Variant report

Variant	esv2757352
Chromosome Location	chr9:115648457-115664299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:298)
CpG islands
(count:490)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115661077-115661500	HepG2	liver:	n/a	n/a
2	BACH1	chr9:115652819-115653393	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:115656385-115656635	GM12878	blood:	n/a	chr9:115656511-115656522
4	BHLHE40	chr9:115649861-115649973	K562	blood:	n/a	n/a
5	CEBPB	chr9:115661033-115661659	MCF-7	breast:	n/a	chr9:115661346-115661357 chr9:115661344-115661357 chr9:115661344-115661355 chr9:115661344-115661357
6	CEBPB	chr9:115661276-115661500	IMR90	lung:	n/a	chr9:115661346-115661357 chr9:115661344-115661357 chr9:115661344-115661355 chr9:115661344-115661357
7	CEBPB	chr9:115657123-115657241	HepG2	liver:	n/a	n/a
8	CEBPB	chr9:115661076-115661521	Hela-S3	cervix:	n/a	chr9:115661346-115661357 chr9:115661344-115661357 chr9:115661344-115661355 chr9:115661344-115661357
9	CEBPB	chr9:115661124-115661585	HepG2	liver:	n/a	chr9:115661346-115661357 chr9:115661344-115661357 chr9:115661344-115661355 chr9:115661344-115661357
10	CEBPB	chr9:115661300-115661520	A549	lung:	n/a	chr9:115661346-115661357 chr9:115661344-115661357 chr9:115661344-115661355 chr9:115661344-115661357
11	CREB1	chr9:115661016-115661446	HepG2	liver:	n/a	n/a
12	CTCF	chr9:115649750-115649975	GM19238	blood:	n/a	n/a
13	CTCF	chr9:115649810-115649912	ProgFib	skin:	n/a	n/a
14	CTCF	chr9:115649800-115649950	GM12868	blood:	n/a	n/a
15	CTCF	chr9:115652540-115652690	HRE	kidney:	n/a	n/a
16	CTCF	chr9:115654713-115654801	K562	blood:	n/a	chr9:115654757-115654775
17	CTCF	chr9:115652521-115652658	MCF-7	breast:	n/a	n/a
18	CTCF	chr9:115649688-115649979	GM12878	blood:	n/a	n/a
19	CTCF	chr9:115649760-115649910	AG04449	skin:	n/a	n/a
20	CTCF	chr9:115649787-115649911	Lung_OC	lung:	n/a	n/a
21	CTCF	chr9:115653060-115653210	HMEC	breast:	n/a	n/a
22	CTCF	chr9:115649797-115649945	Fibrobl	skin:	n/a	n/a
23	CTCF	chr9:115649658-115650032	K562	blood:	n/a	n/a
24	CTCF	chr9:115649752-115649993	IMR90	lung:	n/a	n/a
25	CTCF	chr9:115649760-115649910	AG09319	gingival:	n/a	n/a
26	CTCF	chr9:115649740-115649890	GM12875	blood:	n/a	n/a
27	CTCF	chr9:115649780-115649930	HRE	kidney:	n/a	n/a
28	CTCF	chr9:115649717-115649940	HepG2	liver:	n/a	n/a
29	CTCF	chr9:115654693-115654806	GM12878	blood:	n/a	chr9:115654757-115654775
30	CTCF	chr9:115649880-115650030	HCT-116	colon:	n/a	n/a
31	CTCF	chr9:115649809-115649911	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr9:115649780-115649930	HFF	foreskin:	n/a	n/a
33	CTCF	chr9:115649760-115649910	GM12870	blood:	n/a	n/a
34	CTCF	chr9:115649820-115649970	HepG2	liver:	n/a	n/a
35	CTCF	chr9:115649754-115649961	MCF-7	breast:	n/a	n/a
36	CTCF	chr9:115654780-115654930	HCM	heart:	n/a	n/a
37	CTCF	chr9:115653128-115653141	LNCaP	prostate:	n/a	n/a
38	CTCF	chr9:115649740-115649890	GM12873	blood:	n/a	n/a
39	CTCF	chr9:115649768-115649945	MCF-7	breast:	n/a	n/a
40	CTCF	chr9:115649651-115650020	K562	blood:	n/a	n/a
41	CTCF	chr9:115653100-115653250	GM12866	blood:	n/a	n/a
42	CTCF	chr9:115654758-115654796	GM19240	blood:	n/a	n/a
43	CTCF	chr9:115649680-115649830	HCT-116	colon:	n/a	n/a
44	CTCF	chr9:115649760-115649910	GM12878	blood:	n/a	n/a
45	CTCF	chr9:115654740-115654890	HepG2	liver:	n/a	chr9:115654757-115654775
46	CTCF	chr9:115649740-115649890	AG04450	lung:	n/a	n/a
47	CTCF	chr9:115649740-115649890	HEK293	kidney:	n/a	n/a
48	CTCF	chr9:115649740-115649890	A549	lung:	n/a	n/a
49	CTCF	chr9:115649760-115649910	HMEC	breast:	n/a	n/a
50	CTCF	chr9:115649900-115650050	A549	lung:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115650856-115650906	HRE	kidney:	n/a
2	chr9:115650248-115650298	HRPEpiC	eye:	n/a
3	chr9:115650856-115650906	HRE	kidney:	n/a
4	chr9:115650248-115650298	HRPEpiC	eye:	n/a
5	chr9:115653543-115653593	NB4	blood:	n/a
6	chr9:115650839-115650889	HEK293	kidney:	embryo
7	chr9:115652824-115652874	A549	lung:	n/a
8	chr9:115653026-115653076	AoSMC	blood vessel:	n/a
9	chr9:115653026-115653076	HCPEpiC	choroid plexus:	n/a
10	chr9:115653543-115653593	Hela-S3	cervix:	n/a
11	chr9:115652824-115652874	PFSK-1	brain:	n/a
12	chr9:115653543-115653593	AG04449	skin:	fetal
13	chr9:115653026-115653076	HCT-116	colon:	n/a
14	chr9:115650248-115650298	NH-A	brain:	n/a
15	chr9:115653802-115653852	SK-N-SH	brain:	n/a
16	chr9:115650856-115650906	ProgFib	skin:	n/a
17	chr9:115653802-115653852	HEK293	kidney:	embryo
18	chr9:115650839-115650889	AoSMC	blood vessel:	n/a
19	chr9:115653543-115653593	LNCaP	prostate:	n/a
20	chr9:115650248-115650298	Jurkat	blood:	n/a
21	chr9:115650248-115650298	AG09319	gingival:	n/a
22	chr9:115653802-115653852	NH-A	brain:	n/a
23	chr9:115653802-115653852	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:115650839-115650889	PANC-1	pancreas:	n/a
25	chr9:115653026-115653076	Jurkat	blood:	n/a
26	chr9:115650856-115650906	HRPEpiC	eye:	n/a
27	chr9:115650248-115650298	HAEpiC	amniotic membrane:	n/a
28	chr9:115650839-115650889	HAEpiC	amniotic membrane:	n/a
29	chr9:115650839-115650889	NHDF-neo	bronchial:	n/a
30	chr9:115653026-115653076	AG09319	gingival:	n/a
31	chr9:115653222-115653272	Jurkat	blood:	n/a
32	chr9:115652824-115652874	AG10803	skin:	n/a
33	chr9:115652824-115652874	HMEC	breast:	n/a
34	chr9:115652824-115652874	ECC-1	luminal epithelium:	n/a
35	chr9:115650856-115650906	AoSMC	blood vessel:	n/a
36	chr9:115650856-115650906	GM19239	blood:	n/a
37	chr9:115650248-115650298	HL-60	blood:	n/a
38	chr9:115653222-115653272	HL-60	blood:	n/a
39	chr9:115650856-115650906	AG10803	skin:	n/a
40	chr9:115653222-115653272	Hela-S3	cervix:	n/a
41	chr9:115653026-115653076	NB4	blood:	n/a
42	chr9:115653802-115653852	HepG2	liver:	n/a
43	chr9:115650248-115650298	SAEC	small airway:	n/a
44	chr9:115650856-115650906	HEEpiC	esophagus:	n/a
45	chr9:115650856-115650906	HCM	heart:	n/a
46	chr9:115650839-115650889	RPTEC	kidney:	n/a
47	chr9:115653543-115653593	HRE	kidney:	n/a
48	chr9:115653802-115653852	GM12878	blood:	n/a
49	chr9:115650839-115650889	HCF	heart:	n/a
50	chr9:115650248-115650298	HIPEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:115605115..115608085-chr9:115663970..115666331,4	MCF-7	breast:
2	chr9:115661009..115663181-chr9:115664939..115667779,3	MCF-7	breast:
3	chr9:115647367..115649652-chr9:115652587..115654849,2	MCF-7	breast:
4	chr9:115659389..115661774-chr9:115663212..115665423,2	MCF-7	breast:
5	chr9:115647996..115649794-chr9:115652153..115653845,2	K562	blood:
6	chr9:115653499..115655772-chr9:115659487..115662405,2	MCF-7	breast:
7	chr9:115653499..115655772-chr9:115659487..115662405,2	MCF-7	breast:
8	chr9:115653737..115657233-chr9:115662868..115665778,3	K562	blood:
9	chr9:115653409..115654935-chr9:115663870..115665546,2	MCF-7	breast:
10	chr9:115659389..115661774-chr9:115663212..115665423,2	MCF-7	breast:
11	chr9:115647367..115649652-chr9:115652587..115654849,2	MCF-7	breast:
12	chr9:115653737..115657233-chr9:115662868..115665778,3	K562	blood:
13	chr9:115647996..115651532-chr9:115651792..115654330,5	K562	blood:
14	chr9:115609355..115610986-chr9:115659802..115661844,2	MCF-7	breast:
15	chr9:115658787..115660468-chr9:115666043..115668753,2	K562	blood:
16	chr9:115511803..115513775-chr9:115660401..115662010,2	MCF-7	breast:
17	chr9:115653409..115654935-chr9:115663870..115665546,2	MCF-7	breast:
18	chr9:115606663..115607630-chr9:115649377..115650352,3	K562	blood:
19	chr9:115606376..115607335-chr9:115649571..115650256,3	MCF-7	breast:
20	chr9:115663052..115664958-chr9:115669316..115671393,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC46A2-2	chr9:115661341-115661886	XLOC_007831

No data

Variant related genes	Relation type
SLC46A2	TF binding region
SLC46A2	CpG island
ENSG00000226609	chromatin interactions
ENSG00000271631	chromatin interactions
ENSG00000119457	chromatin interactions
ENSG00000148158	chromatin interactions
ZBTB4	miRNA target sites

Extended variants
information (count: 719 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10817402	chr9:115648457-115648458	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548586504	chr9:115648463-115648464	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568430724	chr9:115648464-115648465	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138822992	chr9:115648488-115648489	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552706032	chr9:115648497-115648498	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566378108	chr9:115648508-115648509	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs181450108	chr9:115648540-115648541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558605093	chr9:115648572-115648573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575513376	chr9:115648581-115648582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530602870	chr9:115648616-115648617	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs78846689	chr9:115648673-115648674	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370864234	chr9:115648690-115648691	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375678235	chr9:115648708-115648709	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368432309	chr9:115648716-115648717	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372725365	chr9:115648725-115648726	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34165711	chr9:115648760-115648761	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs554558725	chr9:115648768-115648769	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs202214849	chr9:115648823-115648824	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144666415	chr9:115648852-115648853	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374764020	chr9:115648855-115648856	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200400658	chr9:115648856-115648857	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148125885	chr9:115648885-115648886	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367632408	chr9:115648922-115648923	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184619781	chr9:115648925-115648926	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs141930369	chr9:115648927-115648928	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371511474	chr9:115648937-115648938	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369874383	chr9:115648949-115648950	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76031056	chr9:115648966-115648967	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529014961	chr9:115648997-115648998	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532049714	chr9:115649002-115649003	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146334753	chr9:115649004-115649005	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568447473	chr9:115649035-115649036	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs11793266	chr9:115649069-115649070	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534672024	chr9:115649114-115649115	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566306906	chr9:115649129-115649130	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374482860	chr9:115649130-115649131	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189710984	chr9:115649246-115649247	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79108252	chr9:115649270-115649271	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538489520	chr9:115649303-115649304	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569015871	chr9:115649341-115649342	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117210829	chr9:115649362-115649363	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554263345	chr9:115649442-115649443	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs75464924	chr9:115649449-115649450	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540315698	chr9:115649453-115649454	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181198751	chr9:115649478-115649479	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs41280195	chr9:115649479-115649480	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs3802493	chr9:115649520-115649521	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs376017853	chr9:115649572-115649573	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186751694	chr9:115649609-115649610	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563108402	chr9:115649661-115649662	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115624200-115652600	Weak transcription	Fetal Heart	heart
2	chr9:115626400-115650800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:115631800-115652200	Weak transcription	Gastric	stomach
4	chr9:115633000-115652600	Weak transcription	Left Ventricle	heart
5	chr9:115633200-115652400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr9:115633200-115652400	Weak transcription	Right Ventricle	heart
7	chr9:115633400-115649200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr9:115633800-115652600	Weak transcription	Liver	Liver
9	chr9:115634800-115651800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr9:115635000-115650800	Weak transcription	Fetal Thymus	thymus
11	chr9:115635600-115649000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr9:115636000-115648600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr9:115638600-115650000	Weak transcription	Fetal Brain Female	brain
14	chr9:115643200-115652600	Weak transcription	Brain Anterior Caudate	brain
15	chr9:115643200-115652800	Weak transcription	Ovary	ovary
16	chr9:115643400-115651600	Weak transcription	Primary B cells from cord blood	blood
17	chr9:115643400-115652400	Weak transcription	Brain Substantia Nigra	brain
18	chr9:115643600-115650000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr9:115643600-115650400	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr9:115643600-115652200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr9:115643600-115652600	Weak transcription	Brain Angular Gyrus	brain
22	chr9:115643800-115650000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr9:115643800-115651800	Weak transcription	Lung	lung
24	chr9:115644000-115649000	Weak transcription	Fetal Intestine Large	intestine
25	chr9:115644000-115649400	Weak transcription	Fetal Muscle Leg	muscle
26	chr9:115644000-115649400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr9:115644000-115649600	Weak transcription	Fetal Intestine Small	intestine
28	chr9:115644000-115650800	Weak transcription	Aorta	Aorta
29	chr9:115644000-115651800	Weak transcription	Spleen	Spleen
30	chr9:115644000-115652000	Weak transcription	Pancreas	Pancrea
31	chr9:115644000-115652800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:115644200-115652200	Weak transcription	Adipose Nuclei	Adipose
33	chr9:115644200-115652200	Weak transcription	Brain Hippocampus Middle	brain
34	chr9:115644200-115652600	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr9:115644800-115650800	Weak transcription	Fetal Stomach	stomach
36	chr9:115645600-115651800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr9:115646000-115649000	Enhancers	Placenta Amnion	Placenta Amnion
38	chr9:115646600-115649600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr9:115646800-115651600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:115646800-115651800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr9:115647000-115652800	Weak transcription	HSMMtube	muscle
42	chr9:115647200-115652600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:115647400-115652200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr9:115647400-115652600	Weak transcription	HMEC	breast
45	chr9:115647400-115652600	Weak transcription	HSMM	muscle
46	chr9:115647600-115652200	Weak transcription	Osteobl	bone
47	chr9:115648600-115649800	Genic enhancers	Monocytes-CD14+_RO01746	blood
48	chr9:115649000-115650000	Genic enhancers	Primary monocytes fromperipheralblood	blood
49	chr9:115649600-115649800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr9:115649600-115650200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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