Variant report

Variant	nsv539621
Chromosome Location	chr8:54631303-54827173
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4435)
CpG islands
(count:3601)
Chromatin interactive
region (count:137)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4435 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:54644917-54645356	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:54754941-54754968	K562	blood:	n/a	n/a
3	ARID3A	chr8:54680405-54681240	K562	blood:	n/a	n/a
4	ARID3A	chr8:54757995-54758100	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:54764007-54764349	K562	blood:	n/a	chr8:54764167-54764183 chr8:54764168-54764184
6	ARID3A	chr8:54764037-54764343	HepG2	liver:	n/a	chr8:54764167-54764183 chr8:54764168-54764184
7	ARID3A	chr8:54755031-54756313	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:54637510-54637700	K562	blood:	n/a	n/a
9	ARID3A	chr8:54691337-54691687	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:54798117-54799189	K562	blood:	n/a	n/a
11	ARID3A	chr8:54797035-54797757	K562	blood:	n/a	n/a
12	ARID3A	chr8:54721367-54721603	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:54777766-54777791	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:54722562-54722623	K562	blood:	n/a	n/a
15	ARID3A	chr8:54647105-54647471	HepG2	liver:	n/a	n/a
16	ATF1	chr8:54775900-54776205	K562	blood:	n/a	n/a
17	ATF1	chr8:54764037-54764232	K562	blood:	n/a	n/a
18	ATF1	chr8:54643653-54644232	K562	blood:	n/a	n/a
19	ATF1	chr8:54806668-54806818	K562	blood:	n/a	n/a
20	ATF1	chr8:54654608-54655219	K562	blood:	n/a	n/a
21	ATF1	chr8:54822337-54822519	K562	blood:	n/a	n/a
22	ATF1	chr8:54649329-54649510	K562	blood:	n/a	n/a
23	ATF1	chr8:54680670-54680980	K562	blood:	n/a	n/a
24	ATF1	chr8:54792417-54792706	K562	blood:	n/a	n/a
25	ATF1	chr8:54722553-54722705	K562	blood:	n/a	n/a
26	ATF1	chr8:54640297-54640735	K562	blood:	n/a	n/a
27	ATF1	chr8:54797091-54797575	K562	blood:	n/a	n/a
28	ATF1	chr8:54785456-54785852	K562	blood:	n/a	n/a
29	ATF1	chr8:54758642-54759219	K562	blood:	n/a	n/a
30	ATF1	chr8:54641216-54641511	K562	blood:	n/a	n/a
31	ATF1	chr8:54788054-54788369	K562	blood:	n/a	n/a
32	ATF2	chr8:54798383-54798865	GM12878	blood:	n/a	n/a
33	ATF2	chr8:54675032-54675540	GM12878	blood:	n/a	n/a
34	ATF2	chr8:54792322-54792805	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr8:54811884-54812833	GM12878	blood:	n/a	n/a
36	ATF2	chr8:54756830-54757321	GM12878	blood:	n/a	n/a
37	ATF2	chr8:54674017-54674831	GM12878	blood:	n/a	n/a
38	ATF2	chr8:54755487-54756106	GM12878	blood:	n/a	n/a
39	ATF2	chr8:54811328-54811876	GM12878	blood:	n/a	n/a
40	ATF2	chr8:54680660-54681618	GM12878	blood:	n/a	n/a
41	ATF2	chr8:54680671-54681379	GM12878	blood:	n/a	n/a
42	ATF2	chr8:54818004-54818462	GM12878	blood:	n/a	n/a
43	ATF2	chr8:54812056-54812828	GM12878	blood:	n/a	n/a
44	ATF2	chr8:54755524-54755924	GM12878	blood:	n/a	n/a
45	ATF2	chr8:54755401-54755938	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr8:54792283-54792730	GM12878	blood:	n/a	n/a
47	ATF3	chr8:54636219-54636386	GM12878	blood:	n/a	n/a
48	ATF3	chr8:54722373-54722713	K562	blood:	n/a	n/a
49	ATF3	chr8:54755658-54756087	A549	lung:	n/a	chr8:54755844-54755853 chr8:54755833-54755853
50	ATF3	chr8:54636102-54636510	GM12878	blood:	n/a	n/a

(count:3601 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:54757132-54757182	MCF10A-Er-Src	breast:	n/a
2	chr8:54755854-54755904	HL-60	blood:	n/a
3	chr8:54757132-54757182	MCF10A-Er-Src	breast:	n/a
4	chr8:54755854-54755904	HL-60	blood:	n/a
5	chr8:54787585-54787635	IMR90	lung:	fetal
6	chr8:54818075-54818125	GM19239	blood:	n/a
7	chr8:54798735-54798785	Hela-S3	cervix:	n/a
8	chr8:54785374-54785424	HEK293	kidney:	embryo
9	chr8:54798735-54798785	SAEC	small airway:	n/a
10	chr8:54790518-54790568	HRE	kidney:	n/a
11	chr8:54756224-54756274	HL-60	blood:	n/a
12	chr8:54790957-54791007	HUVEC	blood vessel:	n/a
13	chr8:54794628-54794678	AoSMC	blood vessel:	n/a
14	chr8:54757048-54757098	H1-hESC	embryonic stem cell:	embryo
15	chr8:54755848-54755898	HepG2	liver:	n/a
16	chr8:54757132-54757182	AG10803	skin:	n/a
17	chr8:54755598-54755648	SAEC	small airway:	n/a
18	chr8:54794348-54794398	NHDF-neo	bronchial:	n/a
19	chr8:54641642-54641692	A549	lung:	n/a
20	chr8:54755419-54755469	Caco-2	colon:	n/a
21	chr8:54817069-54817119	SKMC	muscle:	n/a
22	chr8:54787585-54787635	NHBE	bronchial:	n/a
23	chr8:54792161-54792211	AG04449	skin:	fetal
24	chr8:54720431-54720481	ovcar-3	ovarian:	n/a
25	chr8:54790518-54790568	NT2-D1	testis:	n/a
26	chr8:54791151-54791201	Hepatocyte	liver:	n/a
27	chr8:54790518-54790568	AG09319	gingival:	n/a
28	chr8:54708636-54708686	NH-A	brain:	n/a
29	chr8:54790841-54790891	RPTEC	kidney:	n/a
30	chr8:54789978-54790028	ProgFib	skin:	n/a
31	chr8:54792161-54792211	HepG2	liver:	n/a
32	chr8:54817069-54817119	HUVEC	blood vessel:	n/a
33	chr8:54755419-54755469	U87	brain:	n/a
34	chr8:54756094-54756144	K562	blood:	n/a
35	chr8:54794628-54794678	U87	brain:	n/a
36	chr8:54755585-54755635	AG09309	skin:	n/a
37	chr8:54755577-54755627	SAEC	small airway:	n/a
38	chr8:54687817-54687867	BE2_C	brain:	n/a
39	chr8:54755854-54755904	PFSK-1	brain:	n/a
40	chr8:54658063-54658113	ECC-1	luminal epithelium:	n/a
41	chr8:54789648-54789698	SK-N-SH	brain:	n/a
42	chr8:54755683-54755733	HRCEpiC	kidney:	n/a
43	chr8:54789325-54789375	Hepatocyte	liver:	n/a
44	chr8:54755981-54756031	AG10803	skin:	n/a
45	chr8:54756094-54756144	HCM	heart:	n/a
46	chr8:54792161-54792211	PrEC	prostate:	n/a
47	chr8:54818075-54818125	AG04449	skin:	fetal
48	chr8:54757132-54757182	SK-N-SH	brain:	n/a
49	chr8:54789207-54789257	HEK293	kidney:	embryo
50	chr8:54794875-54794925	PFSK-1	brain:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:54744420..54745965-chr8:54750144..54752140,2	K562	blood:
2	chr8:54669633..54671247-chr8:54674350..54676508,2	K562	blood:
3	chr8:54743278..54745985-chr8:54748911..54752561,4	K562	blood:
4	chr8:54614266..54615818-chr8:54636955..54638612,2	K562	blood:
5	chr8:54736720..54739090-chr8:54754502..54756079,2	K562	blood:
6	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
7	chr8:54792772..54795313-chr8:55047110..55049629,2	MCF-7	breast:
8	chr8:54635896..54638290-chr8:54641065..54643578,3	K562	blood:
9	chr8:54685432..54687285-chr8:54688902..54690630,2	K562	blood:
10	chr8:54620507..54623207-chr8:54638020..54640255,2	K562	blood:
11	chr8:54743278..54745985-chr8:54748911..54752561,4	K562	blood:
12	chr8:54756285..54757983-chr8:54774408..54775966,2	MCF-7	breast:
13	chr8:54755728..54757820-chr8:101732813..101735091,2	MCF-7	breast:
14	chr8:54754476..54757676-chr8:54757839..54759715,3	MCF-7	breast:
15	chr8:54655663..54657675-chr8:54698753..54701327,2	MCF-7	breast:
16	chr8:54650208..54652519-chr8:54653816..54655343,2	MCF-7	breast:
17	chr8:54632819..54637804-chr8:54638171..54641276,4	MCF-7	breast:
18	chr6:36561901..36562650-chr8:54793415..54793991,2	HCT-116	colon:
19	chr8:54726065..54728887-chr8:54733160..54735179,2	MCF-7	breast:
20	chr8:54754073..54756825-chr8:54765433..54767534,2	K562	blood:
21	chr8:54685641..54687590-chr8:54702056..54704049,2	K562	blood:
22	chr12:122240596..122241191-chr8:54755297..54756198,2	HCT-116	colon:
23	chr8:54813329..54816016-chr8:54818127..54820294,2	K562	blood:
24	chr8:54806250..54809119-chr8:54814470..54816413,2	K562	blood:
25	chr8:54667680..54670590-chr8:54671196..54673684,2	K562	blood:
26	chr8:54789285..54792223-chr8:54932900..54934940,2	K562	blood:
27	chr8:54755454..54757105-chr8:54791568..54794141,2	K562	blood:
28	chr8:54651332..54653261-chr8:54754407..54756402,2	MCF-7	breast:
29	chr8:54783474..54786409-chr8:54789438..54792325,2	K562	blood:
30	chr8:54725647..54728988-chr8:54753947..54756397,3	MCF-7	breast:
31	chr8:54802586..54804292-chr8:54811511..54813202,2	K562	blood:
32	chr8:54631323..54633867-chr8:54635784..54637550,2	K562	blood:
33	chr8:54740899..54743524-chr8:54747224..54749984,3	MCF-7	breast:
34	chr8:54748659..54752308-chr8:54753286..54756528,7	K562	blood:
35	chr8:54654556..54656764-chr8:54720675..54722580,2	MCF-7	breast:
36	chr8:54716170..54717689-chr8:54721716..54724539,2	K562	blood:
37	chr8:54652211..54654707-chr8:54657866..54660858,2	MCF-7	breast:
38	chr8:54754676..54757522-chr8:54774455..54776549,2	K562	blood:
39	chr8:54802586..54804292-chr8:54811511..54813202,2	K562	blood:
40	chr8:54716170..54717689-chr8:54721716..54724539,2	K562	blood:
41	chr8:54733544..54735901-chr8:54752993..54755423,2	MCF-7	breast:
42	chr8:54749963..54753631-chr8:54753914..54756219,5	MCF-7	breast:
43	chr8:54635896..54638290-chr8:54641065..54643578,3	K562	blood:
44	chr8:54640506..54642635-chr8:54647079..54648821,2	K562	blood:
45	chr8:54743534..54745842-chr8:54749054..54751844,2	MCF-7	breast:
46	chr8:54785381..54788323-chr8:54789364..54792317,2	MCF-7	breast:
47	chr8:54770995..54772909-chr8:54774285..54777231,3	MCF-7	breast:
48	chr8:54647068..54647713-chr8:54775574..54776093,2	MCF-7	breast:
49	chr8:54788748..54791564-chr8:54792392..54794472,3	K562	blood:
50	chr8:54754073..54757431-chr8:54763114..54767534,4	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCEA1-2	chr8:54745425-54745646	NONHSAT126609
2	lnc-ATP6V1H-3	chr8:54788710-54789209	ENSG00000272457.1
3	lnc-ATP6V1H-5	chr8:54799568-54799804	NONHSAT126614
4	lnc-MRPL15-4	chr8:54826057-54826482	NR_104578
5	lnc-MRPL15-4	chr8:54793432-54793644	NR_104578
6	lnc-MRPL15-1	chr8:54811569-54813639	ENSG00000251475
7	lnc-MRPL15-1	chr8:54821350-54821517	ENSG00000251475
8	lnc-TCEA1-2	chr8:54752185-54752398	NONHSAT126609
9	lnc-MRPL15-4	chr8:54826057-54826482	NONHSAT126613
10	lnc-MRPL15-4	chr8:54793461-54793644	NONHSAT126613

No data

Variant related genes	Relation type
RGS20	TF binding region
ENSG00000272457	TF binding region
ENSG00000244159	TF binding region
RNU6-1331P	TF binding region
ATP6V1H	TF binding region
RGS20	CpG island
ENSG00000272457	CpG island
ENSG00000244159	CpG island
RNU6-1331P	CpG island
ATP6V1H	CpG island
ENSG00000272457	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000165494	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000147509	chromatin interactions
ENSG00000244159	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000187735	chromatin interactions
ENSG00000137547	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000047249	chromatin interactions
ENSG00000023287	chromatin interactions
ENSG00000120992	chromatin interactions
CCNE2	miRNA target sites
KTN1	miRNA target sites

Extended variants
information (count: 7199 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:7199 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191556591	chr8:54631317-54631318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561582531	chr8:54631326-54631327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547598672	chr8:54631400-54631401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369489723	chr8:54631422-54631423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4738701	chr8:54631446-54631447	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573514852	chr8:54631481-54631482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181236191	chr8:54631604-54631605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138494873	chr8:54631680-54631681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530393150	chr8:54631706-54631707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80332917	chr8:54631716-54631717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549938353	chr8:54631721-54631722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372595623	chr8:54631766-54631767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187153974	chr8:54631773-54631774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534386352	chr8:54631781-54631782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10104229	chr8:54631866-54631867	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs4737518	chr8:54631879-54631880	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191580197	chr8:54631916-54631917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148351120	chr8:54631935-54631936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182877397	chr8:54631979-54631980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141660971	chr8:54631998-54631999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575992644	chr8:54632009-54632010	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372852644	chr8:54632010-54632011	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541421837	chr8:54632021-54632022	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150546661	chr8:54632053-54632054	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571782418	chr8:54632095-54632096	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377355932	chr8:54632130-54632131	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540858626	chr8:54632133-54632134	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113606674	chr8:54632148-54632149	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533095532	chr8:54632149-54632150	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138655093	chr8:54632194-54632195	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563387345	chr8:54632202-54632203	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370704352	chr8:54632257-54632258	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552354949	chr8:54632293-54632294	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529295962	chr8:54632378-54632379	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549073332	chr8:54632414-54632415	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186494931	chr8:54632530-54632531	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190935965	chr8:54632549-54632550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182406438	chr8:54632563-54632564	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377751481	chr8:54632568-54632569	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371215361	chr8:54632580-54632581	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537594839	chr8:54632600-54632601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557642088	chr8:54632653-54632654	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574214718	chr8:54632714-54632715	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78084817	chr8:54632767-54632768	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186741260	chr8:54632811-54632812	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142712959	chr8:54632842-54632843	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs59751066	chr8:54632852-54632853	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146504257	chr8:54632855-54632856	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58319533	chr8:54632857-54632858	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182985681	chr8:54632888-54632889	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:6487 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54613600-54634800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:54620800-54636200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:54620800-54636200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:54621400-54643600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:54622200-54632800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:54624200-54635800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:54624200-54640600	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr8:54624200-54643600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:54624600-54639200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr8:54625000-54640000	Weak transcription	Fetal Thymus	thymus
11	chr8:54625000-54642000	Weak transcription	Brain Substantia Nigra	brain
12	chr8:54625200-54634600	Weak transcription	Pancreas	Pancrea
13	chr8:54625200-54635800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:54625200-54639800	Weak transcription	Thymus	Thymus
15	chr8:54625200-54641200	Weak transcription	Brain Angular Gyrus	brain
16	chr8:54625200-54649000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr8:54625200-54649600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr8:54625400-54631800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr8:54625400-54634000	Weak transcription	NHDF-Ad	bronchial
20	chr8:54625400-54634200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr8:54625400-54634600	Weak transcription	Esophagus	oesophagus
22	chr8:54625400-54634800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:54625400-54634800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr8:54625400-54634800	Weak transcription	Left Ventricle	heart
25	chr8:54625400-54636200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:54625400-54636200	Weak transcription	Aorta	Aorta
27	chr8:54625400-54639200	Weak transcription	Brain Anterior Caudate	brain
28	chr8:54625400-54639400	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr8:54625400-54639600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:54625400-54639600	Weak transcription	Fetal Lung	lung
31	chr8:54625400-54639800	Weak transcription	Fetal Intestine Large	intestine
32	chr8:54625400-54639800	Weak transcription	Fetal Muscle Trunk	muscle
33	chr8:54625400-54639800	Weak transcription	HMEC	breast
34	chr8:54625400-54639800	Weak transcription	NH-A	brain
35	chr8:54625400-54640000	Weak transcription	Duodenum Mucosa	Duodenum
36	chr8:54625400-54640600	Weak transcription	Fetal Brain Female	brain
37	chr8:54625400-54640600	Weak transcription	Psoas Muscle	Psoas
38	chr8:54625400-54640600	Weak transcription	Right Ventricle	heart
39	chr8:54625400-54640600	Weak transcription	NHLF	lung
40	chr8:54625400-54641800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr8:54625400-54641800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr8:54625400-54641800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr8:54625400-54642000	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr8:54625400-54642000	Weak transcription	Fetal Muscle Leg	muscle
45	chr8:54625400-54645200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:54625400-54645800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr8:54625400-54646800	Weak transcription	Fetal Kidney	kidney
48	chr8:54625400-54649400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr8:54625600-54634600	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr8:54625600-54635600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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