Variant report

Variant	nsv436326
Chromosome Location	chr20:23757769-23838141
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	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
4	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
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	chr20:23779880-23780030	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr20:23779683-23779759	GM12892	blood:	n/a	n/a
9	CTCF	chr20:23821960-23822110	Caco-2	colon:	n/a	n/a
10	CTCF	chr20:23826250-23826323	MCF-7	breast:	n/a	n/a
11	CTCF	chr20:23805840-23805990	K562	blood:	n/a	n/a
12	CTCF	chr20:23763120-23763270	HEK293	kidney:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
13	CTCF	chr20:23779893-23780429	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
14	CTCF	chr20:23763140-23763290	BJ	skin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
15	CTCF	chr20:23780280-23780430	HepG2	liver:	n/a	chr20:23780320-23780329
16	CTCF	chr20:23779881-23780348	GM12892	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
17	CTCF	chr20:23779960-23780110	GM12878	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
18	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
19	CTCF	chr20:23763039-23763574	MCF-7	breast:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
20	CTCF	chr20:23779960-23780110	AoAF	blood vessel:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
21	CTCF	chr20:23763324-23763334	HepG2	liver:	n/a	n/a
22	CTCF	chr20:23763120-23763270	SK-N-SH_RA	brain:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
23	CTCF	chr20:23763103-23763255	GM13976	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
24	CTCF	chr20:23779960-23780110	GM12874	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
25	CTCF	chr20:23779881-23780172	Medullo	brain:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
26	CTCF	chr20:23779960-23780110	HBMEC	blood vessel:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
27	CTCF	chr20:23832700-23832850	GM12867	blood:	n/a	n/a
28	CTCF	chr20:23779915-23780381	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
29	CTCF	chr20:23779880-23780030	HRE	kidney:	n/a	n/a
30	CTCF	chr20:23762860-23763010	HFF	foreskin:	n/a	n/a
31	CTCF	chr20:23779893-23780175	GM19239	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
32	CTCF	chr20:23780360-23780510	GM12873	blood:	n/a	n/a
33	CTCF	chr20:23832056-23832136	GM13976	blood:	n/a	n/a
34	CTCF	chr20:23763074-23763516	H1-hESC	embryonic stem cell:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
35	CTCF	chr20:23763096-23763361	A549	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
36	CTCF	chr20:23779880-23780030	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr20:23762977-23763623	H1-hESC	embryonic stem cell:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
38	CTCF	chr20:23779896-23780383	ProgFib	skin:	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	chr20:23779920-23780070	HFF	foreskin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
40	CTCF	chr20:23763100-23763250	GM12868	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
41	CTCF	chr20:23779960-23780110	HEEpiC	esophagus:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
42	CTCF	chr20:23763113-23763295	Lung_OC	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
43	CTCF	chr20:23779880-23780030	GM12801	blood:	n/a	n/a
44	CTCF	chr20:23780166-23780406	T-47D	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
45	CTCF	chr20:23763089-23763335	GM19240	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
46	CTCF	chr20:23762846-23762938	GM19238	blood:	n/a	n/a
47	CTCF	chr20:23779878-23780378	GM19238	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
48	CTCF	chr20:23779960-23780110	SK-N-SH_RA	brain:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
49	CTCF	chr20:23780215-23780398	K562	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
50	CTCF	chr20:23806103-23806106	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23807778-23807828	NHDF-neo	bronchial:	n/a
2	chr20:23807778-23807828	BE2_C	brain:	n/a
3	chr20:23807359-23807409	Hepatocyte	liver:	n/a
4	chr20:23807778-23807828	Hepatocyte	liver:	n/a
5	chr20:23807736-23807786	IMR90	lung:	fetal
6	chr20:23806999-23807049	HepG2	liver:	n/a
7	chr20:23807736-23807786	NHBE	bronchial:	n/a
8	chr20:23807736-23807786	HEEpiC	esophagus:	n/a
9	chr20:23807736-23807786	SKMC	muscle:	n/a
10	chr20:23807736-23807786	A549	lung:	n/a
11	chr20:23807306-23807356	SAEC	small airway:	n/a
12	chr20:23806999-23807049	T-47D	breast:	n/a
13	chr20:23806999-23807049	K562	blood:	n/a
14	chr20:23807736-23807786	HRPEpiC	eye:	n/a
15	chr20:23807359-23807409	MCF-7	breast:	n/a
16	chr20:23806999-23807049	AG04450	lung:	fetal
17	chr20:23807306-23807356	RPTEC	kidney:	n/a
18	chr20:23806999-23807049	ovcar-3	ovarian:	n/a
19	chr20:23807306-23807356	ECC-1	luminal epithelium:	n/a
20	chr20:23807778-23807828	SKMC	muscle:	n/a
21	chr20:23807359-23807409	RPTEC	kidney:	n/a
22	chr20:23807778-23807828	PANC-1	pancreas:	n/a
23	chr20:23807359-23807409	K562	blood:	n/a
24	chr20:23807778-23807828	SK-N-SH_RA	brain:	n/a
25	chr20:23806999-23807049	HAEpiC	amniotic membrane:	n/a
26	chr20:23807359-23807409	NH-A	brain:	n/a
27	chr20:23807359-23807409	HEEpiC	esophagus:	n/a
28	chr20:23807736-23807786	HNPCEpiC	eye:	n/a
29	chr20:23807778-23807828	HEEpiC	esophagus:	n/a
30	chr20:23807778-23807828	H1-hESC	embryonic stem cell:	embryo
31	chr20:23807306-23807356	SK-N-SH	brain:	n/a
32	chr20:23807736-23807786	HCPEpiC	choroid plexus:	n/a
33	chr20:23807359-23807409	HRCEpiC	kidney:	n/a
34	chr20:23807359-23807409	HL-60	blood:	n/a
35	chr20:23807736-23807786	U87	brain:	n/a
36	chr20:23807778-23807828	AG09319	gingival:	n/a
37	chr20:23807778-23807828	AG04450	lung:	fetal
38	chr20:23807359-23807409	GM12878	blood:	n/a
39	chr20:23807306-23807356	LNCaP	prostate:	n/a
40	chr20:23807359-23807409	HNPCEpiC	eye:	n/a
41	chr20:23807359-23807409	IMR90	lung:	fetal
42	chr20:23807736-23807786	GM12891	blood:	n/a
43	chr20:23807778-23807828	T-47D	breast:	n/a
44	chr20:23807736-23807786	HRCEpiC	kidney:	n/a
45	chr20:23806999-23807049	IMR90	lung:	fetal
46	chr20:23806999-23807049	Caco-2	colon:	n/a
47	chr20:23807359-23807409	GM12892	blood:	n/a
48	chr20:23806999-23807049	MCF10A-Er-Src	breast:	n/a
49	chr20:23807359-23807409	PANC-1	pancreas:	n/a
50	chr20:23807736-23807786	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
2	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
3	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:
4	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
5	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
6	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
7	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
8	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
9	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
10	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
11	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:

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

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

Extended variants
information (count: 2067 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2067 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140193395	chr20:23757784-23757785	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188313956	chr20:23757814-23757815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530793932	chr20:23757867-23757868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192967384	chr20:23757880-23757881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567669220	chr20:23757881-23757882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529885267	chr20:23757900-23757901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546419777	chr20:23757903-23757904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6049105	chr20:23757914-23757915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs11697006	chr20:23757966-23757967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113083838	chr20:23758023-23758024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140659754	chr20:23758038-23758039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538886455	chr20:23758057-23758058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377379780	chr20:23758058-23758059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182851873	chr20:23758113-23758114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555221733	chr20:23758138-23758139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150087660	chr20:23758144-23758145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6132656	chr20:23758149-23758150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572505634	chr20:23758158-23758159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577361711	chr20:23758159-23758160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6132657	chr20:23758190-23758191	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556571645	chr20:23758197-23758198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186848836	chr20:23758220-23758221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554935200	chr20:23758222-23758223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191256922	chr20:23758238-23758239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561227300	chr20:23758263-23758264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184917484	chr20:23758273-23758274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540377103	chr20:23758276-23758277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559825107	chr20:23758281-23758282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376407002	chr20:23758298-23758299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116108179	chr20:23758368-23758369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4813508	chr20:23758383-23758384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531319479	chr20:23758387-23758388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145535239	chr20:23758401-23758402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189628071	chr20:23758403-23758404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534130837	chr20:23758414-23758415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117693843	chr20:23758438-23758439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141215333	chr20:23758439-23758440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539969512	chr20:23758448-23758449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs193077790	chr20:23758482-23758483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185438377	chr20:23758505-23758506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542205200	chr20:23758512-23758513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111537386	chr20:23758565-23758566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58998030	chr20:23758567-23758568	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs574635022	chr20:23758581-23758582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540069364	chr20:23758597-23758598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6083256	chr20:23758622-23758623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189911343	chr20:23758672-23758673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370762113	chr20:23758678-23758679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545527235	chr20:23758682-23758683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6049106	chr20:23758700-23758701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23756600-23757800	Enhancers	Fetal Kidney	kidney
2	chr20:23757200-23757800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr20:23757200-23758000	Enhancers	Osteobl	bone
4	chr20:23757200-23758200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr20:23757600-23759000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr20:23757600-23759000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr20:23757800-23759000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr20:23758200-23759000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr20:23758800-23760000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr20:23759000-23759800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr20:23759000-23759800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr20:23759000-23759800	Enhancers	NHDF-Ad	bronchial
13	chr20:23759000-23760000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr20:23759000-23760000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr20:23759200-23759400	Flanking Active TSS	Osteobl	bone
16	chr20:23759200-23760000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr20:23759400-23760000	Enhancers	Osteobl	bone
18	chr20:23759800-23760000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr20:23762200-23763600	Enhancers	Dnd41	blood
20	chr20:23775400-23776600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr20:23776200-23776600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr20:23793400-23794000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr20:23794000-23795000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr20:23795000-23795800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23800600-23802400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr20:23801200-23802000	Enhancers	NHDF-Ad	bronchial
27	chr20:23801200-23802200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr20:23801400-23806800	Enhancers	Fetal Thymus	thymus
29	chr20:23802000-23806800	Weak transcription	NHDF-Ad	bronchial
30	chr20:23803800-23804200	Enhancers	Stomach Smooth Muscle	stomach
31	chr20:23803800-23805400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr20:23804000-23804200	Enhancers	Brain Anterior Caudate	brain
33	chr20:23804000-23804200	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr20:23804000-23804400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr20:23804000-23804400	Bivalent Enhancer	Fetal Stomach	stomach
36	chr20:23804000-23804600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr20:23804000-23804600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr20:23804000-23804600	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr20:23804000-23804600	Enhancers	Fetal Muscle Trunk	muscle
40	chr20:23804000-23804800	Enhancers	Dnd41	blood
41	chr20:23804000-23805000	Enhancers	Fetal Muscle Leg	muscle
42	chr20:23804000-23805000	Enhancers	Lung	lung
43	chr20:23804200-23804400	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr20:23804200-23804600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr20:23804200-23804600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr20:23804200-23804800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr20:23804400-23805200	Enhancers	Fetal Stomach	stomach
48	chr20:23804400-23807400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr20:23804600-23806400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:23804600-23806800	Weak transcription	H1 Cell Line	embryonic stem cell

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