Variant report

Variant	nsv879506
Chromosome Location	chr4:80316417-80604625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1093)
CpG islands
(count:978)
Chromatin interactive
region (count:22)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80599630-80600187	K562	blood:	n/a	n/a
2	ARID3A	chr4:80496141-80496176	K562	blood:	n/a	n/a
3	ARID3A	chr4:80573413-80573707	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:80571533-80571550	K562	blood:	n/a	n/a
5	ARID3A	chr4:80541823-80542117	K562	blood:	n/a	n/a
6	ARID3A	chr4:80497603-80497843	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:80497589-80497889	K562	blood:	n/a	n/a
8	ARID3A	chr4:80553365-80553702	K562	blood:	n/a	n/a
9	ATF1	chr4:80435285-80435719	K562	blood:	n/a	n/a
10	ATF1	chr4:80572632-80572652	K562	blood:	n/a	n/a
11	ATF1	chr4:80497516-80497891	K562	blood:	n/a	n/a
12	ATF1	chr4:80484457-80484657	K562	blood:	n/a	n/a
13	ATF1	chr4:80541811-80542045	K562	blood:	n/a	n/a
14	ATF1	chr4:80553273-80553691	K562	blood:	n/a	n/a
15	ATF1	chr4:80524904-80525261	K562	blood:	n/a	n/a
16	ATF1	chr4:80599574-80600070	K562	blood:	n/a	n/a
17	ATF3	chr4:80599406-80600004	K562	blood:	n/a	n/a
18	BACH1	chr4:80599834-80600042	K562	blood:	n/a	n/a
19	BACH1	chr4:80324660-80324853	K562	blood:	n/a	n/a
20	BACH1	chr4:80418339-80418346	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr4:80473623-80473792	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr4:80497562-80497841	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:80553336-80553617	K562	blood:	n/a	n/a
24	BHLHE40	chr4:80497515-80497874	K562	blood:	n/a	n/a
25	BHLHE40	chr4:80599720-80600214	K562	blood:	n/a	n/a
26	BHLHE40	chr4:80496417-80496439	K562	blood:	n/a	n/a
27	BHLHE40	chr4:80544430-80544470	K562	blood:	n/a	n/a
28	BHLHE40	chr4:80321858-80321886	K562	blood:	n/a	n/a
29	BHLHE40	chr4:80449536-80449542	K562	blood:	n/a	n/a
30	BHLHE40	chr4:80532222-80532519	K562	blood:	n/a	n/a
31	BHLHE40	chr4:80413202-80413295	K562	blood:	n/a	n/a
32	BRCA1	chr4:80497726-80497750	HepG2	liver:	n/a	n/a
33	CBX3	chr4:80553248-80553613	K562	blood:	n/a	n/a
34	CBX3	chr4:80599555-80600094	K562	blood:	n/a	n/a
35	CCNT2	chr4:80541582-80542094	K562	blood:	n/a	n/a
36	CCNT2	chr4:80525875-80526041	K562	blood:	n/a	n/a
37	CCNT2	chr4:80599582-80600184	K562	blood:	n/a	n/a
38	CCNT2	chr4:80319985-80320084	K562	blood:	n/a	n/a
39	CCNT2	chr4:80553289-80553615	K562	blood:	n/a	n/a
40	CCNT2	chr4:80551624-80551778	K562	blood:	n/a	n/a
41	CEBPB	chr4:80462261-80462309	K562	blood:	n/a	n/a
42	CEBPB	chr4:80387471-80387474	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:80553233-80553597	K562	blood:	n/a	n/a
44	CEBPB	chr4:80573198-80573821	MCF-7	breast:	n/a	chr4:80573393-80573406
45	CEBPB	chr4:80507006-80507341	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:80572297-80572583	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:80496222-80496357	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:80325973-80326038	H1-hESC	embryonic stem cell:	n/a	chr4:80326023-80326034
49	CEBPB	chr4:80446198-80446286	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:80367856-80368008	K562	blood:	n/a	chr4:80367941-80367954 chr4:80367943-80367952 chr4:80367942-80367953 chr4:80367941-80367952

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80572259-80572309	NB4	blood:	n/a
2	chr4:80329388-80329438	Jurkat	blood:	n/a
3	chr4:80572259-80572309	NB4	blood:	n/a
4	chr4:80329388-80329438	Jurkat	blood:	n/a
5	chr4:80329447-80329497	HCF	heart:	n/a
6	chr4:80327523-80327573	HEK293	kidney:	embryo
7	chr4:80329424-80329474	HMEC	breast:	n/a
8	chr4:80329368-80329418	ECC-1	luminal epithelium:	n/a
9	chr4:80329447-80329497	SK-N-SH	brain:	n/a
10	chr4:80329481-80329531	SK-N-SH_RA	brain:	n/a
11	chr4:80572259-80572309	T-47D	breast:	n/a
12	chr4:80329486-80329536	HRE	kidney:	n/a
13	chr4:80572259-80572309	MCF10A-Er-Src	breast:	n/a
14	chr4:80327523-80327573	HCT-116	colon:	n/a
15	chr4:80329388-80329438	NHBE	bronchial:	n/a
16	chr4:80413489-80413539	MCF10A-Er-Src	breast:	n/a
17	chr4:80329483-80329533	AoSMC	blood vessel:	n/a
18	chr4:80604140-80604190	GM12878	blood:	n/a
19	chr4:80334832-80334882	AG04450	lung:	fetal
20	chr4:80329447-80329497	HCM	heart:	n/a
21	chr4:80329486-80329536	MCF10A-Er-Src	breast:	n/a
22	chr4:80329284-80329334	BJ	skin:	n/a
23	chr4:80329483-80329533	T-47D	breast:	n/a
24	chr4:80572259-80572309	SAEC	small airway:	n/a
25	chr4:80329481-80329531	CMK	blood:	n/a
26	chr4:80329633-80329683	HCPEpiC	choroid plexus:	n/a
27	chr4:80329481-80329531	HAEpiC	amniotic membrane:	n/a
28	chr4:80329368-80329418	BE2_C	brain:	n/a
29	chr4:80329402-80329452	HEK293	kidney:	embryo
30	chr4:80329388-80329438	NH-A	brain:	n/a
31	chr4:80329388-80329438	NB4	blood:	n/a
32	chr4:80329424-80329474	PFSK-1	brain:	n/a
33	chr4:80329284-80329334	SK-N-MC	brain:	n/a
34	chr4:80329486-80329536	Hepatocyte	liver:	n/a
35	chr4:80334832-80334882	SKMC	muscle:	n/a
36	chr4:80329483-80329533	ovcar-3	ovarian:	n/a
37	chr4:80329481-80329531	AG09319	gingival:	n/a
38	chr4:80329388-80329438	SKMC	muscle:	n/a
39	chr4:80573233-80573283	NH-A	brain:	n/a
40	chr4:80329424-80329474	CMK	blood:	n/a
41	chr4:80329368-80329418	Caco-2	colon:	n/a
42	chr4:80413489-80413539	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:80329402-80329452	K562	blood:	n/a
44	chr4:80329483-80329533	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:80329483-80329533	SK-N-SH	brain:	n/a
46	chr4:80327523-80327573	AG09309	skin:	n/a
47	chr4:80329402-80329452	AG09309	skin:	n/a
48	chr4:80329424-80329474	GM12878	blood:	n/a
49	chr4:80329486-80329536	HUVEC	blood vessel:	n/a
50	chr4:80329368-80329418	T-47D	breast:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80317313..80320222-chr4:80322525..80325047,2	K562	blood:
2	chr4:80552394..80554921-chr4:80558193..80559831,2	K562	blood:
3	chr4:80032018..80033796-chr4:80556626..80558164,2	K562	blood:
4	chr4:80349558..80352426-chr4:80355667..80358007,3	K562	blood:
5	chr4:80552394..80554921-chr4:80558193..80559831,2	K562	blood:
6	chr4:80295453..80298446-chr4:80331381..80333559,2	K562	blood:
7	chr17:59884431..59885001-chr4:80544092..80544675,2	MCF-7	breast:
8	chr4:80516564..80518189-chr4:80518557..80520658,2	K562	blood:
9	chr4:80349558..80352426-chr4:80355667..80358007,3	K562	blood:
10	chr4:80509176..80511123-chr4:80514677..80516383,2	K562	blood:
11	chr4:79964140..79964963-chr4:80497048..80497852,2	MCF-7	breast:
12	chr4:80562829..80565369-chr4:80570389..80573368,2	MCF-7	breast:
13	chr4:79963329..79963907-chr4:80497328..80498247,2	K562	blood:
14	chr4:80281030..80283740-chr4:80487916..80490045,2	K562	blood:
15	chr4:79963311..79963867-chr4:80497354..80497886,2	MCF-7	breast:
16	chr4:80241849..80242382-chr4:80497698..80498294,2	MCF-7	breast:
17	chr4:80562829..80565369-chr4:80570389..80573368,2	MCF-7	breast:
18	chr4:80323363..80325719-chr4:80329559..80332370,2	K562	blood:
19	chr4:80323363..80325719-chr4:80329559..80332370,2	K562	blood:
20	chr4:80163067..80163617-chr4:80497361..80497863,2	MCF-7	breast:
21	chr4:80162158..80162658-chr4:80497305..80497853,2	MCF-7	breast:
22	chr4:80317313..80320222-chr4:80322525..80325047,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM8-2	chr4:80588084-80588280	NONHSAT097119
2	lnc-PRDM8-2	chr4:80584915-80585002	XLOC_003588
3	lnc-PRDM8-9	chr4:80472781-80474355	NONHSAT097115
4	lnc-BMP2K-3	chr4:80413570-80413777	ENSG00000250334
5	lnc-BMP2K-3	chr4:80413747-80413928	NONHSAT097114
6	lnc-BMP2K-3	chr4:80434939-80435056	ENSG00000250334
7	lnc-BMP2K-1	chr4:80446864-80446906	l_2674_chr4:80088967-80336103_prostate
8	lnc-PRDM8-3	chr4:80518031-80518327	ENSG00000251399
9	lnc-BMP2K-3	chr4:80414306-80414739	ENSG00000250334
10	lnc-PRDM8-9	chr4:80476639-80477031	NONHSAT097115
11	lnc-PRDM8-2	chr4:80589005-80589731	NONHSAT097119
12	lnc-BMP2K-1	chr4:80448451-80448970	l_2674_chr4:80088967-80336103_prostate
13	lnc-BMP2K-1	chr4:80336248-80336365	l_2674_chr4:80088967-80336103_prostate
14	lnc-BMP2K-3	chr4:80414306-80414739	NONHSAT097114
15	lnc-BMP2K-3	chr4:80413747-80413928	ENSG00000250334
16	lnc-BMP2K-3	chr4:80434939-80435056	NONHSAT097114
17	lnc-BMP2K-3	chr4:80496295-80497614	ENSG00000250334
18	lnc-BMP2K-1	chr4:80336014-80336110	l_2674_chr4:80088967-80336103_prostate
19	lnc-BMP2K-2	chr4:80319090-80319319	XLOC_003586
20	lnc-BMP2K-2	chr4:80320267-80320316	XLOC_003586
21	lnc-PRDM8-3	chr4:80517696-80517753	ENSG00000251399
22	lnc-BMP2K-3	chr4:80434939-80435056	ENSG00000250334
23	lnc-BMP2K-3	chr4:80496295-80497612	ENSG00000250334
24	lnc-PRDM8-2	chr4:80589143-80589281	XLOC_003588
25	lnc-BMP2K-3	chr4:80496295-80497614	NONHSAT097114
26	lnc-PRDM8-2	chr4:80584859-80585002	NONHSAT097119
27	lnc-BMP2K-3	chr4:80414306-80414739	ENSG00000250334

No data

Variant related genes	Relation type
OR7E94P	TF binding region
ENSG00000248408	TF binding region
LINC00989	TF binding region
ENSG00000251399	TF binding region
GK2	TF binding region
OR7E94P	CpG island
ENSG00000248408	CpG island
LINC00989	CpG island
ENSG00000251399	CpG island
GK2	CpG island
ENSG00000251399	chromatin interactions
ENSG00000249646	chromatin interactions

Extended variants
information (count: 7573 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7573 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1484150	chr4:80316417-80316418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538654306	chr4:80316437-80316438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386676474	chr4:80316475-80316476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377664528	chr4:80316478-80316479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376747050	chr4:80316481-80316482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558517209	chr4:80316526-80316527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138605838	chr4:80316542-80316543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537338771	chr4:80316581-80316582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558282077	chr4:80316582-80316583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1484151	chr4:80316628-80316629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573804758	chr4:80316636-80316637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190329603	chr4:80316660-80316661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149293199	chr4:80316673-80316674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572966299	chr4:80316734-80316735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146217342	chr4:80316821-80316822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564852951	chr4:80316902-80316903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183238213	chr4:80316943-80316944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551270552	chr4:80316961-80316962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561394682	chr4:80317023-80317024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371200927	chr4:80317042-80317043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187935471	chr4:80317056-80317057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574037770	chr4:80317067-80317068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546749615	chr4:80317098-80317099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139170579	chr4:80317106-80317107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34630062	chr4:80317157-80317158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35991876	chr4:80317163-80317164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557113904	chr4:80317196-80317197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142356181	chr4:80317198-80317199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13151260	chr4:80317224-80317225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538743533	chr4:80317273-80317274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13151296	chr4:80317278-80317279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573435101	chr4:80317279-80317280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552179951	chr4:80317314-80317315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371139983	chr4:80317331-80317332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569251304	chr4:80317353-80317354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs17003748	chr4:80317371-80317372	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190852004	chr4:80317401-80317402	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs567407421	chr4:80317449-80317450	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs536494698	chr4:80317546-80317547	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs145927067	chr4:80317558-80317559	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs573004732	chr4:80317581-80317582	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs545110370	chr4:80317592-80317593	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs558332886	chr4:80317593-80317594	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs575214492	chr4:80317671-80317672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11930550	chr4:80317724-80317725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs17003749	chr4:80317772-80317773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs148609405	chr4:80317815-80317816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544819044	chr4:80317816-80317817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182310466	chr4:80317835-80317836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534542708	chr4:80317872-80317873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:1009 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80313000-80317000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:80317000-80317400	Enhancers	Adipose Nuclei	Adipose
3	chr4:80317000-80317600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:80317000-80317600	Enhancers	Dnd41	blood
5	chr4:80317400-80317600	Active TSS	Fetal Lung	lung
6	chr4:80317600-80323000	Weak transcription	Fetal Lung	lung
7	chr4:80319000-80319400	Enhancers	Right Atrium	heart
8	chr4:80321600-80321800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr4:80321600-80322000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:80321800-80322000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
11	chr4:80321800-80323000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:80322000-80323200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:80323000-80323800	Enhancers	Fetal Lung	lung
14	chr4:80323200-80323800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:80323200-80324000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:80323200-80324000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:80323600-80323800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:80324400-80324600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:80328800-80329200	Active TSS	Brain Substantia Nigra	brain
20	chr4:80330800-80331000	Enhancers	Psoas Muscle	Psoas
21	chr4:80333600-80335600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:80334000-80334400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:80334000-80334600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:80334000-80335400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr4:80334000-80335600	Enhancers	Brain Germinal Matrix	brain
26	chr4:80334200-80335000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr4:80334200-80335000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:80334400-80335600	Enhancers	Fetal Brain Male	brain
29	chr4:80334600-80335000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:80334600-80335600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:80335200-80335400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:80345800-80346400	Enhancers	Fetal Muscle Leg	muscle
33	chr4:80346400-80347400	Weak transcription	Fetal Muscle Leg	muscle
34	chr4:80347200-80348600	Enhancers	Fetal Stomach	stomach
35	chr4:80347400-80348000	Enhancers	Rectal Smooth Muscle	rectum
36	chr4:80347400-80348800	Enhancers	Fetal Muscle Leg	muscle
37	chr4:80347600-80348600	Enhancers	Fetal Lung	lung
38	chr4:80348000-80348400	Enhancers	Colon Smooth Muscle	Colon
39	chr4:80348800-80351000	Weak transcription	Fetal Muscle Leg	muscle
40	chr4:80349600-80349800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:80350200-80350400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:80350400-80351200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:80350400-80351200	Enhancers	Stomach Smooth Muscle	stomach
44	chr4:80350600-80351200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:80350600-80351400	Enhancers	Adipose Nuclei	Adipose
46	chr4:80351000-80351400	Enhancers	Fetal Muscle Leg	muscle
47	chr4:80351200-80351400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:80351400-80353000	Weak transcription	Adipose Nuclei	Adipose
49	chr4:80351400-80353000	Weak transcription	Fetal Muscle Leg	muscle
50	chr4:80351600-80352000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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