Variant report

Variant	nsv1005152
Chromosome Location	chr4:80549659-80814456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:852)
CpG islands
(count:610)
Chromatin interactive
region (count:30)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80685291-80685539	K562	blood:	n/a	n/a
2	ARID3A	chr4:80573413-80573707	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:80599630-80600187	K562	blood:	n/a	n/a
4	ARID3A	chr4:80553365-80553702	K562	blood:	n/a	n/a
5	ARID3A	chr4:80571533-80571550	K562	blood:	n/a	n/a
6	ATF1	chr4:80599574-80600070	K562	blood:	n/a	n/a
7	ATF1	chr4:80621566-80621751	K562	blood:	n/a	n/a
8	ATF1	chr4:80790831-80791068	K562	blood:	n/a	n/a
9	ATF1	chr4:80685309-80685612	K562	blood:	n/a	n/a
10	ATF1	chr4:80572632-80572652	K562	blood:	n/a	n/a
11	ATF1	chr4:80792382-80792496	K562	blood:	n/a	n/a
12	ATF1	chr4:80553273-80553691	K562	blood:	n/a	n/a
13	ATF1	chr4:80773436-80773735	K562	blood:	n/a	n/a
14	ATF3	chr4:80599406-80600004	K562	blood:	n/a	n/a
15	BACH1	chr4:80599834-80600042	K562	blood:	n/a	n/a
16	BATF	chr4:80681049-80681323	GM12878	blood:	n/a	chr4:80681190-80681201
17	BATF	chr4:80681101-80681304	GM12878	blood:	n/a	chr4:80681190-80681201
18	BHLHE40	chr4:80553336-80553617	K562	blood:	n/a	n/a
19	BHLHE40	chr4:80599720-80600214	K562	blood:	n/a	n/a
20	BRCA1	chr4:80807403-80807424	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:80606631-80606641	HepG2	liver:	n/a	n/a
22	CBX3	chr4:80599555-80600094	K562	blood:	n/a	n/a
23	CBX3	chr4:80710064-80710413	K562	blood:	n/a	n/a
24	CBX3	chr4:80710056-80710422	K562	blood:	n/a	n/a
25	CBX3	chr4:80553248-80553613	K562	blood:	n/a	n/a
26	CBX3	chr4:80688764-80689088	K562	blood:	n/a	n/a
27	CBX3	chr4:80799340-80799593	K562	blood:	n/a	n/a
28	CCNT2	chr4:80553289-80553615	K562	blood:	n/a	n/a
29	CCNT2	chr4:80551624-80551778	K562	blood:	n/a	n/a
30	CCNT2	chr4:80599582-80600184	K562	blood:	n/a	n/a
31	CEBPB	chr4:80599550-80600162	K562	blood:	n/a	chr4:80599946-80599957
32	CEBPB	chr4:80767481-80767657	K562	blood:	n/a	chr4:80767540-80767553 chr4:80767573-80767586 chr4:80767542-80767553 chr4:80767542-80767551
33	CEBPB	chr4:80773356-80773708	K562	blood:	n/a	n/a
34	CEBPB	chr4:80621616-80621838	K562	blood:	n/a	n/a
35	CEBPB	chr4:80706633-80706957	IMR90	lung:	n/a	chr4:80706790-80706801
36	CEBPB	chr4:80618621-80618857	HepG2	liver:	n/a	chr4:80618717-80618728
37	CEBPB	chr4:80553222-80553634	K562	blood:	n/a	n/a
38	CEBPB	chr4:80784213-80784244	K562	blood:	n/a	n/a
39	CEBPB	chr4:80731564-80731880	HepG2	liver:	n/a	chr4:80731709-80731720
40	CEBPB	chr4:80772769-80773720	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:80621582-80621882	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:80773370-80773613	K562	blood:	n/a	n/a
43	CEBPB	chr4:80573234-80573711	Hela-S3	cervix:	n/a	chr4:80573393-80573406
44	CEBPB	chr4:80779116-80779132	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:80772730-80773792	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr4:80741218-80741326	A549	lung:	n/a	chr4:80741308-80741321 chr4:80741310-80741321 chr4:80741308-80741321
47	CEBPB	chr4:80806605-80806770	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:80685475-80685488	K562	blood:	n/a	n/a
49	CEBPB	chr4:80573351-80573590	HepG2	liver:	n/a	chr4:80573393-80573406
50	CEBPB	chr4:80731548-80731883	IMR90	lung:	n/a	chr4:80731709-80731720

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80747387-80747437	NB4	blood:	n/a
2	chr4:80573233-80573283	HMEC	breast:	n/a
3	chr4:80748552-80748602	Caco-2	colon:	n/a
4	chr4:80604140-80604190	HAEpiC	amniotic membrane:	n/a
5	chr4:80747125-80747175	HEK293	kidney:	embryo
6	chr4:80775399-80775449	LNCaP	prostate:	n/a
7	chr4:80775399-80775449	BJ	skin:	n/a
8	chr4:80572259-80572309	HepG2	liver:	n/a
9	chr4:80748660-80748710	BJ	skin:	n/a
10	chr4:80747387-80747437	HCPEpiC	choroid plexus:	n/a
11	chr4:80748660-80748710	HL-60	blood:	n/a
12	chr4:80748660-80748710	SK-N-SH_RA	brain:	n/a
13	chr4:80573233-80573283	HL-60	blood:	n/a
14	chr4:80604140-80604190	Hepatocyte	liver:	n/a
15	chr4:80786707-80786757	NB4	blood:	n/a
16	chr4:80748660-80748710	HepG2	liver:	n/a
17	chr4:80573233-80573283	SAEC	small airway:	n/a
18	chr4:80748552-80748602	SK-N-SH_RA	brain:	n/a
19	chr4:80775399-80775449	AG04449	skin:	fetal
20	chr4:80775399-80775449	GM12878	blood:	n/a
21	chr4:80572259-80572309	RPTEC	kidney:	n/a
22	chr4:80572259-80572309	SK-N-SH_RA	brain:	n/a
23	chr4:80604140-80604190	HIPEpiC	eye:	n/a
24	chr4:80747125-80747175	AG09319	gingival:	n/a
25	chr4:80748552-80748602	MCF-7	breast:	n/a
26	chr4:80786707-80786757	NHDF-neo	bronchial:	n/a
27	chr4:80644890-80644940	HRCEpiC	kidney:	n/a
28	chr4:80573233-80573283	SKMC	muscle:	n/a
29	chr4:80572259-80572309	AG09309	skin:	n/a
30	chr4:80748552-80748602	CMK	blood:	n/a
31	chr4:80747387-80747437	HRE	kidney:	n/a
32	chr4:80748552-80748602	A549	lung:	n/a
33	chr4:80747387-80747437	BJ	skin:	n/a
34	chr4:80644890-80644940	GM12891	blood:	n/a
35	chr4:80747387-80747437	HMEC	breast:	n/a
36	chr4:80786707-80786757	HRCEpiC	kidney:	n/a
37	chr4:80786707-80786757	NHBE	bronchial:	n/a
38	chr4:80747387-80747437	GM19239	blood:	n/a
39	chr4:80747387-80747437	HCF	heart:	n/a
40	chr4:80748552-80748602	U87	brain:	n/a
41	chr4:80747125-80747175	SK-N-SH	brain:	n/a
42	chr4:80604140-80604190	NHDF-neo	bronchial:	n/a
43	chr4:80775399-80775449	SK-N-SH_RA	brain:	n/a
44	chr4:80748552-80748602	HNPCEpiC	eye:	n/a
45	chr4:80747125-80747175	BJ	skin:	n/a
46	chr4:80573233-80573283	CMK	blood:	n/a
47	chr4:80644890-80644940	IMR90	lung:	fetal
48	chr4:80572259-80572309	HRPEpiC	eye:	n/a
49	chr4:80604140-80604190	HCT-116	colon:	n/a
50	chr4:80786707-80786757	MCF-7	breast:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80776733..80778866-chr4:80781108..80783860,2	K562	blood:
2	chr4:80788595..80790337-chr4:80797527..80800434,2	K562	blood:
3	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
4	chr4:80552394..80554921-chr4:80558193..80559831,2	K562	blood:
5	chr4:80604769..80607470-chr4:80609950..80612780,2	K562	blood:
6	chr4:80562829..80565369-chr4:80570389..80573368,2	MCF-7	breast:
7	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
8	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
9	chr4:80799642..80801616-chr4:80802558..80804161,2	K562	blood:
10	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
11	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
12	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
13	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
14	chr4:80809631..80812535-chr4:80813453..80815966,2	K562	blood:
15	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
16	chr4:80562829..80565369-chr4:80570389..80573368,2	MCF-7	breast:
17	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
18	chr4:80788595..80790337-chr4:80797527..80800434,2	K562	blood:
19	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
20	chr4:80799642..80801616-chr4:80802558..80804161,2	K562	blood:
21	chr4:80774526..80776523-chr4:80780097..80782671,2	K562	blood:
22	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
23	chr4:80809631..80812535-chr4:80813453..80815966,2	K562	blood:
24	chr4:80032018..80033796-chr4:80556626..80558164,2	K562	blood:
25	chr4:80552394..80554921-chr4:80558193..80559831,2	K562	blood:
26	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
27	chr4:80774526..80776523-chr4:80780097..80782671,2	K562	blood:
28	chr4:80776733..80778866-chr4:80781108..80783860,2	K562	blood:
29	chr4:80604769..80607470-chr4:80609950..80612780,2	K562	blood:
30	chr4:80799782..80802342-chr4:80814982..80816736,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM8-2	chr4:80584859-80585002	NONHSAT097119
2	lnc-PRDM8-7	chr4:80763406-80763602	l_2676_chr4:80740905-80762602_adipose
3	lnc-PRDM8-8	chr4:80633330-80633763	ucscGeneNc_uc003hlv_2
4	lnc-PRDM8-7	chr4:80740906-80740955	l_2676_chr4:80740905-80762602_adipose
5	lnc-PRDM8-7	chr4:80751264-80751305	l_2676_chr4:80740905-80762602_adipose
6	lnc-PRDM8-2	chr4:80584915-80585002	XLOC_003588
7	lnc-PRDM8-8	chr4:80632771-80632952	ucscGeneNc_uc003hlv_2
8	lnc-PRDM8-2	chr4:80588084-80588280	NONHSAT097119
9	lnc-PRDM8-8	chr4:80715319-80716636	ucscGeneNc_uc003hlv_2
10	lnc-PRDM8-1	chr4:80782444-80784401	ENSG00000251321.1
11	lnc-PRDM8-2	chr4:80589143-80589281	XLOC_003588
12	lnc-PRDM8-7	chr4:80747007-80747134	l_2676_chr4:80740905-80762602_adipose
13	lnc-PRDM8-2	chr4:80611142-80611230	XLOC_003588
14	lnc-PRDM8-1	chr4:80798769-80798924	ENSG00000251321.1
15	lnc-PRDM8-8	chr4:80653963-80654080	ucscGeneNc_uc003hlv_2
16	lnc-PRDM8-2	chr4:80617567-80617991	XLOC_003588
17	lnc-PRDM8-1	chr4:80748625-80748757	ENSG00000251321.1
18	lnc-PRDM8-2	chr4:80589005-80589731	NONHSAT097119
19	lnc-PRDM8-1	chr4:80782444-80782591	ENSG00000251321.1
20	lnc-PRDM8-1	chr4:80748689-80748757	ENSG00000251321.1
21	lnc-PRDM8-7	chr4:80762510-80762602	l_2676_chr4:80740905-80762602_adipose

No data

Variant related genes	Relation type
ENSG00000212620	TF binding region
ENSG00000248408	TF binding region
PCAT4	TF binding region
ENSG00000212620	CpG island
ENSG00000248408	CpG island
PCAT4	CpG island

Extended variants
information (count: 5546 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:5546 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114353807	chr4:80549669-80549670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557085807	chr4:80549697-80549698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142752055	chr4:80549709-80549710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542750951	chr4:80549723-80549724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553532316	chr4:80549755-80549756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573458707	chr4:80549810-80549811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569466971	chr4:80549813-80549814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184846425	chr4:80549834-80549835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570355176	chr4:80549846-80549847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73830568	chr4:80549933-80549934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529099961	chr4:80549941-80549942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374316559	chr4:80549975-80549976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115444167	chr4:80550042-80550043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376583648	chr4:80550067-80550068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72865042	chr4:80550078-80550079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191998723	chr4:80550111-80550112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184818816	chr4:80550119-80550120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189182866	chr4:80550137-80550138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532144172	chr4:80550170-80550171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147370513	chr4:80550219-80550220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139469536	chr4:80550225-80550226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537738566	chr4:80550234-80550235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548509461	chr4:80550264-80550265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567529883	chr4:80550271-80550272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536678366	chr4:80550411-80550412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553469197	chr4:80550419-80550420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11098788	chr4:80550428-80550429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs11098789	chr4:80550505-80550506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs145061439	chr4:80550509-80550510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575843210	chr4:80550611-80550612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544558025	chr4:80550632-80550633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115927554	chr4:80550656-80550657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574320430	chr4:80550658-80550659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180980835	chr4:80550672-80550673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539866525	chr4:80550714-80550715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559766341	chr4:80550721-80550722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72865046	chr4:80550791-80550792	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs551892117	chr4:80550807-80550808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562537975	chr4:80550809-80550810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531560931	chr4:80550819-80550820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113616568	chr4:80550898-80550899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547743020	chr4:80550945-80550946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17004008	chr4:80550946-80550947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113315785	chr4:80550951-80550952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60454622	chr4:80550989-80550990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185760356	chr4:80551003-80551004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539131339	chr4:80551025-80551026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34049528	chr4:80551087-80551088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189874271	chr4:80551212-80551213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575731450	chr4:80551216-80551217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80545000-80551400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr4:80545000-80555400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:80545400-80555200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:80547000-80552800	Weak transcription	K562	blood
5	chr4:80551400-80553000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:80551600-80551800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:80551800-80552800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr4:80551800-80553000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:80552800-80553200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:80552800-80553200	Enhancers	K562	blood
11	chr4:80552800-80553600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:80552800-80553600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:80553000-80553400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:80553000-80559400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:80553200-80553400	Flanking Active TSS	K562	blood
16	chr4:80553200-80553600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr4:80553200-80553600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:80553200-80553800	Enhancers	NHEK	skin
19	chr4:80553200-80555200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr4:80553400-80553600	Enhancers	K562	blood
21	chr4:80553400-80555400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:80553600-80553800	Flanking Active TSS	K562	blood
23	chr4:80553600-80555400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr4:80553800-80554000	Enhancers	K562	blood
25	chr4:80555200-80555600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:80555200-80555600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:80555200-80555600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:80555200-80555600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:80555200-80555800	Enhancers	Brain Germinal Matrix	brain
30	chr4:80555200-80556000	Enhancers	Fetal Brain Female	brain
31	chr4:80555400-80555600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:80555400-80555600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:80555400-80555800	Enhancers	Fetal Brain Male	brain
34	chr4:80555400-80556400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:80555600-80566600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr4:80555600-80566800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr4:80555800-80556800	Weak transcription	Brain Germinal Matrix	brain
38	chr4:80556000-80557000	Weak transcription	Fetal Brain Female	brain
39	chr4:80556400-80559800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr4:80557000-80557200	Enhancers	Brain Germinal Matrix	brain
41	chr4:80557000-80557600	Enhancers	Fetal Brain Female	brain
42	chr4:80558200-80558400	Enhancers	Dnd41	blood
43	chr4:80558400-80559600	Weak transcription	Dnd41	blood
44	chr4:80559400-80559600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:80559600-80560800	Enhancers	Dnd41	blood
46	chr4:80559600-80566600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr4:80559800-80560200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:80562600-80563200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:80563200-80566600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr4:80563400-80563600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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