Variant report

Variant	esv3437172
Chromosome Location	chr12:50478110-50480658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:643)
CpG islands
(count:611)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:50478595-50479030	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:50478676-50479022	K562	blood:	n/a	n/a
3	ATF2	chr12:50478458-50479021	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:50478487-50479212	GM12878	blood:	n/a	n/a
5	BCL3	chr12:50478419-50479168	A549	lung:	n/a	n/a
6	BCL3	chr12:50478436-50479123	A549	lung:	n/a	n/a
7	BCLAF1	chr12:50478603-50479074	K562	blood:	n/a	n/a
8	BCLAF1	chr12:50478617-50479151	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:50478596-50479079	K562	blood:	n/a	n/a
10	BCLAF1	chr12:50478566-50479193	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:50478721-50479118	K562	blood:	n/a	n/a
12	BHLHE40	chr12:50478664-50479170	GM12878	blood:	n/a	n/a
13	BRCA1	chr12:50478596-50479066	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr12:50478568-50479067	K562	blood:	n/a	n/a
15	CCNT2	chr12:50478812-50479252	K562	blood:	n/a	n/a
16	CEBPB	chr12:50478785-50478990	K562	blood:	n/a	n/a
17	CEBPB	chr12:50478415-50479100	GM12878	blood:	n/a	n/a
18	CEBPB	chr12:50478749-50479079	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:50478702-50479009	K562	blood:	n/a	n/a
20	CEBPD	chr12:50478832-50479205	HepG2	liver:	n/a	n/a
21	CHD1	chr12:50478592-50479004	GM12878	blood:	n/a	n/a
22	CHD1	chr12:50478135-50479792	IMR90	lung:	n/a	n/a
23	CHD2	chr12:50478704-50479571	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr12:50478568-50479715	GM12878	blood:	n/a	n/a
25	CHD2	chr12:50479166-50479177	K562	blood:	n/a	n/a
26	CHD2	chr12:50478770-50478974	HepG2	liver:	n/a	n/a
27	CHD2	chr12:50478616-50478960	K562	blood:	n/a	n/a
28	CREB1	chr12:50478756-50479371	A549	lung:	n/a	n/a
29	CREB1	chr12:50478713-50478983	A549	lung:	n/a	n/a
30	CREB1	chr12:50478593-50479176	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr12:50478638-50479030	H1-hESC	embryonic stem cell:	n/a	chr12:50478890-50478903
32	CTCF	chr12:50478820-50478970	GM12874	blood:	n/a	chr12:50478890-50478903
33	CTCF	chr12:50478589-50478615	GM12878	blood:	n/a	n/a
34	CTCF	chr12:50479500-50479650	AG09319	gingival:	n/a	n/a
35	CTCF	chr12:50480214-50480250	GM19240	blood:	n/a	chr12:50480223-50480244 chr12:50480221-50480239
36	CTCF	chr12:50478640-50478790	SAEC	small airway:	n/a	n/a
37	CTCF	chr12:50478840-50478990	HPAF	blood vessel:	n/a	chr12:50478890-50478903
38	CTCF	chr12:50478820-50478970	GM12870	blood:	n/a	chr12:50478890-50478903
39	CTCF	chr12:50478820-50478970	K562	blood:	n/a	chr12:50478890-50478903
40	CTCF	chr12:50478770-50479026	Medullo	brain:	n/a	chr12:50478890-50478903
41	CTCF	chr12:50478800-50478950	HCFaa	heart:	n/a	chr12:50478890-50478903
42	CTCF	chr12:50478773-50479019	H1-hESC	embryonic stem cell:	n/a	chr12:50478890-50478903
43	CTCF	chr12:50480174-50480244	GM12891	blood:	n/a	chr12:50480223-50480244 chr12:50480221-50480239
44	CTCF	chr12:50478797-50479016	Pancreas_OC	pancreas:	n/a	chr12:50478890-50478903
45	CTCF	chr12:50480185-50480273	GM12892	blood:	n/a	chr12:50480223-50480244 chr12:50480221-50480239
46	CTCF	chr12:50478589-50479225	MCF-7	breast:	n/a	chr12:50478890-50478903
47	CTCF	chr12:50478860-50479010	HFF-Myc	foreskin:	n/a	chr12:50478890-50478903
48	CTCF	chr12:50480154-50480258	MCF-7	breast:	n/a	chr12:50480223-50480244 chr12:50480221-50480239
49	CTCF	chr12:50478880-50479030	GM12865	blood:	n/a	chr12:50478890-50478903
50	CTCF	chr12:50478840-50478990	HAc	cerebellar:	n/a	chr12:50478890-50478903

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50479634-50479684	Caco-2	colon:	n/a
2	chr12:50479634-50479684	Caco-2	colon:	n/a
3	chr12:50478887-50478937	SK-N-SH	brain:	n/a
4	chr12:50478901-50478951	HCF	heart:	n/a
5	chr12:50478887-50478937	HRCEpiC	kidney:	n/a
6	chr12:50478976-50479026	SKMC	muscle:	n/a
7	chr12:50478901-50478951	AG04449	skin:	fetal
8	chr12:50478901-50478951	HRPEpiC	eye:	n/a
9	chr12:50478890-50478940	ECC-1	luminal epithelium:	n/a
10	chr12:50479634-50479684	SK-N-SH	brain:	n/a
11	chr12:50478890-50478940	Caco-2	colon:	n/a
12	chr12:50478856-50478906	Caco-2	colon:	n/a
13	chr12:50479003-50479053	NHDF-neo	bronchial:	n/a
14	chr12:50478887-50478937	GM12878	blood:	n/a
15	chr12:50478976-50479026	NT2-D1	testis:	n/a
16	chr12:50479634-50479684	Jurkat	blood:	n/a
17	chr12:50478890-50478940	HNPCEpiC	eye:	n/a
18	chr12:50478887-50478937	NHDF-neo	bronchial:	n/a
19	chr12:50478751-50478801	GM12878	blood:	n/a
20	chr12:50478751-50478801	GM06990	blood:	n/a
21	chr12:50478887-50478937	HepG2	liver:	n/a
22	chr12:50479003-50479053	HEEpiC	esophagus:	n/a
23	chr12:50478890-50478940	T-47D	breast:	n/a
24	chr12:50478751-50478801	MCF-7	breast:	n/a
25	chr12:50478890-50478940	Hepatocyte	liver:	n/a
26	chr12:50478480-50478530	AoSMC	blood vessel:	n/a
27	chr12:50478856-50478906	HCT-116	colon:	n/a
28	chr12:50478901-50478951	HEEpiC	esophagus:	n/a
29	chr12:50478480-50478530	HEEpiC	esophagus:	n/a
30	chr12:50478480-50478530	HCPEpiC	choroid plexus:	n/a
31	chr12:50479634-50479684	NHDF-neo	bronchial:	n/a
32	chr12:50478901-50478951	SK-N-MC	brain:	n/a
33	chr12:50478976-50479026	K562	blood:	n/a
34	chr12:50478856-50478906	SKMC	muscle:	n/a
35	chr12:50479003-50479053	GM12891	blood:	n/a
36	chr12:50478751-50478801	HIPEpiC	eye:	n/a
37	chr12:50478976-50479026	HEK293	kidney:	embryo
38	chr12:50478890-50478940	HCM	heart:	n/a
39	chr12:50478976-50479026	Caco-2	colon:	n/a
40	chr12:50479003-50479053	K562	blood:	n/a
41	chr12:50479634-50479684	HAEpiC	amniotic membrane:	n/a
42	chr12:50479634-50479684	BJ	skin:	n/a
43	chr12:50479003-50479053	NH-A	brain:	n/a
44	chr12:50478751-50478801	U87	brain:	n/a
45	chr12:50478901-50478951	K562	blood:	n/a
46	chr12:50478976-50479026	LNCaP	prostate:	n/a
47	chr12:50478890-50478940	SK-N-MC	brain:	n/a
48	chr12:50478887-50478937	HMEC	breast:	n/a
49	chr12:50478890-50478940	CMK	blood:	n/a
50	chr12:50479197-50479247	BJ	skin:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:50466696..50474949-chr12:50474970..50481457,17	MCF-7	breast:
2	chr12:50478149..50480392-chr17:58677532..58679268,2	MCF-7	breast:
3	chr12:50472028..50474859-chr12:50477717..50480636,3	MCF-7	breast:
4	chr12:50469904..50470842-chr12:50478448..50479302,2	K562	blood:
5	chr12:50477720..50479464-chr12:50594213..50596665,2	MCF-7	breast:
6	chr12:50477580..50479686-chr17:62501151..62502654,2	MCF-7	breast:
7	chr12:50464456..50466840-chr12:50477683..50480596,2	MCF-7	breast:
8	chr12:50279366..50281726-chr12:50476723..50478563,2	MCF-7	breast:
9	chr12:50478583..50479243-chr3:179280120..179280858,2	Hela-S3	cervix:
10	chr12:50477576..50479559-chr12:50526628..50528314,2	MCF-7	breast:
11	chr12:50476185..50478149-chr12:50743107..50745216,2	K562	blood:
12	chr12:50461826..50464798-chr12:50477927..50479451,2	K562	blood:
13	chr12:50477885..50480264-chr12:50559751..50562542,2	K562	blood:
14	chr12:50475132..50479699-chr12:50479828..50484275,5	K562	blood:
15	chr12:50477100..50479136-chr12:50582674..50585443,2	K562	blood:
16	chr12:50475910..50478397-chr12:50494395..50497008,2	K562	blood:
17	chr12:50235441..50237993-chr12:50478392..50480338,2	K562	blood:
18	chr12:50478449..50481902-chr12:50536030..50539935,3	MCF-7	breast:
19	chr12:50477499..50479020-chr12:50528748..50530881,2	MCF-7	breast:
20	chr12:50478705..50480450-chr12:50534679..50536447,2	MCF-7	breast:
21	chr12:50475972..50484033-chr12:50500850..50507517,14	K562	blood:
22	chr12:50477670..50481382-chr12:50495555..50500836,7	K562	blood:
23	chr12:50479656..50481335-chr12:50569381..50571958,2	MCF-7	breast:
24	chr12:50135082..50136603-chr12:50479268..50481708,2	MCF-7	breast:
25	chr12:50476634..50479276-chr12:50493202..50495258,2	K562	blood:
26	chr12:50478595..50483647-chr12:50502911..50507517,7	K562	blood:
27	chr12:50477688..50480373-chr12:50497434..50499573,3	K562	blood:
28	chr12:50477178..50480105-chr12:50648113..50650406,2	K562	blood:
29	chr12:50478513..50480166-chr12:50489047..50490966,2	K562	blood:
30	chr12:50475132..50479699-chr12:50479828..50484275,5	K562	blood:
31	chr12:50478759..50480659-chr12:50481009..50483998,3	K562	blood:
32	chr12:50477567..50484756-chr12:50559008..50565131,16	MCF-7	breast:
33	chr12:49524766..49526462-chr12:50478450..50480251,2	MCF-7	breast:
34	chr12:50477150..50481052-chr12:50559881..50562931,6	MCF-7	breast:

No data

Variant related genes	Relation type
SMARCD1	TF binding region
SMARCD1	CpG island
ENSG00000108654	chromatin interactions
ENSG00000167588	chromatin interactions
ENSG00000257298	chromatin interactions
ENSG00000185958	chromatin interactions
ENSG00000212496	chromatin interactions
ENSG00000110881	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000186666	chromatin interactions
ENSG00000136518	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000178449	chromatin interactions
ENSG00000066117	chromatin interactions
ENSG00000139624	chromatin interactions
ENSG00000050405	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000272368	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200359712	chr12:50478147-50478148	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs540665042	chr12:50478148-50478149	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs2640533	chr12:50478149-50478150	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs568050708	chr12:50478160-50478161	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs367621408	chr12:50478163-50478164	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs564246498	chr12:50478239-50478240	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs147189770	chr12:50478341-50478342	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs10875996	chr12:50478352-50478353	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs569890985	chr12:50478415-50478416	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs529068236	chr12:50478431-50478432	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs4898546	chr12:50478449-50478450	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs565814630	chr12:50478460-50478461	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs534246388	chr12:50478572-50478573	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs553873116	chr12:50478678-50478679	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
15	rs540055188	chr12:50478742-50478743	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
16	rs539565588	chr12:50478835-50478836	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
17	rs556203676	chr12:50478853-50478854	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs576262517	chr12:50478855-50478856	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs76547724	chr12:50478862-50478863	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs556069185	chr12:50478888-50478889	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
21	rs572637520	chr12:50478956-50478957	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
22	rs370455719	chr12:50478962-50478963	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
23	rs552076397	chr12:50478991-50478992	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
24	rs563930077	chr12:50479005-50479006	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
25	rs373317640	chr12:50479022-50479023	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
26	rs532931037	chr12:50479074-50479075	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
27	rs543560456	chr12:50479111-50479112	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs200178915	chr12:50479144-50479145	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs563360016	chr12:50479145-50479146	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs529129659	chr12:50479148-50479149	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs71464994	chr12:50479256-50479257	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs548902421	chr12:50479294-50479295	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs566006926	chr12:50479384-50479385	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs528387075	chr12:50479399-50479400	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs551623873	chr12:50479401-50479402	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs553744546	chr12:50479442-50479443	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs570526816	chr12:50479444-50479445	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs566928546	chr12:50479457-50479458	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs74090049	chr12:50479498-50479499	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556264672	chr12:50479523-50479524	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs386762920	chr12:50479575-50479576	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs189195538	chr12:50479577-50479578	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs555690370	chr12:50479609-50479610	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs572555543	chr12:50479645-50479646	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
45	rs535031779	chr12:50479720-50479721	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs558397503	chr12:50479729-50479730	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs577750634	chr12:50479732-50479733	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs543420481	chr12:50479749-50479750	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs147472384	chr12:50479760-50479761	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs573771727	chr12:50479785-50479786	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
T-cell prolymphocytic leukemia	19278963	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50458200-50478200	Weak transcription	Thymus	Thymus
2	chr12:50464400-50478200	Weak transcription	Fetal Heart	heart
3	chr12:50464400-50478200	Weak transcription	Right Atrium	heart
4	chr12:50464800-50478200	Weak transcription	Colon Smooth Muscle	Colon
5	chr12:50464800-50478200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr12:50464800-50478200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr12:50464800-50478400	Weak transcription	Primary T cells from cord blood	blood
8	chr12:50469400-50478200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:50469400-50478200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr12:50469400-50478200	Weak transcription	Fetal Brain Male	brain
11	chr12:50469600-50478200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:50469600-50478200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:50469600-50478200	Weak transcription	Brain Angular Gyrus	brain
14	chr12:50469600-50478200	Weak transcription	Brain Anterior Caudate	brain
15	chr12:50469600-50478200	Weak transcription	Fetal Lung	lung
16	chr12:50469600-50478200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr12:50469800-50478200	Weak transcription	Gastric	stomach
18	chr12:50470000-50478200	Weak transcription	Liver	Liver
19	chr12:50472600-50478200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr12:50473400-50478200	Enhancers	Fetal Intestine Large	intestine
21	chr12:50474000-50478200	Weak transcription	Brain Hippocampus Middle	brain
22	chr12:50474800-50478200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr12:50475000-50478200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr12:50475200-50478200	Weak transcription	Placenta	Placenta
25	chr12:50475200-50478200	Weak transcription	Right Ventricle	heart
26	chr12:50475200-50478200	Weak transcription	K562	blood
27	chr12:50475200-50478400	Weak transcription	Lung	lung
28	chr12:50475600-50478200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:50475600-50478200	Weak transcription	Fetal Muscle Leg	muscle
30	chr12:50475800-50478200	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr12:50476000-50478200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:50476200-50478200	Weak transcription	Brain Germinal Matrix	brain
33	chr12:50476400-50478200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:50476400-50478200	Enhancers	Adipose Nuclei	Adipose
35	chr12:50476600-50478200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:50477000-50478200	Weak transcription	Fetal Brain Female	brain
37	chr12:50477000-50478200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr12:50477000-50478200	Enhancers	NHDF-Ad	bronchial
39	chr12:50477000-50478200	Enhancers	Osteobl	bone
40	chr12:50477200-50478200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr12:50477200-50478200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:50477200-50478200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr12:50477200-50478200	Enhancers	Fetal Intestine Small	intestine
44	chr12:50477200-50478200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr12:50477400-50478200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:50477400-50478200	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr12:50477400-50478200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr12:50477400-50478200	Weak transcription	Colonic Mucosa	Colon
49	chr12:50477400-50478400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr12:50477600-50478200	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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