Variant report

Variant	nsv1043722
Chromosome Location	chr9:85663674-85747562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:650)
CpG islands
(count:428)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:85734754-85735114	HepG2	liver:	n/a	n/a
2	ATF2	chr9:85677673-85677950	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:85678070-85678255	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:85721244-85721426	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:85677162-85677604	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:85671203-85671338	A549	lung:	n/a	n/a
7	BHLHE40	chr9:85734839-85735064	HepG2	liver:	n/a	n/a
8	BRCA1	chr9:85676918-85677383	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr9:85677713-85678015	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr9:85664226-85664330	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:85677677-85678198	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr9:85674729-85675018	HepG2	liver:	n/a	chr9:85674846-85674857 chr9:85674908-85674921 chr9:85674845-85674858 chr9:85674908-85674921
13	CEBPB	chr9:85676908-85677157	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:85716249-85716437	HepG2	liver:	n/a	chr9:85716348-85716359 chr9:85716348-85716361 chr9:85716349-85716360
15	CEBPB	chr9:85676889-85677191	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:85728472-85728742	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:85734815-85734966	HepG2	liver:	n/a	chr9:85734911-85734922
18	CEBPB	chr9:85676815-85678319	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr9:85675510-85675982	MCF-7	breast:	n/a	chr9:85675784-85675796
20	CEBPB	chr9:85676796-85677244	MCF-7	breast:	n/a	n/a
21	CEBPB	chr9:85734730-85735110	A549	lung:	n/a	chr9:85734911-85734922
22	CEBPB	chr9:85684670-85685000	IMR90	lung:	n/a	chr9:85684823-85684834
23	CEBPB	chr9:85734793-85735008	IMR90	lung:	n/a	chr9:85734911-85734922
24	CEBPB	chr9:85674694-85675037	A549	lung:	n/a	chr9:85674846-85674857 chr9:85674908-85674921 chr9:85674845-85674858 chr9:85674908-85674921
25	CEBPB	chr9:85681763-85682106	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:85734806-85735194	MCF-7	breast:	n/a	chr9:85734911-85734922
27	CEBPB	chr9:85734733-85735093	HepG2	liver:	n/a	chr9:85734911-85734922
28	CEBPB	chr9:85684659-85684986	HepG2	liver:	n/a	chr9:85684823-85684834
29	CEBPB	chr9:85684746-85684999	A549	lung:	n/a	chr9:85684823-85684834
30	CEBPB	chr9:85674756-85675021	Hela-S3	cervix:	n/a	chr9:85674846-85674857 chr9:85674908-85674921 chr9:85674845-85674858 chr9:85674908-85674921
31	CEBPB	chr9:85734654-85735237	A549	lung:	n/a	chr9:85734911-85734922
32	CEBPB	chr9:85698947-85699036	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:85671264-85671490	A549	lung:	n/a	n/a
34	CEBPB	chr9:85698895-85699032	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr9:85676711-85678264	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr9:85677152-85678261	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr9:85677623-85678141	ECC-1	luminal epithelium:	n/a	n/a
38	CREB1	chr9:85676933-85677979	H1-hESC	embryonic stem cell:	n/a	chr9:85677010-85677023
39	CREB1	chr9:85676828-85677223	A549	lung:	n/a	chr9:85677010-85677023
40	CREB1	chr9:85677449-85678259	A549	lung:	n/a	n/a
41	CTBP2	chr9:85676882-85678346	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr9:85677700-85677850	NHEK	skin:	n/a	n/a
43	CTCF	chr9:85696360-85696510	NHDF-neo	bronchial:	n/a	chr9:85696390-85696408 chr9:85696392-85696413
44	CTCF	chr9:85677700-85677850	AG09309	skin:	n/a	n/a
45	CTCF	chr9:85677620-85677770	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr9:85677599-85677985	H1-hESC	embryonic stem cell:	n/a	chr9:85677852-85677865
47	CTCF	chr9:85677710-85677848	LNCaP	prostate:	n/a	n/a
48	CTCF	chr9:85677720-85677870	NHDF-neo	bronchial:	n/a	chr9:85677852-85677865
49	CTCF	chr9:85677632-85677938	MCF-7	breast:	n/a	chr9:85677852-85677865
50	CTCF	chr9:85690942-85691091	MCF-7	breast:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:85678242-85678292	T-47D	breast:	n/a
2	chr9:85678242-85678292	T-47D	breast:	n/a
3	chr9:85678242-85678292	HepG2	liver:	n/a
4	chr9:85678251-85678301	NH-A	brain:	n/a
5	chr9:85678242-85678292	GM12891	blood:	n/a
6	chr9:85677330-85677380	NH-A	brain:	n/a
7	chr9:85677016-85677066	HCM	heart:	n/a
8	chr9:85676358-85676408	Jurkat	blood:	n/a
9	chr9:85677330-85677380	HCT-116	colon:	n/a
10	chr9:85678242-85678292	HCPEpiC	choroid plexus:	n/a
11	chr9:85678242-85678292	HCT-116	colon:	n/a
12	chr9:85677921-85677971	SK-N-SH_RA	brain:	n/a
13	chr9:85676358-85676408	NHDF-neo	bronchial:	n/a
14	chr9:85677330-85677380	Hepatocyte	liver:	n/a
15	chr9:85676358-85676408	SK-N-MC	brain:	n/a
16	chr9:85678251-85678301	IMR90	lung:	fetal
17	chr9:85677921-85677971	SKMC	muscle:	n/a
18	chr9:85678242-85678292	PANC-1	pancreas:	n/a
19	chr9:85677921-85677971	LNCaP	prostate:	n/a
20	chr9:85678242-85678292	GM12892	blood:	n/a
21	chr9:85676358-85676408	HCT-116	colon:	n/a
22	chr9:85679694-85679744	HUVEC	blood vessel:	n/a
23	chr9:85677330-85677380	GM12891	blood:	n/a
24	chr9:85677330-85677380	GM12892	blood:	n/a
25	chr9:85678251-85678301	HNPCEpiC	eye:	n/a
26	chr9:85679694-85679744	HAEpiC	amniotic membrane:	n/a
27	chr9:85679694-85679744	A549	lung:	n/a
28	chr9:85676358-85676408	PFSK-1	brain:	n/a
29	chr9:85677921-85677971	AG04449	skin:	fetal
30	chr9:85677921-85677971	HCPEpiC	choroid plexus:	n/a
31	chr9:85677330-85677380	T-47D	breast:	n/a
32	chr9:85677330-85677380	ovcar-3	ovarian:	n/a
33	chr9:85677921-85677971	NB4	blood:	n/a
34	chr9:85677016-85677066	HMEC	breast:	n/a
35	chr9:85677330-85677380	SKMC	muscle:	n/a
36	chr9:85677330-85677380	SAEC	small airway:	n/a
37	chr9:85676358-85676408	GM06990	blood:	n/a
38	chr9:85677921-85677971	AG04450	lung:	fetal
39	chr9:85678242-85678292	HMEC	breast:	n/a
40	chr9:85678251-85678301	PrEC	prostate:	n/a
41	chr9:85678242-85678292	A549	lung:	n/a
42	chr9:85677921-85677971	Jurkat	blood:	n/a
43	chr9:85679694-85679744	NHBE	bronchial:	n/a
44	chr9:85677330-85677380	NHBE	bronchial:	n/a
45	chr9:85677016-85677066	RPTEC	kidney:	n/a
46	chr9:85678242-85678292	Jurkat	blood:	n/a
47	chr9:85677016-85677066	HUVEC	blood vessel:	n/a
48	chr9:85678242-85678292	U87	brain:	n/a
49	chr9:85677016-85677066	Hela-S3	cervix:	n/a
50	chr9:85678242-85678292	HEEpiC	esophagus:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:85740064..85745263-chr9:85745452..85749700,6	MCF-7	breast:
2	chr9:85675506..85677391-chr9:85694736..85696323,2	MCF-7	breast:
3	chr9:85715783..85717290-chr9:85720395..85722921,2	K562	blood:
4	chr9:85703404..85704350-chrX:71914443..71915103,2	MCF-7	breast:
5	chr9:85676330..85678438-chr9:85720312..85722824,2	MCF-7	breast:
6	chr9:85675258..85677545-chr9:85832289..85835005,2	MCF-7	breast:
7	chr9:85655420..85657921-chr9:85674583..85677127,3	MCF-7	breast:
8	chr9:85567518..85569787-chr9:85676279..85677863,2	MCF-7	breast:
9	chr9:85681699..85685875-chr9:85690492..85692266,3	MCF-7	breast:
10	chr9:85676183..85677844-chr9:85708576..85710898,2	MCF-7	breast:
11	chr9:85670132..85672799-chr9:85673818..85675715,2	MCF-7	breast:
12	chr9:85676183..85677844-chr9:85708576..85710898,2	MCF-7	breast:
13	chr9:85670132..85672799-chr9:85673818..85675715,2	MCF-7	breast:
14	chr9:85696325..85697890-chr9:85697958..85699470,2	MCF-7	breast:
15	chr9:85697664..85699553-chr9:85733756..85736324,2	MCF-7	breast:
16	chr9:85715783..85717290-chr9:85720395..85722921,2	K562	blood:
17	chr9:85697664..85699553-chr9:85733756..85736324,2	MCF-7	breast:
18	chr9:85675506..85677391-chr9:85694736..85696323,2	MCF-7	breast:
19	chr9:85696325..85697890-chr9:85697958..85699470,2	MCF-7	breast:
20	chr9:85517725..85520143-chr9:85676232..85677764,2	MCF-7	breast:
21	chr9:85681699..85685875-chr9:85690492..85692266,3	MCF-7	breast:
22	chr9:85679555..85682048-chr9:85742285..85744042,2	MCF-7	breast:
23	chr9:85722110..85725029-chr9:85812448..85815231,2	MCF-7	breast:
24	chr7:126928309..126929229-chr9:85704406..85705155,2	MCF-7	breast:
25	chr9:85659740..85661503-chr9:85675650..85677677,2	MCF-7	breast:
26	chr9:85740064..85745263-chr9:85745452..85749700,6	MCF-7	breast:
27	chr9:85519169..85522016-chr9:85676128..85677993,2	MCF-7	breast:
28	chr9:85676023..85678265-chr9:85688162..85689853,3	MCF-7	breast:
29	chr9:85734626..85737595-chr9:85745024..85746688,2	MCF-7	breast:
30	chr9:85679555..85682048-chr9:85742285..85744042,2	MCF-7	breast:
31	chr9:85111301..85113649-chr9:85675485..85677870,2	MCF-7	breast:
32	chr9:85615571..85616446-chr9:85674578..85675173,2	MCF-7	breast:
33	chr9:85674686..85677678-chr9:85690780..85693708,2	MCF-7	breast:
34	chr9:85669834..85672672-chr9:85676087..85678737,3	MCF-7	breast:
35	chr9:85677479..85679475-chr9:85708782..85710847,2	MCF-7	breast:
36	chr9:85677455..85679468-chr9:85739045..85741596,2	MCF-7	breast:
37	chr9:85734626..85737595-chr9:85745024..85746688,2	MCF-7	breast:
38	chr9:85674686..85677678-chr9:85690780..85693708,2	MCF-7	breast:
39	chr9:85538017..85538733-chr9:85674545..85675107,2	MCF-7	breast:

No data

Variant related genes	Relation type
RASEF	TF binding region
RASEF	CpG island
ENSG00000229109	chromatin interactions
ENSG00000165105	chromatin interactions

Extended variants
information (count: 1964 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1964 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10116216	chr9:85663674-85663675	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533077517	chr9:85663676-85663677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550013202	chr9:85663677-85663678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545764210	chr9:85663685-85663686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544717848	chr9:85663738-85663739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576415945	chr9:85663841-85663842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543527355	chr9:85663866-85663867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140048760	chr9:85663872-85663873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529039981	chr9:85663907-85663908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181762644	chr9:85663911-85663912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569833797	chr9:85663932-85663933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559660579	chr9:85663989-85663990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144029102	chr9:85664014-85664015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551734766	chr9:85664015-85664016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147319274	chr9:85664017-85664018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537098522	chr9:85664033-85664034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200356817	chr9:85664057-85664058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199938012	chr9:85664068-85664069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113550405	chr9:85664091-85664092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73471429	chr9:85664101-85664102	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567362739	chr9:85664142-85664143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140035540	chr9:85664152-85664153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186844246	chr9:85664164-85664165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34431781	chr9:85664167-85664168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369251564	chr9:85664169-85664170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74982661	chr9:85664177-85664178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149875185	chr9:85664196-85664197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558451031	chr9:85664202-85664203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576354410	chr9:85664235-85664236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543838688	chr9:85664268-85664269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144870995	chr9:85664273-85664274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574204843	chr9:85664280-85664281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548693017	chr9:85664281-85664282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559572836	chr9:85664300-85664301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114932217	chr9:85664319-85664320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545321309	chr9:85664322-85664323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190202369	chr9:85664340-85664341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540495240	chr9:85664349-85664350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78687841	chr9:85664392-85664393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567219650	chr9:85664395-85664396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79813403	chr9:85664414-85664415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546323015	chr9:85664415-85664416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201121922	chr9:85664443-85664444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200712436	chr9:85664444-85664445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10687615	chr9:85664445-85664446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76764544	chr9:85664468-85664469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79100491	chr9:85664471-85664472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80144810	chr9:85664473-85664474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76751658	chr9:85664474-85664475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113201659	chr9:85664491-85664492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Astrocytoma	22246337	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85644800-85670600	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr9:85655200-85671400	Weak transcription	Fetal Intestine Small	intestine
3	chr9:85660400-85664400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr9:85661400-85663800	Enhancers	A549	lung
5	chr9:85662200-85663800	Enhancers	Fetal Heart	heart
6	chr9:85663000-85663800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:85663200-85663800	Enhancers	Pancreas	Pancrea
8	chr9:85663200-85664400	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr9:85663200-85676400	Weak transcription	Gastric	stomach
10	chr9:85663400-85670800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr9:85663600-85664200	Weak transcription	Right Ventricle	heart
12	chr9:85663600-85673400	Weak transcription	Stomach Mucosa	stomach
13	chr9:85663800-85671200	Weak transcription	A549	lung
14	chr9:85663800-85674200	Weak transcription	Pancreas	Pancrea
15	chr9:85664200-85664400	Enhancers	Right Ventricle	heart
16	chr9:85664400-85670400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr9:85664400-85671400	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr9:85670200-85670400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr9:85670200-85670600	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr9:85670400-85670600	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr9:85670400-85670800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr9:85670400-85671200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
23	chr9:85670600-85670800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
24	chr9:85670600-85670800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr9:85670600-85672600	Enhancers	Fetal Intestine Large	intestine
26	chr9:85670800-85671000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr9:85670800-85671000	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr9:85670800-85672000	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr9:85670800-85673200	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr9:85671200-85672400	Enhancers	A549	lung
31	chr9:85671400-85671600	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr9:85671400-85671800	Enhancers	Fetal Intestine Small	intestine
33	chr9:85671600-85673000	Enhancers	Duodenum Mucosa	Duodenum
34	chr9:85671600-85673800	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr9:85671800-85675200	Weak transcription	Fetal Intestine Small	intestine
36	chr9:85672000-85672600	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr9:85672400-85674400	Weak transcription	A549	lung
38	chr9:85672600-85673800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr9:85672600-85676000	Weak transcription	Fetal Intestine Large	intestine
40	chr9:85673000-85674400	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:85673200-85673600	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr9:85673400-85674600	Enhancers	Stomach Mucosa	stomach
43	chr9:85673600-85675800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr9:85673600-85675800	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr9:85673800-85674000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:85673800-85674000	Bivalent Enhancer	Left Ventricle	heart
47	chr9:85673800-85674400	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr9:85673800-85674800	Enhancers	Esophagus	oesophagus
49	chr9:85673800-85674800	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr9:85673800-85675800	Enhancers	HMEC	breast

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