Variant report

Variant	esv1822393
Chromosome Location	chr5:79195538-79260489
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	chr5:79236582-79236650	K562	blood:	n/a	n/a
2	ATF1	chr5:79255260-79255424	K562	blood:	n/a	n/a
3	BACH1	chr5:79259984-79260108	K562	blood:	n/a	n/a
4	CBX3	chr5:79228990-79229294	K562	blood:	n/a	n/a
5	CEBPB	chr5:79250424-79250785	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:79227240-79227611	IMR90	lung:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
7	CEBPB	chr5:79231917-79232117	K562	blood:	n/a	chr5:79232018-79232029
8	CEBPB	chr5:79227240-79227597	HepG2	liver:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
9	CEBPB	chr5:79250411-79250788	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:79227251-79227607	A549	lung:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
11	CEBPB	chr5:79250427-79250783	A549	lung:	n/a	n/a
12	CEBPB	chr5:79231873-79232171	HepG2	liver:	n/a	chr5:79232018-79232029
13	CEBPB	chr5:79215515-79215732	A549	lung:	n/a	chr5:79215617-79215628 chr5:79215647-79215658
14	CEBPB	chr5:79215594-79215653	HepG2	liver:	n/a	chr5:79215617-79215628
15	CEBPB	chr5:79227194-79227634	A549	lung:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
16	CEBPB	chr5:79250358-79250815	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:79246252-79246292	HepG2	liver:	n/a	chr5:79246270-79246281
18	CEBPB	chr5:79250619-79250672	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:79227253-79227589	K562	blood:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
20	CEBPB	chr5:79231855-79232182	IMR90	lung:	n/a	chr5:79232018-79232029
21	CEBPB	chr5:79227255-79227605	H1-hESC	embryonic stem cell:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
22	CEBPB	chr5:79231911-79232111	A549	lung:	n/a	chr5:79232018-79232029
23	CEBPB	chr5:79250466-79250758	K562	blood:	n/a	n/a
24	CEBPB	chr5:79227286-79227598	Hela-S3	cervix:	n/a	chr5:79227419-79227430 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429 chr5:79227418-79227431 chr5:79227420-79227429
25	CHD2	chr5:79234271-79234288	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr5:79255177-79255475	GM12878	blood:	n/a	n/a
27	CTCF	chr5:79257640-79257790	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr5:79220900-79221022	GM13977	blood:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
29	CTCF	chr5:79220859-79221054	GM19238	blood:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
30	CTCF	chr5:79220980-79221130	GM12873	blood:	n/a	chr5:79220983-79220996
31	CTCF	chr5:79220868-79221004	SK-N-SH_RA	brain:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
32	CTCF	chr5:79220880-79221030	A549	lung:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
33	CTCF	chr5:79220960-79221110	GM12871	blood:	n/a	chr5:79220983-79220996
34	CTCF	chr5:79214498-79214506	GM10248	blood:	n/a	n/a
35	CTCF	chr5:79220980-79221130	HFF	foreskin:	n/a	chr5:79220983-79220996
36	CTCF	chr5:79220857-79221053	GM19240	blood:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
37	CTCF	chr5:79220880-79221030	HA-sp	spinal cord:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
38	CTCF	chr5:79220880-79221030	GM06990	blood:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
39	CTCF	chr5:79220840-79220990	HepG2	liver:	n/a	chr5:79220951-79220969
40	CTCF	chr5:79220900-79221050	WERI-Rb-1	eye:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
41	CTCF	chr5:79220878-79221010	Hela-S3	cervix:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
42	CTCF	chr5:79220851-79221069	GM12892	blood:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
43	CTCF	chr5:79257713-79257748	NHEK	skin:	n/a	n/a
44	CTCF	chr5:79220856-79221042	HepG2	liver:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
45	CTCF	chr5:79220860-79221010	NHEK	skin:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
46	CTCF	chr5:79220872-79221034	GM19239	blood:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
47	CTCF	chr5:79220900-79221050	HBMEC	blood vessel:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
48	CTCF	chr5:79220625-79221266	SK-N-SH	brain:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
49	CTCF	chr5:79220880-79221030	AG09319	gingival:	n/a	chr5:79220951-79220969 chr5:79220983-79220996
50	CTCF	chr5:79225020-79225170	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79222121-79222171	PrEC	prostate:	n/a
2	chr5:79251870-79251920	PrEC	prostate:	n/a
3	chr5:79258838-79258888	Caco-2	colon:	n/a
4	chr5:79258838-79258888	HCF	heart:	n/a
5	chr5:79222121-79222171	HMEC	breast:	n/a
6	chr5:79258838-79258888	RPTEC	kidney:	n/a
7	chr5:79251870-79251920	Jurkat	blood:	n/a
8	chr5:79222121-79222171	HRCEpiC	kidney:	n/a
9	chr5:79222121-79222171	NHDF-neo	bronchial:	n/a
10	chr5:79251870-79251920	MCF10A-Er-Src	breast:	n/a
11	chr5:79251870-79251920	GM19239	blood:	n/a
12	chr5:79251870-79251920	K562	blood:	n/a
13	chr5:79258838-79258888	HUVEC	blood vessel:	n/a
14	chr5:79222121-79222171	GM12892	blood:	n/a
15	chr5:79258838-79258888	IMR90	lung:	fetal
16	chr5:79258838-79258888	H1-hESC	embryonic stem cell:	embryo
17	chr5:79222121-79222171	HCT-116	colon:	n/a
18	chr5:79222121-79222171	HepG2	liver:	n/a
19	chr5:79222121-79222171	AG10803	skin:	n/a
20	chr5:79222121-79222171	BE2_C	brain:	n/a
21	chr5:79258838-79258888	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:79222121-79222171	MCF10A-Er-Src	breast:	n/a
23	chr5:79251870-79251920	HL-60	blood:	n/a
24	chr5:79222121-79222171	HCPEpiC	choroid plexus:	n/a
25	chr5:79251870-79251920	NB4	blood:	n/a
26	chr5:79251870-79251920	AG09319	gingival:	n/a
27	chr5:79251870-79251920	NH-A	brain:	n/a
28	chr5:79222121-79222171	BJ	skin:	n/a
29	chr5:79222121-79222171	ovcar-3	ovarian:	n/a
30	chr5:79258838-79258888	HCPEpiC	choroid plexus:	n/a
31	chr5:79222121-79222171	IMR90	lung:	fetal
32	chr5:79222121-79222171	HAEpiC	amniotic membrane:	n/a
33	chr5:79222121-79222171	T-47D	breast:	n/a
34	chr5:79222121-79222171	RPTEC	kidney:	n/a
35	chr5:79222121-79222171	A549	lung:	n/a
36	chr5:79251870-79251920	HUVEC	blood vessel:	n/a
37	chr5:79258838-79258888	HRPEpiC	eye:	n/a
38	chr5:79251870-79251920	CMK	blood:	n/a
39	chr5:79222121-79222171	H1-hESC	embryonic stem cell:	embryo
40	chr5:79222121-79222171	Caco-2	colon:	n/a
41	chr5:79258838-79258888	HEEpiC	esophagus:	n/a
42	chr5:79258838-79258888	AG04449	skin:	fetal
43	chr5:79251870-79251920	HAEpiC	amniotic membrane:	n/a
44	chr5:79258838-79258888	HEK293	kidney:	embryo
45	chr5:79258838-79258888	AG09309	skin:	n/a
46	chr5:79258838-79258888	K562	blood:	n/a
47	chr5:79258838-79258888	AG04450	lung:	fetal
48	chr5:79222121-79222171	U87	brain:	n/a
49	chr5:79222121-79222171	ECC-1	luminal epithelium:	n/a
50	chr5:79251870-79251920	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:79216472..79218715-chr5:79220881..79222567,2	K562	blood:
2	chr5:79216472..79218715-chr5:79220881..79222567,2	K562	blood:
3	chr5:79233060..79235575-chr5:79249554..79252283,4	MCF-7	breast:
4	chr5:79249151..79251519-chr5:79253481..79257590,3	K562	blood:
5	chr5:79224007..79226249-chr5:79227050..79229652,2	MCF-7	breast:
6	chr5:79249151..79251519-chr5:79253481..79257590,3	K562	blood:
7	chr5:79254651..79257793-chr5:79258388..79261777,3	K562	blood:
8	chr5:79225597..79228798-chr5:79376988..79380641,3	MCF-7	breast:
9	chr5:79221384..79223524-chr5:79243090..79245085,2	MCF-7	breast:
10	chr5:79243051..79245888-chr5:79249775..79252734,2	K562	blood:
11	chr5:79224007..79226249-chr5:79227050..79229652,2	MCF-7	breast:
12	chr5:79221102..79221682-chr5:79378398..79379159,2	MCF-7	breast:
13	chr5:79220441..79221400-chr5:79296482..79297375,4	MCF-7	breast:
14	chr5:79249486..79252419-chr5:79253972..79256405,2	MCF-7	breast:
15	chr5:79228008..79229698-chr5:79234534..79237440,2	MCF-7	breast:
16	chr5:79220836..79221589-chr5:79285813..79286607,2	MCF-7	breast:
17	chr5:79253337..79255880-chr5:79257487..79259390,2	MCF-7	breast:
18	chr5:79243051..79245888-chr5:79249775..79252734,2	K562	blood:
19	chr5:79220616..79221598-chr5:79378757..79379944,5	MCF-7	breast:
20	chr5:79251016..79252738-chr5:79254951..79256533,2	MCF-7	breast:
21	chr5:79243470..79245963-chr5:79249243..79251067,2	MCF-7	breast:
22	chr5:79251016..79252738-chr5:79254951..79256533,2	MCF-7	breast:
23	chr5:79257889..79260201-chr5:79261651..79263210,2	K562	blood:
24	chr5:79233060..79235575-chr5:79249554..79252283,4	MCF-7	breast:
25	chr5:79217165..79219101-chr5:79377151..79378778,2	MCF-7	breast:
26	chr5:79220985..79223322-chr5:79242510..79245158,2	K562	blood:
27	chr5:79220985..79223322-chr5:79242510..79245158,2	K562	blood:
28	chr5:79243470..79245963-chr5:79249243..79251067,2	MCF-7	breast:
29	chr5:79252333..79253868-chr5:79285797..79288103,2	MCF-7	breast:
30	chr5:79249284..79251451-chr5:79270809..79273026,3	MCF-7	breast:
31	chr5:79220513..79221401-chr5:79378378..79379197,2	K562	blood:
32	chr5:79254651..79257793-chr5:79258388..79261777,3	K562	blood:
33	chr5:79250469..79253672-chr5:79285038..79288543,6	MCF-7	breast:
34	chr5:79228008..79229698-chr5:79234534..79237440,2	MCF-7	breast:
35	chr5:79196588..79198348-chr5:79339313..79342153,2	K562	blood:
36	chr5:79221384..79223524-chr5:79243090..79245085,2	MCF-7	breast:
37	chr5:79229191..79232150-chr5:79238031..79240460,2	MCF-7	breast:
38	chr5:79249486..79252419-chr5:79253972..79256405,2	MCF-7	breast:
39	chr5:79220191..79221034-chr5:79296621..79297178,2	MCF-7	breast:
40	chr5:79229191..79232150-chr5:79238031..79240460,2	MCF-7	breast:
41	chr5:79253337..79255880-chr5:79257487..79259390,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THBS4-2	chr5:79238234-79238452	XLOC_004442
2	lnc-THBS4-2	chr5:79232402-79232703	XLOC_004442

Variant related genes	Relation type
ENSG00000250888	TF binding region
ENSG00000250888	CpG island
ENSG00000113296	chromatin interactions
ENSG00000249825	chromatin interactions
ENSG00000177034	chromatin interactions

Extended variants
information (count: 1253 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555747082	chr5:79207009-79207010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181506074	chr5:79207014-79207015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535125402	chr5:79207017-79207018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140814563	chr5:79207049-79207050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577900483	chr5:79207062-79207063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13170399	chr5:79207070-79207071	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs111988450	chr5:79207097-79207098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573897346	chr5:79207121-79207122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138667343	chr5:79207138-79207139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186145438	chr5:79207145-79207146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148897760	chr5:79207171-79207172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190072632	chr5:79207186-79207187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181393609	chr5:79207187-79207188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186535350	chr5:79207201-79207202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564674133	chr5:79207203-79207204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372095989	chr5:79207235-79207236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533329245	chr5:79207236-79207237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550372170	chr5:79207243-79207244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570218291	chr5:79207250-79207251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191000422	chr5:79207290-79207291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544546924	chr5:79207291-79207292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549061043	chr5:79207292-79207293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182715781	chr5:79207308-79207309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535056018	chr5:79207324-79207325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13171797	chr5:79207333-79207334	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs369821551	chr5:79207347-79207348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs578162441	chr5:79207370-79207371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111407209	chr5:79207379-79207380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs36114485	chr5:79207384-79207385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs540646167	chr5:79207394-79207395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573809339	chr5:79207407-79207408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542907782	chr5:79207485-79207486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145536174	chr5:79207489-79207490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201221280	chr5:79207491-79207492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553035801	chr5:79207527-79207528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35575130	chr5:79207540-79207541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542522844	chr5:79207559-79207560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386689438	chr5:79207564-79207565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114673226	chr5:79207565-79207566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187655657	chr5:79217168-79217169	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569401555	chr5:79217237-79217238	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538144378	chr5:79217285-79217286	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs147084364	chr5:79217296-79217297	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191554048	chr5:79217303-79217304	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533959577	chr5:79217331-79217332	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533975980	chr5:79217342-79217343	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs78246405	chr5:79217364-79217365	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141588029	chr5:79217365-79217366	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs553947740	chr5:79217409-79217410	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577282613	chr5:79217418-79217419	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79207000-79207600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:79219400-79219600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:79219600-79219800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:79221200-79222200	Bivalent Enhancer	NHDF-Ad	bronchial
5	chr5:79222000-79222800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr5:79222200-79222600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:79222400-79222800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:79223800-79224200	Enhancers	Psoas Muscle	Psoas
9	chr5:79224200-79224600	Weak transcription	Psoas Muscle	Psoas
10	chr5:79224600-79225200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr5:79224600-79225400	Enhancers	Psoas Muscle	Psoas
12	chr5:79225000-79225400	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr5:79225000-79225800	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr5:79225400-79231200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr5:79225600-79225800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr5:79225800-79232600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr5:79227200-79231400	Weak transcription	Right Ventricle	heart
18	chr5:79227400-79228200	Enhancers	NHDF-Ad	bronchial
19	chr5:79227400-79229600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:79227800-79228400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:79227800-79228800	Enhancers	Osteobl	bone
22	chr5:79227800-79229400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:79228000-79229400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:79228200-79228400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:79228200-79228600	Flanking Active TSS	NHDF-Ad	bronchial
26	chr5:79228200-79228800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr5:79228200-79229000	Enhancers	NHEK	skin
28	chr5:79228200-79229200	Enhancers	HMEC	breast
29	chr5:79228400-79228600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:79228400-79228600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr5:79228400-79228800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:79228400-79231200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:79228600-79228800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:79228600-79229400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:79228600-79229400	Enhancers	NHDF-Ad	bronchial
36	chr5:79228800-79230200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr5:79228800-79230600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:79229000-79230400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:79229000-79230400	Weak transcription	NHEK	skin
40	chr5:79229200-79230200	Weak transcription	HMEC	breast
41	chr5:79229400-79231200	Weak transcription	NHDF-Ad	bronchial
42	chr5:79229400-79231400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:79229600-79231000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:79230200-79230400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr5:79230200-79235400	Enhancers	HMEC	breast
46	chr5:79230400-79230800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr5:79230400-79234400	Enhancers	NHEK	skin
48	chr5:79230400-79235000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:79230600-79231200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:79230800-79231000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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