Variant report

Variant	nsv826352
Chromosome Location	chr12:42593124-42675255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1125)
CpG islands
(count:733)
Chromatin interactive
region (count:68)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:42631288-42631488	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:42631893-42631981	K562	blood:	n/a	n/a
3	ARID3A	chr12:42632233-42632433	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:42632492-42632514	K562	blood:	n/a	n/a
5	ATF2	chr12:42631169-42631590	GM12878	blood:	n/a	n/a
6	ATF3	chr12:42632047-42632313	K562	blood:	n/a	chr12:42632174-42632194
7	ATF3	chr12:42632078-42632289	HepG2	liver:	n/a	chr12:42632174-42632194
8	ATF3	chr12:42632070-42632285	H1-hESC	embryonic stem cell:	n/a	chr12:42632174-42632194
9	ATF3	chr12:42631953-42632381	GM12878	blood:	n/a	chr12:42632174-42632194
10	ATF3	chr12:42632079-42632260	GM12878	blood:	n/a	chr12:42632174-42632194
11	BACH1	chr12:42631143-42631510	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr12:42631108-42631617	GM12878	blood:	n/a	chr12:42631292-42631305 chr12:42631324-42631337
13	BCLAF1	chr12:42632060-42632811	GM12878	blood:	n/a	chr12:42632156-42632165 chr12:42632239-42632252 chr12:42632116-42632129
14	BHLHE40	chr12:42626796-42626809	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:42631211-42632605	GM12878	blood:	n/a	chr12:42632198-42632214 chr12:42632174-42632183 chr12:42631556-42631572 chr12:42632175-42632184 chr12:42632172-42632185 chr12:42632174-42632183 chr12:42631564-42631580
16	BHLHE40	chr12:42632197-42632250	A549	lung:	n/a	chr12:42632198-42632214
17	BHLHE40	chr12:42631841-42632958	K562	blood:	n/a	chr12:42632198-42632214 chr12:42632174-42632183 chr12:42632175-42632184 chr12:42632172-42632185 chr12:42632174-42632183
18	BHLHE40	chr12:42631942-42632907	HepG2	liver:	n/a	chr12:42632198-42632214 chr12:42632174-42632183 chr12:42632175-42632184 chr12:42632172-42632185 chr12:42632174-42632183
19	BHLHE40	chr12:42631080-42631577	K562	blood:	n/a	chr12:42631556-42631572
20	BRCA1	chr12:42632290-42632335	HepG2	liver:	n/a	n/a
21	BRCA1	chr12:42631800-42631860	GM12878	blood:	n/a	n/a
22	BRCA1	chr12:42630966-42631541	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr12:42631132-42631605	K562	blood:	n/a	n/a
24	CCNT2	chr12:42631197-42632552	K562	blood:	n/a	n/a
25	CEBPB	chr12:42633269-42633547	IMR90	lung:	n/a	chr12:42633440-42633451
26	CEBPB	chr12:42659414-42659592	HepG2	liver:	n/a	chr12:42659479-42659490
27	CEBPB	chr12:42632015-42632034	K562	blood:	n/a	n/a
28	CEBPB	chr12:42631057-42631631	GM12878	blood:	n/a	n/a
29	CEBPB	chr12:42649194-42650041	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:42614208-42614368	A549	lung:	n/a	n/a
31	CEBPB	chr12:42634204-42634469	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr12:42654972-42655194	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:42609543-42609554	A549	lung:	n/a	n/a
34	CEBPB	chr12:42636347-42636593	K562	blood:	n/a	chr12:42636480-42636491
35	CEBPB	chr12:42665060-42665163	HepG2	liver:	n/a	chr12:42665124-42665135
36	CEBPB	chr12:42633291-42633563	K562	blood:	n/a	chr12:42633440-42633451
37	CEBPB	chr12:42636339-42636557	HepG2	liver:	n/a	chr12:42636480-42636491
38	CEBPB	chr12:42636355-42636555	IMR90	lung:	n/a	chr12:42636480-42636491
39	CEBPB	chr12:42631913-42632751	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr12:42633306-42633582	HepG2	liver:	n/a	chr12:42633440-42633451
41	CEBPB	chr12:42670193-42670506	HepG2	liver:	n/a	chr12:42670358-42670369
42	CEBPB	chr12:42636427-42636531	A549	lung:	n/a	chr12:42636480-42636491
43	CEBPB	chr12:42659379-42659634	IMR90	lung:	n/a	chr12:42659479-42659490
44	CEBPB	chr12:42659373-42659586	K562	blood:	n/a	chr12:42659479-42659490
45	CEBPB	chr12:42631098-42631637	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:42628734-42629370	HepG2	liver:	n/a	chr12:42628906-42628917
47	CEBPB	chr12:42604301-42604464	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:42601829-42602017	HepG2	liver:	n/a	chr12:42601867-42601878
49	CEBPB	chr12:42632577-42632777	K562	blood:	n/a	n/a
50	CEBPD	chr12:42631288-42631567	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:42632618-42632668	HCM	heart:	n/a
2	chr12:42632618-42632668	HCM	heart:	n/a
3	chr12:42632001-42632051	NHBE	bronchial:	n/a
4	chr12:42634807-42634857	HUVEC	blood vessel:	n/a
5	chr12:42632325-42632375	Caco-2	colon:	n/a
6	chr12:42632001-42632051	PANC-1	pancreas:	n/a
7	chr12:42628089-42628139	HL-60	blood:	n/a
8	chr12:42631803-42631853	LNCaP	prostate:	n/a
9	chr12:42634807-42634857	HepG2	liver:	n/a
10	chr12:42632138-42632188	SAEC	small airway:	n/a
11	chr12:42632129-42632179	A549	lung:	n/a
12	chr12:42628089-42628139	SK-N-MC	brain:	n/a
13	chr12:42631803-42631853	HepG2	liver:	n/a
14	chr12:42631401-42631451	HRPEpiC	eye:	n/a
15	chr12:42631401-42631451	Hela-S3	cervix:	n/a
16	chr12:42632907-42632957	LNCaP	prostate:	n/a
17	chr12:42632618-42632668	HRPEpiC	eye:	n/a
18	chr12:42632138-42632188	T-47D	breast:	n/a
19	chr12:42632618-42632668	HPAEpiC	pulmonary alveolar:	n/a
20	chr12:42632618-42632668	HEEpiC	esophagus:	n/a
21	chr12:42632907-42632957	GM12892	blood:	n/a
22	chr12:42631401-42631451	Jurkat	blood:	n/a
23	chr12:42632618-42632668	BE2_C	brain:	n/a
24	chr12:42632001-42632051	HL-60	blood:	n/a
25	chr12:42631803-42631853	SK-N-SH_RA	brain:	n/a
26	chr12:42620681-42620731	SAEC	small airway:	n/a
27	chr12:42632907-42632957	SAEC	small airway:	n/a
28	chr12:42632129-42632179	HRCEpiC	kidney:	n/a
29	chr12:42632907-42632957	BE2_C	brain:	n/a
30	chr12:42632129-42632179	HCM	heart:	n/a
31	chr12:42620681-42620731	PFSK-1	brain:	n/a
32	chr12:42632312-42632362	HRCEpiC	kidney:	n/a
33	chr12:42632312-42632362	H1-hESC	embryonic stem cell:	embryo
34	chr12:42632312-42632362	HL-60	blood:	n/a
35	chr12:42620681-42620731	GM19239	blood:	n/a
36	chr12:42632325-42632375	NHBE	bronchial:	n/a
37	chr12:42632907-42632957	PFSK-1	brain:	n/a
38	chr12:42634807-42634857	SAEC	small airway:	n/a
39	chr12:42632907-42632957	HAEpiC	amniotic membrane:	n/a
40	chr12:42628089-42628139	T-47D	breast:	n/a
41	chr12:42632312-42632362	BJ	skin:	n/a
42	chr12:42632325-42632375	IMR90	lung:	fetal
43	chr12:42620681-42620731	HepG2	liver:	n/a
44	chr12:42631401-42631451	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:42628089-42628139	GM12878	blood:	n/a
46	chr12:42620681-42620731	HL-60	blood:	n/a
47	chr12:42628089-42628139	SAEC	small airway:	n/a
48	chr12:42632129-42632179	HRPEpiC	eye:	n/a
49	chr12:42632907-42632957	Caco-2	colon:	n/a
50	chr12:42620681-42620731	NH-A	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:42652103..42654567-chr12:42656993..42659814,2	MCF-7	breast:
2	chr1:115322980..115323593-chr12:42632513..42633232,2	MCF-7	breast:
3	chr12:42536858..42540358-chr12:42630016..42633914,10	MCF-7	breast:
4	chr12:42537005..42540223-chr12:42630265..42633071,6	MCF-7	breast:
5	chr12:42604514..42606736-chr12:42630600..42632682,2	MCF-7	breast:
6	chr12:42591218..42593294-chr12:42596615..42598964,2	K562	blood:
7	chr12:42597838..42599534-chr12:42630169..42632429,2	MCF-7	breast:
8	chr12:42537474..42540100-chr12:42609019..42612283,3	K562	blood:
9	chr12:42631475..42633841-chr12:42740722..42742775,2	K562	blood:
10	chr12:42631482..42632205-chr5:122758852..122759800,2	Hela-S3	cervix:
11	chr12:42631690..42633240-chr12:42634536..42637417,2	MCF-7	breast:
12	chr12:42615591..42617465-chr12:42626571..42628750,2	MCF-7	breast:
13	chr1:45805626..45806419-chr12:42631018..42631667,2	Hela-S3	cervix:
14	chr12:42625009..42627071-chr12:42627822..42629813,2	MCF-7	breast:
15	chr12:42631376..42634368-chr12:42640313..42643094,3	MCF-7	breast:
16	chr12:42595134..42595826-chr12:42630960..42631860,2	MCF-7	breast:
17	chr12:42536520..42538445-chr12:42636169..42638853,2	MCF-7	breast:
18	chr12:42601252..42603432-chr12:42605930..42608444,2	K562	blood:
19	chr12:42600600..42602301-chr12:42611820..42613323,2	K562	blood:
20	chr12:42633699..42635354-chr12:42650492..42652110,2	K562	blood:
21	chr12:42613730..42615825-chr12:42628835..42630747,2	K562	blood:
22	chr12:42630585..42631302-chr8:144126589..144127131,2	MCF-7	breast:
23	chr12:42536195..42540644-chr12:42629191..42634148,6	K562	blood:
24	chr12:42631690..42633240-chr12:42634536..42637417,2	MCF-7	breast:
25	chr12:42631954..42632456-chr3:72495895..72496648,2	MCF-7	breast:
26	chr12:42631389..42632009-chr2:99224712..99225682,3	Hela-S3	cervix:
27	chr12:42604828..42607249-chr12:42726467..42728548,2	MCF-7	breast:
28	chr12:42615591..42617465-chr12:42626571..42628750,2	MCF-7	breast:
29	chr12:42602650..42606559-chr12:42628357..42633249,5	MCF-7	breast:
30	chr12:42609074..42611841-chr12:42630116..42632105,3	MCF-7	breast:
31	chr12:42537957..42540928-chr12:42622624..42625244,2	MCF-7	breast:
32	chr12:42629382..42633215-chr12:42724719..42729481,4	MCF-7	breast:
33	chr12:42625009..42627071-chr12:42627822..42629813,2	MCF-7	breast:
34	chr12:42605935..42607831-chr12:42611202..42613567,2	K562	blood:
35	chr12:42605935..42607831-chr12:42611202..42613567,2	K562	blood:
36	chr12:42602650..42606559-chr12:42628357..42633249,5	MCF-7	breast:
37	chr12:42652103..42654567-chr12:42656993..42659814,2	MCF-7	breast:
38	chr12:42631956..42632484-chr3:72495796..72496451,3	HCT-116	colon:
39	chr12:42601009..42602619-chr12:42631364..42633589,2	MCF-7	breast:
40	chr12:42625677..42628614-chr12:42630499..42632506,2	MCF-7	breast:
41	chr12:42629596..42634057-chr12:42635851..42641617,6	MCF-7	breast:
42	chr12:42591218..42593294-chr12:42596615..42598964,2	K562	blood:
43	chr12:42617053..42619651-chr12:42629734..42632982,4	MCF-7	breast:
44	chr12:42528143..42530319-chr12:42607718..42609289,2	MCF-7	breast:
45	chr12:42630764..42634412-chr12:42661858..42664112,3	K562	blood:
46	chr12:42613730..42615825-chr12:42628835..42630747,2	K562	blood:
47	chr12:42629683..42634871-chr12:42717173..42721669,10	K562	blood:
48	chr12:42552974..42555837-chr12:42630405..42632767,3	MCF-7	breast:
49	chr12:42612206..42614346-chr12:42630499..42633033,4	MCF-7	breast:
50	chr12:42631625..42634573-chr12:42719114..42721447,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GXYLT1-4	chr12:42592938-42593346	NONHSAT027765
2	lnc-PDZRN4-2	chr12:42636017-42636316	NONHSAT027767

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	YAF2	hsa-miR-103a-3p	chr12:42628062-42628084

Variant related genes	Relation type
RN7SL10P	TF binding region
ENSG00000269367	TF binding region
PPHLN1	TF binding region
YAF2	TF binding region
RN7SL10P	CpG island
ENSG00000269367	CpG island
PPHLN1	CpG island
YAF2	CpG island
ENSG00000163602	chromatin interactions
ENSG00000151233	chromatin interactions
ENSG00000183513	chromatin interactions
ENSG00000241710	chromatin interactions
ENSG00000115446	chromatin interactions
ENSG00000132773	chromatin interactions
ENSG00000134283	chromatin interactions
ENSG00000170540	chromatin interactions
ENSG00000132781	chromatin interactions
ENSG00000052723	chromatin interactions
ENSG00000015153	chromatin interactions
ENSG00000107560	chromatin interactions
ENSG00000260342	chromatin interactions
ENSG00000168944	chromatin interactions
ENSG00000139168	chromatin interactions
ENSG00000252917	chromatin interactions
ENSG00000177640	chromatin interactions

Extended variants
information (count: 2727 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2727 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150446620	chr12:42593290-42593291	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs55699566	chr12:42593300-42593301	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs529263851	chr12:42593318-42593319	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs376932767	chr12:42593385-42593386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs712125	chr12:42593436-42593437	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs539759872	chr12:42593525-42593526	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11181376	chr12:42593529-42593530	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs566804265	chr12:42593574-42593575	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562617288	chr12:42593593-42593594	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35910821	chr12:42593594-42593595	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114513282	chr12:42593693-42593694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558722911	chr12:42593699-42593700	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576915640	chr12:42593735-42593736	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544343773	chr12:42593764-42593765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556257434	chr12:42593777-42593778	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574564267	chr12:42593828-42593829	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77600253	chr12:42593889-42593890	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560181383	chr12:42593968-42593969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533282742	chr12:42593969-42593970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527998225	chr12:42593988-42593989	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143037593	chr12:42594019-42594020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34896304	chr12:42594100-42594101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564727025	chr12:42594123-42594124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80039797	chr12:42594179-42594180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549948028	chr12:42594193-42594194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73281868	chr12:42594207-42594208	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs529341366	chr12:42594212-42594213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190809846	chr12:42594224-42594225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373435357	chr12:42594288-42594289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566860146	chr12:42594301-42594302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534097419	chr12:42594303-42594304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371952464	chr12:42594419-42594420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558543439	chr12:42594473-42594474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78062157	chr12:42594486-42594487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182161640	chr12:42594500-42594501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186782385	chr12:42594501-42594502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs17592715	chr12:42594509-42594510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567060069	chr12:42594517-42594518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535503349	chr12:42594526-42594527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35154804	chr12:42594556-42594557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553735486	chr12:42594589-42594590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567635174	chr12:42594607-42594608	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534930285	chr12:42594609-42594610	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527940246	chr12:42594682-42594683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567622196	chr12:42594703-42594704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564663506	chr12:42594710-42594711	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576304817	chr12:42594713-42594714	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543654213	chr12:42594719-42594720	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77330786	chr12:42594748-42594749	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529353469	chr12:42594793-42594794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:1445 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42539800-42607800	Weak transcription	Pancreas	Pancrea
2	chr12:42547800-42610400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:42550600-42615800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:42552000-42604000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr12:42552200-42613000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr12:42552400-42620000	Weak transcription	Fetal Brain Female	brain
7	chr12:42554000-42607600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:42555000-42628600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr12:42555400-42598000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr12:42556800-42613200	Weak transcription	HMEC	breast
11	chr12:42557000-42604000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:42557200-42606800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:42558000-42602400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr12:42563200-42608000	Weak transcription	Small Intestine	intestine
15	chr12:42568400-42623400	Weak transcription	K562	blood
16	chr12:42568600-42607800	Weak transcription	Right Ventricle	heart
17	chr12:42568800-42630600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr12:42569600-42630800	Weak transcription	Colonic Mucosa	Colon
19	chr12:42569800-42631000	Weak transcription	Gastric	stomach
20	chr12:42571400-42597600	Weak transcription	Esophagus	oesophagus
21	chr12:42571600-42602400	Weak transcription	HepG2	liver
22	chr12:42574800-42615600	Weak transcription	HUVEC	blood vessel
23	chr12:42575600-42607800	Weak transcription	Brain Angular Gyrus	brain
24	chr12:42575600-42628600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:42575800-42607800	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr12:42575800-42607800	Weak transcription	Brain Substantia Nigra	brain
27	chr12:42576600-42607800	Weak transcription	Brain Anterior Caudate	brain
28	chr12:42578000-42606400	Weak transcription	Fetal Heart	heart
29	chr12:42578800-42603600	Weak transcription	Brain Germinal Matrix	brain
30	chr12:42579200-42606800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:42581800-42607800	Weak transcription	Ovary	ovary
32	chr12:42582000-42596000	Weak transcription	NHEK	skin
33	chr12:42582200-42602000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr12:42583800-42606800	Weak transcription	HSMM	muscle
35	chr12:42584400-42594600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr12:42585200-42593400	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr12:42585200-42596400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:42585200-42608000	Weak transcription	Colon Smooth Muscle	Colon
39	chr12:42585400-42595400	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr12:42585600-42604600	Weak transcription	Fetal Brain Male	brain
41	chr12:42586000-42593400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr12:42586200-42593600	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr12:42586400-42603800	Weak transcription	NH-A	brain
44	chr12:42586800-42630000	Weak transcription	Fetal Kidney	kidney
45	chr12:42587200-42607800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr12:42587200-42629600	Weak transcription	Lung	lung
47	chr12:42587400-42597800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:42587400-42620000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr12:42587600-42606800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr12:42587800-42619400	Weak transcription	Fetal Lung	lung

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