Variant report

Variant	nsv912583
Chromosome Location	chr20:873749-926397
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	chr20:892718-892815	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr20:921731-921791	HepG2	liver:	n/a	n/a
3	CBX3	chr20:912147-912383	HCT-116	colon:	n/a	n/a
4	CEBPB	chr20:892274-892474	HepG2	liver:	n/a	chr20:892408-892419
5	CEBPB	chr20:890820-891090	A549	lung:	n/a	n/a
6	CEBPB	chr20:905306-905575	K562	blood:	n/a	chr20:905412-905423
7	CEBPB	chr20:876270-876520	HepG2	liver:	n/a	chr20:876366-876377
8	CEBPB	chr20:890855-891004	K562	blood:	n/a	n/a
9	CEBPB	chr20:890841-891137	IMR90	lung:	n/a	n/a
10	CEBPB	chr20:890846-891143	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:896245-896512	HepG2	liver:	n/a	chr20:896378-896389 chr20:896380-896391 chr20:896378-896391
12	CEBPB	chr20:905276-905535	HepG2	liver:	n/a	chr20:905412-905423
13	CEBPZ	chr20:912151-912386	HepG2	liver:	n/a	n/a
14	CHD2	chr20:925496-925746	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr20:892565-892837	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr20:892580-892730	GM12870	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
17	CTCF	chr20:892606-892791	MCF-7	breast:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
18	CTCF	chr20:892520-892670	A549	lung:	n/a	chr20:892633-892641
19	CTCF	chr20:892470-893007	HCT-116	colon:	n/a	chr20:892887-892895 chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
20	CTCF	chr20:892570-892780	K562	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
21	CTCF	chr20:915178-915401	H1-hESC	embryonic stem cell:	n/a	chr20:915287-915305
22	CTCF	chr20:892680-892830	HepG2	liver:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709
23	CTCF	chr20:892600-892750	GM12872	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
24	CTCF	chr20:892454-892890	H1-hESC	embryonic stem cell:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
25	CTCF	chr20:892566-892820	H1-hESC	embryonic stem cell:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
26	CTCF	chr20:900695-900722	H1-hESC	embryonic stem cell:	n/a	chr20:900711-900720
27	CTCF	chr20:892640-892790	HCT-116	colon:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709
28	CTCF	chr20:892420-892570	NHEK	skin:	n/a	n/a
29	CTCF	chr20:892684-892745	LNCaP	prostate:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709
30	CTCF	chr20:892613-892825	GM19240	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
31	CTCF	chr20:892669-892728	LNCaP	prostate:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709
32	CTCF	chr20:892780-892930	GM12873	blood:	n/a	chr20:892887-892895
33	CTCF	chr20:915240-915390	WERI-Rb-1	eye:	n/a	chr20:915287-915305
34	CTCF	chr20:892530-892821	K562	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
35	CTCF	chr20:884880-885030	GM12872	blood:	n/a	n/a
36	CTCF	chr20:892700-892850	SAEC	small airway:	n/a	n/a
37	CTCF	chr20:892600-892750	GM12865	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
38	CTCF	chr20:892679-892737	A549	lung:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709
39	CTCF	chr20:892616-892793	MCF-7	breast:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
40	CTCF	chr20:892600-892750	HepG2	liver:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
41	CTCF	chr20:915160-915310	HEK293	kidney:	n/a	chr20:915287-915305
42	CTCF	chr20:892620-892770	GM12875	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
43	CTCF	chr20:892589-892810	GM12892	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
44	CTCF	chr20:892479-892793	MCF-7	breast:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
45	CTCF	chr20:892620-892770	Caco-2	colon:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
46	CTCF	chr20:892574-892798	HepG2	liver:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
47	CTCF	chr20:892673-892742	Hela-S3	cervix:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709
48	CTCF	chr20:892620-892770	SAEC	small airway:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
49	CTCF	chr20:892620-892770	GM12868	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709 chr20:892633-892641
50	CTCF	chr20:892676-892751	GM10248	blood:	n/a	chr20:892695-892708 chr20:892693-892711 chr20:892688-892709

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:896349-896399	HepG2	liver:	n/a
2	chr20:896349-896399	T-47D	breast:	n/a
3	chr20:896349-896399	NHBE	bronchial:	n/a
4	chr20:896349-896399	SK-N-SH	brain:	n/a
5	chr20:897050-897100	MCF-7	breast:	n/a
6	chr20:897545-897595	HMEC	breast:	n/a
7	chr20:896564-896614	BE2_C	brain:	n/a
8	chr20:896981-897031	AG04450	lung:	fetal
9	chr20:896876-896926	K562	blood:	n/a
10	chr20:897545-897595	NB4	blood:	n/a
11	chr20:896564-896614	SK-N-SH	brain:	n/a
12	chr20:896564-896614	SKMC	muscle:	n/a
13	chr20:896349-896399	HRE	kidney:	n/a
14	chr20:897600-897650	NHBE	bronchial:	n/a
15	chr20:896564-896614	SK-N-SH_RA	brain:	n/a
16	chr20:897545-897595	ovcar-3	ovarian:	n/a
17	chr20:897024-897074	SK-N-SH	brain:	n/a
18	chr20:896349-896399	ProgFib	skin:	n/a
19	chr20:897024-897074	SAEC	small airway:	n/a
20	chr20:896349-896399	PrEC	prostate:	n/a
21	chr20:897024-897074	HRPEpiC	eye:	n/a
22	chr20:897545-897595	GM06990	blood:	n/a
23	chr20:897600-897650	HPAEpiC	pulmonary alveolar:	n/a
24	chr20:897024-897074	SK-N-SH_RA	brain:	n/a
25	chr20:897024-897074	HUVEC	blood vessel:	n/a
26	chr20:896876-896926	PANC-1	pancreas:	n/a
27	chr20:897050-897100	AG09319	gingival:	n/a
28	chr20:897050-897100	NH-A	brain:	n/a
29	chr20:897545-897595	HCM	heart:	n/a
30	chr20:896564-896614	GM06990	blood:	n/a
31	chr20:896876-896926	U87	brain:	n/a
32	chr20:897050-897100	A549	lung:	n/a
33	chr20:896981-897031	HRCEpiC	kidney:	n/a
34	chr20:896876-896926	AG04449	skin:	fetal
35	chr20:897545-897595	GM12891	blood:	n/a
36	chr20:897600-897650	Jurkat	blood:	n/a
37	chr20:896981-897031	HUVEC	blood vessel:	n/a
38	chr20:896349-896399	SK-N-MC	brain:	n/a
39	chr20:896349-896399	HAEpiC	amniotic membrane:	n/a
40	chr20:897024-897074	Hepatocyte	liver:	n/a
41	chr20:896349-896399	H1-hESC	embryonic stem cell:	embryo
42	chr20:896564-896614	ovcar-3	ovarian:	n/a
43	chr20:897545-897595	HAEpiC	amniotic membrane:	n/a
44	chr20:896564-896614	NT2-D1	testis:	n/a
45	chr20:896564-896614	HL-60	blood:	n/a
46	chr20:897545-897595	NH-A	brain:	n/a
47	chr20:896981-897031	NHBE	bronchial:	n/a
48	chr20:897545-897595	SAEC	small airway:	n/a
49	chr20:897050-897100	PFSK-1	brain:	n/a
50	chr20:897600-897650	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr20:809347..810136-chr20:883815..884702,3	MCF-7	breast:
2	chr20:897191..899627-chr20:903602..905719,2	MCF-7	breast:
3	chr20:873612..875715-chr20:890183..892090,2	MCF-7	breast:
4	chr20:890014..892494-chr20:895153..897440,2	MCF-7	breast:
5	chr20:897191..899627-chr20:903602..905719,2	MCF-7	breast:
6	chr20:899077..901728-chr20:908752..911161,2	K562	blood:
7	chr20:925330..928261-chr20:941058..943608,3	K562	blood:
8	chr20:857198..860086-chr20:873899..876217,2	MCF-7	breast:
9	chr20:825224..827249-chr20:896016..898725,2	MCF-7	breast:
10	chr20:899077..901728-chr20:908752..911161,2	K562	blood:
11	chr20:921972..923694-chr20:931266..933420,2	K562	blood:
12	chr20:914281..915061-chr3:49059512..49060483,2	NB4	blood:
13	chr20:836809..839072-chr20:903298..905274,2	K562	blood:
14	chr20:873612..875715-chr20:890183..892090,2	MCF-7	breast:
15	chr20:847957..850389-chr20:899044..901532,2	K562	blood:

Variant related genes	Relation type
ANGPT4	TF binding region
ANGPT4	CpG island
ENSG00000178057	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000125898	chromatin interactions
ENSG00000101280	chromatin interactions

Extended variants
information (count: 2268 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2268 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4816051	chr20:873749-873750	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs137956730	chr20:873796-873797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182116222	chr20:873844-873845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560319900	chr20:873846-873847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576888812	chr20:873868-873869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551440671	chr20:873885-873886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370491790	chr20:873939-873940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545936565	chr20:873940-873941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186715972	chr20:873968-873969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374540646	chr20:873971-873972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555834401	chr20:874000-874001	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs73078200	chr20:874107-874108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs201395051	chr20:874108-874109	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs80184510	chr20:874126-874127	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs527592329	chr20:874167-874168	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs547528688	chr20:874190-874191	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs570699924	chr20:874204-874205	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs191175583	chr20:874241-874242	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs549927054	chr20:874249-874250	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs569650234	chr20:874252-874253	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs143396584	chr20:874275-874276	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555088645	chr20:874285-874286	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs575031463	chr20:874329-874330	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534235852	chr20:874352-874353	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs113253971	chr20:874373-874374	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147335086	chr20:874377-874378	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs561457296	chr20:874499-874500	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs577072795	chr20:874609-874610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545871157	chr20:874631-874632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376247749	chr20:874713-874714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138952658	chr20:874775-874776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542180634	chr20:874871-874872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149423119	chr20:874891-874892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183786190	chr20:874932-874933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547760342	chr20:874997-874998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564251758	chr20:875022-875023	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs55965819	chr20:875028-875029	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs370353054	chr20:875041-875042	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs374356762	chr20:875093-875094	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs144786605	chr20:875095-875096	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs368571764	chr20:875115-875116	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs569704029	chr20:875129-875130	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs528985470	chr20:875138-875139	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs6118131	chr20:875159-875160	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs148548853	chr20:875197-875198	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs562438550	chr20:875207-875208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114010322	chr20:875238-875239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570698848	chr20:875253-875254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189248490	chr20:875284-875285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144335213	chr20:875328-875329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
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
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	17426248	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:866200-877000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:868800-875600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr20:871600-874600	Enhancers	Primary B cells from peripheral blood	blood
4	chr20:871800-874200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr20:872000-874200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr20:872000-875000	Weak transcription	Brain Substantia Nigra	brain
7	chr20:872400-874200	Weak transcription	Spleen	Spleen
8	chr20:872600-873800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr20:872800-874000	Weak transcription	Adipose Nuclei	Adipose
10	chr20:872800-874000	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr20:872800-874200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr20:872800-876000	Weak transcription	Ovary	ovary
13	chr20:874000-874400	Enhancers	Adipose Nuclei	Adipose
14	chr20:874000-874600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr20:874200-874400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr20:874200-874400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr20:874200-874400	Enhancers	Fetal Brain Male	brain
18	chr20:874200-874400	Flanking Active TSS	Spleen	Spleen
19	chr20:874200-874600	Enhancers	Primary hematopoietic stem cells	blood
20	chr20:874200-874600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr20:874400-874600	Active TSS	Spleen	Spleen
22	chr20:874600-875000	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr20:874600-875400	Weak transcription	Spleen	Spleen
24	chr20:875000-875200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr20:875000-875600	Enhancers	Brain Substantia Nigra	brain
26	chr20:875200-875600	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr20:875400-875600	Enhancers	Spleen	Spleen
28	chr20:877000-877400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr20:878200-879000	Enhancers	Fetal Muscle Leg	muscle
30	chr20:882000-883400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr20:882600-886400	Weak transcription	Ovary	ovary
32	chr20:883400-884200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr20:883400-884200	Enhancers	Brain Substantia Nigra	brain
34	chr20:883400-884200	Enhancers	HMEC	breast
35	chr20:883400-888400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr20:883600-883800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr20:883600-883800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr20:883600-884200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr20:883600-884200	Enhancers	Adipose Nuclei	Adipose
40	chr20:883600-884200	Enhancers	Esophagus	oesophagus
41	chr20:883600-884800	Enhancers	NHEK	skin
42	chr20:883600-885800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr20:883800-884000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr20:883800-884200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr20:883800-884400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr20:883800-885600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr20:883800-886800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr20:884000-884200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr20:884000-884200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr20:884200-884800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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