Variant report

Variant	esv3316001
Chromosome Location	chr17:20770384-20771800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:174 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:20771647-20772028	HepG2	liver:	n/a	n/a
2	ATF1	chr17:20771215-20771847	K562	blood:	n/a	n/a
3	BCLAF1	chr17:20771699-20774204	K562	blood:	n/a	n/a
4	BHLHE40	chr17:20771094-20771527	K562	blood:	n/a	n/a
5	CBX3	chr17:20771289-20772187	K562	blood:	n/a	n/a
6	CCNT2	chr17:20771695-20772039	K562	blood:	n/a	n/a
7	CEBPB	chr17:20771375-20771995	K562	blood:	n/a	n/a
8	CEBPD	chr17:20771738-20772231	K562	blood:	n/a	n/a
9	CEBPD	chr17:20771666-20772111	K562	blood:	n/a	n/a
10	CHD1	chr17:20771782-20772757	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr17:20771438-20771981	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr17:20771264-20772113	K562	blood:	n/a	n/a
13	CHD2	chr17:20771296-20771487	HepG2	liver:	n/a	n/a
14	EGR1	chr17:20771747-20772037	K562	blood:	n/a	n/a
15	EGR1	chr17:20771730-20771956	K562	blood:	n/a	n/a
16	ELF1	chr17:20771727-20772199	K562	blood:	n/a	n/a
17	EP300	chr17:20771375-20772057	GM12878	blood:	n/a	n/a
18	EP300	chr17:20770933-20770935	K562	blood:	n/a	n/a
19	EP300	chr17:20771327-20772060	K562	blood:	n/a	n/a
20	EP300	chr17:20771727-20771968	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr17:20771315-20771530	HepG2	liver:	n/a	n/a
22	FOS	chr17:20771427-20772002	K562	blood:	n/a	n/a
23	GABPA	chr17:20771742-20772097	SK-N-SH	brain:	n/a	n/a
24	GABPA	chr17:20771726-20772061	SK-N-SH	brain:	n/a	n/a
25	GABPA	chr17:20771721-20771968	HepG2	liver:	n/a	n/a
26	GATA2	chr17:20771433-20772109	K562	blood:	n/a	n/a
27	GTF2B	chr17:20771428-20772057	K562	blood:	n/a	n/a
28	GTF2F1	chr17:20771456-20772015	H1-hESC	embryonic stem cell:	n/a	n/a
29	GTF2F1	chr17:20771147-20772038	K562	blood:	n/a	n/a
30	HCFC1	chr17:20771375-20772064	K562	blood:	n/a	n/a
31	HEY1	chr17:20770918-20772102	HepG2	liver:	n/a	n/a
32	HEY1	chr17:20769547-20770521	K562	blood:	n/a	n/a
33	HEY1	chr17:20769307-20776159	K562	blood:	n/a	n/a
34	HEY1	chr17:20771157-20772077	HepG2	liver:	n/a	n/a
35	HEY1	chr17:20770783-20772361	K562	blood:	n/a	n/a
36	IRF1	chr17:20771398-20772101	K562	blood:	n/a	n/a
37	IRF1	chr17:20771329-20772167	K562	blood:	n/a	n/a
38	JUN	chr17:20771447-20772005	K562	blood:	n/a	n/a
39	JUND	chr17:20771321-20772024	K562	blood:	n/a	n/a
40	MAFF	chr17:20771485-20771678	HepG2	liver:	n/a	chr17:20771551-20771569
41	MAFK	chr17:20771651-20771987	K562	blood:	n/a	n/a
42	MAX	chr17:20771743-20772029	SK-N-SH	brain:	n/a	n/a
43	MAX	chr17:20771790-20772026	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr17:20771732-20772127	K562	blood:	n/a	n/a
45	MAX	chr17:20771761-20772048	SK-N-SH	brain:	n/a	n/a
46	MAX	chr17:20771745-20771986	K562	blood:	n/a	n/a
47	MAX	chr17:20770305-20770596	K562	blood:	n/a	n/a
48	MAX	chr17:20771139-20771615	K562	blood:	n/a	n/a
49	MAZ	chr17:20770925-20771109	K562	blood:	n/a	n/a
50	MAZ	chr17:20771435-20772273	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20771551-20771601	AG10803	skin:	n/a
2	chr17:20771377-20771427	Caco-2	colon:	n/a
3	chr17:20771551-20771601	AoSMC	blood vessel:	n/a
4	chr17:20771377-20771427	HCF	heart:	n/a
5	chr17:20771377-20771427	NT2-D1	testis:	n/a
6	chr17:20771551-20771601	A549	lung:	n/a
7	chr17:20771551-20771601	HCM	heart:	n/a
8	chr17:20771377-20771427	T-47D	breast:	n/a
9	chr17:20771377-20771427	HRPEpiC	eye:	n/a
10	chr17:20771377-20771427	HL-60	blood:	n/a
11	chr17:20771377-20771427	NHBE	bronchial:	n/a
12	chr17:20771377-20771427	HUVEC	blood vessel:	n/a
13	chr17:20771377-20771427	MCF-7	breast:	n/a
14	chr17:20771551-20771601	HEEpiC	esophagus:	n/a
15	chr17:20771551-20771601	SK-N-SH	brain:	n/a
16	chr17:20771377-20771427	HAEpiC	amniotic membrane:	n/a
17	chr17:20771551-20771601	HRCEpiC	kidney:	n/a
18	chr17:20771377-20771427	HRCEpiC	kidney:	n/a
19	chr17:20771377-20771427	Jurkat	blood:	n/a
20	chr17:20771377-20771427	HCPEpiC	choroid plexus:	n/a
21	chr17:20771551-20771601	H1-hESC	embryonic stem cell:	embryo
22	chr17:20771551-20771601	HIPEpiC	eye:	n/a
23	chr17:20771551-20771601	Caco-2	colon:	n/a
24	chr17:20771551-20771601	CMK	blood:	n/a
25	chr17:20771551-20771601	ECC-1	luminal epithelium:	n/a
26	chr17:20771377-20771427	LNCaP	prostate:	n/a
27	chr17:20771377-20771427	HRE	kidney:	n/a
28	chr17:20771377-20771427	GM12892	blood:	n/a
29	chr17:20771377-20771427	HMEC	breast:	n/a
30	chr17:20771551-20771601	SK-N-SH_RA	brain:	n/a
31	chr17:20771551-20771601	SAEC	small airway:	n/a
32	chr17:20771551-20771601	HepG2	liver:	n/a
33	chr17:20771551-20771601	PrEC	prostate:	n/a
34	chr17:20771551-20771601	IMR90	lung:	fetal
35	chr17:20771377-20771427	AG09309	skin:	n/a
36	chr17:20771377-20771427	NB4	blood:	n/a
37	chr17:20771551-20771601	HAEpiC	amniotic membrane:	n/a
38	chr17:20771377-20771427	RPTEC	kidney:	n/a
39	chr17:20771377-20771427	SK-N-MC	brain:	n/a
40	chr17:20771551-20771601	NB4	blood:	n/a
41	chr17:20771377-20771427	GM12891	blood:	n/a
42	chr17:20771551-20771601	Jurkat	blood:	n/a
43	chr17:20771377-20771427	AG04450	lung:	fetal
44	chr17:20771551-20771601	HCF	heart:	n/a
45	chr17:20771377-20771427	HEEpiC	esophagus:	n/a
46	chr17:20771551-20771601	HMEC	breast:	n/a
47	chr17:20771377-20771427	U87	brain:	n/a
48	chr17:20771377-20771427	GM19239	blood:	n/a
49	chr17:20771377-20771427	NH-A	brain:	n/a
50	chr17:20771551-20771601	GM12892	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:20766270..20770547-chr17:21518548..21521594,4	K562	blood:
2	chr17:20769754..20771503-chr17:25415743..25417258,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000233098	TF binding region
CCDC144NL	TF binding region
ENSG00000233098	CpG island
CCDC144NL	CpG island

Extended variants
information (count: 167 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:167 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79414585	chr17:20770393-20770394	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs114768187	chr17:20770408-20770409	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77434613	chr17:20770419-20770420	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs72838137	chr17:20770423-20770424	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573177075	chr17:20770449-20770450	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs73298047	chr17:20770453-20770454	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558982988	chr17:20770461-20770462	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs9899981	chr17:20770474-20770475	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs76396285	chr17:20770478-20770479	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562737826	chr17:20770480-20770481	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs80227424	chr17:20770485-20770486	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs530351211	chr17:20770486-20770487	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542100248	chr17:20770498-20770499	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs372283067	chr17:20770501-20770502	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs375814860	chr17:20770504-20770505	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs560736322	chr17:20770506-20770507	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528060750	chr17:20770510-20770511	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs78897158	chr17:20770512-20770513	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs116577386	chr17:20770525-20770526	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs571279243	chr17:20770533-20770534	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs141450311	chr17:20770546-20770547	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs202138290	chr17:20770548-20770549	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs532236283	chr17:20770549-20770550	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs200347724	chr17:20770568-20770569	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189110742	chr17:20770574-20770575	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs569051196	chr17:20770575-20770576	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs536585591	chr17:20770577-20770578	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs115284220	chr17:20770580-20770581	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs373254249	chr17:20770597-20770598	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs114073249	chr17:20770598-20770599	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs114623999	chr17:20770599-20770600	ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs117159141	chr17:20770611-20770612	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs78429114	chr17:20770617-20770618	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs75664468	chr17:20770619-20770620	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs9900429	chr17:20770627-20770628	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs566777531	chr17:20770644-20770645	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs112375141	chr17:20770689-20770690	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558794853	chr17:20770697-20770698	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371241636	chr17:20770708-20770709	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs80093728	chr17:20770739-20770740	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540571385	chr17:20770740-20770741	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs77966516	chr17:20770744-20770745	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369533402	chr17:20770745-20770746	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs72838139	chr17:20770752-20770753	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374309403	chr17:20770756-20770757	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576969820	chr17:20770762-20770763	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs75929647	chr17:20770814-20770815	Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556371009	chr17:20770815-20770816	Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs574656473	chr17:20770825-20770826	Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs74504743	chr17:20770838-20770839	Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:150)

Disease	PMID	Source
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17142309	CNVD
Autism	20808228	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20769400-20778000	Active TSS	K562	blood
2	chr17:20769600-20771000	Active TSS	HepG2	liver
3	chr17:20770200-20772200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:20770400-20770600	Enhancers	Pancreas	Pancrea
5	chr17:20770800-20771800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr17:20771000-20772200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr17:20771000-20773000	Bivalent/Poised TSS	HepG2	liver
8	chr17:20771200-20771400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr17:20771200-20771600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
10	chr17:20771200-20771800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr17:20771200-20773600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr17:20771200-20774000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr17:20771200-20774200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr17:20771200-20774800	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr17:20771200-20775200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr17:20771400-20772000	Weak transcription	Pancreas	Pancrea
17	chr17:20771400-20774600	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr17:20771600-20775000	Active TSS	H1 Cell Line	embryonic stem cell
19	chr17:20771800-20772000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr17:20771800-20772200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr17:20771800-20772400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr17:20771800-20773000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr17:20771800-20774000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr17:20771800-20774200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr17:20771800-20774200	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr17:20771800-20774200	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr17:20771800-20774400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr17:20771800-20774400	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr17:20771800-20775000	Active TSS	HUES6 Cell Line	embryonic stem cell

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