Variant report

Variant	nsv892617
Chromosome Location	chr9:14791348-14889834
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	chr9:14882074-14882476	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14868526-14869963	HepG2	liver:	n/a	chr9:14869168-14869184 chr9:14869167-14869183
3	ARID3A	chr9:14888518-14888791	HepG2	liver:	n/a	n/a
4	ATF1	chr9:14797561-14797747	K562	blood:	n/a	n/a
5	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr9:14812818-14813170	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:14831736-14831957	K562	blood:	n/a	n/a
8	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
9	CEBPB	chr9:14799005-14799390	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
10	CEBPB	chr9:14799044-14799407	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
11	CEBPB	chr9:14868569-14869669	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:14799109-14799362	H1-hESC	embryonic stem cell:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
13	CEBPB	chr9:14827709-14827960	HepG2	liver:	n/a	chr9:14827827-14827838
14	CEBPB	chr9:14884179-14884475	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:14799137-14799326	Hela-S3	cervix:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
16	CEBPB	chr9:14799070-14799407	IMR90	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
17	CEBPB	chr9:14799087-14799406	A549	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
18	CEBPB	chr9:14799060-14799419	K562	blood:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
19	CEBPB	chr9:14877121-14877303	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:14799051-14799431	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
21	CEBPB	chr9:14827792-14827904	IMR90	lung:	n/a	chr9:14827827-14827838
22	CEBPB	chr9:14799112-14799348	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
23	CEBPB	chr9:14799090-14799366	MCF-7	breast:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
24	CEBPD	chr9:14799130-14799332	HepG2	liver:	n/a	n/a
25	CEBPD	chr9:14868715-14869298	HepG2	liver:	n/a	n/a
26	CEBPD	chr9:14869355-14869588	HepG2	liver:	n/a	n/a
27	CHD2	chr9:14846832-14847123	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr9:14846857-14847057	HepG2	liver:	n/a	n/a
29	CHD2	chr9:14818253-14818267	GM12878	blood:	n/a	n/a
30	CHD2	chr9:14868700-14869330	HepG2	liver:	n/a	n/a
31	CREB1	chr9:14846723-14847119	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr9:14846688-14847074	HCT-116	colon:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
33	CTCF	chr9:14846880-14847030	AG04449	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
34	CTCF	chr9:14846780-14846930	HVMF	connective:	n/a	n/a
35	CTCF	chr9:14846763-14847185	GM12878	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
36	CTCF	chr9:14846840-14846990	NHLF	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
37	CTCF	chr9:14882649-14882719	GM20000	blood:	n/a	n/a
38	CTCF	chr9:14846860-14847010	GM12872	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
39	CTCF	chr9:14846900-14847050	NB4	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
40	CTCF	chr9:14846880-14847030	HAc	cerebellar:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
41	CTCF	chr9:14846860-14847010	NHDF-neo	bronchial:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
42	CTCF	chr9:14846880-14847030	HPF	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
43	CTCF	chr9:14846823-14847039	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
44	CTCF	chr9:14846880-14847030	Caco-2	colon:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
45	CTCF	chr9:14846940-14847090	HL-60	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
46	CTCF	chr9:14846880-14847030	SAEC	small airway:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
47	CTCF	chr9:14846837-14847088	GM13977	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
48	CTCF	chr9:14846800-14846950	WI-38	lung:	n/a	n/a
49	CTCF	chr9:14863420-14863570	AG09319	gingival:	n/a	chr9:14863556-14863564 chr9:14863551-14863569
50	CTCF	chr9:14846860-14847010	WERI-Rb-1	eye:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14838752-14838802	Jurkat	blood:	n/a
2	chr9:14883945-14883995	HRPEpiC	eye:	n/a
3	chr9:14883945-14883995	HMEC	breast:	n/a
4	chr9:14838752-14838802	U87	brain:	n/a
5	chr9:14838752-14838802	HepG2	liver:	n/a
6	chr9:14838752-14838802	BJ	skin:	n/a
7	chr9:14838752-14838802	SK-N-MC	brain:	n/a
8	chr9:14883945-14883995	NHDF-neo	bronchial:	n/a
9	chr9:14883945-14883995	U87	brain:	n/a
10	chr9:14838752-14838802	AG09319	gingival:	n/a
11	chr9:14883945-14883995	GM12878	blood:	n/a
12	chr9:14883945-14883995	ovcar-3	ovarian:	n/a
13	chr9:14883945-14883995	HCT-116	colon:	n/a
14	chr9:14838752-14838802	GM12892	blood:	n/a
15	chr9:14883945-14883995	HCPEpiC	choroid plexus:	n/a
16	chr9:14838752-14838802	LNCaP	prostate:	n/a
17	chr9:14838752-14838802	NHDF-neo	bronchial:	n/a
18	chr9:14883945-14883995	BJ	skin:	n/a
19	chr9:14883945-14883995	HCM	heart:	n/a
20	chr9:14838752-14838802	Hepatocyte	liver:	n/a
21	chr9:14838752-14838802	HCF	heart:	n/a
22	chr9:14883945-14883995	ECC-1	luminal epithelium:	n/a
23	chr9:14883945-14883995	NB4	blood:	n/a
24	chr9:14838752-14838802	PFSK-1	brain:	n/a
25	chr9:14838752-14838802	GM12891	blood:	n/a
26	chr9:14838752-14838802	HCM	heart:	n/a
27	chr9:14883945-14883995	HCF	heart:	n/a
28	chr9:14883945-14883995	AG10803	skin:	n/a
29	chr9:14838752-14838802	SAEC	small airway:	n/a
30	chr9:14838752-14838802	IMR90	lung:	fetal
31	chr9:14838752-14838802	HMEC	breast:	n/a
32	chr9:14883945-14883995	HRE	kidney:	n/a
33	chr9:14838752-14838802	AoSMC	blood vessel:	n/a
34	chr9:14883945-14883995	PANC-1	pancreas:	n/a
35	chr9:14883945-14883995	SK-N-MC	brain:	n/a
36	chr9:14883945-14883995	SAEC	small airway:	n/a
37	chr9:14838752-14838802	HRCEpiC	kidney:	n/a
38	chr9:14883945-14883995	HEK293	kidney:	embryo
39	chr9:14883945-14883995	AG09319	gingival:	n/a
40	chr9:14883945-14883995	SK-N-SH	brain:	n/a
41	chr9:14838752-14838802	SK-N-SH_RA	brain:	n/a
42	chr9:14838752-14838802	HEK293	kidney:	embryo
43	chr9:14838752-14838802	PrEC	prostate:	n/a
44	chr9:14883945-14883995	HL-60	blood:	n/a
45	chr9:14838752-14838802	SK-N-SH	brain:	n/a
46	chr9:14883945-14883995	Hela-S3	cervix:	n/a
47	chr9:14883945-14883995	HRCEpiC	kidney:	n/a
48	chr9:14883945-14883995	SKMC	muscle:	n/a
49	chr9:14838752-14838802	HAEpiC	amniotic membrane:	n/a
50	chr9:14883945-14883995	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
2	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:
3	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
4	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
5	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
6	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
7	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
8	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
9	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:

Variant related genes	Relation type
RNU6-1260P	TF binding region
FREM1	TF binding region
RNU6-1260P	CpG island
FREM1	CpG island
ENSG00000175893	chromatin interactions
ENSG00000199814	chromatin interactions
ENSG00000251960	chromatin interactions

Extended variants
information (count: 5172 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5172 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13296345	chr9:14791348-14791349	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368518280	chr9:14791377-14791378	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568234757	chr9:14791415-14791416	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183666464	chr9:14791427-14791428	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529215902	chr9:14791428-14791429	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs16932288	chr9:14791444-14791445	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs561452510	chr9:14791461-14791462	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368162049	chr9:14791504-14791505	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1389734	chr9:14791505-14791506	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543996032	chr9:14791536-14791537	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35006983	chr9:14791558-14791559	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535208293	chr9:14791626-14791627	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4740588	chr9:14791627-14791628	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs143432352	chr9:14791636-14791637	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555030528	chr9:14791642-14791643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527697012	chr9:14791660-14791661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs16932291	chr9:14791678-14791679	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567777243	chr9:14791708-14791709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1389733	chr9:14791715-14791716	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs189291710	chr9:14791728-14791729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7031082	chr9:14791729-14791730	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571773205	chr9:14791731-14791732	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539289687	chr9:14791758-14791759	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560312168	chr9:14791759-14791760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376820059	chr9:14791776-14791777	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552992539	chr9:14791785-14791786	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200311022	chr9:14791818-14791819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371184244	chr9:14791819-14791820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143891787	chr9:14791834-14791835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34769166	chr9:14791839-14791840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117744611	chr9:14791846-14791847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199553182	chr9:14791847-14791848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572460570	chr9:14791865-14791866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141417030	chr9:14791888-14791889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111974505	chr9:14791918-14791919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554986564	chr9:14791921-14791922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180850744	chr9:14791922-14791923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2201379	chr9:14791923-14791924	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs373032431	chr9:14791926-14791927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560465944	chr9:14791928-14791929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187649570	chr9:14791929-14791930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561297793	chr9:14791943-14791944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191916002	chr9:14791953-14791954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377343831	chr9:14791954-14791955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181690152	chr9:14791997-14791998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571776873	chr9:14792004-14792005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56371878	chr9:14792016-14792017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144354617	chr9:14792022-14792023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566024853	chr9:14792024-14792025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536583187	chr9:14792027-14792028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
3	chr9:14758400-14793400	Weak transcription	Aorta	Aorta
4	chr9:14764800-14809600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:14768600-14808800	Weak transcription	Fetal Intestine Small	intestine
6	chr9:14773400-14796400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:14776200-14794000	Weak transcription	Fetal Stomach	stomach
8	chr9:14779200-14798600	Strong transcription	Fetal Kidney	kidney
9	chr9:14779800-14853200	Weak transcription	Placenta	Placenta
10	chr9:14780400-14795800	Weak transcription	Left Ventricle	heart
11	chr9:14780400-14843200	Weak transcription	Fetal Heart	heart
12	chr9:14782000-14822000	Weak transcription	Fetal Brain Male	brain
13	chr9:14782800-14822000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr9:14783600-14800200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:14784400-14791400	Weak transcription	Fetal Muscle Leg	muscle
16	chr9:14786800-14814400	Strong transcription	Fetal Lung	lung
17	chr9:14787200-14793800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr9:14787600-14792000	Strong transcription	Fetal Muscle Trunk	muscle
19	chr9:14788400-14806800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:14789200-14793400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:14789400-14809200	Weak transcription	Fetal Intestine Large	intestine
22	chr9:14790200-14797800	Strong transcription	Adipose Nuclei	Adipose
23	chr9:14790400-14793600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:14790400-14795400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:14790800-14791800	Strong transcription	Duodenum Mucosa	Duodenum
26	chr9:14790800-14792000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:14791000-14791600	Strong transcription	Colon Smooth Muscle	Colon
28	chr9:14791000-14791600	Genic enhancers	HepG2	liver
29	chr9:14791200-14801600	Weak transcription	Small Intestine	intestine
30	chr9:14791400-14791600	Genic enhancers	Fetal Muscle Leg	muscle
31	chr9:14791600-14791800	Enhancers	Fetal Muscle Leg	muscle
32	chr9:14791600-14793800	Weak transcription	Colon Smooth Muscle	Colon
33	chr9:14791600-14799200	Strong transcription	HepG2	liver
34	chr9:14791800-14793200	Weak transcription	Fetal Muscle Leg	muscle
35	chr9:14791800-14796000	Weak transcription	Duodenum Mucosa	Duodenum
36	chr9:14792000-14793400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr9:14792000-14795600	Weak transcription	Fetal Muscle Trunk	muscle
38	chr9:14793000-14822600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr9:14793200-14794000	Strong transcription	Fetal Muscle Leg	muscle
40	chr9:14793400-14794400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr9:14793400-14794600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr9:14793400-14794800	Strong transcription	Aorta	Aorta
43	chr9:14793600-14794000	ZNF genes & repeats	Gastric	stomach
44	chr9:14793600-14799400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:14793800-14795600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr9:14793800-14798200	Strong transcription	Colon Smooth Muscle	Colon
47	chr9:14794000-14794800	Strong transcription	Fetal Stomach	stomach
48	chr9:14794000-14806400	Weak transcription	Fetal Muscle Leg	muscle
49	chr9:14794400-14797200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr9:14794600-14797200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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