo	bronchial:	n/a
12	chr20:13200954-13201004	HL-60	blood:	n/a
13	chr20:13200944-13200994	HRE	kidney:	n/a
14	chr20:13201216-13201266	AG04449	skin:	fetal
15	chr20:13201193-13201243	Hepatocyte	liver:	n/a
16	chr20:13199787-13199837	GM06990	blood:	n/a
17	chr20:13197399-13197449	RPTEC	kidney:	n/a
18	chr20:13201216-13201266	PANC-1	pancreas:	n/a
19	chr20:13200969-13201019	IMR90	lung:	fetal
20	chr20:13200992-13201042	A549	lung:	n/a
21	chr20:13201829-13201879	RPTEC	kidney:	n/a
22	chr20:13199787-13199837	SK-N-SH	brain:	n/a
23	chr20:13201225-13201275	Caco-2	colon:	n/a
24	chr20:13145549-13145599	Caco-2	colon:	n/a
25	chr20:13145549-13145599	ProgFib	skin:	n/a
26	chr20:13201551-13201601	U87	brain:	n/a
27	chr20:13205832-13205882	PrEC	prostate:	n/a
28	chr20:13201670-13201720	SK-N-MC	brain:	n/a
29	chr20:13201456-13201506	SK-N-MC	brain:	n/a
30	chr20:13201225-13201275	NHBE	bronchial:	n/a
31	chr20:13201353-13201403	Jurkat	blood:	n/a
32	chr20:13201670-13201720	ProgFib	skin:	n/a
33	chr20:13200748-13200798	IMR90	lung:	fetal
34	chr20:13201216-13201266	HUVEC	blood vessel:	n/a
35	chr20:13201193-13201243	HRPEpiC	eye:	n/a
36	chr20:13200929-13200979	SK-N-MC	brain:	n/a
37	chr20:13200982-13201032	AG09319	gingival:	n/a
38	chr20:13202225-13202275	CMK	blood:	n/a
39	chr20:13202225-13202275	Caco-2	colon:	n/a
40	chr20:13200069-13200119	BJ	skin:	n/a
41	chr20:13201662-13201712	GM19239	blood:	n/a
42	chr20:13201829-13201879	HCF	heart:	n/a
43	chr20:13201670-13201720	LNCaP	prostate:	n/a
44	chr20:13201551-13201601	NHDF-neo	bronchial:	n/a
45	chr20:13202489-13202539	GM12878	blood:	n/a
46	chr20:13200982-13201032	AG09309	skin:	n/a
47	chr20:13202476-13202526	HRPEpiC	eye:	n/a
48	chr20:13201205-13201255	Caco-2	colon:	n/a
49	chr20:13200748-13200798	RPTEC	kidney:	n/a
50	chr20:13145549-13145599	AG04450	lung:	fetal

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:13222224..13226467-chr20:13226832..13229125,4	MCF-7	breast:
2	chr20:13196643..13199803-chr20:13200089..13202885,4	MCF-7	breast:
3	chr20:13217886..13220237-chr20:13220614..13223071,3	MCF-7	breast:
4	chr20:13187247..13188806-chr20:13192089..13194671,2	MCF-7	breast:
5	chr14:48176778..48178872-chr20:13212572..13214916,2	MCF-7	breast:
6	chr20:13195544..13197787-chr20:13200539..13202622,2	K562	blood:
7	chr20:13186346..13187286-chr20:13242328..13243323,3	MCF-7	breast:
8	chr20:13187247..13188806-chr20:13192089..13194671,2	MCF-7	breast:
9	chr20:13186534..13187312-chr20:13283028..13283706,3	MCF-7	breast:
10	chr20:13224428..13227075-chr20:13229216..13232192,3	MCF-7	breast:
11	chr20:13217886..13220237-chr20:13220614..13223071,3	MCF-7	breast:
12	chr20:13186665..13187313-chr20:13282994..13283540,2	MCF-7	breast:
13	chr20:13138229..13140817-chr20:13161228..13162854,2	MCF-7	breast:
14	chr20:13138229..13140817-chr20:13161228..13162854,2	MCF-7	breast:
15	chr20:13225351..13227078-chr20:13232726..13234413,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TASP1-1	chr20:13224711-13225028	ENSG00000225956.1
2	lnc-TASP1-9	chr20:13167631-13167751	ucscGeneNc_uc002wof_1
3	lnc-ISM1-1	chr20:13200717-13201032	NONHSAT078681
4	lnc-ISM1-1	chr20:13200350-13200585	NONHSAT078681
5	lnc-ISM1-1	chr20:13200350-13200970	NONHSAT078682
6	lnc-TASP1-2	chr20:13218067-13218756	NONHSAT078683
7	lnc-SPTLC3-5	chr20:13229880-13230196	NONHSAT078685
8	lnc-TASP1-1	chr20:13225889-13226016	ENSG00000225956.1
9	lnc-TASP1-2	chr20:13218733-13218756	NONHSAT078684
10	lnc-TASP1-9	chr20:13166068-13166756	ucscGeneNc_uc002wof_1
11	lnc-TASP1-10	chr20:13147713-13148970	ncRnaDb_ncrna_FR082676_1
12	lnc-TASP1-2	chr20:13219631-13219751	NONHSAT078683
13	lnc-SPTLC3-5	chr20:13219374-13219813	NONHSAT078685
14	lnc-TASP1-2	chr20:13220100-13220334	NONHSAT078683
15	lnc-SPTLC3-4	chr20:13148350-13148970	ucscGeneNc_uc002woe_1
16	lnc-TASP1-9	chr20:13168100-13168321	ucscGeneNc_uc002wof_1
17	lnc-TASP1-2	chr20:13219658-13220301	NONHSAT078684

No data

Variant related genes	Relation type
ISM1	TF binding region
ENSG00000225956	TF binding region
ISM1-AS1	TF binding region
ISM1	CpG island
ENSG00000225956	CpG island
ISM1-AS1	CpG island
ENSG00000225956	chromatin interactions
ENSG00000101230	chromatin interactions

Extended variants
information (count: 3198 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3198 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6078938	chr20:13134768-13134769	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370644573	chr20:13134799-13134800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6078939	chr20:13134816-13134817	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6074563	chr20:13134833-13134834	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574507695	chr20:13134856-13134857	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553016504	chr20:13134857-13134858	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557095527	chr20:13134915-13134916	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2073303	chr20:13134931-13134932	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192269163	chr20:13134958-13134959	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs57093302	chr20:13135029-13135030	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6131444	chr20:13135050-13135051	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572575493	chr20:13135054-13135055	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370177311	chr20:13135068-13135069	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544983547	chr20:13135099-13135100	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541380980	chr20:13135135-13135136	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145523044	chr20:13135136-13135137	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564677906	chr20:13135144-13135145	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530048312	chr20:13135162-13135163	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543366805	chr20:13135163-13135164	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563342161	chr20:13135194-13135195	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532540727	chr20:13135195-13135196	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112173447	chr20:13135225-13135226	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552625890	chr20:13135342-13135343	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117960698	chr20:13135349-13135350	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78593740	chr20:13135367-13135368	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548520571	chr20:13135445-13135446	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544491575	chr20:13135491-13135492	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561197454	chr20:13135580-13135581	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112025611	chr20:13135615-13135616	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6033629	chr20:13135654-13135655	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376262131	chr20:13135678-13135679	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11908122	chr20:13135689-13135690	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570446475	chr20:13135769-13135770	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148216991	chr20:13135887-13135888	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540476502	chr20:13135893-13135894	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142776232	chr20:13135932-13135933	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146713967	chr20:13135942-13135943	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554848305	chr20:13135956-13135957	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574843778	chr20:13135982-13135983	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs6074564	chr20:13136043-13136044	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs200380335	chr20:13136047-13136048	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563377488	chr20:13136061-13136062	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188842584	chr20:13136078-13136079	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139212414	chr20:13136088-13136089	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559765121	chr20:13136131-13136132	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528276760	chr20:13136172-13136173	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548450553	chr20:13136200-13136201	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568251517	chr20:13136201-13136202	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530860833	chr20:13136216-13136217	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550870030	chr20:13136229-13136230	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
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
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Autism	22102821	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:13093000-13144600	Weak transcription	Pancreas	Pancrea
2	chr20:13108200-13145000	Weak transcription	Gastric	stomach
3	chr20:13111200-13144000	Weak transcription	Thymus	Thymus
4	chr20:13114200-13149200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr20:13115600-13143400	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr20:13122400-13139200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr20:13122600-13134800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr20:13128000-13148400	Weak transcription	Left Ventricle	heart
9	chr20:13128200-13134800	Weak transcription	Adipose Nuclei	Adipose
10	chr20:13128200-13139000	Weak transcription	Right Atrium	heart
11	chr20:13128400-13136800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr20:13128400-13139600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr20:13128800-13142400	Weak transcription	Fetal Kidney	kidney
14	chr20:13128800-13144000	Weak transcription	Fetal Stomach	stomach
15	chr20:13129200-13138200	Strong transcription	HepG2	liver
16	chr20:13129400-13139000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr20:13129400-13148200	Strong transcription	Placenta	Placenta
18	chr20:13129400-13148800	Weak transcription	Fetal Lung	lung
19	chr20:13129600-13139000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr20:13129600-13144800	Weak transcription	Lung	lung
21	chr20:13130800-13138800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr20:13131200-13137200	Strong transcription	Fetal Intestine Large	intestine
23	chr20:13131200-13144000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr20:13132200-13137600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr20:13132800-13148000	Weak transcription	Primary T cells from cord blood	blood
26	chr20:13133000-13136400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr20:13133400-13136200	Strong transcription	Duodenum Mucosa	Duodenum
28	chr20:13133800-13146800	Strong transcription	Liver	Liver
29	chr20:13134200-13135400	Strong transcription	Aorta	Aorta
30	chr20:13134400-13135400	Strong transcription	Ovary	ovary
31	chr20:13134400-13135800	Strong transcription	Fetal Intestine Small	intestine
32	chr20:13134400-13136400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr20:13134400-13137000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr20:13134600-13135400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr20:13134600-13135400	Strong transcription	Stomach Smooth Muscle	stomach
36	chr20:13134800-13135400	Enhancers	H9 Cell Line	embryonic stem cell
37	chr20:13134800-13136000	Strong transcription	Adipose Nuclei	Adipose
38	chr20:13134800-13136200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr20:13135400-13139000	Weak transcription	Aorta	Aorta
40	chr20:13135400-13139000	Weak transcription	Stomach Smooth Muscle	stomach
41	chr20:13135400-13139200	Weak transcription	Ovary	ovary
42	chr20:13135400-13141000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr20:13135800-13151800	Weak transcription	Fetal Intestine Small	intestine
44	chr20:13136000-13139000	Weak transcription	Adipose Nuclei	Adipose
45	chr20:13136200-13140600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr20:13136200-13141000	Weak transcription	Duodenum Mucosa	Duodenum
47	chr20:13136400-13136600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr20:13136400-13137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr20:13136400-13147400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:13136600-13136800	Enhancers	Skeletal Muscle Male	skeletal muscle

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