Variant report

Variant	esv3449843
Chromosome Location	chr12:103888522-103890420
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	ATF3	chr12:103889903-103890388	A549	lung:	n/a	n/a
2	BATF	chr12:103889725-103890270	GM12878	blood:	n/a	n/a
3	BCL11A	chr12:103889775-103890215	GM12878	blood:	n/a	n/a
4	BCLAF1	chr12:103889660-103890292	GM12878	blood:	n/a	chr12:103889708-103889721
5	BHLHE40	chr12:103889042-103889501	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:103889706-103890379	GM12878	blood:	n/a	n/a
7	CHD1	chr12:103889326-103890149	GM12878	blood:	n/a	chr12:103889448-103889458
8	CHD2	chr12:103888943-103890278	GM12878	blood:	n/a	chr12:103889448-103889458
9	CHD2	chr12:103888976-103889149	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr12:103889087-103889566	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr12:103889240-103889962	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr12:103889760-103889910	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr12:103890060-103890210	HCFaa	heart:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
14	CTCF	chr12:103890060-103890210	HVMF	connective:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
15	CTCF	chr12:103889904-103889908	GM12878	blood:	n/a	n/a
16	CTCF	chr12:103890080-103890230	BE2_C	brain:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
17	CTCF	chr12:103890080-103890230	AG09319	gingival:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
18	CTCF	chr12:103890020-103890170	Hela-S3	cervix:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
19	CTCF	chr12:103890040-103890190	HBMEC	blood vessel:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
20	CTCF	chr12:103889845-103890439	MCF-7	breast:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
21	CTCF	chr12:103890060-103890210	HCPEpiC	choroid plexus:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
22	CTCF	chr12:103889857-103890416	HCT-116	colon:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
23	CTCF	chr12:103890080-103890230	BJ	skin:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
24	CTCF	chr12:103889301-103889354	GM19238	blood:	n/a	n/a
25	CTCF	chr12:103890023-103890239	GM10248	blood:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
26	CTCF	chr12:103890060-103890210	NHLF	lung:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
27	CTCF	chr12:103890020-103890170	WI-38	lung:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
28	CTCF	chr12:103889700-103889881	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:103889640-103889790	GM12874	blood:	n/a	chr12:103889646-103889656
30	CTCF	chr12:103890049-103890234	LNCaP	prostate:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
31	CTCF	chr12:103889225-103890477	SK-N-SH	brain:	n/a	chr12:103889646-103889656 chr12:103890135-103890153 chr12:103890138-103890151
32	CTCF	chr12:103890000-103890150	NHEK	skin:	n/a	n/a
33	CTCF	chr12:103890023-103890233	GM13976	blood:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
34	CTCF	chr12:103888604-103888686	GM19238	blood:	n/a	chr12:103888654-103888672 chr12:103888657-103888670
35	CTCF	chr12:103890006-103890273	H1-hESC	embryonic stem cell:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
36	CTCF	chr12:103889649-103889922	GM19239	blood:	n/a	n/a
37	CTCF	chr12:103889714-103889817	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr12:103890120-103890270	GM12873	blood:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
39	CTCF	chr12:103890060-103890210	HMF	breast:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
40	CTCF	chr12:103890060-103890210	AoAF	blood vessel:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
41	CTCF	chr12:103890041-103890228	HepG2	liver:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
42	CTCF	chr12:103890060-103890210	AG09309	skin:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
43	CTCF	chr12:103890000-103890276	A549	lung:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
44	CTCF	chr12:103889572-103889586	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:103889720-103889870	GM12866	blood:	n/a	n/a
46	CTCF	chr12:103890080-103890230	HVMF	connective:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
47	CTCF	chr12:103890080-103890230	GM06990	blood:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
48	CTCF	chr12:103890040-103890330	WI-38	lung:	n/a	chr12:103890135-103890153 chr12:103890138-103890151
49	CTCF	chr12:103889712-103889719	NHEK	skin:	n/a	n/a
50	CTCF	chr12:103890056-103890241	Lung_OC	lung:	n/a	chr12:103890135-103890153 chr12:103890138-103890151

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:103890083-103890133	GM12891	blood:	n/a
2	chr12:103890083-103890133	GM12891	blood:	n/a
3	chr12:103889516-103889566	HRCEpiC	kidney:	n/a
4	chr12:103889960-103890010	HL-60	blood:	n/a
5	chr12:103889516-103889566	AG04450	lung:	fetal
6	chr12:103889789-103889839	H1-hESC	embryonic stem cell:	embryo
7	chr12:103890274-103890324	AG10803	skin:	n/a
8	chr12:103889960-103890010	NT2-D1	testis:	n/a
9	chr12:103889798-103889848	HCPEpiC	choroid plexus:	n/a
10	chr12:103889903-103889953	HCF	heart:	n/a
11	chr12:103889784-103889834	A549	lung:	n/a
12	chr12:103889789-103889839	NHDF-neo	bronchial:	n/a
13	chr12:103889903-103889953	HL-60	blood:	n/a
14	chr12:103889960-103890010	SK-N-MC	brain:	n/a
15	chr12:103889166-103889216	Caco-2	colon:	n/a
16	chr12:103889307-103889357	HEK293	kidney:	embryo
17	chr12:103889789-103889839	SAEC	small airway:	n/a
18	chr12:103889307-103889357	AG09309	skin:	n/a
19	chr12:103889960-103890010	SK-N-SH	brain:	n/a
20	chr12:103889655-103889705	AG04449	skin:	fetal
21	chr12:103889798-103889848	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:103889928-103889978	HAEpiC	amniotic membrane:	n/a
23	chr12:103889789-103889839	Caco-2	colon:	n/a
24	chr12:103889042-103889092	NHBE	bronchial:	n/a
25	chr12:103890274-103890324	AG04450	lung:	fetal
26	chr12:103889960-103890010	K562	blood:	n/a
27	chr12:103889784-103889834	MCF10A-Er-Src	breast:	n/a
28	chr12:103889960-103890010	HNPCEpiC	eye:	n/a
29	chr12:103889789-103889839	ovcar-3	ovarian:	n/a
30	chr12:103890083-103890133	Hepatocyte	liver:	n/a
31	chr12:103890083-103890133	AG09319	gingival:	n/a
32	chr12:103889042-103889092	AG04450	lung:	fetal
33	chr12:103889166-103889216	SK-N-MC	brain:	n/a
34	chr12:103889516-103889566	NHBE	bronchial:	n/a
35	chr12:103889307-103889357	HNPCEpiC	eye:	n/a
36	chr12:103889960-103890010	AG04449	skin:	fetal
37	chr12:103889798-103889848	T-47D	breast:	n/a
38	chr12:103889307-103889357	GM12891	blood:	n/a
39	chr12:103889960-103890010	A549	lung:	n/a
40	chr12:103889772-103889822	GM12891	blood:	n/a
41	chr12:103889166-103889216	Hela-S3	cervix:	n/a
42	chr12:103889772-103889822	NT2-D1	testis:	n/a
43	chr12:103890083-103890133	HL-60	blood:	n/a
44	chr12:103889772-103889822	CMK	blood:	n/a
45	chr12:103890083-103890133	ECC-1	luminal epithelium:	n/a
46	chr12:103889516-103889566	PANC-1	pancreas:	n/a
47	chr12:103889166-103889216	ProgFib	skin:	n/a
48	chr12:103889307-103889357	NH-A	brain:	n/a
49	chr12:103889042-103889092	HepG2	liver:	n/a
50	chr12:103889655-103889705	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:103868882..103870646-chr12:103889851..103892092,2	MCF-7	breast:
2	chr12:103890051..103890606-chr12:104026106..104027016,2	MCF-7	breast:
3	chr12:103889657..103890710-chr12:103941159..103943032,10	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAH-2	chr12:103889680-103889703	NONHSAT030372
2	lnc-PAH-2	chr12:103889545-103889749	NONHSAT030375
3	lnc-PAH-2	chr12:103889680-103889724	NONHSAT030371
4	lnc-PAH-2	chr12:103889680-103889788	NR_103526
5	lnc-PAH-2	chr12:103889680-103889736	NONHSAT030368

Variant related genes	Relation type
C12orf42	TF binding region
C12orf42	CpG island
ENSG00000257762	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573966683	chr12:103888532-103888533	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs570055120	chr12:103888538-103888539	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs535605797	chr12:103888549-103888550	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs374052449	chr12:103888557-103888558	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs367646419	chr12:103888605-103888606	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs71097982	chr12:103888619-103888620	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs185042238	chr12:103888639-103888640	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs565801130	chr12:103888658-103888659	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs535139258	chr12:103888667-103888668	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs557996704	chr12:103888668-103888669	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs577952656	chr12:103888673-103888674	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs537088886	chr12:103888758-103888759	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs528353839	chr12:103888768-103888769	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs113969226	chr12:103888789-103888790	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs576411341	chr12:103888820-103888821	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546619876	chr12:103888838-103888839	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561881926	chr12:103888841-103888842	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78233823	chr12:103888852-103888853	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375840659	chr12:103888889-103888890	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541100832	chr12:103888899-103888900	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11111609	chr12:103888931-103888932	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567957640	chr12:103888951-103888952	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189413636	chr12:103888977-103888978	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12422517	chr12:103889031-103889032	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563599149	chr12:103889032-103889033	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs181977695	chr12:103889087-103889088	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs186202890	chr12:103889132-103889133	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs115733644	chr12:103889140-103889141	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs549136569	chr12:103889144-103889145	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs566134961	chr12:103889150-103889151	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs556763337	chr12:103889181-103889182	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs528712533	chr12:103889192-103889193	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs551841926	chr12:103889198-103889199	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs564584360	chr12:103889239-103889240	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs571694829	chr12:103889270-103889271	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs537403195	chr12:103889272-103889273	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs376378871	chr12:103889317-103889318	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs369640577	chr12:103889336-103889337	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs527325534	chr12:103889356-103889357	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs12311248	chr12:103889408-103889409	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs188324076	chr12:103889419-103889420	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376911199	chr12:103889478-103889479	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572190697	chr12:103889479-103889480	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540909365	chr12:103889498-103889499	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557831529	chr12:103889548-103889549	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs117706353	chr12:103889581-103889582	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs368714530	chr12:103889590-103889591	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs542978954	chr12:103889624-103889625	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs562966015	chr12:103889673-103889674	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs537247885	chr12:103889692-103889693	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103886400-103888800	Enhancers	NHEK	skin
2	chr12:103886400-103889200	Enhancers	HMEC	breast
3	chr12:103886600-103888800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:103887400-103889400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:103887800-103888800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:103887800-103888800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:103887800-103889000	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr12:103888000-103888600	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr12:103888000-103888800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:103888000-103888800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:103888000-103889000	Flanking Active TSS	Dnd41	blood
12	chr12:103888200-103888600	Enhancers	Primary B cells from peripheral blood	blood
13	chr12:103888200-103888600	Flanking Active TSS	Primary T cells from cord blood	blood
14	chr12:103888200-103888600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr12:103888200-103888800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:103888200-103888800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr12:103888200-103888800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr12:103888200-103889000	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr12:103888200-103889000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr12:103888200-103889000	Flanking Active TSS	Fetal Thymus	thymus
21	chr12:103888200-103889600	Active TSS	Thymus	Thymus
22	chr12:103888400-103888600	Active TSS	H1 Cell Line	embryonic stem cell
23	chr12:103888400-103888600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
24	chr12:103888400-103888600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
25	chr12:103888400-103888600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr12:103888400-103888600	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr12:103888400-103888600	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr12:103888400-103888800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr12:103888400-103888800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr12:103888400-103888800	Bivalent Enhancer	Primary B cells from cord blood	blood
31	chr12:103888400-103888800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
32	chr12:103888400-103888800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:103888400-103888800	Enhancers	GM12878-XiMat	blood
34	chr12:103888400-103889000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:103888400-103889000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr12:103888400-103889000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr12:103888400-103889000	Flanking Active TSS	Fetal Brain Female	brain
38	chr12:103888400-103889200	Enhancers	Fetal Brain Male	brain
39	chr12:103888400-103889800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr12:103888400-103890000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
41	chr12:103888400-103890200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
42	chr12:103888400-103890200	Active TSS	H9 Cell Line	embryonic stem cell
43	chr12:103888400-103890200	Active TSS	Brain Angular Gyrus	brain
44	chr12:103888600-103888800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
45	chr12:103888600-103888800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:103888600-103888800	Active TSS	Primary T cells from cord blood	blood
47	chr12:103888600-103888800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:103888600-103888800	Enhancers	Brain Cingulate Gyrus	brain
49	chr12:103888600-103888800	Active TSS	Brain Germinal Matrix	brain
50	chr12:103888600-103888800	Bivalent Enhancer	Brain Hippocampus Middle	brain

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