Variant report

Variant	esv3337985
Chromosome Location	chr12:26109585-26113883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:580)
CpG islands
(count:794)
Chromatin interactive
region (count:4)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:580 , 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	chr12:26112175-26112984	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr12:26111108-26111522	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr12:26111365-26111532	HepG2	liver:	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	chr12:26112674-26112920	A549	lung:	n/a	n/a
10	CEBPB	chr12:26111997-26112283	A549	lung:	n/a	n/a
11	CEBPB	chr12:26111976-26112392	A549	lung:	n/a	n/a
12	CEBPB	chr12:26111886-26112248	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:26110907-26113412	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:26111941-26112282	A549	lung:	n/a	n/a
15	CEBPB	chr12:26112669-26112946	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:26111941-26112234	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:26111874-26112285	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:26111962-26112210	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:26111935-26112156	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:26112527-26113059	A549	lung:	n/a	n/a
21	CEBPB	chr12:26111833-26112347	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr12:26112002-26112163	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr12:26112585-26112981	IMR90	lung:	n/a	n/a
24	CEBPB	chr12:26112044-26112231	K562	blood:	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	chr12:26110394-26114412	IMR90	lung:	n/a	chr12:26111241-26111251
28	CHD1	chr12:26111776-26111841	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr12:26113051-26113310	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr12:26111193-26111675	HepG2	liver:	n/a	chr12:26111241-26111251
31	CHD2	chr12:26112283-26112306	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr12:26110923-26111653	H1-hESC	embryonic stem cell:	n/a	chr12:26111241-26111251
33	CHD2	chr12:26110731-26113022	Hela-S3	cervix:	n/a	chr12:26111241-26111251
34	CHD2	chr12:26111356-26111688	K562	blood:	n/a	n/a
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	chr12:26111004-26111511	K562	blood:	n/a	n/a
38	CREB1	chr12:26111163-26111483	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr12:26111027-26111852	HepG2	liver:	n/a	n/a
40	CTBP2	chr12:26111692-26112349	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr12:26110974-26111479	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr12:26111408-26111578	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:26113220-26113370	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr12:26113180-26113330	Caco-2	colon:	n/a	n/a
45	CTCF	chr12:26111391-26111546	LNCaP	prostate:	n/a	n/a
46	CTCF	chr12:26111391-26111596	Fibrobl	skin:	n/a	n/a
47	CTCF	chr12:26113180-26113330	HMEC	breast:	n/a	n/a
48	CTCF	chr12:26113180-26113330	HRE	kidney:	n/a	n/a
49	CTCF	chr12:26111399-26111562	GM19238	blood:	n/a	n/a
50	CTCF	chr12:26113200-26113350	HCPEpiC	choroid plexus:	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	chr12:26112065-26112115	HAEpiC	amniotic membrane:	n/a
2	chr12:26112065-26112115	HAEpiC	amniotic membrane:	n/a
3	chr12:26110666-26110716	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:26111697-26111747	HRPEpiC	eye:	n/a
5	chr12:26111213-26111263	AoSMC	blood vessel:	n/a
6	chr12:26110700-26110750	HRPEpiC	eye:	n/a
7	chr12:26112653-26112703	HCPEpiC	choroid plexus:	n/a
8	chr12:26111348-26111398	GM06990	blood:	n/a
9	chr12:26110518-26110568	NB4	blood:	n/a
10	chr12:26111213-26111263	HCM	heart:	n/a
11	chr12:26112065-26112115	HEEpiC	esophagus:	n/a
12	chr12:26112065-26112115	SK-N-MC	brain:	n/a
13	chr12:26111162-26111212	ovcar-3	ovarian:	n/a
14	chr12:26111697-26111747	HUVEC	blood vessel:	n/a
15	chr12:26111348-26111398	NHDF-neo	bronchial:	n/a
16	chr12:26111697-26111747	SK-N-SH	brain:	n/a
17	chr12:26111162-26111212	HRE	kidney:	n/a
18	chr12:26112746-26112796	NT2-D1	testis:	n/a
19	chr12:26112121-26112171	HL-60	blood:	n/a
20	chr12:26112454-26112504	HCT-116	colon:	n/a
21	chr12:26112121-26112171	H1-hESC	embryonic stem cell:	embryo
22	chr12:26112454-26112504	AG10803	skin:	n/a
23	chr12:26111697-26111747	HCT-116	colon:	n/a
24	chr12:26111213-26111263	Jurkat	blood:	n/a
25	chr12:26112065-26112115	Jurkat	blood:	n/a
26	chr12:26112454-26112504	PFSK-1	brain:	n/a
27	chr12:26110518-26110568	HUVEC	blood vessel:	n/a
28	chr12:26110666-26110716	HepG2	liver:	n/a
29	chr12:26111162-26111212	AG04449	skin:	fetal
30	chr12:26110666-26110716	HCM	heart:	n/a
31	chr12:26112653-26112703	IMR90	lung:	fetal
32	chr12:26112454-26112504	GM19239	blood:	n/a
33	chr12:26111348-26111398	NB4	blood:	n/a
34	chr12:26112653-26112703	HIPEpiC	eye:	n/a
35	chr12:26111697-26111747	HIPEpiC	eye:	n/a
36	chr12:26112746-26112796	SK-N-MC	brain:	n/a
37	chr12:26112121-26112171	GM12878	blood:	n/a
38	chr12:26111697-26111747	BJ	skin:	n/a
39	chr12:26110518-26110568	NHDF-neo	bronchial:	n/a
40	chr12:26112121-26112171	HCPEpiC	choroid plexus:	n/a
41	chr12:26112065-26112115	NT2-D1	testis:	n/a
42	chr12:26112454-26112504	BE2_C	brain:	n/a
43	chr12:26112065-26112115	HCPEpiC	choroid plexus:	n/a
44	chr12:26111213-26111263	HEEpiC	esophagus:	n/a
45	chr12:26111821-26111871	AG10803	skin:	n/a
46	chr12:26111213-26111263	HIPEpiC	eye:	n/a
47	chr12:26112121-26112171	U87	brain:	n/a
48	chr12:26111821-26111871	ovcar-3	ovarian:	n/a
49	chr12:26111821-26111871	BE2_C	brain:	n/a
50	chr12:26111821-26111871	LNCaP	prostate:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:26112991..26115825-chr12:26120756..26122747,2	MCF-7	breast:
2	chr12:26110998..26111780-chr19:1251515..1252465,2	Hela-S3	cervix:
3	chr12:26113833..26115366-chr12:26119637..26121899,2	K562	blood:
4	chr12:25986954..25988487-chr12:26111623..26114201,2	MCF-7	breast:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BHLHE41-2	chr12:26111865-26111998	ENSG00000246695
2	lnc-BHLHE41-2	chr12:26110952-26111511	ENSG00000246695
3	lnc-BHLHE41-2	chr12:26112259-26112698	ENSG00000246695
4	lnc-BHLHE41-2	chr12:26111865-26111998	ENSG00000246695
5	lnc-BHLHE41-2	chr12:26110386-26110429	NONHSAT027377
6	lnc-BHLHE41-2	chr12:26112259-26112375	NR_038228
7	lnc-BHLHE41-2	chr12:26110386-26110433	NONHSAT027370
8	lnc-BHLHE41-2	chr12:26110952-26111408	NONHSAT027374
9	lnc-BHLHE41-2	chr12:26110952-26111408	NONHSAT140062
10	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
11	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027371
12	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT140062
13	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027374
14	lnc-BHLHE41-2	chr12:26110386-26110518	ENSG00000246695
15	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
16	lnc-BHLHE41-2	chr12:26112259-26112314	ENSG00000246695
17	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
18	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
19	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
20	lnc-BHLHE41-2	chr12:26112259-26112375	ENSG00000246695
21	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027366
22	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027381
23	lnc-SSPN-6	chr12:26112054-26112081	NONHSAT027387
24	lnc-BHLHE41-2	chr12:26111865-26111975	ENSG00000246695
25	lnc-BHLHE41-2	chr12:26110952-26110979	ENSG00000246695
26	lnc-SSPN-6	chr12:26111991-26112081	NONHSAT027385
27	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027382
28	lnc-BHLHE41-2	chr12:26110952-26111030	NONHSAT027371
29	lnc-BHLHE41-2	chr12:26110952-26111426	NONHSAT027382
30	lnc-BHLHE41-2	chr12:26110386-26110518	NONHSAT027378
31	lnc-BHLHE41-2	chr12:26110952-26111483	NONHSAT027384
32	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027370
33	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027384
34	lnc-BHLHE41-2	chr12:26109572-26109694	NONHSAT027378
35	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
36	lnc-BHLHE41-2	chr12:26110952-26111426	NONHSAT027381
37	lnc-BHLHE41-2	chr12:26109572-26109697	NR_038228
38	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
39	lnc-BHLHE41-2	chr12:26109572-26109694	ENSG00000246695
40	lnc-BHLHE41-2	chr12:26110386-26110518	ENSG00000246695
41	lnc-SSPN-6	chr12:26112054-26112081	NONHSAT027388
42	lnc-BHLHE41-2	chr12:26109572-26109697	ENSG00000246695
43	lnc-BHLHE41-2	chr12:26110952-26111496	NONHSAT027366
44	lnc-BHLHE41-2	chr12:26109572-26109697	NONHSAT027377
45	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
ENSG00000167470	chromatin interactions
RMND5A	miRNA target sites
KAT2B	miRNA target sites
PLEKHA5	miRNA target sites
DOCK5	miRNA target sites
ZADH2	miRNA target sites
NARS	miRNA target sites
CNOT6	miRNA target sites
NOTCH2	miRNA target sites
ZMIZ1	miRNA target sites
VPS4B	miRNA target sites
ZNF638	miRNA target sites
RPH3AL	miRNA target sites
SSU72	miRNA target sites
TMEM41A	miRNA target sites
FNDC3B	miRNA target sites

Extended variants
information (count: 162 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:162 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571020027	chr12:26109586-26109587	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs575154105	chr12:26109631-26109632	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs1149808	chr12:26109635-26109636	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs563828479	chr12:26109653-26109654	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs144089504	chr12:26109670-26109671	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs543496074	chr12:26109753-26109754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56738730	chr12:26109754-26109755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1149807	chr12:26109755-26109756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141494094	chr12:26109780-26109781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs861218	chr12:26109785-26109786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs865507	chr12:26109793-26109794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs864917	chr12:26109799-26109800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75894153	chr12:26109872-26109873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1167547	chr12:26109902-26109903	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113278083	chr12:26109903-26109904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546960243	chr12:26109923-26109924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142444264	chr12:26109946-26109947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186349012	chr12:26109974-26109975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147655573	chr12:26109975-26109976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189380989	chr12:26109981-26109982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181020475	chr12:26109993-26109994	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs140737066	chr12:26110017-26110018	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552616012	chr12:26110041-26110042	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553799875	chr12:26110052-26110053	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs111945881	chr12:26110057-26110058	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs371005340	chr12:26110058-26110059	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs565983002	chr12:26110101-26110102	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs144892165	chr12:26110109-26110110	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs186049860	chr12:26110114-26110115	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs575217085	chr12:26110130-26110131	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534915873	chr12:26110132-26110133	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs117347081	chr12:26110146-26110147	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs191365575	chr12:26110181-26110182	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs28712704	chr12:26110197-26110198	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs575779570	chr12:26110216-26110217	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs543182221	chr12:26110293-26110294	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs146977652	chr12:26110342-26110343	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs565013828	chr12:26110372-26110373	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs74448691	chr12:26110388-26110389	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs79717396	chr12:26110408-26110409	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs540628599	chr12:26110428-26110429	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs76951545	chr12:26110443-26110444	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs368765054	chr12:26110444-26110445	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs140630853	chr12:26110457-26110458	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs4963944	chr12:26110484-26110485	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs181095410	chr12:26110501-26110502	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs113219994	chr12:26110518-26110519	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs185903838	chr12:26110547-26110548	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
49	rs552048701	chr12:26110565-26110566	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
50	rs12424238	chr12:26110610-26110611	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance

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:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr12:26093400-26110400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr12:26095800-26111000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:26097400-26110600	Weak transcription	Right Ventricle	heart
9	chr12:26097600-26110400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:26098000-26110200	Weak transcription	HSMM	muscle
11	chr12:26099800-26110200	Weak transcription	Brain Anterior Caudate	brain
12	chr12:26101400-26110600	Weak transcription	Placenta	Placenta
13	chr12:26104000-26110600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr12:26104200-26110200	Weak transcription	NH-A	brain
15	chr12:26104200-26110200	Weak transcription	NHEK	skin
16	chr12:26104200-26110600	Weak transcription	Liver	Liver
17	chr12:26104400-26110400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr12:26104600-26109600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr12:26104600-26110000	Weak transcription	Hela-S3	cervix
20	chr12:26105400-26110000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr12:26105400-26110200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr12:26105600-26110000	Weak transcription	NHLF	lung
23	chr12:26105800-26110600	Weak transcription	Fetal Intestine Small	intestine
24	chr12:26105800-26110600	Weak transcription	HSMMtube	muscle
25	chr12:26106000-26110800	Weak transcription	Colon Smooth Muscle	Colon
26	chr12:26106400-26110200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr12:26106400-26110600	Weak transcription	Adipose Nuclei	Adipose
28	chr12:26106400-26110600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr12:26106800-26110600	Weak transcription	Fetal Intestine Large	intestine
30	chr12:26107400-26110200	Weak transcription	Fetal Kidney	kidney
31	chr12:26107400-26110600	Weak transcription	Left Ventricle	heart
32	chr12:26107600-26110400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr12:26107800-26110200	Weak transcription	Fetal Lung	lung
34	chr12:26108000-26110600	Weak transcription	Brain Angular Gyrus	brain
35	chr12:26108000-26110600	Weak transcription	Fetal Stomach	stomach
36	chr12:26108200-26110200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:26108200-26110200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:26108400-26110200	Weak transcription	Fetal Muscle Leg	muscle
39	chr12:26108400-26110400	Weak transcription	Fetal Muscle Trunk	muscle
40	chr12:26108800-26110000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:26108800-26110600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr12:26109000-26110000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:26109000-26110000	Weak transcription	NHDF-Ad	bronchial
44	chr12:26109000-26110200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:26109000-26110200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:26109000-26110200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr12:26109000-26110200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:26109000-26110200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr12:26109000-26110600	Weak transcription	Brain Hippocampus Middle	brain
50	chr12:26109200-26110000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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