Variant report

Variant	nsv915982
Chromosome Location	chr12:67050863-67189954
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:983)
CpG islands
(count:551)
Chromatin interactive
region (count:56)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:67170642-67171041	GM12878	blood:	n/a	n/a
2	BACH1	chr12:67076780-67076853	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:67170708-67171069	GM12878	blood:	n/a	n/a
4	BATF	chr12:67055122-67055399	GM12878	blood:	n/a	n/a
5	BATF	chr12:67055171-67055483	GM12878	blood:	n/a	n/a
6	BATF	chr12:67170761-67171074	GM12878	blood:	n/a	n/a
7	BCL11A	chr12:67170768-67171000	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:67170790-67171069	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:67082643-67082952	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:67052791-67052942	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:67087970-67087977	GM12878	blood:	n/a	n/a
12	CEBPB	chr12:67073528-67073838	MCF-7	breast:	n/a	n/a
13	CEBPB	chr12:67073468-67073795	IMR90	lung:	n/a	n/a
14	CEBPB	chr12:67082643-67082935	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:67138715-67138996	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:67113492-67113613	K562	blood:	n/a	n/a
17	CEBPB	chr12:67138695-67138991	K562	blood:	n/a	n/a
18	CEBPB	chr12:67138611-67139048	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:67073473-67073797	A549	lung:	n/a	n/a
20	CEBPB	chr12:67073474-67073755	K562	blood:	n/a	n/a
21	CEBPB	chr12:67131490-67131690	K562	blood:	n/a	n/a
22	CEBPB	chr12:67178069-67178104	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:67138687-67139031	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr12:67130864-67131019	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:67073446-67073794	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:67131609-67131785	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr12:67073457-67073808	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:67170935-67171105	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:67095950-67096156	HepG2	liver:	n/a	chr12:67096084-67096095
30	CEBPB	chr12:67073534-67073750	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:67138648-67139144	MCF-7	breast:	n/a	n/a
32	CEBPB	chr12:67084108-67084286	HepG2	liver:	n/a	chr12:67084134-67084145
33	CHD1	chr12:67127652-67127842	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:67082701-67082981	HepG2	liver:	n/a	n/a
35	CHD2	chr12:67127788-67127973	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr12:67082760-67082910	GM12871	blood:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
37	CTCF	chr12:67138860-67139010	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr12:67088800-67088950	GM06990	blood:	n/a	n/a
39	CTCF	chr12:67082707-67082929	GM13976	blood:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
40	CTCF	chr12:67087800-67087950	GM12878	blood:	n/a	n/a
41	CTCF	chr12:67082760-67082910	Hela-S3	cervix:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
42	CTCF	chr12:67102540-67102690	HA-sp	spinal cord:	n/a	chr12:67102633-67102654 chr12:67102638-67102656 chr12:67102639-67102655
43	CTCF	chr12:67082740-67082890	HA-sp	spinal cord:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
44	CTCF	chr12:67102560-67102710	HUVEC	blood vessel:	n/a	chr12:67102633-67102654 chr12:67102638-67102656 chr12:67102639-67102655
45	CTCF	chr12:67087720-67087870	HCT-116	colon:	n/a	n/a
46	CTCF	chr12:67082680-67082830	A549	lung:	n/a	chr12:67082822-67082830
47	CTCF	chr12:67102620-67102770	A549	lung:	n/a	chr12:67102633-67102654 chr12:67102638-67102656 chr12:67102639-67102655
48	CTCF	chr12:67103332-67103333	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:67082720-67082870	HPF	lung:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
50	CTCF	chr12:67102540-67102690	SAEC	small airway:	n/a	chr12:67102633-67102654 chr12:67102638-67102656 chr12:67102639-67102655

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67072769-67072819	Hela-S3	cervix:	n/a
2	chr12:67127781-67127831	HMEC	breast:	n/a
3	chr12:67072769-67072819	Hela-S3	cervix:	n/a
4	chr12:67127781-67127831	HMEC	breast:	n/a
5	chr12:67072951-67073001	PANC-1	pancreas:	n/a
6	chr12:67072769-67072819	BJ	skin:	n/a
7	chr12:67072769-67072819	RPTEC	kidney:	n/a
8	chr12:67072951-67073001	NH-A	brain:	n/a
9	chr12:67073062-67073112	NB4	blood:	n/a
10	chr12:67072769-67072819	MCF10A-Er-Src	breast:	n/a
11	chr12:67072769-67072819	A549	lung:	n/a
12	chr12:67073062-67073112	GM12891	blood:	n/a
13	chr12:67073022-67073072	PrEC	prostate:	n/a
14	chr12:67073760-67073810	GM12892	blood:	n/a
15	chr12:67160208-67160258	HCT-116	colon:	n/a
16	chr12:67072951-67073001	HCT-116	colon:	n/a
17	chr12:67127781-67127831	MCF10A-Er-Src	breast:	n/a
18	chr12:67072988-67073038	HMEC	breast:	n/a
19	chr12:67073022-67073072	NB4	blood:	n/a
20	chr12:67073760-67073810	NHDF-neo	bronchial:	n/a
21	chr12:67073022-67073072	NHBE	bronchial:	n/a
22	chr12:67073022-67073072	HRCEpiC	kidney:	n/a
23	chr12:67073760-67073810	PFSK-1	brain:	n/a
24	chr12:67073062-67073112	NT2-D1	testis:	n/a
25	chr12:67072951-67073001	GM12878	blood:	n/a
26	chr12:67127781-67127831	NH-A	brain:	n/a
27	chr12:67073022-67073072	HAEpiC	amniotic membrane:	n/a
28	chr12:67073760-67073810	HepG2	liver:	n/a
29	chr12:67127781-67127831	SK-N-SH_RA	brain:	n/a
30	chr12:67127781-67127831	GM12892	blood:	n/a
31	chr12:67072988-67073038	CMK	blood:	n/a
32	chr12:67073062-67073112	H1-hESC	embryonic stem cell:	embryo
33	chr12:67072769-67072819	SAEC	small airway:	n/a
34	chr12:67073062-67073112	GM06990	blood:	n/a
35	chr12:67160208-67160258	HAEpiC	amniotic membrane:	n/a
36	chr12:67127781-67127831	Hepatocyte	liver:	n/a
37	chr12:67072769-67072819	PANC-1	pancreas:	n/a
38	chr12:67160208-67160258	HUVEC	blood vessel:	n/a
39	chr12:67073062-67073112	MCF-7	breast:	n/a
40	chr12:67073062-67073112	LNCaP	prostate:	n/a
41	chr12:67072951-67073001	LNCaP	prostate:	n/a
42	chr12:67160208-67160258	NHDF-neo	bronchial:	n/a
43	chr12:67073266-67073316	CMK	blood:	n/a
44	chr12:67073022-67073072	HCF	heart:	n/a
45	chr12:67073022-67073072	HCPEpiC	choroid plexus:	n/a
46	chr12:67072988-67073038	HRPEpiC	eye:	n/a
47	chr12:67073266-67073316	HEEpiC	esophagus:	n/a
48	chr12:67073022-67073072	HMEC	breast:	n/a
49	chr12:67073760-67073810	NH-A	brain:	n/a
50	chr12:67073266-67073316	SK-N-SH	brain:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:67105154..67107956-chr12:67110716..67113455,2	MCF-7	breast:
2	chr12:67132372..67134745-chr12:67135516..67139525,4	MCF-7	breast:
3	chr12:67109144..67111332-chr12:67122763..67125755,2	K562	blood:
4	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
5	chr12:67092019..67092945-chr12:67254522..67255578,9	MCF-7	breast:
6	chr12:67054441..67056343-chr12:67057026..67059042,3	MCF-7	breast:
7	chr12:67071707..67074499-chr12:67077173..67078844,2	K562	blood:
8	chr12:67092025..67093817-chr12:67096340..67098697,2	MCF-7	breast:
9	chr12:67132372..67134745-chr12:67135516..67139525,4	MCF-7	breast:
10	chr12:67105154..67107956-chr12:67110716..67113455,2	MCF-7	breast:
11	chr12:66745697..66746293-chr12:67082336..67083172,2	MCF-7	breast:
12	chr12:67082373..67083323-chr12:67255078..67255633,2	MCF-7	breast:
13	chr12:67109144..67111332-chr12:67122763..67125755,2	K562	blood:
14	chr12:67075881..67076642-chr12:67254630..67255196,2	MCF-7	breast:
15	chr12:67092981..67095022-chr12:67095390..67096975,2	MCF-7	breast:
16	chr12:67135712..67138658-chr12:67140137..67142202,2	K562	blood:
17	chr12:67092025..67093817-chr12:67096340..67098697,2	MCF-7	breast:
18	chr12:67173926..67176766-chr12:67210508..67212832,2	MCF-7	breast:
19	chr12:67083332..67087175-chr12:67091989..67094050,4	K562	blood:
20	chr12:67076449..67078895-chr12:67089539..67091893,2	MCF-7	breast:
21	chr12:67169597..67171791-chr2:190019336..190021927,2	MCF-7	breast:
22	chr12:67092981..67095022-chr12:67095390..67096975,2	MCF-7	breast:
23	chr12:67071707..67073529-chr12:67076657..67078844,2	K562	blood:
24	chr12:67079528..67081954-chr12:67090312..67092253,2	K562	blood:
25	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
26	chr12:67135712..67138658-chr12:67140137..67142202,2	K562	blood:
27	chr12:67083332..67087175-chr12:67091989..67094050,4	K562	blood:
28	chr12:66924711..66926666-chr12:67101075..67103092,2	MCF-7	breast:
29	chr12:67109764..67110463-chr12:67254735..67255402,2	MCF-7	breast:
30	chr12:67091996..67092975-chr12:67101719..67102723,3	MCF-7	breast:
31	chr12:67091996..67092975-chr12:67101719..67102723,3	MCF-7	breast:
32	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
33	chr12:66745711..66746634-chr12:67087184..67088269,6	MCF-7	breast:
34	chr12:67073537..67076031-chr12:67078174..67080837,2	K562	blood:
35	chr12:67110471..67111538-chr12:67254403..67256131,14	MCF-7	breast:
36	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
37	chr12:67053423..67055434-chr12:67055731..67058319,2	K562	blood:
38	chr12:67155440..67157393-chr12:67158810..67161653,2	MCF-7	breast:
39	chr12:67155440..67157393-chr12:67158810..67161653,2	MCF-7	breast:
40	chr12:67102904..67104726-chr12:67105810..67107426,2	MCF-7	breast:
41	chr12:67103027..67105591-chr12:67109305..67111957,2	K562	blood:
42	chr12:67102904..67104726-chr12:67105810..67107426,2	MCF-7	breast:
43	chr12:67067995..67069958-chr12:67071524..67073123,2	MCF-7	breast:
44	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
45	chr12:67181348..67184002-chr12:67184358..67185894,2	K562	blood:
46	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
47	chr12:67082410..67083294-chr12:67254648..67255604,5	MCF-7	breast:
48	chr12:66942264..66943151-chr12:67082787..67083333,2	MCF-7	breast:
49	chr12:67076449..67078895-chr12:67089539..67091893,2	MCF-7	breast:
50	chr12:67103027..67105591-chr12:67109305..67111957,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMBIM4-4	chr12:67113331-67113418	l_672_chr12:67111893-67114021_adrenal
2	lnc-TMBIM4-4	chr12:67115010-67115062	l_672_chr12:67111893-67114021_adrenal
3	lnc-TMBIM4-4	chr12:67131414-67131624	l_672_chr12:67111893-67114021_adrenal
4	lnc-TMBIM4-4	chr12:67111894-67112178	l_672_chr12:67111893-67114021_adrenal
5	lnc-TMBIM4-4	chr12:67113856-67114021	l_672_chr12:67111893-67114021_adrenal
6	lnc-TMBIM4-4	chr12:67112662-67112726	l_672_chr12:67111893-67114021_adrenal
7	lnc-TMBIM4-4	chr12:67122111-67122188	l_672_chr12:67111893-67114021_adrenal

No data

Variant related genes	Relation type
GRIP1	TF binding region
GRIP1	CpG island
ENSG00000155974	chromatin interactions

Extended variants
information (count: 4765 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4765 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143649664	chr12:67050877-67050878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572351454	chr12:67050918-67050919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113383702	chr12:67050964-67050965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17102788	chr12:67050969-67050970	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73327009	chr12:67050981-67050982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547818808	chr12:67050987-67050988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562179380	chr12:67050999-67051000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529471982	chr12:67051027-67051028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61926117	chr12:67051044-67051045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561616977	chr12:67051057-67051058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs66697612	chr12:67051058-67051059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369238417	chr12:67051060-67051061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372434977	chr12:67051061-67051062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530360517	chr12:67051062-67051063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201780563	chr12:67051065-67051066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559793959	chr12:67051073-67051074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142775325	chr12:67051080-67051081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550366917	chr12:67051088-67051089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17102790	chr12:67051115-67051116	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs570083694	chr12:67051140-67051141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531219909	chr12:67051141-67051142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142541882	chr12:67051200-67051201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538715998	chr12:67051206-67051207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549424142	chr12:67051223-67051224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17181840	chr12:67051225-67051226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11176361	chr12:67051314-67051315	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73128821	chr12:67051323-67051324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17779619	chr12:67051330-67051331	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs539749310	chr12:67051415-67051416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189208511	chr12:67051493-67051494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117225982	chr12:67051494-67051495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537453956	chr12:67051528-67051529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180854019	chr12:67051529-67051530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574127073	chr12:67051535-67051536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541258421	chr12:67051546-67051547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559922488	chr12:67051551-67051552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56159309	chr12:67051584-67051585	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs117619552	chr12:67051616-67051617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563646228	chr12:67051617-67051618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367863335	chr12:67051632-67051633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549411699	chr12:67051654-67051655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187405776	chr12:67051695-67051696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7955786	chr12:67051884-67051885	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs371024497	chr12:67051912-67051913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547254264	chr12:67052000-67052001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79344250	chr12:67052025-67052026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529308452	chr12:67052057-67052058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112372562	chr12:67052065-67052066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4597137	chr12:67052066-67052067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7969621	chr12:67052206-67052207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21569311	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67042600-67055800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:67047600-67051200	Enhancers	Fetal Brain Male	brain
3	chr12:67047800-67052800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:67048000-67052800	Weak transcription	Right Atrium	heart
5	chr12:67048400-67051000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr12:67048400-67052800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr12:67051000-67051200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:67051000-67051600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:67051200-67056000	Weak transcription	Fetal Brain Male	brain
10	chr12:67052800-67053000	Enhancers	Right Atrium	heart
11	chr12:67052800-67053200	Enhancers	H9 Cell Line	embryonic stem cell
12	chr12:67052800-67053200	Enhancers	Fetal Lung	lung
13	chr12:67052800-67053600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:67053000-67062200	Weak transcription	Right Atrium	heart
15	chr12:67053200-67055600	Weak transcription	Fetal Lung	lung
16	chr12:67054600-67059600	Enhancers	Primary B cells from cord blood	blood
17	chr12:67054800-67056800	Enhancers	GM12878-XiMat	blood
18	chr12:67054800-67057800	Enhancers	Primary B cells from peripheral blood	blood
19	chr12:67055000-67055600	Enhancers	NHEK	skin
20	chr12:67055000-67057200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr12:67055200-67058200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:67055600-67055800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:67055600-67056200	Weak transcription	Colon Smooth Muscle	Colon
24	chr12:67055600-67056800	Flanking Active TSS	NHEK	skin
25	chr12:67055600-67057000	Enhancers	Fetal Lung	lung
26	chr12:67055600-67057800	Enhancers	HMEC	breast
27	chr12:67055800-67056000	Enhancers	HSMMtube	muscle
28	chr12:67055800-67056200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:67055800-67058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:67056000-67056800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr12:67056000-67056800	Enhancers	NH-A	brain
32	chr12:67056000-67057000	Enhancers	Fetal Brain Male	brain
33	chr12:67056000-67057000	Enhancers	HSMM	muscle
34	chr12:67056000-67057400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr12:67056000-67057400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:67056000-67057400	Enhancers	HUVEC	blood vessel
37	chr12:67056000-67061600	Weak transcription	HSMMtube	muscle
38	chr12:67056200-67056400	Enhancers	Colon Smooth Muscle	Colon
39	chr12:67056200-67056800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:67056200-67056800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:67056200-67056800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:67056200-67057000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:67056400-67056600	Flanking Active TSS	NHLF	lung
44	chr12:67056400-67056800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:67056400-67057200	Weak transcription	Colon Smooth Muscle	Colon
46	chr12:67056400-67057400	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr12:67056400-67057600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:67056400-67057600	Enhancers	Fetal Heart	heart
49	chr12:67056400-67059400	Enhancers	Brain Germinal Matrix	brain
50	chr12:67056600-67056800	Enhancers	Stomach Smooth Muscle	stomach

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