Variant report

Variant	esv3348501
Chromosome Location	chr5:145543808-145572250
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	chr5:145570492-145570635	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:145561812-145562714	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:145561689-145562556	K562	blood:	n/a	n/a
4	ARID3A	chr5:145548626-145549020	HepG2	liver:	n/a	n/a
5	ATF1	chr5:145551256-145551280	K562	blood:	n/a	n/a
6	ATF1	chr5:145561969-145562643	K562	blood:	n/a	n/a
7	ATF2	chr5:145553057-145553609	GM12878	blood:	n/a	n/a
8	ATF2	chr5:145561959-145562657	H1-hESC	embryonic stem cell:	n/a	chr5:145562365-145562376
9	ATF2	chr5:145561795-145562742	H1-hESC	embryonic stem cell:	n/a	chr5:145562365-145562376
10	ATF2	chr5:145561804-145562616	GM12878	blood:	n/a	chr5:145562365-145562376
11	ATF2	chr5:145561863-145562720	GM12878	blood:	n/a	chr5:145562365-145562376
12	ATF3	chr5:145561794-145562750	A549	lung:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
13	ATF3	chr5:145572119-145572521	K562	blood:	n/a	n/a
14	ATF3	chr5:145561978-145562457	H1-hESC	embryonic stem cell:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
15	ATF3	chr5:145562029-145562500	K562	blood:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
16	ATF3	chr5:145561913-145562552	K562	blood:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
17	ATF3	chr5:145561998-145562564	A549	lung:	n/a	chr5:145562364-145562375 chr5:145562363-145562376 chr5:145562366-145562377 chr5:145562367-145562377 chr5:145562367-145562374 chr5:145562365-145562378 chr5:145562366-145562374 chr5:145562363-145562378 chr5:145562364-145562374 chr5:145562367-145562375 chr5:145562355-145562375
18	BACH1	chr5:145561812-145562672	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr5:145562738-145563155	GM12878	blood:	n/a	n/a
20	BATF	chr5:145562820-145563124	GM12878	blood:	n/a	n/a
21	BATF	chr5:145562035-145562498	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:145553130-145553474	GM12878	blood:	n/a	n/a
23	BCL3	chr5:145561846-145562716	A549	lung:	n/a	n/a
24	BCL3	chr5:145561680-145562656	A549	lung:	n/a	n/a
25	BCLAF1	chr5:145561831-145562759	GM12878	blood:	n/a	n/a
26	BCLAF1	chr5:145552551-145552881	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:145553066-145553628	GM12878	blood:	n/a	n/a
28	BCLAF1	chr5:145561912-145562656	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:145561975-145562630	K562	blood:	n/a	n/a
30	BHLHE40	chr5:145561932-145562592	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:145552650-145553578	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:145561079-145561259	K562	blood:	n/a	n/a
33	BHLHE40	chr5:145561911-145562563	HepG2	liver:	n/a	n/a
34	BRCA1	chr5:145561947-145562566	GM12878	blood:	n/a	n/a
35	BRCA1	chr5:145561843-145562615	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr5:145562058-145562538	HepG2	liver:	n/a	n/a
37	BRCA1	chr5:145561972-145562644	H1-hESC	embryonic stem cell:	n/a	n/a
38	CBX3	chr5:145561920-145562639	K562	blood:	n/a	n/a
39	CBX3	chr5:145561463-145562765	K562	blood:	n/a	n/a
40	CCNT2	chr5:145562125-145562488	K562	blood:	n/a	n/a
41	CEBPB	chr5:145568002-145568252	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:145561986-145562864	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:145561927-145562565	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:145572041-145572576	K562	blood:	n/a	chr5:145572387-145572398
45	CEBPB	chr5:145562013-145562452	A549	lung:	n/a	n/a
46	CEBPB	chr5:145561969-145562307	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr5:145572237-145572544	H1-hESC	embryonic stem cell:	n/a	chr5:145572387-145572398
48	CEBPB	chr5:145572231-145572573	A549	lung:	n/a	chr5:145572387-145572398
49	CEBPB	chr5:145561984-145562549	K562	blood:	n/a	n/a
50	CEBPB	chr5:145561981-145562427	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:145562699-145562749	AG09319	gingival:	n/a
2	chr5:145562699-145562749	AG09319	gingival:	n/a
3	chr5:145562699-145562749	PrEC	prostate:	n/a
4	chr5:145562010-145562060	ovcar-3	ovarian:	n/a
5	chr5:145562428-145562478	H1-hESC	embryonic stem cell:	embryo
6	chr5:145562498-145562548	SK-N-SH	brain:	n/a
7	chr5:145562268-145562318	PrEC	prostate:	n/a
8	chr5:145562010-145562060	HAEpiC	amniotic membrane:	n/a
9	chr5:145562010-145562060	K562	blood:	n/a
10	chr5:145562268-145562318	NHBE	bronchial:	n/a
11	chr5:145562530-145562580	HCM	heart:	n/a
12	chr5:145562498-145562548	CMK	blood:	n/a
13	chr5:145562428-145562478	LNCaP	prostate:	n/a
14	chr5:145562268-145562318	HIPEpiC	eye:	n/a
15	chr5:145562426-145562476	HCF	heart:	n/a
16	chr5:145562370-145562420	HRE	kidney:	n/a
17	chr5:145562010-145562060	Hela-S3	cervix:	n/a
18	chr5:145562530-145562580	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:145562010-145562060	Jurkat	blood:	n/a
20	chr5:145562428-145562478	GM19239	blood:	n/a
21	chr5:145562699-145562749	HCM	heart:	n/a
22	chr5:145562010-145562060	AG09319	gingival:	n/a
23	chr5:145562434-145562484	AoSMC	blood vessel:	n/a
24	chr5:145562010-145562060	ProgFib	skin:	n/a
25	chr5:145562426-145562476	NHBE	bronchial:	n/a
26	chr5:145562498-145562548	HCPEpiC	choroid plexus:	n/a
27	chr5:145562699-145562749	IMR90	lung:	fetal
28	chr5:145562428-145562478	GM12891	blood:	n/a
29	chr5:145562010-145562060	GM12892	blood:	n/a
30	chr5:145562428-145562478	SK-N-SH_RA	brain:	n/a
31	chr5:145562699-145562749	ProgFib	skin:	n/a
32	chr5:145562010-145562060	HMEC	breast:	n/a
33	chr5:145562268-145562318	IMR90	lung:	fetal
34	chr5:145562434-145562484	GM06990	blood:	n/a
35	chr5:145562268-145562318	GM19239	blood:	n/a
36	chr5:145562426-145562476	Hela-S3	cervix:	n/a
37	chr5:145562530-145562580	HUVEC	blood vessel:	n/a
38	chr5:145562010-145562060	HepG2	liver:	n/a
39	chr5:145562010-145562060	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:145562268-145562318	Hepatocyte	liver:	n/a
41	chr5:145562428-145562478	HRPEpiC	eye:	n/a
42	chr5:145562699-145562749	NT2-D1	testis:	n/a
43	chr5:145562010-145562060	RPTEC	kidney:	n/a
44	chr5:145562478-145562528	NHDF-neo	bronchial:	n/a
45	chr5:145562699-145562749	HepG2	liver:	n/a
46	chr5:145562426-145562476	H1-hESC	embryonic stem cell:	embryo
47	chr5:145562699-145562749	SK-N-SH_RA	brain:	n/a
48	chr5:145562428-145562478	PFSK-1	brain:	n/a
49	chr5:145562530-145562580	HRE	kidney:	n/a
50	chr5:145562530-145562580	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:145563092..145566274-chr5:145579879..145584548,5	MCF-7	breast:
2	chr5:145543670..145545508-chr5:145560602..145562850,2	MCF-7	breast:
3	chr5:145559745..145561849-chr5:145588233..145589890,2	K562	blood:
4	chr20:46414738..46416706-chr5:145560925..145562971,2	MCF-7	breast:
5	chr5:145551306..145553774-chr5:145557195..145559625,2	K562	blood:
6	chr5:145540004..145542261-chr5:145544154..145547069,3	K562	blood:
7	chr5:145542821..145544989-chr5:145547735..145549727,2	K562	blood:
8	chr5:145560893..145564215-chr5:145581108..145584712,3	MCF-7	breast:
9	chr5:145559594..145562426-chr5:145581996..145584629,4	MCF-7	breast:
10	chr5:145536432..145538417-chr5:145545755..145548340,2	K562	blood:
11	chr5:145562850..145566563-chr5:145571128..145574037,3	MCF-7	breast:
12	chr5:145556363..145559212-chr5:145560408..145562154,3	K562	blood:
13	chr19:49496287..49496957-chr5:145561885..145562408,2	HCT-116	colon:
14	chr5:145558307..145563846-chr5:145580315..145584343,10	K562	blood:
15	chr5:145558240..145560527-chr5:145600863..145603054,2	K562	blood:
16	chr5:145530712..145532401-chr5:145543556..145545762,2	MCF-7	breast:
17	chr5:145544700..145547234-chr5:145551344..145553851,2	K562	blood:
18	chr5:145560592..145565120-chr5:145580444..145584486,7	K562	blood:
19	chr5:145547972..145550072-chr5:145559815..145562335,2	K562	blood:
20	chr5:145564948..145567866-chr5:145592052..145594140,2	K562	blood:
21	chr5:145562850..145566563-chr5:145571128..145574037,3	MCF-7	breast:
22	chr5:145543973..145545500-chr5:145559065..145562026,2	K562	blood:
23	chr5:145555213..145560576-chr5:145560598..145562206,4	K562	blood:
24	chr5:145542821..145544989-chr5:145547735..145549727,2	K562	blood:
25	chr5:145549719..145552981-chr5:145557063..145560291,4	MCF-7	breast:
26	chr5:145560445..145562806-chr5:145569318..145570972,2	K562	blood:
27	chr5:145559635..145563527-chr5:145825770..145828320,3	K562	blood:
28	chr5:145551516..145553977-chr5:145559737..145562085,2	K562	blood:
29	chr5:145570785..145572816-chr5:145582211..145584363,2	MCF-7	breast:
30	chr5:145525794..145527740-chr5:145551579..145553885,3	K562	blood:
31	chr5:145553826..145555566-chr5:145583178..145584730,2	K562	blood:
32	chr5:145567639..145569805-chr5:145575511..145577560,2	K562	blood:
33	chr5:145544700..145547234-chr5:145551344..145553851,2	K562	blood:
34	chr5:145560642..145563806-chr5:145566350..145569083,3	MCF-7	breast:
35	chr5:145559635..145562318-chr5:145826820..145828574,2	K562	blood:
36	chr5:145543973..145545500-chr5:145559065..145562026,2	K562	blood:
37	chr5:145564650..145566770-chr5:145588134..145589874,2	K562	blood:
38	chr5:145551306..145553774-chr5:145557195..145559625,2	K562	blood:
39	chr5:145555891..145557716-chr5:145560403..145562060,2	MCF-7	breast:
40	chr5:145549719..145552981-chr5:145557063..145560291,4	MCF-7	breast:
41	chr5:145557742..145559707-chr5:145585614..145588262,3	K562	blood:
42	chr5:145551052..145554687-chr5:145559207..145562583,5	K562	blood:

Variant related genes	Relation type
LARS	TF binding region
LARS	CpG island
ENSG00000113649	chromatin interactions
ENSG00000104812	chromatin interactions
ENSG00000183207	chromatin interactions
ENSG00000133706	chromatin interactions
ENSG00000091009	chromatin interactions
ENSG00000196562	chromatin interactions

Extended variants
information (count: 1202 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372050155	chr5:145543809-145543810	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375161107	chr5:145543818-145543819	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200063676	chr5:145543820-145543821	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566017123	chr5:145543831-145543832	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145909725	chr5:145543864-145543865	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369268762	chr5:145543868-145543869	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs199808937	chr5:145543902-145543903	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs3763373	chr5:145543972-145543973	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs372590611	chr5:145543981-145543982	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201463704	chr5:145543989-145543990	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146218818	chr5:145543991-145543992	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200657735	chr5:145544021-145544022	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376134002	chr5:145544022-145544023	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs367618230	chr5:145544045-145544046	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs76839811	chr5:145544046-145544047	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375947593	chr5:145544061-145544062	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577125293	chr5:145544062-145544063	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs186220534	chr5:145544072-145544073	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375962805	chr5:145544114-145544115	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572760052	chr5:145544183-145544184	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112640793	chr5:145544288-145544289	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541503757	chr5:145544306-145544307	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs117183781	chr5:145544342-145544343	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs138850077	chr5:145544350-145544351	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370234759	chr5:145544431-145544432	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543595656	chr5:145544438-145544439	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192032122	chr5:145544457-145544458	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572261210	chr5:145544510-145544511	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs35436549	chr5:145544566-145544567	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs62373794	chr5:145544646-145544647	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
31	rs62373795	chr5:145544647-145544648	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs142733415	chr5:145544664-145544665	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35581472	chr5:145544674-145544675	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs183347195	chr5:145544680-145544681	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568523207	chr5:145544730-145544731	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537507387	chr5:145544742-145544743	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557514270	chr5:145544753-145544754	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs4705398	chr5:145544766-145544767	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs539655984	chr5:145544790-145544791	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553226729	chr5:145544821-145544822	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372367962	chr5:145544828-145544829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186590731	chr5:145544845-145544846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs117223978	chr5:145544897-145544898	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532098545	chr5:145544914-145544915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555104774	chr5:145545018-145545019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574911065	chr5:145545082-145545083	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111593664	chr5:145545102-145545103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551709400	chr5:145545105-145545106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563847875	chr5:145545112-145545113	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532557092	chr5:145545154-145545155	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145481200-145560200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:145491000-145551600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr5:145491000-145553800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:145491000-145560200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr5:145491200-145552600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr5:145491200-145560200	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:145491200-145560200	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr5:145491200-145560800	Weak transcription	Stomach Mucosa	stomach
9	chr5:145491400-145560000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:145491400-145560400	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr5:145491600-145557000	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr5:145491600-145559800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr5:145491800-145546400	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr5:145492000-145552200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:145492200-145560200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr5:145495800-145559200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:145496200-145552200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr5:145499000-145557400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:145510800-145546800	Strong transcription	Primary T cells from cord blood	blood
20	chr5:145511200-145548000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr5:145511600-145552800	Strong transcription	Fetal Thymus	thymus
22	chr5:145511600-145556800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:145515800-145546800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:145515800-145557400	Strong transcription	Liver	Liver
25	chr5:145516800-145545600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:145517000-145553000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr5:145518600-145545200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:145518800-145552800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr5:145519000-145551600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr5:145519200-145558200	Strong transcription	Dnd41	blood
31	chr5:145519400-145545200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:145519400-145551800	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr5:145519600-145546800	Strong transcription	HSMM	muscle
34	chr5:145520000-145551800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr5:145520200-145551800	Strong transcription	Muscle Satellite Cultured Cells	--
36	chr5:145520600-145548400	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr5:145521600-145548000	Strong transcription	A549	lung
38	chr5:145526000-145546200	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr5:145526000-145550800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:145526200-145551600	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr5:145526200-145553000	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr5:145526400-145551800	Strong transcription	Duodenum Mucosa	Duodenum
43	chr5:145526400-145551800	Strong transcription	Placenta	Placenta
44	chr5:145526400-145551800	Strong transcription	Stomach Smooth Muscle	stomach
45	chr5:145526600-145546200	Strong transcription	HUVEC	blood vessel
46	chr5:145526600-145548000	Strong transcription	NH-A	brain
47	chr5:145526800-145551800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:145526800-145554000	Strong transcription	Adipose Nuclei	Adipose
49	chr5:145532000-145545400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:145532200-145559600	Weak transcription	Small Intestine	intestine

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