Variant report

Variant	esv17456
Chromosome Location	chr12:26108846-26114910
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:590)
CpG islands
(count:794)
Chromatin interactive
region (count:7)
LncRNA
region (count:63)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	BHLHE40	chr12:26112213-26112339	HepG2	liver:	n/a	chr12:26112227-26112243
4	BRCA1	chr12:26111365-26111532	HepG2	liver:	n/a	n/a
5	BRCA1	chr12:26112175-26112984	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr12:26111108-26111522	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr12:26111238-26112215	K562	blood:	n/a	n/a
8	CEBPB	chr12:26111890-26112243	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:26111941-26112282	A549	lung:	n/a	n/a
10	CEBPB	chr12:26112527-26113059	A549	lung:	n/a	n/a
11	CEBPB	chr12:26111886-26112248	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:26110907-26113412	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:26111962-26112210	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:26112044-26112231	K562	blood:	n/a	n/a
15	CEBPB	chr12:26111935-26112156	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:26111874-26112285	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:26111833-26112347	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr12:26111997-26112283	A549	lung:	n/a	n/a
19	CEBPB	chr12:26112002-26112163	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr12:26112669-26112946	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:26112585-26112981	IMR90	lung:	n/a	n/a
22	CEBPB	chr12:26112674-26112920	A549	lung:	n/a	n/a
23	CEBPB	chr12:26111976-26112392	A549	lung:	n/a	n/a
24	CEBPB	chr12:26111941-26112234	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPD	chr12:26111949-26112217	HepG2	liver:	n/a	n/a
26	CHD1	chr12:26112224-26112728	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr12:26113051-26113310	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr12:26111776-26111841	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr12:26110394-26114412	IMR90	lung:	n/a	chr12:26111241-26111251
30	CHD2	chr12:26110923-26111653	H1-hESC	embryonic stem cell:	n/a	chr12:26111241-26111251
31	CHD2	chr12:26112283-26112306	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr12:26110731-26113022	Hela-S3	cervix:	n/a	chr12:26111241-26111251
33	CHD2	chr12:26111356-26111688	K562	blood:	n/a	n/a
34	CHD2	chr12:26111193-26111675	HepG2	liver:	n/a	chr12:26111241-26111251
35	CREB1	chr12:26110975-26111517	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr12:26111109-26112471	A549	lung:	n/a	n/a
37	CREB1	chr12:26111027-26111852	HepG2	liver:	n/a	n/a
38	CREB1	chr12:26111004-26111511	K562	blood:	n/a	n/a
39	CREB1	chr12:26111163-26111483	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr12:26110974-26111479	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr12:26111692-26112349	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr12:26113200-26113350	AG04450	lung:	n/a	n/a
43	CTCF	chr12:26113240-26113390	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr12:26111387-26111589	GM19240	blood:	n/a	n/a
45	CTCF	chr12:26113140-26113290	GM12872	blood:	n/a	n/a
46	CTCF	chr12:26111844-26113535	SK-N-SH	brain:	n/a	n/a
47	CTCF	chr12:26113220-26113370	AG09319	gingival:	n/a	n/a
48	CTCF	chr12:26111420-26111570	GM12871	blood:	n/a	n/a
49	CTCF	chr12:26112769-26112868	Lung_OC	lung:	n/a	n/a
50	CTCF	chr12:26113257-26113322	Spleen_OC	spleen:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:26111213-26111263	MCF10A-Er-Src	breast:	n/a
2	chr12:26111213-26111263	MCF10A-Er-Src	breast:	n/a
3	chr12:26110700-26110750	HRCEpiC	kidney:	n/a
4	chr12:26112065-26112115	HCPEpiC	choroid plexus:	n/a
5	chr12:26111348-26111398	HRCEpiC	kidney:	n/a
6	chr12:26112121-26112171	A549	lung:	n/a
7	chr12:26112121-26112171	HCPEpiC	choroid plexus:	n/a
8	chr12:26111213-26111263	GM12878	blood:	n/a
9	chr12:26110700-26110750	PFSK-1	brain:	n/a
10	chr12:26110666-26110716	SKMC	muscle:	n/a
11	chr12:26110700-26110750	HCF	heart:	n/a
12	chr12:26111348-26111398	MCF-7	breast:	n/a
13	chr12:26111348-26111398	PFSK-1	brain:	n/a
14	chr12:26111162-26111212	NH-A	brain:	n/a
15	chr12:26111348-26111398	PrEC	prostate:	n/a
16	chr12:26111348-26111398	HRE	kidney:	n/a
17	chr12:26111697-26111747	HUVEC	blood vessel:	n/a
18	chr12:26112454-26112504	SKMC	muscle:	n/a
19	chr12:26112454-26112504	HIPEpiC	eye:	n/a
20	chr12:26110518-26110568	HAEpiC	amniotic membrane:	n/a
21	chr12:26112065-26112115	SAEC	small airway:	n/a
22	chr12:26110666-26110716	PANC-1	pancreas:	n/a
23	chr12:26112121-26112171	HRE	kidney:	n/a
24	chr12:26112653-26112703	AG04449	skin:	fetal
25	chr12:26110518-26110568	HNPCEpiC	eye:	n/a
26	chr12:26110666-26110716	HepG2	liver:	n/a
27	chr12:26111821-26111871	HCPEpiC	choroid plexus:	n/a
28	chr12:26112454-26112504	RPTEC	kidney:	n/a
29	chr12:26111213-26111263	HCPEpiC	choroid plexus:	n/a
30	chr12:26110700-26110750	NH-A	brain:	n/a
31	chr12:26111348-26111398	PANC-1	pancreas:	n/a
32	chr12:26110666-26110716	GM06990	blood:	n/a
33	chr12:26112653-26112703	SAEC	small airway:	n/a
34	chr12:26112653-26112703	Jurkat	blood:	n/a
35	chr12:26112065-26112115	MCF-7	breast:	n/a
36	chr12:26111162-26111212	HRPEpiC	eye:	n/a
37	chr12:26112121-26112171	GM12892	blood:	n/a
38	chr12:26110700-26110750	SAEC	small airway:	n/a
39	chr12:26111213-26111263	BE2_C	brain:	n/a
40	chr12:26111348-26111398	AG09309	skin:	n/a
41	chr12:26111162-26111212	HCM	heart:	n/a
42	chr12:26112746-26112796	SK-N-MC	brain:	n/a
43	chr12:26112653-26112703	AG09319	gingival:	n/a
44	chr12:26112653-26112703	Hela-S3	cervix:	n/a
45	chr12:26112121-26112171	GM06990	blood:	n/a
46	chr12:26110700-26110750	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:26112653-26112703	SK-N-SH_RA	brain:	n/a
48	chr12:26110518-26110568	AG10803	skin:	n/a
49	chr12:26112121-26112171	PANC-1	pancreas:	n/a
50	chr12:26112653-26112703	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:25986954..25988487-chr12:26111623..26114201,2	MCF-7	breast:
2	chr12:26113833..26115366-chr12:26119637..26121899,2	K562	blood:
3	chr12:26107603..26109573-chr12:26124823..26126965,2	K562	blood:
4	chr12:26112991..26115825-chr12:26120756..26122747,2	MCF-7	breast:
5	chr12:26107125..26109528-chr12:26109576..26111769,2	K562	blood:
6	chr12:26105978..26107821-chr12:26108027..26109546,2	MCF-7	breast:
7	chr12:26110998..26111780-chr19:1251515..1252465,2	Hela-S3	cervix:

(count:63 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BHLHE41-2	chr12:26112259-26112314	ENSG00000246695
2	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
3	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027374
4	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027377
5	lnc-BHLHE41-2	chr12:26109135-26109280	NONHSAT140062
6	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
7	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027374
8	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027371
9	lnc-BHLHE41-2	chr12:26111865-26111998	ENSG00000246695
10	lnc-BHLHE41-2	chr12:26111865-26111998	ENSG00000246695
11	lnc-BHLHE41-2	chr12:26110952-26111408	NONHSAT027374
12	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
13	lnc-BHLHE41-2	chr12:26110386-26110518	ENSG00000246695
14	lnc-BHLHE41-2	chr12:26110952-26111408	NONHSAT140062
15	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027382
16	lnc-BHLHE41-2	chr12:26105691-26109280	NONHSAT027366
17	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
18	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027377
19	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027370
20	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027381
21	lnc-BHLHE41-2	chr12:26110952-26111496	NONHSAT027366
22	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
23	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
24	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027366
25	lnc-BHLHE41-2	chr12:26110952-26111426	NONHSAT027381
26	lnc-BHLHE41-2	chr12:26110952-26111511	ENSG00000246695
27	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
28	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027378
29	lnc-BHLHE41-2	chr12:26112259-26112698	ENSG00000246695
30	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027381
31	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
32	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027370
33	lnc-SSPN-6	chr12:26111991-26112081	NONHSAT027385
34	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT140062
35	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
36	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
37	lnc-BHLHE41-2	chr12:26111865-26111975	ENSG00000246695
38	lnc-BHLHE41-2	chr12:26109160-26109280	NR_038228
39	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
40	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
41	lnc-BHLHE41-2	chr12:26110386-26110518	ENSG00000246695
42	lnc-BHLHE41-2	chr12:26110386-26110433	NONHSAT027370
43	lnc-BHLHE41-2	chr12:26110952-26110979	ENSG00000246695
44	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
45	lnc-BHLHE41-2	chr12:26109160-26109280	ENSG00000246695
46	lnc-SSPN-6	chr12:26112054-26112081	NONHSAT027387
47	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
48	lnc-BHLHE41-2	chr12:26109160-26109280	NONHSAT027378
49	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
50	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695

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
ENSG00000246695	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000123094	chromatin interactions
ADAR	miRNA target sites
FNDC3B	miRNA target sites
E2F7	miRNA target sites
SSU72	miRNA target sites
ZMIZ1	miRNA target sites
PLEKHA5	miRNA target sites
RPH3AL	miRNA target sites
ZNF638	miRNA target sites
ZADH2	miRNA target sites
SRPK1	miRNA target sites
NOTCH2	miRNA target sites
KAT2B	miRNA target sites
VPS4B	miRNA target sites
TMEM41A	miRNA target sites
KIAA1432	miRNA target sites
NARS	miRNA target sites
CNOT6	miRNA target sites
RMND5A	miRNA target sites
BMI1	miRNA target sites
DOCK5	miRNA target sites

Extended variants
information (count: 229 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:229 , 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	rs706518	chr12:26108869-26108870	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35405714	chr12:26108878-26108879	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs530292691	chr12:26108880-26108881	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs79601673	chr12:26108893-26108894	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs560983541	chr12:26108925-26108926	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs531398874	chr12:26108931-26108932	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs77316832	chr12:26108955-26108956	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs571219964	chr12:26108991-26108992	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs76079770	chr12:26109007-26109008	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs373426668	chr12:26109134-26109135	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs77061004	chr12:26109136-26109137	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs565568024	chr12:26109212-26109213	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs370656187	chr12:26109215-26109216	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs184555125	chr12:26109224-26109225	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs11048359	chr12:26109249-26109250	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs34073890	chr12:26109282-26109283	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs568642554	chr12:26109284-26109285	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs7958968	chr12:26109285-26109286	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs386375974	chr12:26109298-26109299	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs71065991	chr12:26109299-26109300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs188922164	chr12:26109320-26109321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs116174890	chr12:26109386-26109387	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577152275	chr12:26109390-26109391	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs181976453	chr12:26109496-26109497	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs149505150	chr12:26109538-26109539	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs571020027	chr12:26109586-26109587	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575154105	chr12:26109631-26109632	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs1149808	chr12:26109635-26109636	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs563828479	chr12:26109653-26109654	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs144089504	chr12:26109670-26109671	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs543496074	chr12:26109753-26109754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56738730	chr12:26109754-26109755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1149807	chr12:26109755-26109756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141494094	chr12:26109780-26109781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs861218	chr12:26109785-26109786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs865507	chr12:26109793-26109794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs864917	chr12:26109799-26109800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75894153	chr12:26109872-26109873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1167547	chr12:26109902-26109903	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs113278083	chr12:26109903-26109904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546960243	chr12:26109923-26109924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142444264	chr12:26109946-26109947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186349012	chr12:26109974-26109975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147655573	chr12:26109975-26109976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189380989	chr12:26109981-26109982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181020475	chr12:26109993-26109994	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs140737066	chr12:26110017-26110018	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs552616012	chr12:26110041-26110042	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs553799875	chr12:26110052-26110053	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111945881	chr12:26110057-26110058	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	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:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26085400-26110600	Weak transcription	Aorta	Aorta
2	chr12:26086800-26110600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:26090200-26110200	Weak transcription	Brain Substantia Nigra	brain
4	chr12:26091400-26110000	Weak transcription	Psoas Muscle	Psoas
5	chr12:26092000-26110600	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:26092800-26109400	Weak transcription	Ovary	ovary
7	chr12:26093400-26110400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr12:26095800-26111000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:26097400-26110600	Weak transcription	Right Ventricle	heart
10	chr12:26097600-26110400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr12:26098000-26110200	Weak transcription	HSMM	muscle
12	chr12:26099800-26110200	Weak transcription	Brain Anterior Caudate	brain
13	chr12:26101400-26110600	Weak transcription	Placenta	Placenta
14	chr12:26104000-26109400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr12:26104000-26110600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:26104200-26110200	Weak transcription	NH-A	brain
17	chr12:26104200-26110200	Weak transcription	NHEK	skin
18	chr12:26104200-26110600	Weak transcription	Liver	Liver
19	chr12:26104400-26110400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr12:26104600-26109600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:26104600-26110000	Weak transcription	Hela-S3	cervix
22	chr12:26105400-26110000	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr12:26105400-26110200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr12:26105600-26109200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr12:26105600-26110000	Weak transcription	NHLF	lung
26	chr12:26105800-26110600	Weak transcription	Fetal Intestine Small	intestine
27	chr12:26105800-26110600	Weak transcription	HSMMtube	muscle
28	chr12:26106000-26110800	Weak transcription	Colon Smooth Muscle	Colon
29	chr12:26106400-26110200	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr12:26106400-26110600	Weak transcription	Adipose Nuclei	Adipose
31	chr12:26106400-26110600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr12:26106600-26109000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:26106800-26109200	Strong transcription	Osteobl	bone
34	chr12:26106800-26110600	Weak transcription	Fetal Intestine Large	intestine
35	chr12:26107000-26109000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:26107000-26109000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr12:26107000-26109000	Strong transcription	NHDF-Ad	bronchial
38	chr12:26107000-26109200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr12:26107000-26109200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr12:26107000-26109200	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr12:26107400-26109200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:26107400-26110200	Weak transcription	Fetal Kidney	kidney
43	chr12:26107400-26110600	Weak transcription	Left Ventricle	heart
44	chr12:26107600-26109000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr12:26107600-26110400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr12:26107800-26109000	Strong transcription	Brain Hippocampus Middle	brain
47	chr12:26107800-26110200	Weak transcription	Fetal Lung	lung
48	chr12:26108000-26110600	Weak transcription	Brain Angular Gyrus	brain
49	chr12:26108000-26110600	Weak transcription	Fetal Stomach	stomach
50	chr12:26108200-26110200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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