Variant report

Variant	esv1822743
Chromosome Location	chr17:20374729-20446160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:20388438-20388633	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr17:20443708-20444186	GM12878	blood:	n/a	n/a
3	BATF	chr17:20443556-20444223	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:20443676-20444145	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:20443777-20444111	GM12878	blood:	n/a	n/a
6	BCL3	chr17:20438566-20438789	GM12878	blood:	n/a	n/a
7	CEBPB	chr17:20432878-20433065	A549	lung:	n/a	chr17:20432946-20432955 chr17:20432944-20432957 chr17:20432944-20432955
8	CEBPB	chr17:20432904-20432946	K562	blood:	n/a	n/a
9	CEBPB	chr17:20388357-20388509	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr17:20428677-20428912	K562	blood:	n/a	n/a
11	CEBPB	chr17:20432902-20433054	IMR90	lung:	n/a	chr17:20432946-20432955 chr17:20432944-20432957 chr17:20432944-20432955
12	CHD1	chr17:20434510-20434553	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr17:20445620-20445770	AG10803	skin:	n/a	n/a
14	CTCF	chr17:20445610-20445723	MCF-7	breast:	n/a	n/a
15	CTCF	chr17:20404993-20405007	Gliobla	brain:	n/a	n/a
16	CTCF	chr17:20405316-20405539	A549	lung:	n/a	n/a
17	CTCF	chr17:20445520-20445670	HMEC	breast:	n/a	n/a
18	CTCF	chr17:20411948-20412055	Medullo	brain:	n/a	n/a
19	CTCF	chr17:20405260-20405410	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr17:20405373-20405396	Medullo	brain:	n/a	n/a
21	CTCF	chr17:20411841-20412098	K562	blood:	n/a	n/a
22	CTCF	chr17:20404997-20405070	GM10266	blood:	n/a	n/a
23	CTCF	chr17:20420883-20420946	GM20000	blood:	n/a	n/a
24	CTCF	chr17:20405281-20405489	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr17:20445604-20445730	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:20405373-20405476	MCF-7	breast:	n/a	n/a
27	CTCF	chr17:20420860-20421010	GM12864	blood:	n/a	n/a
28	CTCF	chr17:20440911-20440950	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr17:20405320-20405470	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr17:20400000-20400073	GM10248	blood:	n/a	n/a
31	CTCF	chr17:20445580-20445730	SAEC	small airway:	n/a	n/a
32	CTCF	chr17:20445637-20445731	Fibrobl	skin:	n/a	n/a
33	CTCF	chr17:20395438-20395742	NHEK	skin:	n/a	chr17:20395527-20395536
34	CTCF	chr17:20399902-20399910	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr17:20445580-20445730	AG09319	gingival:	n/a	n/a
36	CTCF	chr17:20411957-20412008	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr17:20405344-20405485	GM10266	blood:	n/a	n/a
38	CTCF	chr17:20399541-20399560	GM10248	blood:	n/a	n/a
39	CTCF	chr17:20420837-20421005	GM13977	blood:	n/a	n/a
40	CTCF	chr17:20418549-20418655	Medullo	brain:	n/a	n/a
41	CTCF	chr17:20445560-20445710	AG04449	skin:	n/a	n/a
42	CTCF	chr17:20445558-20445742	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr17:20445558-20445726	T-47D	breast:	n/a	n/a
44	CTCF	chr17:20378584-20378697	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr17:20405381-20405534	Gliobla	brain:	n/a	n/a
46	CTCF	chr17:20405080-20405230	RPTEC	kidney:	n/a	n/a
47	CTCF	chr17:20411842-20412144	A549	lung:	n/a	n/a
48	CTCF	chr17:20445560-20445710	AG10803	skin:	n/a	n/a
49	CTCF	chr17:20405370-20405432	GM20000	blood:	n/a	n/a
50	CTCF	chr17:20445600-20445750	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20408772-20408822	NH-A	brain:	n/a
2	chr17:20408772-20408822	HEK293	kidney:	embryo
3	chr17:20433187-20433237	MCF10A-Er-Src	breast:	n/a
4	chr17:20408647-20408697	AG04450	lung:	fetal
5	chr17:20445757-20445807	HRCEpiC	kidney:	n/a
6	chr17:20408772-20408822	AG09319	gingival:	n/a
7	chr17:20409125-20409175	HCPEpiC	choroid plexus:	n/a
8	chr17:20409125-20409175	Caco-2	colon:	n/a
9	chr17:20433187-20433237	NHDF-neo	bronchial:	n/a
10	chr17:20445757-20445807	MCF-7	breast:	n/a
11	chr17:20408772-20408822	HCT-116	colon:	n/a
12	chr17:20445757-20445807	HRPEpiC	eye:	n/a
13	chr17:20408647-20408697	SK-N-SH	brain:	n/a
14	chr17:20408772-20408822	K562	blood:	n/a
15	chr17:20408772-20408822	GM12891	blood:	n/a
16	chr17:20433187-20433237	ProgFib	skin:	n/a
17	chr17:20408772-20408822	RPTEC	kidney:	n/a
18	chr17:20445757-20445807	GM06990	blood:	n/a
19	chr17:20433187-20433237	ECC-1	luminal epithelium:	n/a
20	chr17:20408772-20408822	HL-60	blood:	n/a
21	chr17:20405382-20405432	PANC-1	pancreas:	n/a
22	chr17:20445757-20445807	GM12891	blood:	n/a
23	chr17:20408647-20408697	BE2_C	brain:	n/a
24	chr17:20405382-20405432	ProgFib	skin:	n/a
25	chr17:20433187-20433237	Caco-2	colon:	n/a
26	chr17:20408647-20408697	AG10803	skin:	n/a
27	chr17:20408772-20408822	NHBE	bronchial:	n/a
28	chr17:20445757-20445807	HAEpiC	amniotic membrane:	n/a
29	chr17:20408772-20408822	MCF10A-Er-Src	breast:	n/a
30	chr17:20409125-20409175	ovcar-3	ovarian:	n/a
31	chr17:20408772-20408822	SAEC	small airway:	n/a
32	chr17:20409125-20409175	ProgFib	skin:	n/a
33	chr17:20433187-20433237	SK-N-SH_RA	brain:	n/a
34	chr17:20405382-20405432	HepG2	liver:	n/a
35	chr17:20445757-20445807	AG10803	skin:	n/a
36	chr17:20433187-20433237	NT2-D1	testis:	n/a
37	chr17:20405382-20405432	U87	brain:	n/a
38	chr17:20445757-20445807	H1-hESC	embryonic stem cell:	embryo
39	chr17:20405382-20405432	AG10803	skin:	n/a
40	chr17:20408772-20408822	H1-hESC	embryonic stem cell:	embryo
41	chr17:20433187-20433237	A549	lung:	n/a
42	chr17:20408772-20408822	A549	lung:	n/a
43	chr17:20408772-20408822	AG04449	skin:	fetal
44	chr17:20405382-20405432	HCM	heart:	n/a
45	chr17:20408772-20408822	U87	brain:	n/a
46	chr17:20433187-20433237	Jurkat	blood:	n/a
47	chr17:20408647-20408697	GM12878	blood:	n/a
48	chr17:20405382-20405432	GM12892	blood:	n/a
49	chr17:20445757-20445807	IMR90	lung:	fetal
50	chr17:20445757-20445807	GM19239	blood:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS9B-10	chr17:20435561-20436194	NONHSAT146584
2	lnc-LGALS9B-7	chr17:20410726-20412244	ENSG00000266925.1
3	lnc-LGALS9B-4	chr17:20375554-20376706	ucscGeneNc_uc002gxd_1
4	lnc-LGALS9B-1	chr17:20433355-20434194	ENSG00000260907.1

No data

Variant related genes	Relation type
ENSG00000260907	TF binding region
YWHAEP3	TF binding region
ENSG00000266042	TF binding region
KRT16P5	TF binding region
ENSG00000266925	TF binding region
ENSG00000265916	TF binding region
ENSG00000205215	TF binding region
ENSG00000231645	TF binding region
KRT16P3	TF binding region
ENSG00000229586	TF binding region
LGALS9B	TF binding region
ENSG00000267075	TF binding region
ENSG00000260907	CpG island
YWHAEP3	CpG island
ENSG00000266042	CpG island
KRT16P5	CpG island
ENSG00000266925	CpG island
ENSG00000265916	CpG island
ENSG00000205215	CpG island
ENSG00000231645	CpG island
KRT16P3	CpG island
ENSG00000229586	CpG island
LGALS9B	CpG island
ENSG00000267075	CpG island

Extended variants
information (count: 1512 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:1512 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144237662	chr17:20374729-20374730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562996465	chr17:20374733-20374734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201031702	chr17:20374739-20374740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530311666	chr17:20374794-20374795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548801782	chr17:20374830-20374831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568263802	chr17:20374831-20374832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372353168	chr17:20374922-20374923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190363076	chr17:20374927-20374928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375847524	chr17:20374939-20374940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28406480	chr17:20374951-20374952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369868846	chr17:20374958-20374959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570924994	chr17:20375020-20375021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538279936	chr17:20375089-20375090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556617510	chr17:20375113-20375114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568659282	chr17:20375123-20375124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536049141	chr17:20375141-20375142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182724275	chr17:20375164-20375165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145014334	chr17:20375229-20375230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554758999	chr17:20375329-20375330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573010191	chr17:20375414-20375415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540545143	chr17:20375420-20375421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558960185	chr17:20375455-20375456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577296253	chr17:20375459-20375460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373917432	chr17:20375485-20375486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1725699	chr17:20375640-20375641	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs141434063	chr17:20375643-20375644	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs539698440	chr17:20375658-20375659	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs530224702	chr17:20375663-20375664	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs146941255	chr17:20375670-20375671	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs368400396	chr17:20375671-20375672	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs56086998	chr17:20375683-20375684	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs527943854	chr17:20375705-20375706	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs552818604	chr17:20375762-20375763	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs201624929	chr17:20376166-20376167	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs564466532	chr17:20376253-20376254	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs371956395	chr17:20376279-20376280	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs531979385	chr17:20376754-20376755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550202854	chr17:20376759-20376760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568571837	chr17:20376799-20376800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1725700	chr17:20376844-20376845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548055132	chr17:20376996-20376997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566677864	chr17:20376997-20376998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533783103	chr17:20377041-20377042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558885844	chr17:20377047-20377048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575960616	chr17:20377054-20377055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149411716	chr17:20377076-20377077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62067983	chr17:20377102-20377103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538199370	chr17:20377141-20377142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556598017	chr17:20377229-20377230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574809147	chr17:20377248-20377249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:151)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	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
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20369800-20380000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr17:20370800-20394800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr17:20373800-20377000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr17:20377000-20377400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr17:20378600-20379000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr17:20378600-20379000	Enhancers	NHEK	skin
7	chr17:20378800-20379000	Enhancers	Esophagus	oesophagus
8	chr17:20379000-20379800	Weak transcription	Esophagus	oesophagus
9	chr17:20379000-20396200	Weak transcription	NHEK	skin
10	chr17:20379800-20380600	Enhancers	Esophagus	oesophagus
11	chr17:20380000-20380600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr17:20380200-20380600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr17:20380600-20383600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr17:20381000-20381400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr17:20383000-20383800	Enhancers	Stomach Mucosa	stomach
16	chr17:20383600-20384000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr17:20383600-20384400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr17:20384400-20384600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr17:20384600-20391800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr17:20388200-20388400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr17:20388200-20388600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr17:20388200-20388600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr17:20388200-20388600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr17:20388200-20388600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr17:20388200-20388600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr17:20388200-20388600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr17:20388200-20388600	Active TSS	Hela-S3	cervix
28	chr17:20388200-20388600	Active TSS	Osteobl	bone
29	chr17:20388400-20388600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr17:20391800-20392400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr17:20392400-20394800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr17:20394800-20396200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr17:20394800-20397600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr17:20396200-20396400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr17:20396200-20396600	Flanking Active TSS	NHEK	skin
36	chr17:20396400-20397800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr17:20396600-20396800	Active TSS	NHEK	skin
38	chr17:20397600-20398200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr17:20397800-20398400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr17:20398200-20399200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr17:20420400-20421000	Active TSS	Fetal Thymus	thymus
42	chr17:20421000-20424800	Weak transcription	Fetal Thymus	thymus
43	chr17:20424800-20425200	Enhancers	Fetal Thymus	thymus
44	chr17:20432800-20433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr17:20432800-20433800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr17:20433200-20434400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr17:20433400-20433600	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr17:20433400-20434400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr17:20433600-20433800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr17:20433600-20433800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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