Variant report

Variant	nsv557385
Chromosome Location	chr12:9556721-9577310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:549)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:9574493-9574708	GM12878	blood:	n/a	n/a
2	BATF	chr12:9560636-9560925	GM12878	blood:	n/a	n/a
3	BCL11A	chr12:9564505-9564797	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:9564391-9564639	GM12878	blood:	n/a	n/a
5	CEBPB	chr12:9561882-9562084	HepG2	liver:	n/a	n/a
6	CTCF	chr12:9572556-9572580	GM10248	blood:	n/a	n/a
7	CTCF	chr12:9564865-9565009	K562	blood:	n/a	n/a
8	CTCF	chr12:9571174-9571189	MCF-7	breast:	n/a	n/a
9	CTCF	chr12:9564942-9565007	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr12:9571200-9571280	LNCaP	prostate:	n/a	n/a
11	CTCF	chr12:9576944-9576986	NHEK	skin:	n/a	n/a
12	CTCF	chr12:9564891-9565003	MCF-7	breast:	n/a	n/a
13	CTCF	chr12:9564939-9564974	GM12891	blood:	n/a	n/a
14	CTCF	chr12:9576926-9577031	LNCaP	prostate:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
15	CTCF	chr12:9576937-9576999	H1-hESC	embryonic stem cell:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
16	CTCF	chr12:9576938-9577019	GM12891	blood:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
17	CTCF	chr12:9576950-9576971	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:9564888-9565004	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:9564955-9564994	NHEK	skin:	n/a	n/a
20	CTCF	chr12:9569276-9569366	GM13976	blood:	n/a	n/a
21	CTCF	chr12:9576927-9577004	GM12892	blood:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
22	CTCF	chr12:9576915-9577017	MCF-7	breast:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
23	CTCF	chr12:9576913-9576999	MCF-7	breast:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
24	CTCF	chr12:9573096-9573215	Lung_OC	lung:	n/a	n/a
25	CTCF	chr12:9564895-9565004	GM12878	blood:	n/a	n/a
26	CTCF	chr12:9576880-9577013	MCF-7	breast:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
27	CTCF	chr12:9559898-9559995	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr12:9576896-9577057	GM13976	blood:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
29	CTCF	chr12:9564893-9565003	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:9569018-9569050	GM20000	blood:	n/a	n/a
31	CTCF	chr12:9576914-9577032	GM10266	blood:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
32	CTCF	chr12:9564875-9565007	GM19238	blood:	n/a	n/a
33	CTCF	chr12:9564927-9564999	GM19240	blood:	n/a	n/a
34	CTCF	chr12:9576949-9577065	LNCaP	prostate:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
35	CTCF	chr12:9564896-9565031	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr12:9576911-9577009	HepG2	liver:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
37	CTCF	chr12:9576943-9576949	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:9570603-9570657	GM13976	blood:	n/a	n/a
39	CTCF	chr12:9575168-9575296	GM10248	blood:	n/a	n/a
40	CTCF	chr12:9564884-9565025	GM19239	blood:	n/a	n/a
41	CTCF	chr12:9576942-9576987	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:9568917-9568998	Lung_OC	lung:	n/a	n/a
43	CTCF	chr12:9576944-9577004	Pancreas_OC	pancreas:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
44	CTCF	chr12:9576915-9577007	Hela-S3	cervix:	n/a	chr12:9576967-9576988 chr12:9576972-9576990
45	CTCF	chr12:9564877-9565011	GM12892	blood:	n/a	n/a
46	CTCF	chr12:9557460-9557610	GM12866	blood:	n/a	n/a
47	CTCF	chr12:9564889-9564998	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:9564891-9565000	A549	lung:	n/a	n/a
49	CTCF	chr12:9566834-9566892	GM13976	blood:	n/a	n/a
50	CTCF	chr12:9576494-9576508	GM10248	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9559693-9559743	HNPCEpiC	eye:	n/a
2	chr12:9557316-9557366	AG04450	lung:	fetal
3	chr12:9571130-9571180	T-47D	breast:	n/a
4	chr12:9557316-9557366	A549	lung:	n/a
5	chr12:9557316-9557366	HEEpiC	esophagus:	n/a
6	chr12:9559402-9559452	MCF-7	breast:	n/a
7	chr12:9568315-9568365	NHBE	bronchial:	n/a
8	chr12:9559693-9559743	NHDF-neo	bronchial:	n/a
9	chr12:9571130-9571180	AG04449	skin:	fetal
10	chr12:9573914-9573964	SKMC	muscle:	n/a
11	chr12:9573914-9573964	HIPEpiC	eye:	n/a
12	chr12:9557205-9557255	NB4	blood:	n/a
13	chr12:9571130-9571180	PANC-1	pancreas:	n/a
14	chr12:9557316-9557366	PrEC	prostate:	n/a
15	chr12:9569744-9569794	HEK293	kidney:	embryo
16	chr12:9568315-9568365	AG09319	gingival:	n/a
17	chr12:9557205-9557255	GM06990	blood:	n/a
18	chr12:9557205-9557255	AG10803	skin:	n/a
19	chr12:9568315-9568365	HepG2	liver:	n/a
20	chr12:9573914-9573964	AG09309	skin:	n/a
21	chr12:9559693-9559743	Hepatocyte	liver:	n/a
22	chr12:9568315-9568365	GM12878	blood:	n/a
23	chr12:9556998-9557048	HMEC	breast:	n/a
24	chr12:9556998-9557048	MCF10A-Er-Src	breast:	n/a
25	chr12:9557205-9557255	Jurkat	blood:	n/a
26	chr12:9559693-9559743	NHBE	bronchial:	n/a
27	chr12:9569744-9569794	NH-A	brain:	n/a
28	chr12:9557316-9557366	HCPEpiC	choroid plexus:	n/a
29	chr12:9571130-9571180	SK-N-SH	brain:	n/a
30	chr12:9559402-9559452	NHDF-neo	bronchial:	n/a
31	chr12:9557316-9557366	HCM	heart:	n/a
32	chr12:9568315-9568365	HRCEpiC	kidney:	n/a
33	chr12:9571130-9571180	MCF10A-Er-Src	breast:	n/a
34	chr12:9556998-9557048	NH-A	brain:	n/a
35	chr12:9569744-9569794	GM06990	blood:	n/a
36	chr12:9559402-9559452	HIPEpiC	eye:	n/a
37	chr12:9559402-9559452	NB4	blood:	n/a
38	chr12:9573914-9573964	MCF-7	breast:	n/a
39	chr12:9559402-9559452	T-47D	breast:	n/a
40	chr12:9559693-9559743	AG04450	lung:	fetal
41	chr12:9571130-9571180	Hepatocyte	liver:	n/a
42	chr12:9569744-9569794	SK-N-SH	brain:	n/a
43	chr12:9568315-9568365	BJ	skin:	n/a
44	chr12:9556998-9557048	HRCEpiC	kidney:	n/a
45	chr12:9559402-9559452	NT2-D1	testis:	n/a
46	chr12:9571130-9571180	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:9559693-9559743	HCM	heart:	n/a
48	chr12:9568315-9568365	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:9559693-9559743	HRCEpiC	kidney:	n/a
50	chr12:9559693-9559743	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9471764..9473665-chr12:9564371..9566160,2	MCF-7	breast:
2	chr12:9471846..9472542-chr12:9564639..9565202,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PZP-12	chr12:9561452-9561545	NONHSAT026823
2	lnc-PZP-12	chr12:9559865-9560050	NONHSAT026823
3	lnc-PZP-12	chr12:9566315-9566384	NONHSAT026823
4	lnc-PZP-12	chr12:9564668-9564845	NONHSAT026825
5	lnc-PZP-12	chr12:9565722-9566143	NONHSAT026825
6	lnc-PZP-12	chr12:9567399-9567447	NONHSAT026817
7	lnc-PZP-12	chr12:9558904-9559128	NONHSAT026823
8	lnc-PZP-12	chr12:9565722-9566137	NONHSAT026823
9	lnc-PZP-12	chr12:9561452-9561545	NONHSAT026825

No data

Variant related genes	Relation type
ENSG00000256673	TF binding region
ENSG00000256673	CpG island

Extended variants
information (count: 779 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:779 , 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	rs183080591	chr12:9556735-9556736	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs115631690	chr12:9556745-9556746	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs150520636	chr12:9556761-9556762	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs113710776	chr12:9556766-9556767	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs74062835	chr12:9556783-9556784	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs139581533	chr12:9556786-9556787	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs114532487	chr12:9556816-9556817	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs80167009	chr12:9556834-9556835	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs76498168	chr12:9556841-9556842	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs369273105	chr12:9556852-9556853	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs144506622	chr12:9556853-9556854	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs371673323	chr12:9556871-9556872	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs55971813	chr12:9556875-9556876	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs71450676	chr12:9556876-9556877	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs113997685	chr12:9556947-9556948	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs536614575	chr12:9556948-9556949	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs74062836	chr12:9556956-9556957	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs187207320	chr12:9556991-9556992	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs112515547	chr12:9556994-9556995	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs67356861	chr12:9556999-9557000	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs369591269	chr12:9557009-9557010	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs79179192	chr12:9557014-9557015	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs77841000	chr12:9557020-9557021	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	mRNA abundance
24	rs77138230	chr12:9557029-9557030	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs528894765	chr12:9557050-9557051	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs56222234	chr12:9557062-9557063	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs113191504	chr12:9557069-9557070	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs559222662	chr12:9557121-9557122	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs144540660	chr12:9557122-9557123	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs191291020	chr12:9557126-9557127	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs116955000	chr12:9557187-9557188	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs377532097	chr12:9557206-9557207	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs75836549	chr12:9557243-9557244	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs79593855	chr12:9557247-9557248	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76655007	chr12:9557249-9557250	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs145448205	chr12:9557282-9557283	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs79050883	chr12:9557287-9557288	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs80038428	chr12:9557288-9557289	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs377310494	chr12:9557290-9557291	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs550781143	chr12:9557292-9557293	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs147669247	chr12:9557298-9557299	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs183874885	chr12:9557312-9557313	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs189391288	chr12:9557316-9557317	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs76265690	chr12:9557334-9557335	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs76581120	chr12:9557336-9557337	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs80237452	chr12:9557342-9557343	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs79389737	chr12:9557343-9557344	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs77621531	chr12:9557348-9557349	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs369384769	chr12:9557349-9557350	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs77665813	chr12:9557350-9557351	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	22237106	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
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9541400-9557200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:9541800-9557400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:9544800-9593200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:9545400-9573800	Weak transcription	Fetal Intestine Small	intestine
5	chr12:9545400-9575600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:9546200-9559400	Weak transcription	A549	lung
7	chr12:9547000-9558600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr12:9547200-9556800	Weak transcription	Fetal Stomach	stomach
9	chr12:9547400-9557400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr12:9549400-9558800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:9549400-9559200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr12:9549400-9564000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:9551400-9557000	Weak transcription	Dnd41	blood
14	chr12:9555200-9557600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:9555600-9559400	Weak transcription	Colonic Mucosa	Colon
16	chr12:9555800-9557400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:9555800-9557400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr12:9555800-9557800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:9555800-9558400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr12:9556200-9558400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr12:9556400-9557400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:9556600-9557200	ZNF genes & repeats	Fetal Thymus	thymus
23	chr12:9556600-9557800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:9556800-9557400	ZNF genes & repeats	Fetal Stomach	stomach
25	chr12:9557000-9557600	ZNF genes & repeats	Dnd41	blood
26	chr12:9557200-9557600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:9557200-9557800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:9557200-9557800	Bivalent/Poised TSS	Right Ventricle	heart
29	chr12:9557400-9557600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:9557400-9557600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:9557400-9557800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
32	chr12:9557400-9557800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:9557400-9557800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:9557400-9557800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr12:9557400-9558400	Weak transcription	Fetal Stomach	stomach
36	chr12:9557400-9558600	Strong transcription	Fetal Muscle Trunk	muscle
37	chr12:9557400-9559200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr12:9557400-9559400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:9557400-9564200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:9557600-9557800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr12:9557600-9557800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr12:9557600-9557800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr12:9557600-9558600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:9557600-9559800	Enhancers	Fetal Brain Male	brain
45	chr12:9557600-9564200	Weak transcription	Dnd41	blood
46	chr12:9557600-9572200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr12:9557800-9558600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:9557800-9558800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:9557800-9558800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:9557800-9558800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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