Variant report

Variant	nsv518888
Chromosome Location	chr17:19789453-19804247
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	CEBPB	chr17:19801254-19801738	IMR90	lung:	n/a	n/a
2	CEBPB	chr17:19800341-19800818	MCF-7	breast:	n/a	n/a
3	CEBPB	chr17:19793944-19794205	HepG2	liver:	n/a	n/a
4	CEBPB	chr17:19801206-19802128	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr17:19800111-19800829	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr17:19800274-19800385	A549	lung:	n/a	n/a
7	CEBPB	chr17:19794059-19794174	HepG2	liver:	n/a	n/a
8	CHD2	chr17:19800350-19800852	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr17:19803113-19803323	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr17:19803209-19803281	K562	blood:	n/a	n/a
11	CTCF	chr17:19802880-19803030	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr17:19801920-19802070	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr17:19803274-19803276	MCF-7	breast:	n/a	n/a
14	CTCF	chr17:19803212-19803246	MCF-7	breast:	n/a	n/a
15	CTCF	chr17:19803180-19803330	HEK293	kidney:	n/a	n/a
16	CTCF	chr17:19803168-19803290	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr17:19803188-19803286	MCF-7	breast:	n/a	n/a
18	CTCF	chr17:19801940-19802090	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr17:19803217-19803254	MCF-7	breast:	n/a	n/a
20	CTCF	chr17:19803208-19803273	MCF-7	breast:	n/a	n/a
21	CTCF	chr17:19803181-19803264	MCF-7	breast:	n/a	n/a
22	E2F4	chr17:19801458-19801547	MCF10A-Er-Src	breast:	n/a	n/a
23	EP300	chr17:19801308-19801549	SK-N-SH_RA	brain:	n/a	chr17:19801487-19801496
24	EP300	chr17:19801305-19801677	Hela-S3	cervix:	n/a	chr17:19801487-19801496
25	EP300	chr17:19800164-19800750	Hela-S3	cervix:	n/a	n/a
26	FOS	chr17:19800007-19800709	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr17:19801315-19801642	Hela-S3	cervix:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496 chr17:19801486-19801497
28	FOS	chr17:19804225-19804501	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr17:19801247-19801674	MCF10A-Er-Src	breast:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496 chr17:19801486-19801497
30	FOS	chr17:19801303-19801674	MCF10A-Er-Src	breast:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496 chr17:19801486-19801497
31	FOS	chr17:19801326-19801665	MCF10A-Er-Src	breast:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496 chr17:19801486-19801497
32	FOS	chr17:19800025-19800966	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr17:19801380-19801651	HUVEC	blood vessel:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496 chr17:19801486-19801497
34	FOS	chr17:19804191-19804468	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr17:19800122-19800713	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr17:19801301-19801680	MCF10A-Er-Src	breast:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496 chr17:19801486-19801497
37	FOS	chr17:19799973-19800775	MCF10A-Er-Src	breast:	n/a	n/a
38	FOSL2	chr17:19801238-19801713	A549	lung:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496
39	FOSL2	chr17:19801345-19801649	A549	lung:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496
40	FOSL2	chr17:19801188-19801686	SK-N-SH	brain:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496
41	FOSL2	chr17:19801264-19801727	MCF-7	breast:	n/a	chr17:19801486-19801498 chr17:19801489-19801496 chr17:19801487-19801496
42	FOSL2	chr17:19800406-19800862	HepG2	liver:	n/a	n/a
43	FOSL2	chr17:19801065-19801425	HepG2	liver:	n/a	chr17:19801184-19801193
44	FOXA1	chr17:19803646-19803929	T-47D	breast:	n/a	n/a
45	FOXA1	chr17:19804083-19804458	T-47D	breast:	n/a	chr17:19804293-19804308
46	FOXA1	chr17:19804073-19804507	T-47D	breast:	n/a	chr17:19804293-19804308
47	FOXA2	chr17:19804002-19804623	A549	lung:	n/a	n/a
48	FOXA2	chr17:19804053-19804626	A549	lung:	n/a	n/a
49	GATA2	chr17:19801220-19801503	HUVEC	blood vessel:	n/a	n/a
50	GATA3	chr17:19801207-19801594	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:19801249-19801299	PANC-1	pancreas:	n/a
2	chr17:19801249-19801299	CMK	blood:	n/a
3	chr17:19801249-19801299	Jurkat	blood:	n/a
4	chr17:19801249-19801299	SK-N-SH_RA	brain:	n/a
5	chr17:19801249-19801299	K562	blood:	n/a
6	chr17:19801249-19801299	HCM	heart:	n/a
7	chr17:19801249-19801299	AG04450	lung:	fetal
8	chr17:19801249-19801299	SAEC	small airway:	n/a
9	chr17:19801249-19801299	ProgFib	skin:	n/a
10	chr17:19801249-19801299	Hela-S3	cervix:	n/a
11	chr17:19801249-19801299	HMEC	breast:	n/a
12	chr17:19801249-19801299	MCF10A-Er-Src	breast:	n/a
13	chr17:19801249-19801299	HNPCEpiC	eye:	n/a
14	chr17:19801249-19801299	HL-60	blood:	n/a
15	chr17:19801249-19801299	GM19239	blood:	n/a
16	chr17:19801249-19801299	HEEpiC	esophagus:	n/a
17	chr17:19801249-19801299	SK-N-MC	brain:	n/a
18	chr17:19801249-19801299	A549	lung:	n/a
19	chr17:19801249-19801299	HCF	heart:	n/a
20	chr17:19801249-19801299	SK-N-SH	brain:	n/a
21	chr17:19801249-19801299	AG04449	skin:	fetal
22	chr17:19801249-19801299	HCT-116	colon:	n/a
23	chr17:19801249-19801299	BJ	skin:	n/a
24	chr17:19801249-19801299	NB4	blood:	n/a
25	chr17:19801249-19801299	GM12878	blood:	n/a
26	chr17:19801249-19801299	HCPEpiC	choroid plexus:	n/a
27	chr17:19801249-19801299	HRE	kidney:	n/a
28	chr17:19801249-19801299	NT2-D1	testis:	n/a
29	chr17:19801249-19801299	H1-hESC	embryonic stem cell:	embryo
30	chr17:19801249-19801299	SKMC	muscle:	n/a
31	chr17:19801249-19801299	AoSMC	blood vessel:	n/a
32	chr17:19801249-19801299	PFSK-1	brain:	n/a
33	chr17:19801249-19801299	HRPEpiC	eye:	n/a
34	chr17:19801249-19801299	HIPEpiC	eye:	n/a
35	chr17:19801249-19801299	RPTEC	kidney:	n/a
36	chr17:19801249-19801299	HEK293	kidney:	embryo
37	chr17:19801249-19801299	GM12892	blood:	n/a
38	chr17:19801249-19801299	T-47D	breast:	n/a
39	chr17:19801249-19801299	AG10803	skin:	n/a
40	chr17:19801249-19801299	Hepatocyte	liver:	n/a
41	chr17:19801249-19801299	AG09309	skin:	n/a
42	chr17:19801249-19801299	MCF-7	breast:	n/a
43	chr17:19801249-19801299	GM06990	blood:	n/a
44	chr17:19801249-19801299	GM12891	blood:	n/a
45	chr17:19801249-19801299	PrEC	prostate:	n/a
46	chr17:19801249-19801299	Caco-2	colon:	n/a
47	chr17:19801249-19801299	NHBE	bronchial:	n/a
48	chr17:19801249-19801299	HepG2	liver:	n/a
49	chr17:19801249-19801299	IMR90	lung:	fetal
50	chr17:19801249-19801299	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:19803045..19804628-chr17:19806537..19808845,2	K562	blood:
2	chr17:19770311..19772498-chr17:19797412..19799362,2	MCF-7	breast:
3	chr17:19748663..19750741-chr17:19801498..19804267,2	K562	blood:
4	chr17:19769802..19772027-chr17:19799780..19804333,4	MCF-7	breast:
5	chr17:19768657..19772126-chr17:19801455..19804744,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKAP10-2	chr17:19800037-19800249	ENSG00000270091.1
2	lnc-AKAP10-2	chr17:19800339-19800600	ENSG00000270091.1
3	lnc-AKAP10-2	chr17:19799903-19800583	ENSG00000270091.1
4	lnc-SPECC1-4	chr17:19798712-19799489	NONHSAT146532

Variant related genes	Relation type
ENSG00000270091	TF binding region
ENSG00000270091	CpG island
ENSG00000083290	chromatin interactions

Extended variants
information (count: 579 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:579 , 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	rs281364	chr17:19789453-19789454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144622720	chr17:19789465-19789466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544713134	chr17:19789472-19789473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564870484	chr17:19789481-19789482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs57690073	chr17:19789520-19789521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115741683	chr17:19789560-19789561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560260020	chr17:19789568-19789569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140172257	chr17:19789613-19789614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373619224	chr17:19789618-19789619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202137343	chr17:19789619-19789620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371586035	chr17:19789624-19789625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76893566	chr17:19789625-19789626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9915910	chr17:19789719-19789720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549542384	chr17:19789733-19789734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56116113	chr17:19789742-19789743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141661415	chr17:19789803-19789804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145310873	chr17:19789828-19789829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551509005	chr17:19789906-19789907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571275892	chr17:19789907-19789908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138418788	chr17:19789953-19789954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553605452	chr17:19789955-19789956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190129312	chr17:19789999-19790000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62066264	chr17:19790011-19790012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536098320	chr17:19790026-19790027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74558414	chr17:19790078-19790079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556308640	chr17:19790089-19790090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141919076	chr17:19790103-19790104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181534719	chr17:19790136-19790137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150665639	chr17:19790142-19790143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536537341	chr17:19790248-19790249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572022585	chr17:19790256-19790257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs60365167	chr17:19790259-19790260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541022819	chr17:19790264-19790265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560804760	chr17:19790299-19790300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529593351	chr17:19790328-19790329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140027926	chr17:19790332-19790333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371838774	chr17:19790333-19790334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563072600	chr17:19790358-19790359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531730296	chr17:19790373-19790374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551813622	chr17:19790402-19790403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531937536	chr17:19790409-19790410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527728368	chr17:19790434-19790435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547378969	chr17:19790511-19790512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149427334	chr17:19790524-19790525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536526235	chr17:19790533-19790534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376548200	chr17:19790540-19790541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185658477	chr17:19790554-19790555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538357776	chr17:19790555-19790556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188374939	chr17:19790572-19790573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548559788	chr17:19790608-19790609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:154)

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
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
Colorectal cancer	16774939	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
Autism	22543975	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19787400-19792800	Weak transcription	Fetal Heart	heart
2	chr17:19792800-19793400	Enhancers	Fetal Heart	heart
3	chr17:19793600-19794800	Enhancers	Placenta	Placenta
4	chr17:19793800-19794800	Enhancers	Liver	Liver
5	chr17:19794400-19794800	Enhancers	Spleen	Spleen
6	chr17:19794600-19794800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr17:19794800-19800000	Weak transcription	Liver	Liver
8	chr17:19794800-19800800	Weak transcription	Spleen	Spleen
9	chr17:19796200-19796400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr17:19796400-19809800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr17:19797600-19800400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr17:19797600-19800600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr17:19797800-19800400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr17:19798000-19800400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr17:19798200-19798400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr17:19798200-19800800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr17:19798400-19804000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr17:19799200-19799400	Enhancers	Thymus	Thymus
19	chr17:19799200-19808400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr17:19799400-19803800	Weak transcription	Thymus	Thymus
21	chr17:19799400-19805000	Weak transcription	Fetal Intestine Large	intestine
22	chr17:19799600-19800600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr17:19799600-19803800	Weak transcription	Primary T cells from cord blood	blood
24	chr17:19799800-19805200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr17:19799800-19806800	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr17:19799800-19807000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr17:19800000-19800200	Enhancers	Hela-S3	cervix
28	chr17:19800000-19800400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr17:19800000-19800800	Enhancers	Liver	Liver
30	chr17:19800000-19801600	Enhancers	Fetal Heart	heart
31	chr17:19800000-19802200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr17:19800200-19800400	Weak transcription	NHLF	lung
33	chr17:19800200-19801600	Enhancers	Colon Smooth Muscle	Colon
34	chr17:19800200-19802000	Enhancers	A549	lung
35	chr17:19800200-19802200	Flanking Active TSS	Hela-S3	cervix
36	chr17:19800200-19802200	Enhancers	HSMMtube	muscle
37	chr17:19800200-19804000	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr17:19800400-19800600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr17:19800400-19800600	Enhancers	Brain Angular Gyrus	brain
40	chr17:19800400-19800600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr17:19800400-19800800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr17:19800400-19800800	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr17:19800400-19801000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr17:19800400-19801000	Enhancers	Esophagus	oesophagus
45	chr17:19800400-19801000	Enhancers	Left Ventricle	heart
46	chr17:19800400-19801000	Enhancers	Pancreas	Pancrea
47	chr17:19800400-19801200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr17:19800400-19801200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr17:19800400-19801200	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr17:19800400-19801400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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