Variant report

Variant	nsv458952
Chromosome Location	chr20:23644387-23775819
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	ARID3A	chr20:23649147-23649450	HepG2	liver:	n/a	n/a
2	BRCA1	chr20:23649179-23649335	HepG2	liver:	n/a	n/a
3	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
4	CEBPB	chr20:23684500-23684595	A549	lung:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
5	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
6	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
7	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
8	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
9	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
10	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
11	CEBPB	chr20:23684405-23684588	HepG2	liver:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
12	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
13	CEBPB	chr20:23655411-23655454	HepG2	liver:	n/a	n/a
14	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
15	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
16	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
17	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
18	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
19	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
20	CHD1	chr20:23648812-23649497	IMR90	lung:	n/a	n/a
21	CHD2	chr20:23649288-23649303	GM12878	blood:	n/a	n/a
22	CHD2	chr20:23649131-23649258	HepG2	liver:	n/a	n/a
23	CTCF	chr20:23649160-23649310	GM12871	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
24	CTCF	chr20:23704380-23704530	AG04450	lung:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
25	CTCF	chr20:23649040-23649190	HAc	cerebellar:	n/a	n/a
26	CTCF	chr20:23649100-23649250	HEK293	kidney:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
27	CTCF	chr20:23646960-23647110	HEEpiC	esophagus:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
28	CTCF	chr20:23704420-23704570	HRPEpiC	eye:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
29	CTCF	chr20:23763140-23763290	GM12864	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
30	CTCF	chr20:23646917-23647127	MCF-7	breast:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
31	CTCF	chr20:23763120-23763270	GM12871	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
32	CTCF	chr20:23763120-23763270	GM12873	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
33	CTCF	chr20:23649009-23649586	HepG2	liver:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
34	CTCF	chr20:23763240-23763390	BE2_C	brain:	n/a	n/a
35	CTCF	chr20:23649080-23649332	GM13977	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
36	CTCF	chr20:23754840-23754990	HMEC	breast:	n/a	chr20:23754976-23754989
37	CTCF	chr20:23735680-23735830	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr20:23704080-23704230	GM12873	blood:	n/a	n/a
39	CTCF	chr20:23649120-23649270	HPAF	blood vessel:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
40	CTCF	chr20:23646969-23647025	LNCaP	prostate:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
41	CTCF	chr20:23649140-23649290	GM06990	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
42	CTCF	chr20:23763086-23763342	GM12891	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
43	CTCF	chr20:23704740-23704890	HepG2	liver:	n/a	chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704787-23704796 chr20:23704740-23704758
44	CTCF	chr20:23667636-23668122	K562	blood:	n/a	n/a
45	CTCF	chr20:23704340-23704490	GM12873	blood:	n/a	n/a
46	CTCF	chr20:23649180-23649330	GM06990	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
47	CTCF	chr20:23648680-23648830	AG09309	skin:	n/a	n/a
48	CTCF	chr20:23649396-23649567	GM10248	blood:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649449-23649470
49	CTCF	chr20:23648496-23648510	K562	blood:	n/a	n/a
50	CTCF	chr20:23729640-23729790	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23671108-23671158	ovcar-3	ovarian:	n/a
2	chr20:23670047-23670097	HEK293	kidney:	embryo
3	chr20:23669241-23669291	GM12878	blood:	n/a
4	chr20:23670047-23670097	Jurkat	blood:	n/a
5	chr20:23670047-23670097	AoSMC	blood vessel:	n/a
6	chr20:23732595-23732645	HepG2	liver:	n/a
7	chr20:23732873-23732923	AG10803	skin:	n/a
8	chr20:23670047-23670097	NH-A	brain:	n/a
9	chr20:23671108-23671158	AoSMC	blood vessel:	n/a
10	chr20:23669470-23669520	HCM	heart:	n/a
11	chr20:23732873-23732923	ECC-1	luminal epithelium:	n/a
12	chr20:23669470-23669520	ECC-1	luminal epithelium:	n/a
13	chr20:23728432-23728482	HCT-116	colon:	n/a
14	chr20:23671108-23671158	ECC-1	luminal epithelium:	n/a
15	chr20:23728432-23728482	AG04449	skin:	fetal
16	chr20:23731367-23731417	HL-60	blood:	n/a
17	chr20:23732873-23732923	Jurkat	blood:	n/a
18	chr20:23671108-23671158	SKMC	muscle:	n/a
19	chr20:23670089-23670139	LNCaP	prostate:	n/a
20	chr20:23731367-23731417	HNPCEpiC	eye:	n/a
21	chr20:23731367-23731417	GM12878	blood:	n/a
22	chr20:23671108-23671158	PFSK-1	brain:	n/a
23	chr20:23671108-23671158	T-47D	breast:	n/a
24	chr20:23670047-23670097	RPTEC	kidney:	n/a
25	chr20:23670089-23670139	Caco-2	colon:	n/a
26	chr20:23670047-23670097	HepG2	liver:	n/a
27	chr20:23669241-23669291	AG09319	gingival:	n/a
28	chr20:23732873-23732923	K562	blood:	n/a
29	chr20:23728814-23728864	Hepatocyte	liver:	n/a
30	chr20:23670047-23670097	HRE	kidney:	n/a
31	chr20:23728814-23728864	BJ	skin:	n/a
32	chr20:23670047-23670097	HMEC	breast:	n/a
33	chr20:23670047-23670097	NB4	blood:	n/a
34	chr20:23670047-23670097	AG09319	gingival:	n/a
35	chr20:23728432-23728482	AG09319	gingival:	n/a
36	chr20:23728432-23728482	NHBE	bronchial:	n/a
37	chr20:23732595-23732645	NH-A	brain:	n/a
38	chr20:23669470-23669520	PFSK-1	brain:	n/a
39	chr20:23728814-23728864	ProgFib	skin:	n/a
40	chr20:23732595-23732645	SAEC	small airway:	n/a
41	chr20:23670047-23670097	AG10803	skin:	n/a
42	chr20:23728432-23728482	Hela-S3	cervix:	n/a
43	chr20:23732873-23732923	BJ	skin:	n/a
44	chr20:23669470-23669520	BJ	skin:	n/a
45	chr20:23669470-23669520	NB4	blood:	n/a
46	chr20:23669241-23669291	NH-A	brain:	n/a
47	chr20:23731367-23731417	HIPEpiC	eye:	n/a
48	chr20:23732595-23732645	T-47D	breast:	n/a
49	chr20:23670047-23670097	SK-N-MC	brain:	n/a
50	chr20:23669470-23669520	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
2	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
3	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
4	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
5	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
6	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
7	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
8	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
9	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
10	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
11	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
12	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
13	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
14	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
15	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
16	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
17	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
18	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
19	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
20	chr20:23648842..23649774-chr20:23870335..23871266,4	MCF-7	breast:
21	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
22	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
23	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:

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

Variant related genes	Relation type
CST4	TF binding region
CST2P1	TF binding region
ENSG00000230908	TF binding region
CST1	TF binding region
CST4	CpG island
CST2P1	CpG island
ENSG00000230908	CpG island
CST1	CpG island

Extended variants
information (count: 5147 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5147 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2424595	chr20:23644387-23644388	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533481540	chr20:23644405-23644406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151009305	chr20:23644414-23644415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569954358	chr20:23644438-23644439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529345532	chr20:23644492-23644493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557625432	chr20:23644494-23644495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549021784	chr20:23644518-23644519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566053143	chr20:23644526-23644527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34599074	chr20:23644531-23644532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534984952	chr20:23644586-23644587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576299162	chr20:23644590-23644591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557889414	chr20:23644622-23644623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570703692	chr20:23644658-23644659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11905347	chr20:23644659-23644660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556385320	chr20:23644661-23644662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184515799	chr20:23644673-23644674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190628832	chr20:23644688-23644689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543783014	chr20:23644704-23644705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181931538	chr20:23644711-23644712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs377217498	chr20:23644764-23644765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142223315	chr20:23644785-23644786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540996928	chr20:23644790-23644791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565189694	chr20:23644808-23644809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187434408	chr20:23644881-23644882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563958252	chr20:23644892-23644893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188813914	chr20:23644894-23644895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543751350	chr20:23644900-23644901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563644253	chr20:23644918-23644919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146174204	chr20:23644925-23644926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549329289	chr20:23644978-23644979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536176187	chr20:23644988-23644989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528607280	chr20:23645049-23645050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554530600	chr20:23645078-23645079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571593884	chr20:23645085-23645086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181615694	chr20:23645139-23645140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556455151	chr20:23645152-23645153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147866809	chr20:23645174-23645175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535616682	chr20:23645189-23645190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555298476	chr20:23645193-23645194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78566187	chr20:23645233-23645234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141566002	chr20:23645240-23645241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59733981	chr20:23645248-23645249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150422818	chr20:23645272-23645273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547496529	chr20:23645305-23645306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185392203	chr20:23645310-23645311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138238841	chr20:23645333-23645334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563607524	chr20:23645354-23645355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530170820	chr20:23645356-23645357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574018201	chr20:23645369-23645370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572758372	chr20:23645381-23645382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23637200-23660000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23641800-23647000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr20:23641800-23647200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr20:23641800-23647200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr20:23641800-23652200	Weak transcription	Adipose Nuclei	Adipose
6	chr20:23642400-23644800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr20:23642400-23649400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr20:23642600-23647000	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr20:23642600-23647000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr20:23643200-23646000	Enhancers	HepG2	liver
11	chr20:23643400-23646800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr20:23643800-23647800	Weak transcription	Fetal Muscle Leg	muscle
13	chr20:23644000-23648400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr20:23644800-23645000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr20:23644800-23645400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr20:23645000-23645600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr20:23645400-23646200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr20:23645600-23645800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr20:23645800-23646000	Enhancers	Spleen	Spleen
20	chr20:23645800-23647000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr20:23646000-23647000	Weak transcription	Spleen	Spleen
22	chr20:23646000-23649200	Weak transcription	HepG2	liver
23	chr20:23646800-23647200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr20:23647000-23647200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23647000-23647600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr20:23647000-23647600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr20:23647000-23647600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr20:23647000-23647800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr20:23647000-23648000	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr20:23647000-23648000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr20:23647000-23648000	Enhancers	HUVEC	blood vessel
32	chr20:23647000-23648200	Enhancers	Spleen	Spleen
33	chr20:23647000-23648800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr20:23647200-23647400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr20:23647200-23648000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr20:23647200-23648400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr20:23647400-23648000	Enhancers	HSMMtube	muscle
38	chr20:23647400-23648200	Enhancers	Fetal Lung	lung
39	chr20:23647600-23648600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr20:23647800-23648200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23647800-23648200	Enhancers	Fetal Muscle Leg	muscle
42	chr20:23647800-23648200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr20:23648200-23648400	Weak transcription	Fetal Muscle Leg	muscle
44	chr20:23648200-23648400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr20:23648200-23649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr20:23648200-23650400	Weak transcription	Spleen	Spleen
47	chr20:23648400-23648600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr20:23648400-23648600	Enhancers	Fetal Muscle Trunk	muscle
49	chr20:23648400-23648800	Enhancers	Fetal Muscle Leg	muscle
50	chr20:23648400-23649200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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