Variant report

Variant	esv3377303
Chromosome Location	chr20:23746098-23827552
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	chr20:23747142-23747274	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
3	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
4	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
5	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
6	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
7	CTCF	chr20:23763120-23763270	GM12868	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
8	CTCF	chr20:23763065-23763355	Fibrobl	skin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
9	CTCF	chr20:23779888-23780427	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
10	CTCF	chr20:23762811-23763754	A549	lung:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
11	CTCF	chr20:23779960-23780110	AG04450	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
12	CTCF	chr20:23763120-23763270	HL-60	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
13	CTCF	chr20:23779960-23780110	GM12865	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
14	CTCF	chr20:23776521-23776531	Lung_OC	lung:	n/a	n/a
15	CTCF	chr20:23779900-23780050	HMEC	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
16	CTCF	chr20:23779920-23780070	HVMF	connective:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
17	CTCF	chr20:23763020-23763170	GM12801	blood:	n/a	n/a
18	CTCF	chr20:23779920-23780070	NB4	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
19	CTCF	chr20:23763160-23763310	NHEK	skin:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
20	CTCF	chr20:23780280-23780430	HUVEC	blood vessel:	n/a	chr20:23780320-23780329
21	CTCF	chr20:23779960-23780110	Caco-2	colon:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
22	CTCF	chr20:23780280-23780430	Caco-2	colon:	n/a	chr20:23780320-23780329
23	CTCF	chr20:23779547-23780498	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
24	CTCF	chr20:23779912-23780152	Hela-S3	cervix:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
25	CTCF	chr20:23763140-23763290	GM12867	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
26	CTCF	chr20:23780247-23780339	GM19239	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
27	CTCF	chr20:23780182-23780519	H1-hESC	embryonic stem cell:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
28	CTCF	chr20:23823800-23823950	GM12874	blood:	n/a	n/a
29	CTCF	chr20:23779960-23780110	HRE	kidney:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
30	CTCF	chr20:23762860-23763010	HFF	foreskin:	n/a	n/a
31	CTCF	chr20:23779960-23780110	GM12873	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
32	CTCF	chr20:23779879-23780336	GM19240	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	chr20:23763105-23763292	GM20000	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
34	CTCF	chr20:23756660-23756810	MCF-7	breast:	n/a	chr20:23756767-23756780
35	CTCF	chr20:23805983-23806110	LNCaP	prostate:	n/a	n/a
36	CTCF	chr20:23779880-23780030	HepG2	liver:	n/a	n/a
37	CTCF	chr20:23763120-23763270	HUVEC	blood vessel:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
38	CTCF	chr20:23756640-23756790	HCFaa	heart:	n/a	chr20:23756767-23756780
39	CTCF	chr20:23780340-23780490	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr20:23763120-23763270	AoAF	blood vessel:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
41	CTCF	chr20:23780260-23780410	MCF-7	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
42	CTCF	chr20:23763140-23763290	HBMEC	blood vessel:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
43	CTCF	chr20:23763160-23763310	A549	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
44	CTCF	chr20:23780166-23780406	T-47D	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
45	CTCF	chr20:23763067-23763375	A549	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
46	CTCF	chr20:23763100-23763250	GM12872	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
47	CTCF	chr20:23779931-23780135	Lung_OC	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
48	CTCF	chr20:23779960-23780110	HMF	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
49	CTCF	chr20:23763090-23763322	Pancreas_OC	pancreas:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
50	CTCF	chr20:23779880-23780030	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23807306-23807356	SAEC	small airway:	n/a
2	chr20:23807306-23807356	SAEC	small airway:	n/a
3	chr20:23807359-23807409	ovcar-3	ovarian:	n/a
4	chr20:23807778-23807828	HCM	heart:	n/a
5	chr20:23807359-23807409	HUVEC	blood vessel:	n/a
6	chr20:23806999-23807049	AG09309	skin:	n/a
7	chr20:23807359-23807409	SK-N-MC	brain:	n/a
8	chr20:23807736-23807786	MCF10A-Er-Src	breast:	n/a
9	chr20:23807306-23807356	HRE	kidney:	n/a
10	chr20:23807359-23807409	MCF10A-Er-Src	breast:	n/a
11	chr20:23807306-23807356	HIPEpiC	eye:	n/a
12	chr20:23807306-23807356	LNCaP	prostate:	n/a
13	chr20:23807778-23807828	AG04449	skin:	fetal
14	chr20:23807778-23807828	A549	lung:	n/a
15	chr20:23807736-23807786	BE2_C	brain:	n/a
16	chr20:23807736-23807786	PFSK-1	brain:	n/a
17	chr20:23807736-23807786	AG04449	skin:	fetal
18	chr20:23806999-23807049	PFSK-1	brain:	n/a
19	chr20:23806999-23807049	AG04449	skin:	fetal
20	chr20:23807778-23807828	T-47D	breast:	n/a
21	chr20:23807736-23807786	HepG2	liver:	n/a
22	chr20:23807359-23807409	SK-N-SH	brain:	n/a
23	chr20:23806999-23807049	NHBE	bronchial:	n/a
24	chr20:23807778-23807828	PANC-1	pancreas:	n/a
25	chr20:23807778-23807828	Hela-S3	cervix:	n/a
26	chr20:23807306-23807356	U87	brain:	n/a
27	chr20:23807778-23807828	AG09309	skin:	n/a
28	chr20:23807736-23807786	NB4	blood:	n/a
29	chr20:23807306-23807356	HCT-116	colon:	n/a
30	chr20:23807359-23807409	NHBE	bronchial:	n/a
31	chr20:23807306-23807356	H1-hESC	embryonic stem cell:	embryo
32	chr20:23807306-23807356	HEK293	kidney:	embryo
33	chr20:23807359-23807409	HPAEpiC	pulmonary alveolar:	n/a
34	chr20:23807736-23807786	LNCaP	prostate:	n/a
35	chr20:23807306-23807356	AG09319	gingival:	n/a
36	chr20:23807359-23807409	NB4	blood:	n/a
37	chr20:23807359-23807409	Caco-2	colon:	n/a
38	chr20:23807306-23807356	Hepatocyte	liver:	n/a
39	chr20:23807778-23807828	GM19239	blood:	n/a
40	chr20:23807778-23807828	HUVEC	blood vessel:	n/a
41	chr20:23806999-23807049	GM06990	blood:	n/a
42	chr20:23806999-23807049	Hela-S3	cervix:	n/a
43	chr20:23807778-23807828	HNPCEpiC	eye:	n/a
44	chr20:23806999-23807049	HMEC	breast:	n/a
45	chr20:23807778-23807828	MCF10A-Er-Src	breast:	n/a
46	chr20:23807778-23807828	CMK	blood:	n/a
47	chr20:23807306-23807356	PANC-1	pancreas:	n/a
48	chr20:23807306-23807356	Caco-2	colon:	n/a
49	chr20:23807778-23807828	BE2_C	brain:	n/a
50	chr20:23807359-23807409	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
2	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
3	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
4	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
5	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
6	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
7	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
8	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
9	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
10	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
11	chr20:23779854..23780390-chr20:23870001..23870554,2	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	chr20:23778778-23778924	XLOC_013494
4	lnc-CST8-3	chr20:23784376-23784473	XLOC_013494

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

Extended variants
information (count: 2360 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2360 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6049088	chr20:23746143-23746144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139863320	chr20:23746151-23746152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576659241	chr20:23746155-23746156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561139534	chr20:23746158-23746159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6138058	chr20:23746203-23746204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374939859	chr20:23746218-23746219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555642070	chr20:23746231-23746232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143419167	chr20:23746238-23746239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550064471	chr20:23746284-23746285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146720963	chr20:23746299-23746300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139438920	chr20:23746300-23746301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6114264	chr20:23746310-23746311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149949329	chr20:23746326-23746327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537663435	chr20:23746340-23746341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543431564	chr20:23746380-23746381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562848686	chr20:23746454-23746455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111737906	chr20:23746455-23746456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531499155	chr20:23746495-23746496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189638632	chr20:23746498-23746499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs193245018	chr20:23746522-23746523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6138059	chr20:23746527-23746528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145201600	chr20:23746540-23746541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6106710	chr20:23746543-23746544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35488686	chr20:23746561-23746562	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185309946	chr20:23746567-23746568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149127102	chr20:23746576-23746577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570335461	chr20:23746586-23746587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535730167	chr20:23746604-23746605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555952020	chr20:23746621-23746622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143290602	chr20:23746629-23746630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147914737	chr20:23746638-23746639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577595290	chr20:23746650-23746651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190161517	chr20:23746672-23746673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543840916	chr20:23746678-23746679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545060325	chr20:23746685-23746686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141635651	chr20:23746694-23746695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34270854	chr20:23746707-23746708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576306397	chr20:23746737-23746738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147096226	chr20:23746739-23746740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563406438	chr20:23746742-23746743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181358498	chr20:23746756-23746757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59795194	chr20:23746767-23746768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188203211	chr20:23746783-23746784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138457172	chr20:23746786-23746787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572022673	chr20:23746802-23746803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs386813413	chr20:23746806-23746807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs180670710	chr20:23746807-23746808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116428859	chr20:23746808-23746809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185057610	chr20:23746820-23746821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377456623	chr20:23746851-23746852	Enhancers Weak transcription	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:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23744200-23746400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr20:23744400-23746400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr20:23744400-23754600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr20:23744800-23746200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr20:23744800-23746200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr20:23745000-23746800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr20:23746000-23746200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr20:23746000-23746600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr20:23746200-23747400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr20:23746400-23746600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr20:23746600-23746800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr20:23746600-23747200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr20:23746800-23747400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr20:23747200-23747400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr20:23747400-23747600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr20:23747600-23756200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr20:23748000-23748200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr20:23754600-23755000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr20:23755000-23756000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr20:23756000-23756800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr20:23756000-23757400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr20:23756200-23756400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr20:23756200-23756600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr20:23756200-23757000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr20:23756400-23756800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
26	chr20:23756400-23756800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr20:23756400-23757200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr20:23756400-23757400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr20:23756400-23757600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr20:23756600-23756800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr20:23756600-23756800	Bivalent Enhancer	Fetal Stomach	stomach
32	chr20:23756600-23757000	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr20:23756600-23757600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr20:23756600-23757800	Enhancers	Fetal Kidney	kidney
35	chr20:23756800-23757000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr20:23756800-23757400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr20:23757000-23757400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr20:23757200-23757400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr20:23757200-23757400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr20:23757200-23757400	Enhancers	Fetal Intestine Large	intestine
41	chr20:23757200-23757600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr20:23757200-23757600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr20:23757200-23757600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr20:23757200-23757600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr20:23757200-23757600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr20:23757200-23757800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr20:23757200-23758000	Enhancers	Osteobl	bone
48	chr20:23757200-23758200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr20:23757400-23757600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr20:23757400-23757600	Active TSS	iPS-20b Cell Line	embryonic stem cell

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