Variant report

Variant	nsv549469
Chromosome Location	chr1:242842300-243080523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:928)
CpG islands
(count:611)
Chromatin interactive
region (count:24)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:928 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:242976778-242977056	GM12878	blood:	n/a	n/a
2	BACH1	chr1:242848092-242848258	K562	blood:	n/a	n/a
3	BACH1	chr1:242907415-242907671	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:242918799-242919176	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:242996994-242996997	K562	blood:	n/a	n/a
6	BACH1	chr1:242908535-242908689	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
8	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
9	BCL3	chr1:242843343-242843676	GM12878	blood:	n/a	n/a
10	BCL3	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:243031757-243031938	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:242976782-242977230	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:242954012-242954043	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
16	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
17	CEBPB	chr1:242933600-242934106	A549	lung:	n/a	n/a
18	CEBPB	chr1:242933686-242933998	A549	lung:	n/a	n/a
19	CEBPB	chr1:242914758-242914854	A549	lung:	n/a	chr1:242914783-242914796
20	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
21	CEBPB	chr1:242899978-242900301	A549	lung:	n/a	chr1:242900141-242900152
22	CEBPB	chr1:242933698-242934016	A549	lung:	n/a	n/a
23	CEBPB	chr1:242955789-242955931	A549	lung:	n/a	n/a
24	CEBPB	chr1:242998985-242999533	A549	lung:	n/a	n/a
25	CEBPB	chr1:242899993-242900287	HepG2	liver:	n/a	chr1:242900141-242900152
26	CEBPB	chr1:242874257-242874306	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:242890951-242891053	A549	lung:	n/a	n/a
28	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
29	CEBPB	chr1:242861497-242861649	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
31	CHD1	chr1:242976654-242977278	GM12878	blood:	n/a	n/a
32	CHD2	chr1:243005456-243005619	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr1:242991732-242991777	HepG2	liver:	n/a	n/a
34	CHD2	chr1:242976690-242977268	GM12878	blood:	n/a	n/a
35	CTCF	chr1:242956626-242957056	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:242882408-242882518	H1-hESC	embryonic stem cell:	n/a	chr1:242882453-242882471 chr1:242882459-242882468
37	CTCF	chr1:243005340-243005490	GM12872	blood:	n/a	n/a
38	CTCF	chr1:243005520-243005670	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr1:243049620-243049764	GM19238	blood:	n/a	n/a
40	CTCF	chr1:242991678-242991788	Fibrobl	skin:	n/a	chr1:242991719-242991740
41	CTCF	chr1:243004440-243004467	K562	blood:	n/a	n/a
42	CTCF	chr1:242980516-242980539	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:242991845-242991851	GM19239	blood:	n/a	n/a
44	CTCF	chr1:243005574-243005603	GM13977	blood:	n/a	n/a
45	CTCF	chr1:243005455-243005673	GM12878	blood:	n/a	n/a
46	CTCF	chr1:242853922-242853995	K562	blood:	n/a	n/a
47	CTCF	chr1:242991611-242991888	A549	lung:	n/a	chr1:242991719-242991740
48	CTCF	chr1:243005540-243005690	GM12864	blood:	n/a	n/a
49	CTCF	chr1:242955775-242955849	GM13976	blood:	n/a	n/a
50	CTCF	chr1:242956785-242956973	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243053673-243053723	HIPEpiC	eye:	n/a
2	chr1:243053673-243053723	HIPEpiC	eye:	n/a
3	chr1:242936925-242936975	AG10803	skin:	n/a
4	chr1:243053673-243053723	NT2-D1	testis:	n/a
5	chr1:243057080-243057130	BJ	skin:	n/a
6	chr1:243053934-243053984	HEEpiC	esophagus:	n/a
7	chr1:243054071-243054121	HMEC	breast:	n/a
8	chr1:243053934-243053984	BE2_C	brain:	n/a
9	chr1:243053673-243053723	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:243050875-243050925	SK-N-SH	brain:	n/a
11	chr1:242937866-242937916	K562	blood:	n/a
12	chr1:243053425-243053475	HepG2	liver:	n/a
13	chr1:243054071-243054121	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:243053673-243053723	AG10803	skin:	n/a
15	chr1:242937866-242937916	HNPCEpiC	eye:	n/a
16	chr1:243057080-243057130	AoSMC	blood vessel:	n/a
17	chr1:243057080-243057130	HRE	kidney:	n/a
18	chr1:243053673-243053723	SK-N-SH	brain:	n/a
19	chr1:242874219-242874269	A549	lung:	n/a
20	chr1:243053865-243053915	PFSK-1	brain:	n/a
21	chr1:242936925-242936975	AG04450	lung:	fetal
22	chr1:243053865-243053915	IMR90	lung:	fetal
23	chr1:243053673-243053723	Hepatocyte	liver:	n/a
24	chr1:243057080-243057130	Hela-S3	cervix:	n/a
25	chr1:243054071-243054121	BE2_C	brain:	n/a
26	chr1:243053865-243053915	HRE	kidney:	n/a
27	chr1:242936925-242936975	Hepatocyte	liver:	n/a
28	chr1:243053865-243053915	HCF	heart:	n/a
29	chr1:242937866-242937916	RPTEC	kidney:	n/a
30	chr1:243053934-243053984	PFSK-1	brain:	n/a
31	chr1:242874219-242874269	HepG2	liver:	n/a
32	chr1:243057080-243057130	ProgFib	skin:	n/a
33	chr1:243054071-243054121	SAEC	small airway:	n/a
34	chr1:242874219-242874269	HCT-116	colon:	n/a
35	chr1:243053425-243053475	HEEpiC	esophagus:	n/a
36	chr1:243053934-243053984	HCPEpiC	choroid plexus:	n/a
37	chr1:243057080-243057130	RPTEC	kidney:	n/a
38	chr1:243053673-243053723	GM12878	blood:	n/a
39	chr1:243053425-243053475	NHBE	bronchial:	n/a
40	chr1:242937866-242937916	SAEC	small airway:	n/a
41	chr1:243057080-243057130	PFSK-1	brain:	n/a
42	chr1:243053934-243053984	HIPEpiC	eye:	n/a
43	chr1:243054071-243054121	HIPEpiC	eye:	n/a
44	chr1:242936925-242936975	IMR90	lung:	fetal
45	chr1:243053425-243053475	BJ	skin:	n/a
46	chr1:243050875-243050925	HAEpiC	amniotic membrane:	n/a
47	chr1:243050875-243050925	ProgFib	skin:	n/a
48	chr1:243053934-243053984	GM12878	blood:	n/a
49	chr1:243053425-243053475	AG04450	lung:	fetal
50	chr1:243053934-243053984	AoSMC	blood vessel:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
2	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
3	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
4	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
5	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
6	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
7	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
8	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
9	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
10	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
11	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
12	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
13	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
14	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
15	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
16	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
17	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
18	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
19	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
20	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
21	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
22	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
23	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
24	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
2	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
3	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
4	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
5	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-

No data

Variant related genes	Relation type
ENSG00000270818	TF binding region
RSL24D1P4	TF binding region
ENSG00000264972	TF binding region
ENSG00000270818	CpG island
RSL24D1P4	CpG island
ENSG00000264972	CpG island

Extended variants
information (count: 6241 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:6241 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5020631	chr1:242842300-242842301	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1413208	chr1:242842313-242842314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs1413207	chr1:242842320-242842321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs539612388	chr1:242842353-242842354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574325816	chr1:242842422-242842423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528840588	chr1:242842568-242842569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186633907	chr1:242842614-242842615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147817837	chr1:242842640-242842641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528228996	chr1:242842646-242842647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560508090	chr1:242842660-242842661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557990120	chr1:242842687-242842688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141472667	chr1:242842718-242842719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571839329	chr1:242842724-242842725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10926820	chr1:242842787-242842788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557589083	chr1:242842850-242842851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116201968	chr1:242842878-242842879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536644055	chr1:242842906-242842907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113984735	chr1:242842958-242842959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199687148	chr1:242842960-242842961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200666410	chr1:242842961-242842962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10544129	chr1:242842962-242842963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79607319	chr1:242842965-242842966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371318017	chr1:242842969-242842970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200797574	chr1:242842975-242842976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7547934	chr1:242842981-242842982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572988671	chr1:242842997-242842998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573004261	chr1:242843016-242843017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190254354	chr1:242843060-242843061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558650975	chr1:242843067-242843068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149960732	chr1:242843083-242843084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182465417	chr1:242843090-242843091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145060356	chr1:242843121-242843122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148932089	chr1:242843129-242843130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188487755	chr1:242843147-242843148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116478784	chr1:242843287-242843288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115800086	chr1:242843323-242843324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193052162	chr1:242843344-242843345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143652502	chr1:242843465-242843466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185613027	chr1:242843466-242843467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144035115	chr1:242843543-242843544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550938465	chr1:242843546-242843547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370043721	chr1:242843548-242843549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6674422	chr1:242843549-242843550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188887693	chr1:242843559-242843560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114495744	chr1:242843564-242843565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566501924	chr1:242843570-242843571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111306123	chr1:242843677-242843678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200505282	chr1:242843680-242843681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546936078	chr1:242843686-242843687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200529017	chr1:242843693-242843694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242838200-242854000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr1:242843200-242843600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:242843600-242852600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:242850400-242850600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:242850600-242852800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:242852600-242853200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:242852600-242853200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:242852800-242853200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:242852800-242853200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:242853200-242854400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:242853200-242855000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:242853800-242854400	Enhancers	Ovary	ovary
13	chr1:242854000-242854200	Enhancers	Brain Hippocampus Middle	brain
14	chr1:242854000-242854200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr1:242854000-242854200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr1:242854200-242854400	Enhancers	Brain Angular Gyrus	brain
17	chr1:242854200-242854600	Flanking Active TSS	Brain Hippocampus Middle	brain
18	chr1:242854200-242854600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
19	chr1:242854200-242854600	Enhancers	Gastric	stomach
20	chr1:242854200-242854800	Active TSS	Brain Substantia Nigra	brain
21	chr1:242854200-242854800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
22	chr1:242854200-242854800	Enhancers	Spleen	Spleen
23	chr1:242854200-242855800	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr1:242854400-242854600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:242854400-242854600	Flanking Active TSS	Brain Angular Gyrus	brain
26	chr1:242854400-242854800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr1:242854400-242855000	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr1:242854400-242855000	Active TSS	Brain Anterior Caudate	brain
29	chr1:242854400-242855000	Active TSS	Brain Cingulate Gyrus	brain
30	chr1:242854400-242855000	Enhancers	Fetal Muscle Trunk	muscle
31	chr1:242854400-242855000	Flanking Active TSS	Ovary	ovary
32	chr1:242854400-242855200	Enhancers	Fetal Muscle Leg	muscle
33	chr1:242854400-242855400	Enhancers	Brain Germinal Matrix	brain
34	chr1:242854600-242854800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:242854600-242855000	Enhancers	Primary B cells from peripheral blood	blood
36	chr1:242854600-242855000	Active TSS	Brain Angular Gyrus	brain
37	chr1:242854600-242855000	Active TSS	Brain Hippocampus Middle	brain
38	chr1:242854600-242855000	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr1:242854800-242855000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:242854800-242855200	Flanking Active TSS	Brain Substantia Nigra	brain
41	chr1:242854800-242855200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr1:242855000-242855200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:242855000-242855200	Enhancers	Brain Angular Gyrus	brain
44	chr1:242855000-242855200	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr1:242855000-242855200	Enhancers	Brain Cingulate Gyrus	brain
46	chr1:242855000-242855200	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr1:242855000-242855400	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr1:242855000-242855400	Enhancers	Ovary	ovary
49	chr1:242855200-242855400	Enhancers	Brain Substantia Nigra	brain
50	chr1:242855800-242856200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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