Variant report

Variant	nsv557802
Chromosome Location	chr12:26093161-26112158
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:610)
Chromatin interactive
region (count:9)
LncRNA
region (count:91)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:26111166-26111346	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr12:26111173-26111242	K562	blood:	n/a	n/a
3	BRCA1	chr12:26111108-26111522	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr12:26111365-26111532	HepG2	liver:	n/a	n/a
5	CCNT2	chr12:26111238-26112215	K562	blood:	n/a	n/a
6	CEBPB	chr12:26097904-26098089	HepG2	liver:	n/a	chr12:26098014-26098025
7	CEBPB	chr12:26110907-26113412	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:26111886-26112248	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:26111890-26112243	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:26111935-26112156	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:26111941-26112282	A549	lung:	n/a	n/a
12	CEBPB	chr12:26112002-26112163	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr12:26111874-26112285	IMR90	lung:	n/a	n/a
14	CEBPB	chr12:26111941-26112234	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:26111976-26112392	A549	lung:	n/a	n/a
16	CEBPB	chr12:26111997-26112283	A549	lung:	n/a	n/a
17	CEBPB	chr12:26111962-26112210	MCF-7	breast:	n/a	n/a
18	CEBPB	chr12:26112044-26112231	K562	blood:	n/a	n/a
19	CEBPB	chr12:26111833-26112347	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPD	chr12:26111949-26112217	HepG2	liver:	n/a	n/a
21	CHD1	chr12:26110394-26114412	IMR90	lung:	n/a	chr12:26111241-26111251
22	CHD1	chr12:26111776-26111841	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr12:26111193-26111675	HepG2	liver:	n/a	chr12:26111241-26111251
24	CHD2	chr12:26110731-26113022	Hela-S3	cervix:	n/a	chr12:26111241-26111251
25	CHD2	chr12:26095504-26095582	HepG2	liver:	n/a	n/a
26	CHD2	chr12:26111356-26111688	K562	blood:	n/a	n/a
27	CHD2	chr12:26110923-26111653	H1-hESC	embryonic stem cell:	n/a	chr12:26111241-26111251
28	CREB1	chr12:26111109-26112471	A549	lung:	n/a	n/a
29	CREB1	chr12:26111163-26111483	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr12:26111027-26111852	HepG2	liver:	n/a	n/a
31	CREB1	chr12:26111004-26111511	K562	blood:	n/a	n/a
32	CREB1	chr12:26110975-26111517	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr12:26111692-26112349	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr12:26110974-26111479	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr12:26111357-26111559	A549	lung:	n/a	n/a
36	CTCF	chr12:26111440-26111590	GM12871	blood:	n/a	n/a
37	CTCF	chr12:26111380-26111530	GM12875	blood:	n/a	n/a
38	CTCF	chr12:26111427-26111532	GM13977	blood:	n/a	n/a
39	CTCF	chr12:26111400-26111550	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr12:26111418-26111579	GM12891	blood:	n/a	n/a
41	CTCF	chr12:26111385-26111390	LNCaP	prostate:	n/a	n/a
42	CTCF	chr12:26111400-26111550	GM12866	blood:	n/a	n/a
43	CTCF	chr12:26111373-26111558	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr12:26111399-26111562	GM19238	blood:	n/a	n/a
45	CTCF	chr12:26111391-26111546	LNCaP	prostate:	n/a	n/a
46	CTCF	chr12:26111440-26111590	GM12869	blood:	n/a	n/a
47	CTCF	chr12:26111424-26111551	Gliobla	brain:	n/a	n/a
48	CTCF	chr12:26111440-26111590	GM12870	blood:	n/a	n/a
49	CTCF	chr12:26111460-26111610	Caco-2	colon:	n/a	n/a
50	CTCF	chr12:26111472-26111532	GM13976	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:26111213-26111263	BE2_C	brain:	n/a
2	chr12:26112121-26112171	HIPEpiC	eye:	n/a
3	chr12:26111348-26111398	HEK293	kidney:	embryo
4	chr12:26112121-26112171	MCF10A-Er-Src	breast:	n/a
5	chr12:26111348-26111398	U87	brain:	n/a
6	chr12:26112065-26112115	SAEC	small airway:	n/a
7	chr12:26110518-26110568	GM12878	blood:	n/a
8	chr12:26112065-26112115	HCT-116	colon:	n/a
9	chr12:26110518-26110568	ovcar-3	ovarian:	n/a
10	chr12:26110518-26110568	SK-N-SH_RA	brain:	n/a
11	chr12:26111821-26111871	HNPCEpiC	eye:	n/a
12	chr12:26110666-26110716	BE2_C	brain:	n/a
13	chr12:26111348-26111398	PANC-1	pancreas:	n/a
14	chr12:26112065-26112115	NT2-D1	testis:	n/a
15	chr12:26111213-26111263	ProgFib	skin:	n/a
16	chr12:26112065-26112115	HNPCEpiC	eye:	n/a
17	chr12:26110518-26110568	K562	blood:	n/a
18	chr12:26112065-26112115	ovcar-3	ovarian:	n/a
19	chr12:26111697-26111747	HEEpiC	esophagus:	n/a
20	chr12:26111348-26111398	ProgFib	skin:	n/a
21	chr12:26111213-26111263	HRCEpiC	kidney:	n/a
22	chr12:26112065-26112115	AoSMC	blood vessel:	n/a
23	chr12:26112065-26112115	GM12878	blood:	n/a
24	chr12:26111162-26111212	MCF10A-Er-Src	breast:	n/a
25	chr12:26111821-26111871	BE2_C	brain:	n/a
26	chr12:26110700-26110750	H1-hESC	embryonic stem cell:	embryo
27	chr12:26111697-26111747	HRPEpiC	eye:	n/a
28	chr12:26111697-26111747	IMR90	lung:	fetal
29	chr12:26111821-26111871	SK-N-SH	brain:	n/a
30	chr12:26112121-26112171	GM12892	blood:	n/a
31	chr12:26111213-26111263	AG09319	gingival:	n/a
32	chr12:26111348-26111398	GM06990	blood:	n/a
33	chr12:26111213-26111263	Hela-S3	cervix:	n/a
34	chr12:26110666-26110716	NB4	blood:	n/a
35	chr12:26110518-26110568	IMR90	lung:	fetal
36	chr12:26112121-26112171	BE2_C	brain:	n/a
37	chr12:26111213-26111263	HEK293	kidney:	embryo
38	chr12:26112065-26112115	GM12891	blood:	n/a
39	chr12:26111697-26111747	HIPEpiC	eye:	n/a
40	chr12:26110700-26110750	AG04450	lung:	fetal
41	chr12:26112121-26112171	SKMC	muscle:	n/a
42	chr12:26110518-26110568	HEK293	kidney:	embryo
43	chr12:26111697-26111747	SK-N-SH_RA	brain:	n/a
44	chr12:26110518-26110568	SKMC	muscle:	n/a
45	chr12:26110518-26110568	AG04450	lung:	fetal
46	chr12:26110518-26110568	HL-60	blood:	n/a
47	chr12:26111213-26111263	SK-N-SH_RA	brain:	n/a
48	chr12:26111162-26111212	T-47D	breast:	n/a
49	chr12:26112121-26112171	HNPCEpiC	eye:	n/a
50	chr12:26110700-26110750	HEK293	kidney:	embryo

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:26107125..26109528-chr12:26109576..26111769,2	K562	blood:
2	chr12:26103913..26105665-chr12:26106928..26108647,2	MCF-7	breast:
3	chr12:26105978..26107821-chr12:26108027..26109546,2	MCF-7	breast:
4	chr12:26103913..26105665-chr12:26106928..26108647,2	MCF-7	breast:
5	chr12:26088641..26091375-chr12:26093087..26096585,3	MCF-7	breast:
6	chr12:25986954..25988487-chr12:26111623..26114201,2	MCF-7	breast:
7	chr12:26107603..26109573-chr12:26124823..26126965,2	K562	blood:
8	chr12:26110998..26111780-chr19:1251515..1252465,2	Hela-S3	cervix:
9	chr12:26105978..26107821-chr12:26108027..26109546,2	MCF-7	breast:

(count:91 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
2	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
3	lnc-BHLHE41-2	chr12:26107968-26108174	ENSG00000246695
4	lnc-BHLHE41-2	chr12:26110386-26110433	NONHSAT027370
5	lnc-BHLHE41-2	chr12:26107905-26108174	NONHSAT027381
6	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027370
7	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
8	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
9	lnc-BHLHE41-2	chr12:26111865-26111998	ENSG00000246695
10	lnc-BHLHE41-2	chr12:26107905-26108174	NONHSAT027382
11	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
12	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027377
13	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027381
14	lnc-BHLHE41-2	chr12:26110952-26111511	ENSG00000246695
15	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027370
16	lnc-BHLHE41-2	chr12:26103355-26103430	NONHSAT027370
17	lnc-BHLHE41-2	chr12:26108071-26108174	NONHSAT027371
18	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
19	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027384
20	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
21	lnc-BHLHE41-2	chr12:26097803-26099068	XLOC_010032
22	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
23	lnc-BHLHE41-2	chr12:26100452-26100555	ENSG00000246695
24	lnc-BHLHE41-2	chr12:26105796-26106009	ENSG00000246695
25	lnc-BHLHE41-2	chr12:26107738-26108174	ENSG00000246695
26	lnc-BHLHE41-2	chr12:26109572-26109697	NR_038228
27	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027381
28	lnc-BHLHE41-2	chr12:26108071-26108174	ENSG00000246695
29	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027377
30	lnc-BHLHE41-2	chr12:26105632-26106009	NONHSAT027374
31	lnc-BHLHE41-2	chr12:26103355-26103430	NONHSAT027371
32	lnc-BHLHE41-2	chr12:26107854-26108174	ENSG00000246695
33	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
34	lnc-BHLHE41-2	chr12:26110952-26111483	NONHSAT027384
35	lnc-SSPN-6	chr12:26111991-26112081	NONHSAT027385
36	lnc-BHLHE41-2	chr12:26107892-26108174	ENSG00000246695
37	lnc-BHLHE41-2	chr12:26107854-26108174	ENSG00000246695
38	lnc-BHLHE41-2	chr12:26108071-26108174	NONHSAT027370
39	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
40	lnc-SSPN-6	chr12:26112054-26112081	NONHSAT027387
41	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
42	lnc-BHLHE41-2	chr12:26107588-26108174	NR_038228
43	lnc-BHLHE41-2	chr12:26105691-26106009	ENSG00000246695
44	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
45	lnc-BHLHE41-2	chr12:26110952-26111426	NONHSAT027382
46	lnc-BHLHE41-2	chr12:26097795-26099068	XLOC_010032
47	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027371
48	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT140062
49	lnc-BHLHE41-2	chr12:26097777-26099068	NONHSAT027366
50	lnc-BHLHE41-2	chr12:26110952-26111426	NONHSAT027381

No data

Variant related genes	Relation type
RASSF8-AS1	TF binding region
RASSF8	TF binding region
RASSF8-AS1	CpG island
RASSF8	CpG island
ENSG00000256440	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000246695	chromatin interactions
ENSG00000123094	chromatin interactions
NARS	miRNA target sites
DOCK5	miRNA target sites
C3orf64	miRNA target sites
SSU72	miRNA target sites
TMEM41A	miRNA target sites
MLLT6	miRNA target sites
ADAR	miRNA target sites
PLEKHA5	miRNA target sites
ZNF638	miRNA target sites
ZMIZ1	miRNA target sites
SRPK1	miRNA target sites
SPRY2	miRNA target sites
ACVR1	miRNA target sites
USP28	miRNA target sites
BMI1	miRNA target sites
GPBP1	miRNA target sites
FAT2	miRNA target sites
KIAA1432	miRNA target sites
CNOT6	miRNA target sites
FNDC3B	miRNA target sites
NOTCH2	miRNA target sites
RMND5A	miRNA target sites
E2F7	miRNA target sites
KAT2B	miRNA target sites
ZNF800	miRNA target sites
CAPZA2	miRNA target sites
RPH3AL	miRNA target sites
HSPB7	miRNA target sites

Extended variants
information (count: 768 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:768 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10842638	chr12:26093161-26093162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577848382	chr12:26093239-26093240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377029163	chr12:26093252-26093253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150360250	chr12:26093264-26093265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536525295	chr12:26093288-26093289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369032065	chr12:26093289-26093290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56835737	chr12:26093300-26093301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572617794	chr12:26093301-26093302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540277423	chr12:26093305-26093306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561578104	chr12:26093306-26093307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573574629	chr12:26093337-26093338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7972672	chr12:26093346-26093347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562750868	chr12:26093358-26093359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533236055	chr12:26093361-26093362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117057612	chr12:26093408-26093409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560347671	chr12:26093414-26093415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190370619	chr12:26093427-26093428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112588865	chr12:26093445-26093446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567594075	chr12:26093446-26093447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs58861844	chr12:26093459-26093460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs371655670	chr12:26093472-26093473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550232929	chr12:26093504-26093505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553165347	chr12:26093533-26093534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145629758	chr12:26093538-26093539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71435676	chr12:26093548-26093549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34292473	chr12:26093573-26093574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553951300	chr12:26093576-26093577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143033402	chr12:26093577-26093578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533693934	chr12:26093581-26093582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555428279	chr12:26093612-26093613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373621596	chr12:26093618-26093619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545075853	chr12:26093619-26093620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146154667	chr12:26093640-26093641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544217950	chr12:26093675-26093676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12311346	chr12:26093676-26093677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558399955	chr12:26093693-26093694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372557030	chr12:26093744-26093745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73074854	chr12:26093752-26093753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35465755	chr12:26093759-26093760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376744910	chr12:26093762-26093763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11612824	chr12:26093774-26093775	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs527472311	chr12:26093926-26093927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116163171	chr12:26093956-26093957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148759868	chr12:26094002-26094003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531681584	chr12:26094003-26094004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189172169	chr12:26094031-26094032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563170773	chr12:26094048-26094049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141517797	chr12:26094055-26094056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373475193	chr12:26094145-26094146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150891016	chr12:26094252-26094253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17133270	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26085400-26110600	Weak transcription	Aorta	Aorta
2	chr12:26086800-26095000	Weak transcription	NHDF-Ad	bronchial
3	chr12:26086800-26110600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:26090200-26110200	Weak transcription	Brain Substantia Nigra	brain
5	chr12:26090400-26107800	Weak transcription	Brain Hippocampus Middle	brain
6	chr12:26091000-26107000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr12:26091400-26110000	Weak transcription	Psoas Muscle	Psoas
8	chr12:26091800-26095600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:26092000-26110600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr12:26092400-26095600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr12:26092400-26108600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:26092800-26095400	Weak transcription	Placenta	Placenta
13	chr12:26092800-26096200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr12:26092800-26109400	Weak transcription	Ovary	ovary
15	chr12:26093400-26110400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr12:26093600-26096000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:26094000-26094200	Enhancers	Right Ventricle	heart
18	chr12:26095000-26095800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:26095000-26095800	Enhancers	NHDF-Ad	bronchial
20	chr12:26095200-26095800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr12:26095200-26096200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr12:26095400-26095800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr12:26095400-26095800	Enhancers	Placenta	Placenta
24	chr12:26095400-26096200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr12:26095600-26095800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr12:26095600-26095800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:26095600-26095800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:26095800-26096000	Weak transcription	NHDF-Ad	bronchial
29	chr12:26095800-26096200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:26095800-26096200	Weak transcription	Placenta	Placenta
31	chr12:26095800-26105600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr12:26095800-26108600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr12:26095800-26111000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:26096000-26096200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr12:26096200-26096600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr12:26096200-26103600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:26096200-26107600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr12:26096600-26107000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:26096600-26107000	Weak transcription	Left Ventricle	heart
40	chr12:26096800-26097000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr12:26096800-26098800	Weak transcription	NHDF-Ad	bronchial
42	chr12:26097000-26097400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:26097400-26098600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:26097400-26107000	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr12:26097400-26110600	Weak transcription	Right Ventricle	heart
46	chr12:26097600-26107000	Weak transcription	Fetal Muscle Leg	muscle
47	chr12:26097600-26110400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:26098000-26110200	Weak transcription	HSMM	muscle
49	chr12:26098400-26100200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr12:26098600-26100400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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