Variant report

Variant	nsv976744
Chromosome Location	chr12:50604432-50610917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr12:50607163-50607590	GM12878	blood:	n/a	n/a
2	BCL3	chr12:50607250-50607607	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:50608764-50609466	Hela-S3	cervix:	n/a	n/a
4	CHD2	chr12:50604751-50604839	GM12878	blood:	n/a	n/a
5	CREB1	chr12:50604584-50604830	GM12878	blood:	n/a	n/a
6	CTCF	chr12:50605600-50605750	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr12:50605540-50605690	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr12:50605644-50605675	Medullo	brain:	n/a	n/a
9	CTCF	chr12:50605647-50605704	Lung_OC	lung:	n/a	n/a
10	CTCF	chr12:50605600-50605750	AG10803	skin:	n/a	n/a
11	CTCF	chr12:50605540-50605690	RPTEC	kidney:	n/a	n/a
12	CTCF	chr12:50605671-50605672	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr12:50608340-50608357	GM10266	blood:	n/a	n/a
14	CTCF	chr12:50605607-50605686	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr12:50605627-50605681	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr12:50605588-50605747	GM12878	blood:	n/a	n/a
17	CTCF	chr12:50605580-50605730	AG10803	skin:	n/a	n/a
18	CTCF	chr12:50605484-50605847	GM12878	blood:	n/a	n/a
19	CTCF	chr12:50605580-50605730	AG04449	skin:	n/a	n/a
20	CTCF	chr12:50605520-50605670	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr12:50605534-50605823	K562	blood:	n/a	n/a
22	CTCF	chr12:50605586-50605732	K562	blood:	n/a	n/a
23	CTCF	chr12:50605619-50605670	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr12:50605584-50605718	HUVEC	blood vessel:	n/a	n/a
25	CUX1	chr12:50604766-50604780	GM12878	blood:	n/a	n/a
26	EBF1	chr12:50609001-50609025	GM12878	blood:	n/a	n/a
27	EBF1	chr12:50604678-50604715	GM12878	blood:	n/a	n/a
28	EP300	chr12:50608756-50609255	Hela-S3	cervix:	n/a	chr12:50609100-50609114 chr12:50608963-50608977
29	EP300	chr12:50608888-50609204	SK-N-SH_RA	brain:	n/a	chr12:50609100-50609114 chr12:50608963-50608977
30	EP300	chr12:50608768-50609168	T-47D	breast:	n/a	chr12:50609100-50609114 chr12:50608963-50608977
31	EP300	chr12:50605447-50605478	GM12878	blood:	n/a	n/a
32	FOS	chr12:50607791-50608004	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr12:50608725-50609314	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr12:50607839-50607841	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr12:50605487-50605789	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:50608993-50609273	HUVEC	blood vessel:	n/a	n/a
37	FOS	chr12:50607239-50607594	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr12:50608877-50609245	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr12:50608873-50609170	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr12:50608738-50609303	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr12:50607321-50607548	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr12:50607246-50607520	MCF10A-Er-Src	breast:	n/a	n/a
43	FOXA1	chr12:50608822-50609203	T-47D	breast:	n/a	n/a
44	FOXA1	chr12:50608867-50609237	T-47D	breast:	n/a	n/a
45	GATA2	chr12:50608847-50609239	HUVEC	blood vessel:	n/a	n/a
46	GATA3	chr12:50608584-50609386	SK-N-SH	brain:	n/a	chr12:50608745-50608752 chr12:50608745-50608752 chr12:50608745-50608752 chr12:50608840-50608853
47	GATA3	chr12:50608858-50609212	MCF-7	breast:	n/a	n/a
48	GATA3	chr12:50608649-50609358	MCF-7	breast:	n/a	chr12:50608745-50608752 chr12:50608745-50608752 chr12:50608745-50608752 chr12:50608840-50608853
49	GATA3	chr12:50608783-50609264	T-47D	breast:	n/a	chr12:50608840-50608853
50	GATA3	chr12:50608661-50609366	MCF-7	breast:	n/a	chr12:50608745-50608752 chr12:50608745-50608752 chr12:50608745-50608752 chr12:50608840-50608853

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50606100-50606150	HNPCEpiC	eye:	n/a
2	chr12:50606100-50606150	AG09319	gingival:	n/a
3	chr12:50606100-50606150	PANC-1	pancreas:	n/a
4	chr12:50606100-50606150	PFSK-1	brain:	n/a
5	chr12:50606100-50606150	A549	lung:	n/a
6	chr12:50606100-50606150	RPTEC	kidney:	n/a
7	chr12:50606100-50606150	T-47D	breast:	n/a
8	chr12:50606100-50606150	HIPEpiC	eye:	n/a
9	chr12:50606100-50606150	HL-60	blood:	n/a
10	chr12:50606100-50606150	HCF	heart:	n/a
11	chr12:50606100-50606150	HRPEpiC	eye:	n/a
12	chr12:50606100-50606150	HCPEpiC	choroid plexus:	n/a
13	chr12:50606100-50606150	GM12878	blood:	n/a
14	chr12:50606100-50606150	HCM	heart:	n/a
15	chr12:50606100-50606150	U87	brain:	n/a
16	chr12:50606100-50606150	Hela-S3	cervix:	n/a
17	chr12:50606100-50606150	SK-N-MC	brain:	n/a
18	chr12:50606100-50606150	ovcar-3	ovarian:	n/a
19	chr12:50606100-50606150	BJ	skin:	n/a
20	chr12:50606100-50606150	NB4	blood:	n/a
21	chr12:50606100-50606150	PrEC	prostate:	n/a
22	chr12:50606100-50606150	IMR90	lung:	fetal
23	chr12:50606100-50606150	SAEC	small airway:	n/a
24	chr12:50606100-50606150	Caco-2	colon:	n/a
25	chr12:50606100-50606150	CMK	blood:	n/a
26	chr12:50606100-50606150	ECC-1	luminal epithelium:	n/a
27	chr12:50606100-50606150	LNCaP	prostate:	n/a
28	chr12:50606100-50606150	BE2_C	brain:	n/a
29	chr12:50606100-50606150	K562	blood:	n/a
30	chr12:50606100-50606150	GM06990	blood:	n/a
31	chr12:50606100-50606150	SK-N-SH_RA	brain:	n/a
32	chr12:50606100-50606150	AG09309	skin:	n/a
33	chr12:50606100-50606150	Jurkat	blood:	n/a
34	chr12:50606100-50606150	SK-N-SH	brain:	n/a
35	chr12:50606100-50606150	NT2-D1	testis:	n/a
36	chr12:50606100-50606150	HMEC	breast:	n/a
37	chr12:50606100-50606150	MCF-7	breast:	n/a
38	chr12:50606100-50606150	HEEpiC	esophagus:	n/a
39	chr12:50606100-50606150	GM12891	blood:	n/a
40	chr12:50606100-50606150	HRCEpiC	kidney:	n/a
41	chr12:50606100-50606150	HCT-116	colon:	n/a
42	chr12:50606100-50606150	GM19239	blood:	n/a
43	chr12:50606100-50606150	SKMC	muscle:	n/a
44	chr12:50606100-50606150	NHDF-neo	bronchial:	n/a
45	chr12:50606100-50606150	AG04450	lung:	fetal
46	chr12:50606100-50606150	AG04449	skin:	fetal
47	chr12:50606100-50606150	HUVEC	blood vessel:	n/a
48	chr12:50606100-50606150	AoSMC	blood vessel:	n/a
49	chr12:50606100-50606150	H1-hESC	embryonic stem cell:	embryo
50	chr12:50606100-50606150	HEK293	kidney:	embryo

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:50590614..50593286-chr12:50607491..50609533,2	K562	blood:
2	chr12:50605956..50609957-chr12:50615053..50617813,4	K562	blood:
3	chr12:50595002..50597983-chr12:50604181..50606536,2	MCF-7	breast:
4	chr12:50598358..50601280-chr12:50607490..50609263,3	K562	blood:
5	chr12:50605986..50607646-chr12:50610972..50613007,2	K562	blood:
6	chr12:50603033..50605751-chr12:50607010..50610517,4	K562	blood:
7	chr12:50583595..50586516-chr12:50609733..50613018,3	K562	blood:
8	chr12:50594262..50596200-chr12:50606267..50608502,2	MCF-7	breast:
9	chr12:50608910..50611527-chr12:50617767..50619869,3	MCF-7	breast:
10	chr12:50606569..50608564-chr12:50646645..50648868,2	K562	blood:
11	chr12:50601699..50604230-chr12:50607719..50610299,2	K562	blood:
12	chr12:50597958..50602856-chr12:50604694..50610518,6	K562	blood:
13	chr12:50603033..50605751-chr12:50607010..50610517,4	K562	blood:
14	chr12:50606014..50607851-chr12:50614151..50616956,2	MCF-7	breast:
15	chr12:50605956..50609777-chr12:50614337..50617813,5	K562	blood:
16	chr12:50578015..50580805-chr12:50608079..50609626,2	K562	blood:
17	chr12:50596300..50599334-chr12:50605728..50608989,3	MCF-7	breast:
18	chr12:50583119..50586019-chr12:50610359..50613018,3	K562	blood:
19	chr12:50607002..50609932-chr12:50675818..50679067,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000257256	TF binding region
ENSG00000257256	CpG island
ENSG00000203433	chromatin interactions
ENSG00000257531	chromatin interactions
ENSG00000050405	chromatin interactions
ENSG00000257298	chromatin interactions

Extended variants
information (count: 203 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:203 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566991110	chr12:50604468-50604469	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549591173	chr12:50604478-50604479	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567827353	chr12:50604548-50604549	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17124540	chr12:50604560-50604561	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182716845	chr12:50604564-50604565	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569487250	chr12:50604623-50604624	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368896808	chr12:50604638-50604639	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538563206	chr12:50604653-50604654	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538153776	chr12:50604673-50604674	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555285255	chr12:50604677-50604678	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568301423	chr12:50604688-50604689	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534151561	chr12:50604721-50604722	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559226081	chr12:50604729-50604730	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553423742	chr12:50604745-50604746	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556853097	chr12:50604819-50604820	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187781246	chr12:50604822-50604823	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369676395	chr12:50604829-50604830	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545746777	chr12:50604847-50604848	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs555892151	chr12:50604905-50604906	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs576037430	chr12:50604956-50604957	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373674249	chr12:50604996-50604997	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367850958	chr12:50604998-50604999	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371022880	chr12:50604999-50605000	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375620293	chr12:50605000-50605001	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541740349	chr12:50605049-50605050	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539079090	chr12:50605063-50605064	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561988803	chr12:50605101-50605102	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527452417	chr12:50605102-50605103	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs34045758	chr12:50605114-50605115	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs9706482	chr12:50605115-50605116	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs117585184	chr12:50605133-50605134	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541241341	chr12:50605152-50605153	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192444952	chr12:50605165-50605166	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs1862042	chr12:50605228-50605229	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs35404088	chr12:50605266-50605267	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs397849822	chr12:50605283-50605284	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs79316295	chr12:50605322-50605323	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77404062	chr12:50605345-50605346	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554769368	chr12:50605361-50605362	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531767061	chr12:50605389-50605390	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548451633	chr12:50605410-50605411	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs149978812	chr12:50605440-50605441	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554382172	chr12:50605518-50605519	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145208699	chr12:50605541-50605542	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6144709	chr12:50605576-50605577	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs3073656	chr12:50605596-50605597	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575786546	chr12:50605651-50605652	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12316153	chr12:50605706-50605707	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570167557	chr12:50605707-50605708	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539159082	chr12:50605716-50605717	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Breast cancer	21858162	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50571800-50614200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:50572200-50614000	Weak transcription	Right Ventricle	heart
3	chr12:50582800-50614000	Weak transcription	Brain Angular Gyrus	brain
4	chr12:50582800-50614200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:50583000-50614400	Weak transcription	Brain Anterior Caudate	brain
6	chr12:50591600-50615600	Weak transcription	HepG2	liver
7	chr12:50593400-50614200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr12:50593400-50614200	Weak transcription	Fetal Brain Male	brain
9	chr12:50593400-50614600	Weak transcription	Esophagus	oesophagus
10	chr12:50596200-50613400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:50596600-50604600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:50596600-50605400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr12:50596600-50607200	Strong transcription	Fetal Intestine Small	intestine
14	chr12:50596800-50607600	Weak transcription	Stomach Mucosa	stomach
15	chr12:50596800-50614000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr12:50597000-50604600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:50597800-50605000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr12:50597800-50608800	Strong transcription	Fetal Intestine Large	intestine
19	chr12:50598400-50605800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr12:50598400-50611400	Weak transcription	Spleen	Spleen
21	chr12:50598400-50613400	Weak transcription	K562	blood
22	chr12:50598600-50605200	Weak transcription	Thymus	Thymus
23	chr12:50598600-50605600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr12:50598600-50612400	Weak transcription	Psoas Muscle	Psoas
25	chr12:50598600-50613400	Weak transcription	Aorta	Aorta
26	chr12:50598600-50613400	Weak transcription	Fetal Kidney	kidney
27	chr12:50598600-50614000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:50598600-50614000	Weak transcription	Brain Germinal Matrix	brain
29	chr12:50599000-50605400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr12:50599000-50612000	Weak transcription	Gastric	stomach
31	chr12:50599000-50614200	Weak transcription	Fetal Brain Female	brain
32	chr12:50599200-50614200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr12:50599400-50606000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr12:50599400-50614000	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:50599400-50615000	Weak transcription	Liver	Liver
36	chr12:50599600-50610200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:50599600-50613400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr12:50599600-50613400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:50599600-50614000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:50599600-50614000	Weak transcription	Brain Hippocampus Middle	brain
41	chr12:50599600-50614000	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr12:50599800-50604600	Weak transcription	Hela-S3	cervix
43	chr12:50599800-50604800	Weak transcription	Dnd41	blood
44	chr12:50599800-50604800	Weak transcription	HUVEC	blood vessel
45	chr12:50599800-50605200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr12:50599800-50605200	Weak transcription	Placenta	Placenta
47	chr12:50599800-50608400	Weak transcription	Small Intestine	intestine
48	chr12:50599800-50608800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr12:50599800-50612400	Weak transcription	Colon Smooth Muscle	Colon
50	chr12:50599800-50613400	Weak transcription	Rectal Smooth Muscle	rectum

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