Variant report

Variant	esv1811424
Chromosome Location	chr17:20351030-20394531
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	BACH1	chr17:20388438-20388633	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr17:20354311-20354673	GM12878	blood:	n/a	chr17:20354476-20354487
3	BATF	chr17:20370764-20371076	GM12878	blood:	n/a	n/a
4	BATF	chr17:20354345-20354597	GM12878	blood:	n/a	chr17:20354476-20354487
5	BATF	chr17:20370787-20371117	GM12878	blood:	n/a	n/a
6	BCL11A	chr17:20370709-20371057	GM12878	blood:	n/a	n/a
7	BCL11A	chr17:20371063-20371231	GM12878	blood:	n/a	n/a
8	BCL11A	chr17:20372530-20372862	GM12878	blood:	n/a	n/a
9	BCL11A	chr17:20370806-20371041	GM12878	blood:	n/a	n/a
10	BHLHE40	chr17:20354420-20354612	K562	blood:	n/a	n/a
11	CEBPB	chr17:20388357-20388509	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr17:20378583-20378635	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr17:20381895-20381977	GM10248	blood:	n/a	n/a
14	CTCF	chr17:20379046-20379073	LNCaP	prostate:	n/a	n/a
15	CTCF	chr17:20356410-20356462	GM12892	blood:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356436-20356454
16	CTCF	chr17:20351033-20351117	GM10248	blood:	n/a	n/a
17	CTCF	chr17:20369632-20369730	GM19240	blood:	n/a	chr17:20369674-20369690 chr17:20369675-20369696 chr17:20369673-20369691 chr17:20369678-20369688
18	CTCF	chr17:20378584-20378697	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr17:20369660-20369708	GM19239	blood:	n/a	chr17:20369674-20369690 chr17:20369675-20369696 chr17:20369673-20369691 chr17:20369678-20369688
20	CTCF	chr17:20379002-20379022	LNCaP	prostate:	n/a	n/a
21	CTCF	chr17:20356209-20356635	A549	lung:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356467-20356476 chr17:20356436-20356454
22	CTCF	chr17:20356348-20356663	K562	blood:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356467-20356476 chr17:20356436-20356454
23	CTCF	chr17:20368168-20368198	GM10248	blood:	n/a	n/a
24	CTCF	chr17:20378615-20378663	LNCaP	prostate:	n/a	n/a
25	CTCF	chr17:20368142-20368195	GM13976	blood:	n/a	n/a
26	CTCF	chr17:20356538-20356604	GM10248	blood:	n/a	n/a
27	CTCF	chr17:20351079-20351261	H1-hESC	embryonic stem cell:	n/a	chr17:20351195-20351208
28	CTCF	chr17:20351089-20351186	MCF-7	breast:	n/a	n/a
29	CTCF	chr17:20393678-20393752	GM20000	blood:	n/a	n/a
30	CTCF	chr17:20357964-20357975	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr17:20356297-20356568	A549	lung:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356467-20356476 chr17:20356436-20356454
32	CTCF	chr17:20371945-20371952	LNCaP	prostate:	n/a	n/a
33	CTCF	chr17:20350960-20351110	HEK293	kidney:	n/a	n/a
34	CTCF	chr17:20354237-20354279	NHEK	skin:	n/a	n/a
35	CTCF	chr17:20354535-20354577	LNCaP	prostate:	n/a	n/a
36	CTCF	chr17:20356361-20356676	K562	blood:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356467-20356476 chr17:20356436-20356454
37	CTCF	chr17:20352289-20352330	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr17:20351103-20351121	MCF-7	breast:	n/a	n/a
39	CTCF	chr17:20378949-20379034	NHEK	skin:	n/a	n/a
40	CTCF	chr17:20369656-20369735	MCF-7	breast:	n/a	chr17:20369674-20369690 chr17:20369675-20369696 chr17:20369673-20369691 chr17:20369678-20369688
41	CTCF	chr17:20354452-20354519	Lung_OC	lung:	n/a	n/a
42	CTCF	chr17:20359413-20359524	GM19240	blood:	n/a	n/a
43	CTCF	chr17:20353314-20353404	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr17:20359410-20359533	GM19239	blood:	n/a	n/a
45	CTCF	chr17:20356347-20356704	K562	blood:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356467-20356476 chr17:20356436-20356454
46	CTCF	chr17:20380718-20380769	Lung_OC	lung:	n/a	n/a
47	CTCF	chr17:20356355-20356563	A549	lung:	n/a	chr17:20356439-20356448 chr17:20356439-20356452 chr17:20356467-20356476 chr17:20356436-20356454
48	CTCF	chr17:20380888-20380960	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr17:20377886-20377928	Spleen_OC	spleen:	n/a	n/a
50	E2F6	chr17:20354365-20354470	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20370597-20370647	MCF10A-Er-Src	breast:	n/a
2	chr17:20370597-20370647	AG04450	lung:	fetal
3	chr17:20370597-20370647	AG09309	skin:	n/a
4	chr17:20370597-20370647	ovcar-3	ovarian:	n/a
5	chr17:20370597-20370647	ProgFib	skin:	n/a
6	chr17:20370597-20370647	HRCEpiC	kidney:	n/a
7	chr17:20370597-20370647	NH-A	brain:	n/a
8	chr17:20370597-20370647	Jurkat	blood:	n/a
9	chr17:20370597-20370647	PANC-1	pancreas:	n/a
10	chr17:20370597-20370647	HCT-116	colon:	n/a
11	chr17:20370597-20370647	ECC-1	luminal epithelium:	n/a
12	chr17:20370597-20370647	RPTEC	kidney:	n/a
13	chr17:20370597-20370647	SKMC	muscle:	n/a
14	chr17:20370597-20370647	H1-hESC	embryonic stem cell:	embryo
15	chr17:20370597-20370647	HIPEpiC	eye:	n/a
16	chr17:20370597-20370647	K562	blood:	n/a
17	chr17:20370597-20370647	SK-N-SH_RA	brain:	n/a
18	chr17:20370597-20370647	HepG2	liver:	n/a
19	chr17:20370597-20370647	HL-60	blood:	n/a
20	chr17:20370597-20370647	PrEC	prostate:	n/a
21	chr17:20370597-20370647	HUVEC	blood vessel:	n/a
22	chr17:20370597-20370647	A549	lung:	n/a
23	chr17:20370597-20370647	PFSK-1	brain:	n/a
24	chr17:20370597-20370647	GM12892	blood:	n/a
25	chr17:20370597-20370647	Caco-2	colon:	n/a
26	chr17:20370597-20370647	SK-N-MC	brain:	n/a
27	chr17:20370597-20370647	BE2_C	brain:	n/a
28	chr17:20370597-20370647	MCF-7	breast:	n/a
29	chr17:20370597-20370647	GM19239	blood:	n/a
30	chr17:20370597-20370647	AG09319	gingival:	n/a
31	chr17:20370597-20370647	T-47D	breast:	n/a
32	chr17:20370597-20370647	HCF	heart:	n/a
33	chr17:20370597-20370647	AoSMC	blood vessel:	n/a
34	chr17:20370597-20370647	NHBE	bronchial:	n/a
35	chr17:20370597-20370647	NHDF-neo	bronchial:	n/a
36	chr17:20370597-20370647	HNPCEpiC	eye:	n/a
37	chr17:20370597-20370647	GM12891	blood:	n/a
38	chr17:20370597-20370647	NT2-D1	testis:	n/a
39	chr17:20370597-20370647	HRPEpiC	eye:	n/a
40	chr17:20370597-20370647	LNCaP	prostate:	n/a
41	chr17:20370597-20370647	HMEC	breast:	n/a
42	chr17:20370597-20370647	CMK	blood:	n/a
43	chr17:20370597-20370647	Hepatocyte	liver:	n/a
44	chr17:20370597-20370647	HRE	kidney:	n/a
45	chr17:20370597-20370647	HEK293	kidney:	embryo
46	chr17:20370597-20370647	SK-N-SH	brain:	n/a
47	chr17:20370597-20370647	AG10803	skin:	n/a
48	chr17:20370597-20370647	GM12878	blood:	n/a
49	chr17:20370597-20370647	HCM	heart:	n/a
50	chr17:20370597-20370647	NB4	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS9B-4	chr17:20373955-20374185	ucscGeneNc_uc002gxd_1
2	lnc-CCDC144NL-9	chr17:20354914-20355028	NONHSAT146573
3	lnc-CCDC144NL-9	chr17:20355135-20355196	NONHSAT146574
4	lnc-CCDC144NL-9	chr17:20355108-20355484	NONHSAT146573
5	lnc-CCDC144NL-9	chr17:20356330-20356786	NONHSAT146574
6	lnc-CCDC144NL-9	chr17:20355664-20355708	NONHSAT146574
7	lnc-LGALS9B-4	chr17:20375554-20376706	ucscGeneNc_uc002gxd_1

Variant related genes	Relation type
ENSG00000229586	TF binding region
LGALS9B	TF binding region
ENSG00000229586	CpG island
LGALS9B	CpG island

Extended variants
information (count: 1204 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:1204 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111950186	chr17:20354025-20354026	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs559399402	chr17:20354162-20354163	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs59377975	chr17:20354222-20354223	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs62066950	chr17:20354269-20354270	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs533010776	chr17:20354285-20354286	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs551474678	chr17:20354310-20354311	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs563303642	chr17:20354311-20354312	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs530714276	chr17:20354365-20354366	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs144222133	chr17:20354393-20354394	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs78075074	chr17:20354406-20354407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567217956	chr17:20354466-20354467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57791812	chr17:20354477-20354478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534644699	chr17:20354492-20354493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140292022	chr17:20354549-20354550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146582979	chr17:20354556-20354557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546551782	chr17:20354561-20354562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs56340236	chr17:20354575-20354576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571313322	chr17:20354607-20354608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538732280	chr17:20354612-20354613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557444430	chr17:20354618-20354619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575684327	chr17:20354626-20354627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs56950705	chr17:20354633-20354634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs55872124	chr17:20354642-20354643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1682191	chr17:20354656-20354657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373481585	chr17:20354682-20354683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56386443	chr17:20354704-20354705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185716869	chr17:20354721-20354722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554910917	chr17:20354738-20354739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200108749	chr17:20354747-20354748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573536337	chr17:20354748-20354749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540930799	chr17:20354783-20354784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552975213	chr17:20354787-20354788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577726552	chr17:20354815-20354816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544711227	chr17:20354829-20354830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150485558	chr17:20354836-20354837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143077736	chr17:20354840-20354841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375018266	chr17:20354857-20354858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368813816	chr17:20354860-20354861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200190473	chr17:20354880-20354881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375391623	chr17:20354902-20354903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542795344	chr17:20354909-20354910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368544798	chr17:20354923-20354924	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs528326279	chr17:20354944-20354945	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs144632272	chr17:20354960-20354961	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs546514719	chr17:20354975-20354976	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs371066326	chr17:20354994-20354995	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs373609607	chr17:20354999-20355000	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs367735656	chr17:20355007-20355008	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs532523296	chr17:20355013-20355014	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs550728150	chr17:20355016-20355017	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:151)

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
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20354000-20354200	Active TSS	Hela-S3	cervix
2	chr17:20354000-20355400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr17:20354200-20354400	Flanking Active TSS	Hela-S3	cervix
4	chr17:20354200-20355200	Enhancers	Primary T cells fromperipheralblood	blood
5	chr17:20354400-20355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr17:20354800-20355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr17:20357200-20369000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr17:20358200-20368800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr17:20366000-20366200	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr17:20366200-20369200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr17:20368200-20368400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:20368400-20369000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr17:20368800-20369800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr17:20369000-20369400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr17:20369000-20369600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr17:20369000-20370800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr17:20369200-20370800	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr17:20369400-20369600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr17:20369400-20369800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
20	chr17:20369400-20369800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr17:20369400-20370800	Enhancers	Primary T cells fromperipheralblood	blood
22	chr17:20369600-20370400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr17:20369600-20370400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr17:20369600-20370600	Enhancers	Esophagus	oesophagus
25	chr17:20369800-20370200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr17:20369800-20370400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr17:20369800-20380000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr17:20370200-20370400	Enhancers	GM12878-XiMat	blood
29	chr17:20370200-20370800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr17:20370400-20370600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr17:20370400-20370600	Enhancers	Colonic Mucosa	Colon
32	chr17:20370400-20370800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr17:20370400-20370800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr17:20370400-20370800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr17:20370400-20370800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr17:20370400-20370800	Enhancers	Primary B cells from cord blood	blood
37	chr17:20370400-20370800	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr17:20370400-20370800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr17:20370400-20370800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr17:20370400-20370800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr17:20370400-20370800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr17:20370400-20370800	Active TSS	Duodenum Mucosa	Duodenum
43	chr17:20370400-20370800	Active TSS	Rectal Smooth Muscle	rectum
44	chr17:20370400-20370800	Flanking Active TSS	GM12878-XiMat	blood
45	chr17:20370400-20370800	Enhancers	Hela-S3	cervix
46	chr17:20370400-20370800	Enhancers	HMEC	breast
47	chr17:20370400-20370800	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr17:20370400-20370800	Enhancers	NHEK	skin
49	chr17:20370400-20370800	Enhancers	Osteobl	bone
50	chr17:20370400-20371200	Enhancers	Primary B cells from peripheral blood	blood

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