Variant report

Variant	nsv1012007
Chromosome Location	chr1:242811313-243041351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:946)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:946 , 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	chr1:242996994-242996997	K562	blood:	n/a	n/a
3	BACH1	chr1:242918799-242919176	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:242907415-242907671	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:242848092-242848258	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	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
10	BCL3	chr1:242843343-242843676	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	chr1:242954012-242954043	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:242899993-242900287	HepG2	liver:	n/a	chr1:242900141-242900152
16	CEBPB	chr1:242933686-242933998	A549	lung:	n/a	n/a
17	CEBPB	chr1:242933698-242934016	A549	lung:	n/a	n/a
18	CEBPB	chr1:242815292-242815888	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:242933600-242934106	A549	lung:	n/a	n/a
20	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
21	CEBPB	chr1:242899978-242900301	A549	lung:	n/a	chr1:242900141-242900152
22	CEBPB	chr1:242890951-242891053	A549	lung:	n/a	n/a
23	CEBPB	chr1:242914758-242914854	A549	lung:	n/a	chr1:242914783-242914796
24	CEBPB	chr1:242815630-242815862	A549	lung:	n/a	n/a
25	CEBPB	chr1:242955789-242955931	A549	lung:	n/a	n/a
26	CEBPB	chr1:242998985-242999533	A549	lung:	n/a	n/a
27	CEBPB	chr1:242861497-242861649	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:242874257-242874306	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr1:242976654-242977278	GM12878	blood:	n/a	n/a
30	CHD2	chr1:242991732-242991777	HepG2	liver:	n/a	n/a
31	CHD2	chr1:242976690-242977268	GM12878	blood:	n/a	n/a
32	CHD2	chr1:243005456-243005619	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:242815220-242815370	GM12874	blood:	n/a	n/a
34	CTCF	chr1:242815188-242815323	K562	blood:	n/a	n/a
35	CTCF	chr1:242815220-242815370	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:242991636-242991778	SK-N-SH_RA	brain:	n/a	chr1:242991719-242991740
37	CTCF	chr1:242815198-242815359	A549	lung:	n/a	n/a
38	CTCF	chr1:242815236-242815344	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr1:243005455-243005673	GM12878	blood:	n/a	n/a
40	CTCF	chr1:242952123-242952379	GM12878	blood:	n/a	chr1:242952183-242952204 chr1:242952181-242952199
41	CTCF	chr1:242815200-242815350	RPTEC	kidney:	n/a	n/a
42	CTCF	chr1:242991610-242991869	MCF-7	breast:	n/a	chr1:242991719-242991740
43	CTCF	chr1:242815400-242815550	GM12870	blood:	n/a	n/a
44	CTCF	chr1:242975725-242975802	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr1:242956800-242956950	GM12868	blood:	n/a	n/a
46	CTCF	chr1:242956718-242957008	GM12878	blood:	n/a	n/a
47	CTCF	chr1:242991640-242991790	MCF-7	breast:	n/a	chr1:242991719-242991740
48	CTCF	chr1:242991800-242991950	GM12868	blood:	n/a	n/a
49	CTCF	chr1:242815180-242815330	HL-60	blood:	n/a	n/a
50	CTCF	chr1:242943580-242943730	GM12867	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242937866-242937916	GM12891	blood:	n/a
2	chr1:242936925-242936975	HCT-116	colon:	n/a
3	chr1:242874219-242874269	HIPEpiC	eye:	n/a
4	chr1:242874219-242874269	PFSK-1	brain:	n/a
5	chr1:242874219-242874269	HCF	heart:	n/a
6	chr1:242936925-242936975	LNCaP	prostate:	n/a
7	chr1:242936925-242936975	PrEC	prostate:	n/a
8	chr1:242936925-242936975	RPTEC	kidney:	n/a
9	chr1:242874219-242874269	PrEC	prostate:	n/a
10	chr1:242936925-242936975	NHBE	bronchial:	n/a
11	chr1:242936925-242936975	CMK	blood:	n/a
12	chr1:242874219-242874269	HUVEC	blood vessel:	n/a
13	chr1:242874219-242874269	HCPEpiC	choroid plexus:	n/a
14	chr1:242937866-242937916	NHDF-neo	bronchial:	n/a
15	chr1:242874219-242874269	RPTEC	kidney:	n/a
16	chr1:242937866-242937916	Hepatocyte	liver:	n/a
17	chr1:242936925-242936975	Caco-2	colon:	n/a
18	chr1:242936925-242936975	HEK293	kidney:	embryo
19	chr1:242936925-242936975	HMEC	breast:	n/a
20	chr1:242874219-242874269	AG04450	lung:	fetal
21	chr1:242874219-242874269	H1-hESC	embryonic stem cell:	embryo
22	chr1:242936925-242936975	AG04449	skin:	fetal
23	chr1:242936925-242936975	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:242874219-242874269	LNCaP	prostate:	n/a
25	chr1:242936925-242936975	AG09309	skin:	n/a
26	chr1:242936925-242936975	HCF	heart:	n/a
27	chr1:242937866-242937916	HMEC	breast:	n/a
28	chr1:242937866-242937916	GM12878	blood:	n/a
29	chr1:242936925-242936975	ECC-1	luminal epithelium:	n/a
30	chr1:242937866-242937916	AG04450	lung:	fetal
31	chr1:242874219-242874269	HCT-116	colon:	n/a
32	chr1:242937866-242937916	CMK	blood:	n/a
33	chr1:242874219-242874269	ECC-1	luminal epithelium:	n/a
34	chr1:242874219-242874269	HL-60	blood:	n/a
35	chr1:242936925-242936975	HRPEpiC	eye:	n/a
36	chr1:242874219-242874269	HRE	kidney:	n/a
37	chr1:242937866-242937916	BE2_C	brain:	n/a
38	chr1:242874219-242874269	NH-A	brain:	n/a
39	chr1:242937866-242937916	ProgFib	skin:	n/a
40	chr1:242936925-242936975	GM12878	blood:	n/a
41	chr1:242937866-242937916	HepG2	liver:	n/a
42	chr1:242874219-242874269	HEK293	kidney:	embryo
43	chr1:242874219-242874269	PANC-1	pancreas:	n/a
44	chr1:242874219-242874269	BJ	skin:	n/a
45	chr1:242937866-242937916	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:242936925-242936975	SKMC	muscle:	n/a
47	chr1:242874219-242874269	Jurkat	blood:	n/a
48	chr1:242936925-242936975	HEEpiC	esophagus:	n/a
49	chr1:242937866-242937916	SAEC	small airway:	n/a
50	chr1:242936925-242936975	Jurkat	blood:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SDCCAG8-4	chr1:242834442-242834878	NONHSAT010573

No data

Variant related genes	Relation type
ENSG00000270859	TF binding region
RSL24D1P4	TF binding region
ENSG00000270859	CpG island
RSL24D1P4	CpG island

Extended variants
information (count: 5874 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5874 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182228372	chr1:242811344-242811345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs578025441	chr1:242811422-242811423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186144542	chr1:242811433-242811434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562626485	chr1:242811559-242811560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2184185	chr1:242811594-242811595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs542111628	chr1:242811613-242811614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561984725	chr1:242811623-242811624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528034418	chr1:242811642-242811643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189763591	chr1:242811711-242811712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548120805	chr1:242811806-242811807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547065666	chr1:242811833-242811834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144945911	chr1:242811837-242811838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113825105	chr1:242811883-242811884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187021346	chr1:242811899-242811900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73118685	chr1:242811914-242811915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191361275	chr1:242811946-242811947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540059037	chr1:242811982-242811983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2184184	chr1:242811984-242811985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183220608	chr1:242811988-242811989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72768513	chr1:242812018-242812019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs377504111	chr1:242812032-242812033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138905759	chr1:242812054-242812055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550846649	chr1:242812171-242812172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116574144	chr1:242812179-242812180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372819706	chr1:242812207-242812208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543512726	chr1:242812232-242812233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188495698	chr1:242812251-242812252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576276272	chr1:242812387-242812388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542025921	chr1:242812391-242812392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193059122	chr1:242812420-242812421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12092120	chr1:242812475-242812476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187725697	chr1:242812489-242812490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563883423	chr1:242812612-242812613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145825965	chr1:242812649-242812650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569153317	chr1:242812651-242812652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536317090	chr1:242812710-242812711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563020702	chr1:242812725-242812726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528988194	chr1:242812744-242812745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533434985	chr1:242812768-242812769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12042953	chr1:242812831-242812832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532613351	chr1:242812857-242812858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111482073	chr1:242812861-242812862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12410064	chr1:242812866-242812867	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs77421799	chr1:242812870-242812871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200352576	chr1:242812903-242812904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148135804	chr1:242812971-242812972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571517529	chr1:242812976-242812977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4658492	chr1:242812993-242812994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs12025330	chr1:242812998-242812999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35566688	chr1:242813045-242813046	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242802200-242815400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr1:242807400-242811400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:242807600-242815600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:242811400-242811800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:242815000-242815600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr1:242815000-242815600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:242815000-242816200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:242815400-242815800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr1:242815400-242815800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:242815400-242815800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr1:242815400-242815800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:242815400-242815800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:242815400-242816000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:242815400-242816200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:242815400-242816200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:242815600-242815800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:242820800-242821000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr1:242821200-242822400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr1:242822400-242823000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr1:242832600-242833000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:242833000-242834200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:242833400-242833600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:242835000-242836200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:242836000-242836200	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr1:242836000-242836400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:242836000-242836600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr1:242836000-242837000	Enhancers	Brain Substantia Nigra	brain
28	chr1:242836200-242836400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr1:242836200-242836400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
30	chr1:242836200-242836600	Enhancers	Brain Cingulate Gyrus	brain
31	chr1:242836200-242837000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:242836200-242837000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr1:242836200-242837000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:242836200-242837000	Enhancers	Brain Angular Gyrus	brain
35	chr1:242836200-242837200	Enhancers	Brain Hippocampus Middle	brain
36	chr1:242836400-242836600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr1:242836400-242837000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:242836400-242838200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr1:242836600-242837000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr1:242836600-242838600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr1:242837000-242837200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:242837000-242838000	Weak transcription	Brain Substantia Nigra	brain
43	chr1:242837200-242838400	Weak transcription	Brain Hippocampus Middle	brain
44	chr1:242837200-242838800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:242838000-242838800	Enhancers	Brain Substantia Nigra	brain
46	chr1:242838200-242854000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr1:242838400-242838600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr1:242838600-242838800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:242838600-242838800	Enhancers	Brain Hippocampus Middle	brain
50	chr1:242838600-242839000	Enhancers	Brain Cingulate Gyrus	brain

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