Variant report

Variant	esv1805457
Chromosome Location	chr5:101924774-101940526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:101)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:101 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:101931903-101932108	GM12878	blood:	n/a	chr5:101932024-101932035
2	BATF	chr5:101931890-101932126	GM12878	blood:	n/a	chr5:101932024-101932035
3	BCL11A	chr5:101931847-101932107	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:101931814-101932072	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:101931026-101931318	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:101926209-101926379	HepG2	liver:	n/a	chr5:101926321-101926334
7	CEBPB	chr5:101926218-101926424	A549	lung:	n/a	chr5:101926321-101926334
8	CTCF	chr5:101928428-101928497	Lung_OC	lung:	n/a	n/a
9	CUX1	chr5:101931733-101931971	GM12878	blood:	n/a	n/a
10	E2F4	chr5:101939550-101939749	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr5:101933395-101933558	MCF10A-Er-Src	breast:	n/a	n/a
12	EBF1	chr5:101927390-101927594	GM12878	blood:	n/a	n/a
13	EBF1	chr5:101931703-101932239	GM12878	blood:	n/a	n/a
14	EBF1	chr5:101936863-101937030	GM12878	blood:	n/a	chr5:101936947-101936958 chr5:101936990-101937001
15	EP300	chr5:101936707-101937039	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr5:101931621-101932402	GM12878	blood:	n/a	n/a
17	EP300	chr5:101925569-101925931	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr5:101927358-101927787	GM12878	blood:	n/a	n/a
19	EP300	chr5:101931068-101931369	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr5:101936706-101937069	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr5:101936668-101937043	SK-N-SH	brain:	n/a	n/a
22	EP300	chr5:101925044-101925987	SK-N-SH_RA	brain:	n/a	chr5:101925066-101925080
23	EP300	chr5:101927447-101927753	GM12878	blood:	n/a	n/a
24	EP300	chr5:101931663-101932112	GM12878	blood:	n/a	n/a
25	EP300	chr5:101931758-101932173	GM12878	blood:	n/a	n/a
26	FOS	chr5:101936695-101937015	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr5:101926240-101926525	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr5:101925420-101925709	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:101926160-101926549	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:101936656-101936911	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:101925394-101925705	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:101926215-101926559	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:101936698-101936959	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:101935114-101935314	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:101935005-101935272	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:101925394-101925655	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:101926178-101926559	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr5:101936649-101936998	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr5:101936608-101937157	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr5:101930667-101931642	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr5:101936557-101937201	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr5:101930815-101931569	SK-N-SH	brain:	n/a	n/a
43	HNF4A	chr5:101928386-101928613	HepG2	liver:	n/a	chr5:101928483-101928498
44	IKZF1	chr5:101927342-101927689	GM12878	blood:	n/a	n/a
45	JUND	chr5:101931053-101931507	SK-N-SH	brain:	n/a	n/a
46	JUND	chr5:101936583-101937154	SK-N-SH	brain:	n/a	n/a
47	MAZ	chr5:101927410-101927542	GM12878	blood:	n/a	n/a
48	MXI1	chr5:101931779-101932071	GM12878	blood:	n/a	n/a
49	MYC	chr5:101939359-101939625	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr5:101927484-101927586	NB4	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:101925501-101925551	HCPEpiC	choroid plexus:	n/a
2	chr5:101925501-101925551	HRCEpiC	kidney:	n/a
3	chr5:101925501-101925551	SK-N-SH	brain:	n/a
4	chr5:101925501-101925551	AG10803	skin:	n/a
5	chr5:101925501-101925551	NB4	blood:	n/a
6	chr5:101925501-101925551	HPAEpiC	pulmonary alveolar:	n/a
7	chr5:101925501-101925551	SK-N-SH_RA	brain:	n/a
8	chr5:101925501-101925551	HMEC	breast:	n/a
9	chr5:101925501-101925551	Jurkat	blood:	n/a
10	chr5:101925501-101925551	U87	brain:	n/a
11	chr5:101925501-101925551	SKMC	muscle:	n/a
12	chr5:101925501-101925551	HNPCEpiC	eye:	n/a
13	chr5:101925501-101925551	HCM	heart:	n/a
14	chr5:101925501-101925551	HCF	heart:	n/a
15	chr5:101925501-101925551	GM12891	blood:	n/a
16	chr5:101925501-101925551	PFSK-1	brain:	n/a
17	chr5:101925501-101925551	AG04450	lung:	fetal
18	chr5:101925501-101925551	NH-A	brain:	n/a
19	chr5:101925501-101925551	ovcar-3	ovarian:	n/a
20	chr5:101925501-101925551	Hela-S3	cervix:	n/a
21	chr5:101925501-101925551	HEEpiC	esophagus:	n/a
22	chr5:101925501-101925551	HL-60	blood:	n/a
23	chr5:101925501-101925551	HCT-116	colon:	n/a
24	chr5:101925501-101925551	MCF10A-Er-Src	breast:	n/a
25	chr5:101925501-101925551	BJ	skin:	n/a
26	chr5:101925501-101925551	GM06990	blood:	n/a
27	chr5:101925501-101925551	A549	lung:	n/a
28	chr5:101925501-101925551	RPTEC	kidney:	n/a
29	chr5:101925501-101925551	GM19239	blood:	n/a
30	chr5:101925501-101925551	LNCaP	prostate:	n/a
31	chr5:101925501-101925551	AG09309	skin:	n/a
32	chr5:101925501-101925551	GM12878	blood:	n/a
33	chr5:101925501-101925551	PrEC	prostate:	n/a
34	chr5:101925501-101925551	AG04449	skin:	fetal
35	chr5:101925501-101925551	IMR90	lung:	fetal
36	chr5:101925501-101925551	BE2_C	brain:	n/a
37	chr5:101925501-101925551	SAEC	small airway:	n/a
38	chr5:101925501-101925551	Caco-2	colon:	n/a
39	chr5:101925501-101925551	HRPEpiC	eye:	n/a
40	chr5:101925501-101925551	K562	blood:	n/a
41	chr5:101925501-101925551	AG09319	gingival:	n/a
42	chr5:101925501-101925551	ECC-1	luminal epithelium:	n/a
43	chr5:101925501-101925551	H1-hESC	embryonic stem cell:	embryo
44	chr5:101925501-101925551	MCF-7	breast:	n/a
45	chr5:101925501-101925551	PANC-1	pancreas:	n/a
46	chr5:101925501-101925551	CMK	blood:	n/a
47	chr5:101925501-101925551	NHDF-neo	bronchial:	n/a
48	chr5:101925501-101925551	T-47D	breast:	n/a
49	chr5:101925501-101925551	HIPEpiC	eye:	n/a
50	chr5:101925501-101925551	HAEpiC	amniotic membrane:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:54411410..54412268-chr5:101936573..101937073,2	Hela-S3	cervix:
2	chr5:101917966..101921211-chr5:101923509..101926669,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000247402	TF binding region
ENSG00000247402	CpG island
ENSG00000116212	chromatin interactions
ENSG00000081870	chromatin interactions

Extended variants
information (count: 549 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3105235	chr5:101924774-101924775	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114111883	chr5:101924778-101924779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182318421	chr5:101924779-101924780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141192699	chr5:101924805-101924806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563319883	chr5:101924806-101924807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566712938	chr5:101924827-101924828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534128998	chr5:101924836-101924837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149345712	chr5:101924843-101924844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530881035	chr5:101924847-101924848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9687561	chr5:101924878-101924879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs150887634	chr5:101924886-101924887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534471950	chr5:101924909-101924910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139354473	chr5:101924930-101924931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149652839	chr5:101924945-101924946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146138947	chr5:101924977-101924978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557026346	chr5:101924994-101924995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140029340	chr5:101925015-101925016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538488514	chr5:101925100-101925101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567831891	chr5:101925121-101925122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13164645	chr5:101925126-101925127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13160594	chr5:101925155-101925156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186586112	chr5:101925165-101925166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190944516	chr5:101925187-101925188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28674948	chr5:101925229-101925230	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535935244	chr5:101925239-101925240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143550649	chr5:101925270-101925271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117251268	chr5:101925345-101925346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577741372	chr5:101925358-101925359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183089181	chr5:101925399-101925400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572293296	chr5:101925498-101925499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188379845	chr5:101925501-101925502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541316675	chr5:101925571-101925572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530772123	chr5:101925593-101925594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555708705	chr5:101925595-101925596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560998686	chr5:101925600-101925601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78417908	chr5:101925601-101925602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546852455	chr5:101925657-101925658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143681967	chr5:101925670-101925671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571447365	chr5:101925675-101925676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532296178	chr5:101925706-101925707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550652500	chr5:101925738-101925739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146822944	chr5:101925765-101925766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193198451	chr5:101925830-101925831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116482205	chr5:101925953-101925954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1995572	chr5:101925961-101925962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs6886505	chr5:101925973-101925974	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs148540934	chr5:101925990-101925991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577807381	chr5:101926006-101926007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6869939	chr5:101926008-101926009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558096692	chr5:101926078-101926079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101919800-101925200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:101919800-101925600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:101920000-101925800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:101925200-101925800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:101925200-101926200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr5:101925200-101926200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:101925200-101926400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:101925400-101925800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:101925400-101925800	Enhancers	Brain Cingulate Gyrus	brain
10	chr5:101925400-101926000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:101925400-101926200	Enhancers	HMEC	breast
12	chr5:101925400-101926400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr5:101925600-101926000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr5:101925600-101926000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:101925800-101926200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:101926000-101926200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:101926000-101931600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:101926200-101926400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr5:101926200-101926800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:101926800-101927000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr5:101926800-101927000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:101928200-101929200	Enhancers	HepG2	liver
23	chr5:101929600-101930400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr5:101931400-101931600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:101931400-101931800	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr5:101931400-101932400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr5:101931400-101932400	Enhancers	GM12878-XiMat	blood
28	chr5:101931600-101932200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:101931600-101932400	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr5:101931600-101932600	Enhancers	Primary hematopoietic stem cells	blood
31	chr5:101931600-101933400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:101931800-101932200	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr5:101931800-101932200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr5:101932200-101932400	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr5:101932200-101932600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr5:101932600-101933000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr5:101933000-101935200	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr5:101933400-101933600	Enhancers	Osteobl	bone
39	chr5:101933400-101935400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:101933600-101935400	Weak transcription	Osteobl	bone
41	chr5:101935200-101937800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr5:101935200-101938000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:101935400-101935600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:101935400-101935600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr5:101935400-101935600	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr5:101935400-101935600	Enhancers	NHDF-Ad	bronchial
47	chr5:101935400-101935600	Enhancers	Osteobl	bone
48	chr5:101935400-101935800	ZNF genes & repeats	Pancreas	Pancrea
49	chr5:101935400-101938000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:101935600-101936400	Weak transcription	Osteobl	bone

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