Variant report

Variant	nsv525391
Chromosome Location	chr1:225912620-225928538
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	chr1:225919372-225919570	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:225923238-225923871	HepG2	liver:	n/a	n/a
3	ATF3	chr1:225923121-225923863	A549	lung:	n/a	n/a
4	ATF3	chr1:225923070-225923765	A549	lung:	n/a	n/a
5	BCL3	chr1:225924483-225924702	GM12878	blood:	n/a	n/a
6	BCL3	chr1:225923164-225924035	A549	lung:	n/a	n/a
7	BCL3	chr1:225923169-225924031	A549	lung:	n/a	n/a
8	BRCA1	chr1:225923201-225925446	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:225926291-225926605	A549	lung:	n/a	chr1:225926441-225926452
10	CEBPB	chr1:225922960-225925434	Hela-S3	cervix:	n/a	chr1:225924703-225924714 chr1:225923420-225923433 chr1:225924702-225924715 chr1:225924702-225924715 chr1:225923420-225923431 chr1:225923246-225923258
11	CEBPB	chr1:225924473-225925338	A549	lung:	n/a	chr1:225924703-225924714 chr1:225924702-225924715 chr1:225924702-225924715
12	CEBPB	chr1:225917239-225917308	H1-hESC	embryonic stem cell:	n/a	chr1:225917262-225917273
13	CEBPB	chr1:225926276-225926620	Hela-S3	cervix:	n/a	chr1:225926441-225926452
14	CEBPB	chr1:225926279-225926574	IMR90	lung:	n/a	chr1:225926441-225926452
15	CEBPB	chr1:225926316-225926571	HepG2	liver:	n/a	chr1:225926441-225926452
16	CEBPB	chr1:225917222-225917366	K562	blood:	n/a	chr1:225917262-225917273
17	CEBPB	chr1:225924479-225924892	HepG2	liver:	n/a	chr1:225924703-225924714 chr1:225924702-225924715 chr1:225924702-225924715
18	CEBPB	chr1:225924313-225925235	A549	lung:	n/a	chr1:225924703-225924714 chr1:225924702-225924715 chr1:225924702-225924715
19	CEBPB	chr1:225917156-225917377	HepG2	liver:	n/a	chr1:225917262-225917273
20	CEBPB	chr1:225922916-225923985	ECC-1	luminal epithelium:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
21	CEBPB	chr1:225924985-225925268	MCF-7	breast:	n/a	n/a
22	CEBPB	chr1:225922980-225924038	A549	lung:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
23	CEBPB	chr1:225926285-225926608	K562	blood:	n/a	chr1:225926441-225926452
24	CEBPB	chr1:225924469-225925031	IMR90	lung:	n/a	chr1:225924703-225924714 chr1:225924702-225924715 chr1:225924702-225924715
25	CEBPB	chr1:225923039-225923956	A549	lung:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
26	CEBPB	chr1:225923170-225923929	HepG2	liver:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
27	CEBPB	chr1:225923027-225923992	IMR90	lung:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
28	CEBPB	chr1:225917176-225917352	HepG2	liver:	n/a	chr1:225917262-225917273
29	CEBPB	chr1:225923035-225923661	ECC-1	luminal epithelium:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
30	CEBPB	chr1:225923059-225923964	A549	lung:	n/a	chr1:225923420-225923433 chr1:225923420-225923431 chr1:225923246-225923258
31	CEBPB	chr1:225917227-225917309	IMR90	lung:	n/a	chr1:225917262-225917273
32	CEBPB	chr1:225926398-225926590	H1-hESC	embryonic stem cell:	n/a	chr1:225926441-225926452
33	CHD2	chr1:225924423-225925310	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr1:225923133-225923913	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr1:225923380-225923900	A549	lung:	n/a	n/a
36	CREB1	chr1:225924915-225925130	A549	lung:	n/a	n/a
37	CTCF	chr1:225923660-225923810	BE2_C	brain:	n/a	chr1:225923737-225923758
38	CTCF	chr1:225923640-225923790	AG10803	skin:	n/a	chr1:225923737-225923758
39	CTCF	chr1:225923680-225923830	AG04450	lung:	n/a	chr1:225923737-225923758
40	CTCF	chr1:225923640-225923790	AG09319	gingival:	n/a	chr1:225923737-225923758
41	CTCF	chr1:225923672-225923767	A549	lung:	n/a	chr1:225923737-225923758
42	CTCF	chr1:225923640-225923790	AG04449	skin:	n/a	chr1:225923737-225923758
43	CTCF	chr1:225923680-225923830	SK-N-SH_RA	brain:	n/a	chr1:225923737-225923758
44	CTCF	chr1:225923680-225923830	HEEpiC	esophagus:	n/a	chr1:225923737-225923758
45	CTCF	chr1:225923620-225923770	AG10803	skin:	n/a	chr1:225923737-225923758
46	CTCF	chr1:225923619-225923825	NHEK	skin:	n/a	chr1:225923737-225923758
47	CTCF	chr1:225923600-225923750	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr1:225923684-225923793	Hela-S3	cervix:	n/a	chr1:225923737-225923758
49	CTCF	chr1:225923720-225923870	AoAF	blood vessel:	n/a	chr1:225923737-225923758
50	CTCF	chr1:225923680-225923830	HFF	foreskin:	n/a	chr1:225923737-225923758

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225924665-225924715	SK-N-SH	brain:	n/a
2	chr1:225924665-225924715	SK-N-SH	brain:	n/a
3	chr1:225924665-225924715	SKMC	muscle:	n/a
4	chr1:225924665-225924715	MCF10A-Er-Src	breast:	n/a
5	chr1:225924665-225924715	MCF-7	breast:	n/a
6	chr1:225924665-225924715	H1-hESC	embryonic stem cell:	embryo
7	chr1:225924665-225924715	AG04449	skin:	fetal
8	chr1:225924665-225924715	GM19239	blood:	n/a
9	chr1:225924665-225924715	HIPEpiC	eye:	n/a
10	chr1:225924665-225924715	ovcar-3	ovarian:	n/a
11	chr1:225924665-225924715	AG09309	skin:	n/a
12	chr1:225924665-225924715	BE2_C	brain:	n/a
13	chr1:225924665-225924715	NHDF-neo	bronchial:	n/a
14	chr1:225924665-225924715	NHBE	bronchial:	n/a
15	chr1:225924665-225924715	AG04450	lung:	fetal
16	chr1:225924665-225924715	Hepatocyte	liver:	n/a
17	chr1:225924665-225924715	HUVEC	blood vessel:	n/a
18	chr1:225924665-225924715	SAEC	small airway:	n/a
19	chr1:225924665-225924715	GM12878	blood:	n/a
20	chr1:225924665-225924715	HCT-116	colon:	n/a
21	chr1:225924665-225924715	GM12892	blood:	n/a
22	chr1:225924665-225924715	HCM	heart:	n/a
23	chr1:225924665-225924715	RPTEC	kidney:	n/a
24	chr1:225924665-225924715	ECC-1	luminal epithelium:	n/a
25	chr1:225924665-225924715	HRPEpiC	eye:	n/a
26	chr1:225924665-225924715	NH-A	brain:	n/a
27	chr1:225924665-225924715	LNCaP	prostate:	n/a
28	chr1:225924665-225924715	SK-N-SH_RA	brain:	n/a
29	chr1:225924665-225924715	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:225924665-225924715	ProgFib	skin:	n/a
31	chr1:225924665-225924715	IMR90	lung:	fetal
32	chr1:225924665-225924715	BJ	skin:	n/a
33	chr1:225924665-225924715	PFSK-1	brain:	n/a
34	chr1:225924665-225924715	AoSMC	blood vessel:	n/a
35	chr1:225924665-225924715	HEEpiC	esophagus:	n/a
36	chr1:225924665-225924715	HRE	kidney:	n/a
37	chr1:225924665-225924715	HL-60	blood:	n/a
38	chr1:225924665-225924715	NB4	blood:	n/a
39	chr1:225924665-225924715	CMK	blood:	n/a
40	chr1:225924665-225924715	K562	blood:	n/a
41	chr1:225924665-225924715	SK-N-MC	brain:	n/a
42	chr1:225924665-225924715	AG09319	gingival:	n/a
43	chr1:225924665-225924715	NT2-D1	testis:	n/a
44	chr1:225924665-225924715	Caco-2	colon:	n/a
45	chr1:225924665-225924715	T-47D	breast:	n/a
46	chr1:225924665-225924715	PrEC	prostate:	n/a
47	chr1:225924665-225924715	HepG2	liver:	n/a
48	chr1:225924665-225924715	HAEpiC	amniotic membrane:	n/a
49	chr1:225924665-225924715	GM12891	blood:	n/a
50	chr1:225924665-225924715	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr1:225913658..225916157-chr1:225919498..225921239,2	K562	blood:
2	chr1:225907924..225909713-chr1:225913248..225915976,2	MCF-7	breast:
3	chr1:225917984..225919874-chr1:225923037..225925878,2	K562	blood:
4	chr1:225905015..225908642-chr1:225910651..225913920,4	K562	blood:
5	chr1:225918372..225920081-chr5:167531170..167532671,2	K562	blood:
6	chr1:225909033..225912009-chr1:225915381..225917178,2	K562	blood:
7	chr1:225914654..225917472-chr1:225922608..225924968,2	MCF-7	breast:
8	chr1:225840236..225841834-chr1:225925182..225927781,2	MCF-7	breast:
9	chr1:225839526..225841681-chr1:225921806..225923361,2	MCF-7	breast:
10	chr1:225917342..225919874-chr1:225923037..225925175,2	K562	blood:
11	chr1:225913658..225916157-chr1:225919498..225921239,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRP9-1	chr1:225925797-225925899	ENSG00000227496.1
2	lnc-ENAH-1	chr1:225923815-225923976	XLOC_001231
3	lnc-ENAH-1	chr1:225923079-225923197	XLOC_001231

Variant related genes	Relation type
RNU6-1304P	TF binding region
ENSG00000226349	TF binding region
RNU6-1304P	CpG island
ENSG00000226349	CpG island
ENSG00000154380	chromatin interactions
ENSG00000226349	chromatin interactions

Extended variants
information (count: 551 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4653659	chr1:225912620-225912621	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141460650	chr1:225912674-225912675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578104923	chr1:225912694-225912695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545670829	chr1:225912695-225912696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560778308	chr1:225912702-225912703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371680033	chr1:225912713-225912714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572644759	chr1:225912733-225912734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542830551	chr1:225912734-225912735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561562094	chr1:225912851-225912852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531297288	chr1:225912854-225912855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs58032328	chr1:225912865-225912866	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs564491299	chr1:225912897-225912898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183721278	chr1:225912922-225912923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74148660	chr1:225912933-225912934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565661487	chr1:225912951-225912952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530032398	chr1:225912963-225912964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548067940	chr1:225912999-225913000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569875856	chr1:225913089-225913090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537950471	chr1:225913091-225913092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535055713	chr1:225913107-225913108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571629081	chr1:225913128-225913129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539051895	chr1:225913156-225913157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150862114	chr1:225913175-225913176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551003460	chr1:225913176-225913177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543344968	chr1:225913207-225913208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189259718	chr1:225913241-225913242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112880288	chr1:225913249-225913250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182296973	chr1:225913262-225913263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112392518	chr1:225913269-225913270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564651939	chr1:225913319-225913320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531951146	chr1:225913322-225913323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143787799	chr1:225913352-225913353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570750208	chr1:225913369-225913370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10915868	chr1:225913472-225913473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs111713678	chr1:225913513-225913514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548513626	chr1:225913523-225913524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186954825	chr1:225913536-225913537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140987232	chr1:225913603-225913604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373474672	chr1:225913616-225913617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117487371	chr1:225913648-225913649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557733630	chr1:225913668-225913669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189988830	chr1:225913750-225913751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554197576	chr1:225913757-225913758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566111520	chr1:225913786-225913787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536495365	chr1:225913837-225913838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181113832	chr1:225913862-225913863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185754693	chr1:225913889-225913890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189731280	chr1:225913959-225913960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558756359	chr1:225913971-225913972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576516642	chr1:225914084-225914085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	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
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	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
Prostate cancer	18632612	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
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	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
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225899400-225915000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:225912000-225913000	Enhancers	Fetal Lung	lung
3	chr1:225912400-225924200	Weak transcription	Spleen	Spleen
4	chr1:225915000-225915200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:225915200-225933600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:225918800-225919400	Enhancers	HepG2	liver
7	chr1:225918800-225919600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:225919000-225919400	Enhancers	Aorta	Aorta
9	chr1:225919000-225919400	Enhancers	Osteobl	bone
10	chr1:225919200-225923000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr1:225919400-225921000	Weak transcription	HepG2	liver
12	chr1:225919400-225923000	Weak transcription	Osteobl	bone
13	chr1:225919600-225922800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:225920400-225921400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:225920600-225921400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr1:225920600-225921600	Enhancers	A549	lung
17	chr1:225920800-225921800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:225921000-225921200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr1:225921000-225921200	Enhancers	NHLF	lung
20	chr1:225921000-225921400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:225921000-225921400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:225921000-225921400	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr1:225921000-225921400	Enhancers	HepG2	liver
24	chr1:225921000-225921600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:225921000-225921600	Enhancers	Fetal Lung	lung
26	chr1:225921000-225921800	Enhancers	Liver	Liver
27	chr1:225921000-225922000	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr1:225921000-225922000	Enhancers	Brain Germinal Matrix	brain
29	chr1:225921000-225922400	Enhancers	Hela-S3	cervix
30	chr1:225921200-225921400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
31	chr1:225921200-225921400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:225921200-225921400	Enhancers	Adipose Nuclei	Adipose
33	chr1:225921200-225921400	Enhancers	Brain Substantia Nigra	brain
34	chr1:225921200-225921400	Enhancers	Esophagus	oesophagus
35	chr1:225921200-225921400	Enhancers	Fetal Heart	heart
36	chr1:225921200-225921400	Enhancers	Fetal Muscle Trunk	muscle
37	chr1:225921200-225921400	Enhancers	Fetal Stomach	stomach
38	chr1:225921200-225921400	Enhancers	Left Ventricle	heart
39	chr1:225921200-225921400	Enhancers	Pancreas	Pancrea
40	chr1:225921200-225921400	Enhancers	Psoas Muscle	Psoas
41	chr1:225921200-225921800	Enhancers	Right Atrium	heart
42	chr1:225921400-225921600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr1:225921400-225922200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:225921400-225922800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:225921400-225922800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr1:225921400-225923000	Weak transcription	Fetal Stomach	stomach
47	chr1:225921400-225923000	Weak transcription	Psoas Muscle	Psoas
48	chr1:225921400-225923000	Weak transcription	HepG2	liver
49	chr1:225921400-225925600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:225921400-225934400	Weak transcription	Esophagus	oesophagus

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