Variant report

Variant	nsv1060247
Chromosome Location	chr20:29860167-29969913
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	chr20:29901133-29901495	HepG2	liver:	n/a	n/a
2	ATF1	chr20:29901261-29901460	K562	blood:	n/a	n/a
3	CEBPB	chr20:29891404-29891489	IMR90	lung:	n/a	chr20:29891449-29891460
4	CEBPB	chr20:29891290-29891604	HepG2	liver:	n/a	chr20:29891449-29891460
5	CEBPB	chr20:29886446-29886770	HepG2	liver:	n/a	chr20:29886585-29886596
6	CEBPB	chr20:29886470-29886721	A549	lung:	n/a	chr20:29886585-29886596
7	CEBPB	chr20:29901179-29901489	IMR90	lung:	n/a	n/a
8	CEBPB	chr20:29886588-29886598	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr20:29926865-29926997	HepG2	liver:	n/a	n/a
10	CEBPB	chr20:29901178-29901527	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:29939648-29939720	HepG2	liver:	n/a	chr20:29939667-29939678
12	CEBPB	chr20:29929046-29929296	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr20:29929475-29929483	K562	blood:	n/a	n/a
14	CEBPB	chr20:29901113-29901610	MCF-7	breast:	n/a	n/a
15	CEBPB	chr20:29930995-29931186	HepG2	liver:	n/a	chr20:29931087-29931098
16	CHD2	chr20:29952144-29952438	HepG2	liver:	n/a	n/a
17	CHD2	chr20:29952083-29952448	K562	blood:	n/a	n/a
18	CTCF	chr20:29901300-29901450	HVMF	connective:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
19	CTCF	chr20:29901280-29901430	GM12878	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
20	CTCF	chr20:29901269-29901510	ProgFib	skin:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
21	CTCF	chr20:29901185-29901436	H1-hESC	embryonic stem cell:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
22	CTCF	chr20:29901320-29901470	AG09319	gingival:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
23	CTCF	chr20:29901252-29901420	GM20000	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
24	CTCF	chr20:29901300-29901450	HPAF	blood vessel:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
25	CTCF	chr20:29941100-29941250	HepG2	liver:	n/a	n/a
26	CTCF	chr20:29900986-29901031	GM19239	blood:	n/a	n/a
27	CTCF	chr20:29900991-29901074	GM19240	blood:	n/a	n/a
28	CTCF	chr20:29901020-29901170	Caco-2	colon:	n/a	n/a
29	CTCF	chr20:29901260-29901410	HRPEpiC	eye:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
30	CTCF	chr20:29901260-29901410	WERI-Rb-1	eye:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
31	CTCF	chr20:29901300-29901450	AoAF	blood vessel:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
32	CTCF	chr20:29900700-29900850	HCT-116	colon:	n/a	n/a
33	CTCF	chr20:29901155-29901484	T-47D	breast:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
34	CTCF	chr20:29901280-29901430	GM12874	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
35	CTCF	chr20:29901060-29901210	HMEC	breast:	n/a	n/a
36	CTCF	chr20:29900936-29901684	HCT-116	colon:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
37	CTCF	chr20:29860380-29860530	HEK293	kidney:	n/a	n/a
38	CTCF	chr20:29900940-29901090	GM12866	blood:	n/a	n/a
39	CTCF	chr20:29901280-29901430	GM12868	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
40	CTCF	chr20:29900986-29901043	GM12892	blood:	n/a	n/a
41	CTCF	chr20:29900960-29901110	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr20:29901471-29901498	GM19239	blood:	n/a	n/a
43	CTCF	chr20:29900780-29901549	K562	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
44	CTCF	chr20:29901260-29901410	GM12865	blood:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
45	CTCF	chr20:29865700-29865850	HepG2	liver:	n/a	n/a
46	CTCF	chr20:29901100-29901250	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr20:29901220-29901370	HCM	heart:	n/a	chr20:29901332-29901353 chr20:29901350-29901368
48	CTCF	chr20:29901020-29901170	GM12869	blood:	n/a	n/a
49	CTCF	chr20:29901300-29901450	MCF-7	breast:	n/a	chr20:29901352-29901373 chr20:29901332-29901353 chr20:29901350-29901368
50	CTCF	chr20:29901200-29901350	WI-38	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:29955259-29955309	Hela-S3	cervix:	n/a
2	chr20:29955259-29955309	Hela-S3	cervix:	n/a
3	chr20:29956585-29956635	Jurkat	blood:	n/a
4	chr20:29956330-29956380	SK-N-MC	brain:	n/a
5	chr20:29896928-29896978	PrEC	prostate:	n/a
6	chr20:29956028-29956078	H1-hESC	embryonic stem cell:	embryo
7	chr20:29956062-29956112	AoSMC	blood vessel:	n/a
8	chr20:29960982-29961032	NHDF-neo	bronchial:	n/a
9	chr20:29892486-29892536	Hela-S3	cervix:	n/a
10	chr20:29960982-29961032	AG10803	skin:	n/a
11	chr20:29956585-29956635	SK-N-MC	brain:	n/a
12	chr20:29956330-29956380	HPAEpiC	pulmonary alveolar:	n/a
13	chr20:29892486-29892536	Jurkat	blood:	n/a
14	chr20:29896479-29896529	HEEpiC	esophagus:	n/a
15	chr20:29896479-29896529	AoSMC	blood vessel:	n/a
16	chr20:29896456-29896506	HUVEC	blood vessel:	n/a
17	chr20:29896456-29896506	MCF10A-Er-Src	breast:	n/a
18	chr20:29896456-29896506	MCF-7	breast:	n/a
19	chr20:29956585-29956635	HL-60	blood:	n/a
20	chr20:29892486-29892536	HIPEpiC	eye:	n/a
21	chr20:29956330-29956380	PFSK-1	brain:	n/a
22	chr20:29892486-29892536	AG04449	skin:	fetal
23	chr20:29956028-29956078	AG09309	skin:	n/a
24	chr20:29896928-29896978	GM12878	blood:	n/a
25	chr20:29956330-29956380	HCPEpiC	choroid plexus:	n/a
26	chr20:29965177-29965227	PrEC	prostate:	n/a
27	chr20:29960982-29961032	AG04449	skin:	fetal
28	chr20:29956585-29956635	HAEpiC	amniotic membrane:	n/a
29	chr20:29956028-29956078	NT2-D1	testis:	n/a
30	chr20:29956062-29956112	ProgFib	skin:	n/a
31	chr20:29956585-29956635	AG09319	gingival:	n/a
32	chr20:29896456-29896506	HCT-116	colon:	n/a
33	chr20:29896456-29896506	AG09319	gingival:	n/a
34	chr20:29892486-29892536	MCF-7	breast:	n/a
35	chr20:29956330-29956380	HAEpiC	amniotic membrane:	n/a
36	chr20:29956062-29956112	ovcar-3	ovarian:	n/a
37	chr20:29956585-29956635	SKMC	muscle:	n/a
38	chr20:29960982-29961032	HEEpiC	esophagus:	n/a
39	chr20:29896456-29896506	K562	blood:	n/a
40	chr20:29896928-29896978	Hela-S3	cervix:	n/a
41	chr20:29896456-29896506	NHDF-neo	bronchial:	n/a
42	chr20:29896456-29896506	AG10803	skin:	n/a
43	chr20:29896479-29896529	Hela-S3	cervix:	n/a
44	chr20:29896928-29896978	BJ	skin:	n/a
45	chr20:29892486-29892536	GM12878	blood:	n/a
46	chr20:29965177-29965227	Hela-S3	cervix:	n/a
47	chr20:29960982-29961032	ovcar-3	ovarian:	n/a
48	chr20:29956330-29956380	SK-N-SH	brain:	n/a
49	chr20:29956062-29956112	HEEpiC	esophagus:	n/a
50	chr20:29965177-29965227	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:29933564..29935935-chr20:29935958..29938008,2	MCF-7	breast:
2	chr20:29940769..29942399-chr20:29945457..29948097,2	MCF-7	breast:
3	chr20:29874751..29877240-chr20:29903779..29906129,2	K562	blood:
4	chr20:29874751..29877240-chr20:29903779..29906129,2	K562	blood:
5	chr20:29933564..29935935-chr20:29935958..29938008,2	MCF-7	breast:
6	chr20:29900644..29901274-chr20:30041865..30042847,4	MCF-7	breast:
7	chr20:29905971..29908391-chr20:29910613..29913391,2	K562	blood:
8	chr20:29900827..29901742-chr20:30090593..30091579,4	MCF-7	breast:
9	chr20:29955069..29955719-chr20:29963915..29964847,2	MCF-7	breast:
10	chr20:29940769..29942399-chr20:29945457..29948097,2	MCF-7	breast:
11	chr20:29900754..29901422-chr20:30042008..30042651,2	MCF-7	breast:
12	chr20:29960399..29962900-chr20:29964371..29965877,2	MCF-7	breast:
13	chr20:29905971..29908391-chr20:29910613..29913391,2	K562	blood:
14	chr20:29960399..29962900-chr20:29964371..29965877,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB119-2	chr20:29929174-29929962	NONHSAT079285
2	lnc-DEFB119-1	chr20:29966155-29966194	NR_073153
3	lnc-DEFB119-2	chr20:29930249-29931017	NONHSAT079285
4	lnc-DEFB119-2	chr20:29931121-29931202	NONHSAT079285
5	lnc-DEFB116-4	chr20:29899106-29899362	NONHSAT079284
6	lnc-DEFB119-1	chr20:29964966-29965165	NONHSAT079290
7	lnc-DEFB119-1	chr20:29966155-29966194	NONHSAT079289
8	lnc-DEFB119-1	chr20:29964966-29965242	NR_073153
9	lnc-DEFB119-1	chr20:29964966-29965242	NONHSAT079289
10	lnc-DEFB116-4	chr20:29899691-29899765	NONHSAT079284
11	lnc-DEFB119-2	chr20:29931511-29932274	NONHSAT079285

Variant related genes	Relation type
HAUS6P2	TF binding region
RPL31P3	TF binding region
DEFB116	TF binding region
ENSG00000212134	TF binding region
DEFB118	TF binding region
RNA5SP480	TF binding region
ENSG00000224628	TF binding region
DKKL1P1	TF binding region
DEFB117	TF binding region
HAUS6P2	CpG island
RPL31P3	CpG island
DEFB116	CpG island
ENSG00000212134	CpG island
DEFB118	CpG island
RNA5SP480	CpG island
ENSG00000224628	CpG island
DKKL1P1	CpG island
DEFB117	CpG island
ENSG00000212134	chromatin interactions

Extended variants
information (count: 850 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6119722	chr20:29860167-29860168	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115281318	chr20:29860233-29860234	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs546029936	chr20:29860260-29860261	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs562626384	chr20:29860266-29860267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs576301227	chr20:29860269-29860270	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs541988814	chr20:29860297-29860298	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs1884743	chr20:29860298-29860299	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527311809	chr20:29860301-29860302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs547051612	chr20:29860305-29860306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs11905764	chr20:29860306-29860307	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs116536446	chr20:29860322-29860323	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs186533074	chr20:29860333-29860334	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs569147147	chr20:29860366-29860367	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs531771875	chr20:29860372-29860373	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs528804075	chr20:29860393-29860394	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs370763530	chr20:29860397-29860398	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs188176234	chr20:29860425-29860426	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs568432736	chr20:29860483-29860484	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112289578	chr20:29860513-29860514	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536279664	chr20:29860609-29860610	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs553840428	chr20:29860618-29860619	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs180931059	chr20:29860649-29860650	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs570763357	chr20:29860675-29860676	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs6121224	chr20:29860684-29860685	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs4911529	chr20:29860698-29860699	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs576340409	chr20:29860722-29860723	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs538704285	chr20:29860737-29860738	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs542025822	chr20:29860748-29860749	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs555462578	chr20:29860759-29860760	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs536338106	chr20:29860813-29860814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541033442	chr20:29860819-29860820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563970606	chr20:29860843-29860844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149064909	chr20:29860845-29860846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112536337	chr20:29860881-29860882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185547383	chr20:29860883-29860884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115384205	chr20:29860895-29860896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4911530	chr20:29860933-29860934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs115755871	chr20:29860969-29860970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576282600	chr20:29860988-29860989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547867915	chr20:29860993-29860994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538968378	chr20:29861038-29861039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143093670	chr20:29861081-29861082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367671706	chr20:29861093-29861094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576131778	chr20:29861100-29861101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371228437	chr20:29861139-29861140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539828584	chr20:29861204-29861205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556526589	chr20:29861214-29861215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569939891	chr20:29861223-29861224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116761135	chr20:29861235-29861236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148216097	chr20:29861258-29861259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20688871	CNVD
Gastric cancer	22014070	CNVD
Cancer	20164919	CNVD

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29859000-29860600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
2	chr20:29859600-29860800	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr20:29860000-29860800	ZNF genes & repeats	Gastric	stomach
4	chr20:29860200-29860600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr20:29860600-29862000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr20:29862000-29862600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr20:29865000-29866600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr20:29865800-29866000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr20:29865800-29866800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr20:29867400-29868000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr20:29901000-29901400	Active TSS	A549	lung
12	chr20:29901000-29901600	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr20:29901200-29901400	Enhancers	Hela-S3	cervix
14	chr20:29901800-29902200	Active TSS	Fetal Heart	heart
15	chr20:29912400-29912800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:29918400-29919800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr20:29935800-29937200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr20:29956200-29956800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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