Variant report

Variant	esv3339962
Chromosome Location	chr12:42982685-42984683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:42982800-42983141	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:42984246-42984643	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:42983611-42983906	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr12:42983564-42983826	GM12878	blood:	n/a	chr12:42983763-42983776
5	CCNT2	chr12:42983171-42983827	K562	blood:	n/a	n/a
6	CHD1	chr12:42983449-42983494	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr12:42983639-42983711	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr12:42983333-42983795	A549	lung:	n/a	n/a
9	CTBP2	chr12:42982768-42984725	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:42984520-42984670	HMEC	breast:	n/a	chr12:42984591-42984609
11	CTCF	chr12:42982800-42982950	AG09319	gingival:	n/a	chr12:42982868-42982889
12	CTCF	chr12:42982800-42982950	HepG2	liver:	n/a	chr12:42982868-42982889
13	CTCF	chr12:42982740-42983016	H1-hESC	embryonic stem cell:	n/a	chr12:42982868-42982889
14	CTCF	chr12:42982786-42982964	GM12892	blood:	n/a	chr12:42982868-42982889
15	CTCF	chr12:42984500-42984650	HPAF	blood vessel:	n/a	chr12:42984591-42984609
16	CTCF	chr12:42982780-42982930	NB4	blood:	n/a	chr12:42982868-42982889
17	CTCF	chr12:42982745-42983006	Medullo	brain:	n/a	chr12:42982868-42982889
18	CTCF	chr12:42982780-42982930	GM12869	blood:	n/a	chr12:42982868-42982889
19	CTCF	chr12:42982780-42982930	GM12868	blood:	n/a	chr12:42982868-42982889
20	CTCF	chr12:42984540-42984690	HCFaa	heart:	n/a	chr12:42984591-42984609
21	CTCF	chr12:42982820-42982970	HMF	breast:	n/a	chr12:42982868-42982889
22	CTCF	chr12:42983632-42983677	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr12:42982800-42982950	AG04449	skin:	n/a	chr12:42982868-42982889
24	CTCF	chr12:42984560-42984710	SAEC	small airway:	n/a	chr12:42984591-42984609
25	CTCF	chr12:42982820-42982970	Caco-2	colon:	n/a	chr12:42982868-42982889
26	CTCF	chr12:42982820-42982970	HRE	kidney:	n/a	chr12:42982868-42982889
27	CTCF	chr12:42982784-42982979	Pancreas_OC	pancreas:	n/a	chr12:42982868-42982889
28	CTCF	chr12:42984500-42984650	MCF-7	breast:	n/a	chr12:42984591-42984609
29	CTCF	chr12:42982781-42982969	SK-N-SH_RA	brain:	n/a	chr12:42982868-42982889
30	CTCF	chr12:42982748-42983006	H1-hESC	embryonic stem cell:	n/a	chr12:42982868-42982889
31	CTCF	chr12:42984520-42984670	HPAF	blood vessel:	n/a	chr12:42984591-42984609
32	CTCF	chr12:42982820-42982970	HCFaa	heart:	n/a	chr12:42982868-42982889
33	CTCF	chr12:42984580-42984730	AG04449	skin:	n/a	chr12:42984591-42984609
34	CTCF	chr12:42982773-42982949	GM13976	blood:	n/a	chr12:42982868-42982889
35	CTCF	chr12:42982780-42982930	GM12874	blood:	n/a	chr12:42982868-42982889
36	CTCF	chr12:42984500-42984689	MCF-7	breast:	n/a	chr12:42984591-42984609
37	CTCF	chr12:42982763-42983060	K562	blood:	n/a	chr12:42982868-42982889
38	CTCF	chr12:42984548-42984622	GM13977	blood:	n/a	chr12:42984591-42984609
39	CTCF	chr12:42982787-42982995	Kidney_OC	kidney:	n/a	chr12:42982868-42982889
40	CTCF	chr12:42982800-42982950	HL-60	blood:	n/a	chr12:42982868-42982889
41	CTCF	chr12:42982698-42983051	GM12878	blood:	n/a	chr12:42982868-42982889
42	CTCF	chr12:42984531-42984647	GM19239	blood:	n/a	chr12:42984591-42984609
43	CTCF	chr12:42982800-42982950	GM12875	blood:	n/a	chr12:42982868-42982889
44	CTCF	chr12:42982745-42983024	NHEK	skin:	n/a	chr12:42982868-42982889
45	CTCF	chr12:42984500-42984650	HCPEpiC	choroid plexus:	n/a	chr12:42984591-42984609
46	CTCF	chr12:42982800-42982950	Caco-2	colon:	n/a	chr12:42982868-42982889
47	CTCF	chr12:42982800-42982950	K562	blood:	n/a	chr12:42982868-42982889
48	CTCF	chr12:42984500-42984650	SK-N-SH_RA	brain:	n/a	chr12:42984591-42984609
49	CTCF	chr12:42982750-42983004	GM19239	blood:	n/a	chr12:42982868-42982889
50	CTCF	chr12:42982800-42982950	HBMEC	blood vessel:	n/a	chr12:42982868-42982889

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:42984114-42984164	PANC-1	pancreas:	n/a
2	chr12:42984236-42984286	HMEC	breast:	n/a
3	chr12:42982649-42982699	NHDF-neo	bronchial:	n/a
4	chr12:42982649-42982699	HCPEpiC	choroid plexus:	n/a
5	chr12:42982929-42982979	ProgFib	skin:	n/a
6	chr12:42983805-42983855	A549	lung:	n/a
7	chr12:42982929-42982979	AG10803	skin:	n/a
8	chr12:42983360-42983410	GM12892	blood:	n/a
9	chr12:42984337-42984387	AG09309	skin:	n/a
10	chr12:42984114-42984164	GM12878	blood:	n/a
11	chr12:42984093-42984143	HAEpiC	amniotic membrane:	n/a
12	chr12:42984093-42984143	MCF10A-Er-Src	breast:	n/a
13	chr12:42982929-42982979	HRPEpiC	eye:	n/a
14	chr12:42984224-42984274	GM12878	blood:	n/a
15	chr12:42984114-42984164	GM19239	blood:	n/a
16	chr12:42983805-42983855	PFSK-1	brain:	n/a
17	chr12:42982929-42982979	H1-hESC	embryonic stem cell:	embryo
18	chr12:42984466-42984516	H1-hESC	embryonic stem cell:	embryo
19	chr12:42984224-42984274	SK-N-SH_RA	brain:	n/a
20	chr12:42984236-42984286	HCT-116	colon:	n/a
21	chr12:42982649-42982699	HNPCEpiC	eye:	n/a
22	chr12:42982929-42982979	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:42984337-42984387	HMEC	breast:	n/a
24	chr12:42984466-42984516	HUVEC	blood vessel:	n/a
25	chr12:42984224-42984274	HepG2	liver:	n/a
26	chr12:42984093-42984143	Caco-2	colon:	n/a
27	chr12:42982649-42982699	PFSK-1	brain:	n/a
28	chr12:42984337-42984387	NB4	blood:	n/a
29	chr12:42984466-42984516	SKMC	muscle:	n/a
30	chr12:42983360-42983410	AG09319	gingival:	n/a
31	chr12:42983360-42983410	SK-N-MC	brain:	n/a
32	chr12:42984093-42984143	BJ	skin:	n/a
33	chr12:42984466-42984516	GM06990	blood:	n/a
34	chr12:42984224-42984274	AoSMC	blood vessel:	n/a
35	chr12:42984114-42984164	NHBE	bronchial:	n/a
36	chr12:42983805-42983855	HCT-116	colon:	n/a
37	chr12:42984093-42984143	GM12892	blood:	n/a
38	chr12:42984466-42984516	HIPEpiC	eye:	n/a
39	chr12:42984236-42984286	NT2-D1	testis:	n/a
40	chr12:42984337-42984387	HCT-116	colon:	n/a
41	chr12:42983805-42983855	HRE	kidney:	n/a
42	chr12:42982649-42982699	SK-N-MC	brain:	n/a
43	chr12:42984224-42984274	AG09309	skin:	n/a
44	chr12:42984466-42984516	Jurkat	blood:	n/a
45	chr12:42984337-42984387	HAEpiC	amniotic membrane:	n/a
46	chr12:42984224-42984274	GM19239	blood:	n/a
47	chr12:42984236-42984286	BE2_C	brain:	n/a
48	chr12:42984337-42984387	SAEC	small airway:	n/a
49	chr12:42984236-42984286	HL-60	blood:	n/a
50	chr12:42982649-42982699	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:42982454..42982981-chr12:43675696..43676627,2	MCF-7	breast:
2	chr12:42984197..42984716-chr12:43676086..43676642,2	MCF-7	breast:
3	chr12:42982822..42983322-chr12:43730434..43730991,2	MCF-7	breast:
4	chr12:42982698..42983359-chr12:43198437..43199068,2	MCF-7	breast:
5	chr12:42975394..42979509-chr12:42980340..42982880,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZCRB1-2	chr12:42983267-42983546	NONHSAT027781

Variant related genes	Relation type
PRICKLE1	TF binding region
PRICKLE1	CpG island

Extended variants
information (count: 49 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:49 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190383510	chr12:42982763-42982764	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74362389	chr12:42982801-42982802	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182546608	chr12:42982884-42982885	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548587005	chr12:42982904-42982905	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373100898	chr12:42982907-42982908	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566887415	chr12:42983027-42983028	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs144868398	chr12:42983069-42983070	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs188063876	chr12:42983081-42983082	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs552392019	chr12:42983098-42983099	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs75377998	chr12:42983135-42983136	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs2141929	chr12:42983138-42983139	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs79374882	chr12:42983159-42983160	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs556367191	chr12:42983160-42983161	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs568399443	chr12:42983248-42983249	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561368128	chr12:42983324-42983325	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs545930952	chr12:42983341-42983342	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs117521428	chr12:42983399-42983400	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs145508056	chr12:42983408-42983409	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs548377394	chr12:42983422-42983423	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs557557453	chr12:42983431-42983432	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs576131579	chr12:42983434-42983435	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs543617300	chr12:42983467-42983468	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs561895960	chr12:42983542-42983543	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs573947148	chr12:42983607-42983608	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs11837158	chr12:42983762-42983763	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs536986417	chr12:42983767-42983768	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370260611	chr12:42983780-42983781	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs190800488	chr12:42983795-42983796	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs112357144	chr12:42983812-42983813	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs5797813	chr12:42983891-42983892	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs560478560	chr12:42983926-42983927	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527693850	chr12:42983931-42983932	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs183902352	chr12:42983949-42983950	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564403108	chr12:42983991-42983992	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs74818946	chr12:42983995-42983996	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs549929214	chr12:42984059-42984060	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs568340682	chr12:42984075-42984076	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140035748	chr12:42984088-42984089	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs547696061	chr12:42984101-42984102	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs566401981	chr12:42984114-42984115	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs149848693	chr12:42984216-42984217	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs556119906	chr12:42984235-42984236	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs557760115	chr12:42984390-42984391	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs576038873	chr12:42984454-42984455	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs537158982	chr12:42984525-42984526	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187834664	chr12:42984541-42984542	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573882173	chr12:42984559-42984560	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs541286329	chr12:42984637-42984638	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs559385862	chr12:42984652-42984653	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42980000-42985000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr12:42980600-42984200	Active TSS	HSMMtube	muscle
3	chr12:42980800-42984200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr12:42981000-42984000	Active TSS	Brain Angular Gyrus	brain
5	chr12:42981000-42984000	Active TSS	Fetal Muscle Leg	muscle
6	chr12:42981200-42983000	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr12:42981200-42983800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
8	chr12:42981200-42984000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr12:42981200-42985000	Active TSS	Right Atrium	heart
10	chr12:42981400-42984000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:42981400-42984000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
12	chr12:42981400-42984200	Active TSS	Brain Anterior Caudate	brain
13	chr12:42981400-42984800	Active TSS	Right Ventricle	heart
14	chr12:42981600-42982800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr12:42981600-42982800	Active TSS	Fetal Muscle Trunk	muscle
16	chr12:42981600-42982800	Active TSS	Fetal Stomach	stomach
17	chr12:42981600-42983000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:42981600-42983200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:42981600-42983200	Active TSS	Fetal Heart	heart
20	chr12:42981600-42983200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr12:42981600-42984200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:42981600-42984400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
23	chr12:42981600-42985000	Active TSS	Fetal Kidney	kidney
24	chr12:42981800-42982800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:42981800-42982800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:42981800-42983200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
27	chr12:42981800-42983200	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
28	chr12:42981800-42983200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr12:42981800-42984600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:42981800-42984800	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
31	chr12:42982000-42982800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr12:42982000-42982800	Active TSS	Placenta	Placenta
33	chr12:42982000-42982800	Bivalent/Poised TSS	NHLF	lung
34	chr12:42982000-42983000	Bivalent/Poised TSS	Brain Substantia Nigra	brain
35	chr12:42982000-42983400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
36	chr12:42982000-42984000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:42982000-42984000	Bivalent/Poised TSS	Colonic Mucosa	Colon
38	chr12:42982000-42984000	Active TSS	HSMM	muscle
39	chr12:42982000-42984000	Active TSS	HUVEC	blood vessel
40	chr12:42982000-42984000	Active TSS	NH-A	brain
41	chr12:42982000-42984800	Active TSS	Aorta	Aorta
42	chr12:42982000-42984800	Active TSS	Left Ventricle	heart
43	chr12:42982000-42984800	Active TSS	Ovary	ovary
44	chr12:42982000-42985000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
45	chr12:42982200-42982800	Bivalent Enhancer	Liver	Liver
46	chr12:42982200-42982800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
47	chr12:42982200-42983400	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr12:42982200-42984000	Active TSS	Fetal Lung	lung
49	chr12:42982200-42984000	Active TSS	HMEC	breast
50	chr12:42982200-42984000	Active TSS	Osteobl	bone

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