Variant report

Variant	nsv997505
Chromosome Location	chr4:63025663-63575696
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	chr4:63316519-63316715	GM12878	blood:	n/a	n/a
6	BATF	chr4:63320363-63320586	GM12878	blood:	n/a	chr4:63320448-63320461
7	BATF	chr4:63265074-63265292	GM12878	blood:	n/a	n/a
8	BATF	chr4:63295109-63295356	GM12878	blood:	n/a	chr4:63295282-63295292
9	BATF	chr4:63461066-63461353	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:63461083-63461365	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:63461102-63461277	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:63258394-63258425	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:63280760-63280912	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:63360833-63361155	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:63210093-63210259	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:63408838-63408903	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:63265023-63265324	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:63167297-63167554	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:63461101-63461115	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:63268010-63268204	GM12878	blood:	n/a	n/a
21	CCNT2	chr4:63279209-63279409	K562	blood:	n/a	n/a
22	CEBPB	chr4:63298894-63299142	HepG2	liver:	n/a	chr4:63299025-63299036 chr4:63299024-63299035
23	CEBPB	chr4:63575018-63575321	IMR90	lung:	n/a	chr4:63575164-63575177
24	CEBPB	chr4:63364784-63365082	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:63492830-63493164	HepG2	liver:	n/a	chr4:63492976-63492989 chr4:63492976-63492987 chr4:63492978-63492989
26	CEBPB	chr4:63366022-63366367	K562	blood:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
27	CEBPB	chr4:63159669-63159844	H1-hESC	embryonic stem cell:	n/a	chr4:63159690-63159701
28	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
29	CEBPB	chr4:63228228-63228454	HepG2	liver:	n/a	chr4:63228379-63228396 chr4:63228382-63228393
30	CEBPB	chr4:63410255-63410445	H1-hESC	embryonic stem cell:	n/a	chr4:63410258-63410269 chr4:63410256-63410269 chr4:63410375-63410386
31	CEBPB	chr4:63060116-63060394	HepG2	liver:	n/a	chr4:63060242-63060253
32	CEBPB	chr4:63366019-63366339	IMR90	lung:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
33	CEBPB	chr4:63413815-63414108	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:63446573-63446898	HepG2	liver:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
35	CEBPB	chr4:63318348-63318604	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:63311320-63311637	HepG2	liver:	n/a	chr4:63311445-63311456
37	CEBPB	chr4:63446674-63446874	A549	lung:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
38	CEBPB	chr4:63159616-63159869	HepG2	liver:	n/a	chr4:63159690-63159701
39	CEBPB	chr4:63446697-63446790	K562	blood:	n/a	chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
40	CEBPB	chr4:63300397-63300639	HepG2	liver:	n/a	chr4:63300537-63300548
41	CEBPB	chr4:63320833-63320835	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:63181778-63181932	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:63173967-63174138	HepG2	liver:	n/a	chr4:63174058-63174069
44	CEBPB	chr4:63165514-63165713	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:63060156-63060317	K562	blood:	n/a	chr4:63060242-63060253
46	CEBPB	chr4:63446579-63446929	IMR90	lung:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
47	CEBPB	chr4:63311317-63311630	IMR90	lung:	n/a	chr4:63311445-63311456
48	CEBPB	chr4:63446580-63446900	ECC-1	luminal epithelium:	n/a	chr4:63446794-63446806 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754 chr4:63446745-63446754
49	CEBPB	chr4:63366031-63366359	HepG2	liver:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
50	CEBPB	chr4:63297137-63297651	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:63380813-63380863	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:63380813-63380863	HUVEC	blood vessel:	n/a
3	chr4:63075650-63075700	HEK293	kidney:	embryo
4	chr4:63357670-63357720	NT2-D1	testis:	n/a
5	chr4:63380813-63380863	U87	brain:	n/a
6	chr4:63357670-63357720	GM12878	blood:	n/a
7	chr4:63075650-63075700	A549	lung:	n/a
8	chr4:63357670-63357720	BE2_C	brain:	n/a
9	chr4:63380813-63380863	HepG2	liver:	n/a
10	chr4:63380813-63380863	NT2-D1	testis:	n/a
11	chr4:63357670-63357720	RPTEC	kidney:	n/a
12	chr4:63380813-63380863	HEK293	kidney:	embryo
13	chr4:63357670-63357720	AG04450	lung:	fetal
14	chr4:63357670-63357720	GM12891	blood:	n/a
15	chr4:63380813-63380863	LNCaP	prostate:	n/a
16	chr4:63416083-63416133	AoSMC	blood vessel:	n/a
17	chr4:63416083-63416133	SAEC	small airway:	n/a
18	chr4:63075650-63075700	NHBE	bronchial:	n/a
19	chr4:63075650-63075700	HEEpiC	esophagus:	n/a
20	chr4:63075650-63075700	AG09309	skin:	n/a
21	chr4:63380813-63380863	GM19239	blood:	n/a
22	chr4:63357670-63357720	HEEpiC	esophagus:	n/a
23	chr4:63075650-63075700	BE2_C	brain:	n/a
24	chr4:63357670-63357720	K562	blood:	n/a
25	chr4:63075650-63075700	HUVEC	blood vessel:	n/a
26	chr4:63075650-63075700	HRE	kidney:	n/a
27	chr4:63416083-63416133	HEEpiC	esophagus:	n/a
28	chr4:63075650-63075700	ProgFib	skin:	n/a
29	chr4:63416083-63416133	HRE	kidney:	n/a
30	chr4:63075650-63075700	Caco-2	colon:	n/a
31	chr4:63357670-63357720	HCPEpiC	choroid plexus:	n/a
32	chr4:63380813-63380863	Caco-2	colon:	n/a
33	chr4:63416083-63416133	AG04449	skin:	fetal
34	chr4:63416083-63416133	NB4	blood:	n/a
35	chr4:63380813-63380863	ProgFib	skin:	n/a
36	chr4:63380813-63380863	A549	lung:	n/a
37	chr4:63075650-63075700	HRCEpiC	kidney:	n/a
38	chr4:63380813-63380863	GM12891	blood:	n/a
39	chr4:63380813-63380863	T-47D	breast:	n/a
40	chr4:63416083-63416133	NT2-D1	testis:	n/a
41	chr4:63075650-63075700	AG04450	lung:	fetal
42	chr4:63357670-63357720	PFSK-1	brain:	n/a
43	chr4:63380813-63380863	AoSMC	blood vessel:	n/a
44	chr4:63075650-63075700	PANC-1	pancreas:	n/a
45	chr4:63357670-63357720	LNCaP	prostate:	n/a
46	chr4:63357670-63357720	SK-N-SH_RA	brain:	n/a
47	chr4:63075650-63075700	LNCaP	prostate:	n/a
48	chr4:63357670-63357720	HCM	heart:	n/a
49	chr4:63075650-63075700	H1-hESC	embryonic stem cell:	embryo
50	chr4:63075650-63075700	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
2	chr4:63217903..63219990-chr4:63223283..63224981,2	K562	blood:
3	chr4:63129483..63131734-chr4:63132033..63135396,3	MCF-7	breast:
4	chr12:6147357..6147998-chr4:63072523..63073523,2	MCF-7	breast:
5	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
6	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
7	chr4:57988251..57990415-chr4:63557022..63559873,2	K562	blood:
8	chr4:63083250..63085262-chr4:63091048..63093534,2	K562	blood:
9	chr4:63123536..63126256-chr4:63130076..63132728,2	K562	blood:
10	chr4:63217903..63219990-chr4:63223283..63224981,2	K562	blood:
11	chr4:63460707..63461284-chr4:63575044..63575829,2	MCF-7	breast:
12	chr4:61671439..61672303-chr4:63574939..63575465,2	MCF-7	breast:
13	chr4:63474723..63477283-chr4:63485203..63487821,2	K562	blood:
14	chr4:63443389..63444065-chr8:95958966..95959897,2	MCF-7	breast:
15	chr4:63474723..63477283-chr4:63485203..63487821,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TECRL-15	chr4:63355213-63355936	NONHSAT096630
2	lnc-TECRL-3	chr4:63316228-63316413	XLOC_003967
3	lnc-LPHN3-10	chr4:63157280-63157310	NONHSAT096628
4	lnc-TECRL-4	chr4:63031232-63031272	ENSG00000248692.1
5	lnc-LPHN3-9	chr4:63114012-63114488	NONHSAT096627
6	lnc-LPHN3-2	chr4:63027476-63027983	NONHSAT096620
7	lnc-TECRL-4	chr4:63031232-63031272	ENSG00000248692.1
8	lnc-LPHN3-12	chr4:63376187-63376489	NONHSAT096631
9	lnc-LPHN3-3	chr4:63031380-63031732	XLOC_003556
10	lnc-TECRL-4	chr4:63027465-63027581	ENSG00000248692.1
11	lnc-TECRL-4	chr4:63027465-63027581	ENSG00000248692.1
12	lnc-TECRL-4	chr4:63031232-63031263	ENSG00000248692.1
13	lnc-LPHN3-3	chr4:63036128-63036192	XLOC_003556
14	lnc-TECRL-3	chr4:63320310-63320355	XLOC_003967
15	lnc-LPHN3-2	chr4:63027477-63027983	XLOC_003555
16	lnc-LPHN3-10	chr4:63157734-63158055	NONHSAT096628

Variant related genes	Relation type
ENSG00000248692	TF binding region
HMGN1P11	TF binding region
ENSG00000250249	TF binding region
RPL21P47	TF binding region
ENSG00000248847	TF binding region
ENSG00000265085	TF binding region
ENSG00000248692	CpG island
HMGN1P11	CpG island
ENSG00000250249	CpG island
RPL21P47	CpG island
ENSG00000248847	CpG island
ENSG00000265085	CpG island
ENSG00000265085	chromatin interactions

Extended variants
information (count: 7635 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:7635 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568897841	chr4:63025665-63025666	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144645494	chr4:63025669-63025670	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75387146	chr4:63025789-63025790	Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs950313	chr4:63025823-63025824	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35723471	chr4:63025841-63025842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533992288	chr4:63025858-63025859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555100225	chr4:63025872-63025873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73825635	chr4:63025922-63025923	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535530217	chr4:63025959-63025960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74774009	chr4:63025977-63025978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565994460	chr4:63025980-63025981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575630443	chr4:63025991-63025992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545869918	chr4:63026001-63026002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558476632	chr4:63026008-63026009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77228608	chr4:63026018-63026019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78625307	chr4:63026032-63026033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189442958	chr4:63026046-63026047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548573613	chr4:63026047-63026048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141225093	chr4:63026104-63026105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568375146	chr4:63026123-63026124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150349068	chr4:63026130-63026131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532988412	chr4:63026152-63026153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529583642	chr4:63026167-63026168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540053024	chr4:63026169-63026170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560403724	chr4:63026182-63026183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527559482	chr4:63026192-63026193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181868346	chr4:63026198-63026199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138036425	chr4:63026306-63026307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537635958	chr4:63026316-63026317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374948013	chr4:63026378-63026379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186120951	chr4:63026385-63026386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539324288	chr4:63026405-63026406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199537935	chr4:63026407-63026408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539823078	chr4:63026427-63026428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557827763	chr4:63026454-63026455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs80019415	chr4:63026476-63026477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74630864	chr4:63026533-63026534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556078056	chr4:63026555-63026556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574323597	chr4:63026592-63026593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544813980	chr4:63026594-63026595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28661714	chr4:63026600-63026601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562604802	chr4:63026618-63026619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7680436	chr4:63026644-63026645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs376469200	chr4:63026659-63026660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189298238	chr4:63026695-63026696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559868844	chr4:63026716-63026717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527275230	chr4:63026725-63026726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548901568	chr4:63026785-63026786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114133707	chr4:63026791-63026792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558200283	chr4:63026851-63026852	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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	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:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63015000-63029600	Weak transcription	Left Ventricle	heart
2	chr4:63025400-63025800	Flanking Active TSS	Fetal Heart	heart
3	chr4:63025800-63026000	Enhancers	Fetal Heart	heart
4	chr4:63026000-63031800	Weak transcription	Fetal Heart	heart
5	chr4:63029600-63029800	Enhancers	Left Ventricle	heart
6	chr4:63031800-63032600	ZNF genes & repeats	Fetal Heart	heart
7	chr4:63040200-63041000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:63040200-63041200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:63040200-63042200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr4:63040200-63042800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:63040400-63041400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:63040400-63042400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:63040600-63041000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr4:63040600-63041000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:63040600-63041000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:63040600-63041400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:63041000-63042000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr4:63041000-63042000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:63041000-63042000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr4:63041400-63041800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr4:63041800-63042200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:63042000-63042200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr4:63042000-63042600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr4:63042200-63042400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:63043600-63044000	Weak transcription	Left Ventricle	heart
26	chr4:63044000-63044200	ZNF genes & repeats	Left Ventricle	heart
27	chr4:63044200-63047400	Weak transcription	Left Ventricle	heart
28	chr4:63047400-63048200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:63047400-63048200	Enhancers	Left Ventricle	heart
30	chr4:63047400-63048200	Enhancers	Ovary	ovary
31	chr4:63047800-63048400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:63056600-63057400	Enhancers	Brain Germinal Matrix	brain
33	chr4:63056800-63058000	Enhancers	Fetal Heart	heart
34	chr4:63057400-63064600	Weak transcription	Brain Germinal Matrix	brain
35	chr4:63058000-63059200	Weak transcription	Fetal Heart	heart
36	chr4:63059200-63059800	Enhancers	Fetal Heart	heart
37	chr4:63059800-63075600	Weak transcription	Fetal Heart	heart
38	chr4:63064600-63065000	Enhancers	Brain Germinal Matrix	brain
39	chr4:63064800-63065400	Enhancers	Fetal Muscle Leg	muscle
40	chr4:63064800-63066000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr4:63065000-63065400	Flanking Active TSS	Brain Germinal Matrix	brain
42	chr4:63065000-63065800	Enhancers	Fetal Brain Male	brain
43	chr4:63065200-63066000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:63065200-63066000	Enhancers	Fetal Brain Female	brain
45	chr4:63065400-63067800	Enhancers	Brain Germinal Matrix	brain
46	chr4:63065400-63074400	Weak transcription	Fetal Muscle Leg	muscle
47	chr4:63067600-63067800	Enhancers	Fetal Brain Male	brain
48	chr4:63069600-63070000	Enhancers	Right Ventricle	heart
49	chr4:63070000-63075600	Weak transcription	Right Ventricle	heart
50	chr4:63072000-63072400	Enhancers	HUES48 Cell Line	embryonic stem cell

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