Variant report

Variant	esv1793746
Chromosome Location	chr12:1702470-1704325
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	chr12:1703921-1704219	HepG2	liver:	n/a	n/a
2	ATF3	chr12:1703979-1704186	K562	blood:	n/a	n/a
3	ATF3	chr12:1703905-1704290	A549	lung:	n/a	n/a
4	ATF3	chr12:1703691-1704192	A549	lung:	n/a	n/a
5	BACH1	chr12:1704012-1704359	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr12:1702399-1703218	A549	lung:	n/a	n/a
7	BCL3	chr12:1702811-1703565	GM12878	blood:	n/a	chr12:1703277-1703290 chr12:1703246-1703255 chr12:1703251-1703264
8	BCLAF1	chr12:1702596-1703225	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:1703961-1704290	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:1703326-1703559	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:1703541-1704274	HepG2	liver:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
12	BHLHE40	chr12:1703673-1704161	A549	lung:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
13	BHLHE40	chr12:1703132-1704326	GM12878	blood:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703282-1703298 chr12:1703887-1703903
14	BHLHE40	chr12:1701573-1702554	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:1703615-1704317	K562	blood:	n/a	chr12:1703756-1703772 chr12:1703860-1703876 chr12:1703887-1703903
16	BHLHE40	chr12:1702937-1703126	K562	blood:	n/a	n/a
17	BRCA1	chr12:1703950-1704220	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr12:1704097-1704217	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr12:1704098-1704155	HepG2	liver:	n/a	n/a
20	CBX3	chr12:1704032-1704330	K562	blood:	n/a	n/a
21	CCNT2	chr12:1701679-1704259	K562	blood:	n/a	chr12:1701691-1701700 chr12:1704222-1704231
22	CEBPB	chr12:1702761-1702791	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:1702722-1702807	HepG2	liver:	n/a	n/a
24	CEBPB	chr12:1703958-1704201	Hela-S3	cervix:	n/a	n/a
25	CEBPD	chr12:1703267-1703620	HepG2	liver:	n/a	n/a
26	CHD1	chr12:1702663-1704334	GM12878	blood:	n/a	chr12:1703237-1703247 chr12:1703259-1703269 chr12:1703926-1703936
27	CHD1	chr12:1702989-1703140	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr12:1703705-1704169	H1-hESC	embryonic stem cell:	n/a	chr12:1703926-1703936
29	CHD1	chr12:1701397-1706266	IMR90	lung:	n/a	chr12:1703237-1703247 chr12:1704434-1704444 chr12:1703259-1703269 chr12:1703926-1703936
30	CHD2	chr12:1702293-1702483	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr12:1702835-1704367	Hela-S3	cervix:	n/a	chr12:1703237-1703247 chr12:1703259-1703269 chr12:1703926-1703936
32	CHD2	chr12:1703861-1704103	HepG2	liver:	n/a	chr12:1703926-1703936
33	CHD2	chr12:1702989-1703142	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:1703767-1704188	K562	blood:	n/a	chr12:1703926-1703936
35	CHD2	chr12:1702913-1703012	K562	blood:	n/a	n/a
36	CHD2	chr12:1702923-1702926	HepG2	liver:	n/a	n/a
37	CHD2	chr12:1701565-1703513	GM12878	blood:	n/a	chr12:1703237-1703247 chr12:1703259-1703269
38	CREB1	chr12:1702782-1703562	A549	lung:	n/a	n/a
39	CREB1	chr12:1703583-1704242	A549	lung:	n/a	n/a
40	CTBP2	chr12:1703753-1704215	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr12:1701629-1703245	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr12:1702400-1702550	GM12875	blood:	n/a	n/a
43	CTCF	chr12:1702648-1702741	LNCaP	prostate:	n/a	n/a
44	CTCF	chr12:1704020-1704170	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr12:1702682-1702701	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:1704040-1704190	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr12:1704040-1704190	HRE	kidney:	n/a	n/a
48	CTCF	chr12:1704060-1704210	GM12864	blood:	n/a	n/a
49	CTCF	chr12:1704114-1704187	GM12878	blood:	n/a	n/a
50	CTCF	chr12:1703200-1703297	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1703704-1703754	GM12892	blood:	n/a
2	chr12:1703704-1703754	HCPEpiC	choroid plexus:	n/a
3	chr12:1704263-1704313	U87	brain:	n/a
4	chr12:1704263-1704313	SK-N-MC	brain:	n/a
5	chr12:1703704-1703754	GM12892	blood:	n/a
6	chr12:1703704-1703754	HCPEpiC	choroid plexus:	n/a
7	chr12:1704263-1704313	U87	brain:	n/a
8	chr12:1704263-1704313	SK-N-MC	brain:	n/a
9	chr12:1704263-1704313	HMEC	breast:	n/a
10	chr12:1703181-1703231	NHBE	bronchial:	n/a
11	chr12:1704263-1704313	HRCEpiC	kidney:	n/a
12	chr12:1703169-1703219	BJ	skin:	n/a
13	chr12:1704080-1704130	HCM	heart:	n/a
14	chr12:1702874-1702924	SAEC	small airway:	n/a
15	chr12:1703169-1703219	PANC-1	pancreas:	n/a
16	chr12:1704080-1704130	Hepatocyte	liver:	n/a
17	chr12:1704156-1704206	GM12892	blood:	n/a
18	chr12:1704080-1704130	NHDF-neo	bronchial:	n/a
19	chr12:1704263-1704313	HCPEpiC	choroid plexus:	n/a
20	chr12:1704156-1704206	PANC-1	pancreas:	n/a
21	chr12:1704065-1704115	K562	blood:	n/a
22	chr12:1704156-1704206	MCF10A-Er-Src	breast:	n/a
23	chr12:1703169-1703219	H1-hESC	embryonic stem cell:	embryo
24	chr12:1704263-1704313	HRPEpiC	eye:	n/a
25	chr12:1704156-1704206	HRPEpiC	eye:	n/a
26	chr12:1704065-1704115	BE2_C	brain:	n/a
27	chr12:1704065-1704115	GM12878	blood:	n/a
28	chr12:1704156-1704206	ovcar-3	ovarian:	n/a
29	chr12:1704080-1704130	ECC-1	luminal epithelium:	n/a
30	chr12:1704263-1704313	NH-A	brain:	n/a
31	chr12:1703169-1703219	HIPEpiC	eye:	n/a
32	chr12:1704156-1704206	GM12891	blood:	n/a
33	chr12:1702874-1702924	GM06990	blood:	n/a
34	chr12:1704156-1704206	AoSMC	blood vessel:	n/a
35	chr12:1704156-1704206	HEK293	kidney:	embryo
36	chr12:1703704-1703754	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:1704263-1704313	SAEC	small airway:	n/a
38	chr12:1703181-1703231	ECC-1	luminal epithelium:	n/a
39	chr12:1703704-1703754	H1-hESC	embryonic stem cell:	embryo
40	chr12:1702874-1702924	Hela-S3	cervix:	n/a
41	chr12:1704065-1704115	HCPEpiC	choroid plexus:	n/a
42	chr12:1703169-1703219	IMR90	lung:	fetal
43	chr12:1702874-1702924	HRE	kidney:	n/a
44	chr12:1704065-1704115	GM12892	blood:	n/a
45	chr12:1703169-1703219	HCF	heart:	n/a
46	chr12:1703169-1703219	GM12892	blood:	n/a
47	chr12:1703181-1703231	HepG2	liver:	n/a
48	chr12:1704263-1704313	MCF-7	breast:	n/a
49	chr12:1703169-1703219	HRCEpiC	kidney:	n/a
50	chr12:1702874-1702924	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1703157..1705505-chr12:1739226..1741204,2	MCF-7	breast:
2	chr12:1224466..1226137-chr12:1702484..1704918,2	MCF-7	breast:
3	chr12:1703685..1705372-chr12:1898619..1900530,2	K562	blood:
4	chr12:1700363..1702369-chr12:1703399..1707703,4	K562	blood:
5	chr12:1057714..1059446-chr12:1702277..1704204,2	MCF-7	breast:
6	chr11:64645557..64646112-chr12:1703529..1704108,2	Hela-S3	cervix:
7	chr12:547432..549780-chr12:1702241..1704941,2	MCF-7	breast:
8	chr12:1703426..1704364-chr18:71959175..71959778,2	NB4	blood:
9	chr12:1703565..1707939-chr12:1709383..1712701,6	MCF-7	breast:
10	chr12:1703509..1704108-chr6:26216519..26217376,2	Hela-S3	cervix:

Variant related genes	Relation type
FBXL14	TF binding region
FBXL14	CpG island
ENSG00000110047	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000166347	chromatin interactions
ENSG00000171823	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000002016	chromatin interactions
ENSG00000111186	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000082805	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34042069	chr12:1702470-1702471	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs139247471	chr12:1702474-1702475	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs192581158	chr12:1702488-1702489	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs143067327	chr12:1702498-1702499	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs200460280	chr12:1702522-1702523	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs17852502	chr12:1702545-1702546	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs35510932	chr12:1702549-1702550	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540327437	chr12:1702555-1702556	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs35524129	chr12:1702561-1702562	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs565300536	chr12:1702570-1702571	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs35571553	chr12:1702575-1702576	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs532761796	chr12:1702592-1702593	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs188789144	chr12:1702621-1702622	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs559895406	chr12:1702629-1702630	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs141855790	chr12:1702645-1702646	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs201421380	chr12:1702716-1702717	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs148182443	chr12:1702724-1702725	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs370898543	chr12:1702752-1702753	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs374158833	chr12:1702771-1702772	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs532374578	chr12:1702786-1702787	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs150585689	chr12:1702852-1702853	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs530748229	chr12:1702855-1702856	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs377115030	chr12:1702871-1702872	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs139660751	chr12:1702873-1702874	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs189581771	chr12:1702876-1702877	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs370486272	chr12:1702888-1702889	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs374965564	chr12:1702903-1702904	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs369693385	chr12:1702906-1702907	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs35466364	chr12:1702912-1702913	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs546251283	chr12:1702926-1702927	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs117331652	chr12:1702929-1702930	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs139319635	chr12:1702936-1702937	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs144026355	chr12:1702948-1702949	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs367626654	chr12:1702951-1702952	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs199753406	chr12:1702957-1702958	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs144961632	chr12:1702971-1702972	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs149028748	chr12:1702981-1702982	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs556714680	chr12:1703017-1703018	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs142082890	chr12:1703019-1703020	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs151115535	chr12:1703040-1703041	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs575209928	chr12:1703064-1703065	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs376933643	chr12:1703077-1703078	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs368750848	chr12:1703095-1703096	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs373403328	chr12:1703097-1703098	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs376652993	chr12:1703167-1703168	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs577325408	chr12:1703185-1703186	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs201556394	chr12:1703226-1703227	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs111814721	chr12:1703246-1703247	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs541686360	chr12:1703264-1703265	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs548123930	chr12:1703281-1703282	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1699200-1703200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:1699400-1703000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
3	chr12:1699400-1703000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
4	chr12:1699400-1703000	Flanking Active TSS	Osteobl	bone
5	chr12:1699600-1703200	Flanking Active TSS	HMEC	breast
6	chr12:1699800-1703000	Transcr. at gene 5' and 3'	Dnd41	blood
7	chr12:1699800-1703200	Flanking Active TSS	HUVEC	blood vessel
8	chr12:1700000-1703200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:1700400-1703200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:1700400-1703200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr12:1700600-1702600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
12	chr12:1700600-1702600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
13	chr12:1700600-1703000	Flanking Active TSS	K562	blood
14	chr12:1700600-1703200	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr12:1700600-1704400	Active TSS	Brain Germinal Matrix	brain
16	chr12:1700800-1702800	Flanking Active TSS	Fetal Intestine Large	intestine
17	chr12:1700800-1703000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr12:1700800-1703000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
19	chr12:1700800-1703000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr12:1700800-1703000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
21	chr12:1700800-1704600	Active TSS	Ovary	ovary
22	chr12:1701000-1703000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:1701000-1704800	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr12:1701200-1702600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:1701200-1703200	Active TSS	Stomach Mucosa	stomach
26	chr12:1701200-1704200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr12:1701400-1702600	Flanking Active TSS	HepG2	liver
28	chr12:1701400-1703000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr12:1701400-1703000	Flanking Active TSS	NHEK	skin
30	chr12:1701400-1703200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
31	chr12:1701400-1703200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr12:1701600-1702600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:1701600-1702600	Flanking Active TSS	Left Ventricle	heart
34	chr12:1701600-1702600	Flanking Active TSS	Lung	lung
35	chr12:1701600-1702600	Flanking Active TSS	Rectal Smooth Muscle	rectum
36	chr12:1701600-1702600	Flanking Active TSS	A549	lung
37	chr12:1701600-1702800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:1701600-1702800	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:1701600-1702800	Flanking Active TSS	Esophagus	oesophagus
40	chr12:1701600-1702800	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
41	chr12:1701600-1702800	Flanking Active TSS	Hela-S3	cervix
42	chr12:1701600-1703000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
43	chr12:1701600-1703000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:1701600-1703000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:1701600-1703000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:1701600-1703000	Flanking Active TSS	Primary B cells from peripheral blood	blood
47	chr12:1701600-1703000	Flanking Active TSS	Primary hematopoietic stem cells	blood
48	chr12:1701600-1703000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
49	chr12:1701600-1703000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:1701600-1703000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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