Variant report

Variant	esv3321912
Chromosome Location	chr9:72286882-72288180
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	ARID3A	chr9:72287778-72288055	HepG2	liver:	n/a	chr9:72287860-72287868
2	ATF2	chr9:72287724-72288162	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr9:72287881-72288378	A549	lung:	n/a	n/a
4	BACH1	chr9:72287312-72288183	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr9:72287701-72288096	GM12878	blood:	n/a	chr9:72287806-72287819
6	BHLHE40	chr9:72287817-72288069	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:72287749-72288045	K562	blood:	n/a	n/a
8	BRCA1	chr9:72287860-72288060	HepG2	liver:	n/a	n/a
9	CHD1	chr9:72287885-72287990	GM12878	blood:	n/a	n/a
10	CHD1	chr9:72287698-72288163	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr9:72287842-72288051	GM12878	blood:	n/a	n/a
12	CHD2	chr9:72286831-72286895	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr9:72287763-72288178	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr9:72287661-72288242	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr9:72287806-72288128	A549	lung:	n/a	n/a
16	CREB1	chr9:72287746-72288169	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTBP2	chr9:72287423-72288203	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr9:72286573-72287153	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:72287840-72287990	HRPEpiC	eye:	n/a	chr9:72287953-72287962
20	CTCF	chr9:72287168-72287173	LNCaP	prostate:	n/a	n/a
21	CTCF	chr9:72287000-72287150	GM12871	blood:	n/a	n/a
22	CTCF	chr9:72287840-72287990	HRE	kidney:	n/a	chr9:72287953-72287962
23	CTCF	chr9:72287821-72288074	GM13976	blood:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
24	CTCF	chr9:72287822-72288096	Kidney_OC	kidney:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
25	CTCF	chr9:72287046-72287126	GM19238	blood:	n/a	n/a
26	CTCF	chr9:72287736-72288126	K562	blood:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
27	CTCF	chr9:72287860-72288010	GM12874	blood:	n/a	chr9:72287953-72287962
28	CTCF	chr9:72287830-72288075	HUVEC	blood vessel:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
29	CTCF	chr9:72287860-72288010	AG04450	lung:	n/a	chr9:72287953-72287962
30	CTCF	chr9:72287880-72288030	AG04449	skin:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
31	CTCF	chr9:72287860-72288010	A549	lung:	n/a	chr9:72287953-72287962
32	CTCF	chr9:72286860-72287010	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr9:72287860-72288010	HVMF	connective:	n/a	chr9:72287953-72287962
34	CTCF	chr9:72287598-72287599	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:72287735-72288173	K562	blood:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
36	CTCF	chr9:72287840-72287990	RPTEC	kidney:	n/a	chr9:72287953-72287962
37	CTCF	chr9:72287555-72288102	GM12892	blood:	n/a	chr9:72287629-72287642 chr9:72287953-72287962 chr9:72288010-72288019
38	CTCF	chr9:72287008-72287197	MCF-7	breast:	n/a	n/a
39	CTCF	chr9:72286920-72287070	HMF	breast:	n/a	n/a
40	CTCF	chr9:72287880-72288030	GM12869	blood:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
41	CTCF	chr9:72286899-72287238	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:72287900-72288050	AG09309	skin:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
43	CTCF	chr9:72287880-72288030	GM12868	blood:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
44	CTCF	chr9:72287880-72288030	HCPEpiC	choroid plexus:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
45	CTCF	chr9:72287880-72288030	AG10803	skin:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
46	CTCF	chr9:72287860-72288010	GM12866	blood:	n/a	chr9:72287953-72287962
47	CTCF	chr9:72287900-72288050	GM12872	blood:	n/a	chr9:72287953-72287962 chr9:72288010-72288019
48	CTCF	chr9:72287860-72288010	BJ	skin:	n/a	chr9:72287953-72287962
49	CTCF	chr9:72287860-72288010	HMF	breast:	n/a	chr9:72287953-72287962
50	CTCF	chr9:72287840-72287990	SK-N-SH_RA	brain:	n/a	chr9:72287953-72287962

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72288179-72288229	ECC-1	luminal epithelium:	n/a
2	chr9:72288179-72288229	ECC-1	luminal epithelium:	n/a
3	chr9:72287772-72287822	AG09309	skin:	n/a
4	chr9:72287772-72287822	PFSK-1	brain:	n/a
5	chr9:72287123-72287173	HAEpiC	amniotic membrane:	n/a
6	chr9:72287152-72287202	H1-hESC	embryonic stem cell:	embryo
7	chr9:72287821-72287871	PANC-1	pancreas:	n/a
8	chr9:72287772-72287822	HAEpiC	amniotic membrane:	n/a
9	chr9:72287152-72287202	HepG2	liver:	n/a
10	chr9:72288156-72288206	A549	lung:	n/a
11	chr9:72287821-72287871	BE2_C	brain:	n/a
12	chr9:72287772-72287822	ECC-1	luminal epithelium:	n/a
13	chr9:72287152-72287202	Hepatocyte	liver:	n/a
14	chr9:72287821-72287871	HRPEpiC	eye:	n/a
15	chr9:72287772-72287822	HMEC	breast:	n/a
16	chr9:72288156-72288206	Hepatocyte	liver:	n/a
17	chr9:72288069-72288119	PrEC	prostate:	n/a
18	chr9:72288098-72288148	SK-N-SH	brain:	n/a
19	chr9:72288098-72288148	K562	blood:	n/a
20	chr9:72287123-72287173	ovcar-3	ovarian:	n/a
21	chr9:72287772-72287822	T-47D	breast:	n/a
22	chr9:72287152-72287202	U87	brain:	n/a
23	chr9:72288098-72288148	AoSMC	blood vessel:	n/a
24	chr9:72287152-72287202	HIPEpiC	eye:	n/a
25	chr9:72288179-72288229	HIPEpiC	eye:	n/a
26	chr9:72288156-72288206	SK-N-SH_RA	brain:	n/a
27	chr9:72288098-72288148	RPTEC	kidney:	n/a
28	chr9:72287772-72287822	HRPEpiC	eye:	n/a
29	chr9:72288179-72288229	NT2-D1	testis:	n/a
30	chr9:72287772-72287822	RPTEC	kidney:	n/a
31	chr9:72288179-72288229	PANC-1	pancreas:	n/a
32	chr9:72288069-72288119	SK-N-SH_RA	brain:	n/a
33	chr9:72287772-72287822	GM12892	blood:	n/a
34	chr9:72287821-72287871	HRE	kidney:	n/a
35	chr9:72287152-72287202	HRPEpiC	eye:	n/a
36	chr9:72287152-72287202	SK-N-SH	brain:	n/a
37	chr9:72288179-72288229	HAEpiC	amniotic membrane:	n/a
38	chr9:72288098-72288148	Hepatocyte	liver:	n/a
39	chr9:72288098-72288148	Caco-2	colon:	n/a
40	chr9:72287821-72287871	SKMC	muscle:	n/a
41	chr9:72288156-72288206	HIPEpiC	eye:	n/a
42	chr9:72288069-72288119	MCF10A-Er-Src	breast:	n/a
43	chr9:72288069-72288119	HCT-116	colon:	n/a
44	chr9:72287152-72287202	NB4	blood:	n/a
45	chr9:72288098-72288148	HRE	kidney:	n/a
46	chr9:72287123-72287173	SK-N-MC	brain:	n/a
47	chr9:72287821-72287871	HNPCEpiC	eye:	n/a
48	chr9:72287123-72287173	T-47D	breast:	n/a
49	chr9:72288156-72288206	MCF-7	breast:	n/a
50	chr9:72288069-72288119	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:144137145..144137665-chr9:72287895..72288430,2	MCF-7	breast:
2	chr9:72286195..72289118-chr9:72373474..72376010,3	MCF-7	breast:
3	chr9:72287056..72289421-chr9:72373634..72375235,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf135-2	chr9:72287665-72288629	ENSG00000261447.1

Variant related genes	Relation type
ENSG00000261447	TF binding region
APBA1	TF binding region
ENSG00000261447	CpG island
APBA1	CpG island
ENSG00000188647	chromatin interactions

Extended variants
information (count: 38 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551216130	chr9:72286906-72286907	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs12348441	chr9:72286945-72286946	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563101156	chr9:72286956-72286957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2309517	chr9:72287026-72287027	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs138398728	chr9:72287163-72287164	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs566751222	chr9:72287197-72287198	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs534204868	chr9:72287251-72287252	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs111848252	chr9:72287357-72287358	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs549167775	chr9:72287376-72287377	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs567764067	chr9:72287380-72287381	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs537623379	chr9:72287406-72287407	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs7862740	chr9:72287437-72287438	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs577455452	chr9:72287498-72287499	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs538543220	chr9:72287500-72287501	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs554037504	chr9:72287501-72287502	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571903510	chr9:72287503-72287504	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs542621503	chr9:72287515-72287516	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs4744930	chr9:72287581-72287582	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs200452330	chr9:72287635-72287636	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs143624667	chr9:72287652-72287653	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs563065782	chr9:72287690-72287691	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs4744931	chr9:72287790-72287791	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs148048051	chr9:72287808-72287809	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs145673070	chr9:72287836-72287837	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs560849163	chr9:72287844-72287845	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs527653247	chr9:72287910-72287911	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs549380849	chr9:72287918-72287919	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs142570347	chr9:72287937-72287938	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs531682460	chr9:72287960-72287961	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs549908807	chr9:72287982-72287983	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs370840227	chr9:72288013-72288014	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs386734797	chr9:72288028-72288029	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs373518599	chr9:72288032-72288033	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs538836940	chr9:72288070-72288071	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs3069283	chr9:72288127-72288128	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs34300435	chr9:72288128-72288129	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs397722187	chr9:72288129-72288130	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs553746492	chr9:72288136-72288137	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Melanoma	22183965	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
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72285400-72288400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr9:72286000-72287000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr9:72286000-72287600	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr9:72286000-72288200	Active TSS	Brain Substantia Nigra	brain
5	chr9:72286200-72287000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr9:72286200-72287000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
7	chr9:72286200-72287000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr9:72286200-72287000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
9	chr9:72286200-72287200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
10	chr9:72286200-72287200	Flanking Active TSS	Stomach Smooth Muscle	stomach
11	chr9:72286200-72287600	Active TSS	Osteobl	bone
12	chr9:72286200-72288000	Active TSS	Colonic Mucosa	Colon
13	chr9:72286200-72288200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr9:72286200-72288200	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr9:72286200-72288600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:72286400-72287000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
17	chr9:72286400-72287000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
18	chr9:72286400-72287000	Flanking Active TSS	Esophagus	oesophagus
19	chr9:72286400-72287200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
20	chr9:72286400-72287200	Flanking Active TSS	Placenta	Placenta
21	chr9:72286400-72287600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr9:72286400-72287600	Active TSS	Primary T cells from cord blood	blood
23	chr9:72286400-72287800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
24	chr9:72286400-72288000	Active TSS	Rectal Smooth Muscle	rectum
25	chr9:72286400-72288000	Active TSS	HSMM	muscle
26	chr9:72286400-72288200	Active TSS	Brain Cingulate Gyrus	brain
27	chr9:72286400-72288200	Active TSS	Brain Hippocampus Middle	brain
28	chr9:72286400-72288400	Active TSS	Aorta	Aorta
29	chr9:72286400-72288400	Active TSS	HSMMtube	muscle
30	chr9:72286400-72288600	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr9:72286600-72287000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr9:72286600-72287000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
33	chr9:72286600-72287000	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr9:72286600-72287000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
35	chr9:72286600-72287000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:72286600-72287000	Flanking Active TSS	Lung	lung
37	chr9:72286600-72287000	Flanking Active TSS	Pancreas	Pancrea
38	chr9:72286600-72287000	Flanking Bivalent TSS/Enh	Spleen	Spleen
39	chr9:72286600-72287200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr9:72286600-72287200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr9:72286600-72287200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
42	chr9:72286600-72287200	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
43	chr9:72286600-72287200	Bivalent/Poised TSS	Fetal Stomach	stomach
44	chr9:72286600-72287200	Flanking Active TSS	HMEC	breast
45	chr9:72286600-72287600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:72286600-72287600	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr9:72286600-72287600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:72286600-72287600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:72286600-72287600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr9:72286600-72287600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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