Variant report

Variant	esv3331113
Chromosome Location	chr9:86431782-86433830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:244)
Chromatin interactive
region (count:4)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr9:86432260-86432688	K562	blood:	n/a	chr9:86432477-86432493
2	BHLHE40	chr9:86432167-86432635	GM12878	blood:	n/a	chr9:86432477-86432493
3	BHLHE40	chr9:86432362-86432520	HepG2	liver:	n/a	chr9:86432477-86432493
4	CCNT2	chr9:86432252-86432698	K562	blood:	n/a	chr9:86432668-86432677
5	CHD1	chr9:86432239-86432282	GM12878	blood:	n/a	n/a
6	CHD1	chr9:86431789-86432598	IMR90	lung:	n/a	chr9:86432468-86432478 chr9:86431865-86431875
7	CHD2	chr9:86432754-86432816	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr9:86432265-86432364	GM12878	blood:	n/a	n/a
9	CHD2	chr9:86432810-86432972	GM12878	blood:	n/a	n/a
10	CREB1	chr9:86432803-86432995	A549	lung:	n/a	n/a
11	CREB1	chr9:86432235-86433076	A549	lung:	n/a	n/a
12	CTCF	chr9:86432268-86432459	A549	lung:	n/a	n/a
13	CTCF	chr9:86432362-86432379	HepG2	liver:	n/a	n/a
14	CTCF	chr9:86432300-86432450	GM12873	blood:	n/a	n/a
15	CTCF	chr9:86432300-86432450	GM12874	blood:	n/a	n/a
16	CTCF	chr9:86432240-86432420	GM10266	blood:	n/a	n/a
17	CTCF	chr9:86432280-86432430	GM12864	blood:	n/a	n/a
18	CTCF	chr9:86432235-86432482	GM19238	blood:	n/a	n/a
19	CTCF	chr9:86432240-86432390	GM12874	blood:	n/a	n/a
20	CTCF	chr9:86432180-86432330	AG04450	lung:	n/a	n/a
21	CTCF	chr9:86432280-86432430	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr9:86432280-86432430	HMEC	breast:	n/a	n/a
23	CTCF	chr9:86432300-86432450	GM12865	blood:	n/a	n/a
24	CTCF	chr9:86432300-86432450	SAEC	small airway:	n/a	n/a
25	CTCF	chr9:86431960-86432110	GM12875	blood:	n/a	n/a
26	CTCF	chr9:86432278-86432457	ProgFib	skin:	n/a	n/a
27	CTCF	chr9:86432237-86432470	GM12892	blood:	n/a	n/a
28	CTCF	chr9:86432300-86432450	GM12875	blood:	n/a	n/a
29	CTCF	chr9:86432260-86432410	HVMF	connective:	n/a	n/a
30	CTCF	chr9:86432260-86432410	GM12872	blood:	n/a	n/a
31	CTCF	chr9:86432301-86432432	K562	blood:	n/a	n/a
32	CTCF	chr9:86432291-86432433	MCF-7	breast:	n/a	n/a
33	CTCF	chr9:86432220-86432370	GM12869	blood:	n/a	n/a
34	CTCF	chr9:86432290-86432431	GM13976	blood:	n/a	n/a
35	CTCF	chr9:86432281-86432438	MCF-7	breast:	n/a	n/a
36	CTCF	chr9:86432300-86432450	GM12864	blood:	n/a	n/a
37	CTCF	chr9:86432900-86433050	HEK293	kidney:	n/a	n/a
38	CTCF	chr9:86432246-86432470	GM19239	blood:	n/a	n/a
39	CTCF	chr9:86432240-86432390	GM12867	blood:	n/a	n/a
40	CTCF	chr9:86432316-86432421	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr9:86432280-86432430	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr9:86432280-86432430	GM12878	blood:	n/a	n/a
43	CTCF	chr9:86432287-86432443	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:86432280-86432430	HAc	cerebellar:	n/a	n/a
45	CTCF	chr9:86432220-86432370	NHLF	lung:	n/a	n/a
46	CTCF	chr9:86432333-86432408	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:86432285-86432422	GM13977	blood:	n/a	n/a
48	CTCF	chr9:86432254-86432531	Fibrobl	skin:	n/a	n/a
49	CTCF	chr9:86432780-86432930	GM12867	blood:	n/a	n/a
50	CTCF	chr9:86432260-86432410	GM12866	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:86432031-86432081	HCM	heart:	n/a
2	chr9:86432031-86432081	K562	blood:	n/a
3	chr9:86432031-86432081	MCF-7	breast:	n/a
4	chr9:86433081-86433131	PFSK-1	brain:	n/a
5	chr9:86432031-86432081	AG04450	lung:	fetal
6	chr9:86433764-86433814	HCM	heart:	n/a
7	chr9:86432031-86432081	HIPEpiC	eye:	n/a
8	chr9:86433764-86433814	SAEC	small airway:	n/a
9	chr9:86433764-86433814	AG09309	skin:	n/a
10	chr9:86432031-86432081	Caco-2	colon:	n/a
11	chr9:86432854-86432904	HRCEpiC	kidney:	n/a
12	chr9:86433764-86433814	NHDF-neo	bronchial:	n/a
13	chr9:86432031-86432081	HCPEpiC	choroid plexus:	n/a
14	chr9:86433081-86433131	HL-60	blood:	n/a
15	chr9:86433764-86433814	HRCEpiC	kidney:	n/a
16	chr9:86433764-86433814	AG09319	gingival:	n/a
17	chr9:86433764-86433814	GM12892	blood:	n/a
18	chr9:86432854-86432904	NHDF-neo	bronchial:	n/a
19	chr9:86433764-86433814	Jurkat	blood:	n/a
20	chr9:86433081-86433131	HRCEpiC	kidney:	n/a
21	chr9:86432031-86432081	T-47D	breast:	n/a
22	chr9:86432031-86432081	PrEC	prostate:	n/a
23	chr9:86432854-86432904	HCPEpiC	choroid plexus:	n/a
24	chr9:86432031-86432081	MCF10A-Er-Src	breast:	n/a
25	chr9:86433081-86433131	GM06990	blood:	n/a
26	chr9:86432854-86432904	AG04450	lung:	fetal
27	chr9:86432031-86432081	SK-N-SH_RA	brain:	n/a
28	chr9:86432854-86432904	K562	blood:	n/a
29	chr9:86433764-86433814	GM12878	blood:	n/a
30	chr9:86433081-86433131	ProgFib	skin:	n/a
31	chr9:86433764-86433814	ovcar-3	ovarian:	n/a
32	chr9:86433764-86433814	BJ	skin:	n/a
33	chr9:86433764-86433814	Hepatocyte	liver:	n/a
34	chr9:86433081-86433131	NHDF-neo	bronchial:	n/a
35	chr9:86432854-86432904	H1-hESC	embryonic stem cell:	embryo
36	chr9:86433081-86433131	ovcar-3	ovarian:	n/a
37	chr9:86433081-86433131	HRPEpiC	eye:	n/a
38	chr9:86433081-86433131	HRE	kidney:	n/a
39	chr9:86432854-86432904	A549	lung:	n/a
40	chr9:86433081-86433131	SK-N-MC	brain:	n/a
41	chr9:86432854-86432904	HCT-116	colon:	n/a
42	chr9:86432854-86432904	HMEC	breast:	n/a
43	chr9:86432854-86432904	AG09319	gingival:	n/a
44	chr9:86433081-86433131	NB4	blood:	n/a
45	chr9:86432854-86432904	RPTEC	kidney:	n/a
46	chr9:86432854-86432904	IMR90	lung:	fetal
47	chr9:86433081-86433131	IMR90	lung:	fetal
48	chr9:86433081-86433131	Jurkat	blood:	n/a
49	chr9:86433081-86433131	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:86432854-86432904	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:86321469..86324662-chr9:86431245..86433854,3	MCF-7	breast:
2	chr9:86321555..86324208-chr9:86431445..86433817,2	MCF-7	breast:
3	chr9:86430622..86432919-chr9:86535075..86537489,2	MCF-7	breast:
4	chr9:86429346..86431861-chr9:86535994..86537805,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RMI1-6	chr9:86433316-86433488	NONHSAT132748
2	lnc-RMI1-6	chr9:86432881-86432983	ENSG00000245608
3	lnc-KIF27-1	chr9:86432900-86433036	NONHSAT132747
4	lnc-RMI1-6	chr9:86432881-86432983	NONHSAT132748
5	lnc-KIF27-1	chr9:86431911-86432042	NONHSAT132747
6	lnc-RMI1-6	chr9:86433316-86433488	ENSG00000245608

No data

Variant related genes	Relation type
GKAP1	TF binding region
GKAP1	CpG island
ENSG00000254473	chromatin interactions
ENSG00000135018	chromatin interactions
ENSG00000165115	chromatin interactions
RNF182	miRNA target sites
RUNX1	miRNA target sites

Extended variants
information (count: 68 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533017603	chr9:86431832-86431833	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs200247613	chr9:86431837-86431838	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551650520	chr9:86431972-86431973	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs569892796	chr9:86431989-86431990	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs537237012	chr9:86431993-86431994	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs555302596	chr9:86432004-86432005	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs201469010	chr9:86432055-86432056	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs557372267	chr9:86432072-86432073	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs577442825	chr9:86432103-86432104	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs567342955	chr9:86432135-86432136	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs376614610	chr9:86432136-86432137	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs114992551	chr9:86432252-86432253	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs534725294	chr9:86432257-86432258	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs552966766	chr9:86432291-86432292	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs577717771	chr9:86432296-86432297	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs3119914	chr9:86432387-86432388	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs544723172	chr9:86432393-86432394	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs558416214	chr9:86432400-86432401	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs145098995	chr9:86432404-86432405	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs543971904	chr9:86432476-86432477	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs561965585	chr9:86432477-86432478	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs3119915	chr9:86432504-86432505	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs9410885	chr9:86432579-86432580	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7041731	chr9:86432595-86432596	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541136589	chr9:86432599-86432600	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs559275664	chr9:86432633-86432634	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs533147534	chr9:86432660-86432661	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs2909286	chr9:86432677-86432678	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs551519261	chr9:86432685-86432686	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs2909287	chr9:86432690-86432691	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs563577849	chr9:86432739-86432740	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs530737018	chr9:86432791-86432792	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs549129203	chr9:86432795-86432796	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs2909288	chr9:86432819-86432820	Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376322311	chr9:86432835-86432836	Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs534661301	chr9:86432873-86432874	Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs2909289	chr9:86432911-86432912	Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs546711822	chr9:86432921-86432922	Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs571404635	chr9:86432956-86432957	Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs369932825	chr9:86433025-86433026	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs295272	chr9:86433037-86433038	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs561620833	chr9:86433046-86433047	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs530680068	chr9:86433051-86433052	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs537359660	chr9:86433063-86433064	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs550287631	chr9:86433077-86433078	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs2780107	chr9:86433083-86433084	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2780108	chr9:86433094-86433095	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs2780109	chr9:86433103-86433104	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs189174991	chr9:86433124-86433125	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559406383	chr9:86433153-86433154	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86353000-86432000	Weak transcription	Lung	lung
2	chr9:86377200-86432000	Weak transcription	Gastric	stomach
3	chr9:86392000-86431800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:86399400-86431800	Weak transcription	Esophagus	oesophagus
5	chr9:86399400-86431800	Weak transcription	Pancreas	Pancrea
6	chr9:86410400-86432000	Weak transcription	Small Intestine	intestine
7	chr9:86412200-86432000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:86417800-86431800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:86431000-86431800	Enhancers	Fetal Brain Male	brain
10	chr9:86431000-86431800	Enhancers	Fetal Heart	heart
11	chr9:86431000-86431800	Weak transcription	Left Ventricle	heart
12	chr9:86431000-86431800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr9:86431000-86433000	Active TSS	A549	lung
14	chr9:86431000-86433200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr9:86431000-86433200	Active TSS	Aorta	Aorta
16	chr9:86431000-86433200	Active TSS	GM12878-XiMat	blood
17	chr9:86431000-86433200	Active TSS	Hela-S3	cervix
18	chr9:86431200-86431800	Enhancers	Primary B cells from peripheral blood	blood
19	chr9:86431200-86431800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:86431200-86432000	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr9:86431200-86433000	Active TSS	NHDF-Ad	bronchial
22	chr9:86431200-86433200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:86431200-86433400	Active TSS	Thymus	Thymus
24	chr9:86431400-86431800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr9:86431400-86431800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr9:86431400-86431800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr9:86431400-86431800	Flanking Active TSS	Liver	Liver
28	chr9:86431400-86431800	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr9:86431400-86431800	Flanking Active TSS	HUVEC	blood vessel
30	chr9:86431400-86432000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr9:86431400-86432000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr9:86431400-86432400	Flanking Active TSS	Primary B cells from cord blood	blood
33	chr9:86431400-86433000	Active TSS	NHLF	lung
34	chr9:86431400-86433200	Active TSS	Fetal Muscle Leg	muscle
35	chr9:86431400-86433200	Active TSS	HepG2	liver
36	chr9:86431400-86433400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:86431400-86433400	Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr9:86431400-86433400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr9:86431600-86431800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:86431600-86431800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr9:86431600-86431800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr9:86431600-86431800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
43	chr9:86431600-86431800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:86431600-86431800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
45	chr9:86431600-86431800	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr9:86431600-86431800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr9:86431600-86431800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr9:86431600-86431800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr9:86431600-86431800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr9:86431600-86431800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

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