Variant report

Variant	nsv832332
Chromosome Location	chr12:12344027-12484966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1789)
CpG islands
(count:1405)
Chromatin interactive
region (count:111)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1789 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:12359846-12359983	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:12466883-12467373	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:12393777-12394301	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:12354491-12354691	K562	blood:	n/a	n/a
5	ARID3A	chr12:12347191-12347512	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:12461439-12461810	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:12369904-12370283	K562	blood:	n/a	n/a
8	ARID3A	chr12:12369128-12369556	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:12420034-12420752	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:12480758-12481101	K562	blood:	n/a	n/a
11	ARID3A	chr12:12409216-12409479	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:12369324-12369605	K562	blood:	n/a	n/a
13	ARID3A	chr12:12419869-12420069	K562	blood:	n/a	n/a
14	ARID3A	chr12:12480753-12481084	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:12377289-12377680	K562	blood:	n/a	n/a
16	ATF1	chr12:12354359-12354658	K562	blood:	n/a	n/a
17	ATF1	chr12:12480817-12481032	K562	blood:	n/a	n/a
18	ATF2	chr12:12377116-12377664	GM12878	blood:	n/a	n/a
19	ATF2	chr12:12419798-12420286	H1-hESC	embryonic stem cell:	n/a	chr12:12419870-12419884
20	ATF2	chr12:12419809-12420566	H1-hESC	embryonic stem cell:	n/a	chr12:12419870-12419884
21	ATF2	chr12:12377175-12377535	GM12878	blood:	n/a	n/a
22	ATF2	chr12:12354050-12354550	GM12878	blood:	n/a	n/a
23	ATF2	chr12:12354115-12354564	GM12878	blood:	n/a	n/a
24	ATF2	chr12:12419719-12420191	GM12878	blood:	n/a	chr12:12419870-12419884
25	ATF3	chr12:12419726-12420546	A549	lung:	n/a	n/a
26	ATF3	chr12:12419668-12420553	A549	lung:	n/a	n/a
27	BACH1	chr12:12369300-12369578	K562	blood:	n/a	n/a
28	BACH1	chr12:12419820-12420083	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr12:12431863-12432183	GM12878	blood:	n/a	chr12:12432057-12432068
30	BATF	chr12:12369353-12369559	GM12878	blood:	n/a	chr12:12369470-12369481
31	BATF	chr12:12377170-12377567	GM12878	blood:	n/a	chr12:12377379-12377390
32	BATF	chr12:12452527-12452730	GM12878	blood:	n/a	n/a
33	BATF	chr12:12377234-12377470	GM12878	blood:	n/a	chr12:12377379-12377390
34	BATF	chr12:12464721-12464983	GM12878	blood:	n/a	chr12:12464748-12464756
35	BATF	chr12:12403189-12403436	GM12878	blood:	n/a	n/a
36	BATF	chr12:12452554-12452706	GM12878	blood:	n/a	n/a
37	BATF	chr12:12354086-12354417	GM12878	blood:	n/a	n/a
38	BATF	chr12:12354117-12354567	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:12377253-12377490	GM12878	blood:	n/a	n/a
40	BCL11A	chr12:12354120-12354591	GM12878	blood:	n/a	n/a
41	BCL11A	chr12:12364043-12364271	GM12878	blood:	n/a	n/a
42	BCL11A	chr12:12464735-12464957	GM12878	blood:	n/a	n/a
43	BCL11A	chr12:12402210-12402539	GM12878	blood:	n/a	n/a
44	BCL3	chr12:12369064-12370169	A549	lung:	n/a	n/a
45	BCL3	chr12:12377220-12377472	GM12878	blood:	n/a	n/a
46	BCL3	chr12:12419715-12420587	A549	lung:	n/a	chr12:12419734-12419747 chr12:12419738-12419751 chr12:12419740-12419753 chr12:12419848-12419861 chr12:12419910-12419923 chr12:12419746-12419759 chr12:12419741-12419754 chr12:12420312-12420325
47	BCL3	chr12:12419832-12420627	A549	lung:	n/a	chr12:12419848-12419861 chr12:12419910-12419923 chr12:12420312-12420325
48	BCLAF1	chr12:12419830-12420549	GM12878	blood:	n/a	chr12:12419848-12419861 chr12:12419910-12419923 chr12:12420312-12420325
49	BCLAF1	chr12:12354127-12354555	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:12377214-12377576	GM12878	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12421246-12421296	GM06990	blood:	n/a
2	chr12:12473531-12473581	Hela-S3	cervix:	n/a
3	chr12:12421246-12421296	GM06990	blood:	n/a
4	chr12:12473531-12473581	Hela-S3	cervix:	n/a
5	chr12:12484680-12484730	HUVEC	blood vessel:	n/a
6	chr12:12473531-12473581	AG09309	skin:	n/a
7	chr12:12420514-12420564	HL-60	blood:	n/a
8	chr12:12423496-12423546	HRE	kidney:	n/a
9	chr12:12418545-12418595	HEK293	kidney:	embryo
10	chr12:12419201-12419251	HEEpiC	esophagus:	n/a
11	chr12:12446971-12447021	U87	brain:	n/a
12	chr12:12419209-12419259	HAEpiC	amniotic membrane:	n/a
13	chr12:12420135-12420185	Hela-S3	cervix:	n/a
14	chr12:12419053-12419103	NT2-D1	testis:	n/a
15	chr12:12435302-12435352	AG09319	gingival:	n/a
16	chr12:12419752-12419802	MCF-7	breast:	n/a
17	chr12:12484680-12484730	HCT-116	colon:	n/a
18	chr12:12419921-12419971	PrEC	prostate:	n/a
19	chr12:12419921-12419971	A549	lung:	n/a
20	chr12:12418545-12418595	MCF10A-Er-Src	breast:	n/a
21	chr12:12419201-12419251	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:12391574-12391624	BE2_C	brain:	n/a
23	chr12:12418005-12418055	PANC-1	pancreas:	n/a
24	chr12:12419921-12419971	ProgFib	skin:	n/a
25	chr12:12416946-12416996	HMEC	breast:	n/a
26	chr12:12484680-12484730	HepG2	liver:	n/a
27	chr12:12473531-12473581	SAEC	small airway:	n/a
28	chr12:12420574-12420624	HAEpiC	amniotic membrane:	n/a
29	chr12:12421246-12421296	Hepatocyte	liver:	n/a
30	chr12:12418545-12418595	AG04449	skin:	fetal
31	chr12:12446971-12447021	BE2_C	brain:	n/a
32	chr12:12416946-12416996	SK-N-SH	brain:	n/a
33	chr12:12419053-12419103	SAEC	small airway:	n/a
34	chr12:12416946-12416996	HNPCEpiC	eye:	n/a
35	chr12:12473531-12473581	K562	blood:	n/a
36	chr12:12418943-12418993	NB4	blood:	n/a
37	chr12:12418005-12418055	HepG2	liver:	n/a
38	chr12:12418005-12418055	NHBE	bronchial:	n/a
39	chr12:12418545-12418595	ProgFib	skin:	n/a
40	chr12:12416946-12416996	HAEpiC	amniotic membrane:	n/a
41	chr12:12419921-12419971	BJ	skin:	n/a
42	chr12:12421246-12421296	SK-N-MC	brain:	n/a
43	chr12:12420135-12420185	HCT-116	colon:	n/a
44	chr12:12419765-12419815	Caco-2	colon:	n/a
45	chr12:12421246-12421296	HL-60	blood:	n/a
46	chr12:12418005-12418055	HRE	kidney:	n/a
47	chr12:12391574-12391624	HRCEpiC	kidney:	n/a
48	chr12:12446971-12447021	HRCEpiC	kidney:	n/a
49	chr12:12419765-12419815	U87	brain:	n/a
50	chr12:12416946-12416996	HRE	kidney:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:12411511..12414541-chr12:12419188..12422648,4	MCF-7	breast:
2	chr12:12418888..12421558-chr12:12875681..12878464,3	MCF-7	breast:
3	chr12:12336035..12338491-chr12:12459842..12461495,2	K562	blood:
4	chr12:12369208..12371594-chr12:12405892..12408383,3	K562	blood:
5	chr12:12378227..12379810-chr12:12418939..12421766,2	K562	blood:
6	chr12:12449043..12450589-chr12:12452243..12454502,2	MCF-7	breast:
7	chr12:12393044..12397840-chr12:12419223..12421821,5	MCF-7	breast:
8	chr12:12419688..12421380-chr12:12433411..12435070,2	MCF-7	breast:
9	chr12:12353652..12355834-chr12:12365732..12367284,2	K562	blood:
10	chr12:12410568..12413506-chr12:12416541..12418558,2	MCF-7	breast:
11	chr12:12406030..12408982-chr12:12413928..12415647,2	MCF-7	breast:
12	chr12:12418815..12421655-chr12:12424332..12429486,6	MCF-7	breast:
13	chr12:12419134..12421122-chr12:12441823..12443690,2	MCF-7	breast:
14	chr12:12395975..12398553-chr12:12399397..12402094,2	MCF-7	breast:
15	chr12:12419697..12421689-chr12:12437095..12439954,3	MCF-7	breast:
16	chr12:12402726..12404762-chr12:12408084..12410910,2	K562	blood:
17	chr12:12413166..12415033-chr12:12416431..12418396,2	K562	blood:
18	chr12:12420321..12422188-chr12:12434856..12437059,2	MCF-7	breast:
19	chr12:12428303..12430629-chr12:12434266..12436457,2	MCF-7	breast:
20	chr12:12364652..12367428-chr12:12369707..12372537,2	K562	blood:
21	chr12:12234308..12235009-chr12:12480762..12481311,2	MCF-7	breast:
22	chr12:12399729..12401467-chr12:12407423..12408972,2	K562	blood:
23	chr12:12435921..12437917-chr12:12447331..12449825,2	MCF-7	breast:
24	chr12:12420258..12422244-chr12:12868437..12870930,2	K562	blood:
25	chr12:12419774..12421330-chr12:12508637..12511348,2	MCF-7	breast:
26	chr12:12395975..12398553-chr12:12399397..12402094,2	MCF-7	breast:
27	chr12:12389441..12390958-chr12:12394768..12397080,2	K562	blood:
28	chr12:12420321..12422188-chr12:12434856..12437059,2	MCF-7	breast:
29	chr12:12418062..12421378-chr12:12712958..12715949,4	MCF-7	breast:
30	chr12:12418368..12422296-chr12:12423665..12427518,5	K562	blood:
31	chr12:12419781..12420755-chr17:33569952..33570461,2	Hela-S3	cervix:
32	chr12:12390182..12397827-chr12:12417123..12421502,7	MCF-7	breast:
33	chr12:12188663..12189590-chr12:12480372..12481301,2	K562	blood:
34	chr12:12450993..12453297-chr12:12461726..12464649,2	MCF-7	breast:
35	chr12:12358286..12360439-chr12:12418199..12420506,2	MCF-7	breast:
36	chr12:12419210..12421739-chr12:12479012..12482155,4	MCF-7	breast:
37	chr12:12435889..12438304-chr12:12442980..12444764,2	MCF-7	breast:
38	chr12:12419370..12422118-chr12:12510348..12512093,2	MCF-7	breast:
39	chr12:12480106..12480918-chr12:27090779..27091584,2	Hela-S3	cervix:
40	chr12:12234582..12235322-chr12:12482615..12483543,2	K562	blood:
41	chr12:12364652..12367428-chr12:12369707..12372537,2	K562	blood:
42	chr12:12399860..12402436-chr12:12417674..12420343,2	K562	blood:
43	chr12:12419999..12420724-chr7:48018768..48019330,2	Hela-S3	cervix:
44	chr12:12401717..12403470-chr12:12410305..12412865,2	MCF-7	breast:
45	chr12:12401851..12404835-chr12:12418306..12421349,3	MCF-7	breast:
46	chr12:12419769..12421659-chr12:12478987..12480796,2	MCF-7	breast:
47	chr12:12479190..12481721-chr12:12482518..12485352,2	MCF-7	breast:
48	chr12:12347779..12350511-chr12:12354038..12356966,2	MCF-7	breast:
49	chr12:12410046..12415348-chr12:12416072..12422539,9	MCF-7	breast:
50	chr12:12230786..12232660-chr12:12419937..12421467,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL2L14-2	chr12:12401925-12402361	NONHSAT026966
2	lnc-MANSC1-1	chr12:12399611-12401006	l_612_NR_024061
3	lnc-MANSC1-1	chr12:12401129-12401268	l_612_NR_024061

No data

Variant related genes	Relation type
RNU6-545P	TF binding region
ENSG00000270857	TF binding region
LRP6	TF binding region
RNU6-1295P	TF binding region
RNU6-545P	CpG island
ENSG00000270857	CpG island
LRP6	CpG island
RNU6-1295P	CpG island
ENSG00000166750	chromatin interactions
ENSG00000070018	chromatin interactions
ENSG00000199551	chromatin interactions
ENSG00000111266	chromatin interactions
ENSG00000266947	chromatin interactions
ENSG00000136273	chromatin interactions
ENSG00000256658	chromatin interactions
ENSG00000207010	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000141458	chromatin interactions
ENSG00000111276	chromatin interactions
ENSG00000121380	chromatin interactions
ENSG00000270857	chromatin interactions
ENSG00000111790	chromatin interactions
ENSG00000064102	chromatin interactions
ENSG00000205791	chromatin interactions

Extended variants
information (count: 5941 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5941 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571938526	chr12:12344033-12344034	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs539365133	chr12:12344040-12344041	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs557485313	chr12:12344088-12344089	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs575755878	chr12:12344090-12344091	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs536888808	chr12:12344095-12344096	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs151087119	chr12:12344104-12344105	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs573429132	chr12:12344137-12344138	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs191490034	chr12:12344162-12344163	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs552564924	chr12:12344186-12344187	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs141019614	chr12:12344195-12344196	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs544912320	chr12:12344196-12344197	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs563640952	chr12:12344264-12344265	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs367804764	chr12:12344344-12344345	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs371193863	chr12:12344420-12344421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530613913	chr12:12344469-12344470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540702448	chr12:12344514-12344515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112684262	chr12:12344558-12344559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561208315	chr12:12344577-12344578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370839289	chr12:12344610-12344611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374466128	chr12:12344728-12344729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116715447	chr12:12344731-12344732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546985274	chr12:12344732-12344733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571669718	chr12:12344735-12344736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34672789	chr12:12344793-12344794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532817095	chr12:12344795-12344796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550985563	chr12:12344920-12344921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569582752	chr12:12344921-12344922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536426043	chr12:12344941-12344942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370093505	chr12:12345021-12345022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368865749	chr12:12345025-12345026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566990034	chr12:12345045-12345046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146868085	chr12:12345095-12345096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371859368	chr12:12345098-12345099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577208727	chr12:12345142-12345143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545034244	chr12:12345180-12345181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373809500	chr12:12345181-12345182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556953518	chr12:12345261-12345262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575528008	chr12:12345288-12345289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542421448	chr12:12345317-12345318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561086453	chr12:12345318-12345319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528545651	chr12:12345342-12345343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183260898	chr12:12345374-12345375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565422387	chr12:12345408-12345409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532549977	chr12:12345415-12345416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376601331	chr12:12345425-12345426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550983160	chr12:12345490-12345491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187529781	chr12:12345527-12345528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530440763	chr12:12345530-12345531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140735913	chr12:12345544-12345545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367995235	chr12:12345560-12345561	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	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
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	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 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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:2884 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12272200-12344600	Weak transcription	Primary B cells from cord blood	blood
2	chr12:12304000-12353000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr12:12312000-12350600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr12:12312200-12355800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:12312200-12362000	Weak transcription	Hela-S3	cervix
6	chr12:12315400-12371600	Weak transcription	Lung	lung
7	chr12:12325400-12360000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr12:12334200-12350800	Weak transcription	Fetal Thymus	thymus
9	chr12:12334400-12348400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:12334400-12349200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr12:12334400-12349600	Weak transcription	Dnd41	blood
12	chr12:12334400-12351200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr12:12334400-12352000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:12334400-12354000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr12:12334400-12367600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr12:12334600-12349200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr12:12334800-12346800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:12334800-12352800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr12:12335200-12352000	Weak transcription	HSMM	muscle
20	chr12:12335200-12365800	Weak transcription	NHEK	skin
21	chr12:12335800-12354000	Weak transcription	HSMMtube	muscle
22	chr12:12336000-12352000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr12:12336000-12354200	Weak transcription	Primary T cells from cord blood	blood
24	chr12:12336000-12355600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr12:12336200-12347000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr12:12336200-12360000	Weak transcription	Aorta	Aorta
27	chr12:12336200-12363200	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr12:12336200-12369800	Weak transcription	Left Ventricle	heart
29	chr12:12336200-12381000	Weak transcription	Pancreas	Pancrea
30	chr12:12336400-12348800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:12336400-12349600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr12:12336400-12357400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr12:12337000-12345200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:12337600-12348200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr12:12337800-12348400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr12:12338200-12349000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr12:12338200-12355800	Weak transcription	Stomach Mucosa	stomach
38	chr12:12339000-12350800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr12:12339200-12357600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr12:12339800-12350600	Weak transcription	Fetal Intestine Small	intestine
41	chr12:12339800-12350600	Weak transcription	Fetal Stomach	stomach
42	chr12:12340000-12346600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr12:12340000-12348600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:12340200-12349600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr12:12340400-12345400	Weak transcription	Fetal Muscle Leg	muscle
46	chr12:12340600-12349600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:12340600-12359400	Weak transcription	Ovary	ovary
48	chr12:12340800-12349600	Weak transcription	Liver	Liver
49	chr12:12341000-12346400	Weak transcription	HepG2	liver
50	chr12:12341400-12344200	Enhancers	Colon Smooth Muscle	Colon

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