Variant report

Variant	nsv537114
Chromosome Location	chr4:63049885-63568580
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	chr4:63294757-63294788	K562	blood:	n/a	n/a
2	ATF2	chr4:63320277-63320601	GM12878	blood:	n/a	n/a
3	BACH1	chr4:63384357-63384360	K562	blood:	n/a	n/a
4	BATF	chr4:63295100-63295326	GM12878	blood:	n/a	chr4:63295282-63295292
5	BATF	chr4:63295109-63295356	GM12878	blood:	n/a	chr4:63295282-63295292
6	BATF	chr4:63320363-63320586	GM12878	blood:	n/a	chr4:63320448-63320461
7	BATF	chr4:63461066-63461353	GM12878	blood:	n/a	n/a
8	BATF	chr4:63316519-63316715	GM12878	blood:	n/a	n/a
9	BATF	chr4:63265074-63265292	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:63461102-63461277	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:63461083-63461365	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:63360833-63361155	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:63210093-63210259	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:63280760-63280912	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:63461101-63461115	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:63258394-63258425	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:63167297-63167554	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:63268010-63268204	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:63408838-63408903	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:63265023-63265324	GM12878	blood:	n/a	n/a
21	CCNT2	chr4:63279209-63279409	K562	blood:	n/a	n/a
22	CEBPB	chr4:63364801-63365006	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:63298894-63299142	HepG2	liver:	n/a	chr4:63299025-63299036 chr4:63299024-63299035
24	CEBPB	chr4:63487872-63488170	HepG2	liver:	n/a	chr4:63488026-63488037
25	CEBPB	chr4:63446565-63446908	H1-hESC	embryonic stem cell:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
26	CEBPB	chr4:63235073-63235279	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:63413777-63414204	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:63413815-63414108	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:63163872-63164135	HepG2	liver:	n/a	chr4:63163993-63164004
30	CEBPB	chr4:63446603-63446869	ECC-1	luminal epithelium:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
31	CEBPB	chr4:63506138-63506482	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr4:63446674-63446874	A549	lung:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
33	CEBPB	chr4:63366031-63366359	HepG2	liver:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
34	CEBPB	chr4:63060116-63060394	HepG2	liver:	n/a	chr4:63060242-63060253
35	CEBPB	chr4:63446573-63446898	HepG2	liver:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
36	CEBPB	chr4:63446579-63446929	IMR90	lung:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
37	CEBPB	chr4:63366019-63366339	IMR90	lung:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
38	CEBPB	chr4:63410255-63410445	H1-hESC	embryonic stem cell:	n/a	chr4:63410258-63410269 chr4:63410256-63410269 chr4:63410375-63410386
39	CEBPB	chr4:63243558-63243875	HepG2	liver:	n/a	chr4:63243712-63243723
40	CEBPB	chr4:63506145-63506397	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr4:63165514-63165713	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:63411339-63411580	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:63364784-63365082	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:63300397-63300639	HepG2	liver:	n/a	chr4:63300537-63300548
45	CEBPB	chr4:63318348-63318604	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:63412665-63412944	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:63228228-63228454	HepG2	liver:	n/a	chr4:63228379-63228396 chr4:63228382-63228393
48	CEBPB	chr4:63366058-63366371	H1-hESC	embryonic stem cell:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
49	CEBPB	chr4:63517639-63517827	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:63446615-63446915	Hela-S3	cervix:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:63416083-63416133	T-47D	breast:	n/a
2	chr4:63416083-63416133	IMR90	lung:	fetal
3	chr4:63357670-63357720	MCF-7	breast:	n/a
4	chr4:63357670-63357720	HIPEpiC	eye:	n/a
5	chr4:63380813-63380863	K562	blood:	n/a
6	chr4:63380813-63380863	HCF	heart:	n/a
7	chr4:63416083-63416133	HUVEC	blood vessel:	n/a
8	chr4:63357670-63357720	GM19239	blood:	n/a
9	chr4:63357670-63357720	HCM	heart:	n/a
10	chr4:63075650-63075700	T-47D	breast:	n/a
11	chr4:63075650-63075700	HCPEpiC	choroid plexus:	n/a
12	chr4:63357670-63357720	Hela-S3	cervix:	n/a
13	chr4:63380813-63380863	PFSK-1	brain:	n/a
14	chr4:63380813-63380863	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:63075650-63075700	NH-A	brain:	n/a
16	chr4:63357670-63357720	PANC-1	pancreas:	n/a
17	chr4:63416083-63416133	BE2_C	brain:	n/a
18	chr4:63380813-63380863	HCM	heart:	n/a
19	chr4:63416083-63416133	H1-hESC	embryonic stem cell:	embryo
20	chr4:63416083-63416133	BJ	skin:	n/a
21	chr4:63416083-63416133	HRE	kidney:	n/a
22	chr4:63380813-63380863	NHBE	bronchial:	n/a
23	chr4:63075650-63075700	RPTEC	kidney:	n/a
24	chr4:63075650-63075700	CMK	blood:	n/a
25	chr4:63380813-63380863	H1-hESC	embryonic stem cell:	embryo
26	chr4:63357670-63357720	PFSK-1	brain:	n/a
27	chr4:63357670-63357720	HCPEpiC	choroid plexus:	n/a
28	chr4:63075650-63075700	HMEC	breast:	n/a
29	chr4:63380813-63380863	HCT-116	colon:	n/a
30	chr4:63416083-63416133	NB4	blood:	n/a
31	chr4:63380813-63380863	HepG2	liver:	n/a
32	chr4:63075650-63075700	GM12892	blood:	n/a
33	chr4:63357670-63357720	SK-N-MC	brain:	n/a
34	chr4:63416083-63416133	PANC-1	pancreas:	n/a
35	chr4:63357670-63357720	AG09319	gingival:	n/a
36	chr4:63416083-63416133	K562	blood:	n/a
37	chr4:63380813-63380863	HIPEpiC	eye:	n/a
38	chr4:63380813-63380863	SK-N-SH	brain:	n/a
39	chr4:63075650-63075700	AG09309	skin:	n/a
40	chr4:63075650-63075700	MCF10A-Er-Src	breast:	n/a
41	chr4:63416083-63416133	SKMC	muscle:	n/a
42	chr4:63075650-63075700	ovcar-3	ovarian:	n/a
43	chr4:63075650-63075700	BJ	skin:	n/a
44	chr4:63416083-63416133	A549	lung:	n/a
45	chr4:63357670-63357720	K562	blood:	n/a
46	chr4:63416083-63416133	HCPEpiC	choroid plexus:	n/a
47	chr4:63357670-63357720	HepG2	liver:	n/a
48	chr4:63416083-63416133	Jurkat	blood:	n/a
49	chr4:63380813-63380863	GM12878	blood:	n/a
50	chr4:63380813-63380863	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
2	chr4:63443389..63444065-chr8:95958966..95959897,2	MCF-7	breast:
3	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
4	chr4:57988251..57990415-chr4:63557022..63559873,2	K562	blood:
5	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
6	chr12:6147357..6147998-chr4:63072523..63073523,2	MCF-7	breast:
7	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
8	chr4:63474723..63477283-chr4:63485203..63487821,2	K562	blood:
9	chr4:63217903..63219990-chr4:63223283..63224981,2	K562	blood:
10	chr4:63474723..63477283-chr4:63485203..63487821,2	K562	blood:
11	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
12	chr4:63217903..63219990-chr4:63223283..63224981,2	K562	blood:
13	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TECRL-3	chr4:63320310-63320355	XLOC_003967
2	lnc-TECRL-15	chr4:63355213-63355936	NONHSAT096630
3	lnc-LPHN3-9	chr4:63114012-63114488	NONHSAT096627
4	lnc-LPHN3-10	chr4:63157280-63157310	NONHSAT096628
5	lnc-TECRL-3	chr4:63316228-63316413	XLOC_003967
6	lnc-LPHN3-10	chr4:63157734-63158055	NONHSAT096628
7	lnc-LPHN3-12	chr4:63376187-63376489	NONHSAT096631

Variant related genes	Relation type
HMGN1P11	TF binding region
ENSG00000250249	TF binding region
RPL21P47	TF binding region
ENSG00000248847	TF binding region
ENSG00000265085	TF binding region
HMGN1P11	CpG island
ENSG00000250249	CpG island
RPL21P47	CpG island
ENSG00000248847	CpG island
ENSG00000265085	CpG island

Extended variants
information (count: 6964 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6964 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199519875	chr4:63056628-63056629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368505953	chr4:63056629-63056630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368918685	chr4:63056630-63056631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200584340	chr4:63056631-63056632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538635607	chr4:63056633-63056634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386400254	chr4:63056642-63056643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs397687834	chr4:63056643-63056644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35208580	chr4:63056659-63056660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181250239	chr4:63056724-63056725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7664142	chr4:63056729-63056730	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs186132654	chr4:63056819-63056820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555152235	chr4:63056852-63056853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7698238	chr4:63056880-63056881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs112965912	chr4:63056922-63056923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558675356	chr4:63056952-63056953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576947197	chr4:63056962-63056963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17082585	chr4:63056963-63056964	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs536438317	chr4:63056981-63056982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190522059	chr4:63057038-63057039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574686570	chr4:63057049-63057050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539341564	chr4:63057090-63057091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541711721	chr4:63057112-63057113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148371875	chr4:63057191-63057192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555191045	chr4:63057231-63057232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530611627	chr4:63057254-63057255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572978929	chr4:63057255-63057256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540360063	chr4:63057289-63057290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115896845	chr4:63057334-63057335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565018362	chr4:63057363-63057364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532443726	chr4:63057374-63057375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140641162	chr4:63057492-63057493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181964258	chr4:63057523-63057524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557989434	chr4:63057554-63057555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530421572	chr4:63057631-63057632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548595696	chr4:63057638-63057639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187612755	chr4:63057639-63057640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537625301	chr4:63057659-63057660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558712155	chr4:63057671-63057672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570581786	chr4:63057684-63057685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534665396	chr4:63057719-63057720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552938538	chr4:63057770-63057771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs77705692	chr4:63057789-63057790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369211225	chr4:63057815-63057816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542148020	chr4:63057830-63057831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556962064	chr4:63057831-63057832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150086357	chr4:63057932-63057933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545617141	chr4:63058074-63058075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17226496	chr4:63058080-63058081	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs532477780	chr4:63058083-63058084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138382963	chr4:63058095-63058096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Medulloblastoma	21163964	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63056600-63057400	Enhancers	Brain Germinal Matrix	brain
2	chr4:63056800-63058000	Enhancers	Fetal Heart	heart
3	chr4:63057400-63064600	Weak transcription	Brain Germinal Matrix	brain
4	chr4:63058000-63059200	Weak transcription	Fetal Heart	heart
5	chr4:63059200-63059800	Enhancers	Fetal Heart	heart
6	chr4:63059800-63075600	Weak transcription	Fetal Heart	heart
7	chr4:63064600-63065000	Enhancers	Brain Germinal Matrix	brain
8	chr4:63064800-63065400	Enhancers	Fetal Muscle Leg	muscle
9	chr4:63064800-63066000	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr4:63065000-63065400	Flanking Active TSS	Brain Germinal Matrix	brain
11	chr4:63065000-63065800	Enhancers	Fetal Brain Male	brain
12	chr4:63065200-63066000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:63065200-63066000	Enhancers	Fetal Brain Female	brain
14	chr4:63065400-63067800	Enhancers	Brain Germinal Matrix	brain
15	chr4:63065400-63074400	Weak transcription	Fetal Muscle Leg	muscle
16	chr4:63067600-63067800	Enhancers	Fetal Brain Male	brain
17	chr4:63069600-63070000	Enhancers	Right Ventricle	heart
18	chr4:63070000-63075600	Weak transcription	Right Ventricle	heart
19	chr4:63072000-63072400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:63072200-63072600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:63072200-63072600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:63072400-63072600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:63072400-63073000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:63072400-63075600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr4:63072600-63074800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr4:63072600-63075400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:63074400-63074800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:63074400-63075800	Enhancers	Fetal Muscle Leg	muscle
29	chr4:63074800-63075000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:63075000-63075600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr4:63075200-63076000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:63075200-63076000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr4:63075400-63075800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:63075400-63075800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:63075400-63076000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:63075400-63076600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:63075600-63075800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr4:63075600-63075800	Enhancers	Right Ventricle	heart
39	chr4:63075600-63076000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:63075600-63076000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr4:63075600-63076000	Enhancers	Fetal Heart	heart
42	chr4:63075600-63076200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:63075800-63076800	Enhancers	Fetal Lung	lung
44	chr4:63086200-63086600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:63086200-63086800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:63086400-63086800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr4:63086400-63087000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:63091000-63092000	Enhancers	Fetal Brain Male	brain
49	chr4:63091000-63092200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:63091000-63092200	Enhancers	Fetal Heart	heart

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