Variant report

Variant	nsv893561
Chromosome Location	chr9:92732368-92802101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:806)
CpG islands
(count:0)
Chromatin interactive
region (count:67)
LncRNA
region (count:26)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:92762370-92762818	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:92756383-92756918	HepG2	liver:	n/a	n/a
3	BACH1	chr9:92796450-92796595	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr9:92745701-92746017	GM12878	blood:	n/a	n/a
5	BATF	chr9:92745702-92746064	GM12878	blood:	n/a	n/a
6	BCL3	chr9:92745787-92746081	GM12878	blood:	n/a	n/a
7	BCL3	chr9:92755734-92756327	GM12878	blood:	n/a	n/a
8	BCL3	chr9:92732679-92733033	GM12878	blood:	n/a	n/a
9	BCL3	chr9:92755431-92756238	GM12878	blood:	n/a	n/a
10	BCLAF1	chr9:92761871-92762374	GM12878	blood:	n/a	chr9:92761889-92761902 chr9:92762159-92762168 chr9:92762232-92762241 chr9:92761978-92761987
11	BCLAF1	chr9:92761927-92762343	GM12878	blood:	n/a	chr9:92762159-92762168 chr9:92762232-92762241 chr9:92761978-92761987
12	BHLHE40	chr9:92757341-92757620	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:92756388-92756830	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:92786693-92787056	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:92740616-92740650	K562	blood:	n/a	n/a
16	BRCA1	chr9:92758580-92758641	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:92732634-92732861	Hela-S3	cervix:	n/a	chr9:92732758-92732769
18	CEBPB	chr9:92756389-92756965	HepG2	liver:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
19	CEBPB	chr9:92746649-92746829	HepG2	liver:	n/a	chr9:92746765-92746776
20	CEBPB	chr9:92756301-92756831	Hela-S3	cervix:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
21	CEBPB	chr9:92791585-92791785	A549	lung:	n/a	n/a
22	CEBPB	chr9:92756354-92756841	HepG2	liver:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
23	CEBPB	chr9:92732686-92732830	HepG2	liver:	n/a	chr9:92732758-92732769
24	CEBPB	chr9:92737903-92738118	HepG2	liver:	n/a	chr9:92737943-92737954
25	CEBPB	chr9:92746595-92746911	IMR90	lung:	n/a	chr9:92746765-92746776
26	CEBPB	chr9:92756405-92756815	A549	lung:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
27	CEBPB	chr9:92756421-92756841	MCF-7	breast:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
28	CEBPB	chr9:92732662-92732891	IMR90	lung:	n/a	chr9:92732758-92732769
29	CEBPB	chr9:92756284-92756896	A549	lung:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
30	CEBPB	chr9:92756295-92756807	MCF-7	breast:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
31	CEBPB	chr9:92740503-92740773	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr9:92794303-92794503	HepG2	liver:	n/a	chr9:92794441-92794452
33	CEBPB	chr9:92756385-92756762	HepG2	liver:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
34	CEBPB	chr9:92749014-92749199	HepG2	liver:	n/a	chr9:92749154-92749167 chr9:92749058-92749069
35	CEBPB	chr9:92732633-92732931	A549	lung:	n/a	chr9:92732758-92732769
36	CEBPB	chr9:92756404-92756800	A549	lung:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
37	CEBPB	chr9:92756482-92756742	HepG2	liver:	n/a	chr9:92756597-92756608 chr9:92756598-92756609 chr9:92756553-92756564
38	CEBPB	chr9:92799609-92799774	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPD	chr9:92756480-92756755	HepG2	liver:	n/a	chr9:92756597-92756608
40	CEBPD	chr9:92756405-92756795	HepG2	liver:	n/a	chr9:92756597-92756608
41	CHD2	chr9:92756365-92756722	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr9:92762065-92762197	GM12878	blood:	n/a	n/a
43	CHD2	chr9:92756574-92756794	HepG2	liver:	n/a	n/a
44	CREB1	chr9:92756335-92756934	HepG2	liver:	n/a	n/a
45	CREB1	chr9:92756275-92756924	HepG2	liver:	n/a	n/a
46	CTCF	chr9:92784879-92785054	MCF-7	breast:	n/a	chr9:92784969-92784990 chr9:92784971-92784978 chr9:92784967-92784985
47	CTCF	chr9:92759069-92759194	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr9:92740565-92740771	NHEK	skin:	n/a	n/a
49	CTCF	chr9:92740580-92740730	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr9:92792440-92792590	GM12867	blood:	n/a	n/a

No data

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:92779076..92781069-chr9:92783497..92785199,2	MCF-7	breast:
2	chr9:92793117..92794767-chr9:92795692..92798106,2	MCF-7	breast:
3	chr9:92743937..92746213-chr9:92746702..92748214,2	MCF-7	breast:
4	chr9:92766437..92768027-chr9:92770302..92772264,2	MCF-7	breast:
5	chr9:92779076..92781069-chr9:92783497..92785199,2	MCF-7	breast:
6	chr9:92736111..92738739-chr9:92755408..92756984,2	MCF-7	breast:
7	chr9:92230289..92231170-chr9:92758244..92759563,4	MCF-7	breast:
8	chr9:92741964..92746302-chr9:92752977..92756296,4	MCF-7	breast:
9	chr9:92220536..92222914-chr9:92732906..92734901,2	MCF-7	breast:
10	chr9:92218418..92219230-chr9:92758601..92759142,2	MCF-7	breast:
11	chr9:92756890..92759147-chr9:92762216..92764609,2	MCF-7	breast:
12	chr9:92774758..92776459-chr9:92788172..92789725,2	MCF-7	breast:
13	chr9:92681447..92682404-chr9:92758846..92759379,3	MCF-7	breast:
14	chr9:92219780..92221429-chr9:92776141..92778037,2	MCF-7	breast:
15	chr9:92741195..92742880-chr9:92743389..92745456,2	MCF-7	breast:
16	chr9:92742006..92743926-chr9:92747160..92749518,2	K562	blood:
17	chr9:92761640..92763658-chr9:92766942..92769443,2	MCF-7	breast:
18	chr9:92755082..92756623-chr9:92757434..92759681,2	MCF-7	breast:
19	chr9:92753705..92756579-chr9:92759778..92762031,2	MCF-7	breast:
20	chr9:92774758..92776459-chr9:92788172..92789725,2	MCF-7	breast:
21	chr9:92779670..92782151-chr9:92784242..92786135,2	MCF-7	breast:
22	chr9:92766437..92768027-chr9:92770302..92772264,2	MCF-7	breast:
23	chr9:92748187..92750208-chr9:92758862..92760801,2	MCF-7	breast:
24	chr9:92776616..92778176-chr9:92780846..92782771,2	MCF-7	breast:
25	chr9:92218567..92220178-chr9:92756424..92758715,2	MCF-7	breast:
26	chr9:92216705..92219095-chr9:92730005..92732968,2	MCF-7	breast:
27	chr9:92743278..92746160-chr9:92749145..92750890,2	MCF-7	breast:
28	chr9:92793900..92797470-chr9:92799837..92802623,4	MCF-7	breast:
29	chr9:92775713..92778575-chr9:92781169..92782694,2	MCF-7	breast:
30	chr9:92775713..92778575-chr9:92781169..92782694,2	MCF-7	breast:
31	chr9:92218708..92219342-chr9:92758550..92759211,2	MCF-7	breast:
32	chr9:92681495..92682068-chr9:92758708..92759575,3	MCF-7	breast:
33	chr9:92761640..92763658-chr9:92766942..92769443,2	MCF-7	breast:
34	chr9:92739296..92741808-chr9:92758775..92761522,2	MCF-7	breast:
35	chr9:92217989..92218568-chr9:92758907..92759509,2	MCF-7	breast:
36	chr9:92217272..92218834-chr9:92763919..92766631,2	MCF-7	breast:
37	chr9:92736111..92738739-chr9:92755408..92756984,2	MCF-7	breast:
38	chr9:92213129..92215525-chr9:92775217..92778427,3	MCF-7	breast:
39	chr9:92741195..92742880-chr9:92743389..92745456,2	MCF-7	breast:
40	chr9:92753705..92756579-chr9:92759778..92762031,2	MCF-7	breast:
41	chr9:92758301..92760371-chr9:92760953..92763123,2	MCF-7	breast:
42	chr9:92216749..92221414-chr9:92756839..92763409,10	MCF-7	breast:
43	chr9:92748243..92750612-chr9:92751364..92753556,2	MCF-7	breast:
44	chr9:92741964..92746302-chr9:92752977..92756296,4	MCF-7	breast:
45	chr9:92218211..92220844-chr9:92785604..92787367,2	MCF-7	breast:
46	chr9:92743278..92746160-chr9:92749145..92750890,2	MCF-7	breast:
47	chr9:92218340..92220049-chr9:92760293..92762561,2	MCF-7	breast:
48	chr9:92756890..92759147-chr9:92762216..92764609,2	MCF-7	breast:
49	chr9:92776616..92778176-chr9:92780846..92782771,2	MCF-7	breast:
50	chr9:92217619..92218164-chr9:92758824..92759396,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GADD45G-5	chr9:92740558-92740714	XLOC_007451
2	lnc-GADD45G-5	chr9:92749463-92749768	XLOC_007451
3	lnc-GADD45G-5	chr9:92765767-92765789	NONHSAT132986
4	lnc-GADD45G-5	chr9:92750970-92751077	NONHSAT132986
5	lnc-DIRAS2-4	chr9:92786845-92788381	ENSG00000227555
6	lnc-GADD45G-5	chr9:92762923-92763500	XLOC_007451
7	lnc-GADD45G-5	chr9:92749463-92749768	NR_109791
8	lnc-GADD45G-6	chr9:92777663-92777861	XLOC_007452
9	lnc-DIRAS2-4	chr9:92798330-92798413	ENSG00000227555
10	lnc-GADD45G-5	chr9:92749463-92749730	XLOC_007451
11	lnc-GADD45G-5	chr9:92740564-92740714	XLOC_007451
12	lnc-GADD45G-5	chr9:92762923-92763500	NONHSAT132986
13	lnc-GADD45G-5	chr9:92749463-92749730	NONHSAT132983
14	lnc-GADD45G-5	chr9:92740558-92740714	NONHSAT132983
15	lnc-GADD45G-6	chr9:92777662-92777861	NONHSAT132988
16	lnc-GADD45G-5	chr9:92740558-92740714	NR_109791
17	lnc-GADD45G-5	chr9:92762923-92763500	NONHSAT132983
18	lnc-GADD45G-6	chr9:92768990-92769070	NONHSAT132988
19	lnc-GADD45G-6	chr9:92768991-92769070	XLOC_007452
20	lnc-GADD45G-5	chr9:92767231-92767420	XLOC_007451
21	lnc-DIRAS2-16	chr9:92767367-92767496	NONHSAT132987
22	lnc-GADD45G-5	chr9:92765767-92765789	NONHSAT132983
23	lnc-GADD45G-5	chr9:92763074-92763500	XLOC_007451
24	lnc-DIRAS2-4	chr9:92782936-92783827	ENSG00000227555
25	lnc-GADD45G-5	chr9:92767231-92767272	XLOC_007451
26	lnc-DIRAS2-16	chr9:92759363-92759527	NONHSAT132987

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4290	chr9:92785733-92785751	MIMAT0016921

No data

Variant related genes	Relation type
MIR4290	TF binding region
ENSG00000237626	TF binding region
ENSG00000130222	chromatin interactions
ENSG00000263967	chromatin interactions
ENSG00000237626	chromatin interactions
TPCN2	miRNA target sites
CHSY1	miRNA target sites

Extended variants
information (count: 2860 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2860 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12353168	chr9:92732368-92732369	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs548760818	chr9:92732370-92732371	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs150936556	chr9:92732387-92732388	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs544511106	chr9:92732403-92732404	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs556250895	chr9:92732415-92732416	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs7038428	chr9:92732443-92732444	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs370490576	chr9:92732448-92732449	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs56693333	chr9:92732458-92732459	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs373970235	chr9:92732493-92732494	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs377238816	chr9:92732551-92732552	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs117807929	chr9:92732599-92732600	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs189596100	chr9:92732608-92732609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532343328	chr9:92732636-92732637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545895640	chr9:92732643-92732644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78006928	chr9:92732660-92732661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571271859	chr9:92732663-92732664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78895243	chr9:92732678-92732679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180831884	chr9:92732757-92732758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527606503	chr9:92732765-92732766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10993510	chr9:92732792-92732793	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs74305889	chr9:92732830-92732831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567737177	chr9:92732850-92732851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539401281	chr9:92732855-92732856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140761890	chr9:92732870-92732871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556188177	chr9:92732921-92732922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569695844	chr9:92732925-92732926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144916956	chr9:92732943-92732944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186758598	chr9:92732963-92732964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555990133	chr9:92732998-92732999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76841835	chr9:92733058-92733059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553997978	chr9:92733141-92733142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61344087	chr9:92733142-92733143	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545832435	chr9:92733175-92733176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138745354	chr9:92733182-92733183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72752995	chr9:92733217-92733218	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs188569311	chr9:92733228-92733229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374062384	chr9:92733246-92733247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181062606	chr9:92733284-92733285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185941256	chr9:92733322-92733323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79587706	chr9:92733342-92733343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543250183	chr9:92733396-92733397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1999100	chr9:92733432-92733433	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs145442787	chr9:92733453-92733454	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs138012453	chr9:92733466-92733467	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs115882023	chr9:92733491-92733492	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs60994320	chr9:92733519-92733520	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs535210591	chr9:92733536-92733537	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs10118050	chr9:92733538-92733539	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs75318562	chr9:92733559-92733560	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs534086750	chr9:92733572-92733573	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Glioma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1230 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92724800-92732400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr9:92725600-92738200	Weak transcription	Lung	lung
3	chr9:92727400-92732800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr9:92729600-92733800	Enhancers	Fetal Intestine Small	intestine
5	chr9:92730800-92733800	Enhancers	Fetal Intestine Large	intestine
6	chr9:92731000-92732600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr9:92731400-92732400	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr9:92731600-92732600	Enhancers	Small Intestine	intestine
9	chr9:92731600-92732600	Enhancers	Stomach Mucosa	stomach
10	chr9:92731600-92732800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:92731600-92732800	Enhancers	HepG2	liver
12	chr9:92731800-92732600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
13	chr9:92732000-92733400	Weak transcription	HSMMtube	muscle
14	chr9:92732200-92732400	Flanking Active TSS	Colonic Mucosa	Colon
15	chr9:92732200-92733000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr9:92732400-92732600	Enhancers	Colonic Mucosa	Colon
17	chr9:92732400-92732600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
18	chr9:92732400-92733400	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr9:92732600-92733000	Weak transcription	Colonic Mucosa	Colon
20	chr9:92732600-92733400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr9:92732600-92733600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr9:92732800-92733400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr9:92733000-92733600	Enhancers	Colonic Mucosa	Colon
24	chr9:92733000-92736600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr9:92733200-92733400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:92733400-92733600	ZNF genes & repeats	HSMMtube	muscle
27	chr9:92733400-92740200	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr9:92733800-92738000	Weak transcription	Fetal Intestine Small	intestine
29	chr9:92734200-92734600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:92736600-92738200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr9:92737400-92738800	Enhancers	Fetal Lung	lung
32	chr9:92738000-92738400	Enhancers	Fetal Intestine Small	intestine
33	chr9:92738000-92738600	Enhancers	Fetal Muscle Leg	muscle
34	chr9:92738200-92738400	Enhancers	Aorta	Aorta
35	chr9:92738200-92738400	Enhancers	Lung	lung
36	chr9:92738200-92738400	Enhancers	Ovary	ovary
37	chr9:92738200-92740400	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr9:92738400-92743000	Weak transcription	Aorta	Aorta
39	chr9:92738800-92740200	Weak transcription	Fetal Lung	lung
40	chr9:92739000-92739400	Enhancers	Left Ventricle	heart
41	chr9:92740200-92740800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr9:92740400-92740600	Enhancers	Fetal Intestine Small	intestine
43	chr9:92740400-92740600	Enhancers	Fetal Lung	lung
44	chr9:92740400-92740800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr9:92740400-92740800	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr9:92740600-92740800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:92740600-92740800	Enhancers	Adipose Nuclei	Adipose
48	chr9:92740600-92741000	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr9:92740600-92741400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr9:92740800-92744200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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