Variant report

Variant	nsv907883
Chromosome Location	chr17:20487047-20613642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:794)
Chromatin interactive
region (count:1)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr17:20552417-20552929	GM12878	blood:	n/a	n/a
2	ATF2	chr17:20552401-20552830	GM12878	blood:	n/a	n/a
3	BATF	chr17:20552419-20552811	GM12878	blood:	n/a	n/a
4	BATF	chr17:20573899-20574074	GM12878	blood:	n/a	n/a
5	BATF	chr17:20602187-20602524	GM12878	blood:	n/a	n/a
6	BATF	chr17:20552423-20552925	GM12878	blood:	n/a	n/a
7	BATF	chr17:20602164-20602479	GM12878	blood:	n/a	n/a
8	BATF	chr17:20568713-20568948	GM12878	blood:	n/a	chr17:20568784-20568795
9	BATF	chr17:20554357-20554645	GM12878	blood:	n/a	n/a
10	BCL11A	chr17:20554373-20554609	GM12878	blood:	n/a	n/a
11	BCL11A	chr17:20602137-20602533	GM12878	blood:	n/a	n/a
12	BCL11A	chr17:20602069-20602629	GM12878	blood:	n/a	n/a
13	BCL11A	chr17:20581794-20582050	GM12878	blood:	n/a	chr17:20582005-20582012
14	BCL11A	chr17:20552438-20552751	GM12878	blood:	n/a	n/a
15	BCL11A	chr17:20559489-20559685	GM12878	blood:	n/a	n/a
16	BCL11A	chr17:20554375-20554592	GM12878	blood:	n/a	n/a
17	BCL11A	chr17:20552374-20552875	GM12878	blood:	n/a	n/a
18	BCL11A	chr17:20603932-20604264	GM12878	blood:	n/a	n/a
19	BHLHE40	chr17:20552469-20552691	GM12878	blood:	n/a	n/a
20	BHLHE40	chr17:20602321-20602362	GM12878	blood:	n/a	n/a
21	BHLHE40	chr17:20514794-20515059	K562	blood:	n/a	chr17:20514926-20514939 chr17:20514929-20514938 chr17:20514928-20514937
22	CEBPB	chr17:20557555-20557814	IMR90	lung:	n/a	chr17:20557790-20557807
23	CEBPB	chr17:20557457-20557822	Hela-S3	cervix:	n/a	chr17:20557790-20557807
24	CEBPB	chr17:20516625-20516934	HepG2	liver:	n/a	n/a
25	CEBPB	chr17:20568666-20568987	K562	blood:	n/a	chr17:20568791-20568804
26	CHD1	chr17:20552549-20552628	GM12878	blood:	n/a	n/a
27	CHD2	chr17:20602331-20602356	GM12878	blood:	n/a	n/a
28	CTCF	chr17:20550440-20550590	HCM	heart:	n/a	n/a
29	CTCF	chr17:20570060-20570210	NB4	blood:	n/a	n/a
30	CTCF	chr17:20550120-20550270	Caco-2	colon:	n/a	chr17:20550147-20550160
31	CTCF	chr17:20570040-20570190	GM12864	blood:	n/a	n/a
32	CTCF	chr17:20550040-20550190	HRPEpiC	eye:	n/a	chr17:20550147-20550160
33	CTCF	chr17:20550040-20550190	HCT-116	colon:	n/a	chr17:20550147-20550160
34	CTCF	chr17:20550000-20550150	AG04450	lung:	n/a	n/a
35	CTCF	chr17:20487357-20487462	K562	blood:	n/a	n/a
36	CTCF	chr17:20570080-20570230	GM12869	blood:	n/a	chr17:20570200-20570213
37	CTCF	chr17:20514680-20514830	GM12875	blood:	n/a	n/a
38	CTCF	chr17:20492974-20493087	MCF-7	breast:	n/a	n/a
39	CTCF	chr17:20570139-20570200	GM10266	blood:	n/a	n/a
40	CTCF	chr17:20601940-20602090	HMEC	breast:	n/a	chr17:20602002-20602023
41	CTCF	chr17:20487387-20487440	LNCaP	prostate:	n/a	n/a
42	CTCF	chr17:20550000-20550150	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr17:20487298-20487527	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr17:20604315-20604361	GM10266	blood:	n/a	n/a
45	CTCF	chr17:20532375-20532499	Gliobla	brain:	n/a	n/a
46	CTCF	chr17:20550100-20550250	GM12872	blood:	n/a	chr17:20550147-20550160
47	CTCF	chr17:20549973-20550244	HepG2	liver:	n/a	chr17:20550147-20550160
48	CTCF	chr17:20550048-20550246	SK-N-SH_RA	brain:	n/a	chr17:20550147-20550160
49	CTCF	chr17:20550036-20550306	GM12892	blood:	n/a	chr17:20550147-20550160
50	CTCF	chr17:20570040-20570190	GM12870	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20516019-20516069	ECC-1	luminal epithelium:	n/a
2	chr17:20516019-20516069	ECC-1	luminal epithelium:	n/a
3	chr17:20536885-20536935	HEK293	kidney:	embryo
4	chr17:20516820-20516870	SAEC	small airway:	n/a
5	chr17:20493503-20493553	Hepatocyte	liver:	n/a
6	chr17:20516172-20516222	HL-60	blood:	n/a
7	chr17:20536885-20536935	NHBE	bronchial:	n/a
8	chr17:20516172-20516222	U87	brain:	n/a
9	chr17:20536948-20536998	HAEpiC	amniotic membrane:	n/a
10	chr17:20493503-20493553	GM12891	blood:	n/a
11	chr17:20516019-20516069	CMK	blood:	n/a
12	chr17:20489071-20489121	GM19239	blood:	n/a
13	chr17:20516019-20516069	HNPCEpiC	eye:	n/a
14	chr17:20493503-20493553	AG10803	skin:	n/a
15	chr17:20493386-20493436	CMK	blood:	n/a
16	chr17:20516820-20516870	HAEpiC	amniotic membrane:	n/a
17	chr17:20493503-20493553	AG04450	lung:	fetal
18	chr17:20516019-20516069	HEK293	kidney:	embryo
19	chr17:20516917-20516967	ECC-1	luminal epithelium:	n/a
20	chr17:20516019-20516069	AoSMC	blood vessel:	n/a
21	chr17:20491042-20491092	Hela-S3	cervix:	n/a
22	chr17:20516917-20516967	Hepatocyte	liver:	n/a
23	chr17:20516917-20516967	GM06990	blood:	n/a
24	chr17:20516820-20516870	NT2-D1	testis:	n/a
25	chr17:20493386-20493436	MCF10A-Er-Src	breast:	n/a
26	chr17:20516172-20516222	PANC-1	pancreas:	n/a
27	chr17:20516019-20516069	SK-N-SH	brain:	n/a
28	chr17:20491042-20491092	AG04450	lung:	fetal
29	chr17:20492631-20492681	A549	lung:	n/a
30	chr17:20536885-20536935	HRE	kidney:	n/a
31	chr17:20516172-20516222	NH-A	brain:	n/a
32	chr17:20517129-20517179	HRPEpiC	eye:	n/a
33	chr17:20489071-20489121	MCF-7	breast:	n/a
34	chr17:20517129-20517179	HL-60	blood:	n/a
35	chr17:20516917-20516967	HAEpiC	amniotic membrane:	n/a
36	chr17:20516019-20516069	GM12891	blood:	n/a
37	chr17:20491042-20491092	MCF-7	breast:	n/a
38	chr17:20515873-20515923	AG04450	lung:	fetal
39	chr17:20516820-20516870	A549	lung:	n/a
40	chr17:20516820-20516870	PFSK-1	brain:	n/a
41	chr17:20517129-20517179	GM12891	blood:	n/a
42	chr17:20536885-20536935	GM12892	blood:	n/a
43	chr17:20516820-20516870	AoSMC	blood vessel:	n/a
44	chr17:20536948-20536998	HepG2	liver:	n/a
45	chr17:20516820-20516870	AG09309	skin:	n/a
46	chr17:20516917-20516967	BJ	skin:	n/a
47	chr17:20492631-20492681	PANC-1	pancreas:	n/a
48	chr17:20516917-20516967	CMK	blood:	n/a
49	chr17:20516820-20516870	MCF10A-Er-Src	breast:	n/a
50	chr17:20493386-20493436	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:20610050..20610947-chr17:30454022..30454629,2	Hela-S3	cervix:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS9B-3	chr17:20516225-20516387	ENSG00000227685.1
2	lnc-LGALS9B-3	chr17:20534785-20534862	ENSG00000227685.1
3	lnc-LGALS9B-3	chr17:20536350-20536547	ENSG00000227685.1
4	lnc-LGALS9B-3	chr17:20536347-20536572	NONHSAT146828
5	lnc-LGALS9B-3	chr17:20517801-20517981	ENSG00000227685.1

No data

Variant related genes	Relation type
ENSG00000227685	TF binding region
ENSG00000264422	TF binding region
ZSWIM5P2	TF binding region
ENSG00000232889	TF binding region
ENSG00000235546	TF binding region
ENSG00000266364	TF binding region
MEIS3P2	TF binding region
ENSG00000236504	TF binding region
ENSG00000226096	TF binding region
ENSG00000227685	CpG island
ENSG00000264422	CpG island
ZSWIM5P2	CpG island
ENSG00000232889	CpG island
ENSG00000235546	CpG island
ENSG00000266364	CpG island
MEIS3P2	CpG island
ENSG00000236504	CpG island
ENSG00000226096	CpG island

Extended variants
information (count: 2724 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:2724 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs688282	chr17:20487047-20487048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559109448	chr17:20487055-20487056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377638845	chr17:20487119-20487120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576527479	chr17:20487120-20487121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371380593	chr17:20487143-20487144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181477237	chr17:20487186-20487187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376029239	chr17:20487215-20487216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574034949	chr17:20487220-20487221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541408579	chr17:20487240-20487241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368449354	chr17:20487345-20487346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527302674	chr17:20487380-20487381	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551950289	chr17:20487413-20487414	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs564215546	chr17:20487461-20487462	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs531356955	chr17:20487467-20487468	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs550044783	chr17:20487496-20487497	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568356086	chr17:20487540-20487541	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs529241570	chr17:20487559-20487560	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs547792176	chr17:20487565-20487566	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs148741763	chr17:20487572-20487573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs141740927	chr17:20487578-20487579	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557931257	chr17:20487590-20487591	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570138405	chr17:20487598-20487599	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs537238016	chr17:20487649-20487650	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555574116	chr17:20487653-20487654	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs573971721	chr17:20487656-20487657	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs541296516	chr17:20487741-20487742	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111795578	chr17:20487756-20487757	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs553266072	chr17:20487768-20487769	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs370346133	chr17:20487852-20487853	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs545783921	chr17:20487883-20487884	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs564019801	chr17:20487923-20487924	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs531477288	chr17:20487927-20487928	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs530616230	chr17:20487972-20487973	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550930741	chr17:20487974-20487975	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs147181078	chr17:20487975-20487976	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs201373331	chr17:20488022-20488023	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs76850913	chr17:20488023-20488024	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs56834160	chr17:20488024-20488025	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs529125438	chr17:20488155-20488156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547681148	chr17:20488181-20488182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185333507	chr17:20488197-20488198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377475353	chr17:20488213-20488214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533129311	chr17:20488218-20488219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189752374	chr17:20488242-20488243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140635868	chr17:20488349-20488350	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs537176008	chr17:20488354-20488355	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs555462900	chr17:20488430-20488431	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375268711	chr17:20488466-20488467	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs180684749	chr17:20488488-20488489	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs58220184	chr17:20488489-20488490	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20472800-20492200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:20484800-20492200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:20491400-20491800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr17:20491600-20492000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr17:20491800-20492000	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr17:20491800-20492000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr17:20491800-20492600	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr17:20491800-20492600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr17:20491800-20492800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr17:20491800-20492800	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr17:20491800-20492800	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr17:20492000-20492400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr17:20492000-20492400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr17:20492000-20492600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr17:20492000-20492600	Active TSS	Ovary	ovary
16	chr17:20492000-20492600	Active TSS	Psoas Muscle	Psoas
17	chr17:20492000-20492800	Active TSS	H9 Cell Line	embryonic stem cell
18	chr17:20492000-20492800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr17:20492000-20492800	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr17:20492000-20492800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr17:20492000-20492800	Active TSS	Brain Germinal Matrix	brain
22	chr17:20492000-20492800	Active TSS	Right Atrium	heart
23	chr17:20492000-20493000	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr17:20492000-20493000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr17:20492200-20492600	Active TSS	H1 Cell Line	embryonic stem cell
26	chr17:20492200-20492600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr17:20492200-20492600	Active TSS	Right Ventricle	heart
28	chr17:20492200-20492800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr17:20492200-20492800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr17:20492200-20492800	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr17:20492200-20492800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr17:20492200-20492800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr17:20492200-20492800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr17:20492200-20492800	Active TSS	Fetal Brain Female	brain
35	chr17:20492200-20493000	Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr17:20492400-20492600	Enhancers	Primary hematopoietic stem cells	blood
37	chr17:20492400-20492600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr17:20492400-20492600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr17:20492400-20492600	Active TSS	Fetal Muscle Trunk	muscle
40	chr17:20492400-20492600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
41	chr17:20492400-20492800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr17:20492400-20492800	Active TSS	Adipose Nuclei	Adipose
43	chr17:20492400-20492800	Bivalent/Poised TSS	Fetal Stomach	stomach
44	chr17:20492400-20493000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr17:20492400-20493000	Active TSS	Fetal Intestine Small	intestine
46	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
47	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
48	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
49	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
50	chr17:20492600-20493000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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