Variant report

Variant	esv3390684
Chromosome Location	chr12:30906885-30909083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:767)
CpG islands
(count:611)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:30907773-30908303	K562	blood:	n/a	n/a
2	ARID3A	chr12:30908801-30909399	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:30907876-30908587	HepG2	liver:	n/a	n/a
4	ATF2	chr12:30907703-30908214	GM12878	blood:	n/a	n/a
5	ATF2	chr12:30908055-30908473	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:30907301-30908343	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr12:30907744-30908518	A549	lung:	n/a	n/a
8	BCLAF1	chr12:30907820-30908342	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:30907694-30908258	K562	blood:	n/a	chr12:30907701-30907714 chr12:30907706-30907719
10	BCLAF1	chr12:30907629-30908418	GM12878	blood:	n/a	chr12:30907647-30907656 chr12:30907644-30907653 chr12:30907701-30907714 chr12:30907706-30907719
11	BHLHE40	chr12:30907212-30908520	K562	blood:	n/a	chr12:30907990-30908006 chr12:30907709-30907725 chr12:30907703-30907719 chr12:30907591-30907607
12	BHLHE40	chr12:30907644-30908275	GM12878	blood:	n/a	chr12:30907990-30908006 chr12:30907709-30907725 chr12:30907703-30907719
13	BRCA1	chr12:30907912-30908264	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr12:30906876-30906925	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr12:30907800-30908128	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr12:30907929-30908168	K562	blood:	n/a	n/a
17	CBX3	chr12:30907642-30908483	K562	blood:	n/a	n/a
18	CCNT2	chr12:30907301-30908316	K562	blood:	n/a	n/a
19	CEBPB	chr12:30909038-30909261	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:30907990-30908248	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr12:30907595-30908867	Hela-S3	cervix:	n/a	chr12:30908831-30908844
22	CEBPB	chr12:30907975-30908530	K562	blood:	n/a	n/a
23	CEBPD	chr12:30907529-30908099	HepG2	liver:	n/a	n/a
24	CHD1	chr12:30906854-30907356	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr12:30908088-30908355	H1-hESC	embryonic stem cell:	n/a	chr12:30908309-30908316
26	CHD2	chr12:30908997-30909107	HepG2	liver:	n/a	n/a
27	CHD2	chr12:30907659-30908224	HepG2	liver:	n/a	chr12:30907872-30907882
28	CHD2	chr12:30906805-30907079	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr12:30907901-30908282	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr12:30907342-30908383	GM12878	blood:	n/a	chr12:30907554-30907564 chr12:30907872-30907882 chr12:30908309-30908316
31	CHD2	chr12:30907350-30908460	Hela-S3	cervix:	n/a	chr12:30907554-30907564 chr12:30907872-30907882 chr12:30908309-30908316
32	CHD2	chr12:30907401-30907441	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr12:30907745-30908411	K562	blood:	n/a	chr12:30907872-30907882 chr12:30908309-30908316
34	CREB1	chr12:30907133-30908325	A549	lung:	n/a	n/a
35	CREB1	chr12:30907389-30908454	HepG2	liver:	n/a	n/a
36	CREB1	chr12:30907498-30908382	K562	blood:	n/a	n/a
37	CREB1	chr12:30907873-30908174	A549	lung:	n/a	n/a
38	CREB1	chr12:30907696-30908487	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr12:30907200-30908370	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:30907940-30908090	HCT-116	colon:	n/a	n/a
41	CTCF	chr12:30907980-30908130	GM12864	blood:	n/a	n/a
42	CTCF	chr12:30907960-30908110	AG04450	lung:	n/a	n/a
43	CTCF	chr12:30907960-30908110	GM12868	blood:	n/a	n/a
44	CTCF	chr12:30907920-30908070	HAc	cerebellar:	n/a	n/a
45	CTCF	chr12:30907674-30907837	Fibrobl	skin:	n/a	n/a
46	CTCF	chr12:30907516-30908228	IMR90	lung:	n/a	n/a
47	CTCF	chr12:30905966-30908651	A549	lung:	n/a	chr12:30907136-30907144
48	CTCF	chr12:30908160-30908310	GM12873	blood:	n/a	n/a
49	CTCF	chr12:30907920-30908070	GM12865	blood:	n/a	n/a
50	CTCF	chr12:30907900-30908050	MCF-7	breast:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30907366-30907416	HNPCEpiC	eye:	n/a
2	chr12:30907366-30907416	HNPCEpiC	eye:	n/a
3	chr12:30908115-30908165	HRE	kidney:	n/a
4	chr12:30907545-30907595	T-47D	breast:	n/a
5	chr12:30907849-30907899	Hela-S3	cervix:	n/a
6	chr12:30907545-30907595	HUVEC	blood vessel:	n/a
7	chr12:30908115-30908165	AG09309	skin:	n/a
8	chr12:30908310-30908360	HL-60	blood:	n/a
9	chr12:30907596-30907646	GM12878	blood:	n/a
10	chr12:30907260-30907310	HAEpiC	amniotic membrane:	n/a
11	chr12:30907849-30907899	AG09309	skin:	n/a
12	chr12:30907260-30907310	MCF-7	breast:	n/a
13	chr12:30908244-30908294	LNCaP	prostate:	n/a
14	chr12:30908115-30908165	HRPEpiC	eye:	n/a
15	chr12:30908115-30908165	HEK293	kidney:	embryo
16	chr12:30907191-30907241	Hepatocyte	liver:	n/a
17	chr12:30907260-30907310	RPTEC	kidney:	n/a
18	chr12:30907545-30907595	MCF-7	breast:	n/a
19	chr12:30908244-30908294	HL-60	blood:	n/a
20	chr12:30907545-30907595	MCF10A-Er-Src	breast:	n/a
21	chr12:30907596-30907646	NB4	blood:	n/a
22	chr12:30907596-30907646	Caco-2	colon:	n/a
23	chr12:30907599-30907649	AG04449	skin:	fetal
24	chr12:30908244-30908294	HCT-116	colon:	n/a
25	chr12:30907260-30907310	NT2-D1	testis:	n/a
26	chr12:30907366-30907416	H1-hESC	embryonic stem cell:	embryo
27	chr12:30907545-30907595	Hepatocyte	liver:	n/a
28	chr12:30907849-30907899	AG04450	lung:	fetal
29	chr12:30907599-30907649	ECC-1	luminal epithelium:	n/a
30	chr12:30907191-30907241	RPTEC	kidney:	n/a
31	chr12:30907366-30907416	A549	lung:	n/a
32	chr12:30907366-30907416	ProgFib	skin:	n/a
33	chr12:30908244-30908294	HCM	heart:	n/a
34	chr12:30907596-30907646	AG04450	lung:	fetal
35	chr12:30908244-30908294	Hepatocyte	liver:	n/a
36	chr12:30908310-30908360	SKMC	muscle:	n/a
37	chr12:30907366-30907416	HRE	kidney:	n/a
38	chr12:30907260-30907310	ECC-1	luminal epithelium:	n/a
39	chr12:30908310-30908360	NB4	blood:	n/a
40	chr12:30907599-30907649	AG04450	lung:	fetal
41	chr12:30907191-30907241	HRE	kidney:	n/a
42	chr12:30908115-30908165	HNPCEpiC	eye:	n/a
43	chr12:30907191-30907241	NB4	blood:	n/a
44	chr12:30907366-30907416	SK-N-SH	brain:	n/a
45	chr12:30907599-30907649	GM19239	blood:	n/a
46	chr12:30908310-30908360	H1-hESC	embryonic stem cell:	embryo
47	chr12:30907260-30907310	BJ	skin:	n/a
48	chr12:30908244-30908294	HUVEC	blood vessel:	n/a
49	chr12:30907260-30907310	HEK293	kidney:	embryo
50	chr12:30907596-30907646	HCPEpiC	choroid plexus:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:30906304..30909589-chr12:30948532..30951386,3	K562	blood:
2	chr12:30907673..30908756-chr12:30947349..30948500,4	Hela-S3	cervix:
3	chr12:30845389..30848478-chr12:30907681..30910609,3	K562	blood:
4	chr12:30907774..30908278-chr5:32585524..32586521,2	Hela-S3	cervix:
5	chr1:161129253..161129757-chr12:30907615..30908521,2	Hela-S3	cervix:
6	chr12:30907876..30908507-chr17:37356246..37356998,2	Hela-S3	cervix:
7	chr12:30908038..30909570-chr12:30918182..30920609,2	K562	blood:
8	chr12:30902650..30905580-chr12:30906095..30908998,3	MCF-7	breast:
9	chr1:45187119..45187880-chr12:30907389..30908146,2	HCT-116	colon:
10	chr12:30901889..30903622-chr12:30908915..30911162,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN11-3	chr12:30908008-30908205	XLOC_009701
2	lnc-TSPAN11-3	chr12:30908008-30908205	ENSG00000246331

No data

Variant related genes	Relation type
ENSG00000246331	TF binding region
CAPRIN2	TF binding region
ENSG00000246331	CpG island
CAPRIN2	CpG island
ENSG00000113387	chromatin interactions
ENSG00000110888	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000133704	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000143258	chromatin interactions
ENSG00000235884	chromatin interactions
MSN	miRNA target sites

Extended variants
information (count: 86 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76953403	chr12:30906915-30906916	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs181538242	chr12:30906984-30906985	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs560430543	chr12:30906989-30906990	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs200108812	chr12:30907009-30907010	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs143398960	chr12:30907011-30907012	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs375954500	chr12:30907013-30907014	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs567348427	chr12:30907110-30907111	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs537493531	chr12:30907128-30907129	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs556104037	chr12:30907139-30907140	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs184891680	chr12:30907216-30907217	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs539707960	chr12:30907229-30907230	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs33254	chr12:30907238-30907239	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs557948303	chr12:30907271-30907272	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs573052017	chr12:30907274-30907275	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs540338897	chr12:30907307-30907308	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs150059543	chr12:30907316-30907317	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs116979159	chr12:30907317-30907318	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs189406055	chr12:30907362-30907363	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs544316502	chr12:30907374-30907375	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs146167357	chr12:30907387-30907388	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs534570224	chr12:30907409-30907410	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs545277635	chr12:30907420-30907421	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs74961653	chr12:30907427-30907428	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs527526570	chr12:30907533-30907534	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs35425801	chr12:30907548-30907549	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs11051058	chr12:30907573-30907574	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs549159900	chr12:30907590-30907591	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs1485346	chr12:30907594-30907595	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs531417666	chr12:30907621-30907622	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs549524758	chr12:30907727-30907728	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs1485345	chr12:30907740-30907741	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs539744655	chr12:30907749-30907750	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs551616976	chr12:30907783-30907784	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs566813527	chr12:30907812-30907813	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs534173813	chr12:30907860-30907861	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs555905195	chr12:30907874-30907875	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs574067986	chr12:30907879-30907880	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs538309563	chr12:30907890-30907891	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs376337459	chr12:30907930-30907931	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs373941368	chr12:30907968-30907969	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs556601369	chr12:30907972-30907973	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs376562254	chr12:30907987-30907988	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs578041747	chr12:30907988-30907989	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs545414602	chr12:30907995-30907996	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs560477870	chr12:30908000-30908001	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs572350723	chr12:30908003-30908004	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs542492997	chr12:30908005-30908006	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs561101475	chr12:30908007-30908008	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs550271029	chr12:30908062-30908063	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
50	rs181339343	chr12:30908066-30908067	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30903800-30908400	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr12:30905400-30907200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
3	chr12:30905600-30907000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
4	chr12:30905600-30907000	Flanking Active TSS	NH-A	brain
5	chr12:30905600-30907200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr12:30905600-30908600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:30905800-30907000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr12:30905800-30907000	Flanking Active TSS	A549	lung
9	chr12:30905800-30907200	Flanking Active TSS	Osteobl	bone
10	chr12:30905800-30908800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:30906000-30907400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:30906000-30908600	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr12:30906200-30907000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:30906200-30907000	Enhancers	Primary B cells from peripheral blood	blood
15	chr12:30906200-30907000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:30906200-30907000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:30906200-30907000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr12:30906200-30907000	Flanking Active TSS	Brain Angular Gyrus	brain
19	chr12:30906200-30907200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:30906200-30907200	Flanking Active TSS	HMEC	breast
21	chr12:30906200-30907200	Flanking Active TSS	K562	blood
22	chr12:30906200-30907400	Flanking Active TSS	Dnd41	blood
23	chr12:30906200-30908600	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr12:30906200-30908600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr12:30906200-30908800	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr12:30906400-30907000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:30906400-30907000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:30906400-30907000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:30906400-30907000	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr12:30906400-30907000	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr12:30906400-30907000	Flanking Active TSS	Brain Substantia Nigra	brain
32	chr12:30906400-30907000	Flanking Active TSS	Fetal Brain Male	brain
33	chr12:30906400-30907000	Flanking Active TSS	Fetal Kidney	kidney
34	chr12:30906400-30907000	Enhancers	Left Ventricle	heart
35	chr12:30906400-30907000	Enhancers	Lung	lung
36	chr12:30906400-30907000	Enhancers	Ovary	ovary
37	chr12:30906400-30907000	Enhancers	Pancreas	Pancrea
38	chr12:30906400-30907000	Enhancers	Stomach Mucosa	stomach
39	chr12:30906400-30907000	Flanking Active TSS	GM12878-XiMat	blood
40	chr12:30906400-30907000	Flanking Active TSS	NHLF	lung
41	chr12:30906400-30907200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:30906400-30907200	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr12:30906400-30907200	Flanking Active TSS	Brain Germinal Matrix	brain
44	chr12:30906400-30907200	Flanking Active TSS	Fetal Lung	lung
45	chr12:30906400-30907200	Flanking Active TSS	Fetal Muscle Leg	muscle
46	chr12:30906400-30907200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr12:30906400-30907200	Flanking Active TSS	Thymus	Thymus
48	chr12:30906400-30907200	Enhancers	Spleen	Spleen
49	chr12:30906400-30907200	Flanking Active TSS	Hela-S3	cervix
50	chr12:30906400-30907200	Flanking Active TSS	HUVEC	blood vessel

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