Variant report

Variant	esv2760892
Chromosome Location	chr4:75073700-75085646
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	BACH1	chr4:75083263-75083307	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:75073601-75073728	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr4:75073753-75073963	GM12878	blood:	n/a	n/a
4	CCNT2	chr4:75083118-75083643	K562	blood:	n/a	n/a
5	CHD1	chr4:75073764-75073956	GM12878	blood:	n/a	n/a
6	CHD2	chr4:75073616-75073752	GM12878	blood:	n/a	n/a
7	CTCF	chr4:75081156-75081304	MCF-7	breast:	n/a	n/a
8	CTCF	chr4:75074614-75074645	K562	blood:	n/a	n/a
9	CTCF	chr4:75081198-75081281	MCF-7	breast:	n/a	n/a
10	CTCF	chr4:75081190-75081230	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:75081159-75081257	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:75073580-75073730	AG04449	skin:	n/a	n/a
13	CTCF	chr4:75073660-75073810	BJ	skin:	n/a	n/a
14	CUX1	chr4:75085084-75085088	K562	blood:	n/a	n/a
15	E2F4	chr4:75083926-75084267	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr4:75073565-75073765	GM12878	blood:	n/a	n/a
17	ELF1	chr4:75080536-75080767	K562	blood:	n/a	n/a
18	FOS	chr4:75083120-75083467	MCF10A-Er-Src	breast:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
19	FOS	chr4:75085093-75085214	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr4:75073590-75073740	MCF10A-Er-Src	breast:	n/a	chr4:75073720-75073729
21	FOS	chr4:75085048-75085198	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr4:75083977-75084208	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr4:75083972-75084186	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr4:75073540-75073722	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr4:75083121-75083462	MCF10A-Er-Src	breast:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
26	FOS	chr4:75083955-75084226	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:75083121-75083441	MCF10A-Er-Src	breast:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
28	FOS	chr4:75083969-75084243	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:75083119-75083467	MCF10A-Er-Src	breast:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
30	FOS	chr4:75073522-75073786	MCF10A-Er-Src	breast:	n/a	chr4:75073720-75073729
31	FOS	chr4:75084988-75085277	MCF10A-Er-Src	breast:	n/a	n/a
32	FOSL1	chr4:75083019-75083511	HCT-116	colon:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
33	FOSL1	chr4:75083080-75083521	HCT-116	colon:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
34	FOXA1	chr4:75080453-75080954	HepG2	liver:	n/a	n/a
35	FOXA1	chr4:75080478-75080851	HepG2	liver:	n/a	n/a
36	FOXA1	chr4:75080534-75080850	HepG2	liver:	n/a	n/a
37	FOXA1	chr4:75080549-75080917	HepG2	liver:	n/a	n/a
38	FOXA1	chr4:75080582-75080809	T-47D	breast:	n/a	n/a
39	FOXA2	chr4:75080381-75080999	A549	lung:	n/a	n/a
40	FOXA2	chr4:75080465-75080840	A549	lung:	n/a	n/a
41	FOXA2	chr4:75080605-75080764	HepG2	liver:	n/a	n/a
42	IRF1	chr4:75085580-75085934	K562	blood:	n/a	chr4:75085784-75085798 chr4:75085791-75085802 chr4:75085784-75085791 chr4:75085785-75085798 chr4:75085789-75085803 chr4:75085786-75085796 chr4:75085790-75085801 chr4:75085791-75085805 chr4:75085782-75085796 chr4:75085785-75085798 chr4:75085786-75085800 chr4:75085788-75085802 chr4:75085785-75085798 chr4:75085800-75085814 chr4:75085784-75085804 chr4:75085786-75085803 chr4:75085785-75085798 chr4:75085785-75085796 chr4:75085785-75085799 chr4:75085791-75085804
43	JUN	chr4:75083209-75083448	K562	blood:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
44	JUN	chr4:75083121-75083537	K562	blood:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
45	JUND	chr4:75083112-75083574	HCT-116	colon:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
46	JUND	chr4:75083098-75083502	K562	blood:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
47	JUND	chr4:75083075-75083610	HCT-116	colon:	n/a	chr4:75083273-75083280 chr4:75083273-75083281 chr4:75083272-75083282 chr4:75083273-75083281 chr4:75083271-75083283 chr4:75083272-75083282
48	JUND	chr4:75074219-75074277	HepG2	liver:	n/a	n/a
49	JUND	chr4:75073574-75073862	H1-hESC	embryonic stem cell:	n/a	chr4:75073720-75073729
50	MAFF	chr4:75083149-75083477	K562	blood:	n/a	chr4:75083364-75083378

No.	Distal block	Cell Line	Cell type
1	chr4:75071138..75073600-chr4:75079457..75081137,2	MCF-7	breast:
2	chr4:75081253..75083346-chr4:75120623..75122127,2	K562	blood:
3	chr4:75072066..75073934-chr4:75080235..75082986,2	K562	blood:
4	chr4:75072066..75073934-chr4:75080235..75082986,2	K562	blood:

Variant related genes	Relation type
MTHFD2L	TF binding region

Extended variants
information (count: 415 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs478987	chr4:75073700-75073701	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577796959	chr4:75073730-75073731	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs143129165	chr4:75073799-75073800	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs577526662	chr4:75073860-75073861	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs370658528	chr4:75073910-75073911	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs148283254	chr4:75073978-75073979	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs374950062	chr4:75073992-75073993	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs369104764	chr4:75074009-75074010	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11427502	chr4:75074020-75074021	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs373690456	chr4:75074021-75074022	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs398107511	chr4:75074022-75074023	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs201691408	chr4:75074037-75074038	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs71219374	chr4:75074038-75074039	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs375202603	chr4:75074039-75074040	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs575201809	chr4:75074072-75074073	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs542219175	chr4:75074083-75074084	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs560860598	chr4:75074095-75074096	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs577802512	chr4:75074096-75074097	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs540513155	chr4:75074112-75074113	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565111104	chr4:75074117-75074118	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs475236	chr4:75074131-75074132	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551855072	chr4:75074154-75074155	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs189270458	chr4:75074162-75074163	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs113468339	chr4:75074187-75074188	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs549155181	chr4:75074268-75074269	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs576509123	chr4:75074281-75074282	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs369512085	chr4:75074283-75074284	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs567297976	chr4:75074288-75074289	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs535017876	chr4:75074331-75074332	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs553215005	chr4:75074342-75074343	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558871600	chr4:75074378-75074379	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs538813461	chr4:75074388-75074389	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs113242201	chr4:75074424-75074425	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575286481	chr4:75074441-75074442	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536343732	chr4:75074499-75074500	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181946227	chr4:75074500-75074501	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563448715	chr4:75074535-75074536	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572860705	chr4:75074553-75074554	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371865961	chr4:75074554-75074555	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79824144	chr4:75074571-75074572	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565128887	chr4:75074592-75074593	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576977181	chr4:75074633-75074634	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542302357	chr4:75074644-75074645	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185951948	chr4:75074693-75074694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530934974	chr4:75074717-75074718	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555515104	chr4:75074820-75074821	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7676371	chr4:75074853-75074854	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs560959797	chr4:75074867-75074868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189154513	chr4:75074929-75074930	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34974385	chr4:75074937-75074938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-small cell lung cancer	21829676	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	20952505	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75024800-75080600	Weak transcription	Left Ventricle	heart
2	chr4:75056800-75096600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:75059200-75081000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr4:75060000-75080200	Weak transcription	Dnd41	blood
5	chr4:75063800-75076600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:75064200-75096400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr4:75064400-75075000	Weak transcription	Spleen	Spleen
8	chr4:75065000-75086200	Weak transcription	Psoas Muscle	Psoas
9	chr4:75066200-75075000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr4:75066600-75074800	Weak transcription	Fetal Brain Female	brain
11	chr4:75067600-75074800	Weak transcription	Brain Germinal Matrix	brain
12	chr4:75067800-75097000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr4:75068400-75075600	Weak transcription	Brain Hippocampus Middle	brain
14	chr4:75068400-75076800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:75068400-75082400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr4:75068400-75093000	Weak transcription	Thymus	Thymus
17	chr4:75068400-75096600	Weak transcription	Adipose Nuclei	Adipose
18	chr4:75068600-75075200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:75069600-75091000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:75070600-75074000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr4:75070800-75073800	Enhancers	NHDF-Ad	bronchial
22	chr4:75070800-75074400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:75071000-75074000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr4:75071000-75074200	Enhancers	NH-A	brain
25	chr4:75071400-75074000	Enhancers	Fetal Heart	heart
26	chr4:75071400-75074800	Enhancers	NHEK	skin
27	chr4:75071800-75074000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:75071800-75074200	Enhancers	HMEC	breast
29	chr4:75071800-75096400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr4:75072000-75075000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:75072200-75074000	Enhancers	HSMM	muscle
32	chr4:75072200-75075000	Enhancers	K562	blood
33	chr4:75072200-75080200	Weak transcription	Fetal Intestine Small	intestine
34	chr4:75072200-75099200	Weak transcription	Ovary	ovary
35	chr4:75072400-75073800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:75072400-75074000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:75072400-75074200	Enhancers	Placenta Amnion	Placenta Amnion
38	chr4:75072400-75074600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:75072600-75074400	Flanking Active TSS	GM12878-XiMat	blood
40	chr4:75072600-75074600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:75072800-75074000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:75072800-75074200	Strong transcription	Fetal Thymus	thymus
43	chr4:75072800-75074400	Enhancers	HSMMtube	muscle
44	chr4:75072800-75074600	Strong transcription	Liver	Liver
45	chr4:75072800-75075800	Weak transcription	Fetal Muscle Leg	muscle
46	chr4:75072800-75076000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr4:75072800-75080200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:75072800-75080400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:75073000-75073800	Strong transcription	Brain Angular Gyrus	brain
50	chr4:75073000-75074000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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