Variant report

Variant	nsv540055
Chromosome Location	chr9:12031527-12302913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:12170667-12170713	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:12292536-12292567	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:12230772-12231081	GM12878	blood:	n/a	n/a
4	CBX3	chr9:12054451-12054644	K562	blood:	n/a	n/a
5	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
7	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
8	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
9	CEBPB	chr9:12119993-12120079	A549	lung:	n/a	chr9:12120059-12120068 chr9:12120057-12120070 chr9:12120057-12120068
10	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
11	CEBPB	chr9:12129071-12129335	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:12288039-12288167	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084
14	CEBPB	chr9:12208833-12209071	HepG2	liver:	n/a	chr9:12208898-12208909 chr9:12208899-12208908 chr9:12208897-12208910
15	CTCF	chr9:12101680-12101830	GM12869	blood:	n/a	n/a
16	CTCF	chr9:12148949-12149036	Fibrobl	skin:	n/a	n/a
17	CTCF	chr9:12224065-12224152	GM13976	blood:	n/a	n/a
18	CTCF	chr9:12092315-12092389	MCF-7	breast:	n/a	n/a
19	CTCF	chr9:12215488-12215552	GM13977	blood:	n/a	n/a
20	CTCF	chr9:12076206-12076321	GM10266	blood:	n/a	n/a
21	CTCF	chr9:12195600-12195750	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr9:12092280-12092430	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr9:12076187-12076204	GM10248	blood:	n/a	n/a
24	CTCF	chr9:12115897-12115954	GM10248	blood:	n/a	n/a
25	CTCF	chr9:12195520-12195670	HMF	breast:	n/a	n/a
26	CTCF	chr9:12053853-12053871	GM20000	blood:	n/a	n/a
27	CTCF	chr9:12219290-12219372	GM13976	blood:	n/a	n/a
28	CTCF	chr9:12195560-12195710	HEK293	kidney:	n/a	n/a
29	CTCF	chr9:12230966-12231007	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr9:12195560-12195710	HMF	breast:	n/a	n/a
31	CTCF	chr9:12100160-12100310	NB4	blood:	n/a	n/a
32	CTCF	chr9:12210667-12210803	GM10248	blood:	n/a	n/a
33	CTCF	chr9:12041004-12041085	GM20000	blood:	n/a	n/a
34	CTCF	chr9:12180880-12181030	HEK293	kidney:	n/a	n/a
35	CTCF	chr9:12092304-12092357	MCF-7	breast:	n/a	n/a
36	CTCF	chr9:12055107-12055140	GM13976	blood:	n/a	n/a
37	CTCF	chr9:12210677-12210803	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr9:12219074-12219108	GM10248	blood:	n/a	n/a
39	CTCF	chr9:12078782-12078864	LNCaP	prostate:	n/a	n/a
40	CTCF	chr9:12264400-12264550	HFF	foreskin:	n/a	n/a
41	CTCF	chr9:12041600-12041634	GM20000	blood:	n/a	n/a
42	CTCF	chr9:12231143-12231170	GM20000	blood:	n/a	n/a
43	CTCF	chr9:12045540-12045690	HPF	lung:	n/a	n/a
44	CTCF	chr9:12142395-12142451	LNCaP	prostate:	n/a	n/a
45	CTCF	chr9:12180880-12181030	GM12878	blood:	n/a	n/a
46	CTCF	chr9:12195600-12195750	NHEK	skin:	n/a	n/a
47	CTCF	chr9:12195560-12195710	AoAF	blood vessel:	n/a	n/a
48	CUX1	chr9:12116986-12116993	GM12878	blood:	n/a	n/a
49	CUX1	chr9:12230853-12230855	GM12878	blood:	n/a	n/a
50	E2F4	chr9:12185683-12185754	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
2	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
3	chr18:21570976..21573123-chr9:12145530..12147030,2	MCF-7	breast:
4	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
5	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
6	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
7	chr16:89002000..89004763-chr9:12244429..12246932,2	MCF-7	breast:
8	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TYRP1-4	chr9:12287320-12288238	NONHSAT130222
2	lnc-MPDZ-9	chr9:12088660-12089015	NONHSAT130219
3	lnc-MPDZ-2	chr9:12139007-12139044	XLOC_007648
4	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
5	lnc-MPDZ-9	chr9:12136273-12136401	NONHSAT130219
6	lnc-MPDZ-9	chr9:12106821-12106865	NONHSAT130219
7	lnc-MPDZ-2	chr9:12146273-12146401	XLOC_007648
8	lnc-MPDZ-2	chr9:12098660-12099015	XLOC_007648
9	lnc-MPDZ-2	chr9:12098714-12099015	XLOC_007648
10	lnc-MPDZ-9	chr9:12149117-12149147	NONHSAT130219
11	lnc-MPDZ-2	chr9:12159117-12159147	XLOC_007648
12	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648

No data

Variant related genes	Relation type
ENSG00000231491	TF binding region
ENSG00000224935	TF binding region
RNU2-47P	TF binding region
ENSG00000168234	chromatin interactions
ENSG00000261226	chromatin interactions

Extended variants
information (count: 4148 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4148 , 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	rs528852537	chr9:12046404-12046405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs7020425	chr9:12046411-12046412	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs534097114	chr9:12046417-12046418	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs566014967	chr9:12046437-12046438	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs534914173	chr9:12046441-12046442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs557924683	chr9:12046446-12046447	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs150147222	chr9:12046465-12046466	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs537155793	chr9:12046468-12046469	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs557401386	chr9:12046520-12046521	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs573968496	chr9:12046606-12046607	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs191538847	chr9:12046652-12046653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs555728371	chr9:12046714-12046715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs572368846	chr9:12046721-12046722	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs185359804	chr9:12046746-12046747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs76000719	chr9:12046755-12046756	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs577865693	chr9:12046770-12046771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs79328172	chr9:12046780-12046781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs561530657	chr9:12046782-12046783	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs138585241	chr9:12046785-12046786	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs374471262	chr9:12046796-12046797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs548940541	chr9:12046798-12046799	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs559664908	chr9:12046802-12046803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528748104	chr9:12046803-12046804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1446270	chr9:12046808-12046809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12339814	chr9:12046842-12046843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs79607502	chr9:12046852-12046853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149287702	chr9:12046917-12046918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147274012	chr9:12046940-12046941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75156649	chr9:12046965-12046966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540100973	chr9:12046966-12046967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573234581	chr9:12046986-12046987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374274245	chr9:12047004-12047005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4741200	chr9:12047033-12047034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs140789212	chr9:12047047-12047048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188177574	chr9:12047054-12047055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75559880	chr9:12047069-12047070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116390018	chr9:12047095-12047096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78367083	chr9:12047098-12047099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573675909	chr9:12047105-12047106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193260559	chr9:12047115-12047116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73646869	chr9:12047131-12047132	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185511427	chr9:12047135-12047136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75794439	chr9:12047146-12047147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565225532	chr9:12047158-12047159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531041026	chr9:12047159-12047160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140220846	chr9:12047182-12047183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567695406	chr9:12047203-12047204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367613507	chr9:12047253-12047254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542252318	chr9:12047255-12047256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189650557	chr9:12047258-12047259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Disorders of sex development	21048976	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
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12046400-12046800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:12046800-12048000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:12048000-12048400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:12054200-12054600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:12057600-12059000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:12058400-12060400	Enhancers	Fetal Intestine Large	intestine
7	chr9:12059000-12060000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr9:12060000-12065800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:12060200-12060400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr9:12060400-12061400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:12060400-12065000	Weak transcription	Fetal Intestine Large	intestine
12	chr9:12061400-12061800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr9:12061400-12062000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr9:12061600-12061800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr9:12061800-12064200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr9:12064200-12065600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr9:12065000-12065800	Enhancers	Fetal Intestine Large	intestine
18	chr9:12076400-12076600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
19	chr9:12076400-12076800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:12076600-12076800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
21	chr9:12091200-12096400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr9:12091600-12092600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:12091800-12092200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr9:12092600-12096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:12096200-12096400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:12096400-12101600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:12101600-12102200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr9:12101600-12102400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr9:12101800-12102800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:12102400-12104200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr9:12104200-12104400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr9:12135800-12137400	Enhancers	Fetal Heart	heart
33	chr9:12137600-12138400	Enhancers	Placenta Amnion	Placenta Amnion
34	chr9:12137800-12138200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr9:12139800-12142600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr9:12142400-12144000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:12155400-12156200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:12156200-12161400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:12161400-12167200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:12161600-12164800	Enhancers	Brain Germinal Matrix	brain
41	chr9:12162200-12162400	Active TSS	Brain Anterior Caudate	brain
42	chr9:12162200-12162600	Active TSS	Brain Angular Gyrus	brain
43	chr9:12162200-12162800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr9:12162200-12163200	Enhancers	Fetal Brain Female	brain
45	chr9:12162400-12162600	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr9:12162400-12162600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr9:12162400-12162800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:12162400-12163000	Enhancers	Brain Hippocampus Middle	brain
49	chr9:12162600-12162800	Enhancers	Brain Anterior Caudate	brain
50	chr9:12162600-12163000	Enhancers	Brain Angular Gyrus	brain

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