Variant report

Variant	esv3486172
Chromosome Location	chr20:23719874-23796522
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	ATF1	chr20:23781355-23781508	K562	blood:	n/a	n/a
2	CEBPB	chr20:23747045-23747345	HepG2	liver:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
3	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
4	CEBPB	chr20:23747142-23747274	K562	blood:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
5	CEBPB	chr20:23747026-23747352	A549	lung:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747029-23747041 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
6	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
7	CTCF	chr20:23779880-23780030	GM06990	blood:	n/a	n/a
8	CTCF	chr20:23763100-23763250	NB4	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
9	CTCF	chr20:23780240-23780390	GM12872	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
10	CTCF	chr20:23780260-23780410	GM12867	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
11	CTCF	chr20:23763020-23763170	RPTEC	kidney:	n/a	n/a
12	CTCF	chr20:23779831-23780203	IMR90	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
13	CTCF	chr20:23763120-23763270	HFF-Myc	foreskin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
14	CTCF	chr20:23729640-23729790	HRE	kidney:	n/a	n/a
15	CTCF	chr20:23754840-23754990	HMEC	breast:	n/a	chr20:23754976-23754989
16	CTCF	chr20:23763341-23763554	HepG2	liver:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763449-23763465
17	CTCF	chr20:23779879-23780428	HepG2	liver:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
18	CTCF	chr20:23729780-23729930	HMF	breast:	n/a	n/a
19	CTCF	chr20:23763040-23763190	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr20:23763060-23763210	GM12865	blood:	n/a	chr20:23763195-23763204 chr20:23763192-23763210
21	CTCF	chr20:23729557-23729559	GM12891	blood:	n/a	n/a
22	CTCF	chr20:23763220-23763370	NHLF	lung:	n/a	n/a
23	CTCF	chr20:23763120-23763270	HEEpiC	esophagus:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
24	CTCF	chr20:23779900-23780050	HA-sp	spinal cord:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
25	CTCF	chr20:23756600-23756750	HRE	kidney:	n/a	n/a
26	CTCF	chr20:23779880-23780030	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr20:23763020-23763170	HMF	breast:	n/a	n/a
28	CTCF	chr20:23779880-23780030	HL-60	blood:	n/a	n/a
29	CTCF	chr20:23763089-23763335	GM19240	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
30	CTCF	chr20:23780260-23780410	HRE	kidney:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
31	CTCF	chr20:23780182-23780519	H1-hESC	embryonic stem cell:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
32	CTCF	chr20:23779893-23780376	GM12891	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
33	CTCF	chr20:23763015-23763537	SK-N-SH	brain:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
34	CTCF	chr20:23780480-23780630	A549	lung:	n/a	n/a
35	CTCF	chr20:23779960-23780110	HMF	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
36	CTCF	chr20:23774782-23774860	MCF-7	breast:	n/a	n/a
37	CTCF	chr20:23779900-23780050	GM12868	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
38	CTCF	chr20:23779800-23779950	GM12873	blood:	n/a	n/a
39	CTCF	chr20:23779833-23780212	GM12878	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
40	CTCF	chr20:23779899-23780423	H1-hESC	embryonic stem cell:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
41	CTCF	chr20:23779960-23780110	AG09309	skin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
42	CTCF	chr20:23763020-23763170	HepG2	liver:	n/a	n/a
43	CTCF	chr20:23763160-23763310	NHEK	skin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
44	CTCF	chr20:23756740-23756890	HCPEpiC	choroid plexus:	n/a	chr20:23756767-23756780
45	CTCF	chr20:23762978-23763660	HepG2	liver:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
46	CTCF	chr20:23763078-23763348	GM19238	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
47	CTCF	chr20:23774795-23774834	GM19239	blood:	n/a	n/a
48	CTCF	chr20:23763080-23763230	GM12870	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
49	CTCF	chr20:23779880-23780030	GM12872	blood:	n/a	n/a
50	CTCF	chr20:23779723-23779757	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23731367-23731417	K562	blood:	n/a
2	chr20:23732873-23732923	HIPEpiC	eye:	n/a
3	chr20:23728432-23728482	Hela-S3	cervix:	n/a
4	chr20:23728432-23728482	Jurkat	blood:	n/a
5	chr20:23731367-23731417	CMK	blood:	n/a
6	chr20:23731367-23731417	HCF	heart:	n/a
7	chr20:23731367-23731417	SAEC	small airway:	n/a
8	chr20:23728432-23728482	HCM	heart:	n/a
9	chr20:23731367-23731417	HL-60	blood:	n/a
10	chr20:23728432-23728482	HEK293	kidney:	embryo
11	chr20:23731367-23731417	RPTEC	kidney:	n/a
12	chr20:23732873-23732923	GM19239	blood:	n/a
13	chr20:23732595-23732645	PANC-1	pancreas:	n/a
14	chr20:23728814-23728864	HAEpiC	amniotic membrane:	n/a
15	chr20:23728432-23728482	HMEC	breast:	n/a
16	chr20:23728432-23728482	RPTEC	kidney:	n/a
17	chr20:23732873-23732923	GM12892	blood:	n/a
18	chr20:23732595-23732645	RPTEC	kidney:	n/a
19	chr20:23732873-23732923	A549	lung:	n/a
20	chr20:23728814-23728864	AG04450	lung:	fetal
21	chr20:23731367-23731417	HNPCEpiC	eye:	n/a
22	chr20:23732873-23732923	NT2-D1	testis:	n/a
23	chr20:23728814-23728864	SKMC	muscle:	n/a
24	chr20:23732595-23732645	MCF-7	breast:	n/a
25	chr20:23728814-23728864	Caco-2	colon:	n/a
26	chr20:23728432-23728482	H1-hESC	embryonic stem cell:	embryo
27	chr20:23732873-23732923	T-47D	breast:	n/a
28	chr20:23732595-23732645	HAEpiC	amniotic membrane:	n/a
29	chr20:23728814-23728864	HRPEpiC	eye:	n/a
30	chr20:23732873-23732923	Hela-S3	cervix:	n/a
31	chr20:23731367-23731417	HCPEpiC	choroid plexus:	n/a
32	chr20:23728432-23728482	ProgFib	skin:	n/a
33	chr20:23731367-23731417	HepG2	liver:	n/a
34	chr20:23728814-23728864	NHDF-neo	bronchial:	n/a
35	chr20:23732873-23732923	CMK	blood:	n/a
36	chr20:23728432-23728482	HUVEC	blood vessel:	n/a
37	chr20:23728432-23728482	HIPEpiC	eye:	n/a
38	chr20:23731367-23731417	HUVEC	blood vessel:	n/a
39	chr20:23728814-23728864	HCM	heart:	n/a
40	chr20:23732595-23732645	GM19239	blood:	n/a
41	chr20:23732595-23732645	U87	brain:	n/a
42	chr20:23732873-23732923	HRCEpiC	kidney:	n/a
43	chr20:23732873-23732923	AG09319	gingival:	n/a
44	chr20:23731367-23731417	AG04449	skin:	fetal
45	chr20:23728814-23728864	ECC-1	luminal epithelium:	n/a
46	chr20:23728814-23728864	GM12891	blood:	n/a
47	chr20:23732595-23732645	GM06990	blood:	n/a
48	chr20:23732595-23732645	HCPEpiC	choroid plexus:	n/a
49	chr20:23732873-23732923	HCF	heart:	n/a
50	chr20:23728432-23728482	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
2	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
3	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
4	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
5	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
6	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
7	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
8	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
9	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
10	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
11	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-3	chr20:23785160-23785281	XLOC_013494
2	lnc-CST8-3	chr20:23785871-23786300	XLOC_013494
3	lnc-CST8-3	chr20:23784376-23784473	XLOC_013494
4	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083
5	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083
6	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083
7	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
8	lnc-CST8-3	chr20:23778778-23778924	XLOC_013494

Variant related genes	Relation type
ENSG00000230908	TF binding region
CST1	TF binding region
ENSG00000230908	CpG island
CST1	CpG island
XIAP	miRNA target sites
WWC2	miRNA target sites
WWP2	miRNA target sites

Extended variants
information (count: 2604 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2604 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543089341	chr20:23724835-23724836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567023024	chr20:23724839-23724840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369811562	chr20:23724848-23724849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543667440	chr20:23724868-23724869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113457266	chr20:23724895-23724896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562275279	chr20:23724906-23724907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528823496	chr20:23724914-23724915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549287425	chr20:23724921-23724922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566315965	chr20:23724928-23724929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534639374	chr20:23724943-23724944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528688046	chr20:23724944-23724945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140322713	chr20:23724952-23724953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191912584	chr20:23724972-23724973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537570636	chr20:23724976-23724977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201725493	chr20:23724991-23724992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4134385	chr20:23725019-23725020	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs567681378	chr20:23725083-23725084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115021058	chr20:23725084-23725085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183235716	chr20:23725085-23725086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188643570	chr20:23725092-23725093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556591340	chr20:23725097-23725098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534607453	chr20:23725118-23725119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191893636	chr20:23725126-23725127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575403883	chr20:23725139-23725140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577744822	chr20:23725146-23725147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182601186	chr20:23725148-23725149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543127930	chr20:23725289-23725290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545653306	chr20:23725306-23725307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563015182	chr20:23725310-23725311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6036512	chr20:23725315-23725316	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542175451	chr20:23725337-23725338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559076789	chr20:23725338-23725339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186878078	chr20:23725343-23725344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550914598	chr20:23725359-23725360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191300147	chr20:23725361-23725362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144153922	chr20:23725365-23725366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184961187	chr20:23725368-23725369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369072204	chr20:23725419-23725420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567716932	chr20:23725441-23725442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372146552	chr20:23725461-23725462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547015785	chr20:23725463-23725464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6049055	chr20:23725464-23725465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376796073	chr20:23725475-23725476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566728520	chr20:23725486-23725487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146501468	chr20:23725487-23725488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557731920	chr20:23725496-23725497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149110308	chr20:23725501-23725502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536823824	chr20:23725506-23725507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190205649	chr20:23725507-23725508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6049056	chr20:23725515-23725516	Enhancers	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
3	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr20:23725400-23725800	Enhancers	Osteobl	bone
5	chr20:23725400-23726000	Enhancers	NHLF	lung
6	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
7	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
13	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr20:23728600-23729200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr20:23728800-23731400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23729200-23730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr20:23730600-23730800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr20:23730600-23731000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr20:23730800-23731000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr20:23731000-23731200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr20:23731200-23731400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
34	chr20:23731400-23731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr20:23731600-23733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr20:23731800-23732000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr20:23731800-23732200	Enhancers	HUVEC	blood vessel
38	chr20:23732000-23732800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr20:23732200-23734200	Weak transcription	HUVEC	blood vessel
40	chr20:23732600-23734000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23732800-23733200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:23733200-23733600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:23733600-23737000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr20:23733800-23736600	Enhancers	NHDF-Ad	bronchial
45	chr20:23733800-23736800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr20:23734000-23736400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr20:23734000-23736400	Enhancers	Osteobl	bone
48	chr20:23734000-23736800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr20:23734200-23734400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr20:23734200-23736600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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