Variant report

Variant	nsv574504
Chromosome Location	chr17:16688280-16718225
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	BATF	chr17:16710949-16711369	GM12878	blood:	n/a	chr17:16711188-16711198 chr17:16711187-16711198
2	BATF	chr17:16711019-16711268	GM12878	blood:	n/a	chr17:16711188-16711198 chr17:16711187-16711198
3	CTCF	chr17:16709100-16709250	K562	blood:	n/a	n/a
4	CTCF	chr17:16693920-16694070	HMEC	breast:	n/a	n/a
5	CTCF	chr17:16693580-16693730	SAEC	small airway:	n/a	n/a
6	CTCF	chr17:16693746-16693757	K562	blood:	n/a	n/a
7	CTCF	chr17:16693580-16693730	HVMF	connective:	n/a	n/a
8	CTCF	chr17:16693742-16693846	GM10266	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
9	CTCF	chr17:16693743-16693772	HepG2	liver:	n/a	n/a
10	CTCF	chr17:16693860-16694010	SAEC	small airway:	n/a	n/a
11	CTCF	chr17:16693540-16693690	Caco-2	colon:	n/a	n/a
12	CTCF	chr17:16693769-16693797	Lung_OC	lung:	n/a	chr17:16693771-16693787
13	CTCF	chr17:16713824-16713893	GM13976	blood:	n/a	n/a
14	CTCF	chr17:16693608-16693964	A549	lung:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
15	CTCF	chr17:16693701-16693855	GM13977	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
16	CTCF	chr17:16709080-16709230	AG09319	gingival:	n/a	n/a
17	CTCF	chr17:16693613-16693949	K562	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
18	CTCF	chr17:16693636-16693890	K562	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
19	CTCF	chr17:16716458-16716534	GM13976	blood:	n/a	n/a
20	CTCF	chr17:16693733-16693826	GM20000	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
21	CTCF	chr17:16693736-16693844	LNCaP	prostate:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
22	CTCF	chr17:16693600-16693750	HCM	heart:	n/a	n/a
23	CTCF	chr17:16718040-16718190	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr17:16693920-16694070	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr17:16709100-16709250	MCF-7	breast:	n/a	n/a
26	CTCF	chr17:16693690-16693882	Medullo	brain:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
27	CTCF	chr17:16709100-16709250	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr17:16693711-16693841	GM10248	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
29	CTCF	chr17:16693540-16693690	GM06990	blood:	n/a	n/a
30	CTCF	chr17:16693560-16693710	HVMF	connective:	n/a	n/a
31	CTCF	chr17:16693590-16693959	A549	lung:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
32	CTCF	chr17:16693666-16693776	Gliobla	brain:	n/a	n/a
33	CTCF	chr17:16701275-16701353	A549	lung:	n/a	n/a
34	CTCF	chr17:16709080-16709230	HMF	breast:	n/a	n/a
35	CTCF	chr17:16693534-16693984	A549	lung:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
36	CTCF	chr17:16693682-16693912	Kidney_OC	kidney:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
37	CTCF	chr17:16693703-16693870	LNCaP	prostate:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
38	CTCF	chr17:16714100-16714250	NB4	blood:	n/a	n/a
39	CTCF	chr17:16693582-16693901	A549	lung:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
40	CTCF	chr17:16693659-16693884	Pancreas_OC	pancreas:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
41	CTCF	chr17:16693640-16693918	K562	blood:	n/a	chr17:16693765-16693786 chr17:16693771-16693787
42	CTCF	chr17:16693900-16694050	HMEC	breast:	n/a	n/a
43	FOXA1	chr17:16715538-16715748	T-47D	breast:	n/a	n/a
44	FOXA1	chr17:16708436-16708696	T-47D	breast:	n/a	n/a
45	GATA2	chr17:16697238-16697635	K562	blood:	n/a	chr17:16697444-16697465 chr17:16697438-16697451
46	HCFC1	chr17:16715633-16715667	K562	blood:	n/a	n/a
47	IRF4	chr17:16710910-16711331	GM12878	blood:	n/a	n/a
48	IRF4	chr17:16710955-16711450	GM12878	blood:	n/a	n/a
49	MAX	chr17:16715522-16715744	K562	blood:	n/a	n/a
50	MAX	chr17:16715518-16715782	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16690169-16690219	LNCaP	prostate:	n/a
2	chr17:16693633-16693683	SK-N-MC	brain:	n/a
3	chr17:16690169-16690219	HEK293	kidney:	embryo
4	chr17:16690169-16690219	HEEpiC	esophagus:	n/a
5	chr17:16690169-16690219	NHBE	bronchial:	n/a
6	chr17:16690169-16690219	SK-N-MC	brain:	n/a
7	chr17:16690169-16690219	Hepatocyte	liver:	n/a
8	chr17:16688816-16688866	HEEpiC	esophagus:	n/a
9	chr17:16690169-16690219	K562	blood:	n/a
10	chr17:16693633-16693683	SAEC	small airway:	n/a
11	chr17:16688816-16688866	HPAEpiC	pulmonary alveolar:	n/a
12	chr17:16688816-16688866	LNCaP	prostate:	n/a
13	chr17:16688816-16688866	AG04450	lung:	fetal
14	chr17:16690173-16690223	AoSMC	blood vessel:	n/a
15	chr17:16690173-16690223	NT2-D1	testis:	n/a
16	chr17:16693633-16693683	RPTEC	kidney:	n/a
17	chr17:16690169-16690219	A549	lung:	n/a
18	chr17:16688816-16688866	Hela-S3	cervix:	n/a
19	chr17:16688816-16688866	MCF10A-Er-Src	breast:	n/a
20	chr17:16690173-16690223	PFSK-1	brain:	n/a
21	chr17:16690169-16690219	RPTEC	kidney:	n/a
22	chr17:16693633-16693683	BE2_C	brain:	n/a
23	chr17:16690169-16690219	HRCEpiC	kidney:	n/a
24	chr17:16693633-16693683	BJ	skin:	n/a
25	chr17:16688816-16688866	NHDF-neo	bronchial:	n/a
26	chr17:16693633-16693683	ECC-1	luminal epithelium:	n/a
27	chr17:16690169-16690219	MCF-7	breast:	n/a
28	chr17:16690169-16690219	SKMC	muscle:	n/a
29	chr17:16693633-16693683	SK-N-SH	brain:	n/a
30	chr17:16688816-16688866	MCF-7	breast:	n/a
31	chr17:16690169-16690219	Hela-S3	cervix:	n/a
32	chr17:16688816-16688866	GM06990	blood:	n/a
33	chr17:16690173-16690223	RPTEC	kidney:	n/a
34	chr17:16693633-16693683	HCPEpiC	choroid plexus:	n/a
35	chr17:16688816-16688866	AoSMC	blood vessel:	n/a
36	chr17:16688816-16688866	SAEC	small airway:	n/a
37	chr17:16688816-16688866	HNPCEpiC	eye:	n/a
38	chr17:16690169-16690219	AG04449	skin:	fetal
39	chr17:16690169-16690219	CMK	blood:	n/a
40	chr17:16688816-16688866	ovcar-3	ovarian:	n/a
41	chr17:16688816-16688866	Caco-2	colon:	n/a
42	chr17:16688816-16688866	AG09319	gingival:	n/a
43	chr17:16688816-16688866	ECC-1	luminal epithelium:	n/a
44	chr17:16690173-16690223	HCF	heart:	n/a
45	chr17:16693633-16693683	GM12878	blood:	n/a
46	chr17:16690169-16690219	AoSMC	blood vessel:	n/a
47	chr17:16693633-16693683	NH-A	brain:	n/a
48	chr17:16690173-16690223	HAEpiC	amniotic membrane:	n/a
49	chr17:16690169-16690219	GM19239	blood:	n/a
50	chr17:16690173-16690223	Caco-2	colon:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRT17P1-1	chr17:16691562-16691620	ENSG00000264673.1
2	lnc-AC104024.2.1-3	chr17:16692057-16693815	NONHSAT146006
3	lnc-AC104024.2.1-3	chr17:16692215-16692721	NONHSAT146007
4	lnc-CCDC144A-1	chr17:16707941-16707992	ENSG00000264729.1
5	lnc-CCDC144A-1	chr17:16708772-16709021	ENSG00000264729.1
6	lnc-KRT17P1-1	chr17:16691922-16692548	ENSG00000264673.1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LOC162632	hsa-miR-26b-5p	chr17:16707023-16707045

Variant related genes	Relation type
FAM106CP	TF binding region
ENSG00000264673	TF binding region
USP32P1	TF binding region
ENSG00000272815	TF binding region
SRP68P1	TF binding region
ENSG00000264892	TF binding region
ENSG00000264729	TF binding region
FAM106CP	CpG island
ENSG00000264673	CpG island
USP32P1	CpG island
ENSG00000272815	CpG island
SRP68P1	CpG island
ENSG00000264892	CpG island
ENSG00000264729	CpG island

Extended variants
information (count: 865 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7222574	chr17:16688280-16688281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566628989	chr17:16688362-16688363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529088743	chr17:16688395-16688396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs59823299	chr17:16688436-16688437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373756641	chr17:16688476-16688477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569146296	chr17:16688519-16688520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142515014	chr17:16688541-16688542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557303406	chr17:16688633-16688634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570559810	chr17:16688647-16688648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539539388	chr17:16688702-16688703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187100485	chr17:16688808-16688809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573054298	chr17:16688864-16688865	Weak transcription	CpG island	3 gene(s)	Overlapped CNVs	n/a
13	rs9895733	chr17:16688865-16688866	Weak transcription	CpG island	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555751661	chr17:16688934-16688935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150954823	chr17:16689024-16689025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544625036	chr17:16689125-16689126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564060391	chr17:16689134-16689135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577722102	chr17:16689177-16689178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540284643	chr17:16689195-16689196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560308788	chr17:16689381-16689382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529043631	chr17:16689472-16689473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549143529	chr17:16689501-16689502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562567647	chr17:16689512-16689513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531632678	chr17:16689704-16689705	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
25	rs192162063	chr17:16689720-16689721	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
26	rs551305434	chr17:16689729-16689730	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
27	rs141703044	chr17:16689738-16689739	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
28	rs570474343	chr17:16689792-16689793	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs111334241	chr17:16689815-16689816	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
30	rs539454347	chr17:16689832-16689833	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
31	rs2948628	chr17:16689862-16689863	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
32	rs2948627	chr17:16689870-16689871	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
33	rs113578165	chr17:16689874-16689875	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
34	rs183934883	chr17:16689878-16689879	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs550938379	chr17:16689879-16689880	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs778669	chr17:16689888-16689889	Weak transcription	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555908972	chr17:16689931-16689932	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs187374667	chr17:16689955-16689956	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs654177	chr17:16689971-16689972	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs558492307	chr17:16690149-16690150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577684723	chr17:16690169-16690170	Weak transcription	CpG island	3 gene(s)	Overlapped CNVs	n/a
42	rs540246096	chr17:16690197-16690198	Weak transcription	CpG island	3 gene(s)	Overlapped CNVs	n/a
43	rs560222195	chr17:16690221-16690222	Weak transcription	CpG island	3 gene(s)	Overlapped CNVs	n/a
44	rs112570190	chr17:16690240-16690241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573657581	chr17:16690393-16690394	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
46	rs542406929	chr17:16690394-16690395	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
47	rs562696232	chr17:16690402-16690403	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
48	rs531417975	chr17:16690410-16690411	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
49	rs551217753	chr17:16690656-16690657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564857881	chr17:16690684-16690685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:158)

Disease	PMID	Source
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
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
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
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	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
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16685200-16695400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr17:16689000-16697600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr17:16689600-16711600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr17:16690000-16706000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr17:16690400-16696000	Weak transcription	Brain Anterior Caudate	brain
6	chr17:16691200-16691600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr17:16692800-16693000	Enhancers	Duodenum Mucosa	Duodenum
8	chr17:16693000-16697600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr17:16695400-16695600	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr17:16697600-16698000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr17:16697600-16698000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr17:16697600-16698000	Enhancers	Duodenum Mucosa	Duodenum
13	chr17:16697600-16698000	Enhancers	A549	lung
14	chr17:16697600-16698000	Enhancers	K562	blood
15	chr17:16697800-16698000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr17:16698000-16704200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:16698000-16710800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr17:16698000-16711800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr17:16698800-16705200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr17:16700000-16700200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr17:16700200-16708200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr17:16708200-16708600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr17:16708200-16708600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr17:16708200-16708600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr17:16711600-16711800	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr17:16716600-16723200	Weak transcription	Right Atrium	heart
27	chr17:16717200-16720000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr17:16717400-16717600	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr17:16717400-16717800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr17:16717600-16717800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr17:16717600-16718000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr17:16717600-16718200	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr17:16717600-16718200	Enhancers	Right Ventricle	heart
34	chr17:16717600-16718200	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr17:16717800-16719000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr17:16718000-16719000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
37	chr17:16718000-16719000	ZNF genes & repeats	Spleen	Spleen

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