Variant report

Variant	nsv592206
Chromosome Location	chr3:162305516-162380954
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	BRCA1	chr3:162343607-162343624	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr3:162318973-162319104	HepG2	liver:	n/a	n/a
3	CEBPB	chr3:162364026-162364261	Hela-S3	cervix:	n/a	chr3:162364112-162364123
4	CEBPB	chr3:162363990-162364207	A549	lung:	n/a	chr3:162364112-162364123 chr3:162364019-162364030
5	CEBPB	chr3:162375840-162376163	A549	lung:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
6	CEBPB	chr3:162375783-162376266	MCF-7	breast:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
7	CEBPB	chr3:162375805-162376171	Hela-S3	cervix:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
8	CEBPB	chr3:162318597-162318906	IMR90	lung:	n/a	chr3:162318771-162318782 chr3:162318770-162318783 chr3:162318770-162318783 chr3:162318770-162318781 chr3:162318772-162318781
9	CEBPB	chr3:162323772-162323878	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr3:162375834-162376167	IMR90	lung:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
11	CEBPB	chr3:162375820-162376163	HepG2	liver:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
12	CEBPB	chr3:162328054-162328397	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:162375910-162376151	ECC-1	luminal epithelium:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
14	CEBPB	chr3:162375773-162376159	MCF-7	breast:	n/a	chr3:162375998-162376009 chr3:162375998-162376011 chr3:162375960-162375971 chr3:162375999-162376010 chr3:162375998-162376011 chr3:162375998-162376009
15	CEBPB	chr3:162318673-162319181	HepG2	liver:	n/a	chr3:162318771-162318782 chr3:162318770-162318783 chr3:162318770-162318783 chr3:162318770-162318781 chr3:162318772-162318781
16	CEBPB	chr3:162363967-162364264	HepG2	liver:	n/a	chr3:162364112-162364123 chr3:162364019-162364030
17	CTCF	chr3:162357965-162358027	GM20000	blood:	n/a	n/a
18	CTCF	chr3:162377836-162377844	MCF-7	breast:	n/a	n/a
19	CTCF	chr3:162323516-162323574	GM10248	blood:	n/a	n/a
20	CTCF	chr3:162361763-162361785	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:162323510-162323512	GM10248	blood:	n/a	n/a
22	CTCF	chr3:162314580-162314730	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr3:162361738-162361757	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:162338003-162338037	GM20000	blood:	n/a	n/a
25	CTCF	chr3:162377841-162377879	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:162361320-162361351	GM13976	blood:	n/a	n/a
27	CUX1	chr3:162317068-162317249	GM12878	blood:	n/a	n/a
28	E2F4	chr3:162305466-162305564	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F6	chr3:162322845-162323143	H1-hESC	embryonic stem cell:	n/a	n/a
30	EP300	chr3:162359766-162360068	SK-N-SH_RA	brain:	n/a	chr3:162359885-162359894
31	EP300	chr3:162318951-162319326	HepG2	liver:	n/a	n/a
32	EP300	chr3:162318845-162319183	HepG2	liver:	n/a	n/a
33	EP300	chr3:162316293-162316729	H1-hESC	embryonic stem cell:	n/a	n/a
34	EP300	chr3:162359807-162360166	SK-N-SH_RA	brain:	n/a	chr3:162359885-162359894
35	EP300	chr3:162320533-162320738	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr3:162344052-162344238	GM12878	blood:	n/a	chr3:162344133-162344147
37	FAM48A	chr3:162309676-162310084	GM12878	blood:	n/a	n/a
38	FAM48A	chr3:162344662-162344768	GM12878	blood:	n/a	n/a
39	FAM48A	chr3:162330895-162331091	GM12878	blood:	n/a	n/a
40	FOS	chr3:162359735-162360032	MCF10A-Er-Src	breast:	n/a	chr3:162359885-162359893 chr3:162359885-162359892 chr3:162359884-162359894
41	FOS	chr3:162321020-162321039	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:162320520-162320764	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:162320468-162320740	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:162320491-162320782	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:162320460-162320766	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr3:162375974-162376051	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:162375939-162376040	MCF10A-Er-Src	breast:	n/a	n/a
48	FOSL2	chr3:162320464-162320747	MCF-7	breast:	n/a	n/a
49	FOXA1	chr3:162318847-162319303	HepG2	liver:	n/a	n/a
50	GABPA	chr3:162342108-162342155	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:162317560-162317610	BJ	skin:	n/a
2	chr3:162317560-162317610	AG09319	gingival:	n/a
3	chr3:162317560-162317610	HRE	kidney:	n/a
4	chr3:162317560-162317610	HCF	heart:	n/a
5	chr3:162317560-162317610	HCT-116	colon:	n/a
6	chr3:162317560-162317610	PrEC	prostate:	n/a
7	chr3:162317560-162317610	ProgFib	skin:	n/a
8	chr3:162317560-162317610	HUVEC	blood vessel:	n/a
9	chr3:162317560-162317610	HRPEpiC	eye:	n/a
10	chr3:162317560-162317610	IMR90	lung:	fetal
11	chr3:162317560-162317610	HCM	heart:	n/a
12	chr3:162317560-162317610	MCF-7	breast:	n/a
13	chr3:162317560-162317610	Hepatocyte	liver:	n/a
14	chr3:162317560-162317610	AG04450	lung:	fetal
15	chr3:162317560-162317610	HAEpiC	amniotic membrane:	n/a
16	chr3:162317560-162317610	NT2-D1	testis:	n/a
17	chr3:162317560-162317610	BE2_C	brain:	n/a
18	chr3:162317560-162317610	GM19239	blood:	n/a
19	chr3:162317560-162317610	RPTEC	kidney:	n/a
20	chr3:162317560-162317610	GM06990	blood:	n/a
21	chr3:162317560-162317610	ovcar-3	ovarian:	n/a
22	chr3:162317560-162317610	Jurkat	blood:	n/a
23	chr3:162317560-162317610	MCF10A-Er-Src	breast:	n/a
24	chr3:162317560-162317610	SK-N-MC	brain:	n/a
25	chr3:162317560-162317610	HEK293	kidney:	embryo
26	chr3:162317560-162317610	ECC-1	luminal epithelium:	n/a
27	chr3:162317560-162317610	NH-A	brain:	n/a
28	chr3:162317560-162317610	HIPEpiC	eye:	n/a
29	chr3:162317560-162317610	GM12892	blood:	n/a
30	chr3:162317560-162317610	HCPEpiC	choroid plexus:	n/a
31	chr3:162317560-162317610	PANC-1	pancreas:	n/a
32	chr3:162317560-162317610	AoSMC	blood vessel:	n/a
33	chr3:162317560-162317610	SK-N-SH_RA	brain:	n/a
34	chr3:162317560-162317610	HEEpiC	esophagus:	n/a
35	chr3:162317560-162317610	H1-hESC	embryonic stem cell:	embryo
36	chr3:162317560-162317610	HMEC	breast:	n/a
37	chr3:162317560-162317610	AG10803	skin:	n/a
38	chr3:162317560-162317610	HepG2	liver:	n/a
39	chr3:162317560-162317610	AG04449	skin:	fetal
40	chr3:162317560-162317610	AG09309	skin:	n/a
41	chr3:162317560-162317610	Caco-2	colon:	n/a
42	chr3:162317560-162317610	NB4	blood:	n/a
43	chr3:162317560-162317610	K562	blood:	n/a
44	chr3:162317560-162317610	GM12878	blood:	n/a
45	chr3:162317560-162317610	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:162317560-162317610	NHBE	bronchial:	n/a
47	chr3:162317560-162317610	HNPCEpiC	eye:	n/a
48	chr3:162317560-162317610	LNCaP	prostate:	n/a
49	chr3:162317560-162317610	SAEC	small airway:	n/a
50	chr3:162317560-162317610	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:162268890..162270552-chr3:162314764..162316650,2	MCF-7	breast:
2	chr3:162307801..162310469-chr3:162314134..162316904,3	MCF-7	breast:
3	chr3:162367684..162370185-chr3:162370811..162372665,2	MCF-7	breast:
4	chr3:162307801..162310469-chr3:162314134..162316904,3	MCF-7	breast:
5	chr3:162367684..162370185-chr3:162370811..162372665,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000243044	TF binding region
ENSG00000243044	CpG island

Extended variants
information (count: 2229 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2229 , 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	rs16850831	chr3:162305516-162305517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543261331	chr3:162305532-162305533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185565204	chr3:162305544-162305545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs16850834	chr3:162305549-162305550	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs190442333	chr3:162305556-162305557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573144589	chr3:162305561-162305562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs180787175	chr3:162305573-162305574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185188958	chr3:162305614-162305615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555051479	chr3:162305622-162305623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533709880	chr3:162305657-162305658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543870376	chr3:162305688-162305689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564168696	chr3:162305698-162305699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577336587	chr3:162305708-162305709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188535387	chr3:162305723-162305724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560343123	chr3:162305758-162305759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529528949	chr3:162305769-162305770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549691581	chr3:162305814-162305815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13321457	chr3:162305835-162305836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs13066627	chr3:162305920-162305921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531683306	chr3:162305947-162305948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551494470	chr3:162305953-162305954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576683567	chr3:162305996-162305997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375121661	chr3:162305998-162305999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534306890	chr3:162306003-162306004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546792757	chr3:162306047-162306048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566705601	chr3:162306051-162306052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535375040	chr3:162306061-162306062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555591439	chr3:162306074-162306075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544138011	chr3:162306101-162306102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13318622	chr3:162306139-162306140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs537817091	chr3:162306146-162306147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59339763	chr3:162306196-162306197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370680280	chr3:162306242-162306243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577297560	chr3:162306266-162306267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373489445	chr3:162306299-162306300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181325596	chr3:162306329-162306330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148034557	chr3:162306347-162306348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573943625	chr3:162306432-162306433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375618571	chr3:162306453-162306454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376843604	chr3:162306457-162306458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546403727	chr3:162306495-162306496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563155219	chr3:162306541-162306542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531927883	chr3:162306565-162306566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9834927	chr3:162306574-162306575	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565305823	chr3:162306645-162306646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77149246	chr3:162306665-162306666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2169728	chr3:162306711-162306712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547949962	chr3:162306723-162306724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564961097	chr3:162306759-162306760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59141791	chr3:162306760-162306761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162305200-162305600	Weak transcription	Dnd41	blood
2	chr3:162305600-162305800	Enhancers	Dnd41	blood
3	chr3:162305800-162307600	Weak transcription	Dnd41	blood
4	chr3:162307600-162308400	Genic enhancers	Dnd41	blood
5	chr3:162308400-162308800	Weak transcription	Dnd41	blood
6	chr3:162308800-162310400	Enhancers	Dnd41	blood
7	chr3:162310400-162311400	Weak transcription	Dnd41	blood
8	chr3:162311400-162312800	Genic enhancers	Dnd41	blood
9	chr3:162312800-162314400	Enhancers	Dnd41	blood
10	chr3:162313800-162317200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr3:162314200-162316400	Enhancers	Brain Substantia Nigra	brain
12	chr3:162314200-162317200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr3:162314400-162315200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr3:162314400-162315800	Flanking Active TSS	Dnd41	blood
15	chr3:162314400-162316400	Enhancers	Brain Hippocampus Middle	brain
16	chr3:162314400-162318800	Weak transcription	HSMM	muscle
17	chr3:162314800-162315200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr3:162314800-162315600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr3:162314800-162315600	Enhancers	Brain Angular Gyrus	brain
20	chr3:162314800-162316200	Enhancers	Brain Cingulate Gyrus	brain
21	chr3:162314800-162316600	Enhancers	Brain Anterior Caudate	brain
22	chr3:162314800-162316800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:162315000-162315200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:162315000-162315600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:162315000-162315800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr3:162315000-162315800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr3:162315000-162316200	Enhancers	GM12878-XiMat	blood
28	chr3:162315200-162315600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:162315200-162316000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:162315200-162316000	Enhancers	Brain Germinal Matrix	brain
31	chr3:162315200-162316600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:162315600-162316000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr3:162315600-162317400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr3:162315800-162316200	Enhancers	Dnd41	blood
35	chr3:162316000-162316200	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr3:162316000-162316400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:162316200-162316400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr3:162316200-162316400	Flanking Active TSS	GM12878-XiMat	blood
39	chr3:162316200-162316800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr3:162316200-162316800	Enhancers	Fetal Muscle Leg	muscle
41	chr3:162316200-162317000	Enhancers	Fetal Heart	heart
42	chr3:162316200-162317400	Flanking Active TSS	Dnd41	blood
43	chr3:162316400-162317000	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr3:162316400-162317000	Active TSS	GM12878-XiMat	blood
45	chr3:162316600-162317000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:162317000-162317200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:162317000-162317200	Enhancers	GM12878-XiMat	blood
48	chr3:162317000-162318400	Weak transcription	Fetal Heart	heart
49	chr3:162317400-162317600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:162317400-162318000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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