Variant report

Variant	nsv832328
Chromosome Location	chr12:10398071-10620443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2550)
CpG islands
(count:1648)
Chromatin interactive
region (count:49)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2550 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

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	chr12:10513720-10513857	K562	blood:	n/a	n/a
3	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:10536954-10536986	K562	blood:	n/a	n/a
6	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
9	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
10	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
11	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
12	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
13	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
14	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
15	ATF2	chr12:10445690-10446665	GM12878	blood:	n/a	n/a
16	ATF2	chr12:10470741-10471136	GM12878	blood:	n/a	n/a
17	ATF2	chr12:10402618-10403042	GM12878	blood:	n/a	n/a
18	ATF2	chr12:10456577-10457005	GM12878	blood:	n/a	n/a
19	ATF2	chr12:10470709-10471203	GM12878	blood:	n/a	n/a
20	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
21	ATF2	chr12:10438561-10438911	GM12878	blood:	n/a	n/a
22	ATF2	chr12:10544776-10545621	GM12878	blood:	n/a	n/a
23	ATF2	chr12:10441581-10442005	GM12878	blood:	n/a	n/a
24	ATF2	chr12:10473155-10473759	GM12878	blood:	n/a	n/a
25	ATF2	chr12:10438421-10438980	GM12878	blood:	n/a	n/a
26	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
28	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
30	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
31	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
32	ATF3	chr12:10515933-10516347	K562	blood:	n/a	n/a
33	BACH1	chr12:10517085-10517124	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr12:10441065-10441159	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr12:10402621-10403044	GM12878	blood:	n/a	n/a
36	BATF	chr12:10473160-10473741	GM12878	blood:	n/a	n/a
37	BATF	chr12:10470851-10471221	GM12878	blood:	n/a	chr12:10471022-10471030
38	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
39	BATF	chr12:10445758-10446130	GM12878	blood:	n/a	n/a
40	BATF	chr12:10473216-10473419	GM12878	blood:	n/a	n/a
41	BATF	chr12:10445763-10446190	GM12878	blood:	n/a	n/a
42	BATF	chr12:10438523-10438850	GM12878	blood:	n/a	n/a
43	BATF	chr12:10516901-10517786	GM12878	blood:	n/a	n/a
44	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
45	BATF	chr12:10473434-10473653	GM12878	blood:	n/a	n/a
46	BATF	chr12:10456621-10457029	GM12878	blood:	n/a	n/a
47	BATF	chr12:10455627-10455902	GM12878	blood:	n/a	chr12:10455749-10455760
48	BATF	chr12:10441546-10441886	GM12878	blood:	n/a	n/a
49	BCL11A	chr12:10473293-10473615	GM12878	blood:	n/a	n/a
50	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10525233-10525283	SK-N-SH	brain:	n/a
2	chr12:10525233-10525283	SK-N-SH	brain:	n/a
3	chr12:10570179-10570229	K562	blood:	n/a
4	chr12:10465272-10465322	Hela-S3	cervix:	n/a
5	chr12:10543073-10543123	PFSK-1	brain:	n/a
6	chr12:10459923-10459973	H1-hESC	embryonic stem cell:	embryo
7	chr12:10459923-10459973	K562	blood:	n/a
8	chr12:10560602-10560652	AG04449	skin:	fetal
9	chr12:10532046-10532096	HUVEC	blood vessel:	n/a
10	chr12:10455788-10455838	NHDF-neo	bronchial:	n/a
11	chr12:10516240-10516290	CMK	blood:	n/a
12	chr12:10516240-10516290	MCF-7	breast:	n/a
13	chr12:10608067-10608117	HepG2	liver:	n/a
14	chr12:10543073-10543123	AG04449	skin:	fetal
15	chr12:10560602-10560652	GM19239	blood:	n/a
16	chr12:10586130-10586180	HL-60	blood:	n/a
17	chr12:10456885-10456935	Jurkat	blood:	n/a
18	chr12:10607538-10607588	HNPCEpiC	eye:	n/a
19	chr12:10560602-10560652	AG10803	skin:	n/a
20	chr12:10583355-10583405	Hepatocyte	liver:	n/a
21	chr12:10515574-10515624	MCF10A-Er-Src	breast:	n/a
22	chr12:10608067-10608117	SK-N-SH	brain:	n/a
23	chr12:10460639-10460689	HCM	heart:	n/a
24	chr12:10460639-10460689	K562	blood:	n/a
25	chr12:10460612-10460662	AG10803	skin:	n/a
26	chr12:10607538-10607588	SKMC	muscle:	n/a
27	chr12:10515574-10515624	HUVEC	blood vessel:	n/a
28	chr12:10532046-10532096	AG10803	skin:	n/a
29	chr12:10570179-10570229	HCM	heart:	n/a
30	chr12:10469147-10469197	HepG2	liver:	n/a
31	chr12:10588483-10588533	AG10803	skin:	n/a
32	chr12:10570179-10570229	RPTEC	kidney:	n/a
33	chr12:10525233-10525283	GM12892	blood:	n/a
34	chr12:10515574-10515624	IMR90	lung:	fetal
35	chr12:10607364-10607414	PFSK-1	brain:	n/a
36	chr12:10607538-10607588	HL-60	blood:	n/a
37	chr12:10465272-10465322	NT2-D1	testis:	n/a
38	chr12:10459912-10459962	HRPEpiC	eye:	n/a
39	chr12:10608067-10608117	AG09319	gingival:	n/a
40	chr12:10515574-10515624	GM12891	blood:	n/a
41	chr12:10525233-10525283	CMK	blood:	n/a
42	chr12:10515574-10515624	NHBE	bronchial:	n/a
43	chr12:10544636-10544686	ovcar-3	ovarian:	n/a
44	chr12:10605936-10605986	SK-N-SH_RA	brain:	n/a
45	chr12:10532046-10532096	AG09319	gingival:	n/a
46	chr12:10515091-10515141	HRPEpiC	eye:	n/a
47	chr12:10460639-10460689	PFSK-1	brain:	n/a
48	chr12:10515091-10515141	LNCaP	prostate:	n/a
49	chr12:10456885-10456935	BE2_C	brain:	n/a
50	chr12:10588483-10588533	HEK293	kidney:	embryo

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10442366..10444908-chr12:10450816..10453146,2	K562	blood:
2	chr12:10424917..10427474-chr12:10431900..10433911,2	K562	blood:
3	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
4	chr12:10424917..10427474-chr12:10431900..10433911,2	K562	blood:
5	chr12:10515701..10519228-chr12:10526352..10529377,4	K562	blood:
6	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
7	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
8	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
9	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
10	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
11	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
12	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
13	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
14	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
15	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
16	chr12:10483978..10484906-chr12:10714545..10715159,3	MCF-7	breast:
17	chr12:10506746..10508549-chr12:10514255..10516412,2	K562	blood:
18	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
19	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
20	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
21	chr12:10483953..10484953-chr12:10826469..10827411,2	K562	blood:
22	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
23	chr12:10453243..10455277-chr12:10460503..10462364,2	K562	blood:
24	chr12:10445022..10447315-chr12:10448355..10450390,2	K562	blood:
25	chr12:10484385..10484963-chr12:10714626..10715246,2	MCF-7	breast:
26	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
27	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
28	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
29	chr12:10442366..10444908-chr12:10450816..10453146,2	K562	blood:
30	chr12:10407362..10410201-chr12:10824046..10826886,2	K562	blood:
31	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
32	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
33	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
34	chr12:10445022..10447315-chr12:10448355..10450390,2	K562	blood:
35	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
36	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
37	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:
38	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
39	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
40	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
41	chr12:10484044..10484911-chr12:10711156..10712037,3	MCF-7	breast:
42	chr12:10484518..10485026-chr12:10826902..10827419,2	MCF-7	breast:
43	chr12:10604438..10606172-chr12:10606795..10608691,2	K562	blood:
44	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
45	chr12:10528733..10530247-chr12:10762165..10764402,2	K562	blood:
46	chr12:10484283..10485072-chr12:10714510..10715568,4	K562	blood:
47	chr12:10515701..10517485-chr12:10526352..10529351,3	K562	blood:
48	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
49	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-277P12.7.1-2	chr12:10490644-10490891	ENSG00000256288
2	lnc-GABARAPL1-3	chr12:10462225-10462287	NONHSAT026878
3	lnc-GABARAPL1-3	chr12:10467272-10467608	NONHSAT026875
4	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648
5	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
6	lnc-GABARAPL1-3	chr12:10466009-10466112	NONHSAT026875
7	lnc-RP11-277P12.7.1-3	chr12:10433068-10433194	XLOC_010016
8	lnc-EIF2S3L.1-6	chr12:10601202-10602083	l_610_chr12:10597245-10602083_whiteBloodCell
9	lnc-GABARAPL1-3	chr12:10457065-10457146	NONHSAT026875
10	lnc-RP11-277P12.7.1-2	chr12:10488711-10488908	ENSG00000256288
11	lnc-GABARAPL1-3	chr12:10464063-10464214	NONHSAT026875
12	lnc-RP11-277P12.7.1-2	chr12:10485460-10485662	ENSG00000256288
13	lnc-GABARAPL1-3	chr12:10460544-10460683	NONHSAT026878
14	lnc-KLRD1-1	chr12:10526634-10526735	ENSG00000245648
15	lnc-KLRD1-1	chr12:10548778-10551105	ENSG00000245648
16	lnc-GABARAPL1-3	chr12:10464063-10464282	NONHSAT026878
17	lnc-GABARAPL1-3	chr12:10460577-10462287	NONHSAT026875
18	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell
19	lnc-KLRD1-1	chr12:10532301-10532435	ENSG00000245648
20	lnc-GABARAPL1-1	chr12:10412867-10412929	XLOC_009659
21	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155
22	lnc-RP11-277P12.7.1-3	chr12:10443737-10443823	XLOC_010016

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLRK1	hsa-miR-9-5p	chr12:10525600-10525624

Variant related genes	Relation type
ENSG00000256288	TF binding region
KLRC3	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000245648	TF binding region
KLRD1	TF binding region
ENSG00000255641	TF binding region
KLRC2	TF binding region
KLRK1	TF binding region
KLRC1	TF binding region
ENSG00000256155	TF binding region
ENSG00000256288	CpG island
KLRC3	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000245648	CpG island
KLRD1	CpG island
ENSG00000255641	CpG island
KLRC2	CpG island
KLRK1	CpG island
KLRC1	CpG island
ENSG00000256155	CpG island
ENSG00000205810	chromatin interactions
ENSG00000213809	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000256888	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000134539	chromatin interactions
ENSG00000060140	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000255641	chromatin interactions
ENSG00000134545	chromatin interactions
RNF111	miRNA target sites
E2F3	miRNA target sites
FZD4	miRNA target sites
KIAA1967	miRNA target sites
SMAD4	miRNA target sites
LPHN2	miRNA target sites
ZEB2	miRNA target sites
NFIB	miRNA target sites
ESR1	miRNA target sites

Extended variants
information (count: 9201 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:9201 , 50 per page) page: 1 2 3 4 5 6 7 ... 185

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571373472	chr12:10398145-10398146	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs367959075	chr12:10398208-10398209	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10772249	chr12:10398248-10398249	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs113488882	chr12:10398273-10398274	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374326437	chr12:10398289-10398290	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185996634	chr12:10398293-10398294	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533043285	chr12:10398316-10398317	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546447860	chr12:10398361-10398362	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10845085	chr12:10398392-10398393	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs528808157	chr12:10398407-10398408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561224789	chr12:10398484-10398485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548870430	chr12:10398493-10398494	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568443433	chr12:10398502-10398503	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200612977	chr12:10398503-10398504	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530770016	chr12:10398544-10398545	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76761385	chr12:10398563-10398564	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550946109	chr12:10398601-10398602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557978156	chr12:10398604-10398605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568805337	chr12:10398626-10398627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574833855	chr12:10398687-10398688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11053708	chr12:10398700-10398701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552785703	chr12:10398810-10398811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531305678	chr12:10398830-10398831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548308541	chr12:10398857-10398858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566296832	chr12:10398858-10398859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7978029	chr12:10398891-10398892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555327255	chr12:10398895-10398896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11053709	chr12:10398906-10398907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs189277591	chr12:10398942-10398943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34841287	chr12:10398974-10398975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12581993	chr12:10399039-10399040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540293137	chr12:10399049-10399050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146539885	chr12:10399078-10399079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552435621	chr12:10399094-10399095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573425778	chr12:10399100-10399101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7953558	chr12:10399108-10399109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7953662	chr12:10399142-10399143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182216562	chr12:10399145-10399146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550729996	chr12:10399253-10399254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372408577	chr12:10399264-10399265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74240395	chr12:10399292-10399293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76567358	chr12:10399328-10399329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546662003	chr12:10399365-10399366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566333775	chr12:10399428-10399429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535233675	chr12:10399450-10399451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568072911	chr12:10399465-10399466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141461226	chr12:10399496-10399497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147043860	chr12:10399513-10399514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569083230	chr12:10399514-10399515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138486754	chr12:10399521-10399522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10377200-10399000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr12:10377800-10404400	Weak transcription	Left Ventricle	heart
3	chr12:10393400-10398200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:10395800-10402400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:10396800-10398800	Strong transcription	Placenta	Placenta
6	chr12:10396800-10400200	Weak transcription	Right Atrium	heart
7	chr12:10397000-10398600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:10397200-10399600	Weak transcription	GM12878-XiMat	blood
9	chr12:10397200-10400200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:10397200-10400200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr12:10397200-10400200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:10397200-10401800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr12:10397200-10402200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:10397200-10402400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr12:10397200-10402400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr12:10397200-10402400	Weak transcription	Dnd41	blood
17	chr12:10397200-10403000	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr12:10398600-10399400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr12:10398800-10436200	Weak transcription	Placenta	Placenta
20	chr12:10399400-10405200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:10399600-10399800	Enhancers	GM12878-XiMat	blood
22	chr12:10399800-10400200	Weak transcription	GM12878-XiMat	blood
23	chr12:10400200-10400400	Enhancers	Right Atrium	heart
24	chr12:10400200-10400400	Enhancers	GM12878-XiMat	blood
25	chr12:10400200-10400600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr12:10400200-10400800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr12:10400200-10400800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:10400400-10402400	Weak transcription	GM12878-XiMat	blood
29	chr12:10400600-10402000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr12:10400800-10401600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr12:10401600-10403800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10401800-10402800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr12:10402000-10403200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr12:10402200-10402400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:10402200-10403000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:10402400-10402600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:10402400-10402800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr12:10402400-10402800	Enhancers	Primary T cells from cord blood	blood
39	chr12:10402400-10402800	Enhancers	GM12878-XiMat	blood
40	chr12:10402400-10403000	Enhancers	Primary hematopoietic stem cells	blood
41	chr12:10402400-10403200	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr12:10402400-10403200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:10402400-10403200	Enhancers	Dnd41	blood
44	chr12:10402600-10402800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:10403000-10403200	Enhancers	Primary T cells fromperipheralblood	blood
46	chr12:10403200-10404400	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr12:10404400-10404600	Enhancers	Primary T cells fromperipheralblood	blood
48	chr12:10404400-10404600	Enhancers	Left Ventricle	heart
49	chr12:10426000-10426200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:10429000-10429400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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