Variant report

Variant	nsv585729
Chromosome Location	chr20:23766096-23836124
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	BACH1	chr20:23832673-23832794	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr20:23828408-23828598	A549	lung:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
4	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
5	CEBPB	chr20:23828412-23828599	HepG2	liver:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
6	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
7	CTCF	chr20:23779920-23780070	BE2_C	brain:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
8	CTCF	chr20:23822953-23822998	GM10266	blood:	n/a	n/a
9	CTCF	chr20:23779888-23780347	NHEK	skin:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
10	CTCF	chr20:23779880-23780030	HepG2	liver:	n/a	n/a
11	CTCF	chr20:23779800-23779950	GM12864	blood:	n/a	n/a
12	CTCF	chr20:23779890-23780385	Fibrobl	skin:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
13	CTCF	chr20:23805801-23806056	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr20:23826271-23826333	Medullo	brain:	n/a	n/a
15	CTCF	chr20:23810371-23810443	GM13976	blood:	n/a	n/a
16	CTCF	chr20:23779960-23780110	AoAF	blood vessel:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
17	CTCF	chr20:23779801-23780482	A549	lung:	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	chr20:23834070-23834125	GM10266	blood:	n/a	n/a
19	CTCF	chr20:23780300-23780450	GM12871	blood:	n/a	chr20:23780320-23780329
20	CTCF	chr20:23805913-23806106	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr20:23779920-23780070	NHDF-neo	bronchial:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
22	CTCF	chr20:23779900-23780050	HMEC	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
23	CTCF	chr20:23779880-23780030	GM12864	blood:	n/a	n/a
24	CTCF	chr20:23778940-23779090	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr20:23779837-23780510	MCF-7	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
26	CTCF	chr20:23779880-23780030	SAEC	small airway:	n/a	n/a
27	CTCF	chr20:23779900-23780050	HFF-Myc	foreskin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
28	CTCF	chr20:23780309-23780608	MCF-7	breast:	n/a	chr20:23780320-23780329
29	CTCF	chr20:23805840-23805990	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr20:23805960-23806110	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr20:23821960-23822110	Caco-2	colon:	n/a	n/a
32	CTCF	chr20:23779960-23780110	AG04450	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
33	CTCF	chr20:23779900-23780050	AG04450	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
34	CTCF	chr20:23779898-23780151	GM10248	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
35	CTCF	chr20:23780204-23780345	Hela-S3	cervix:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
36	CTCF	chr20:23779880-23780030	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr20:23779831-23780203	IMR90	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
38	CTCF	chr20:23779907-23780379	GM13977	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
39	CTCF	chr20:23779888-23780179	K562	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
40	CTCF	chr20:23826243-23826366	LNCaP	prostate:	n/a	n/a
41	CTCF	chr20:23806035-23806099	GM13976	blood:	n/a	n/a
42	CTCF	chr20:23779960-23780110	AG09309	skin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
43	CTCF	chr20:23779900-23780050	HCT-116	colon:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
44	CTCF	chr20:23779960-23780110	HEEpiC	esophagus:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
45	CTCF	chr20:23780260-23780410	Caco-2	colon:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
46	CTCF	chr20:23779931-23780147	Spleen_OC	spleen:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
47	CTCF	chr20:23779940-23780090	GM12878	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
48	CTCF	chr20:23780240-23780390	GM12872	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
49	CTCF	chr20:23780260-23780410	HepG2	liver:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
50	CTCF	chr20:23825740-23825890	GM12867	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23807778-23807828	SK-N-SH	brain:	n/a
2	chr20:23806999-23807049	HRE	kidney:	n/a
3	chr20:23807778-23807828	PrEC	prostate:	n/a
4	chr20:23807736-23807786	PANC-1	pancreas:	n/a
5	chr20:23807778-23807828	NH-A	brain:	n/a
6	chr20:23807778-23807828	Hela-S3	cervix:	n/a
7	chr20:23807778-23807828	Hepatocyte	liver:	n/a
8	chr20:23807359-23807409	BJ	skin:	n/a
9	chr20:23806999-23807049	AoSMC	blood vessel:	n/a
10	chr20:23807306-23807356	GM12878	blood:	n/a
11	chr20:23807359-23807409	HRCEpiC	kidney:	n/a
12	chr20:23807736-23807786	HEEpiC	esophagus:	n/a
13	chr20:23807736-23807786	HCT-116	colon:	n/a
14	chr20:23807306-23807356	HCPEpiC	choroid plexus:	n/a
15	chr20:23807359-23807409	HRE	kidney:	n/a
16	chr20:23806999-23807049	ProgFib	skin:	n/a
17	chr20:23806999-23807049	HRPEpiC	eye:	n/a
18	chr20:23807306-23807356	AG09309	skin:	n/a
19	chr20:23806999-23807049	CMK	blood:	n/a
20	chr20:23807778-23807828	SKMC	muscle:	n/a
21	chr20:23807736-23807786	HRPEpiC	eye:	n/a
22	chr20:23807736-23807786	Hepatocyte	liver:	n/a
23	chr20:23807778-23807828	IMR90	lung:	fetal
24	chr20:23807736-23807786	NH-A	brain:	n/a
25	chr20:23807306-23807356	SK-N-MC	brain:	n/a
26	chr20:23807359-23807409	K562	blood:	n/a
27	chr20:23807778-23807828	HCM	heart:	n/a
28	chr20:23807359-23807409	HMEC	breast:	n/a
29	chr20:23807359-23807409	PFSK-1	brain:	n/a
30	chr20:23807359-23807409	T-47D	breast:	n/a
31	chr20:23806999-23807049	H1-hESC	embryonic stem cell:	embryo
32	chr20:23806999-23807049	NHDF-neo	bronchial:	n/a
33	chr20:23807306-23807356	MCF-7	breast:	n/a
34	chr20:23807359-23807409	AoSMC	blood vessel:	n/a
35	chr20:23807736-23807786	HEK293	kidney:	embryo
36	chr20:23806999-23807049	GM12892	blood:	n/a
37	chr20:23807306-23807356	Caco-2	colon:	n/a
38	chr20:23807359-23807409	SK-N-MC	brain:	n/a
39	chr20:23807778-23807828	BE2_C	brain:	n/a
40	chr20:23807736-23807786	K562	blood:	n/a
41	chr20:23806999-23807049	ovcar-3	ovarian:	n/a
42	chr20:23807306-23807356	GM19239	blood:	n/a
43	chr20:23806999-23807049	T-47D	breast:	n/a
44	chr20:23807736-23807786	HRCEpiC	kidney:	n/a
45	chr20:23807736-23807786	BJ	skin:	n/a
46	chr20:23807778-23807828	AoSMC	blood vessel:	n/a
47	chr20:23807736-23807786	NHDF-neo	bronchial:	n/a
48	chr20:23807736-23807786	ProgFib	skin:	n/a
49	chr20:23807778-23807828	AG10803	skin:	n/a
50	chr20:23807736-23807786	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
2	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
3	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
4	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
5	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-3	chr20:23778778-23778924	XLOC_013494
2	lnc-CST8-3	chr20:23784376-23784473	XLOC_013494
3	lnc-CST8-3	chr20:23785871-23786300	XLOC_013494
4	lnc-CST8-3	chr20:23785160-23785281	XLOC_013494

Variant related genes	Relation type
CST2	TF binding region
ENSG00000230908	TF binding region
CST2	CpG island
ENSG00000230908	CpG island
WWC2	miRNA target sites
WWP2	miRNA target sites
XIAP	miRNA target sites

Extended variants
information (count: 1720 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1720 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556991108	chr20:23773923-23773924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs144617602	chr20:23774116-23774117	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs4591413	chr20:23774138-23774139	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535366760	chr20:23774139-23774140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542713514	chr20:23774737-23774738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201940303	chr20:23774760-23774761	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs559146069	chr20:23774776-23774777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528093819	chr20:23774806-23774807	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149223029	chr20:23774818-23774819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564518457	chr20:23774821-23774822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs143374013	chr20:23774825-23774826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs550853461	chr20:23774834-23774835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567895781	chr20:23774860-23774861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs182996726	chr20:23774873-23774874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs547086617	chr20:23774874-23774875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs6106718	chr20:23774885-23774886	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs556332835	chr20:23774905-23774906	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs137884118	chr20:23774920-23774921	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs114962993	chr20:23774961-23774962	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs140846301	chr20:23774983-23774984	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs556926993	chr20:23775040-23775041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs115673844	chr20:23775041-23775042	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs187289903	chr20:23775056-23775057	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553057101	chr20:23775065-23775066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs5841006	chr20:23775101-23775102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572633603	chr20:23775105-23775106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs191760850	chr20:23775108-23775109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs113480423	chr20:23775130-23775131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs552698966	chr20:23775404-23775405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138613660	chr20:23775410-23775411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538205399	chr20:23775443-23775444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4319988	chr20:23775453-23775454	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs114057982	chr20:23775469-23775470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4549173	chr20:23775488-23775489	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192534463	chr20:23775550-23775551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572692924	chr20:23775553-23775554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538394046	chr20:23775597-23775598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558183392	chr20:23775626-23775627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574909067	chr20:23775628-23775629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560828851	chr20:23775643-23775644	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376893313	chr20:23775663-23775664	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs543833844	chr20:23775680-23775681	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs371551640	chr20:23775683-23775684	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544963531	chr20:23775689-23775690	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs184348350	chr20:23775695-23775696	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs531630954	chr20:23775719-23775720	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563459408	chr20:23775732-23775733	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs190807652	chr20:23775735-23775736	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs543054308	chr20:23775741-23775742	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs79850732	chr20:23775742-23775743	Enhancers	TF binding region	1 gene(s)	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:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23775400-23776600	Enhancers	Placenta Amnion	Placenta Amnion
2	chr20:23776200-23776600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr20:23793400-23794000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr20:23794000-23795000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:23795000-23795800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:23800600-23802400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr20:23801200-23802000	Enhancers	NHDF-Ad	bronchial
8	chr20:23801200-23802200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr20:23801400-23806800	Enhancers	Fetal Thymus	thymus
10	chr20:23802000-23806800	Weak transcription	NHDF-Ad	bronchial
11	chr20:23803800-23804200	Enhancers	Stomach Smooth Muscle	stomach
12	chr20:23803800-23805400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr20:23804000-23804200	Enhancers	Brain Anterior Caudate	brain
14	chr20:23804000-23804200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr20:23804000-23804400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:23804000-23804400	Bivalent Enhancer	Fetal Stomach	stomach
17	chr20:23804000-23804600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr20:23804000-23804600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr20:23804000-23804600	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr20:23804000-23804600	Enhancers	Fetal Muscle Trunk	muscle
21	chr20:23804000-23804800	Enhancers	Dnd41	blood
22	chr20:23804000-23805000	Enhancers	Fetal Muscle Leg	muscle
23	chr20:23804000-23805000	Enhancers	Lung	lung
24	chr20:23804200-23804400	Flanking Active TSS	Stomach Smooth Muscle	stomach
25	chr20:23804200-23804600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr20:23804200-23804600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr20:23804200-23804800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr20:23804400-23805200	Enhancers	Fetal Stomach	stomach
29	chr20:23804400-23807400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr20:23804600-23806400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr20:23804600-23806800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr20:23804600-23806800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr20:23804800-23805200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr20:23804800-23807400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr20:23805000-23806800	Weak transcription	Fetal Muscle Leg	muscle
36	chr20:23805200-23805400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr20:23805400-23806400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr20:23805400-23807000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr20:23806400-23807600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr20:23806400-23807800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr20:23806400-23807800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr20:23806600-23807400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr20:23806600-23807400	Enhancers	NHLF	lung
44	chr20:23806600-23807800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr20:23806800-23807400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr20:23806800-23807400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr20:23806800-23807400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr20:23806800-23807400	Enhancers	Fetal Muscle Leg	muscle
49	chr20:23806800-23807800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr20:23806800-23807800	Enhancers	NHDF-Ad	bronchial

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