Variant report

Variant	nsv3921
Chromosome Location	chr1:189668405-189810638
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:503)
CpG islands
(count:122)
Chromatin interactive
region (count:19)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:189743917-189744230	HepG2	liver:	n/a	n/a
2	ATF1	chr1:189692607-189692756	K562	blood:	n/a	n/a
3	ATF1	chr1:189759191-189759268	K562	blood:	n/a	n/a
4	BACH1	chr1:189774960-189775194	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr1:189743704-189744394	A549	lung:	n/a	chr1:189744338-189744347
6	CEBPB	chr1:189688196-189688361	H1-hESC	embryonic stem cell:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
7	CEBPB	chr1:189688098-189688417	A549	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
8	CEBPB	chr1:189769201-189769380	A549	lung:	n/a	chr1:189769331-189769342 chr1:189769332-189769343
9	CEBPB	chr1:189738671-189738934	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:189675218-189675345	A549	lung:	n/a	chr1:189675255-189675266
11	CEBPB	chr1:189739895-189740150	A549	lung:	n/a	n/a
12	CEBPB	chr1:189672613-189673256	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:189731420-189731730	HepG2	liver:	n/a	chr1:189731575-189731586
14	CEBPB	chr1:189689001-189689131	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:189738746-189738942	A549	lung:	n/a	n/a
16	CEBPB	chr1:189675215-189675438	HepG2	liver:	n/a	chr1:189675255-189675266
17	CEBPB	chr1:189738790-189738826	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:189738620-189739003	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:189688107-189688436	HepG2	liver:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
20	CEBPB	chr1:189769228-189769482	HepG2	liver:	n/a	chr1:189769331-189769342 chr1:189769332-189769343
21	CEBPB	chr1:189688106-189688428	IMR90	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
22	CEBPB	chr1:189743808-189744388	MCF-7	breast:	n/a	chr1:189743903-189743914
23	CEBPB	chr1:189731505-189731602	K562	blood:	n/a	chr1:189731575-189731586
24	CEBPB	chr1:189743902-189744361	MCF-7	breast:	n/a	chr1:189743903-189743914
25	CEBPB	chr1:189718442-189718647	HepG2	liver:	n/a	chr1:189718486-189718497
26	CEBPB	chr1:189718405-189718652	A549	lung:	n/a	chr1:189718486-189718497
27	CEBPB	chr1:189688868-189689176	MCF-7	breast:	n/a	n/a
28	CEBPB	chr1:189743808-189744409	A549	lung:	n/a	chr1:189743903-189743914
29	CHD2	chr1:189703140-189703285	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:189677880-189678030	NHEK	skin:	n/a	n/a
31	CTCF	chr1:189772560-189772710	GM12873	blood:	n/a	n/a
32	CTCF	chr1:189677880-189678030	HMEC	breast:	n/a	n/a
33	CTCF	chr1:189677820-189677970	HCT-116	colon:	n/a	n/a
34	CTCF	chr1:189677880-189678030	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:189677840-189677990	GM12865	blood:	n/a	n/a
36	CTCF	chr1:189677880-189678030	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr1:189677918-189678033	GM12892	blood:	n/a	n/a
38	CTCF	chr1:189677880-189678030	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr1:189677760-189677910	HMEC	breast:	n/a	n/a
40	CTCF	chr1:189728266-189728301	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:189677840-189677990	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr1:189772640-189772790	HEK293	kidney:	n/a	n/a
43	CTCF	chr1:189693530-189693582	GM13976	blood:	n/a	n/a
44	CTCF	chr1:189677840-189677990	HRE	kidney:	n/a	n/a
45	CTCF	chr1:189677863-189678104	T-47D	breast:	n/a	n/a
46	CTCF	chr1:189677500-189677650	A549	lung:	n/a	n/a
47	CTCF	chr1:189756934-189756961	GM10248	blood:	n/a	n/a
48	CTCF	chr1:189677802-189678142	GM12878	blood:	n/a	n/a
49	CTCF	chr1:189677860-189678010	HAc	cerebellar:	n/a	n/a
50	CTCF	chr1:189677860-189678010	HPAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189744005-189744055	Hela-S3	cervix:	n/a
2	chr1:189744005-189744055	HCF	heart:	n/a
3	chr1:189722103-189722153	AG04450	lung:	fetal
4	chr1:189722103-189722153	PrEC	prostate:	n/a
5	chr1:189722103-189722153	HUVEC	blood vessel:	n/a
6	chr1:189722103-189722153	PFSK-1	brain:	n/a
7	chr1:189722103-189722153	AG09309	skin:	n/a
8	chr1:189744005-189744055	HEK293	kidney:	embryo
9	chr1:189722103-189722153	ECC-1	luminal epithelium:	n/a
10	chr1:189722103-189722153	SK-N-MC	brain:	n/a
11	chr1:189722103-189722153	SKMC	muscle:	n/a
12	chr1:189744005-189744055	NHDF-neo	bronchial:	n/a
13	chr1:189744005-189744055	IMR90	lung:	fetal
14	chr1:189744005-189744055	HIPEpiC	eye:	n/a
15	chr1:189722103-189722153	SK-N-SH	brain:	n/a
16	chr1:189722103-189722153	HRCEpiC	kidney:	n/a
17	chr1:189722103-189722153	Jurkat	blood:	n/a
18	chr1:189744005-189744055	SAEC	small airway:	n/a
19	chr1:189744005-189744055	PrEC	prostate:	n/a
20	chr1:189744005-189744055	CMK	blood:	n/a
21	chr1:189722103-189722153	NHDF-neo	bronchial:	n/a
22	chr1:189744005-189744055	HRPEpiC	eye:	n/a
23	chr1:189722103-189722153	HAEpiC	amniotic membrane:	n/a
24	chr1:189744005-189744055	SKMC	muscle:	n/a
25	chr1:189722103-189722153	CMK	blood:	n/a
26	chr1:189722103-189722153	GM12878	blood:	n/a
27	chr1:189722103-189722153	Hepatocyte	liver:	n/a
28	chr1:189722103-189722153	AG10803	skin:	n/a
29	chr1:189744005-189744055	HRCEpiC	kidney:	n/a
30	chr1:189744005-189744055	NH-A	brain:	n/a
31	chr1:189744005-189744055	HNPCEpiC	eye:	n/a
32	chr1:189744005-189744055	Caco-2	colon:	n/a
33	chr1:189722103-189722153	A549	lung:	n/a
34	chr1:189722103-189722153	HCM	heart:	n/a
35	chr1:189722103-189722153	GM19239	blood:	n/a
36	chr1:189744005-189744055	HL-60	blood:	n/a
37	chr1:189722103-189722153	T-47D	breast:	n/a
38	chr1:189744005-189744055	NHBE	bronchial:	n/a
39	chr1:189744005-189744055	BJ	skin:	n/a
40	chr1:189722103-189722153	SK-N-SH_RA	brain:	n/a
41	chr1:189722103-189722153	LNCaP	prostate:	n/a
42	chr1:189722103-189722153	GM06990	blood:	n/a
43	chr1:189744005-189744055	HRE	kidney:	n/a
44	chr1:189744005-189744055	HEEpiC	esophagus:	n/a
45	chr1:189744005-189744055	GM06990	blood:	n/a
46	chr1:189722103-189722153	HIPEpiC	eye:	n/a
47	chr1:189722103-189722153	GM12891	blood:	n/a
48	chr1:189744005-189744055	Hepatocyte	liver:	n/a
49	chr1:189722103-189722153	U87	brain:	n/a
50	chr1:189722103-189722153	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr1:189790429..189793066-chr1:189800961..189802500,2	MCF-7	breast:
2	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
3	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
4	chr1:189677420..189678491-chr1:190289916..190290952,3	MCF-7	breast:
5	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
6	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
7	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
8	chr1:189790429..189793066-chr1:189800961..189802500,2	MCF-7	breast:
9	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
10	chr1:189778329..189781313-chr1:189784587..189786793,2	MCF-7	breast:
11	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
12	chr1:189778329..189781313-chr1:189784587..189786793,2	MCF-7	breast:
13	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
14	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
15	chr1:189677502..189678569-chr1:190053452..190054228,3	MCF-7	breast:
16	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
17	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
18	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
19	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-7	chr1:189760709-189760893	XLOC_000503
2	lnc-RGS18-7	chr1:189746390-189746467	XLOC_000503
3	lnc-RGS18-7	chr1:189744595-189744695	XLOC_000503
4	lnc-RGS18-7	chr1:189783962-189784048	XLOC_000503

No data

Variant related genes	Relation type
ENSG00000232212	TF binding region
ENSG00000232212	CpG island
SOX13	miRNA target sites
SOX11	miRNA target sites
SOX2	miRNA target sites

Extended variants
information (count: 1358 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567170464	chr1:189675223-189675224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538481953	chr1:189675254-189675255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528862415	chr1:189675315-189675316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535335459	chr1:189675370-189675371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373517205	chr1:189675388-189675389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191598609	chr1:189675403-189675404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10919607	chr1:189675416-189675417	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs577815747	chr1:189675466-189675467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181806170	chr1:189675469-189675470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551983812	chr1:189675502-189675503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186571651	chr1:189675519-189675520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189846360	chr1:189675528-189675529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117392076	chr1:189675548-189675549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541213	chr1:189675575-189675576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536687562	chr1:189675709-189675710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542223	chr1:189675716-189675717	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138917074	chr1:189675719-189675720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141169897	chr1:189675753-189675754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375278407	chr1:189675765-189675766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367879874	chr1:189675782-189675783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182410406	chr1:189675783-189675784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543166611	chr1:189675806-189675807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187639309	chr1:189675817-189675818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191304810	chr1:189675901-189675902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113521528	chr1:189675922-189675923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572878305	chr1:189675924-189675925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs66529483	chr1:189675935-189675936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372450435	chr1:189675972-189675973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2038652	chr1:189675987-189675988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540391796	chr1:189675988-189675989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139009489	chr1:189675990-189675991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528054448	chr1:189676005-189676006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183007116	chr1:189676052-189676053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551208464	chr1:189676091-189676092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57979130	chr1:189676148-189676149	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs149488732	chr1:189676157-189676158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576048084	chr1:189676161-189676162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561772634	chr1:189676176-189676177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150219280	chr1:189678030-189678031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532837166	chr1:189678045-189678046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552181948	chr1:189678085-189678086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568926668	chr1:189678098-189678099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537820558	chr1:189678104-189678105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554645988	chr1:189678126-189678127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568498811	chr1:189678165-189678166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566727647	chr1:189678183-189678184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562491074	chr1:189678212-189678213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2902583	chr1:189678231-189678232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs184309220	chr1:189678235-189678236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147901882	chr1:189678269-189678270	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	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
Hepatocellular carcinoma	18803288	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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189675200-189676200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr1:189678000-189678200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:189678000-189678400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:189688000-189688600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:189720600-189720800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:189720800-189721600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:189721600-189722400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:189721600-189722600	Enhancers	Fetal Heart	heart
9	chr1:189721600-189723000	Enhancers	Fetal Lung	lung
10	chr1:189721800-189722000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:189722000-189722600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:189722000-189722600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr1:189722400-189723000	Enhancers	Hela-S3	cervix
14	chr1:189722600-189722800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:189733200-189734200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:189733400-189734000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:189733400-189734000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr1:189733400-189734400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr1:189743400-189743600	Enhancers	A549	lung
20	chr1:189743600-189744800	Flanking Active TSS	A549	lung
21	chr1:189744000-189744600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:189744000-189745000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr1:189744000-189745200	Enhancers	Fetal Heart	heart
24	chr1:189744200-189745000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:189744200-189745000	Enhancers	NH-A	brain
26	chr1:189744400-189744800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:189744400-189745000	Enhancers	Hela-S3	cervix
28	chr1:189744800-189745000	Enhancers	A549	lung
29	chr1:189745000-189745200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:189745200-189746200	Weak transcription	Fetal Heart	heart
31	chr1:189746200-189746800	Enhancers	Fetal Heart	heart
32	chr1:189751000-189751800	Enhancers	Fetal Brain Male	brain
33	chr1:189751400-189751800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:189751800-189754800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:189754600-189755600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:189754800-189756200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:189755600-189756000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:189756000-189756200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:189756200-189756400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:189756200-189756600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:189756200-189756600	Active TSS	Fetal Brain Female	brain
42	chr1:189756400-189756600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:189756400-189756600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:189756400-189756800	Active TSS	Brain Substantia Nigra	brain
45	chr1:189756600-189757600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:189757200-189757600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr1:189761800-189765400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr1:189773400-189773800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:189773400-189773800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:189773400-189773800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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