Variant report

Variant	nsv1005770
Chromosome Location	chr4:62344379-62398798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:673)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 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	ATF2	chr4:62382805-62383235	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:62388087-62388393	HepG2	liver:	n/a	chr4:62388250-62388261
3	CEBPB	chr4:62350625-62350991	A549	lung:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
4	CEBPB	chr4:62377819-62378206	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:62350575-62350948	IMR90	lung:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
6	CEBPB	chr4:62396998-62397232	HepG2	liver:	n/a	chr4:62397139-62397156
7	CEBPB	chr4:62350601-62350882	H1-hESC	embryonic stem cell:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
8	CEBPB	chr4:62382807-62383257	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:62377827-62378189	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr4:62382956-62383180	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:62397064-62397291	H1-hESC	embryonic stem cell:	n/a	chr4:62397139-62397156
12	CEBPB	chr4:62396845-62397323	HepG2	liver:	n/a	chr4:62397139-62397156
13	CEBPB	chr4:62377886-62377996	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:62377822-62378208	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:62377920-62378118	A549	lung:	n/a	n/a
16	CEBPB	chr4:62382873-62383280	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:62388092-62388415	IMR90	lung:	n/a	chr4:62388250-62388261
18	CEBPB	chr4:62382989-62383289	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:62388120-62388412	A549	lung:	n/a	chr4:62388250-62388261
20	CEBPB	chr4:62350577-62350924	HepG2	liver:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
21	CEBPB	chr4:62350663-62351071	Hela-S3	cervix:	n/a	chr4:62350749-62350762 chr4:62350998-62351015 chr4:62350749-62350760
22	CEBPB	chr4:62382897-62383261	HepG2	liver:	n/a	n/a
23	CEBPD	chr4:62397074-62397221	HepG2	liver:	n/a	n/a
24	CEBPD	chr4:62382908-62383163	HepG2	liver:	n/a	n/a
25	CHD2	chr4:62380571-62380609	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr4:62382886-62383175	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr4:62382798-62383410	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:62366740-62366890	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr4:62366860-62367010	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr4:62366780-62366930	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr4:62355800-62355950	HMEC	breast:	n/a	n/a
32	CTCF	chr4:62388280-62388430	HMEC	breast:	n/a	n/a
33	CTCF	chr4:62383000-62383150	HRE	kidney:	n/a	n/a
34	CTCF	chr4:62383044-62383143	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:62366740-62366890	SAEC	small airway:	n/a	n/a
36	CTCF	chr4:62366740-62366890	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr4:62355800-62355950	RPTEC	kidney:	n/a	n/a
38	CTCF	chr4:62386020-62386170	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr4:62366740-62366890	HMF	breast:	n/a	n/a
40	CTCF	chr4:62383030-62383156	A549	lung:	n/a	n/a
41	CTCF	chr4:62383059-62383136	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:62366820-62366970	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr4:62383020-62383170	HRE	kidney:	n/a	n/a
44	CTCF	chr4:62383038-62383182	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:62388300-62388450	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr4:62366740-62366890	HCM	heart:	n/a	n/a
47	CTCF	chr4:62366730-62366909	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:62366760-62366910	RPTEC	kidney:	n/a	n/a
49	CTCF	chr4:62383038-62383154	GM13977	blood:	n/a	n/a
50	CTCF	chr4:62389807-62389872	LNCaP	prostate:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:62362347-62362397	GM12892	blood:	n/a
2	chr4:62362347-62362397	HCT-116	colon:	n/a
3	chr4:62362347-62362397	GM12892	blood:	n/a
4	chr4:62362347-62362397	HCT-116	colon:	n/a
5	chr4:62383240-62383290	HCM	heart:	n/a
6	chr4:62384183-62384233	HMEC	breast:	n/a
7	chr4:62383028-62383078	SAEC	small airway:	n/a
8	chr4:62382932-62382982	NT2-D1	testis:	n/a
9	chr4:62397911-62397961	Hela-S3	cervix:	n/a
10	chr4:62359523-62359573	RPTEC	kidney:	n/a
11	chr4:62384183-62384233	GM12892	blood:	n/a
12	chr4:62383240-62383290	K562	blood:	n/a
13	chr4:62397911-62397961	SK-N-SH_RA	brain:	n/a
14	chr4:62362347-62362397	A549	lung:	n/a
15	chr4:62359523-62359573	HRPEpiC	eye:	n/a
16	chr4:62359523-62359573	AoSMC	blood vessel:	n/a
17	chr4:62379822-62379872	BE2_C	brain:	n/a
18	chr4:62359523-62359573	T-47D	breast:	n/a
19	chr4:62382932-62382982	HNPCEpiC	eye:	n/a
20	chr4:62383028-62383078	GM12891	blood:	n/a
21	chr4:62384183-62384233	ECC-1	luminal epithelium:	n/a
22	chr4:62379822-62379872	HRPEpiC	eye:	n/a
23	chr4:62384183-62384233	PANC-1	pancreas:	n/a
24	chr4:62382932-62382982	Jurkat	blood:	n/a
25	chr4:62383028-62383078	ECC-1	luminal epithelium:	n/a
26	chr4:62379822-62379872	HCT-116	colon:	n/a
27	chr4:62362455-62362505	HL-60	blood:	n/a
28	chr4:62362347-62362397	NB4	blood:	n/a
29	chr4:62387003-62387053	SK-N-SH_RA	brain:	n/a
30	chr4:62383146-62383196	RPTEC	kidney:	n/a
31	chr4:62362455-62362505	NHBE	bronchial:	n/a
32	chr4:62362347-62362397	ovcar-3	ovarian:	n/a
33	chr4:62383240-62383290	GM19239	blood:	n/a
34	chr4:62383146-62383196	SKMC	muscle:	n/a
35	chr4:62359523-62359573	GM12878	blood:	n/a
36	chr4:62384183-62384233	AG10803	skin:	n/a
37	chr4:62383240-62383290	SK-N-SH_RA	brain:	n/a
38	chr4:62383028-62383078	A549	lung:	n/a
39	chr4:62384183-62384233	HUVEC	blood vessel:	n/a
40	chr4:62387003-62387053	NT2-D1	testis:	n/a
41	chr4:62383240-62383290	BE2_C	brain:	n/a
42	chr4:62382932-62382982	U87	brain:	n/a
43	chr4:62387003-62387053	ovcar-3	ovarian:	n/a
44	chr4:62362455-62362505	HAEpiC	amniotic membrane:	n/a
45	chr4:62383240-62383290	HNPCEpiC	eye:	n/a
46	chr4:62362455-62362505	SKMC	muscle:	n/a
47	chr4:62383240-62383290	HIPEpiC	eye:	n/a
48	chr4:62387003-62387053	BJ	skin:	n/a
49	chr4:62383028-62383078	PFSK-1	brain:	n/a
50	chr4:62397911-62397961	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:62355800..62358187-chr4:62359806..62361871,2	K562	blood:
2	chr4:62349743..62350606-chr8:100642196..100642782,2	MCF-7	breast:
3	chr4:62340392..62342899-chr4:62384568..62386458,2	MCF-7	breast:
4	chr4:62355800..62358187-chr4:62359806..62361871,2	K562	blood:

No data

Variant related genes	Relation type
LPHN3	TF binding region
LPHN3	CpG island

Extended variants
information (count: 1767 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1767 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75432559	chr4:62344381-62344382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs335329	chr4:62344387-62344388	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs335328	chr4:62344439-62344440	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370456343	chr4:62344452-62344453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528922990	chr4:62344470-62344471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140379308	chr4:62344474-62344475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374423957	chr4:62344506-62344507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146182248	chr4:62344510-62344511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373591444	chr4:62344513-62344514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532896260	chr4:62344538-62344539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551409535	chr4:62344551-62344552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566571839	chr4:62344574-62344575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533957216	chr4:62344656-62344657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549045319	chr4:62344684-62344685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532207697	chr4:62344739-62344740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184997187	chr4:62344829-62344830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528272320	chr4:62344909-62344910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386675077	chr4:62344927-62344928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs66603708	chr4:62344928-62344929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539568972	chr4:62344949-62344950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558194468	chr4:62344957-62344958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532111062	chr4:62344978-62344979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs137898128	chr4:62345017-62345018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs335327	chr4:62345024-62345025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574376800	chr4:62345042-62345043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544881151	chr4:62345046-62345047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185941661	chr4:62345151-62345152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189474331	chr4:62345174-62345175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142441780	chr4:62345177-62345178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs335326	chr4:62345189-62345190	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs527524518	chr4:62345276-62345277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74523641	chr4:62345332-62345333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567080145	chr4:62345348-62345349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145975026	chr4:62345398-62345399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182078121	chr4:62345402-62345403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186407996	chr4:62345451-62345452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77881553	chr4:62345503-62345504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374529269	chr4:62345514-62345515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557998600	chr4:62345552-62345553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566952669	chr4:62345593-62345594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534167600	chr4:62345597-62345598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556006465	chr4:62345607-62345608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535880919	chr4:62345636-62345637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550628070	chr4:62345650-62345651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148657739	chr4:62345664-62345665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544943603	chr4:62345720-62345721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189984275	chr4:62345791-62345792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577604028	chr4:62345812-62345813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544971041	chr4:62345876-62345877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182468866	chr4:62345912-62345913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62341200-62348000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr4:62344200-62344600	Enhancers	Brain Anterior Caudate	brain
3	chr4:62348000-62348600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr4:62354600-62356000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:62355600-62356200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:62355600-62356200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:62355800-62356200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:62355800-62356200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:62355800-62356200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr4:62355800-62356400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:62356000-62359200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:62356200-62356400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:62356200-62358400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:62356200-62358400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:62356200-62358600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:62356200-62359400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:62356400-62358400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr4:62356800-62358000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:62358000-62359000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr4:62358200-62359800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr4:62358400-62359800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:62358400-62359800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:62358400-62360000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:62358400-62360200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:62358600-62359200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr4:62358600-62359800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr4:62358600-62360200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:62359000-62359600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr4:62359000-62360200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:62359200-62360400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr4:62359400-62359600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:62359400-62360200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:62359400-62360200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:62359600-62359800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr4:62359600-62363000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:62360000-62363000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr4:62360200-62363000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:62363000-62363200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:62363000-62363200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr4:62363000-62365000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:62363200-62363800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:62363800-62364000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:62363800-62370600	Weak transcription	Fetal Stomach	stomach
44	chr4:62364000-62364200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:62364200-62372800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:62364600-62365000	Enhancers	Brain Anterior Caudate	brain
47	chr4:62364600-62365000	Enhancers	Brain Substantia Nigra	brain
48	chr4:62364800-62365000	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr4:62365000-62366200	Weak transcription	Brain Substantia Nigra	brain
50	chr4:62365000-62367600	Weak transcription	Brain Anterior Caudate	brain

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