Variant report

Variant	nsv892092
Chromosome Location	chr9:3565211-3687942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:369)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr9:3607963-3608436	GM12878	blood:	n/a	n/a
3	BACH1	chr9:3604433-3604472	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr9:3608014-3608345	GM12878	blood:	n/a	n/a
5	BATF	chr9:3656298-3656558	GM12878	blood:	n/a	n/a
6	BATF	chr9:3656318-3656576	GM12878	blood:	n/a	n/a
7	BATF	chr9:3607987-3608334	GM12878	blood:	n/a	n/a
8	BATF	chr9:3631375-3631642	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:3608133-3608328	GM12878	blood:	n/a	n/a
10	BCL3	chr9:3651345-3651710	GM12878	blood:	n/a	n/a
11	BCLAF1	chr9:3608009-3608344	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:3651100-3651575	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:3607905-3608488	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:3661642-3661842	K562	blood:	n/a	n/a
15	BHLHE40	chr9:3648954-3649126	K562	blood:	n/a	n/a
16	CEBPB	chr9:3649161-3649459	IMR90	lung:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
17	CEBPB	chr9:3578803-3579146	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:3570813-3571048	HepG2	liver:	n/a	chr9:3570924-3570935
19	CEBPB	chr9:3649224-3649451	Hela-S3	cervix:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
20	CEBPB	chr9:3650762-3650973	HepG2	liver:	n/a	chr9:3650859-3650872 chr9:3650856-3650873 chr9:3650859-3650870
21	CEBPB	chr9:3649158-3649446	A549	lung:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
22	CEBPB	chr9:3633690-3633806	K562	blood:	n/a	n/a
23	CEBPB	chr9:3570806-3570986	K562	blood:	n/a	chr9:3570924-3570935
24	CEBPB	chr9:3671154-3671354	A549	lung:	n/a	n/a
25	CEBPB	chr9:3667020-3667258	K562	blood:	n/a	chr9:3667147-3667158
26	CEBPB	chr9:3603761-3603960	A549	lung:	n/a	chr9:3603896-3603907 chr9:3603896-3603909 chr9:3603896-3603909 chr9:3603896-3603907 chr9:3603874-3603886
27	CEBPB	chr9:3649165-3649500	HepG2	liver:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
28	CEBPB	chr9:3570787-3571080	IMR90	lung:	n/a	chr9:3570924-3570935
29	CEBPB	chr9:3649628-3649648	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:3596987-3597185	A549	lung:	n/a	chr9:3597142-3597155 chr9:3597143-3597154 chr9:3597142-3597153
31	CEBPB	chr9:3642748-3642878	K562	blood:	n/a	chr9:3642822-3642833
32	CEBPB	chr9:3667036-3667296	IMR90	lung:	n/a	chr9:3667147-3667158
33	CEBPB	chr9:3597102-3597242	HepG2	liver:	n/a	chr9:3597142-3597155 chr9:3597143-3597154 chr9:3597142-3597153
34	CEBPB	chr9:3594978-3595127	HepG2	liver:	n/a	chr9:3595051-3595068
35	CEBPB	chr9:3667066-3667291	H1-hESC	embryonic stem cell:	n/a	chr9:3667147-3667158
36	CEBPB	chr9:3649175-3649477	K562	blood:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
37	CEBPB	chr9:3633564-3633808	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:3570795-3571076	A549	lung:	n/a	chr9:3570924-3570935
39	CEBPB	chr9:3667037-3667287	A549	lung:	n/a	chr9:3667147-3667158
40	CEBPB	chr9:3671067-3671327	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:3667017-3667275	HepG2	liver:	n/a	chr9:3667147-3667158
42	CEBPB	chr9:3651301-3651734	GM12878	blood:	n/a	n/a
43	CEBPB	chr9:3642733-3642933	HepG2	liver:	n/a	chr9:3642822-3642833
44	CEBPB	chr9:3618064-3618264	HepG2	liver:	n/a	chr9:3618137-3618148
45	CHD1	chr9:3572466-3572512	GM12878	blood:	n/a	n/a
46	CHD1	chr9:3651104-3651525	GM12878	blood:	n/a	n/a
47	CHD2	chr9:3651207-3651583	GM12878	blood:	n/a	n/a
48	CTCF	chr9:3652374-3652449	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr9:3647780-3647922	GM12878	blood:	n/a	n/a
50	CTCF	chr9:3647880-3648030	HRPEpiC	eye:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:3655163..3657660-chr9:3672402..3674386,2	K562	blood:
2	chr9:3632578..3635092-chr9:3639764..3642505,2	MCF-7	breast:
3	chr9:3605941..3608408-chr9:3657516..3659534,2	K562	blood:
4	chr13:45496976..45497802-chr9:3627604..3628338,2	Hela-S3	cervix:
5	chr9:3532661..3534867-chr9:3592564..3594236,2	K562	blood:
6	chr9:3594034..3597239-chr9:3602535..3604961,3	K562	blood:
7	chr9:3649975..3652712-chr9:3654160..3655972,2	K562	blood:
8	chr9:3684957..3686893-chr9:3690032..3691953,2	MCF-7	breast:
9	chr9:3605941..3608408-chr9:3657516..3659534,2	K562	blood:
10	chr9:3594034..3597239-chr9:3602535..3604961,3	K562	blood:
11	chr9:3632578..3635092-chr9:3639764..3642505,2	MCF-7	breast:
12	chr9:3566363..3569263-chr9:3574839..3576405,2	MCF-7	breast:
13	chr9:3649975..3652712-chr9:3654160..3655972,2	K562	blood:
14	chr9:3531967..3534867-chr9:3591369..3594064,2	K562	blood:
15	chr9:3526287..3529194-chr9:3646038..3648964,2	K562	blood:
16	chr9:3525115..3527683-chr9:3647759..3649608,2	MCF-7	breast:
17	chr9:3561040..3563255-chr9:3569242..3571583,2	K562	blood:
18	chr9:3566363..3569263-chr9:3574839..3576405,2	MCF-7	breast:
19	chr9:3655163..3657660-chr9:3672402..3674386,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC1A1-5	chr9:3647754-3648338	ENSG00000237359
2	lnc-KCNV2-3	chr9:3602535-3602584	ENSG00000232104
3	lnc-KCNV2-3	chr9:3671477-3671634	ENSG00000232104.2
4	lnc-GLIS3-1	chr9:3684076-3684459	ENSG00000226669.2
5	lnc-KCNV2-3	chr9:3568794-3568889	ENSG00000232104.2
6	lnc-SLC1A1-12	chr9:3681504-3681814	NONHSAT130030
7	lnc-SLC1A1-12	chr9:3680837-3680959	NONHSAT130030
8	lnc-SLC1A1-5	chr9:3647335-3647477	ENSG00000237359
9	lnc-KCNV2-3	chr9:3668086-3668408	ENSG00000232104
10	lnc-SLC1A1-4	chr9:3674546-3674648	ENSG00000235326
11	lnc-KCNV2-3	chr9:3606693-3606738	ENSG00000232104
12	lnc-KCNV2-3	chr9:3602523-3602584	ENSG00000232104.2
13	lnc-SLC1A1-12	chr9:3664546-3664648	NONHSAT130030
14	lnc-KCNV2-3	chr9:3606693-3606738	ENSG00000232104.2
15	lnc-GLIS3-1	chr9:3684076-3684459	XLOC_007633
16	lnc-KCNV2-3	chr9:3671474-3671646	ENSG00000232104
17	lnc-GLIS3-3	chr9:3674076-3674459	NONHSAT130032
18	lnc-KCNV2-3	chr9:3671477-3671624	ENSG00000232104
19	lnc-KCNV2-3	chr9:3568794-3568890	ENSG00000232104
20	lnc-SLC1A1-12	chr9:3661474-3661660	l_3729_chr9:3656973-3664950_testes
21	lnc-GLIS3-3	chr9:3679335-3679626	NONHSAT130032
22	lnc-SLC1A1-12	chr9:3656974-3658408	l_3729_chr9:3656973-3664950_testes
23	lnc-SLC1A1-13	chr9:3637335-3637477	NONHSAT130028
24	lnc-SLC1A1-12	chr9:3664411-3665024	l_3729_chr9:3656973-3664950_testes
25	lnc-SLC1A1-13	chr9:3637754-3638338	NONHSAT130028

No data

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

Extended variants
information (count: 4342 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4342 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7864107	chr9:3565211-3565212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572146783	chr9:3565216-3565217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375577378	chr9:3565222-3565223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541052124	chr9:3565227-3565228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561651799	chr9:3565255-3565256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575051080	chr9:3565291-3565292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34249659	chr9:3565334-3565335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76139618	chr9:3565367-3565368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563880301	chr9:3565470-3565471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs117597155	chr9:3565475-3565476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193105848	chr9:3565483-3565484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150296927	chr9:3565492-3565493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185878656	chr9:3565498-3565499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547855294	chr9:3565515-3565516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76858461	chr9:3565531-3565532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138678680	chr9:3565532-3565533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550421656	chr9:3565574-3565575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137858429	chr9:3565606-3565607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556176927	chr9:3565625-3565626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114270533	chr9:3565632-3565633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572185533	chr9:3565645-3565646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149460884	chr9:3565650-3565651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180996282	chr9:3565717-3565718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs202033203	chr9:3565725-3565726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574732959	chr9:3565824-3565825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543761475	chr9:3565838-3565839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185176342	chr9:3565884-3565885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577555363	chr9:3565892-3565893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188773296	chr9:3565897-3565898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78285005	chr9:3565958-3565959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548209851	chr9:3565974-3565975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528196153	chr9:3566011-3566012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181109533	chr9:3566041-3566042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555448504	chr9:3566052-3566053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561539033	chr9:3566068-3566069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530480618	chr9:3566072-3566073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373625261	chr9:3566077-3566078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530736413	chr9:3566084-3566085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186800770	chr9:3566103-3566104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117016816	chr9:3566110-3566111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532987694	chr9:3566151-3566152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371097179	chr9:3566210-3566211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147316731	chr9:3566323-3566324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369860241	chr9:3566328-3566329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566623625	chr9:3566329-3566330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554999192	chr9:3566351-3566352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568410401	chr9:3566452-3566453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372262408	chr9:3566465-3566466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537445482	chr9:3566511-3566512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557724097	chr9:3566514-3566515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3527400-3567600	Weak transcription	Ovary	ovary
2	chr9:3529000-3579000	Weak transcription	HSMMtube	muscle
3	chr9:3531000-3575800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr9:3531800-3579000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:3547600-3572800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:3549400-3570200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr9:3549800-3572800	Weak transcription	Right Ventricle	heart
8	chr9:3550000-3566000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:3550000-3593000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr9:3551000-3571200	Weak transcription	Thymus	Thymus
11	chr9:3554400-3576000	Weak transcription	Adipose Nuclei	Adipose
12	chr9:3554400-3576400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr9:3554400-3579400	Weak transcription	Left Ventricle	heart
14	chr9:3554600-3569400	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr9:3554800-3578000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:3560800-3571000	Weak transcription	Fetal Muscle Trunk	muscle
17	chr9:3560800-3571400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr9:3562800-3568000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr9:3563200-3565400	Weak transcription	Lung	lung
20	chr9:3563600-3566000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr9:3563800-3566000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr9:3563800-3567200	Weak transcription	Primary B cells from peripheral blood	blood
23	chr9:3563800-3576200	Weak transcription	Primary B cells from cord blood	blood
24	chr9:3563800-3578200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr9:3565200-3568400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:3567600-3568000	Enhancers	Fetal Heart	heart
27	chr9:3567600-3568800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr9:3568400-3569800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr9:3568800-3571600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr9:3569400-3570400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr9:3569600-3570400	Enhancers	Psoas Muscle	Psoas
32	chr9:3569800-3572400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:3570000-3570200	Enhancers	Aorta	Aorta
34	chr9:3570200-3570400	Enhancers	Stomach Smooth Muscle	stomach
35	chr9:3570200-3579400	Weak transcription	Aorta	Aorta
36	chr9:3570400-3579200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr9:3571200-3573000	Enhancers	HUVEC	blood vessel
38	chr9:3571600-3571800	Enhancers	Fetal Brain Female	brain
39	chr9:3571600-3571800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr9:3572200-3573400	Weak transcription	Fetal Brain Female	brain
41	chr9:3572400-3572800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr9:3572400-3572800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:3572800-3575600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:3572800-3575800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:3573400-3574200	Enhancers	Fetal Brain Female	brain
46	chr9:3575600-3576400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr9:3575800-3576000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr9:3575800-3576000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr9:3575800-3576800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr9:3575800-3576800	Enhancers	Primary hematopoietic stem cells	blood

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