Variant report

Variant	nsv1056210
Chromosome Location	chr20:23645826-23697939
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	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
5	CEBPB	chr20:23655411-23655454	HepG2	liver:	n/a	n/a
6	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
7	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
8	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
9	CHD1	chr20:23648812-23649497	IMR90	lung:	n/a	n/a
10	CHD2	chr20:23649131-23649258	HepG2	liver:	n/a	n/a
11	CHD2	chr20:23649288-23649303	GM12878	blood:	n/a	n/a
12	CTCF	chr20:23646861-23647158	K562	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
13	CTCF	chr20:23649072-23649571	K562	blood:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
14	CTCF	chr20:23649140-23649290	GM12874	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
15	CTCF	chr20:23646920-23647070	AoAF	blood vessel:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
16	CTCF	chr20:23648999-23649545	IMR90	lung:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
17	CTCF	chr20:23649140-23649290	HA-sp	spinal cord:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
18	CTCF	chr20:23649416-23649540	GM12892	blood:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649449-23649470
19	CTCF	chr20:23646940-23647090	AG04449	skin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
20	CTCF	chr20:23646900-23647050	BE2_C	brain:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
21	CTCF	chr20:23648540-23648690	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr20:23646920-23647070	HRPEpiC	eye:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
23	CTCF	chr20:23646960-23647110	RPTEC	kidney:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
24	CTCF	chr20:23649079-23649346	Spleen_OC	spleen:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
25	CTCF	chr20:23649140-23649290	HVMF	connective:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
26	CTCF	chr20:23648560-23648710	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr20:23649140-23649290	AG04449	skin:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
28	CTCF	chr20:23646880-23647030	A549	lung:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
29	CTCF	chr20:23646880-23647030	Hela-S3	cervix:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
30	CTCF	chr20:23646952-23647072	GM12878	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
31	CTCF	chr20:23649160-23649310	HCT-116	colon:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
32	CTCF	chr20:23649100-23649250	HCM	heart:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
33	CTCF	chr20:23649077-23649323	H1-hESC	embryonic stem cell:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
34	CTCF	chr20:23649064-23649336	MCF-7	breast:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
35	CTCF	chr20:23649160-23649310	HEEpiC	esophagus:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
36	CTCF	chr20:23646940-23647090	HPAF	blood vessel:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
37	CTCF	chr20:23649120-23649270	GM12801	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
38	CTCF	chr20:23649100-23649250	HCT-116	colon:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
39	CTCF	chr20:23648994-23649635	H1-hESC	embryonic stem cell:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
40	CTCF	chr20:23646920-23647070	HAc	cerebellar:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
41	CTCF	chr20:23648527-23649805	A549	lung:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
42	CTCF	chr20:23646880-23647030	HRE	kidney:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
43	CTCF	chr20:23646980-23647130	GM12873	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
44	CTCF	chr20:23649067-23649580	HUVEC	blood vessel:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
45	CTCF	chr20:23646920-23647070	SAEC	small airway:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
46	CTCF	chr20:23646920-23647070	MCF-7	breast:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
47	CTCF	chr20:23649346-23649553	A549	lung:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649449-23649470
48	CTCF	chr20:23649062-23649368	GM12891	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
49	CTCF	chr20:23667840-23667990	HEK293	kidney:	n/a	n/a
50	CTCF	chr20:23649041-23649632	K562	blood:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23670047-23670097	PrEC	prostate:	n/a
2	chr20:23666505-23666555	HCPEpiC	choroid plexus:	n/a
3	chr20:23669241-23669291	GM19239	blood:	n/a
4	chr20:23669241-23669291	SKMC	muscle:	n/a
5	chr20:23671108-23671158	HCT-116	colon:	n/a
6	chr20:23669241-23669291	GM06990	blood:	n/a
7	chr20:23669470-23669520	HNPCEpiC	eye:	n/a
8	chr20:23669470-23669520	Hela-S3	cervix:	n/a
9	chr20:23670047-23670097	A549	lung:	n/a
10	chr20:23671108-23671158	PFSK-1	brain:	n/a
11	chr20:23666505-23666555	Jurkat	blood:	n/a
12	chr20:23670089-23670139	Hela-S3	cervix:	n/a
13	chr20:23669241-23669291	HIPEpiC	eye:	n/a
14	chr20:23670089-23670139	Hepatocyte	liver:	n/a
15	chr20:23669241-23669291	NHDF-neo	bronchial:	n/a
16	chr20:23669241-23669291	RPTEC	kidney:	n/a
17	chr20:23671108-23671158	Hela-S3	cervix:	n/a
18	chr20:23670089-23670139	CMK	blood:	n/a
19	chr20:23671108-23671158	AG10803	skin:	n/a
20	chr20:23670047-23670097	HRE	kidney:	n/a
21	chr20:23671108-23671158	AoSMC	blood vessel:	n/a
22	chr20:23671108-23671158	HCM	heart:	n/a
23	chr20:23671108-23671158	NT2-D1	testis:	n/a
24	chr20:23669241-23669291	AG04450	lung:	fetal
25	chr20:23671108-23671158	HepG2	liver:	n/a
26	chr20:23670089-23670139	HMEC	breast:	n/a
27	chr20:23670089-23670139	MCF10A-Er-Src	breast:	n/a
28	chr20:23669470-23669520	HIPEpiC	eye:	n/a
29	chr20:23669470-23669520	AoSMC	blood vessel:	n/a
30	chr20:23666505-23666555	HRPEpiC	eye:	n/a
31	chr20:23670047-23670097	Caco-2	colon:	n/a
32	chr20:23670047-23670097	SK-N-SH_RA	brain:	n/a
33	chr20:23670047-23670097	SKMC	muscle:	n/a
34	chr20:23670089-23670139	AG09319	gingival:	n/a
35	chr20:23669241-23669291	HMEC	breast:	n/a
36	chr20:23670047-23670097	LNCaP	prostate:	n/a
37	chr20:23670047-23670097	ECC-1	luminal epithelium:	n/a
38	chr20:23670089-23670139	ProgFib	skin:	n/a
39	chr20:23670089-23670139	GM19239	blood:	n/a
40	chr20:23669241-23669291	IMR90	lung:	fetal
41	chr20:23666505-23666555	A549	lung:	n/a
42	chr20:23670089-23670139	H1-hESC	embryonic stem cell:	embryo
43	chr20:23670047-23670097	Hepatocyte	liver:	n/a
44	chr20:23669470-23669520	AG10803	skin:	n/a
45	chr20:23670047-23670097	NHBE	bronchial:	n/a
46	chr20:23666505-23666555	K562	blood:	n/a
47	chr20:23669241-23669291	SK-N-SH_RA	brain:	n/a
48	chr20:23671108-23671158	HRE	kidney:	n/a
49	chr20:23669470-23669520	HUVEC	blood vessel:	n/a
50	chr20:23670047-23670097	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
2	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
3	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
4	chr20:23648842..23649774-chr20:23870335..23871266,4	MCF-7	breast:
5	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:
6	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
7	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
8	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
9	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:

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

Extended variants
information (count: 2206 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2206 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8117359	chr20:23645826-23645827	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571079448	chr20:23645847-23645848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529114125	chr20:23645885-23645886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371181262	chr20:23645889-23645890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115421599	chr20:23645941-23645942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185757707	chr20:23645954-23645955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565349011	chr20:23645987-23645988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535287840	chr20:23646019-23646020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547173848	chr20:23646060-23646061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550976300	chr20:23646087-23646088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146398309	chr20:23646123-23646124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529183682	chr20:23646158-23646159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139798929	chr20:23646173-23646174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553518943	chr20:23646196-23646197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141165994	chr20:23646226-23646227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534485729	chr20:23646264-23646265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551186944	chr20:23646280-23646281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570990527	chr20:23646286-23646287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536784535	chr20:23646300-23646301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376192588	chr20:23646328-23646329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191057640	chr20:23646330-23646331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183697853	chr20:23646345-23646346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559263414	chr20:23646421-23646422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536248962	chr20:23646467-23646468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553355228	chr20:23646477-23646478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116093642	chr20:23646486-23646487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571982890	chr20:23646497-23646498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367653362	chr20:23646528-23646529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536007303	chr20:23646553-23646554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150742347	chr20:23646555-23646556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201698380	chr20:23646616-23646617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139118183	chr20:23646630-23646631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554696799	chr20:23646659-23646660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187976954	chr20:23646687-23646688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371880396	chr20:23646721-23646722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544760358	chr20:23646781-23646782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190547985	chr20:23646782-23646783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149905646	chr20:23646793-23646794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2424597	chr20:23646809-23646810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs183154603	chr20:23646828-23646829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528417320	chr20:23646839-23646840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140519357	chr20:23646840-23646841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144485785	chr20:23646844-23646845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530518585	chr20:23646862-23646863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187125426	chr20:23646891-23646892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6138031	chr20:23646900-23646901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191943262	chr20:23646970-23646971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577078530	chr20:23646991-23646992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373560783	chr20:23646994-23646995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147857144	chr20:23646996-23646997	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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

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	chr20:23642400-23649400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr20:23642600-23647000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr20:23642600-23647000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr20:23643200-23646000	Enhancers	HepG2	liver
10	chr20:23643400-23646800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr20:23643800-23647800	Weak transcription	Fetal Muscle Leg	muscle
12	chr20:23644000-23648400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr20:23645400-23646200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:23645800-23646000	Enhancers	Spleen	Spleen
15	chr20:23645800-23647000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr20:23646000-23647000	Weak transcription	Spleen	Spleen
17	chr20:23646000-23649200	Weak transcription	HepG2	liver
18	chr20:23646800-23647200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr20:23647000-23647200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr20:23647000-23647600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr20:23647000-23647600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr20:23647000-23647600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr20:23647000-23647800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr20:23647000-23648000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr20:23647000-23648000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr20:23647000-23648000	Enhancers	HUVEC	blood vessel
27	chr20:23647000-23648200	Enhancers	Spleen	Spleen
28	chr20:23647000-23648800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr20:23647200-23647400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr20:23647200-23648000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr20:23647200-23648400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr20:23647400-23648000	Enhancers	HSMMtube	muscle
33	chr20:23647400-23648200	Enhancers	Fetal Lung	lung
34	chr20:23647600-23648600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr20:23647800-23648200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr20:23647800-23648200	Enhancers	Fetal Muscle Leg	muscle
37	chr20:23647800-23648200	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr20:23648200-23648400	Weak transcription	Fetal Muscle Leg	muscle
39	chr20:23648200-23648400	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr20:23648200-23649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23648200-23650400	Weak transcription	Spleen	Spleen
42	chr20:23648400-23648600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr20:23648400-23648600	Enhancers	Fetal Muscle Trunk	muscle
44	chr20:23648400-23648800	Enhancers	Fetal Muscle Leg	muscle
45	chr20:23648400-23649200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr20:23648600-23648800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr20:23648600-23649000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr20:23648800-23649200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr20:23649000-23650400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr20:23649200-23649400	Enhancers	Skeletal Muscle Female	skeletal muscle

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