Variant report

Variant	nsv613652
Chromosome Location	chr9:15579744-15661859
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	chr9:15642421-15642732	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15606729-15607013	HepG2	liver:	n/a	n/a
3	ATF1	chr9:15606159-15606277	K562	blood:	n/a	n/a
4	ATF3	chr9:15587162-15587411	K562	blood:	n/a	n/a
5	BATF	chr9:15612994-15613254	GM12878	blood:	n/a	chr9:15613158-15613169
6	BATF	chr9:15613003-15613305	GM12878	blood:	n/a	chr9:15613158-15613169
7	CEBPB	chr9:15634699-15634857	A549	lung:	n/a	chr9:15634719-15634730
8	CEBPB	chr9:15587156-15587411	K562	blood:	n/a	chr9:15587301-15587312
9	CEBPB	chr9:15587130-15587433	IMR90	lung:	n/a	chr9:15587301-15587312
10	CEBPB	chr9:15634610-15635086	IMR90	lung:	n/a	chr9:15634719-15634730
11	CEBPB	chr9:15587167-15587391	HepG2	liver:	n/a	chr9:15587301-15587312
12	CEBPB	chr9:15616839-15617368	HepG2	liver:	n/a	chr9:15617185-15617196
13	CEBPB	chr9:15634650-15635051	HepG2	liver:	n/a	chr9:15634719-15634730
14	CREB1	chr9:15612874-15613444	GM12878	blood:	n/a	n/a
15	CREB1	chr9:15613014-15613393	GM12878	blood:	n/a	n/a
16	CTCF	chr9:15617123-15617222	GM10248	blood:	n/a	n/a
17	CTCF	chr9:15642377-15642663	HepG2	liver:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
18	CTCF	chr9:15606780-15606930	GM12864	blood:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
19	CTCF	chr9:15620260-15620410	HMF	breast:	n/a	n/a
20	CTCF	chr9:15642400-15642550	HBMEC	blood vessel:	n/a	chr9:15642528-15642549 chr9:15642535-15642548
21	CTCF	chr9:15620520-15620670	HVMF	connective:	n/a	n/a
22	CTCF	chr9:15620280-15620550	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr9:15642420-15642570	GM12871	blood:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
24	CTCF	chr9:15642420-15642570	AG04449	skin:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
25	CTCF	chr9:15606740-15606890	HCM	heart:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
26	CTCF	chr9:15606720-15606870	GM12870	blood:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
27	CTCF	chr9:15606760-15606910	HEK293	kidney:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
28	CTCF	chr9:15622740-15622890	HMEC	breast:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
29	CTCF	chr9:15622740-15622890	HMF	breast:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
30	CTCF	chr9:15656120-15656270	MCF-7	breast:	n/a	n/a
31	CTCF	chr9:15606820-15606970	GM12872	blood:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
32	CTCF	chr9:15607000-15607150	HAc	cerebellar:	n/a	n/a
33	CTCF	chr9:15656244-15656294	GM12892	blood:	n/a	n/a
34	CTCF	chr9:15606740-15606890	MCF-7	breast:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
35	CTCF	chr9:15606708-15607006	Spleen_OC	spleen:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
36	CTCF	chr9:15622720-15622870	HMEC	breast:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
37	CTCF	chr9:15642500-15642650	HCT-116	colon:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
38	CTCF	chr9:15606720-15606870	SAEC	small airway:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
39	CTCF	chr9:15642432-15642569	GM20000	blood:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
40	CTCF	chr9:15642440-15642590	Hela-S3	cervix:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
41	CTCF	chr9:15606760-15606910	NB4	blood:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
42	CTCF	chr9:15642360-15642510	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr9:15606780-15606930	HFF	foreskin:	n/a	chr9:15606836-15606849 chr9:15606829-15606850 chr9:15606834-15606852 chr9:15606835-15606851 chr9:15606839-15606847
44	CTCF	chr9:15606800-15606950	AG04450	lung:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
45	CTCF	chr9:15642460-15642610	WERI-Rb-1	eye:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
46	CTCF	chr9:15642371-15642780	HCT-116	colon:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
47	CTCF	chr9:15642560-15642710	HAc	cerebellar:	n/a	n/a
48	CTCF	chr9:15642480-15642630	HBMEC	blood vessel:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
49	CTCF	chr9:15622700-15622850	HA-sp	spinal cord:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
50	CTCF	chr9:15606800-15606950	HPF	lung:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850

No.	Distal block	Cell Line	Cell type
1	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
2	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
3	chr9:15421567..15424446-chr9:15606338..15608598,2	MCF-7	breast:
4	chr9:15551543..15553297-chr9:15600119..15601625,2	MCF-7	breast:
5	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
6	chr9:15509144..15511285-chr9:15608383..15610950,2	MCF-7	breast:
7	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-4	chr9:15588353-15588613	NONHSAT130276

Variant related genes	Relation type
HMGN2P16	TF binding region
ENSG00000164985	chromatin interactions
ENSG00000164975	chromatin interactions
ENSG00000164989	chromatin interactions

Extended variants
information (count: 4418 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4418 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3129710	chr9:15579744-15579745	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550831304	chr9:15579845-15579846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569366825	chr9:15579881-15579882	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143188585	chr9:15579882-15579883	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571422548	chr9:15579928-15579929	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551708485	chr9:15579943-15579944	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566765412	chr9:15579974-15579975	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534476733	chr9:15579975-15579976	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148263449	chr9:15580029-15580030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140113064	chr9:15580071-15580072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538039397	chr9:15580072-15580073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189386996	chr9:15580100-15580101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537109329	chr9:15580122-15580123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181702851	chr9:15580123-15580124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557703107	chr9:15580169-15580170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185122307	chr9:15580210-15580211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150304208	chr9:15580285-15580286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190020490	chr9:15580287-15580288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574026757	chr9:15580302-15580303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544419053	chr9:15580328-15580329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563645312	chr9:15580431-15580432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs137889705	chr9:15580454-15580455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181082723	chr9:15580482-15580483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10120805	chr9:15580509-15580510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557425850	chr9:15580511-15580512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189576178	chr9:15580541-15580542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536634008	chr9:15580550-15580551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567615158	chr9:15580567-15580568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375829942	chr9:15580571-15580572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538152285	chr9:15580573-15580574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549921352	chr9:15580574-15580575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562285277	chr9:15580644-15580645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201690767	chr9:15580645-15580646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528019855	chr9:15580661-15580662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181947942	chr9:15580669-15580670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143566340	chr9:15580721-15580722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147165475	chr9:15580765-15580766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138480006	chr9:15580810-15580811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186411501	chr9:15580842-15580843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190860046	chr9:15580862-15580863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183850833	chr9:15580887-15580888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188189514	chr9:15580896-15580897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368862474	chr9:15580952-15580953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544530228	chr9:15580965-15580966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191469939	chr9:15580969-15580970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201560263	chr9:15581081-15581082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577888164	chr9:15581097-15581098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200006252	chr9:15581211-15581212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545221518	chr9:15581213-15581214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560372781	chr9:15581264-15581265	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
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15553800-15580600	Weak transcription	Ovary	ovary
2	chr9:15553800-15592600	Weak transcription	Left Ventricle	heart
3	chr9:15554000-15590200	Weak transcription	Fetal Stomach	stomach
4	chr9:15554600-15580800	Weak transcription	Brain Anterior Caudate	brain
5	chr9:15562200-15588200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr9:15562400-15583800	Weak transcription	Thymus	Thymus
7	chr9:15572400-15580800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:15574600-15580000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr9:15578600-15580000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:15578800-15580400	Strong transcription	Fetal Thymus	thymus
11	chr9:15579400-15590200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr9:15580000-15587000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr9:15580000-15587600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr9:15580400-15581000	Weak transcription	Fetal Thymus	thymus
15	chr9:15580800-15582200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:15581000-15581600	Strong transcription	Fetal Thymus	thymus
17	chr9:15581600-15583000	Weak transcription	Fetal Thymus	thymus
18	chr9:15582200-15583200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:15583000-15583400	ZNF genes & repeats	Fetal Thymus	thymus
20	chr9:15583200-15584400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:15583400-15584800	Enhancers	Fetal Thymus	thymus
22	chr9:15583600-15584800	Enhancers	Placenta	Placenta
23	chr9:15583800-15586000	Enhancers	Thymus	Thymus
24	chr9:15584000-15585000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr9:15584400-15584800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr9:15584400-15585000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr9:15584400-15585800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr9:15584400-15588600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr9:15584600-15584800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr9:15584600-15585400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr9:15584600-15585400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr9:15584600-15585600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr9:15584600-15585800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:15584800-15585200	Weak transcription	Fetal Thymus	thymus
35	chr9:15584800-15585600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr9:15584800-15585600	Weak transcription	Placenta	Placenta
37	chr9:15585200-15585600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr9:15585200-15586000	Enhancers	Fetal Thymus	thymus
39	chr9:15585400-15585600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr9:15585600-15585800	Enhancers	Placenta	Placenta
41	chr9:15586000-15587000	Weak transcription	Fetal Thymus	thymus
42	chr9:15586000-15588200	Weak transcription	Thymus	Thymus
43	chr9:15587000-15587200	ZNF genes & repeats	Fetal Thymus	thymus
44	chr9:15587000-15588400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:15587000-15620400	Weak transcription	Pancreas	Pancrea
46	chr9:15587200-15588200	Weak transcription	Fetal Thymus	thymus
47	chr9:15587600-15588600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr9:15588200-15588600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr9:15588200-15589400	Enhancers	Fetal Thymus	thymus
50	chr9:15588200-15589400	Enhancers	Thymus	Thymus

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