Variant report

Variant	nsv933370
Chromosome Location	chr4:80641162-80856064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:872)
CpG islands
(count:611)
Chromatin interactive
region (count:28)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:872 , 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	chr4:80833114-80833129	K562	blood:	n/a	n/a
3	ATF1	chr4:80792382-80792496	K562	blood:	n/a	n/a
4	ATF1	chr4:80685309-80685612	K562	blood:	n/a	n/a
5	ATF1	chr4:80790831-80791068	K562	blood:	n/a	n/a
6	ATF1	chr4:80773436-80773735	K562	blood:	n/a	n/a
7	BACH1	chr4:80835268-80835271	K562	blood:	n/a	n/a
8	BATF	chr4:80681049-80681323	GM12878	blood:	n/a	chr4:80681190-80681201
9	BATF	chr4:80681101-80681304	GM12878	blood:	n/a	chr4:80681190-80681201
10	BHLHE40	chr4:80844337-80844352	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:80807403-80807424	GM12878	blood:	n/a	n/a
12	CBX3	chr4:80799340-80799593	K562	blood:	n/a	n/a
13	CBX3	chr4:80839504-80839840	K562	blood:	n/a	n/a
14	CBX3	chr4:80688764-80689088	K562	blood:	n/a	n/a
15	CBX3	chr4:80839348-80839823	K562	blood:	n/a	n/a
16	CBX3	chr4:80710056-80710422	K562	blood:	n/a	n/a
17	CBX3	chr4:80710064-80710413	K562	blood:	n/a	n/a
18	CEBPB	chr4:80825811-80826045	K562	blood:	n/a	n/a
19	CEBPB	chr4:80773350-80773719	K562	blood:	n/a	n/a
20	CEBPB	chr4:80741210-80741367	K562	blood:	n/a	chr4:80741308-80741321 chr4:80741310-80741321 chr4:80741308-80741321
21	CEBPB	chr4:80773356-80773708	K562	blood:	n/a	n/a
22	CEBPB	chr4:80685475-80685488	K562	blood:	n/a	n/a
23	CEBPB	chr4:80773387-80773711	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:80731564-80731880	HepG2	liver:	n/a	chr4:80731709-80731720
25	CEBPB	chr4:80845083-80845342	HepG2	liver:	n/a	chr4:80845200-80845211
26	CEBPB	chr4:80779116-80779132	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:80741218-80741326	A549	lung:	n/a	chr4:80741308-80741321 chr4:80741310-80741321 chr4:80741308-80741321
28	CEBPB	chr4:80773247-80773927	HCT-116	colon:	n/a	n/a
29	CEBPB	chr4:80773353-80773733	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:80773370-80773613	K562	blood:	n/a	n/a
31	CEBPB	chr4:80706714-80706914	A549	lung:	n/a	chr4:80706790-80706801
32	CEBPB	chr4:80772769-80773720	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:80773198-80773899	HCT-116	colon:	n/a	n/a
34	CEBPB	chr4:80845071-80845363	K562	blood:	n/a	chr4:80845200-80845211
35	CEBPB	chr4:80841566-80841603	HepG2	liver:	n/a	chr4:80841567-80841578 chr4:80841566-80841579
36	CEBPB	chr4:80767481-80767657	K562	blood:	n/a	chr4:80767540-80767553 chr4:80767573-80767586 chr4:80767542-80767553 chr4:80767542-80767551
37	CEBPB	chr4:80806605-80806770	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:80769907-80770099	HepG2	liver:	n/a	chr4:80769965-80769978
39	CEBPB	chr4:80784213-80784244	K562	blood:	n/a	n/a
40	CEBPB	chr4:80725691-80725968	HepG2	liver:	n/a	chr4:80725802-80725813
41	CEBPB	chr4:80845089-80845121	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:80706633-80706957	IMR90	lung:	n/a	chr4:80706790-80706801
43	CEBPB	chr4:80706630-80706962	HepG2	liver:	n/a	chr4:80706790-80706801
44	CEBPB	chr4:80772730-80773792	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:80771303-80771333	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:80731548-80731883	IMR90	lung:	n/a	chr4:80731709-80731720
47	CEBPD	chr4:80685349-80685623	K562	blood:	n/a	n/a
48	CHD2	chr4:80655647-80655866	K562	blood:	n/a	n/a
49	CTCF	chr4:80838415-80838618	Medullo	brain:	n/a	chr4:80838510-80838531 chr4:80838509-80838525 chr4:80838508-80838526 chr4:80838511-80838524
50	CTCF	chr4:80741700-80741850	GM12864	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80748552-80748602	PANC-1	pancreas:	n/a
2	chr4:80748552-80748602	PANC-1	pancreas:	n/a
3	chr4:80747125-80747175	ProgFib	skin:	n/a
4	chr4:80747387-80747437	SKMC	muscle:	n/a
5	chr4:80786707-80786757	HCPEpiC	choroid plexus:	n/a
6	chr4:80748660-80748710	HRCEpiC	kidney:	n/a
7	chr4:80747125-80747175	HRE	kidney:	n/a
8	chr4:80775399-80775449	AG04449	skin:	fetal
9	chr4:80747125-80747175	IMR90	lung:	fetal
10	chr4:80775399-80775449	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:80823062-80823112	HAEpiC	amniotic membrane:	n/a
12	chr4:80747125-80747175	GM19239	blood:	n/a
13	chr4:80747125-80747175	BJ	skin:	n/a
14	chr4:80775399-80775449	Caco-2	colon:	n/a
15	chr4:80644890-80644940	T-47D	breast:	n/a
16	chr4:80786707-80786757	AoSMC	blood vessel:	n/a
17	chr4:80832187-80832237	GM12878	blood:	n/a
18	chr4:80747125-80747175	NT2-D1	testis:	n/a
19	chr4:80786707-80786757	HAEpiC	amniotic membrane:	n/a
20	chr4:80775399-80775449	HCF	heart:	n/a
21	chr4:80644890-80644940	SK-N-MC	brain:	n/a
22	chr4:80832187-80832237	HEEpiC	esophagus:	n/a
23	chr4:80832187-80832237	HCM	heart:	n/a
24	chr4:80836552-80836602	HCPEpiC	choroid plexus:	n/a
25	chr4:80823062-80823112	T-47D	breast:	n/a
26	chr4:80786707-80786757	LNCaP	prostate:	n/a
27	chr4:80644890-80644940	NHDF-neo	bronchial:	n/a
28	chr4:80747387-80747437	GM06990	blood:	n/a
29	chr4:80775399-80775449	NHDF-neo	bronchial:	n/a
30	chr4:80775399-80775449	MCF-7	breast:	n/a
31	chr4:80823062-80823112	Caco-2	colon:	n/a
32	chr4:80644890-80644940	MCF10A-Er-Src	breast:	n/a
33	chr4:80747387-80747437	CMK	blood:	n/a
34	chr4:80823062-80823112	Hela-S3	cervix:	n/a
35	chr4:80775399-80775449	ECC-1	luminal epithelium:	n/a
36	chr4:80644890-80644940	HCT-116	colon:	n/a
37	chr4:80747125-80747175	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:80747387-80747437	HRPEpiC	eye:	n/a
39	chr4:80836552-80836602	AG04449	skin:	fetal
40	chr4:80836552-80836602	AG09319	gingival:	n/a
41	chr4:80748552-80748602	AG04450	lung:	fetal
42	chr4:80747125-80747175	SK-N-SH_RA	brain:	n/a
43	chr4:80832187-80832237	SK-N-MC	brain:	n/a
44	chr4:80747125-80747175	HUVEC	blood vessel:	n/a
45	chr4:80836552-80836602	Caco-2	colon:	n/a
46	chr4:80748660-80748710	AoSMC	blood vessel:	n/a
47	chr4:80832187-80832237	RPTEC	kidney:	n/a
48	chr4:80748552-80748602	GM12891	blood:	n/a
49	chr4:80775399-80775449	K562	blood:	n/a
50	chr4:80832187-80832237	HRPEpiC	eye:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80815942..80817955-chr4:80819970..80822494,2	K562	blood:
2	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
3	chr4:80809631..80812535-chr4:80813453..80815966,2	K562	blood:
4	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
5	chr4:80815942..80817955-chr4:80819970..80822494,2	K562	blood:
6	chr4:80819415..80820177-chr9:2843573..2844496,2	NB4	blood:
7	chr4:80825221..80827189-chr4:80827685..80831029,3	K562	blood:
8	chr4:80776733..80778866-chr4:80781108..80783860,2	K562	blood:
9	chr4:80826854..80828654-chr4:80829651..80832192,2	K562	blood:
10	chr4:80799642..80801616-chr4:80802558..80804161,2	K562	blood:
11	chr4:80788595..80790337-chr4:80797527..80800434,2	K562	blood:
12	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
13	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
14	chr4:80774526..80776523-chr4:80780097..80782671,2	K562	blood:
15	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:
16	chr4:80776733..80778866-chr4:80781108..80783860,2	K562	blood:
17	chr4:80799782..80802342-chr4:80814982..80816736,2	K562	blood:
18	chr4:80732058..80734998-chr4:80735708..80738719,4	K562	blood:
19	chr4:80825221..80827189-chr4:80827685..80831029,3	K562	blood:
20	chr4:80826854..80828654-chr4:80829651..80832192,2	K562	blood:
21	chr4:80799642..80801616-chr4:80802558..80804161,2	K562	blood:
22	chr4:80732058..80735312-chr4:80735956..80738909,3	K562	blood:
23	chr4:80788595..80790337-chr4:80797527..80800434,2	K562	blood:
24	chr4:80809631..80812535-chr4:80813453..80815966,2	K562	blood:
25	chr4:80799782..80802342-chr4:80814982..80816736,2	K562	blood:
26	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
27	chr4:80774526..80776523-chr4:80780097..80782671,2	K562	blood:
28	chr4:80670243..80673451-chr4:80674141..80676694,3	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM8-7	chr4:80747007-80747134	l_2676_chr4:80740905-80762602_adipose
2	lnc-PRDM8-1	chr4:80782444-80782591	ENSG00000251321.1
3	lnc-PRDM8-8	chr4:80653963-80654080	ucscGeneNc_uc003hlv_2
4	lnc-PRDM8-1	chr4:80798769-80798924	ENSG00000251321.1
5	lnc-PRDM8-7	chr4:80762510-80762602	l_2676_chr4:80740905-80762602_adipose
6	lnc-GK2-2	chr4:80828324-80828621	NONHSAT097126
7	lnc-PRDM8-1	chr4:80748625-80748757	ENSG00000251321.1
8	lnc-PRDM8-8	chr4:80715319-80716636	ucscGeneNc_uc003hlv_2
9	lnc-PRDM8-7	chr4:80740906-80740955	l_2676_chr4:80740905-80762602_adipose
10	lnc-PRDM8-7	chr4:80751264-80751305	l_2676_chr4:80740905-80762602_adipose
11	lnc-PRDM8-1	chr4:80748689-80748757	ENSG00000251321.1
12	lnc-PRDM8-7	chr4:80763406-80763602	l_2676_chr4:80740905-80762602_adipose
13	lnc-PRDM8-1	chr4:80782444-80784401	ENSG00000251321.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ANTXR2	hsa-miR-186-5p	chr4:80825752-80825746

Variant related genes	Relation type
ENSG00000212620	TF binding region
PCAT4	TF binding region
ENSG00000212620	CpG island
PCAT4	CpG island
ENSG00000080608	chromatin interactions

Extended variants
information (count: 4830 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4830 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140393350	chr4:80641164-80641165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566572302	chr4:80641167-80641168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532172366	chr4:80641224-80641225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145281835	chr4:80641247-80641248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186387790	chr4:80641273-80641274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371033740	chr4:80641288-80641289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115756713	chr4:80641311-80641312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62297334	chr4:80641347-80641348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536652481	chr4:80641350-80641351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78836613	chr4:80641353-80641354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527895785	chr4:80641354-80641355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78198598	chr4:80641366-80641367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77970597	chr4:80641369-80641370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs398063730	chr4:80641370-80641371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553150085	chr4:80641392-80641393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375056978	chr4:80641407-80641408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs33981611	chr4:80641490-80641491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573311597	chr4:80641505-80641506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545200876	chr4:80641554-80641555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7686701	chr4:80641575-80641576	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs577852481	chr4:80641647-80641648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575953080	chr4:80641653-80641654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568444619	chr4:80641656-80641657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529250114	chr4:80641658-80641659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113145352	chr4:80641659-80641660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75632988	chr4:80641676-80641677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142202853	chr4:80641728-80641729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371864901	chr4:80641735-80641736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533146811	chr4:80641765-80641766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532212845	chr4:80641770-80641771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145922114	chr4:80641777-80641778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116341849	chr4:80641782-80641783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531446479	chr4:80641827-80641828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548032287	chr4:80641881-80641882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138556885	chr4:80641905-80641906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191589819	chr4:80641923-80641924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182522351	chr4:80641924-80641925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566790338	chr4:80641933-80641934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9997382	chr4:80641981-80641982	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs543093155	chr4:80642035-80642036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148848354	chr4:80642061-80642062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374511288	chr4:80642065-80642066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10009183	chr4:80642095-80642096	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555267579	chr4:80642127-80642128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575097720	chr4:80642171-80642172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375965674	chr4:80642173-80642174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563018646	chr4:80642199-80642200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540596237	chr4:80642233-80642234	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs187479205	chr4:80642242-80642243	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs576804786	chr4:80642269-80642270	Weak transcription Enhancers Active TSS	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	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	20952505	CNVD

Chromatin state (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80636200-80644800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:80642000-80642600	Enhancers	Duodenum Smooth Muscle	Duodenum
3	chr4:80642200-80642600	Enhancers	Rectal Smooth Muscle	rectum
4	chr4:80642200-80642600	Active TSS	Stomach Smooth Muscle	stomach
5	chr4:80644600-80644800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:80644600-80645200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr4:80644600-80645200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:80644600-80645400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:80644800-80645000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr4:80644800-80645000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:80644800-80645000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:80644800-80645200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr4:80644800-80645200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:80645000-80645200	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr4:80657800-80658000	Enhancers	Placenta	Placenta
16	chr4:80658400-80661000	Weak transcription	Placenta	Placenta
17	chr4:80660600-80661400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:80661000-80661200	Enhancers	Placenta	Placenta
19	chr4:80661000-80661400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:80661000-80661600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:80661200-80661600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr4:80663600-80664000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:80663600-80664400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:80669000-80669200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:80669400-80671000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:80669800-80670200	Enhancers	Placenta	Placenta
27	chr4:80670000-80670200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:80670000-80670400	Enhancers	Pancreas	Pancrea
29	chr4:80670000-80670400	Enhancers	K562	blood
30	chr4:80671000-80671200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:80671200-80672000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:80675400-80675800	Enhancers	Colon Smooth Muscle	Colon
33	chr4:80675800-80676600	Enhancers	Rectal Smooth Muscle	rectum
34	chr4:80675800-80677600	Weak transcription	Colon Smooth Muscle	Colon
35	chr4:80676600-80677800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr4:80677200-80677600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:80677600-80678800	Enhancers	Colon Smooth Muscle	Colon
38	chr4:80677800-80678800	Enhancers	Rectal Smooth Muscle	rectum
39	chr4:80678200-80679000	Enhancers	Placenta Amnion	Placenta Amnion
40	chr4:80678200-80679400	Enhancers	Placenta	Placenta
41	chr4:80678600-80679400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:80678800-80679400	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr4:80683200-80683600	Enhancers	Dnd41	blood
44	chr4:80684800-80685400	Enhancers	K562	blood
45	chr4:80685600-80685800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:80691200-80697200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:80697200-80697400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:80697400-80701800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:80701800-80702000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:80703600-80704200	Enhancers	Colon Smooth Muscle	Colon

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