Variant report

Variant	nsv1033417
Chromosome Location	chr9:3594189-3732530
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	chr9:3607966-3608348	GM12878	blood:	n/a	n/a
2	ATF2	chr9:3730328-3731026	GM12878	blood:	n/a	n/a
3	ATF2	chr9:3607963-3608436	GM12878	blood:	n/a	n/a
4	ATF2	chr9:3730258-3731050	GM12878	blood:	n/a	n/a
5	BACH1	chr9:3604433-3604472	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:3689736-3689800	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:3730393-3730769	GM12878	blood:	n/a	n/a
8	BATF	chr9:3656298-3656558	GM12878	blood:	n/a	n/a
9	BATF	chr9:3730359-3730752	GM12878	blood:	n/a	n/a
10	BATF	chr9:3631375-3631642	GM12878	blood:	n/a	n/a
11	BATF	chr9:3608014-3608345	GM12878	blood:	n/a	n/a
12	BATF	chr9:3656318-3656576	GM12878	blood:	n/a	n/a
13	BATF	chr9:3607987-3608334	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:3608133-3608328	GM12878	blood:	n/a	n/a
15	BCL3	chr9:3651345-3651710	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:3608009-3608344	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:3651100-3651575	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:3730503-3730941	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:3661642-3661842	K562	blood:	n/a	n/a
20	BHLHE40	chr9:3648954-3649126	K562	blood:	n/a	n/a
21	BHLHE40	chr9:3607905-3608488	GM12878	blood:	n/a	n/a
22	CEBPB	chr9:3706611-3706974	HepG2	liver:	n/a	chr9:3706784-3706797 chr9:3706784-3706797 chr9:3706785-3706796 chr9:3706783-3706800 chr9:3706784-3706795
23	CEBPB	chr9:3706629-3706948	A549	lung:	n/a	chr9:3706784-3706797 chr9:3706784-3706797 chr9:3706785-3706796 chr9:3706783-3706800 chr9:3706784-3706795
24	CEBPB	chr9:3706616-3706966	IMR90	lung:	n/a	chr9:3706784-3706797 chr9:3706784-3706797 chr9:3706785-3706796 chr9:3706783-3706800 chr9:3706784-3706795
25	CEBPB	chr9:3650762-3650973	HepG2	liver:	n/a	chr9:3650859-3650872 chr9:3650856-3650873 chr9:3650859-3650870
26	CEBPB	chr9:3704902-3705209	HepG2	liver:	n/a	chr9:3705057-3705068 chr9:3705058-3705069 chr9:3705057-3705070 chr9:3705057-3705070 chr9:3705057-3705068
27	CEBPB	chr9:3618064-3618264	HepG2	liver:	n/a	chr9:3618137-3618148
28	CEBPB	chr9:3671154-3671354	A549	lung:	n/a	n/a
29	CEBPB	chr9:3704996-3705199	A549	lung:	n/a	chr9:3705057-3705068 chr9:3705058-3705069 chr9:3705057-3705070 chr9:3705057-3705070 chr9:3705057-3705068
30	CEBPB	chr9:3597102-3597242	HepG2	liver:	n/a	chr9:3597142-3597155 chr9:3597143-3597154 chr9:3597142-3597153
31	CEBPB	chr9:3649161-3649459	IMR90	lung:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
32	CEBPB	chr9:3642748-3642878	K562	blood:	n/a	chr9:3642822-3642833
33	CEBPB	chr9:3667036-3667296	IMR90	lung:	n/a	chr9:3667147-3667158
34	CEBPB	chr9:3649628-3649648	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr9:3649224-3649451	Hela-S3	cervix:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
36	CEBPB	chr9:3649165-3649500	HepG2	liver:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
37	CEBPB	chr9:3667037-3667287	A549	lung:	n/a	chr9:3667147-3667158
38	CEBPB	chr9:3649158-3649446	A549	lung:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
39	CEBPB	chr9:3603761-3603960	A549	lung:	n/a	chr9:3603896-3603907 chr9:3603896-3603909 chr9:3603896-3603909 chr9:3603896-3603907 chr9:3603874-3603886
40	CEBPB	chr9:3706657-3706902	K562	blood:	n/a	chr9:3706784-3706797 chr9:3706784-3706797 chr9:3706785-3706796 chr9:3706783-3706800 chr9:3706784-3706795
41	CEBPB	chr9:3704937-3705235	ECC-1	luminal epithelium:	n/a	chr9:3705057-3705068 chr9:3705058-3705069 chr9:3705057-3705070 chr9:3705057-3705070 chr9:3705057-3705068
42	CEBPB	chr9:3633690-3633806	K562	blood:	n/a	n/a
43	CEBPB	chr9:3633564-3633808	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:3642733-3642933	HepG2	liver:	n/a	chr9:3642822-3642833
45	CEBPB	chr9:3730360-3731175	GM12878	blood:	n/a	chr9:3730629-3730642
46	CEBPB	chr9:3708532-3709297	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr9:3667017-3667275	HepG2	liver:	n/a	chr9:3667147-3667158
48	CEBPB	chr9:3596987-3597185	A549	lung:	n/a	chr9:3597142-3597155 chr9:3597143-3597154 chr9:3597142-3597153
49	CEBPB	chr9:3651301-3651734	GM12878	blood:	n/a	n/a
50	CEBPB	chr9:3667066-3667291	H1-hESC	embryonic stem cell:	n/a	chr9:3667147-3667158

No.	Distal block	Cell Line	Cell type
1	chr9:3690355..3691926-chr9:3696454..3698344,2	MCF-7	breast:
2	chr9:3525115..3527683-chr9:3647759..3649608,2	MCF-7	breast:
3	chr9:3732366..3733251-chr9:4117087..4118391,3	K562	blood:
4	chr9:3605941..3608408-chr9:3657516..3659534,2	K562	blood:
5	chr9:3690355..3691926-chr9:3696454..3698344,2	MCF-7	breast:
6	chr9:3732396..3733264-chr9:3993863..3994418,3	MCF-7	breast:
7	chr9:3526118..3527672-chr9:3696360..3698362,2	MCF-7	breast:
8	chr9:3526287..3529194-chr9:3646038..3648964,2	K562	blood:
9	chr9:3710815..3712584-chr9:3716346..3718840,2	K562	blood:
10	chr9:3732447..3733442-chr9:4375097..4375609,2	MCF-7	breast:
11	chr9:3532661..3534867-chr9:3592564..3594236,2	K562	blood:
12	chr9:3732377..3733427-chr9:3848513..3849486,3	MCF-7	breast:
13	chr9:3594034..3597239-chr9:3602535..3604961,3	K562	blood:
14	chr13:45496976..45497802-chr9:3627604..3628338,2	Hela-S3	cervix:
15	chr9:3697208..3698903-chr9:3702495..3704955,2	MCF-7	breast:
16	chr9:3649975..3652712-chr9:3654160..3655972,2	K562	blood:
17	chr9:3684957..3686893-chr9:3690032..3691953,2	MCF-7	breast:
18	chr9:3732376..3733230-chr9:4197636..4198214,2	MCF-7	breast:
19	chr9:3732415..3733255-chr9:4228331..4229005,2	MCF-7	breast:
20	chr9:3684957..3686893-chr9:3690032..3691953,2	MCF-7	breast:
21	chr9:3605941..3608408-chr9:3657516..3659534,2	K562	blood:
22	chr9:3710815..3712584-chr9:3716346..3718840,2	K562	blood:
23	chr9:3697208..3698903-chr9:3702495..3704955,2	MCF-7	breast:
24	chr9:3655163..3657660-chr9:3672402..3674386,2	K562	blood:
25	chr9:3632578..3635092-chr9:3639764..3642505,2	MCF-7	breast:
26	chr9:3594034..3597239-chr9:3602535..3604961,3	K562	blood:
27	chr9:3632578..3635092-chr9:3639764..3642505,2	MCF-7	breast:
28	chr9:3649975..3652712-chr9:3654160..3655972,2	K562	blood:
29	chr9:3655163..3657660-chr9:3672402..3674386,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV2-3	chr9:3668086-3668408	ENSG00000232104
2	lnc-SLC1A1-5	chr9:3647754-3648338	ENSG00000237359
3	lnc-SLC1A1-4	chr9:3691504-3691814	ENSG00000235326
4	lnc-SLC1A1-13	chr9:3637335-3637477	NONHSAT130028
5	lnc-SLC1A1-4	chr9:3674546-3674648	ENSG00000235326
6	lnc-SLC1A1-12	chr9:3681504-3681814	NONHSAT130030
7	lnc-SLC1A1-12	chr9:3664411-3665024	l_3729_chr9:3656973-3664950_testes
8	lnc-KCNV2-3	chr9:3602523-3602584	ENSG00000232104.2
9	lnc-KCNV2-3	chr9:3606693-3606738	ENSG00000232104.2
10	lnc-GLIS3-1	chr9:3684076-3684459	XLOC_007633
11	lnc-SLC1A1-4	chr9:3690837-3690959	ENSG00000235326
12	lnc-SLC1A1-12	chr9:3664546-3664648	NONHSAT130030
13	lnc-KCNV2-3	chr9:3606693-3606738	ENSG00000232104
14	lnc-KCNV2-3	chr9:3671477-3671624	ENSG00000232104
15	lnc-SLC1A1-13	chr9:3637754-3638338	NONHSAT130028
16	lnc-SLC1A1-12	chr9:3680837-3680959	NONHSAT130030
17	lnc-SLC1A1-12	chr9:3661474-3661660	l_3729_chr9:3656973-3664950_testes
18	lnc-GLIS3-3	chr9:3679335-3679626	NONHSAT130032
19	lnc-GLIS3-1	chr9:3689335-3689626	XLOC_007633
20	lnc-SLC1A1-12	chr9:3656974-3658408	l_3729_chr9:3656973-3664950_testes
21	lnc-KCNV2-3	chr9:3671477-3671634	ENSG00000232104.2
22	lnc-SLC1A1-5	chr9:3647335-3647477	ENSG00000237359
23	lnc-GLIS3-1	chr9:3684076-3684459	ENSG00000226669.2
24	lnc-GLIS3-3	chr9:3674076-3674459	NONHSAT130032
25	lnc-KCNV2-3	chr9:3602535-3602584	ENSG00000232104
26	lnc-KCNV2-3	chr9:3671474-3671646	ENSG00000232104
27	lnc-GLIS3-1	chr9:3689332-3689626	ENSG00000226669.2

Variant related genes	Relation type
ENSG00000226669	TF binding region
ENSG00000232104	TF binding region
ENSG00000237359	TF binding region
ENSG00000235326	TF binding region
ENSG00000080298	chromatin interactions
ENSG00000107249	chromatin interactions
ENSG00000232104	chromatin interactions
KLF4	miRNA target sites

Extended variants
information (count: 4137 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:4137 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536946864	chr9:3600800-3600801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150466531	chr9:3600817-3600818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386731821	chr9:3600907-3600908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576955377	chr9:3600942-3600943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10120801	chr9:3600970-3600971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564347666	chr9:3600978-3600979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559029470	chr9:3601016-3601017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369188766	chr9:3601042-3601043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572523019	chr9:3601050-3601051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111951762	chr9:3601071-3601072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373165886	chr9:3601083-3601084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561256586	chr9:3601086-3601087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138210565	chr9:3601098-3601099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544072231	chr9:3601124-3601125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563763839	chr9:3601125-3601126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377054167	chr9:3601164-3601165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532962326	chr9:3601181-3601182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532764325	chr9:3601202-3601203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372930357	chr9:3601228-3601229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552449593	chr9:3601281-3601282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565447260	chr9:3601286-3601287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528165983	chr9:3601287-3601288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547830726	chr9:3601294-3601295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34499742	chr9:3601338-3601339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10758333	chr9:3601355-3601356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs190293573	chr9:3601364-3601365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117606290	chr9:3601403-3601404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570623150	chr9:3601436-3601437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551270621	chr9:3601445-3601446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180989826	chr9:3601466-3601467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183665660	chr9:3601587-3601588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149575707	chr9:3601698-3601699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541532822	chr9:3601716-3601717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146094322	chr9:3601762-3601763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138794692	chr9:3601782-3601783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188760059	chr9:3601789-3601790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543417468	chr9:3601807-3601808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530442581	chr9:3601814-3601815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546537137	chr9:3601821-3601822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577426331	chr9:3601871-3601872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550627241	chr9:3601880-3601881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546418480	chr9:3601998-3601999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559518977	chr9:3602010-3602011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1334069	chr9:3602018-3602019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs547867320	chr9:3602066-3602067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561414772	chr9:3602078-3602079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370765063	chr9:3602115-3602116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12346979	chr9:3602137-3602138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs7852723	chr9:3602147-3602148	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs7867712	chr9:3602170-3602171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
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
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
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3600800-3620400	Weak transcription	Ovary	ovary
2	chr9:3603400-3603800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr9:3603400-3603800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr9:3606400-3640400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr9:3607800-3608200	Enhancers	Primary B cells from peripheral blood	blood
6	chr9:3607800-3608400	Enhancers	GM12878-XiMat	blood
7	chr9:3610800-3611000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:3611600-3628000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr9:3611800-3612800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:3612600-3612800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:3612800-3613600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr9:3613000-3613400	Enhancers	HSMMtube	muscle
13	chr9:3613600-3619600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:3619600-3625600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:3619800-3620000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:3621400-3629600	Weak transcription	Brain Substantia Nigra	brain
17	chr9:3621800-3627800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:3622600-3626200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:3622800-3626000	Weak transcription	Pancreas	Pancrea
20	chr9:3623800-3625800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
21	chr9:3624000-3624800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:3624000-3626200	Weak transcription	Spleen	Spleen
23	chr9:3624000-3629800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr9:3624200-3627000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:3624800-3626400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:3625600-3626400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
27	chr9:3625800-3626000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
28	chr9:3626000-3626800	ZNF genes & repeats	Pancreas	Pancrea
29	chr9:3626000-3629400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr9:3626200-3626800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:3626200-3626800	ZNF genes & repeats	Spleen	Spleen
32	chr9:3626400-3627200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:3626400-3629400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr9:3626800-3627600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:3627000-3627400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr9:3627800-3628800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:3627800-3629800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:3628000-3630000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:3628000-3630000	Enhancers	Osteobl	bone
40	chr9:3628200-3629800	Enhancers	Adipose Nuclei	Adipose
41	chr9:3628200-3630000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr9:3628800-3629200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:3629000-3630000	Enhancers	Stomach Smooth Muscle	stomach
44	chr9:3629200-3629400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr9:3629400-3629600	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr9:3629400-3630000	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr9:3629600-3630000	Enhancers	Brain Substantia Nigra	brain
48	chr9:3629800-3630000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr9:3632200-3633600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr9:3644400-3644600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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