Variant report

Variant	nsv830317
Chromosome Location	chr5:61298840-61478113
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	ATF1	chr5:61378560-61378712	K562	blood:	n/a	n/a
2	ATF1	chr5:61303457-61303611	K562	blood:	n/a	n/a
3	ATF2	chr5:61370480-61371346	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:61370493-61371261	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:61339400-61339775	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr5:61360992-61361187	K562	blood:	n/a	n/a
7	BATF	chr5:61401781-61401944	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:61339418-61339689	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr5:61339417-61339760	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr5:61370927-61371194	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr5:61389871-61389963	K562	blood:	n/a	n/a
12	BRCA1	chr5:61419948-61419994	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:61429174-61429235	GM12878	blood:	n/a	n/a
14	CEBPB	chr5:61466469-61466739	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:61360944-61361194	HepG2	liver:	n/a	chr5:61361086-61361097
16	CEBPB	chr5:61409672-61409729	K562	blood:	n/a	chr5:61409696-61409709 chr5:61409696-61409707
17	CEBPB	chr5:61426019-61426298	ECC-1	luminal epithelium:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
18	CEBPB	chr5:61459905-61460138	K562	blood:	n/a	n/a
19	CEBPB	chr5:61435688-61435816	K562	blood:	n/a	chr5:61435701-61435712
20	CEBPB	chr5:61435638-61435838	HepG2	liver:	n/a	chr5:61435701-61435712
21	CEBPB	chr5:61434610-61434737	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:61425968-61426306	H1-hESC	embryonic stem cell:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
23	CEBPB	chr5:61357259-61357548	Hela-S3	cervix:	n/a	chr5:61357397-61357408 chr5:61357397-61357410
24	CEBPB	chr5:61325166-61325551	A549	lung:	n/a	n/a
25	CEBPB	chr5:61465307-61465380	HepG2	liver:	n/a	chr5:61465317-61465328
26	CEBPB	chr5:61378145-61378767	HCT-116	colon:	n/a	chr5:61378293-61378306
27	CEBPB	chr5:61357356-61357559	HepG2	liver:	n/a	chr5:61357397-61357408 chr5:61357397-61357410
28	CEBPB	chr5:61384963-61385162	K562	blood:	n/a	n/a
29	CEBPB	chr5:61425966-61426192	K562	blood:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
30	CEBPB	chr5:61426038-61426233	MCF-7	breast:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
31	CEBPB	chr5:61357287-61357514	A549	lung:	n/a	chr5:61357397-61357408 chr5:61357397-61357410
32	CEBPB	chr5:61384949-61385134	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr5:61469329-61469562	HepG2	liver:	n/a	chr5:61469407-61469418
34	CEBPB	chr5:61354792-61355011	HepG2	liver:	n/a	chr5:61354939-61354950
35	CEBPB	chr5:61425949-61426306	HepG2	liver:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
36	CEBPB	chr5:61475101-61475678	A549	lung:	n/a	chr5:61475260-61475269 chr5:61475260-61475271 chr5:61475260-61475269 chr5:61475258-61475269 chr5:61475260-61475269 chr5:61475258-61475271 chr5:61475260-61475269
37	CEBPB	chr5:61428083-61428425	Hela-S3	cervix:	n/a	chr5:61428233-61428244 chr5:61428231-61428244
38	CEBPB	chr5:61378164-61378611	Hela-S3	cervix:	n/a	chr5:61378293-61378306
39	CEBPB	chr5:61303442-61303605	K562	blood:	n/a	n/a
40	CEBPB	chr5:61369119-61369319	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:61475068-61475454	K562	blood:	n/a	chr5:61475260-61475269 chr5:61475260-61475271 chr5:61475260-61475269 chr5:61475258-61475269 chr5:61475260-61475269 chr5:61475258-61475271 chr5:61475260-61475269
42	CEBPB	chr5:61425913-61426319	MCF-7	breast:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
43	CEBPB	chr5:61425935-61426316	K562	blood:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
44	CEBPB	chr5:61325456-61325479	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:61466571-61466632	K562	blood:	n/a	n/a
46	CEBPB	chr5:61357295-61357455	H1-hESC	embryonic stem cell:	n/a	chr5:61357397-61357408 chr5:61357397-61357410
47	CEBPB	chr5:61475157-61475424	Hela-S3	cervix:	n/a	chr5:61475260-61475269 chr5:61475260-61475271 chr5:61475260-61475269 chr5:61475258-61475269 chr5:61475260-61475269 chr5:61475258-61475271 chr5:61475260-61475269
48	CEBPB	chr5:61425964-61426295	Hela-S3	cervix:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131
49	CEBPB	chr5:61475106-61475686	IMR90	lung:	n/a	chr5:61475260-61475269 chr5:61475260-61475271 chr5:61475260-61475269 chr5:61475258-61475269 chr5:61475260-61475269 chr5:61475258-61475271 chr5:61475260-61475269
50	CEBPB	chr5:61425945-61426327	ECC-1	luminal epithelium:	n/a	chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131 chr5:61426122-61426131

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61370304-61370354	HUVEC	blood vessel:	n/a
2	chr5:61374735-61374785	HCT-116	colon:	n/a
3	chr5:61337620-61337670	HIPEpiC	eye:	n/a
4	chr5:61337620-61337670	AG04450	lung:	fetal
5	chr5:61439790-61439840	GM19239	blood:	n/a
6	chr5:61420932-61420982	MCF10A-Er-Src	breast:	n/a
7	chr5:61439790-61439840	HRPEpiC	eye:	n/a
8	chr5:61420932-61420982	ProgFib	skin:	n/a
9	chr5:61433576-61433626	AoSMC	blood vessel:	n/a
10	chr5:61374735-61374785	Hepatocyte	liver:	n/a
11	chr5:61298898-61298948	SK-N-SH_RA	brain:	n/a
12	chr5:61370304-61370354	NHDF-neo	bronchial:	n/a
13	chr5:61374735-61374785	H1-hESC	embryonic stem cell:	embryo
14	chr5:61439790-61439840	HCPEpiC	choroid plexus:	n/a
15	chr5:61370304-61370354	HRPEpiC	eye:	n/a
16	chr5:61420932-61420982	Caco-2	colon:	n/a
17	chr5:61439790-61439840	RPTEC	kidney:	n/a
18	chr5:61374735-61374785	HCF	heart:	n/a
19	chr5:61298898-61298948	K562	blood:	n/a
20	chr5:61370304-61370354	SK-N-SH	brain:	n/a
21	chr5:61370304-61370354	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:61374735-61374785	AG04449	skin:	fetal
23	chr5:61420932-61420982	NHBE	bronchial:	n/a
24	chr5:61439790-61439840	CMK	blood:	n/a
25	chr5:61374735-61374785	SKMC	muscle:	n/a
26	chr5:61298898-61298948	MCF-7	breast:	n/a
27	chr5:61439790-61439840	BJ	skin:	n/a
28	chr5:61433576-61433626	Jurkat	blood:	n/a
29	chr5:61439790-61439840	K562	blood:	n/a
30	chr5:61433576-61433626	RPTEC	kidney:	n/a
31	chr5:61374735-61374785	HRCEpiC	kidney:	n/a
32	chr5:61370304-61370354	AG10803	skin:	n/a
33	chr5:61433576-61433626	T-47D	breast:	n/a
34	chr5:61374735-61374785	RPTEC	kidney:	n/a
35	chr5:61370304-61370354	HAEpiC	amniotic membrane:	n/a
36	chr5:61337620-61337670	HNPCEpiC	eye:	n/a
37	chr5:61439790-61439840	AG09309	skin:	n/a
38	chr5:61433576-61433626	HCT-116	colon:	n/a
39	chr5:61374735-61374785	AG09309	skin:	n/a
40	chr5:61439790-61439840	NH-A	brain:	n/a
41	chr5:61298898-61298948	GM12892	blood:	n/a
42	chr5:61433576-61433626	PFSK-1	brain:	n/a
43	chr5:61298898-61298948	CMK	blood:	n/a
44	chr5:61370304-61370354	HCF	heart:	n/a
45	chr5:61433576-61433626	Hela-S3	cervix:	n/a
46	chr5:61433576-61433626	HRPEpiC	eye:	n/a
47	chr5:61374735-61374785	GM06990	blood:	n/a
48	chr5:61420932-61420982	BJ	skin:	n/a
49	chr5:61439790-61439840	SAEC	small airway:	n/a
50	chr5:61433576-61433626	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:61424317..61428011-chr5:61428590..61430862,3	K562	blood:
2	chr5:61437415..61439852-chr5:61446212..61449062,2	K562	blood:
3	chr1:190820569..190821089-chr5:61468212..61468732,2	MCF-7	breast:
4	chr5:61437415..61439852-chr5:61446212..61449062,2	K562	blood:
5	chr5:61366065..61368035-chr5:61368040..61370720,2	K562	blood:
6	chr5:61439485..61439993-chr5:61501806..61502567,2	MCF-7	breast:
7	chr5:61296910..61298928-chr5:61315407..61317934,2	MCF-7	breast:
8	chr5:61229619..61230608-chr5:61439489..61440182,2	MCF-7	breast:
9	chr5:61366065..61368035-chr5:61368040..61370720,2	K562	blood:
10	chr5:61426729..61428623-chr5:61433121..61435714,2	K562	blood:
11	chr5:61354756..61356477-chr5:61362437..61365300,2	MCF-7	breast:
12	chr5:61426729..61428623-chr5:61433121..61435714,2	K562	blood:
13	chr5:61334280..61336026-chr5:61338071..61340993,2	MCF-7	breast:
14	chr5:61471386..61473482-chr5:61474946..61477299,2	MCF-7	breast:
15	chr5:61442438..61445370-chr5:61445571..61447544,2	MCF-7	breast:
16	chr5:61422681..61424219-chr5:61436524..61438145,2	MCF-7	breast:
17	chr5:61422681..61424219-chr5:61436524..61438145,2	MCF-7	breast:
18	chr5:61471386..61473482-chr5:61474946..61477299,2	MCF-7	breast:
19	chr5:61424317..61428011-chr5:61428590..61430862,3	K562	blood:
20	chr5:61354756..61356477-chr5:61362437..61365300,2	MCF-7	breast:
21	chr5:61008135..61009057-chr5:61470844..61471443,2	K562	blood:
22	chr12:125398291..125400539-chr5:61461576..61463918,2	MCF-7	breast:
23	chr5:61334280..61336026-chr5:61338071..61340993,2	MCF-7	breast:
24	chr5:61296910..61298928-chr5:61315407..61317934,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF2A-2	chr5:61442492-61442773	NONHSAT101705

Variant related genes	Relation type
RN7SKP157	TF binding region
RN7SKP157	CpG island
ENSG00000150991	chromatin interactions
ENSG00000251983	chromatin interactions
ENSG00000265345	chromatin interactions

Extended variants
information (count: 4621 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4621 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114878850	chr5:61298842-61298843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182806576	chr5:61298862-61298863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554071671	chr5:61298877-61298878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151065793	chr5:61298898-61298899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557706096	chr5:61298905-61298906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577478854	chr5:61298908-61298909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565931250	chr5:61298946-61298947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369244184	chr5:61298975-61298976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs202075731	chr5:61298977-61298978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397997955	chr5:61298986-61298987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62367065	chr5:61298989-61298990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141274083	chr5:61299040-61299041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145011578	chr5:61299069-61299070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541999557	chr5:61299148-61299149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187244212	chr5:61299157-61299158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138795809	chr5:61299164-61299165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75905166	chr5:61299277-61299278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552071626	chr5:61299300-61299301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570281394	chr5:61299360-61299361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs968159	chr5:61299442-61299443	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs565775335	chr5:61299447-61299448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534670931	chr5:61299448-61299449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547981948	chr5:61299453-61299454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191652943	chr5:61299465-61299466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537059262	chr5:61299486-61299487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557028447	chr5:61299524-61299525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369563183	chr5:61299569-61299570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577591297	chr5:61299614-61299615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141942057	chr5:61299629-61299630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577812522	chr5:61299653-61299654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536571619	chr5:61299748-61299749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115117243	chr5:61299802-61299803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553523261	chr5:61299805-61299806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573367329	chr5:61299911-61299912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143350126	chr5:61299937-61299938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55638110	chr5:61300006-61300007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189262624	chr5:61300090-61300091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138644054	chr5:61300133-61300134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575202914	chr5:61300214-61300215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193147938	chr5:61300218-61300219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555053668	chr5:61300226-61300227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532436006	chr5:61300228-61300229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149307742	chr5:61300230-61300231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111739539	chr5:61300239-61300240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs3922059	chr5:61300266-61300267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541332581	chr5:61300290-61300291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528295227	chr5:61300298-61300299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548270486	chr5:61300345-61300346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568145561	chr5:61300357-61300358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530649470	chr5:61300370-61300371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	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
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	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
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
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61294800-61299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:61295000-61299000	Enhancers	HMEC	breast
3	chr5:61296400-61299000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:61298600-61301200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:61298800-61301000	Weak transcription	NHEK	skin
6	chr5:61299000-61299400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:61299000-61299400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr5:61299000-61299400	Weak transcription	HMEC	breast
9	chr5:61299400-61299600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:61299400-61299600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:61299400-61299600	Enhancers	HMEC	breast
12	chr5:61299600-61301000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:61299600-61301000	Weak transcription	HMEC	breast
14	chr5:61299600-61301200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:61301000-61302000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:61301000-61302000	Enhancers	HMEC	breast
17	chr5:61301000-61302000	Enhancers	NHEK	skin
18	chr5:61301200-61302000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr5:61301200-61302000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:61302000-61306200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:61303000-61303400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:61303000-61304000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:61304000-61305800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:61304400-61305400	Enhancers	Fetal Brain Male	brain
25	chr5:61305800-61306400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:61306200-61306800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:61306200-61308800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:61306400-61306600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:61306400-61307000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr5:61306400-61308000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:61306400-61308000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr5:61306600-61307200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr5:61306600-61307600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:61306800-61307400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:61306800-61324400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:61307000-61307400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:61307200-61307400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr5:61307400-61308400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr5:61307400-61308800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:61308000-61309000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:61308800-61309200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:61308800-61309400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr5:61309000-61309200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr5:61309000-61309600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr5:61312000-61312400	Enhancers	Placenta	Placenta
46	chr5:61312600-61313800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:61312800-61313600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:61312800-61314000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:61313000-61313400	Enhancers	Colon Smooth Muscle	Colon
50	chr5:61323400-61324600	Weak transcription	NHEK	skin

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