Variant report

Variant	nsv898764
Chromosome Location	chr12:10537269-10698255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1396)
CpG islands
(count:979)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10548121-10548681	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
3	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:10653777-10653877	K562	blood:	n/a	n/a
5	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
6	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
7	ATF2	chr12:10693152-10694036	GM12878	blood:	n/a	n/a
8	ATF2	chr12:10695894-10696491	GM12878	blood:	n/a	n/a
9	ATF2	chr12:10695883-10696624	GM12878	blood:	n/a	n/a
10	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
11	ATF2	chr12:10544776-10545621	GM12878	blood:	n/a	n/a
12	ATF2	chr12:10693081-10694102	GM12878	blood:	n/a	n/a
13	BATF	chr12:10641906-10642182	GM12878	blood:	n/a	chr12:10642014-10642025
14	BATF	chr12:10696036-10696487	GM12878	blood:	n/a	n/a
15	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
16	BATF	chr12:10693317-10693939	GM12878	blood:	n/a	chr12:10693650-10693661
17	BATF	chr12:10641882-10642185	GM12878	blood:	n/a	chr12:10642014-10642025
18	BATF	chr12:10693300-10693868	GM12878	blood:	n/a	chr12:10693650-10693661
19	BATF	chr12:10696061-10696446	GM12878	blood:	n/a	n/a
20	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
21	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:10696076-10696426	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:10547875-10548349	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:10547793-10548282	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:10696199-10696390	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:10671811-10671985	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:10693354-10693625	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:10598783-10598965	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:10693310-10693858	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:10544909-10545281	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a
32	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
33	BCL3	chr12:10693360-10693849	GM12878	blood:	n/a	n/a
34	BCL3	chr12:10695995-10696628	GM12878	blood:	n/a	n/a
35	BCL3	chr12:10693210-10693959	GM12878	blood:	n/a	n/a
36	BCL3	chr12:10696031-10696586	GM12878	blood:	n/a	n/a
37	BCLAF1	chr12:10547846-10548369	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:10544936-10545515	GM12878	blood:	n/a	chr12:10545490-10545499
39	BCLAF1	chr12:10696071-10696445	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:10693217-10694044	GM12878	blood:	n/a	n/a
41	BCLAF1	chr12:10693241-10693808	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:10544894-10545448	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:10559427-10559772	K562	blood:	n/a	n/a
44	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
45	BHLHE40	chr12:10693305-10693679	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:10547847-10548665	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
48	BRCA1	chr12:10562044-10562186	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr12:10676248-10676302	GM12878	blood:	n/a	n/a
50	BRCA1	chr12:10544899-10545539	Hela-S3	cervix:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10658539-10658589	HUVEC	blood vessel:	n/a
2	chr12:10605936-10605986	HMEC	breast:	n/a
3	chr12:10607538-10607588	Hepatocyte	liver:	n/a
4	chr12:10658539-10658589	HUVEC	blood vessel:	n/a
5	chr12:10605936-10605986	HMEC	breast:	n/a
6	chr12:10607538-10607588	Hepatocyte	liver:	n/a
7	chr12:10607538-10607588	BE2_C	brain:	n/a
8	chr12:10658425-10658475	AG04450	lung:	fetal
9	chr12:10543073-10543123	NH-A	brain:	n/a
10	chr12:10607538-10607588	ProgFib	skin:	n/a
11	chr12:10599740-10599790	Hepatocyte	liver:	n/a
12	chr12:10605936-10605986	HEEpiC	esophagus:	n/a
13	chr12:10570179-10570229	AG04450	lung:	fetal
14	chr12:10586130-10586180	HCT-116	colon:	n/a
15	chr12:10658539-10658589	H1-hESC	embryonic stem cell:	embryo
16	chr12:10583355-10583405	NT2-D1	testis:	n/a
17	chr12:10560602-10560652	GM12891	blood:	n/a
18	chr12:10583355-10583405	BJ	skin:	n/a
19	chr12:10605936-10605986	HNPCEpiC	eye:	n/a
20	chr12:10608067-10608117	ovcar-3	ovarian:	n/a
21	chr12:10608067-10608117	HepG2	liver:	n/a
22	chr12:10605936-10605986	HRE	kidney:	n/a
23	chr12:10545083-10545133	HAEpiC	amniotic membrane:	n/a
24	chr12:10607538-10607588	PFSK-1	brain:	n/a
25	chr12:10545083-10545133	BE2_C	brain:	n/a
26	chr12:10588483-10588533	HRE	kidney:	n/a
27	chr12:10588483-10588533	GM19239	blood:	n/a
28	chr12:10608067-10608117	Caco-2	colon:	n/a
29	chr12:10599740-10599790	HEEpiC	esophagus:	n/a
30	chr12:10658425-10658475	Hela-S3	cervix:	n/a
31	chr12:10544636-10544686	ECC-1	luminal epithelium:	n/a
32	chr12:10545083-10545133	PrEC	prostate:	n/a
33	chr12:10570179-10570229	HEEpiC	esophagus:	n/a
34	chr12:10583355-10583405	HNPCEpiC	eye:	n/a
35	chr12:10607538-10607588	H1-hESC	embryonic stem cell:	embryo
36	chr12:10586130-10586180	PFSK-1	brain:	n/a
37	chr12:10560602-10560652	Hela-S3	cervix:	n/a
38	chr12:10607538-10607588	SK-N-SH	brain:	n/a
39	chr12:10605936-10605986	PANC-1	pancreas:	n/a
40	chr12:10658281-10658331	BE2_C	brain:	n/a
41	chr12:10583355-10583405	K562	blood:	n/a
42	chr12:10545083-10545133	HEEpiC	esophagus:	n/a
43	chr12:10607364-10607414	MCF-7	breast:	n/a
44	chr12:10570179-10570229	AG09309	skin:	n/a
45	chr12:10599740-10599790	U87	brain:	n/a
46	chr12:10658539-10658589	K562	blood:	n/a
47	chr12:10560602-10560652	LNCaP	prostate:	n/a
48	chr12:10545083-10545133	AG10803	skin:	n/a
49	chr12:10545083-10545133	GM19239	blood:	n/a
50	chr12:10543073-10543123	HMEC	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
2	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
3	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
4	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
5	chr12:10693047..10695502-chr12:10698886..10701191,2	K562	blood:
6	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
7	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
8	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
9	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
10	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
11	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
12	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
13	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
14	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
15	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
16	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
17	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
18	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
19	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
20	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
21	chr12:10388252..10388816-chr12:10653557..10654233,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRD1-1	chr12:10548778-10551105	ENSG00000245648
2	lnc-EIF2S3L.1-6	chr12:10601202-10602083	l_610_chr12:10597245-10602083_whiteBloodCell
3	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell

No data

Variant related genes	Relation type
ENSG00000180574	TF binding region
KLRC2	TF binding region
KLRC3	TF binding region
KLRK1	TF binding region
KLRC4	TF binding region
KLRC1	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000255641	TF binding region
ENSG00000180574	CpG island
KLRC2	CpG island
KLRC3	CpG island
KLRK1	CpG island
KLRC4	CpG island
KLRC1	CpG island
KLRC4-KLRK1	CpG island
ENSG00000255641	CpG island
ENSG00000167900	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000213809	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000255641	chromatin interactions
ENSG00000134545	chromatin interactions
ENSG00000205810	chromatin interactions
ENSG00000245648	chromatin interactions
ESR1	miRNA target sites

Extended variants
information (count: 4667 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4667 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11053781	chr12:10537269-10537270	Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571950886	chr12:10537328-10537329	Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs527963022	chr12:10537345-10537346	Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547830098	chr12:10537433-10537434	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567610360	chr12:10537434-10537435	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536351299	chr12:10537458-10537459	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556611203	chr12:10537511-10537512	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs556038225	chr12:10537555-10537556	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs60077215	chr12:10537569-10537570	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2927561	chr12:10537573-10537574	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs558301703	chr12:10537574-10537575	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187926121	chr12:10537597-10537598	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540885241	chr12:10537602-10537603	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192355218	chr12:10537611-10537612	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs78172402	chr12:10537678-10537679	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543196300	chr12:10537715-10537716	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs184619975	chr12:10537729-10537730	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1904123	chr12:10537780-10537781	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs190106747	chr12:10537861-10537862	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181680403	chr12:10537870-10537871	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs2126889	chr12:10537879-10537880	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs572081442	chr12:10537904-10537905	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541145545	chr12:10537928-10537929	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs370640178	chr12:10537944-10537945	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145204994	chr12:10537966-10537967	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs200419975	chr12:10537967-10537968	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200704443	chr12:10537970-10537971	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs71049092	chr12:10537988-10537989	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3055416	chr12:10537995-10537996	Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs561971740	chr12:10538015-10538016	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs548064721	chr12:10538027-10538028	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs567592361	chr12:10538033-10538034	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs140773359	chr12:10538090-10538091	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs550034341	chr12:10538155-10538156	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs373309176	chr12:10538225-10538226	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs376395094	chr12:10538230-10538231	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570154692	chr12:10538254-10538255	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs185000810	chr12:10538273-10538274	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs2617159	chr12:10538286-10538287	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs371276389	chr12:10538289-10538290	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs80018829	chr12:10538305-10538306	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs35744198	chr12:10538451-10538452	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs150101030	chr12:10538480-10538481	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs576657445	chr12:10538505-10538506	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75180586	chr12:10538519-10538520	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs199732034	chr12:10538585-10538586	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs536084771	chr12:10538586-10538587	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs398018396	chr12:10538600-10538601	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554840840	chr12:10538631-10538632	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574386297	chr12:10538637-10538638	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10519600-10547800	Weak transcription	Colon Smooth Muscle	Colon
2	chr12:10525400-10547200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:10527600-10538600	Weak transcription	Brain Hippocampus Middle	brain
4	chr12:10531200-10544400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr12:10533200-10541400	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
6	chr12:10533600-10538000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:10533600-10538600	Active TSS	Primary T helper naive cells from peripheral blood	blood
8	chr12:10533800-10537800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:10533800-10538200	Weak transcription	Fetal Intestine Large	intestine
10	chr12:10533800-10539000	Weak transcription	Fetal Intestine Small	intestine
11	chr12:10533800-10544600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:10534600-10544600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr12:10534800-10537600	Weak transcription	Osteobl	bone
14	chr12:10534800-10537800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
15	chr12:10534800-10542000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr12:10534800-10544400	Weak transcription	NHEK	skin
17	chr12:10534800-10548800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:10535000-10537600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:10535200-10537400	Weak transcription	Hela-S3	cervix
20	chr12:10536200-10537400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr12:10536200-10542800	Active TSS	Primary T cells fromperipheralblood	blood
22	chr12:10536600-10537400	ZNF genes & repeats	Primary T cells from cord blood	blood
23	chr12:10537200-10538000	Strong transcription	Primary B cells from cord blood	blood
24	chr12:10537200-10542800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr12:10537400-10538000	Enhancers	Primary T cells from cord blood	blood
26	chr12:10537400-10538800	Enhancers	Hela-S3	cervix
27	chr12:10537400-10543000	Active TSS	Primary T killer memory cells from peripheral blood	blood
28	chr12:10537600-10538400	Enhancers	Osteobl	bone
29	chr12:10537600-10538600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:10537600-10540000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr12:10537800-10538400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10537800-10538400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:10537800-10538800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:10538000-10538400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:10538000-10538400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:10538000-10538400	Enhancers	HMEC	breast
37	chr12:10538000-10539600	Weak transcription	Primary B cells from cord blood	blood
38	chr12:10538000-10541200	Active TSS	Primary T cells from cord blood	blood
39	chr12:10538200-10538400	Enhancers	Fetal Intestine Large	intestine
40	chr12:10538400-10538600	Enhancers	HSMM	muscle
41	chr12:10538400-10539400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:10538400-10542800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr12:10538400-10544400	Weak transcription	Osteobl	bone
44	chr12:10538400-10544600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr12:10538400-10544800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:10538600-10538800	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
47	chr12:10538600-10539400	Weak transcription	HSMM	muscle
48	chr12:10538600-10544400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:10538800-10539400	Weak transcription	Hela-S3	cervix
50	chr12:10538800-10543200	Active TSS	Primary T helper naive cells from peripheral blood	blood

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