Variant report

Variant	nsv613047
Chromosome Location	chr9:802801-855091
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	ATF2	chr9:840342-840725	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:841437-841715	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
4	BATF	chr9:847470-847844	GM12878	blood:	n/a	n/a
5	BATF	chr9:847504-847840	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:840410-840568	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:852632-852864	GM12878	blood:	n/a	n/a
9	CEBPB	chr9:838394-838547	MCF-7	breast:	n/a	chr9:838455-838466
10	CEBPB	chr9:819788-820128	IMR90	lung:	n/a	chr9:819810-819821
11	CEBPB	chr9:819796-819940	K562	blood:	n/a	chr9:819810-819821
12	CEBPB	chr9:819922-820082	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:819807-820076	A549	lung:	n/a	chr9:819810-819821
14	CEBPB	chr9:838431-838470	HepG2	liver:	n/a	chr9:838455-838466
15	CEBPB	chr9:819700-819839	HepG2	liver:	n/a	chr9:819810-819821
16	CEBPB	chr9:812281-812423	HepG2	liver:	n/a	chr9:812339-812350
17	CEBPB	chr9:836594-836631	HepG2	liver:	n/a	chr9:836599-836610
18	CHD2	chr9:826666-826799	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr9:852634-852834	GM12878	blood:	n/a	n/a
20	CREB1	chr9:843173-843475	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr9:841342-842260	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr9:842540-843394	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr9:840294-840738	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr9:806990-807078	A549	lung:	n/a	n/a
25	CTCF	chr9:806620-806770	WI-38	lung:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
26	CTCF	chr9:806519-806969	GM12878	blood:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
27	CTCF	chr9:806660-806810	SAEC	small airway:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
28	CTCF	chr9:806680-806830	GM12864	blood:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
29	CTCF	chr9:847060-847210	GM12865	blood:	n/a	n/a
30	CTCF	chr9:840540-840690	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr9:806660-806810	GM12865	blood:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
32	CTCF	chr9:806993-807135	GM19238	blood:	n/a	n/a
33	CTCF	chr9:806660-806810	BJ	skin:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
34	CTCF	chr9:847123-847143	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:807100-807250	WI-38	lung:	n/a	n/a
36	CTCF	chr9:830221-830241	LNCaP	prostate:	n/a	n/a
37	CTCF	chr9:806660-806810	HBMEC	blood vessel:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
38	CTCF	chr9:815588-815656	GM10248	blood:	n/a	n/a
39	CTCF	chr9:806290-807165	A549	lung:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
40	CTCF	chr9:840434-840492	HUVEC	blood vessel:	n/a	chr9:840475-840488
41	CTCF	chr9:806700-806850	GM12865	blood:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
42	CTCF	chr9:806640-806790	RPTEC	kidney:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
43	CTCF	chr9:806639-806873	LNCaP	prostate:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
44	CTCF	chr9:806660-806810	HEEpiC	esophagus:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
45	CTCF	chr9:806658-806863	GM13977	blood:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
46	CTCF	chr9:806700-806850	HepG2	liver:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
47	CTCF	chr9:806700-806850	HRPEpiC	eye:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
48	CTCF	chr9:807017-807069	GM19240	blood:	n/a	n/a
49	CTCF	chr9:806680-806830	HCFaa	heart:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759
50	CTCF	chr9:806654-806882	Gliobla	brain:	n/a	chr9:806742-806758 chr9:806736-806757 chr9:806741-806759

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:843748-843798	MCF10A-Er-Src	breast:	n/a
2	chr9:841340-841390	HAEpiC	amniotic membrane:	n/a
3	chr9:843748-843798	MCF10A-Er-Src	breast:	n/a
4	chr9:841340-841390	HAEpiC	amniotic membrane:	n/a
5	chr9:841850-841900	BE2_C	brain:	n/a
6	chr9:839557-839607	GM12891	blood:	n/a
7	chr9:845427-845477	RPTEC	kidney:	n/a
8	chr9:842799-842849	GM19239	blood:	n/a
9	chr9:843179-843229	H1-hESC	embryonic stem cell:	embryo
10	chr9:843179-843229	CMK	blood:	n/a
11	chr9:841559-841609	ProgFib	skin:	n/a
12	chr9:845427-845477	MCF-7	breast:	n/a
13	chr9:841850-841900	NB4	blood:	n/a
14	chr9:842914-842964	NB4	blood:	n/a
15	chr9:843179-843229	HMEC	breast:	n/a
16	chr9:841559-841609	HUVEC	blood vessel:	n/a
17	chr9:845427-845477	HCF	heart:	n/a
18	chr9:841436-841486	GM12892	blood:	n/a
19	chr9:841850-841900	AG09319	gingival:	n/a
20	chr9:839126-839176	ECC-1	luminal epithelium:	n/a
21	chr9:841436-841486	SK-N-SH_RA	brain:	n/a
22	chr9:826657-826707	HEEpiC	esophagus:	n/a
23	chr9:841436-841486	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:841850-841900	NHDF-neo	bronchial:	n/a
25	chr9:841850-841900	GM12878	blood:	n/a
26	chr9:841340-841390	NHBE	bronchial:	n/a
27	chr9:843748-843798	Hepatocyte	liver:	n/a
28	chr9:841636-841686	ovcar-3	ovarian:	n/a
29	chr9:843179-843229	MCF10A-Er-Src	breast:	n/a
30	chr9:841559-841609	Hela-S3	cervix:	n/a
31	chr9:841632-841682	MCF10A-Er-Src	breast:	n/a
32	chr9:826657-826707	HCPEpiC	choroid plexus:	n/a
33	chr9:839126-839176	MCF-7	breast:	n/a
34	chr9:839557-839607	AG04449	skin:	fetal
35	chr9:839557-839607	GM19239	blood:	n/a
36	chr9:843748-843798	HEK293	kidney:	embryo
37	chr9:841850-841900	NH-A	brain:	n/a
38	chr9:841436-841486	HRCEpiC	kidney:	n/a
39	chr9:842799-842849	HCF	heart:	n/a
40	chr9:842799-842849	PrEC	prostate:	n/a
41	chr9:841850-841900	PrEC	prostate:	n/a
42	chr9:845427-845477	BE2_C	brain:	n/a
43	chr9:842799-842849	AG10803	skin:	n/a
44	chr9:843179-843229	HCF	heart:	n/a
45	chr9:841340-841390	RPTEC	kidney:	n/a
46	chr9:841340-841390	HRPEpiC	eye:	n/a
47	chr9:839126-839176	U87	brain:	n/a
48	chr9:841559-841609	PANC-1	pancreas:	n/a
49	chr9:842799-842849	AG09309	skin:	n/a
50	chr9:845427-845477	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
2	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
3	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
4	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
5	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
6	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
7	chr9:852085..854136-chr9:910104..912950,2	K562	blood:
8	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
9	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
10	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
11	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
12	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
13	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
14	chr9:845876..848526-chr9:868544..871068,2	MCF-7	breast:
15	chr9:706377..708156-chr9:805249..808005,2	MCF-7	breast:
16	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
17	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
18	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:

Variant related genes	Relation type
DMRT1	TF binding region
DMRT1	CpG island
ENSG00000107104	chromatin interactions

Extended variants
information (count: 1608 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2370200	chr9:802801-802802	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577567349	chr9:802814-802815	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538649066	chr9:802850-802851	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs558552127	chr9:802949-802950	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544455824	chr9:802982-802983	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs572067013	chr9:802991-802992	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs13288334	chr9:802999-803000	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs35396494	chr9:803003-803004	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs13285288	chr9:803008-803009	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543356537	chr9:803026-803027	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs554307766	chr9:803054-803055	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373173085	chr9:803064-803065	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs567611954	chr9:803078-803079	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs376376586	chr9:803079-803080	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs563242932	chr9:803081-803082	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs536663313	chr9:803091-803092	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs74910769	chr9:803095-803096	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs545815662	chr9:803134-803135	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs10976679	chr9:803158-803159	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs143165833	chr9:803183-803184	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs180976795	chr9:803187-803188	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs78932677	chr9:803236-803237	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs531141314	chr9:803237-803238	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs551156492	chr9:803269-803270	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368044409	chr9:803291-803292	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs377434205	chr9:803342-803343	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571178433	chr9:803350-803351	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs551675079	chr9:803367-803368	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs10976681	chr9:803442-803443	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs76769238	chr9:803445-803446	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs184207683	chr9:803471-803472	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs146708045	chr9:803473-803474	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs574402669	chr9:803475-803476	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs10120425	chr9:803481-803482	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs370736004	chr9:803493-803494	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs370873999	chr9:803497-803498	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs545678330	chr9:803505-803506	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs10815720	chr9:803506-803507	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs541813974	chr9:803507-803508	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs562223151	chr9:803522-803523	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs530993592	chr9:803567-803568	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs567501044	chr9:803579-803580	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs10119680	chr9:803606-803607	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs139374183	chr9:803614-803615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142722840	chr9:803619-803620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533700642	chr9:803623-803624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547301510	chr9:803625-803626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs60587682	chr9:803634-803635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561054184	chr9:803635-803636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565585733	chr9:803657-803658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Ependymoma	20639864	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:794600-809600	Weak transcription	Right Atrium	heart
2	chr9:801400-803600	Flanking Active TSS	HUVEC	blood vessel
3	chr9:802200-805000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr9:802400-803000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr9:802600-805000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:802800-804200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:802800-804200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:802800-805000	Weak transcription	NHEK	skin
9	chr9:802800-808800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:802800-811600	Weak transcription	HMEC	breast
11	chr9:803000-808800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:803600-804000	Enhancers	HUVEC	blood vessel
13	chr9:804000-804600	Flanking Active TSS	HUVEC	blood vessel
14	chr9:804200-804400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:804200-804400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:804400-804800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr9:804600-805800	Enhancers	HUVEC	blood vessel
18	chr9:804800-805600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr9:805000-805600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:805000-805600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr9:805000-805600	Enhancers	NHEK	skin
22	chr9:805600-810200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:805600-810600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:805600-810800	Weak transcription	NHEK	skin
25	chr9:805800-806200	Weak transcription	HUVEC	blood vessel
26	chr9:806200-806800	Enhancers	Dnd41	blood
27	chr9:806200-806800	Enhancers	HUVEC	blood vessel
28	chr9:806400-807200	Enhancers	HepG2	liver
29	chr9:806800-807000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:807000-810200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:808800-809000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr9:808800-809200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:808800-809200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
34	chr9:809000-809200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr9:809200-811200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:810200-811400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:810200-811800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr9:810400-811000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:810400-811800	Enhancers	Colon Smooth Muscle	Colon
40	chr9:810400-811800	Enhancers	A549	lung
41	chr9:810600-811400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr9:810600-811800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr9:810800-811600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr9:810800-811800	Enhancers	NHEK	skin
45	chr9:811000-811800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr9:811000-811800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr9:811200-811600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr9:811200-811600	Enhancers	NH-A	brain
49	chr9:811400-811800	Enhancers	Rectal Smooth Muscle	rectum
50	chr9:811600-811800	Enhancers	HMEC	breast

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