Variant report

Variant	nsv442410
Chromosome Location	chr17:15650630-15674005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:427)
Chromatin interactive
region (count:1)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:15672304-15672497	Pancreas_OC	pancreas:	n/a	n/a
2	CTCF	chr17:15672282-15672486	GM12891	blood:	n/a	n/a
3	CTCF	chr17:15652603-15652660	A549	lung:	n/a	chr17:15652623-15652636
4	CTCF	chr17:15672328-15672471	HepG2	liver:	n/a	n/a
5	CTCF	chr17:15654856-15654909	GM13976	blood:	n/a	n/a
6	CTCF	chr17:15655205-15655263	GM13977	blood:	n/a	n/a
7	CTCF	chr17:15672250-15672516	GM12878	blood:	n/a	n/a
8	CTCF	chr17:15653788-15653894	LNCaP	prostate:	n/a	n/a
9	CTCF	chr17:15671235-15671316	GM13977	blood:	n/a	n/a
10	CTCF	chr17:15672060-15672210	HAc	cerebellar:	n/a	n/a
11	CTCF	chr17:15672440-15672590	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr17:15672278-15672492	MCF-7	breast:	n/a	n/a
13	CTCF	chr17:15672365-15672431	GM19239	blood:	n/a	n/a
14	CTCF	chr17:15653545-15653592	GM13976	blood:	n/a	n/a
15	CTCF	chr17:15655194-15655285	GM13976	blood:	n/a	n/a
16	CTCF	chr17:15672315-15672472	ProgFib	skin:	n/a	n/a
17	CTCF	chr17:15672311-15672497	Fibrobl	skin:	n/a	n/a
18	CTCF	chr17:15672313-15672454	GM19240	blood:	n/a	n/a
19	CTCF	chr17:15672264-15672508	MCF-7	breast:	n/a	n/a
20	CTCF	chr17:15672266-15672501	MCF-7	breast:	n/a	n/a
21	CTCF	chr17:15672262-15672511	MCF-7	breast:	n/a	n/a
22	CTCF	chr17:15672270-15672499	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr17:15672366-15672430	K562	blood:	n/a	n/a
24	CTCF	chr17:15672340-15672469	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr17:15672295-15672488	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr17:15672282-15672499	GM12892	blood:	n/a	n/a
27	CTCF	chr17:15672364-15672419	Medullo	brain:	n/a	n/a
28	CTCF	chr17:15672290-15672483	A549	lung:	n/a	n/a
29	CTCF	chr17:15668468-15668555	Lung_OC	lung:	n/a	n/a
30	CTCF	chr17:15672291-15672439	LNCaP	prostate:	n/a	n/a
31	CTCF	chr17:15672330-15672420	GM19238	blood:	n/a	n/a
32	CTCF	chr17:15672364-15672436	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr17:15672261-15672504	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:15672282-15672486	NHEK	skin:	n/a	n/a
35	CTCF	chr17:15672228-15672496	A549	lung:	n/a	n/a
36	CTCF	chr17:15672277-15672498	Gliobla	brain:	n/a	n/a
37	CTCF	chr17:15672440-15672590	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr17:15666698-15666753	Spleen_OC	spleen:	n/a	n/a
39	EBF1	chr17:15651959-15652279	GM12878	blood:	n/a	n/a
40	EBF1	chr17:15651996-15652216	GM12878	blood:	n/a	n/a
41	ESR1	chr17:15658091-15658495	T-47D	breast:	n/a	chr17:15658257-15658274 chr17:15658256-15658273
42	ESR1	chr17:15658120-15658430	T-47D	breast:	n/a	chr17:15658257-15658274 chr17:15658256-15658273
43	FOXA2	chr17:15651919-15652290	A549	lung:	n/a	n/a
44	POLR2A	chr17:15652594-15652680	A549	lung:	n/a	n/a
45	POLR2A	chr17:15659746-15660144	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr17:15672443-15672736	SK-N-SH	brain:	n/a	n/a
47	POLR2A	chr17:15672399-15672805	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr17:15659903-15660140	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr17:15652593-15652715	A549	lung:	n/a	n/a
50	POLR2A	chr17:15656456-15656607	A549	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15653096-15653146	SK-N-MC	brain:	n/a
2	chr17:15653096-15653146	Hela-S3	cervix:	n/a
3	chr17:15652329-15652379	H1-hESC	embryonic stem cell:	embryo
4	chr17:15653096-15653146	Caco-2	colon:	n/a
5	chr17:15652329-15652379	Jurkat	blood:	n/a
6	chr17:15652715-15652765	HCT-116	colon:	n/a
7	chr17:15652715-15652765	HCPEpiC	choroid plexus:	n/a
8	chr17:15653096-15653146	SKMC	muscle:	n/a
9	chr17:15655637-15655687	AG09309	skin:	n/a
10	chr17:15653096-15653146	AG09319	gingival:	n/a
11	chr17:15652715-15652765	NHDF-neo	bronchial:	n/a
12	chr17:15653473-15653523	HCF	heart:	n/a
13	chr17:15652329-15652379	HCM	heart:	n/a
14	chr17:15653473-15653523	PANC-1	pancreas:	n/a
15	chr17:15653096-15653146	U87	brain:	n/a
16	chr17:15653548-15653598	BJ	skin:	n/a
17	chr17:15653548-15653598	AoSMC	blood vessel:	n/a
18	chr17:15653473-15653523	NHDF-neo	bronchial:	n/a
19	chr17:15653548-15653598	ovcar-3	ovarian:	n/a
20	chr17:15653473-15653523	HMEC	breast:	n/a
21	chr17:15652715-15652765	AG10803	skin:	n/a
22	chr17:15652715-15652765	BE2_C	brain:	n/a
23	chr17:15652329-15652379	HAEpiC	amniotic membrane:	n/a
24	chr17:15655637-15655687	Jurkat	blood:	n/a
25	chr17:15653473-15653523	PrEC	prostate:	n/a
26	chr17:15652329-15652379	SKMC	muscle:	n/a
27	chr17:15652329-15652379	BJ	skin:	n/a
28	chr17:15653096-15653146	NT2-D1	testis:	n/a
29	chr17:15652854-15652904	HEK293	kidney:	embryo
30	chr17:15652329-15652379	Hela-S3	cervix:	n/a
31	chr17:15653548-15653598	K562	blood:	n/a
32	chr17:15653473-15653523	SAEC	small airway:	n/a
33	chr17:15653473-15653523	HCPEpiC	choroid plexus:	n/a
34	chr17:15653096-15653146	AoSMC	blood vessel:	n/a
35	chr17:15652854-15652904	HRPEpiC	eye:	n/a
36	chr17:15653473-15653523	SK-N-SH	brain:	n/a
37	chr17:15652854-15652904	AG09319	gingival:	n/a
38	chr17:15652715-15652765	HRPEpiC	eye:	n/a
39	chr17:15655637-15655687	AG04449	skin:	fetal
40	chr17:15655637-15655687	BJ	skin:	n/a
41	chr17:15652715-15652765	Hela-S3	cervix:	n/a
42	chr17:15655637-15655687	HUVEC	blood vessel:	n/a
43	chr17:15652854-15652904	ovcar-3	ovarian:	n/a
44	chr17:15653096-15653146	GM12878	blood:	n/a
45	chr17:15655637-15655687	NB4	blood:	n/a
46	chr17:15653548-15653598	RPTEC	kidney:	n/a
47	chr17:15652854-15652904	BJ	skin:	n/a
48	chr17:15653473-15653523	HRE	kidney:	n/a
49	chr17:15652854-15652904	SAEC	small airway:	n/a
50	chr17:15652329-15652379	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15646677..15648283-chr17:15650856..15653224,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM16-1	chr17:15652017-15652629	NONHSAT145866
2	lnc-TRIM16-2	chr17:15652075-15652506	ENSG00000233002.2
3	lnc-TRIM16-7	chr17:15664746-15664857	NONHSAT145868
4	lnc-TRIM16-6	chr17:15661567-15661668	NONHSAT145865
5	lnc-TRIM16-3	chr17:15664928-15665158	ENSG00000233193
6	lnc-TRIM16-6	chr17:15661567-15661699	ucscGeneNc_uc010cow_1
7	lnc-TRIM16-7	chr17:15663778-15664123	NONHSAT145868
8	lnc-TRIM16-1	chr17:15666900-15669134	NONHSAT145863
9	lnc-TRIM16-6	chr17:15660004-15660081	ucscGeneNc_uc010cow_1
10	lnc-TRIM16-6	chr17:15650705-15650937	NONHSAT145865
11	lnc-TRIM16-6	chr17:15660004-15660081	NONHSAT145865
12	lnc-TRIM16-3	chr17:15666900-15667083	ENSG00000233193
13	lnc-TRIM16-6	chr17:15650514-15650937	ucscGeneNc_uc010cow_1

No data

Variant related genes	Relation type
ENSG00000233002	TF binding region
ENSG00000267227	TF binding region
CDRT15P2	TF binding region
ENSG00000233193	TF binding region
ENSG00000233002	CpG island
ENSG00000267227	CpG island
CDRT15P2	CpG island
ENSG00000233193	CpG island
ENSG00000233002	chromatin interactions

Extended variants
information (count: 361 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148842499	chr17:15650635-15650636	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs557390437	chr17:15650649-15650650	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs143452286	chr17:15650704-15650705	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs56053384	chr17:15650728-15650729	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs75299246	chr17:15650737-15650738	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs55673041	chr17:15650742-15650743	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs371332571	chr17:15650779-15650780	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs547949881	chr17:15650780-15650781	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs369407230	chr17:15650810-15650811	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs569240585	chr17:15650824-15650825	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs536889335	chr17:15650829-15650830	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs556739438	chr17:15650843-15650844	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs373341205	chr17:15650908-15650909	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs137942965	chr17:15650920-15650921	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs545706996	chr17:15650922-15650923	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs552818308	chr17:15650938-15650939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572824575	chr17:15650950-15650951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541446274	chr17:15650951-15650952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561861943	chr17:15651025-15651026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11657430	chr17:15651090-15651091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184787566	chr17:15651124-15651125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529689860	chr17:15651132-15651133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530519636	chr17:15651154-15651155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72821710	chr17:15651192-15651193	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs11652541	chr17:15651231-15651232	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs79893156	chr17:15651247-15651248	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533532556	chr17:15651280-15651281	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368992634	chr17:15651362-15651363	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs370827783	chr17:15651438-15651439	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372446492	chr17:15651484-15651485	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547341891	chr17:15651655-15651656	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143396345	chr17:15651674-15651675	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541006358	chr17:15651715-15651716	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529326865	chr17:15651755-15651756	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146258166	chr17:15651769-15651770	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs138917223	chr17:15651780-15651781	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565874904	chr17:15651796-15651797	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557794448	chr17:15651829-15651830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141264529	chr17:15651860-15651861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150759611	chr17:15651863-15651864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553265946	chr17:15651876-15651877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573045161	chr17:15651883-15651884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557822350	chr17:15651887-15651888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191400197	chr17:15651904-15651905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555072343	chr17:15651905-15651906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144165489	chr17:15651919-15651920	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs59623326	chr17:15651933-15651934	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374782159	chr17:15651934-15651935	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs58699635	chr17:15651939-15651940	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201170427	chr17:15651943-15651944	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	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
Acute myeloid leukemia	17237825	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
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15648800-15652800	Weak transcription	Ovary	ovary
2	chr17:15651400-15651800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr17:15651400-15651800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr17:15652600-15653000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
5	chr17:15652800-15653000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr17:15652800-15653000	Flanking Active TSS	Ovary	ovary
7	chr17:15652800-15653000	Flanking Active TSS	Psoas Muscle	Psoas
8	chr17:15652800-15653200	Enhancers	Placenta Amnion	Placenta Amnion
9	chr17:15652800-15653400	Active TSS	Right Ventricle	heart
10	chr17:15653000-15654000	Active TSS	Ovary	ovary
11	chr17:15671800-15672000	Enhancers	Fetal Muscle Leg	muscle
12	chr17:15672000-15672800	Weak transcription	Fetal Muscle Leg	muscle
13	chr17:15672000-15673200	Enhancers	Fetal Muscle Trunk	muscle
14	chr17:15672600-15674200	Enhancers	Stomach Smooth Muscle	stomach
15	chr17:15672800-15673000	Bivalent Enhancer	Fetal Stomach	stomach
16	chr17:15672800-15674000	Enhancers	Fetal Muscle Leg	muscle
17	chr17:15672800-15674400	Enhancers	Left Ventricle	heart
18	chr17:15672800-15674800	Enhancers	Fetal Heart	heart
19	chr17:15673200-15673600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr17:15673600-15674000	Enhancers	Fetal Muscle Trunk	muscle
21	chr17:15674000-15674200	Enhancers	Fetal Stomach	stomach

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