Variant report

Variant	nsv457705
Chromosome Location	chr17:20483882-20527718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:675)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr17:20514794-20515059	K562	blood:	n/a	chr17:20514926-20514939 chr17:20514929-20514938 chr17:20514928-20514937
2	CEBPB	chr17:20516625-20516934	HepG2	liver:	n/a	n/a
3	CTCF	chr17:20514940-20515090	MCF-7	breast:	n/a	n/a
4	CTCF	chr17:20514732-20514926	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr17:20514758-20514893	MCF-7	breast:	n/a	n/a
6	CTCF	chr17:20514740-20514883	GM12891	blood:	n/a	n/a
7	CTCF	chr17:20487394-20487465	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr17:20514740-20514890	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr17:20487302-20487541	MCF-7	breast:	n/a	n/a
10	CTCF	chr17:20514766-20514861	MCF-7	breast:	n/a	n/a
11	CTCF	chr17:20514773-20514830	GM19238	blood:	n/a	n/a
12	CTCF	chr17:20514760-20514910	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr17:20514760-20514910	GM12868	blood:	n/a	n/a
14	CTCF	chr17:20487301-20487561	MCF-7	breast:	n/a	n/a
15	CTCF	chr17:20514680-20514830	GM12875	blood:	n/a	n/a
16	CTCF	chr17:20487312-20487526	GM12891	blood:	n/a	n/a
17	CTCF	chr17:20487356-20487475	GM19239	blood:	n/a	n/a
18	CTCF	chr17:20487262-20487496	A549	lung:	n/a	n/a
19	CTCF	chr17:20487336-20487504	ProgFib	skin:	n/a	n/a
20	CTCF	chr17:20514640-20514790	GM12865	blood:	n/a	n/a
21	CTCF	chr17:20487305-20487537	MCF-7	breast:	n/a	n/a
22	CTCF	chr17:20487298-20487527	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr17:20492983-20493096	MCF-7	breast:	n/a	n/a
24	CTCF	chr17:20487375-20487526	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr17:20519907-20519910	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr17:20487326-20487535	GM12878	blood:	n/a	n/a
27	CTCF	chr17:20514740-20514890	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr17:20487360-20487490	HepG2	liver:	n/a	n/a
29	CTCF	chr17:20487308-20487542	Gliobla	brain:	n/a	n/a
30	CTCF	chr17:20493004-20493104	MCF-7	breast:	n/a	n/a
31	CTCF	chr17:20514680-20514830	GM12865	blood:	n/a	n/a
32	CTCF	chr17:20487327-20487528	A549	lung:	n/a	n/a
33	CTCF	chr17:20514762-20514838	K562	blood:	n/a	n/a
34	CTCF	chr17:20514740-20514890	HepG2	liver:	n/a	n/a
35	CTCF	chr17:20514768-20514848	GM12878	blood:	n/a	n/a
36	CTCF	chr17:20520462-20520500	GM10248	blood:	n/a	n/a
37	CTCF	chr17:20487287-20487548	MCF-7	breast:	n/a	n/a
38	CTCF	chr17:20487480-20487630	GM12873	blood:	n/a	n/a
39	CTCF	chr17:20487480-20487630	HEK293	kidney:	n/a	n/a
40	CTCF	chr17:20514740-20514890	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr17:20492974-20493087	MCF-7	breast:	n/a	n/a
42	CTCF	chr17:20515860-20515911	H1-hESC	embryonic stem cell:	n/a	chr17:20515882-20515898 chr17:20515881-20515899
43	CTCF	chr17:20487353-20487496	GM19240	blood:	n/a	n/a
44	CTCF	chr17:20492996-20493099	MCF-7	breast:	n/a	n/a
45	CTCF	chr17:20487440-20487590	SAEC	small airway:	n/a	n/a
46	CTCF	chr17:20487387-20487440	LNCaP	prostate:	n/a	n/a
47	CTCF	chr17:20514720-20514870	A549	lung:	n/a	n/a
48	CTCF	chr17:20487293-20487541	MCF-7	breast:	n/a	n/a
49	CTCF	chr17:20487329-20487520	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr17:20487351-20487529	Fibrobl	skin:	n/a	n/a

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20517129-20517179	ECC-1	luminal epithelium:	n/a
2	chr17:20493503-20493553	GM12892	blood:	n/a
3	chr17:20492631-20492681	AG10803	skin:	n/a
4	chr17:20516917-20516967	AG09319	gingival:	n/a
5	chr17:20517129-20517179	ECC-1	luminal epithelium:	n/a
6	chr17:20493503-20493553	GM12892	blood:	n/a
7	chr17:20492631-20492681	AG10803	skin:	n/a
8	chr17:20516917-20516967	AG09319	gingival:	n/a
9	chr17:20493386-20493436	LNCaP	prostate:	n/a
10	chr17:20491042-20491092	SKMC	muscle:	n/a
11	chr17:20491042-20491092	NHBE	bronchial:	n/a
12	chr17:20517129-20517179	HIPEpiC	eye:	n/a
13	chr17:20491042-20491092	PrEC	prostate:	n/a
14	chr17:20517129-20517179	HRPEpiC	eye:	n/a
15	chr17:20516172-20516222	MCF10A-Er-Src	breast:	n/a
16	chr17:20493503-20493553	NHBE	bronchial:	n/a
17	chr17:20515873-20515923	SAEC	small airway:	n/a
18	chr17:20491042-20491092	HepG2	liver:	n/a
19	chr17:20491042-20491092	NHDF-neo	bronchial:	n/a
20	chr17:20493503-20493553	GM12878	blood:	n/a
21	chr17:20516019-20516069	SK-N-MC	brain:	n/a
22	chr17:20489071-20489121	HIPEpiC	eye:	n/a
23	chr17:20493386-20493436	AG09309	skin:	n/a
24	chr17:20515873-20515923	PrEC	prostate:	n/a
25	chr17:20516019-20516069	BJ	skin:	n/a
26	chr17:20492631-20492681	HMEC	breast:	n/a
27	chr17:20492631-20492681	HRCEpiC	kidney:	n/a
28	chr17:20516172-20516222	HCF	heart:	n/a
29	chr17:20516172-20516222	Caco-2	colon:	n/a
30	chr17:20515873-20515923	GM06990	blood:	n/a
31	chr17:20489071-20489121	HRPEpiC	eye:	n/a
32	chr17:20493503-20493553	HCM	heart:	n/a
33	chr17:20516019-20516069	Hela-S3	cervix:	n/a
34	chr17:20489071-20489121	MCF10A-Er-Src	breast:	n/a
35	chr17:20515873-20515923	T-47D	breast:	n/a
36	chr17:20492631-20492681	HepG2	liver:	n/a
37	chr17:20491042-20491092	LNCaP	prostate:	n/a
38	chr17:20489071-20489121	NHBE	bronchial:	n/a
39	chr17:20517129-20517179	BE2_C	brain:	n/a
40	chr17:20516820-20516870	AG04450	lung:	fetal
41	chr17:20492631-20492681	NHBE	bronchial:	n/a
42	chr17:20493503-20493553	HRE	kidney:	n/a
43	chr17:20516820-20516870	HPAEpiC	pulmonary alveolar:	n/a
44	chr17:20516820-20516870	K562	blood:	n/a
45	chr17:20516917-20516967	HEK293	kidney:	embryo
46	chr17:20493386-20493436	PANC-1	pancreas:	n/a
47	chr17:20489071-20489121	LNCaP	prostate:	n/a
48	chr17:20516820-20516870	NB4	blood:	n/a
49	chr17:20491042-20491092	HCT-116	colon:	n/a
50	chr17:20491042-20491092	GM12891	blood:	n/a

No data

(count:2 , 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	chr17:20517801-20517981	ENSG00000227685.1

No data

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

Extended variants
information (count: 572 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11868057	chr17:20483882-20483883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572846761	chr17:20483898-20483899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142233315	chr17:20483901-20483902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531163364	chr17:20483934-20483935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397834842	chr17:20483978-20483979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532477016	chr17:20484011-20484012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144207782	chr17:20484029-20484030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562851193	chr17:20484118-20484119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551132303	chr17:20484203-20484204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530267722	chr17:20484265-20484266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548848151	chr17:20484283-20484284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567163386	chr17:20484332-20484333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534532690	chr17:20484365-20484366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567907719	chr17:20484396-20484397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571197190	chr17:20484542-20484543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536939834	chr17:20484751-20484752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538274092	chr17:20484799-20484800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556973805	chr17:20484825-20484826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568859621	chr17:20484836-20484837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536033012	chr17:20484888-20484889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186835042	chr17:20484908-20484909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572783681	chr17:20484925-20484926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143511811	chr17:20484978-20484979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558599311	chr17:20485016-20485017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112068673	chr17:20485102-20485103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577134698	chr17:20485112-20485113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557757575	chr17:20485116-20485117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs609551	chr17:20485140-20485141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150956226	chr17:20485163-20485164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562997298	chr17:20485203-20485204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530259914	chr17:20485220-20485221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542428039	chr17:20485254-20485255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560696956	chr17:20485294-20485295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191254599	chr17:20485339-20485340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552872699	chr17:20485358-20485359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571070996	chr17:20485364-20485365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141064838	chr17:20485368-20485369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550349132	chr17:20485443-20485444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568923171	chr17:20485450-20485451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112003067	chr17:20485512-20485513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575315815	chr17:20485562-20485563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554320873	chr17:20485646-20485647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566302724	chr17:20485655-20485656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533753261	chr17:20485672-20485673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558769767	chr17:20485710-20485711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577111945	chr17:20485718-20485719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544585143	chr17:20485721-20485722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556319312	chr17:20485735-20485736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574967236	chr17:20485756-20485757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542317497	chr17:20485766-20485767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:150)

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

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20472800-20492200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr17:20484600-20484800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:20484800-20492200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr17:20491400-20491800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr17:20491600-20492000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr17:20491800-20492000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr17:20491800-20492000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr17:20491800-20492600	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr17:20491800-20492600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr17:20491800-20492800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr17:20491800-20492800	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr17:20491800-20492800	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr17:20492000-20492400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr17:20492000-20492400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr17:20492000-20492600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr17:20492000-20492600	Active TSS	Ovary	ovary
17	chr17:20492000-20492600	Active TSS	Psoas Muscle	Psoas
18	chr17:20492000-20492800	Active TSS	H9 Cell Line	embryonic stem cell
19	chr17:20492000-20492800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr17:20492000-20492800	Active TSS	Cortex derived primary cultured neurospheres	brain
21	chr17:20492000-20492800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr17:20492000-20492800	Active TSS	Brain Germinal Matrix	brain
23	chr17:20492000-20492800	Active TSS	Right Atrium	heart
24	chr17:20492000-20493000	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr17:20492000-20493000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr17:20492200-20492600	Active TSS	H1 Cell Line	embryonic stem cell
27	chr17:20492200-20492600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr17:20492200-20492600	Active TSS	Right Ventricle	heart
29	chr17:20492200-20492800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr17:20492200-20492800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr17:20492200-20492800	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr17:20492200-20492800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr17:20492200-20492800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr17:20492200-20492800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr17:20492200-20492800	Active TSS	Fetal Brain Female	brain
36	chr17:20492200-20493000	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr17:20492400-20492600	Enhancers	Primary hematopoietic stem cells	blood
38	chr17:20492400-20492600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:20492400-20492600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr17:20492400-20492600	Active TSS	Fetal Muscle Trunk	muscle
41	chr17:20492400-20492600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
42	chr17:20492400-20492800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr17:20492400-20492800	Active TSS	Adipose Nuclei	Adipose
44	chr17:20492400-20492800	Bivalent/Poised TSS	Fetal Stomach	stomach
45	chr17:20492400-20493000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr17:20492400-20493000	Active TSS	Fetal Intestine Small	intestine
47	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
48	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
49	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
50	chr17:20492600-20492800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle

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