Variant report

Variant	nsv830354
Chromosome Location	chr5:75074143-75259398
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	ARID3A	chr5:75190340-75190539	HepG2	liver:	n/a	n/a
2	ATF1	chr5:75114533-75114536	K562	blood:	n/a	n/a
3	ATF1	chr5:75231556-75231599	K562	blood:	n/a	n/a
4	ATF2	chr5:75181091-75181566	GM12878	blood:	n/a	n/a
5	ATF2	chr5:75143016-75143983	GM12878	blood:	n/a	n/a
6	ATF2	chr5:75133129-75133647	GM12878	blood:	n/a	n/a
7	ATF2	chr5:75143015-75143908	GM12878	blood:	n/a	n/a
8	BATF	chr5:75143260-75143829	GM12878	blood:	n/a	n/a
9	BATF	chr5:75231434-75231714	GM12878	blood:	n/a	n/a
10	BATF	chr5:75186426-75186707	GM12878	blood:	n/a	n/a
11	BATF	chr5:75143255-75143843	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:75143279-75143764	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
13	BCL11A	chr5:75143255-75143876	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
14	BCL3	chr5:75143295-75143812	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
15	BCLAF1	chr5:75143072-75143934	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
16	BCLAF1	chr5:75143147-75143817	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
17	BHLHE40	chr5:75182182-75182311	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:75143332-75143767	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:75133202-75133334	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:75201528-75201544	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:75147851-75147873	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:75143364-75143717	GM12878	blood:	n/a	n/a
23	CEBPB	chr5:75162122-75162123	K562	blood:	n/a	n/a
24	CEBPB	chr5:75182177-75182351	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:75143152-75144063	GM12878	blood:	n/a	n/a
26	CHD1	chr5:75143178-75144080	GM12878	blood:	n/a	n/a
27	CHD2	chr5:75221095-75221100	K562	blood:	n/a	n/a
28	CHD2	chr5:75143202-75143804	GM12878	blood:	n/a	n/a
29	CHD2	chr5:75182165-75182374	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr5:75133413-75133557	GM12878	blood:	n/a	n/a
31	CREB1	chr5:75181054-75181565	GM12878	blood:	n/a	n/a
32	CTCF	chr5:75182160-75182310	GM12870	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
33	CTCF	chr5:75182180-75182330	GM12864	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
34	CTCF	chr5:75182104-75182331	GM19240	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
35	CTCF	chr5:75182126-75182304	GM19239	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
36	CTCF	chr5:75181740-75181890	HRE	kidney:	n/a	n/a
37	CTCF	chr5:75182120-75182270	HepG2	liver:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
38	CTCF	chr5:75182140-75182290	GM12872	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
39	CTCF	chr5:75182160-75182310	NB4	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
40	CTCF	chr5:75182094-75182354	MCF-7	breast:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
41	CTCF	chr5:75183938-75184045	K562	blood:	n/a	n/a
42	CTCF	chr5:75182142-75182310	GM13976	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
43	CTCF	chr5:75182140-75182290	BE2_C	brain:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
44	CTCF	chr5:75182065-75182385	K562	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
45	CTCF	chr5:75119973-75120054	GM12878	blood:	n/a	chr5:75120010-75120018 chr5:75120011-75120019 chr5:75120008-75120026
46	CTCF	chr5:75182084-75182376	H1-hESC	embryonic stem cell:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
47	CTCF	chr5:75182120-75182270	GM06990	blood:	n/a	chr5:75182217-75182226 chr5:75182216-75182237
48	CTCF	chr5:75184060-75184210	GM12869	blood:	n/a	n/a
49	CTCF	chr5:75207016-75207157	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:75182080-75182230	HRPEpiC	eye:	n/a	chr5:75182217-75182226

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75127929-75127979	AG09319	gingival:	n/a
2	chr5:75127862-75127912	LNCaP	prostate:	n/a
3	chr5:75127862-75127912	ovcar-3	ovarian:	n/a
4	chr5:75127929-75127979	ProgFib	skin:	n/a
5	chr5:75127862-75127912	AG10803	skin:	n/a
6	chr5:75127929-75127979	NHDF-neo	bronchial:	n/a
7	chr5:75127929-75127979	HRE	kidney:	n/a
8	chr5:75127929-75127979	GM12878	blood:	n/a
9	chr5:75127929-75127979	LNCaP	prostate:	n/a
10	chr5:75127929-75127979	CMK	blood:	n/a
11	chr5:75127929-75127979	MCF10A-Er-Src	breast:	n/a
12	chr5:75127929-75127979	ECC-1	luminal epithelium:	n/a
13	chr5:75127862-75127912	NH-A	brain:	n/a
14	chr5:75127862-75127912	BJ	skin:	n/a
15	chr5:75127862-75127912	AG09309	skin:	n/a
16	chr5:75127929-75127979	HepG2	liver:	n/a
17	chr5:75127862-75127912	NT2-D1	testis:	n/a
18	chr5:75127862-75127912	HAEpiC	amniotic membrane:	n/a
19	chr5:75127929-75127979	GM12892	blood:	n/a
20	chr5:75127929-75127979	SKMC	muscle:	n/a
21	chr5:75127862-75127912	ProgFib	skin:	n/a
22	chr5:75127929-75127979	SK-N-SH	brain:	n/a
23	chr5:75127862-75127912	IMR90	lung:	fetal
24	chr5:75127929-75127979	HIPEpiC	eye:	n/a
25	chr5:75127929-75127979	PFSK-1	brain:	n/a
26	chr5:75127929-75127979	SAEC	small airway:	n/a
27	chr5:75127862-75127912	AoSMC	blood vessel:	n/a
28	chr5:75127929-75127979	A549	lung:	n/a
29	chr5:75127862-75127912	HCPEpiC	choroid plexus:	n/a
30	chr5:75127862-75127912	T-47D	breast:	n/a
31	chr5:75127862-75127912	MCF-7	breast:	n/a
32	chr5:75127862-75127912	HCM	heart:	n/a
33	chr5:75127929-75127979	HMEC	breast:	n/a
34	chr5:75127862-75127912	HEK293	kidney:	embryo
35	chr5:75127862-75127912	RPTEC	kidney:	n/a
36	chr5:75127862-75127912	SK-N-MC	brain:	n/a
37	chr5:75127929-75127979	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:75127929-75127979	GM19239	blood:	n/a
39	chr5:75127929-75127979	HCPEpiC	choroid plexus:	n/a
40	chr5:75127862-75127912	NHBE	bronchial:	n/a
41	chr5:75127929-75127979	MCF-7	breast:	n/a
42	chr5:75127862-75127912	HNPCEpiC	eye:	n/a
43	chr5:75127929-75127979	Jurkat	blood:	n/a
44	chr5:75127929-75127979	AG09309	skin:	n/a
45	chr5:75127929-75127979	NT2-D1	testis:	n/a
46	chr5:75127862-75127912	BE2_C	brain:	n/a
47	chr5:75127862-75127912	HRPEpiC	eye:	n/a
48	chr5:75127929-75127979	ovcar-3	ovarian:	n/a
49	chr5:75127929-75127979	HCT-116	colon:	n/a
50	chr5:75127862-75127912	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:75199631..75200148-chr5:75897260..75897978,2	K562	blood:
2	chr5:75188593..75190683-chr5:75197067..75199658,2	MCF-7	breast:
3	chr5:75199618..75202080-chr5:75204295..75207273,2	MCF-7	breast:
4	chr20:49340007..49342985-chr5:75118339..75121338,3	MCF-7	breast:
5	chr5:75181800..75182723-chr5:75551788..75552375,3	K562	blood:
6	chr5:75012994..75014594-chr5:75126997..75129169,2	K562	blood:
7	chr5:75011495..75013611-chr5:75196806..75199543,2	K562	blood:
8	chr20:49341351..49342130-chr5:75119338..75119859,2	MCF-7	breast:
9	chr5:75030809..75031718-chr5:75181454..75182073,2	MCF-7	breast:
10	chr5:75182130..75182669-chr5:75470688..75471450,3	MCF-7	breast:
11	chr5:75188593..75190683-chr5:75197067..75199658,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POC5-5	chr5:75206108-75206401	NONHSAT102225

Variant related genes	Relation type
ENSG00000251419	TF binding region
ENSG00000228367	TF binding region
ENSG00000249301	TF binding region
BIN2P2	TF binding region
ENSG00000251419	CpG island
ENSG00000228367	CpG island
ENSG00000249301	CpG island
BIN2P2	CpG island
ENSG00000249301	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000248684	chromatin interactions

Extended variants
information (count: 1948 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1948 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138000470	chr5:75075877-75075878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs367698767	chr5:75075907-75075908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556397962	chr5:75075911-75075912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117001394	chr5:75075915-75075916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374382123	chr5:75075929-75075930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542360575	chr5:75075946-75075947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115254274	chr5:75075955-75075956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35382970	chr5:75075963-75075964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs398064912	chr5:75075975-75075976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397697811	chr5:75075976-75075977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62368366	chr5:75075978-75075979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142075235	chr5:75076023-75076024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150856204	chr5:75076046-75076047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186421395	chr5:75076060-75076061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370413598	chr5:75076095-75076096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199940028	chr5:75076100-75076101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549718680	chr5:75076101-75076102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564615249	chr5:75076116-75076117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191040827	chr5:75076145-75076146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541718333	chr5:75076148-75076149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138196703	chr5:75076153-75076154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149564021	chr5:75076154-75076155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182119221	chr5:75076178-75076179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186848807	chr5:75076180-75076181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553321650	chr5:75076187-75076188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369700007	chr5:75076192-75076193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192856981	chr5:75076203-75076204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570113491	chr5:75076214-75076215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539311839	chr5:75076221-75076222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539768245	chr5:75076263-75076264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144208981	chr5:75076266-75076267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556413122	chr5:75076291-75076292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569852104	chr5:75076305-75076306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535676176	chr5:75076364-75076365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182895516	chr5:75076380-75076381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141066485	chr5:75076387-75076388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534669976	chr5:75076389-75076390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372504638	chr5:75076390-75076391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191407454	chr5:75094009-75094010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs182299857	chr5:75094032-75094033	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs543937948	chr5:75094041-75094042	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs187003611	chr5:75094048-75094049	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs191825486	chr5:75094072-75094073	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs376272215	chr5:75094084-75094085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs529697267	chr5:75094091-75094092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs550142940	chr5:75094102-75094103	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs376292891	chr5:75094103-75094104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs185182788	chr5:75094115-75094116	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs189911094	chr5:75094119-75094120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs117196271	chr5:75094120-75094121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75075800-75076400	Weak transcription	Right Atrium	heart
2	chr5:75094000-75094600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:75110000-75110400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:75110400-75110600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:75119600-75120400	Enhancers	Primary B cells from peripheral blood	blood
6	chr5:75119600-75120800	Enhancers	GM12878-XiMat	blood
7	chr5:75123000-75123800	Enhancers	Stomach Mucosa	stomach
8	chr5:75127400-75127600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:75127400-75127800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:75127600-75128000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:75133000-75133600	Enhancers	Primary B cells from peripheral blood	blood
12	chr5:75133600-75135600	Weak transcription	Primary B cells from peripheral blood	blood
13	chr5:75135600-75135800	Enhancers	Primary B cells from peripheral blood	blood
14	chr5:75138200-75138400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:75138200-75143000	Enhancers	Fetal Heart	heart
16	chr5:75138400-75139600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr5:75139200-75140200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:75139600-75140000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr5:75140000-75144000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr5:75140200-75144600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:75141200-75142400	Enhancers	GM12878-XiMat	blood
22	chr5:75141200-75145200	Enhancers	Primary B cells from peripheral blood	blood
23	chr5:75141600-75144600	Enhancers	Primary B cells from cord blood	blood
24	chr5:75141800-75142000	Enhancers	Pancreas	Pancrea
25	chr5:75141800-75142000	Enhancers	Spleen	Spleen
26	chr5:75142000-75143200	Weak transcription	Pancreas	Pancrea
27	chr5:75142400-75144200	Flanking Active TSS	GM12878-XiMat	blood
28	chr5:75143000-75143400	Flanking Active TSS	Fetal Heart	heart
29	chr5:75143000-75144000	Enhancers	Stomach Mucosa	stomach
30	chr5:75143200-75144000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr5:75143200-75144200	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr5:75143200-75144200	Enhancers	Gastric	stomach
33	chr5:75143200-75144200	Enhancers	Pancreas	Pancrea
34	chr5:75143200-75144200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr5:75143400-75143800	Enhancers	Fetal Heart	heart
36	chr5:75143600-75143800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr5:75143800-75144200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr5:75143800-75144200	Flanking Active TSS	Fetal Heart	heart
39	chr5:75143800-75144200	Enhancers	Spleen	Spleen
40	chr5:75144000-75144800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr5:75144200-75144600	Active TSS	Fetal Heart	heart
42	chr5:75144200-75145000	Enhancers	GM12878-XiMat	blood
43	chr5:75144600-75145200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:75144600-75146800	Enhancers	Fetal Heart	heart
45	chr5:75146800-75147200	Flanking Active TSS	Fetal Heart	heart
46	chr5:75147200-75147400	Enhancers	Fetal Heart	heart
47	chr5:75158400-75159000	Enhancers	Pancreas	Pancrea
48	chr5:75158400-75159600	Enhancers	HepG2	liver
49	chr5:75158600-75159200	Enhancers	Fetal Kidney	kidney
50	chr5:75158600-75159200	Enhancers	Stomach Mucosa	stomach

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