Variant report

Variant	esv2757119
Chromosome Location	chr5:75426863-75474780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:718)
CpG islands
(count:550)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:75458345-75458529	K562	blood:	n/a	n/a
2	ATF1	chr5:75442283-75442385	K562	blood:	n/a	n/a
3	ATF1	chr5:75471623-75472170	K562	blood:	n/a	n/a
4	ATF2	chr5:75474597-75475178	GM12878	blood:	n/a	n/a
5	ATF2	chr5:75474650-75475133	GM12878	blood:	n/a	n/a
6	ATF2	chr5:75471452-75472442	GM12878	blood:	n/a	n/a
7	ATF2	chr5:75471604-75472348	GM12878	blood:	n/a	n/a
8	ATF3	chr5:75471599-75472016	K562	blood:	n/a	n/a
9	BATF	chr5:75474748-75475148	GM12878	blood:	n/a	n/a
10	BATF	chr5:75471890-75472287	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:75440843-75440979	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr5:75474738-75475112	GM12878	blood:	n/a	n/a
13	BCL3	chr5:75473860-75474199	GM12878	blood:	n/a	n/a
14	BCL3	chr5:75474685-75475133	GM12878	blood:	n/a	n/a
15	BCL3	chr5:75471555-75472304	GM12878	blood:	n/a	n/a
16	BCLAF1	chr5:75470838-75471335	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:75471604-75472393	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:75471619-75472026	K562	blood:	n/a	n/a
19	BHLHE40	chr5:75470933-75471235	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:75471965-75472226	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:75441876-75442076	K562	blood:	n/a	n/a
22	CBX3	chr5:75471552-75472056	K562	blood:	n/a	n/a
23	CCNT2	chr5:75471729-75471951	K562	blood:	n/a	chr5:75471940-75471949
24	CEBPB	chr5:75439721-75440086	HepG2	liver:	n/a	chr5:75439901-75439912
25	CEBPB	chr5:75444208-75444493	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:75439719-75440089	IMR90	lung:	n/a	chr5:75439901-75439912
27	CEBPB	chr5:75452257-75452426	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:75471319-75472430	GM12878	blood:	n/a	chr5:75472082-75472093
29	CEBPB	chr5:75439723-75440097	H1-hESC	embryonic stem cell:	n/a	chr5:75439901-75439912
30	CEBPB	chr5:75439724-75440079	A549	lung:	n/a	chr5:75439901-75439912
31	CEBPB	chr5:75439722-75440030	MCF-7	breast:	n/a	chr5:75439901-75439912
32	CEBPB	chr5:75471561-75471990	K562	blood:	n/a	n/a
33	CEBPB	chr5:75439750-75440070	Hela-S3	cervix:	n/a	chr5:75439901-75439912
34	CEBPB	chr5:75471615-75472408	K562	blood:	n/a	chr5:75472082-75472093
35	CEBPB	chr5:75439719-75440084	K562	blood:	n/a	chr5:75439901-75439912
36	CEBPB	chr5:75439743-75440041	K562	blood:	n/a	chr5:75439901-75439912
37	CEBPB	chr5:75444202-75444422	MCF-7	breast:	n/a	n/a
38	CEBPB	chr5:75439766-75440023	ECC-1	luminal epithelium:	n/a	chr5:75439901-75439912
39	CEBPD	chr5:75471581-75472156	K562	blood:	n/a	n/a
40	CEBPD	chr5:75471616-75472089	K562	blood:	n/a	n/a
41	CHD2	chr5:75470986-75471111	HepG2	liver:	n/a	n/a
42	CREB1	chr5:75462653-75463210	GM12878	blood:	n/a	n/a
43	CREB1	chr5:75462671-75463124	GM12878	blood:	n/a	n/a
44	CTCF	chr5:75470660-75470810	GM12867	blood:	n/a	n/a
45	CTCF	chr5:75470980-75471130	HEK293	kidney:	n/a	chr5:75471073-75471082 chr5:75471062-75471083 chr5:75471067-75471085
46	CTCF	chr5:75441847-75442054	MCF-7	breast:	n/a	chr5:75441948-75441966
47	CTCF	chr5:75442100-75442250	HRE	kidney:	n/a	n/a
48	CTCF	chr5:75441860-75442010	Pancreas_OC	pancreas:	n/a	chr5:75441948-75441966
49	CTCF	chr5:75471000-75471150	AG10803	skin:	n/a	chr5:75471073-75471082 chr5:75471062-75471083 chr5:75471067-75471085
50	CTCF	chr5:75470860-75471290	A549	lung:	n/a	chr5:75471073-75471082 chr5:75471062-75471083 chr5:75471067-75471085

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75470039-75470089	RPTEC	kidney:	n/a
2	chr5:75470039-75470089	RPTEC	kidney:	n/a
3	chr5:75469969-75470019	GM12878	blood:	n/a
4	chr5:75471166-75471216	AoSMC	blood vessel:	n/a
5	chr5:75469904-75469954	BJ	skin:	n/a
6	chr5:75464408-75464458	ProgFib	skin:	n/a
7	chr5:75472143-75472193	AG04449	skin:	fetal
8	chr5:75469969-75470019	HEK293	kidney:	embryo
9	chr5:75464408-75464458	GM12878	blood:	n/a
10	chr5:75464408-75464458	SAEC	small airway:	n/a
11	chr5:75469826-75469876	HUVEC	blood vessel:	n/a
12	chr5:75469969-75470019	H1-hESC	embryonic stem cell:	embryo
13	chr5:75464408-75464458	PFSK-1	brain:	n/a
14	chr5:75469826-75469876	Hela-S3	cervix:	n/a
15	chr5:75469826-75469876	HRE	kidney:	n/a
16	chr5:75464408-75464458	ECC-1	luminal epithelium:	n/a
17	chr5:75472143-75472193	HRPEpiC	eye:	n/a
18	chr5:75464408-75464458	NB4	blood:	n/a
19	chr5:75471166-75471216	PFSK-1	brain:	n/a
20	chr5:75470039-75470089	A549	lung:	n/a
21	chr5:75469969-75470019	HepG2	liver:	n/a
22	chr5:75471166-75471216	SK-N-SH	brain:	n/a
23	chr5:75465603-75465653	SK-N-SH	brain:	n/a
24	chr5:75465603-75465653	PFSK-1	brain:	n/a
25	chr5:75465603-75465653	NH-A	brain:	n/a
26	chr5:75464408-75464458	H1-hESC	embryonic stem cell:	embryo
27	chr5:75470039-75470089	HEEpiC	esophagus:	n/a
28	chr5:75469826-75469876	MCF-7	breast:	n/a
29	chr5:75469826-75469876	AoSMC	blood vessel:	n/a
30	chr5:75464408-75464458	HRPEpiC	eye:	n/a
31	chr5:75465603-75465653	HRPEpiC	eye:	n/a
32	chr5:75469969-75470019	GM06990	blood:	n/a
33	chr5:75465603-75465653	MCF-7	breast:	n/a
34	chr5:75471166-75471216	SK-N-SH_RA	brain:	n/a
35	chr5:75465603-75465653	HUVEC	blood vessel:	n/a
36	chr5:75469826-75469876	HRCEpiC	kidney:	n/a
37	chr5:75473201-75473251	HRE	kidney:	n/a
38	chr5:75470039-75470089	NHBE	bronchial:	n/a
39	chr5:75471166-75471216	K562	blood:	n/a
40	chr5:75465603-75465653	Hepatocyte	liver:	n/a
41	chr5:75473201-75473251	K562	blood:	n/a
42	chr5:75469904-75469954	ECC-1	luminal epithelium:	n/a
43	chr5:75469904-75469954	NHBE	bronchial:	n/a
44	chr5:75473201-75473251	HCF	heart:	n/a
45	chr5:75469826-75469876	SK-N-SH_RA	brain:	n/a
46	chr5:75469969-75470019	NB4	blood:	n/a
47	chr5:75465603-75465653	LNCaP	prostate:	n/a
48	chr5:75464408-75464458	GM12891	blood:	n/a
49	chr5:75469904-75469954	SK-N-SH_RA	brain:	n/a
50	chr5:75469826-75469876	Caco-2	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
2	chr5:75011937..75013471-chr5:75474552..75477211,2	MCF-7	breast:
3	chr5:75182130..75182669-chr5:75470688..75471450,3	MCF-7	breast:
4	chr5:75031130..75031721-chr5:75470748..75471418,2	MCF-7	breast:
5	chr5:75470625..75471456-chr5:75551799..75552684,5	MCF-7	breast:
6	chr2:175960283..175962736-chr5:75428852..75431360,2	MCF-7	breast:
7	chr5:75370258..75370917-chr5:75470691..75471438,2	MCF-7	breast:
8	chr5:75370002..75370997-chr5:75470399..75471572,8	MCF-7	breast:
9	chr5:75369710..75371593-chr5:75472300..75473889,2	K562	blood:
10	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
11	chr5:75441859..75445534-chr5:75469171..75472141,3	K562	blood:
12	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
13	chr5:75030911..75031730-chr5:75470555..75471416,3	MCF-7	breast:
14	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000251668	TF binding region
ENSG00000254893	TF binding region
ENSG00000251668	CpG island
ENSG00000254893	CpG island
ENSG00000254893	chromatin interactions
ENSG00000249777	chromatin interactions
ENSG00000152359	chromatin interactions

Extended variants
information (count: 1114 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371722323	chr5:75428011-75428012	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs200407202	chr5:75428021-75428022	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528331991	chr5:75428044-75428045	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73130289	chr5:75428070-75428071	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs143178564	chr5:75428074-75428075	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370011561	chr5:75428097-75428098	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373545330	chr5:75428098-75428099	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199759329	chr5:75428108-75428109	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370586925	chr5:75428130-75428131	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182655756	chr5:75428164-75428165	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537436682	chr5:75428166-75428167	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376084851	chr5:75428181-75428182	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370097334	chr5:75428190-75428191	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557623516	chr5:75430812-75430813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574200044	chr5:75430814-75430815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192291936	chr5:75430910-75430911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368603665	chr5:75430973-75430974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530790993	chr5:75431034-75431035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182301046	chr5:75431041-75431042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372688347	chr5:75431126-75431127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550594017	chr5:75431138-75431139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186022798	chr5:75431164-75431165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570608193	chr5:75431194-75431195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577879825	chr5:75431198-75431199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543394943	chr5:75431199-75431200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563575534	chr5:75431249-75431250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529132452	chr5:75431267-75431268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189828077	chr5:75431272-75431273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559905746	chr5:75431290-75431291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34681499	chr5:75431316-75431317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76132001	chr5:75431350-75431351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539293576	chr5:75431352-75431353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139227019	chr5:75431385-75431386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114978829	chr5:75431414-75431415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12657223	chr5:75431439-75431440	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs551018640	chr5:75431448-75431449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199671286	chr5:75431559-75431560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17746851	chr5:75433601-75433602	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs6863226	chr5:75433638-75433639	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546520749	chr5:75433653-75433654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563018286	chr5:75433775-75433776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191953216	chr5:75433831-75433832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76908770	chr5:75433874-75433875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535931263	chr5:75433878-75433879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560987538	chr5:75433926-75433927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12659363	chr5:75433933-75433934	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs34715685	chr5:75433939-75433940	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566504815	chr5:75433940-75433941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185247358	chr5:75433963-75433964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35273704	chr5:75433966-75433967	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	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
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75428000-75428200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:75428000-75428200	Enhancers	Pancreas	Pancrea
3	chr5:75430800-75431600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:75433600-75434200	Enhancers	Placenta	Placenta
5	chr5:75438000-75440400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:75439200-75439400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:75439400-75439600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:75439600-75441400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:75439800-75442400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:75440000-75440200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr5:75440000-75440600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:75440000-75441800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr5:75440200-75442200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr5:75440400-75440600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:75440400-75442200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:75440400-75442600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:75440600-75440800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr5:75440600-75441000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:75440800-75442400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:75441000-75441600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:75441000-75441800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr5:75441000-75441800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:75441400-75442200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr5:75441400-75442400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr5:75442200-75449800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr5:75442400-75443200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr5:75442600-75443200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr5:75443200-75443400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:75443200-75443400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr5:75443200-75443400	Enhancers	Pancreas	Pancrea
31	chr5:75443200-75445400	Enhancers	Ovary	ovary
32	chr5:75443400-75444000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr5:75443400-75444600	Weak transcription	Pancreas	Pancrea
34	chr5:75444600-75445400	Enhancers	Pancreas	Pancrea
35	chr5:75444600-75447800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:75445400-75447200	Weak transcription	Pancreas	Pancrea
37	chr5:75447200-75447800	Enhancers	Pancreas	Pancrea
38	chr5:75447200-75448800	Enhancers	HUVEC	blood vessel
39	chr5:75447200-75449000	Enhancers	Gastric	stomach
40	chr5:75449200-75449400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr5:75449800-75450600	Enhancers	H9 Cell Line	embryonic stem cell
42	chr5:75449800-75450600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr5:75450000-75450400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr5:75450200-75451000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr5:75450200-75451200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr5:75450200-75451400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr5:75450400-75451200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr5:75450400-75451400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr5:75450600-75451000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr5:75450600-75451600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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