Variant report

Variant	nsv907725
Chromosome Location	chr17:16699832-16743852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:252)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:16719169-16719457	K562	blood:	n/a	n/a
2	BACH1	chr17:16719341-16719384	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr17:16710949-16711369	GM12878	blood:	n/a	chr17:16711188-16711198 chr17:16711187-16711198
4	BATF	chr17:16711019-16711268	GM12878	blood:	n/a	chr17:16711188-16711198 chr17:16711187-16711198
5	CTCF	chr17:16722140-16722290	MCF-7	breast:	n/a	n/a
6	CTCF	chr17:16733600-16733825	LNCaP	prostate:	n/a	n/a
7	CTCF	chr17:16733720-16733870	HepG2	liver:	n/a	n/a
8	CTCF	chr17:16719220-16719370	SAEC	small airway:	n/a	n/a
9	CTCF	chr17:16733614-16733838	Medullo	brain:	n/a	n/a
10	CTCF	chr17:16733640-16733790	A549	lung:	n/a	n/a
11	CTCF	chr17:16733645-16733834	GM12891	blood:	n/a	n/a
12	CTCF	chr17:16733647-16733833	A549	lung:	n/a	n/a
13	CTCF	chr17:16733526-16733849	K562	blood:	n/a	n/a
14	CTCF	chr17:16733600-16733750	HCFaa	heart:	n/a	n/a
15	CTCF	chr17:16719921-16719989	GM13976	blood:	n/a	n/a
16	CTCF	chr17:16709080-16709230	AG09319	gingival:	n/a	n/a
17	CTCF	chr17:16732536-16732650	LNCaP	prostate:	n/a	n/a
18	CTCF	chr17:16720520-16720577	GM12892	blood:	n/a	n/a
19	CTCF	chr17:16733620-16733770	GM12869	blood:	n/a	n/a
20	CTCF	chr17:16733439-16733929	A549	lung:	n/a	n/a
21	CTCF	chr17:16722240-16722327	Fibrobl	skin:	n/a	n/a
22	CTCF	chr17:16740288-16740357	GM10248	blood:	n/a	n/a
23	CTCF	chr17:16722128-16722338	A549	lung:	n/a	n/a
24	CTCF	chr17:16733563-16733841	GM10248	blood:	n/a	n/a
25	CTCF	chr17:16733700-16733850	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr17:16719240-16719390	HCT-116	colon:	n/a	n/a
27	CTCF	chr17:16733664-16733837	GM12892	blood:	n/a	n/a
28	CTCF	chr17:16733621-16733856	Gliobla	brain:	n/a	n/a
29	CTCF	chr17:16739909-16739984	GM10248	blood:	n/a	chr17:16739926-16739944 chr17:16739929-16739942
30	CTCF	chr17:16733566-16733843	GM13977	blood:	n/a	n/a
31	CTCF	chr17:16722187-16722392	MCF-7	breast:	n/a	n/a
32	CTCF	chr17:16726027-16726055	LNCaP	prostate:	n/a	n/a
33	CTCF	chr17:16733658-16733837	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:16725222-16725241	GM13976	blood:	n/a	n/a
35	CTCF	chr17:16714100-16714250	NB4	blood:	n/a	n/a
36	CTCF	chr17:16722282-16722309	GM12878	blood:	n/a	n/a
37	CTCF	chr17:16733629-16733838	K562	blood:	n/a	n/a
38	CTCF	chr17:16742054-16742198	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr17:16733671-16733828	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr17:16726160-16726218	GM20000	blood:	n/a	n/a
41	CTCF	chr17:16719394-16719507	LNCaP	prostate:	n/a	n/a
42	CTCF	chr17:16734499-16734511	GM10248	blood:	n/a	n/a
43	CTCF	chr17:16735283-16735344	GM10248	blood:	n/a	n/a
44	CTCF	chr17:16713824-16713893	GM13976	blood:	n/a	n/a
45	CTCF	chr17:16733711-16733761	HepG2	liver:	n/a	n/a
46	CTCF	chr17:16733679-16733836	GM12878	blood:	n/a	n/a
47	CTCF	chr17:16709100-16709250	K562	blood:	n/a	n/a
48	CTCF	chr17:16733677-16733842	MCF-7	breast:	n/a	n/a
49	CTCF	chr17:16722175-16722391	MCF-7	breast:	n/a	n/a
50	CTCF	chr17:16740285-16740372	Spleen_OC	spleen:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16736463-16736513	MCF-7	breast:	n/a
2	chr17:16737096-16737146	HCPEpiC	choroid plexus:	n/a
3	chr17:16734819-16734869	IMR90	lung:	fetal
4	chr17:16734819-16734869	MCF10A-Er-Src	breast:	n/a
5	chr17:16737096-16737146	A549	lung:	n/a
6	chr17:16734819-16734869	NHDF-neo	bronchial:	n/a
7	chr17:16734819-16734869	AoSMC	blood vessel:	n/a
8	chr17:16734819-16734869	K562	blood:	n/a
9	chr17:16736463-16736513	AG04450	lung:	fetal
10	chr17:16734819-16734869	Hela-S3	cervix:	n/a
11	chr17:16736463-16736513	GM12892	blood:	n/a
12	chr17:16736463-16736513	HCF	heart:	n/a
13	chr17:16737096-16737146	Hepatocyte	liver:	n/a
14	chr17:16737096-16737146	CMK	blood:	n/a
15	chr17:16736463-16736513	HRCEpiC	kidney:	n/a
16	chr17:16736463-16736513	AG09309	skin:	n/a
17	chr17:16736463-16736513	CMK	blood:	n/a
18	chr17:16736463-16736513	Hepatocyte	liver:	n/a
19	chr17:16736463-16736513	AG09319	gingival:	n/a
20	chr17:16734819-16734869	HCT-116	colon:	n/a
21	chr17:16736463-16736513	NH-A	brain:	n/a
22	chr17:16734819-16734869	BJ	skin:	n/a
23	chr17:16734819-16734869	HepG2	liver:	n/a
24	chr17:16734819-16734869	Jurkat	blood:	n/a
25	chr17:16736463-16736513	HMEC	breast:	n/a
26	chr17:16737096-16737146	SAEC	small airway:	n/a
27	chr17:16737096-16737146	AG04450	lung:	fetal
28	chr17:16736463-16736513	K562	blood:	n/a
29	chr17:16737096-16737146	H1-hESC	embryonic stem cell:	embryo
30	chr17:16736463-16736513	ovcar-3	ovarian:	n/a
31	chr17:16734819-16734869	LNCaP	prostate:	n/a
32	chr17:16737096-16737146	HRPEpiC	eye:	n/a
33	chr17:16734819-16734869	HCF	heart:	n/a
34	chr17:16736463-16736513	Hela-S3	cervix:	n/a
35	chr17:16736463-16736513	HPAEpiC	pulmonary alveolar:	n/a
36	chr17:16736463-16736513	A549	lung:	n/a
37	chr17:16736463-16736513	SK-N-MC	brain:	n/a
38	chr17:16734819-16734869	GM12878	blood:	n/a
39	chr17:16737096-16737146	PrEC	prostate:	n/a
40	chr17:16734819-16734869	HRPEpiC	eye:	n/a
41	chr17:16734819-16734869	HMEC	breast:	n/a
42	chr17:16736463-16736513	GM12878	blood:	n/a
43	chr17:16734819-16734869	ovcar-3	ovarian:	n/a
44	chr17:16736463-16736513	PFSK-1	brain:	n/a
45	chr17:16734819-16734869	HEK293	kidney:	embryo
46	chr17:16736463-16736513	SKMC	muscle:	n/a
47	chr17:16734819-16734869	A549	lung:	n/a
48	chr17:16734819-16734869	GM12892	blood:	n/a
49	chr17:16737096-16737146	NH-A	brain:	n/a
50	chr17:16737096-16737146	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:16721818..16722353-chr17:16776583..16777108,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC144A-4	chr17:16735634-16735881	NONHSAT146016
2	lnc-CCDC144A-4	chr17:16734662-16734742	NONHSAT146016
3	lnc-CCDC144A-1	chr17:16708772-16709021	ENSG00000264729.1
4	lnc-CCDC144A-1	chr17:16707941-16707992	ENSG00000264729.1

No data

(count:1 , 50 per page) page: 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
USP32P1	TF binding region
ENSG00000264729	TF binding region
ENSG00000226145	TF binding region
KRT16P2	TF binding region
ENSG00000264892	TF binding region
USP32P1	CpG island
ENSG00000264729	CpG island
ENSG00000226145	CpG island
KRT16P2	CpG island
ENSG00000264892	CpG island

Extended variants
information (count: 1361 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs778672	chr17:16699832-16699833	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62075091	chr17:16699858-16699859	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558753497	chr17:16699867-16699868	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572244548	chr17:16699962-16699963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541353926	chr17:16700051-16700052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185936433	chr17:16700125-16700126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573980037	chr17:16700136-16700137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543115269	chr17:16700153-16700154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562985802	chr17:16700170-16700171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531876376	chr17:16700172-16700173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573719546	chr17:16700194-16700195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4034471	chr17:16700213-16700214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2688044	chr17:16700214-16700215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551982481	chr17:16700215-16700216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3114290	chr17:16700283-16700284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2621738	chr17:16700288-16700289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565520731	chr17:16700362-16700363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9906035	chr17:16700383-16700384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527969588	chr17:16700400-16700401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548079875	chr17:16700418-16700419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567105700	chr17:16700467-16700468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs583179	chr17:16700517-16700518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371929398	chr17:16700526-16700527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535869135	chr17:16700528-16700529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190802114	chr17:16700545-16700546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563374980	chr17:16700553-16700554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs582783	chr17:16700573-16700574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569399107	chr17:16700637-16700638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538377647	chr17:16700680-16700681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs778673	chr17:16700723-16700724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148892070	chr17:16700782-16700783	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572212923	chr17:16700806-16700807	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs534566516	chr17:16700833-16700834	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs554869070	chr17:16700836-16700837	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574046867	chr17:16700837-16700838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs9907213	chr17:16700863-16700864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs4924867	chr17:16700875-16700876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139799467	chr17:16700876-16700877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182397333	chr17:16700881-16700882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9908540	chr17:16700882-16700883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111924085	chr17:16700883-16700884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61106631	chr17:16700889-16700890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143552316	chr17:16700916-16700917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2621737	chr17:16700930-16700931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527891389	chr17:16700946-16700947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs678620	chr17:16700954-16700955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541335929	chr17:16700969-16700970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561643781	chr17:16700999-16701000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397833933	chr17:16701008-16701009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs678522	chr17:16701025-16701026	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
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16689600-16711600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr17:16690000-16706000	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr17:16698000-16704200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr17:16698000-16710800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr17:16698000-16711800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr17:16698800-16705200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:16700000-16700200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr17:16700200-16708200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr17:16708200-16708600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr17:16708200-16708600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr17:16708200-16708600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr17:16711600-16711800	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr17:16716600-16723200	Weak transcription	Right Atrium	heart
14	chr17:16717200-16720000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr17:16717400-16717600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr17:16717400-16717800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:16717600-16717800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr17:16717600-16718000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr17:16717600-16718200	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr17:16717600-16718200	Enhancers	Right Ventricle	heart
21	chr17:16717600-16718200	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr17:16717800-16719000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr17:16718000-16719000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr17:16718000-16719000	ZNF genes & repeats	Spleen	Spleen
25	chr17:16718600-16719200	Enhancers	A549	lung
26	chr17:16718600-16720600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr17:16719000-16719200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr17:16719000-16719200	Enhancers	NHEK	skin
29	chr17:16719000-16719400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr17:16719000-16723200	Weak transcription	Spleen	Spleen
31	chr17:16719000-16724000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr17:16719200-16720600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:16719200-16723600	Weak transcription	NHEK	skin
34	chr17:16719400-16720200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr17:16720200-16722400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr17:16720600-16722200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr17:16720600-16723000	Strong transcription	Placenta Amnion	Placenta Amnion
38	chr17:16720600-16723200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr17:16721400-16724600	Enhancers	Adipose Nuclei	Adipose
40	chr17:16721600-16723800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr17:16721800-16722000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr17:16722000-16722600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr17:16722000-16723200	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr17:16722000-16724800	Enhancers	Right Ventricle	heart
45	chr17:16722200-16723000	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr17:16722200-16724200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr17:16722400-16722600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr17:16722400-16722800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr17:16722400-16722800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr17:16722400-16723400	Enhancers	Skeletal Muscle Female	skeletal muscle

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