Variant report

Variant	nsv4811
Chromosome Location	chr5:41844522-41887353
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:1038)
Chromatin interactive
region (count:95)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:41878679-41879141	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:41870536-41870561	K562	blood:	n/a	n/a
3	ARID3A	chr5:41868957-41869144	K562	blood:	n/a	n/a
4	ARID3A	chr5:41856684-41857005	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:41856827-41857171	K562	blood:	n/a	n/a
6	ARID3A	chr5:41883234-41883684	K562	blood:	n/a	n/a
7	ATF1	chr5:41864061-41864213	K562	blood:	n/a	n/a
8	ATF1	chr5:41883246-41883735	K562	blood:	n/a	n/a
9	ATF1	chr5:41869979-41870803	K562	blood:	n/a	chr5:41870565-41870579
10	ATF2	chr5:41870475-41870815	H1-hESC	embryonic stem cell:	n/a	chr5:41870565-41870579
11	ATF2	chr5:41870176-41870804	GM12878	blood:	n/a	chr5:41870565-41870579
12	ATF2	chr5:41870243-41870794	GM12878	blood:	n/a	chr5:41870565-41870579
13	ATF3	chr5:41869978-41870295	K562	blood:	n/a	n/a
14	BACH1	chr5:41870219-41870842	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr5:41864066-41864306	GM12878	blood:	n/a	chr5:41864169-41864179 chr5:41864168-41864179
16	BCL3	chr5:41870282-41870909	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:41870120-41870971	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:41875502-41875510	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:41870066-41871151	K562	blood:	n/a	n/a
20	BHLHE40	chr5:41870204-41870967	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:41856835-41857125	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:41882920-41883615	K562	blood:	n/a	n/a
23	BHLHE40	chr5:41856869-41857091	K562	blood:	n/a	n/a
24	BHLHE40	chr5:41864071-41864354	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:41869209-41869562	K562	blood:	n/a	n/a
26	BRCA1	chr5:41856938-41857091	HepG2	liver:	n/a	n/a
27	BRCA1	chr5:41870412-41870596	GM12878	blood:	n/a	n/a
28	BRCA1	chr5:41870383-41870740	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr5:41869888-41870164	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr5:41870037-41870964	K562	blood:	n/a	n/a
31	CBX3	chr5:41883202-41883708	K562	blood:	n/a	n/a
32	CCNT2	chr5:41883318-41883778	K562	blood:	n/a	n/a
33	CCNT2	chr5:41869530-41870923	K562	blood:	n/a	n/a
34	CCNT2	chr5:41879167-41879481	K562	blood:	n/a	n/a
35	CCNT2	chr5:41849243-41849443	K562	blood:	n/a	chr5:41849341-41849361
36	CEBPB	chr5:41879955-41879993	A549	lung:	n/a	n/a
37	CEBPB	chr5:41869894-41870094	K562	blood:	n/a	n/a
38	CEBPB	chr5:41869713-41870897	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:41883418-41883749	K562	blood:	n/a	n/a
40	CEBPB	chr5:41869145-41869209	K562	blood:	n/a	n/a
41	CEBPB	chr5:41856906-41857065	K562	blood:	n/a	n/a
42	CEBPB	chr5:41884190-41884504	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:41883319-41883672	K562	blood:	n/a	n/a
44	CEBPB	chr5:41870714-41870780	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr5:41883712-41883758	A549	lung:	n/a	n/a
46	CEBPD	chr5:41883262-41883729	K562	blood:	n/a	n/a
47	CEBPD	chr5:41883256-41883796	K562	blood:	n/a	n/a
48	CEBPD	chr5:41849092-41849455	K562	blood:	n/a	n/a
49	CHD1	chr5:41870219-41870725	GM12878	blood:	n/a	n/a
50	CHD1	chr5:41864030-41864350	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:41874348-41874398	HUVEC	blood vessel:	n/a
2	chr5:41874348-41874398	HUVEC	blood vessel:	n/a
3	chr5:41870081-41870131	LNCaP	prostate:	n/a
4	chr5:41870081-41870131	ProgFib	skin:	n/a
5	chr5:41869963-41870013	K562	blood:	n/a
6	chr5:41870875-41870925	HCPEpiC	choroid plexus:	n/a
7	chr5:41870860-41870910	AG10803	skin:	n/a
8	chr5:41871189-41871239	MCF-7	breast:	n/a
9	chr5:41870860-41870910	SKMC	muscle:	n/a
10	chr5:41871189-41871239	BJ	skin:	n/a
11	chr5:41869963-41870013	HCF	heart:	n/a
12	chr5:41866725-41866775	BE2_C	brain:	n/a
13	chr5:41870875-41870925	AG10803	skin:	n/a
14	chr5:41870860-41870910	U87	brain:	n/a
15	chr5:41870796-41870846	RPTEC	kidney:	n/a
16	chr5:41870746-41870796	NT2-D1	testis:	n/a
17	chr5:41866725-41866775	HepG2	liver:	n/a
18	chr5:41870081-41870131	AG09309	skin:	n/a
19	chr5:41870796-41870846	HNPCEpiC	eye:	n/a
20	chr5:41870316-41870366	PrEC	prostate:	n/a
21	chr5:41870856-41870906	HCT-116	colon:	n/a
22	chr5:41870910-41870960	ProgFib	skin:	n/a
23	chr5:41870316-41870366	NHDF-neo	bronchial:	n/a
24	chr5:41870081-41870131	HNPCEpiC	eye:	n/a
25	chr5:41870860-41870910	MCF10A-Er-Src	breast:	n/a
26	chr5:41870910-41870960	HCPEpiC	choroid plexus:	n/a
27	chr5:41869679-41869729	HepG2	liver:	n/a
28	chr5:41870746-41870796	HRPEpiC	eye:	n/a
29	chr5:41870910-41870960	AoSMC	blood vessel:	n/a
30	chr5:41870796-41870846	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:41869679-41869729	PANC-1	pancreas:	n/a
32	chr5:41869963-41870013	NHBE	bronchial:	n/a
33	chr5:41866725-41866775	HCPEpiC	choroid plexus:	n/a
34	chr5:41868227-41868277	HL-60	blood:	n/a
35	chr5:41870316-41870366	GM12892	blood:	n/a
36	chr5:41869963-41870013	AG04449	skin:	fetal
37	chr5:41870875-41870925	AG09309	skin:	n/a
38	chr5:41871189-41871239	ovcar-3	ovarian:	n/a
39	chr5:41874348-41874398	AG09309	skin:	n/a
40	chr5:41869679-41869729	K562	blood:	n/a
41	chr5:41870860-41870910	NT2-D1	testis:	n/a
42	chr5:41869679-41869729	HEK293	kidney:	embryo
43	chr5:41870746-41870796	SK-N-SH_RA	brain:	n/a
44	chr5:41874348-41874398	HRPEpiC	eye:	n/a
45	chr5:41874348-41874398	SK-N-MC	brain:	n/a
46	chr5:41874348-41874398	HAEpiC	amniotic membrane:	n/a
47	chr5:41870856-41870906	AoSMC	blood vessel:	n/a
48	chr5:41870875-41870925	PANC-1	pancreas:	n/a
49	chr5:41870860-41870910	HIPEpiC	eye:	n/a
50	chr5:41870796-41870846	LNCaP	prostate:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:41856921..41859678-chr5:41902862..41906383,3	K562	blood:
2	chr5:41881132..41883774-chr5:41884323..41886903,2	K562	blood:
3	chr21:26979740..26980706-chr5:41869727..41870577,2	Hela-S3	cervix:
4	chr12:56551419..56552000-chr5:41870278..41870895,2	Hela-S3	cervix:
5	chr5:41865404..41878163-chr5:41900217..41908471,28	K562	blood:
6	chr5:41856471..41857410-chr5:42656558..42657380,2	MCF-7	breast:
7	chr5:41870254..41870956-chr5:179049882..179050830,2	Hela-S3	cervix:
8	chr1:153935318..153936274-chr5:41870150..41870705,2	Hela-S3	cervix:
9	chr19:41256382..41257161-chr5:41869993..41870560,2	Hela-S3	cervix:
10	chr12:52444516..52445216-chr5:41870286..41870902,2	Hela-S3	cervix:
11	chr17:7475963..7476627-chr5:41869655..41870189,2	Hela-S3	cervix:
12	chr5:41883917..41886978-chr5:41887352..41891327,3	K562	blood:
13	chr5:41676941..41679139-chr5:41866132..41868129,2	K562	blood:
14	chr5:41872879..41875448-chr5:41895436..41897906,2	K562	blood:
15	chr5:41871626..41873159-chr5:41881683..41883592,2	K562	blood:
16	chr5:41856847..41857569-chr5:42057071..42057972,2	MCF-7	breast:
17	chr5:41885203..41888121-chr5:41889501..41892447,3	K562	blood:
18	chr5:41868991..41872715-chr5:41873991..41877809,9	K562	blood:
19	chr5:41866693..41874585-chr5:41920680..41930326,14	K562	blood:
20	chr5:41881132..41883774-chr5:41884323..41886903,2	K562	blood:
21	chr5:41866709..41868950-chr5:41930527..41932665,2	K562	blood:
22	chr5:41868727..41870919-chr5:41887155..41888776,2	K562	blood:
23	chr20:39657405..39657909-chr5:41870172..41871003,2	Hela-S3	cervix:
24	chr5:41870733..41872720-chr5:41882349..41885044,2	MCF-7	breast:
25	chr2:24306797..24307765-chr5:41870107..41870774,2	Hela-S3	cervix:
26	chr5:41879598..41881638-chr5:41943324..41944878,2	K562	blood:
27	chr5:41869502..41870457-chr7:134576191..134576878,2	Hela-S3	cervix:
28	chr5:34007552..34008327-chr5:41870117..41870711,2	Hela-S3	cervix:
29	chr19:39420991..39421729-chr5:41870292..41870960,2	Hela-S3	cervix:
30	chr5:41870219..41871078-chr6:44355052..44355939,2	Hela-S3	cervix:
31	chr5:41870117..41870830-chr6:160114180..160114700,2	Hela-S3	cervix:
32	chr5:40833527..40835162-chr5:41861192..41862978,2	MCF-7	breast:
33	chr5:41874167..41876175-chr5:41878438..41881219,2	MCF-7	breast:
34	chr5:41865564..41868288-chr5:41873378..41876329,4	K562	blood:
35	chr5:41871626..41873159-chr5:41881683..41883592,2	K562	blood:
36	chr5:41882384..41891851-chr5:41900562..41907560,15	K562	blood:
37	chr5:41851290..41853624-chr5:41855397..41858252,2	K562	blood:
38	chr5:41850949..41853870-chr5:41854462..41856684,2	MCF-7	breast:
39	chr5:41869775..41870984-chr5:41903748..41904904,5	Hela-S3	cervix:
40	chr5:41866734..41868498-chr5:41868516..41871487,2	MCF-7	breast:
41	chr5:41870733..41872720-chr5:41882349..41885044,2	MCF-7	breast:
42	chr5:41875191..41876862-chr5:41878614..41881383,3	K562	blood:
43	chr5:41857377..41859702-chr5:41923897..41925458,2	K562	blood:
44	chr5:41859110..41859726-chr5:42056831..42057996,3	K562	blood:
45	chr5:41870798..41872531-chr5:41879112..41881533,2	K562	blood:
46	chr5:41867500..41871930-chr5:41901815..41908844,17	K562	blood:
47	chr5:41875191..41876862-chr5:41878614..41881383,3	K562	blood:
48	chr14:21572468..21572981-chr5:41870321..41871052,2	HCT-116	colon:
49	chr5:41843846..41845908-chr5:42054612..42056725,2	K562	blood:
50	chr5:41887319..41889409-chr5:41922980..41925910,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf51-1	chr5:41870222-41870294	ENSG00000248668.1
2	lnc-C5orf51-1	chr5:41870132-41870294	NR_046635
3	lnc-C5orf51-1	chr5:41870393-41870484	ENSG00000248668.1
4	lnc-C5orf51-1	chr5:41870393-41870818	ENSG00000248668.1
5	lnc-C5orf51-1	chr5:41870868-41872338	NR_046635
6	lnc-C5orf51-1	chr5:41870393-41870484	NR_046635
7	lnc-C5orf51-1	chr5:41870868-41871059	ENSG00000248668.1
8	lnc-C5orf51-1	chr5:41870132-41870294	ENSG00000248668.1

No data

Variant related genes	Relation type
OXCT1	TF binding region
OXCT1-AS1	TF binding region
OXCT1	CpG island
OXCT1-AS1	CpG island
ENSG00000119953	chromatin interactions
ENSG00000221990	chromatin interactions
ENSG00000205765	chromatin interactions
ENSG00000104835	chromatin interactions
ENSG00000163527	chromatin interactions
ENSG00000083720	chromatin interactions
ENSG00000198900	chromatin interactions
ENSG00000128626	chromatin interactions
ENSG00000248668	chromatin interactions
ENSG00000157617	chromatin interactions
ENSG00000161960	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000130856	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000112078	chromatin interactions
ENSG00000188493	chromatin interactions
ENSG00000264278	chromatin interactions
ENSG00000069849	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000180104	chromatin interactions
ENSG00000077312	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000151876	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000269891	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000166965	chromatin interactions
ENSG00000258384	chromatin interactions
ENSG00000165804	chromatin interactions
ENSG00000213390	chromatin interactions
ENSG00000242110	chromatin interactions
ENSG00000112096	chromatin interactions
ENSG00000108848	chromatin interactions
ENSG00000096401	chromatin interactions
ENSG00000240281	chromatin interactions
ENSG00000179165	chromatin interactions
ENSG00000115129	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000122786	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000154719	chromatin interactions

Extended variants
information (count: 1400 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575223666	chr5:41844550-41844551	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs373529226	chr5:41844580-41844581	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542227492	chr5:41844595-41844596	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs187387409	chr5:41844600-41844601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190878361	chr5:41844614-41844615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546526362	chr5:41844633-41844634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1112842	chr5:41844634-41844635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182310225	chr5:41844657-41844658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546023488	chr5:41844688-41844689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149958381	chr5:41844696-41844697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145187435	chr5:41844705-41844706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549589549	chr5:41844716-41844717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559798034	chr5:41844728-41844729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571276788	chr5:41844742-41844743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377267143	chr5:41844780-41844781	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs561615559	chr5:41844806-41844807	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs373312271	chr5:41844817-41844818	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529185615	chr5:41844821-41844822	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369059610	chr5:41844849-41844850	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547347608	chr5:41844898-41844899	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs187064352	chr5:41844900-41844901	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372980059	chr5:41844948-41844949	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376124610	chr5:41844953-41844954	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs569788427	chr5:41844961-41844962	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs538405757	chr5:41844990-41844991	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs550789251	chr5:41845029-41845030	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs190182708	chr5:41845041-41845042	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs552992378	chr5:41845044-41845045	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs375518219	chr5:41845061-41845062	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568745860	chr5:41845072-41845073	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs142363411	chr5:41845106-41845107	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs554129484	chr5:41845140-41845141	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs77435205	chr5:41845206-41845207	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs146505237	chr5:41845234-41845235	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs147895691	chr5:41845247-41845248	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs182775510	chr5:41845272-41845273	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs11739106	chr5:41845274-41845275	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs543199440	chr5:41845275-41845276	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs561574807	chr5:41845278-41845279	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141662378	chr5:41845321-41845322	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540927548	chr5:41845335-41845336	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559601190	chr5:41845376-41845377	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs188643395	chr5:41845461-41845462	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs111612288	chr5:41845471-41845472	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs569750273	chr5:41845485-41845486	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530937098	chr5:41845489-41845490	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550645104	chr5:41845504-41845505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs376021038	chr5:41845508-41845509	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs192980828	chr5:41845539-41845540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550391458	chr5:41845561-41845562	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Bladder cancer	21909424	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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1242 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41801000-41849200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr5:41801200-41849200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr5:41801200-41849200	Weak transcription	Fetal Brain Male	brain
4	chr5:41818400-41852000	Weak transcription	Small Intestine	intestine
5	chr5:41819200-41852800	Weak transcription	Pancreas	Pancrea
6	chr5:41822600-41849200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:41824600-41859400	Weak transcription	Spleen	Spleen
8	chr5:41825800-41849200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr5:41827800-41849800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr5:41828600-41849200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr5:41828800-41849000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr5:41829400-41851000	Weak transcription	Fetal Intestine Small	intestine
13	chr5:41830800-41849200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr5:41830800-41849800	Weak transcription	Gastric	stomach
15	chr5:41831200-41849200	Weak transcription	Brain Germinal Matrix	brain
16	chr5:41831200-41854400	Weak transcription	Colonic Mucosa	Colon
17	chr5:41831400-41849200	Weak transcription	Placenta	Placenta
18	chr5:41832200-41849200	Weak transcription	Fetal Kidney	kidney
19	chr5:41832800-41849200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr5:41832800-41850000	Weak transcription	Esophagus	oesophagus
21	chr5:41832800-41869200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr5:41833400-41849200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr5:41834000-41849200	Weak transcription	Duodenum Mucosa	Duodenum
24	chr5:41834600-41849200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr5:41835800-41845600	Strong transcription	Dnd41	blood
26	chr5:41836000-41857200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr5:41836200-41849200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr5:41836400-41849200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:41836400-41849200	Weak transcription	Brain Anterior Caudate	brain
30	chr5:41836400-41849200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr5:41836400-41849200	Weak transcription	Brain Substantia Nigra	brain
32	chr5:41836400-41849200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr5:41836400-41849200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr5:41836400-41849400	Weak transcription	Colon Smooth Muscle	Colon
35	chr5:41836600-41849000	Weak transcription	NHDF-Ad	bronchial
36	chr5:41836600-41849200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:41836600-41849200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:41836600-41849200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr5:41836600-41849200	Weak transcription	Ovary	ovary
40	chr5:41836600-41849200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr5:41836600-41849200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr5:41836600-41849200	Weak transcription	Osteobl	bone
43	chr5:41836600-41849400	Weak transcription	HSMM	muscle
44	chr5:41836600-41863800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr5:41837000-41849200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr5:41837000-41849200	Weak transcription	Fetal Heart	heart
47	chr5:41837000-41849200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr5:41837000-41850000	Weak transcription	Brain Angular Gyrus	brain
49	chr5:41837200-41858600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr5:41837600-41849200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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