Variant report

Variant	nsv1002031
Chromosome Location	chr4:80459528-80759113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1142)
CpG islands
(count:491)
Chromatin interactive
region (count:29)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1142 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80553365-80553702	K562	blood:	n/a	n/a
2	ARID3A	chr4:80599630-80600187	K562	blood:	n/a	n/a
3	ARID3A	chr4:80497589-80497889	K562	blood:	n/a	n/a
4	ARID3A	chr4:80685291-80685539	K562	blood:	n/a	n/a
5	ARID3A	chr4:80573413-80573707	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:80571533-80571550	K562	blood:	n/a	n/a
7	ARID3A	chr4:80541823-80542117	K562	blood:	n/a	n/a
8	ARID3A	chr4:80497603-80497843	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:80496141-80496176	K562	blood:	n/a	n/a
10	ATF1	chr4:80685309-80685612	K562	blood:	n/a	n/a
11	ATF1	chr4:80621566-80621751	K562	blood:	n/a	n/a
12	ATF1	chr4:80572632-80572652	K562	blood:	n/a	n/a
13	ATF1	chr4:80524904-80525261	K562	blood:	n/a	n/a
14	ATF1	chr4:80497516-80497891	K562	blood:	n/a	n/a
15	ATF1	chr4:80553273-80553691	K562	blood:	n/a	n/a
16	ATF1	chr4:80541811-80542045	K562	blood:	n/a	n/a
17	ATF1	chr4:80599574-80600070	K562	blood:	n/a	n/a
18	ATF1	chr4:80484457-80484657	K562	blood:	n/a	n/a
19	ATF3	chr4:80599406-80600004	K562	blood:	n/a	n/a
20	BACH1	chr4:80599834-80600042	K562	blood:	n/a	n/a
21	BATF	chr4:80681049-80681323	GM12878	blood:	n/a	chr4:80681190-80681201
22	BATF	chr4:80681101-80681304	GM12878	blood:	n/a	chr4:80681190-80681201
23	BCL11A	chr4:80473623-80473792	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr4:80497562-80497841	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:80497515-80497874	K562	blood:	n/a	n/a
26	BHLHE40	chr4:80544430-80544470	K562	blood:	n/a	n/a
27	BHLHE40	chr4:80599720-80600214	K562	blood:	n/a	n/a
28	BHLHE40	chr4:80496417-80496439	K562	blood:	n/a	n/a
29	BHLHE40	chr4:80553336-80553617	K562	blood:	n/a	n/a
30	BHLHE40	chr4:80532222-80532519	K562	blood:	n/a	n/a
31	BRCA1	chr4:80497726-80497750	HepG2	liver:	n/a	n/a
32	BRCA1	chr4:80606631-80606641	HepG2	liver:	n/a	n/a
33	CBX3	chr4:80710056-80710422	K562	blood:	n/a	n/a
34	CBX3	chr4:80599555-80600094	K562	blood:	n/a	n/a
35	CBX3	chr4:80688764-80689088	K562	blood:	n/a	n/a
36	CBX3	chr4:80710064-80710413	K562	blood:	n/a	n/a
37	CBX3	chr4:80553248-80553613	K562	blood:	n/a	n/a
38	CCNT2	chr4:80599582-80600184	K562	blood:	n/a	n/a
39	CCNT2	chr4:80553289-80553615	K562	blood:	n/a	n/a
40	CCNT2	chr4:80541582-80542094	K562	blood:	n/a	n/a
41	CCNT2	chr4:80525875-80526041	K562	blood:	n/a	n/a
42	CCNT2	chr4:80551624-80551778	K562	blood:	n/a	n/a
43	CEBPB	chr4:80559741-80559908	K562	blood:	n/a	n/a
44	CEBPB	chr4:80599550-80600162	K562	blood:	n/a	chr4:80599946-80599957
45	CEBPB	chr4:80496222-80496357	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:80507006-80507341	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr4:80621582-80621882	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:80541810-80542102	K562	blood:	n/a	chr4:80541937-80541950
49	CEBPB	chr4:80516663-80516889	HepG2	liver:	n/a	chr4:80516800-80516813
50	CEBPB	chr4:80494897-80495230	K562	blood:	n/a	chr4:80495054-80495065 chr4:80495053-80495066

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80748660-80748710	PFSK-1	brain:	n/a
2	chr4:80573233-80573283	BE2_C	brain:	n/a
3	chr4:80748552-80748602	GM06990	blood:	n/a
4	chr4:80748660-80748710	PFSK-1	brain:	n/a
5	chr4:80573233-80573283	BE2_C	brain:	n/a
6	chr4:80748552-80748602	GM06990	blood:	n/a
7	chr4:80748552-80748602	PFSK-1	brain:	n/a
8	chr4:80747125-80747175	IMR90	lung:	fetal
9	chr4:80644890-80644940	SK-N-MC	brain:	n/a
10	chr4:80747125-80747175	NH-A	brain:	n/a
11	chr4:80573233-80573283	AoSMC	blood vessel:	n/a
12	chr4:80572259-80572309	HEK293	kidney:	embryo
13	chr4:80573233-80573283	HCPEpiC	choroid plexus:	n/a
14	chr4:80747387-80747437	ProgFib	skin:	n/a
15	chr4:80572259-80572309	HIPEpiC	eye:	n/a
16	chr4:80747387-80747437	HepG2	liver:	n/a
17	chr4:80748552-80748602	RPTEC	kidney:	n/a
18	chr4:80573233-80573283	MCF10A-Er-Src	breast:	n/a
19	chr4:80572259-80572309	PrEC	prostate:	n/a
20	chr4:80604140-80604190	HCPEpiC	choroid plexus:	n/a
21	chr4:80748552-80748602	Jurkat	blood:	n/a
22	chr4:80573233-80573283	HepG2	liver:	n/a
23	chr4:80573233-80573283	HRPEpiC	eye:	n/a
24	chr4:80573233-80573283	HIPEpiC	eye:	n/a
25	chr4:80644890-80644940	MCF-7	breast:	n/a
26	chr4:80748660-80748710	CMK	blood:	n/a
27	chr4:80747125-80747175	GM12878	blood:	n/a
28	chr4:80644890-80644940	SAEC	small airway:	n/a
29	chr4:80748552-80748602	NH-A	brain:	n/a
30	chr4:80572259-80572309	HCPEpiC	choroid plexus:	n/a
31	chr4:80747387-80747437	T-47D	breast:	n/a
32	chr4:80747387-80747437	AG04449	skin:	fetal
33	chr4:80644890-80644940	HAEpiC	amniotic membrane:	n/a
34	chr4:80572259-80572309	SK-N-MC	brain:	n/a
35	chr4:80748552-80748602	HUVEC	blood vessel:	n/a
36	chr4:80748660-80748710	IMR90	lung:	fetal
37	chr4:80747387-80747437	HL-60	blood:	n/a
38	chr4:80747125-80747175	HCT-116	colon:	n/a
39	chr4:80604140-80604190	AoSMC	blood vessel:	n/a
40	chr4:80573233-80573283	SKMC	muscle:	n/a
41	chr4:80748552-80748602	CMK	blood:	n/a
42	chr4:80748552-80748602	MCF-7	breast:	n/a
43	chr4:80572259-80572309	AG10803	skin:	n/a
44	chr4:80604140-80604190	SK-N-MC	brain:	n/a
45	chr4:80748660-80748710	PrEC	prostate:	n/a
46	chr4:80748552-80748602	HCT-116	colon:	n/a
47	chr4:80573233-80573283	Hela-S3	cervix:	n/a
48	chr4:80748660-80748710	HCT-116	colon:	n/a
49	chr4:80573233-80573283	HAEpiC	amniotic membrane:	n/a
50	chr4:80604140-80604190	T-47D	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
2	chr4:80509176..80511123-chr4:80514677..80516383,2	K562	blood:
3	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
4	chr4:80552394..80554921-chr4:80558193..80559831,2	K562	blood:
5	chr4:80241849..80242382-chr4:80497698..80498294,2	MCF-7	breast:
6	chr4:80562829..80565369-chr4:80570389..80573368,2	MCF-7	breast:
7	chr4:80552394..80554921-chr4:80558193..80559831,2	K562	blood:
8	chr4:80516564..80518189-chr4:80518557..80520658,2	K562	blood:
9	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
10	chr4:79963329..79963907-chr4:80497328..80498247,2	K562	blood:
11	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
12	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
13	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
14	chr4:80162158..80162658-chr4:80497305..80497853,2	MCF-7	breast:
15	chr4:80604769..80607470-chr4:80609950..80612780,2	K562	blood:
16	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
17	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
18	chr17:59884431..59885001-chr4:80544092..80544675,2	MCF-7	breast:
19	chr4:79963311..79963867-chr4:80497354..80497886,2	MCF-7	breast:
20	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
21	chr4:79964140..79964963-chr4:80497048..80497852,2	MCF-7	breast:
22	chr4:80163067..80163617-chr4:80497361..80497863,2	MCF-7	breast:
23	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
24	chr4:80604769..80607470-chr4:80609950..80612780,2	K562	blood:
25	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
26	chr4:80032018..80033796-chr4:80556626..80558164,2	K562	blood:
27	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
28	chr4:80562829..80565369-chr4:80570389..80573368,2	MCF-7	breast:
29	chr4:80281030..80283740-chr4:80487916..80490045,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM8-7	chr4:80740906-80740955	l_2676_chr4:80740905-80762602_adipose
2	lnc-PRDM8-7	chr4:80751264-80751305	l_2676_chr4:80740905-80762602_adipose
3	lnc-PRDM8-2	chr4:80611142-80611230	XLOC_003588
4	lnc-PRDM8-2	chr4:80584915-80585002	XLOC_003588
5	lnc-PRDM8-3	chr4:80517696-80517753	ENSG00000251399
6	lnc-PRDM8-2	chr4:80588084-80588280	NONHSAT097119
7	lnc-PRDM8-3	chr4:80518031-80518327	ENSG00000251399
8	lnc-PRDM8-2	chr4:80589005-80589731	NONHSAT097119
9	lnc-PRDM8-8	chr4:80632771-80632952	ucscGeneNc_uc003hlv_2
10	lnc-PRDM8-1	chr4:80748689-80748757	ENSG00000251321.1
11	lnc-PRDM8-2	chr4:80617567-80617991	XLOC_003588
12	lnc-PRDM8-8	chr4:80633330-80633763	ucscGeneNc_uc003hlv_2
13	lnc-PRDM8-8	chr4:80653963-80654080	ucscGeneNc_uc003hlv_2
14	lnc-PRDM8-9	chr4:80476639-80477031	NONHSAT097115
15	lnc-PRDM8-7	chr4:80747007-80747134	l_2676_chr4:80740905-80762602_adipose
16	lnc-BMP2K-3	chr4:80496295-80497614	NONHSAT097114
17	lnc-PRDM8-9	chr4:80472781-80474355	NONHSAT097115
18	lnc-BMP2K-3	chr4:80496295-80497614	ENSG00000250334
19	lnc-PRDM8-8	chr4:80715319-80716636	ucscGeneNc_uc003hlv_2
20	lnc-PRDM8-2	chr4:80584859-80585002	NONHSAT097119
21	lnc-BMP2K-3	chr4:80496295-80497612	ENSG00000250334
22	lnc-PRDM8-1	chr4:80748625-80748757	ENSG00000251321.1
23	lnc-PRDM8-2	chr4:80589143-80589281	XLOC_003588

No data

Variant related genes	Relation type
OR7E94P	TF binding region
ENSG00000248408	TF binding region
PCAT4	TF binding region
ENSG00000251399	TF binding region
OR7E94P	CpG island
ENSG00000248408	CpG island
PCAT4	CpG island
ENSG00000251399	CpG island
ENSG00000249646	chromatin interactions
ENSG00000251399	chromatin interactions

Extended variants
information (count: 6956 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6956 , 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	rs536519096	chr4:80461238-80461239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553157292	chr4:80461283-80461284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115183559	chr4:80461287-80461288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115937202	chr4:80461335-80461336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145498227	chr4:80461464-80461465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148828415	chr4:80461480-80461481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543813803	chr4:80461489-80461490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376327525	chr4:80461506-80461507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554110231	chr4:80461530-80461531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574812814	chr4:80461534-80461535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540547564	chr4:80461570-80461571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370970047	chr4:80461599-80461600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529647651	chr4:80465006-80465007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76446229	chr4:80465008-80465009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113177681	chr4:80465010-80465011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575846940	chr4:80465014-80465015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566188469	chr4:80465080-80465081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142148987	chr4:80465092-80465093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558028316	chr4:80465093-80465094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571424695	chr4:80465102-80465103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548711581	chr4:80465149-80465150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111991695	chr4:80465176-80465177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536591674	chr4:80465182-80465183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573683935	chr4:80465183-80465184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534633402	chr4:80465186-80465187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191184239	chr4:80465204-80465205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555634334	chr4:80465213-80465214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572203555	chr4:80465245-80465246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183446210	chr4:80465297-80465298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564243633	chr4:80465315-80465316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533085964	chr4:80465395-80465396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187938565	chr4:80465405-80465406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571095111	chr4:80465428-80465429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528891771	chr4:80465439-80465440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548655936	chr4:80465440-80465441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566373278	chr4:80465449-80465450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528747397	chr4:80465452-80465453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111765473	chr4:80465458-80465459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555322125	chr4:80465498-80465499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140222688	chr4:80465523-80465524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537184232	chr4:80465524-80465525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550654895	chr4:80465529-80465530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567371898	chr4:80465618-80465619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573589886	chr4:80465620-80465621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536655926	chr4:80465676-80465677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113240644	chr4:80465685-80465686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572324688	chr4:80465777-80465778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554854685	chr4:80465815-80465816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559208137	chr4:80465924-80465925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572627789	chr4:80466026-80466027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:849 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80461200-80461600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:80465000-80478200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:80466600-80467000	Enhancers	K562	blood
4	chr4:80466800-80467000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr4:80466800-80467200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
6	chr4:80466800-80467600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
7	chr4:80467000-80468200	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:80467200-80468200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:80467600-80485600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr4:80467800-80468400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr4:80468200-80468400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr4:80468200-80468800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:80468200-80469200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr4:80468400-80469200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:80468400-80470000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr4:80468400-80471800	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr4:80468600-80469400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:80468800-80469400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr4:80468800-80469600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr4:80469200-80470600	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:80469400-80470200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr4:80469400-80471800	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr4:80469600-80470000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr4:80470000-80475200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr4:80470200-80470600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr4:80470600-80471200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:80470600-80473400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr4:80471200-80473600	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr4:80471200-80474800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:80471800-80473200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr4:80471800-80473200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
32	chr4:80473200-80473800	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr4:80473200-80474600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr4:80473400-80473800	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr4:80473600-80474000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:80473600-80474200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr4:80473600-80474200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr4:80473600-80474400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:80473800-80474600	Genic enhancers	HUES64 Cell Line	embryonic stem cell
40	chr4:80473800-80475000	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
41	chr4:80474000-80474200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:80474200-80474600	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr4:80474200-80480000	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr4:80474200-80481600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr4:80474600-80474800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:80474600-80475000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
47	chr4:80474600-80475000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr4:80474800-80475200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:80474800-80478400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr4:80475000-80475200	Strong transcription	HUES6 Cell Line	embryonic stem cell

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