Variant report

Variant	esv3414346
Chromosome Location	chr20:23699402-23774974
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	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
2	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
3	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
4	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
5	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
6	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
7	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
8	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
9	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
10	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
11	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
12	CTCF	chr20:23763080-23763230	GM12864	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
13	CTCF	chr20:23763120-23763270	HFF-Myc	foreskin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
14	CTCF	chr20:23763034-23763366	K562	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
15	CTCF	chr20:23763140-23763290	GM12869	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
16	CTCF	chr20:23763100-23763250	MCF-7	breast:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
17	CTCF	chr20:23744462-23744492	GM10266	blood:	n/a	n/a
18	CTCF	chr20:23703820-23703970	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr20:23704337-23704656	GM12878	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
20	CTCF	chr20:23704420-23704570	Hela-S3	cervix:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
21	CTCF	chr20:23704308-23704679	GM12878	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
22	CTCF	chr20:23729517-23729596	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr20:23729640-23729790	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr20:23705020-23705170	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr20:23704194-23704202	MCF-7	breast:	n/a	n/a
26	CTCF	chr20:23763080-23763230	AG04450	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
27	CTCF	chr20:23763045-23763506	Gliobla	brain:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
28	CTCF	chr20:23704340-23704490	SAEC	small airway:	n/a	n/a
29	CTCF	chr20:23704360-23704510	HMF	breast:	n/a	chr20:23704496-23704505
30	CTCF	chr20:23763080-23763230	HRPEpiC	eye:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
31	CTCF	chr20:23756660-23756810	A549	lung:	n/a	chr20:23756767-23756780
32	CTCF	chr20:23763140-23763290	GM12864	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
33	CTCF	chr20:23729760-23729910	HEK293	kidney:	n/a	n/a
34	CTCF	chr20:23704685-23704688	GM19239	blood:	n/a	n/a
35	CTCF	chr20:23703638-23703722	MCF-7	breast:	n/a	n/a
36	CTCF	chr20:23763324-23763334	HepG2	liver:	n/a	n/a
37	CTCF	chr20:23704336-23704930	MCF-7	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
38	CTCF	chr20:23729640-23729790	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr20:23704375-23704634	Spleen_OC	spleen:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
40	CTCF	chr20:23762900-23762938	A549	lung:	n/a	n/a
41	CTCF	chr20:23763120-23763270	HL-60	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
42	CTCF	chr20:23762965-23763740	MCF-7	breast:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
43	CTCF	chr20:23704402-23704572	SK-N-SH_RA	brain:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
44	CTCF	chr20:23704122-23704692	SK-N-SH	brain:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
45	CTCF	chr20:23754906-23755044	MCF-7	breast:	n/a	chr20:23754976-23754989
46	CTCF	chr20:23704265-23704588	MCF-7	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
47	CTCF	chr20:23704340-23704490	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr20:23704355-23704882	A549	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
49	CTCF	chr20:23763120-23763270	AG10803	skin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
50	CTCF	chr20:23763113-23763295	Lung_OC	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23728432-23728482	ECC-1	luminal epithelium:	n/a
2	chr20:23731367-23731417	ovcar-3	ovarian:	n/a
3	chr20:23732873-23732923	NHBE	bronchial:	n/a
4	chr20:23728432-23728482	H1-hESC	embryonic stem cell:	embryo
5	chr20:23732595-23732645	GM06990	blood:	n/a
6	chr20:23732595-23732645	Caco-2	colon:	n/a
7	chr20:23731367-23731417	SAEC	small airway:	n/a
8	chr20:23728814-23728864	ProgFib	skin:	n/a
9	chr20:23732873-23732923	HL-60	blood:	n/a
10	chr20:23728432-23728482	HL-60	blood:	n/a
11	chr20:23728814-23728864	HEEpiC	esophagus:	n/a
12	chr20:23731367-23731417	BE2_C	brain:	n/a
13	chr20:23728432-23728482	GM12878	blood:	n/a
14	chr20:23728814-23728864	HepG2	liver:	n/a
15	chr20:23731367-23731417	IMR90	lung:	fetal
16	chr20:23731367-23731417	HCPEpiC	choroid plexus:	n/a
17	chr20:23732595-23732645	GM12892	blood:	n/a
18	chr20:23732873-23732923	T-47D	breast:	n/a
19	chr20:23728814-23728864	AoSMC	blood vessel:	n/a
20	chr20:23728432-23728482	NHBE	bronchial:	n/a
21	chr20:23732873-23732923	HUVEC	blood vessel:	n/a
22	chr20:23728814-23728864	HCM	heart:	n/a
23	chr20:23732873-23732923	HEK293	kidney:	embryo
24	chr20:23728814-23728864	HCT-116	colon:	n/a
25	chr20:23728432-23728482	NHDF-neo	bronchial:	n/a
26	chr20:23731367-23731417	SKMC	muscle:	n/a
27	chr20:23732873-23732923	GM12891	blood:	n/a
28	chr20:23732873-23732923	NHDF-neo	bronchial:	n/a
29	chr20:23732873-23732923	HPAEpiC	pulmonary alveolar:	n/a
30	chr20:23728814-23728864	HRE	kidney:	n/a
31	chr20:23728432-23728482	IMR90	lung:	fetal
32	chr20:23728432-23728482	BE2_C	brain:	n/a
33	chr20:23728814-23728864	Jurkat	blood:	n/a
34	chr20:23728814-23728864	U87	brain:	n/a
35	chr20:23728814-23728864	IMR90	lung:	fetal
36	chr20:23728814-23728864	Hepatocyte	liver:	n/a
37	chr20:23728814-23728864	CMK	blood:	n/a
38	chr20:23731367-23731417	GM12892	blood:	n/a
39	chr20:23731367-23731417	ProgFib	skin:	n/a
40	chr20:23728814-23728864	NHDF-neo	bronchial:	n/a
41	chr20:23731367-23731417	RPTEC	kidney:	n/a
42	chr20:23731367-23731417	LNCaP	prostate:	n/a
43	chr20:23732595-23732645	Hepatocyte	liver:	n/a
44	chr20:23732595-23732645	GM12891	blood:	n/a
45	chr20:23731367-23731417	SK-N-SH_RA	brain:	n/a
46	chr20:23732595-23732645	BJ	skin:	n/a
47	chr20:23728814-23728864	HRCEpiC	kidney:	n/a
48	chr20:23728814-23728864	HL-60	blood:	n/a
49	chr20:23732595-23732645	NHDF-neo	bronchial:	n/a
50	chr20:23732873-23732923	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
2	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
3	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
4	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
5	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
6	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
7	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
8	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
9	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
10	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
11	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
12	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
13	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
2	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083
3	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083
4	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083

Variant related genes	Relation type
CST1	TF binding region
ENSG00000230908	TF binding region
CST1	CpG island
ENSG00000230908	CpG island

Extended variants
information (count: 2744 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2744 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139684169	chr20:23700203-23700204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116038975	chr20:23700213-23700214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547063882	chr20:23700220-23700221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143707533	chr20:23700226-23700227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540112201	chr20:23700236-23700237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6106698	chr20:23700244-23700245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556799732	chr20:23700246-23700247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562724413	chr20:23700265-23700266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533373089	chr20:23700287-23700288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6049018	chr20:23700289-23700290	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs139687374	chr20:23700292-23700293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11697789	chr20:23700320-23700321	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372575268	chr20:23700327-23700328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35632085	chr20:23700330-23700331	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs377432436	chr20:23700359-23700360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557696011	chr20:23700387-23700388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139578621	chr20:23700392-23700393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545643615	chr20:23700416-23700417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189681729	chr20:23700418-23700419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6083232	chr20:23700419-23700420	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs144312583	chr20:23700435-23700436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561857701	chr20:23700456-23700457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527364400	chr20:23700560-23700561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567848506	chr20:23700564-23700565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146598608	chr20:23700602-23700603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570416396	chr20:23700619-23700620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373118084	chr20:23700630-23700631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4349407	chr20:23700631-23700632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34180040	chr20:23700633-23700634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116103104	chr20:23700658-23700659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4614993	chr20:23700663-23700664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs369028326	chr20:23700674-23700675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536072859	chr20:23700681-23700682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74477632	chr20:23700682-23700683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566180577	chr20:23700714-23700715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534780469	chr20:23700720-23700721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539068917	chr20:23700750-23700751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180862090	chr20:23700752-23700753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4377399	chr20:23700757-23700758	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs543401225	chr20:23700779-23700780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73314097	chr20:23700794-23700795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576244194	chr20:23700808-23700809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542025363	chr20:23700822-23700823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7266357	chr20:23700824-23700825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs13041947	chr20:23700832-23700833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145154815	chr20:23700859-23700860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34344461	chr20:23700864-23700865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4629230	chr20:23700872-23700873	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs151337148	chr20:23700877-23700878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533006601	chr20:23700904-23700905	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23700200-23701000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr20:23702200-23702400	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr20:23703600-23704000	Enhancers	Left Ventricle	heart
4	chr20:23713600-23714200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:23714200-23719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:23715200-23716000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:23715400-23716400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr20:23719000-23719400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
11	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr20:23725400-23725800	Enhancers	Osteobl	bone
13	chr20:23725400-23726000	Enhancers	NHLF	lung
14	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
15	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
21	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:23728600-23729200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr20:23728800-23731400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr20:23729200-23730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr20:23730600-23730800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr20:23730600-23731000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr20:23730800-23731000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr20:23731000-23731200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr20:23731200-23731400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
42	chr20:23731400-23731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr20:23731600-23733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr20:23731800-23732000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr20:23731800-23732200	Enhancers	HUVEC	blood vessel
46	chr20:23732000-23732800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr20:23732200-23734200	Weak transcription	HUVEC	blood vessel
48	chr20:23732600-23734000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr20:23732800-23733200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr20:23733200-23733600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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