Variant report

Variant	esv34096
Chromosome Location	chr12:8927520-8968810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 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	ATF2	chr12:8948585-8948825	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr12:8949511-8950085	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:8941185-8941680	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:8948844-8950141	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:8966665-8966680	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr12:8934027-8934153	K562	blood:	n/a	n/a
7	CBX3	chr12:8946893-8947158	K562	blood:	n/a	n/a
8	CEBPB	chr12:8937416-8937695	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:8932505-8932833	K562	blood:	n/a	chr12:8932667-8932678
10	CEBPB	chr12:8929390-8929631	HepG2	liver:	n/a	chr12:8929553-8929564
11	CEBPB	chr12:8932505-8932846	H1-hESC	embryonic stem cell:	n/a	chr12:8932667-8932678
12	CEBPB	chr12:8932433-8932881	MCF-7	breast:	n/a	chr12:8932667-8932678
13	CEBPB	chr12:8932501-8932835	HepG2	liver:	n/a	chr12:8932667-8932678
14	CEBPB	chr12:8945902-8946055	A549	lung:	n/a	n/a
15	CEBPB	chr12:8932426-8932841	MCF-7	breast:	n/a	chr12:8932667-8932678
16	CEBPB	chr12:8945828-8946029	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:8932543-8932792	A549	lung:	n/a	chr12:8932667-8932678
18	CEBPB	chr12:8932526-8932794	Hela-S3	cervix:	n/a	chr12:8932667-8932678
19	CEBPB	chr12:8932421-8932898	HCT-116	colon:	n/a	chr12:8932667-8932678
20	CEBPB	chr12:8945916-8946023	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:8962787-8962961	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr12:8943024-8943372	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr12:8941302-8942576	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr12:8950973-8951423	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr12:8948876-8950157	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr12:8943084-8943112	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr12:8933230-8933380	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:8933160-8933310	GM12865	blood:	n/a	n/a
29	CTCF	chr12:8933017-8933347	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr12:8932520-8932670	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:8933160-8933310	BE2_C	brain:	n/a	n/a
32	CTCF	chr12:8933120-8933270	Caco-2	colon:	n/a	n/a
33	CTCF	chr12:8932900-8933050	GM12872	blood:	n/a	n/a
34	CTCF	chr12:8933080-8933230	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr12:8933100-8933250	GM12869	blood:	n/a	n/a
36	CTCF	chr12:8933100-8933250	BE2_C	brain:	n/a	n/a
37	CTCF	chr12:8933080-8933230	HCM	heart:	n/a	n/a
38	CTCF	chr12:8933100-8933250	GM12866	blood:	n/a	n/a
39	CTCF	chr12:8962216-8962295	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:8933100-8933250	Caco-2	colon:	n/a	n/a
41	CTCF	chr12:8938526-8938548	ProgFib	skin:	n/a	n/a
42	CTCF	chr12:8933100-8933250	HPF	lung:	n/a	n/a
43	CTCF	chr12:8933080-8933230	HAc	cerebellar:	n/a	n/a
44	CTCF	chr12:8933120-8933270	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr12:8947521-8947575	GM13976	blood:	n/a	n/a
46	CTCF	chr12:8933160-8933310	NHEK	skin:	n/a	n/a
47	CTCF	chr12:8933122-8933243	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr12:8938900-8939050	GM12869	blood:	n/a	n/a
49	CTCF	chr12:8933121-8933262	GM13977	blood:	n/a	n/a
50	CTCF	chr12:8933149-8933249	Kidney_OC	kidney:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8940171-8940221	AG04450	lung:	fetal
2	chr12:8931239-8931289	NB4	blood:	n/a
3	chr12:8932036-8932086	GM12892	blood:	n/a
4	chr12:8932036-8932086	GM19239	blood:	n/a
5	chr12:8947385-8947435	GM19239	blood:	n/a
6	chr12:8931477-8931527	HL-60	blood:	n/a
7	chr12:8931239-8931289	HCF	heart:	n/a
8	chr12:8931239-8931289	IMR90	lung:	fetal
9	chr12:8947385-8947435	NH-A	brain:	n/a
10	chr12:8940171-8940221	GM06990	blood:	n/a
11	chr12:8940075-8940125	HCM	heart:	n/a
12	chr12:8932036-8932086	SK-N-SH	brain:	n/a
13	chr12:8940171-8940221	MCF10A-Er-Src	breast:	n/a
14	chr12:8931239-8931289	A549	lung:	n/a
15	chr12:8932036-8932086	Hepatocyte	liver:	n/a
16	chr12:8931477-8931527	GM19239	blood:	n/a
17	chr12:8947385-8947435	GM12891	blood:	n/a
18	chr12:8940075-8940125	SK-N-SH	brain:	n/a
19	chr12:8940171-8940221	HNPCEpiC	eye:	n/a
20	chr12:8947385-8947435	AG09309	skin:	n/a
21	chr12:8932036-8932086	HCM	heart:	n/a
22	chr12:8932036-8932086	ovcar-3	ovarian:	n/a
23	chr12:8940075-8940125	HUVEC	blood vessel:	n/a
24	chr12:8932036-8932086	GM12891	blood:	n/a
25	chr12:8940171-8940221	NT2-D1	testis:	n/a
26	chr12:8931477-8931527	PFSK-1	brain:	n/a
27	chr12:8940075-8940125	NH-A	brain:	n/a
28	chr12:8931239-8931289	AoSMC	blood vessel:	n/a
29	chr12:8931239-8931289	HEEpiC	esophagus:	n/a
30	chr12:8947385-8947435	HL-60	blood:	n/a
31	chr12:8940171-8940221	Hepatocyte	liver:	n/a
32	chr12:8947385-8947435	SAEC	small airway:	n/a
33	chr12:8932036-8932086	HCT-116	colon:	n/a
34	chr12:8931477-8931527	GM12891	blood:	n/a
35	chr12:8931239-8931289	HRCEpiC	kidney:	n/a
36	chr12:8947385-8947435	PFSK-1	brain:	n/a
37	chr12:8931477-8931527	HepG2	liver:	n/a
38	chr12:8940171-8940221	SK-N-SH_RA	brain:	n/a
39	chr12:8947385-8947435	GM12878	blood:	n/a
40	chr12:8940171-8940221	GM19239	blood:	n/a
41	chr12:8940075-8940125	HepG2	liver:	n/a
42	chr12:8931239-8931289	NT2-D1	testis:	n/a
43	chr12:8932036-8932086	MCF-7	breast:	n/a
44	chr12:8940171-8940221	HCPEpiC	choroid plexus:	n/a
45	chr12:8940075-8940125	HRCEpiC	kidney:	n/a
46	chr12:8940171-8940221	HAEpiC	amniotic membrane:	n/a
47	chr12:8931239-8931289	GM12891	blood:	n/a
48	chr12:8940075-8940125	RPTEC	kidney:	n/a
49	chr12:8940075-8940125	HCPEpiC	choroid plexus:	n/a
50	chr12:8932036-8932086	SK-N-SH_RA	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:8933396..8934033-chr12:8976044..8976692,2	MCF-7	breast:
2	chr12:8932743..8934022-chr12:9012782..9013946,5	MCF-7	breast:
3	chr12:8932764..8933606-chr12:9042861..9043830,2	MCF-7	breast:
4	chr12:8966691..8968770-chr12:8970773..8972791,2	K562	blood:
5	chr12:8848676..8851094-chr12:8930285..8932392,2	MCF-7	breast:
6	chr12:8928693..8931429-chr12:8932088..8934674,2	K562	blood:
7	chr12:8849261..8852154-chr12:8937447..8939184,2	K562	blood:
8	chr12:8849666..8851674-chr12:8967931..8970598,2	MCF-7	breast:
9	chr12:8954325..8956641-chr12:8972949..8974486,2	MCF-7	breast:
10	chr12:8925479..8928412-chr12:8982610..8985503,2	MCF-7	breast:
11	chr12:8932585..8933638-chr12:8975858..8976715,6	MCF-7	breast:
12	chr12:8928693..8931429-chr12:8932088..8934674,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-A2ML1-1	chr12:8929964-8930398	NONHSAT026362
2	lnc-A2ML1-1	chr12:8931627-8933335	NONHSAT026365
3	lnc-M6PR-3	chr12:8928815-8928980	ENSG00000256661.1
4	lnc-A2ML1-1	chr12:8935508-8935681	ENSG00000248882
5	lnc-A2ML1-1	chr12:8935508-8935691	NONHSAT026364
6	lnc-A2ML1-1	chr12:8935508-8935681	NONHSAT026362
7	lnc-A2ML1-1	chr12:8932408-8932708	NONHSAT026366
8	lnc-A2ML1-1	chr12:8932408-8932708	ENSG00000248882
9	lnc-MFAP5-1	chr12:8930460-8931191	ENSG00000249118
10	lnc-A2ML1-1	chr12:8930161-8930398	NONHSAT026363
11	lnc-A2ML1-1	chr12:8932631-8932708	NONHSAT026364
12	lnc-A2ML1-1	chr12:8933174-8933335	NONHSAT026363
13	lnc-A2ML1-1	chr12:8933171-8933335	NONHSAT026364
14	lnc-A2ML1-1	chr12:8935508-8935679	ENSG00000248882
15	lnc-A2ML1-1	chr12:8931627-8933335	ENSG00000248882
16	lnc-MFAP5-1	chr12:8929764-8930258	ENSG00000249118
17	lnc-A2ML1-1	chr12:8935508-8935691	NONHSAT026366
18	lnc-A2ML1-1	chr12:8935508-8935691	NONHSAT026365
19	lnc-A2ML1-1	chr12:8933171-8933335	NONHSAT026362
20	lnc-A2ML1-1	chr12:8933171-8933335	ENSG00000248882
21	lnc-A2ML1-1	chr12:8933171-8933335	NONHSAT026366
22	lnc-A2ML1-1	chr12:8930186-8930398	NONHSAT026364
23	lnc-A2ML1-1	chr12:8935508-8935682	NONHSAT026363

No data

Variant related genes	Relation type
RIMKLB	TF binding region
ENSG00000249790	TF binding region
RIMKLB	CpG island
ENSG00000249790	CpG island
ENSG00000256661	chromatin interactions
ENSG00000166535	chromatin interactions
ENSG00000166532	chromatin interactions
ENSG00000256904	chromatin interactions
ABCC3	miRNA target sites
PEX13	miRNA target sites
HNRNPD	miRNA target sites
PAFAH1B2	miRNA target sites
GALNT1	miRNA target sites

Extended variants
information (count: 1302 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1302 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9783460	chr12:8927520-8927521	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541721743	chr12:8927556-8927557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs202197030	chr12:8927571-8927572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148153196	chr12:8927582-8927583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531900677	chr12:8927710-8927711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs147418862	chr12:8927756-8927757	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182623919	chr12:8927770-8927771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186336552	chr12:8927804-8927805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141034003	chr12:8927976-8927977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548838302	chr12:8927999-8928000	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570155554	chr12:8928038-8928039	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150333388	chr12:8928173-8928174	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199751953	chr12:8928221-8928222	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568566501	chr12:8928283-8928284	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs368088232	chr12:8928333-8928334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs370221926	chr12:8928335-8928336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374575980	chr12:8928352-8928353	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs137965008	chr12:8928387-8928388	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560222200	chr12:8928407-8928408	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191041126	chr12:8928456-8928457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1476902	chr12:8928462-8928463	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566597247	chr12:8928488-8928489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538719566	chr12:8928505-8928506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117662233	chr12:8928552-8928553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371063742	chr12:8928580-8928581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114882326	chr12:8928668-8928669	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74061813	chr12:8928681-8928682	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs144920337	chr12:8928764-8928765	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575281962	chr12:8928773-8928774	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201556222	chr12:8928848-8928849	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs1056770	chr12:8928850-8928851	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs143440633	chr12:8928860-8928861	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs182881427	chr12:8928861-8928862	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs138723846	chr12:8928909-8928910	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs574635159	chr12:8928921-8928922	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs9783480	chr12:8929162-8929163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs540467355	chr12:8929173-8929174	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187652599	chr12:8929234-8929235	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147128275	chr12:8929251-8929252	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201084850	chr12:8929332-8929333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs58866787	chr12:8929382-8929383	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191768429	chr12:8929471-8929472	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs9783524	chr12:8929508-8929509	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs183380468	chr12:8929517-8929518	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs532504000	chr12:8929650-8929651	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs369508564	chr12:8929699-8929700	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs11554711	chr12:8929716-8929717	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs199731936	chr12:8929811-8929812	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs71045208	chr12:8929812-8929813	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs398018351	chr12:8929836-8929837	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8853200-8934000	Weak transcription	K562	blood
2	chr12:8875800-8933200	Weak transcription	Fetal Kidney	kidney
3	chr12:8878400-8937200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr12:8882200-8938400	Weak transcription	Spleen	Spleen
5	chr12:8882200-8939400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:8883400-8938800	Weak transcription	Primary B cells from cord blood	blood
7	chr12:8888800-8932000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr12:8889200-8935800	Weak transcription	A549	lung
9	chr12:8889200-8936600	Weak transcription	Brain Angular Gyrus	brain
10	chr12:8890600-8937000	Weak transcription	Colon Smooth Muscle	Colon
11	chr12:8894200-8937800	Weak transcription	Esophagus	oesophagus
12	chr12:8895400-8927600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr12:8895600-8935200	Weak transcription	HMEC	breast
14	chr12:8895600-8937800	Weak transcription	HSMMtube	muscle
15	chr12:8895600-8941200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:8897000-8931400	Weak transcription	Brain Anterior Caudate	brain
17	chr12:8899400-8941200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:8903000-8941200	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr12:8904600-8932000	Weak transcription	Gastric	stomach
20	chr12:8904600-8933200	Weak transcription	Fetal Brain Male	brain
21	chr12:8905000-8938400	Weak transcription	Pancreas	Pancrea
22	chr12:8905800-8941200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr12:8906000-8941200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr12:8906400-8937400	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr12:8906800-8941200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr12:8907000-8935600	Weak transcription	HSMM	muscle
27	chr12:8907000-8935600	Weak transcription	Osteobl	bone
28	chr12:8907000-8938200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr12:8907200-8928000	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr12:8907200-8934000	Weak transcription	Brain Substantia Nigra	brain
31	chr12:8907200-8936000	Weak transcription	Primary B cells from peripheral blood	blood
32	chr12:8907200-8937600	Weak transcription	NH-A	brain
33	chr12:8907400-8928600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:8907400-8930200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr12:8908200-8930000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr12:8908600-8931800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr12:8908600-8932000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr12:8908600-8941000	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr12:8908600-8941200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr12:8908600-8941200	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr12:8909800-8936400	Weak transcription	Brain Hippocampus Middle	brain
42	chr12:8911600-8937800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr12:8911800-8935600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr12:8913800-8938400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:8918400-8935800	Weak transcription	NHLF	lung
46	chr12:8918400-8937200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:8921000-8936200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr12:8921000-8937200	Weak transcription	Duodenum Mucosa	Duodenum
49	chr12:8922200-8936200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:8922800-8928600	Weak transcription	NHDF-Ad	bronchial

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