Variant report

Variant	nsv898810
Chromosome Location	chr12:12600080-12627410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:12602378-12603101	HepG2	liver:	n/a	n/a
2	BHLHE40	chr12:12617905-12618306	K562	blood:	n/a	n/a
3	BHLHE40	chr12:12614941-12615141	GM12878	blood:	n/a	chr12:12615057-12615066 chr12:12615056-12615065 chr12:12615051-12615072 chr12:12615057-12615066
4	BHLHE40	chr12:12602553-12603149	HepG2	liver:	n/a	n/a
5	CCNT2	chr12:12617885-12618266	K562	blood:	n/a	n/a
6	CEBPB	chr12:12609667-12610019	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:12602348-12603049	A549	lung:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
8	CEBPB	chr12:12602457-12602990	A549	lung:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
9	CEBPB	chr12:12602506-12603432	HepG2	liver:	n/a	chr12:12603282-12603295 chr12:12603282-12603293 chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
10	CEBPB	chr12:12619872-12619933	K562	blood:	n/a	chr12:12619918-12619929
11	CEBPB	chr12:12602677-12602848	H1-hESC	embryonic stem cell:	n/a	chr12:12602731-12602742 chr12:12602732-12602741
12	CEBPB	chr12:12619833-12620048	IMR90	lung:	n/a	chr12:12619918-12619929
13	CEBPB	chr12:12602529-12602947	ECC-1	luminal epithelium:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
14	CEBPB	chr12:12602666-12602822	K562	blood:	n/a	chr12:12602731-12602742 chr12:12602732-12602741
15	CEBPB	chr12:12603165-12603359	HepG2	liver:	n/a	chr12:12603282-12603295 chr12:12603282-12603293
16	CEBPB	chr12:12609717-12609982	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:12609712-12609983	K562	blood:	n/a	n/a
18	CEBPB	chr12:12619774-12620049	A549	lung:	n/a	chr12:12619918-12619929
19	CEBPB	chr12:12602408-12602999	Hela-S3	cervix:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
20	CEBPB	chr12:12603147-12603388	MCF-7	breast:	n/a	chr12:12603282-12603295 chr12:12603282-12603293
21	CEBPB	chr12:12602556-12602897	IMR90	lung:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
22	CEBPB	chr12:12619796-12619975	HepG2	liver:	n/a	chr12:12619918-12619929
23	CEBPB	chr12:12602408-12602904	HepG2	liver:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
24	CEBPB	chr12:12602477-12602908	ECC-1	luminal epithelium:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
25	CEBPB	chr12:12602392-12603024	MCF-7	breast:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
26	CEBPB	chr12:12603039-12603353	HepG2	liver:	n/a	chr12:12603282-12603295 chr12:12603282-12603293
27	CEBPB	chr12:12619855-12619939	Hela-S3	cervix:	n/a	chr12:12619918-12619929
28	CEBPB	chr12:12602580-12602842	HepG2	liver:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
29	CEBPB	chr12:12602415-12602993	MCF-7	breast:	n/a	chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
30	CEBPB	chr12:12602491-12603431	A549	lung:	n/a	chr12:12603282-12603295 chr12:12603282-12603293 chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
31	CEBPB	chr12:12602423-12603463	HepG2	liver:	n/a	chr12:12603282-12603295 chr12:12603282-12603293 chr12:12602731-12602742 chr12:12602732-12602741 chr12:12602654-12602671
32	CEBPD	chr12:12602565-12602909	HepG2	liver:	n/a	chr12:12602730-12602741
33	CEBPD	chr12:12617883-12618256	K562	blood:	n/a	n/a
34	CEBPD	chr12:12602467-12602904	HepG2	liver:	n/a	chr12:12602730-12602741
35	CEBPD	chr12:12617962-12618258	K562	blood:	n/a	n/a
36	CHD2	chr12:12602588-12603160	HepG2	liver:	n/a	n/a
37	CREB1	chr12:12602513-12603430	HepG2	liver:	n/a	n/a
38	CREB1	chr12:12602588-12602866	A549	lung:	n/a	n/a
39	CREB1	chr12:12602363-12603419	HepG2	liver:	n/a	n/a
40	CREB1	chr12:12602510-12602878	A549	lung:	n/a	n/a
41	CTCF	chr12:12602684-12602761	Lung_OC	lung:	n/a	chr12:12602739-12602760
42	CTCF	chr12:12620820-12620970	GM12864	blood:	n/a	n/a
43	CTCF	chr12:12609257-12609341	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr12:12618581-12618646	H1-hESC	embryonic stem cell:	n/a	n/a
45	E2F4	chr12:12609629-12609768	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr12:12622332-12622631	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr12:12602559-12602933	MCF10A-Er-Src	breast:	n/a	n/a
48	ELF1	chr12:12602586-12602919	HepG2	liver:	n/a	n/a
49	ELK4	chr12:12602531-12602882	Hela-S3	cervix:	n/a	n/a
50	EP300	chr12:12602457-12603381	HepG2	liver:	n/a	chr12:12603043-12603052

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12620523-12620573	AG04450	lung:	fetal
2	chr12:12605465-12605515	PFSK-1	brain:	n/a
3	chr12:12625652-12625702	AG09309	skin:	n/a
4	chr12:12619103-12619153	T-47D	breast:	n/a
5	chr12:12601972-12602022	NHDF-neo	bronchial:	n/a
6	chr12:12605465-12605515	GM12891	blood:	n/a
7	chr12:12618591-12618641	SKMC	muscle:	n/a
8	chr12:12605470-12605520	Jurkat	blood:	n/a
9	chr12:12625652-12625702	NH-A	brain:	n/a
10	chr12:12620523-12620573	SKMC	muscle:	n/a
11	chr12:12605426-12605476	HMEC	breast:	n/a
12	chr12:12618833-12618883	A549	lung:	n/a
13	chr12:12620789-12620839	HIPEpiC	eye:	n/a
14	chr12:12601972-12602022	SKMC	muscle:	n/a
15	chr12:12601972-12602022	K562	blood:	n/a
16	chr12:12619103-12619153	ECC-1	luminal epithelium:	n/a
17	chr12:12618833-12618883	HRPEpiC	eye:	n/a
18	chr12:12618833-12618883	AoSMC	blood vessel:	n/a
19	chr12:12618833-12618883	SK-N-SH_RA	brain:	n/a
20	chr12:12620789-12620839	T-47D	breast:	n/a
21	chr12:12605426-12605476	MCF-7	breast:	n/a
22	chr12:12618833-12618883	HMEC	breast:	n/a
23	chr12:12620523-12620573	HMEC	breast:	n/a
24	chr12:12601972-12602022	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:12618750-12618800	HCT-116	colon:	n/a
26	chr12:12605465-12605515	NH-A	brain:	n/a
27	chr12:12605470-12605520	HMEC	breast:	n/a
28	chr12:12618833-12618883	Hepatocyte	liver:	n/a
29	chr12:12605426-12605476	SKMC	muscle:	n/a
30	chr12:12618591-12618641	RPTEC	kidney:	n/a
31	chr12:12620789-12620839	A549	lung:	n/a
32	chr12:12605426-12605476	Hela-S3	cervix:	n/a
33	chr12:12620789-12620839	RPTEC	kidney:	n/a
34	chr12:12618750-12618800	HIPEpiC	eye:	n/a
35	chr12:12618833-12618883	AG09319	gingival:	n/a
36	chr12:12619103-12619153	NB4	blood:	n/a
37	chr12:12620789-12620839	HRCEpiC	kidney:	n/a
38	chr12:12620789-12620839	SAEC	small airway:	n/a
39	chr12:12601972-12602022	GM12892	blood:	n/a
40	chr12:12620523-12620573	NHDF-neo	bronchial:	n/a
41	chr12:12605426-12605476	AoSMC	blood vessel:	n/a
42	chr12:12605465-12605515	RPTEC	kidney:	n/a
43	chr12:12619103-12619153	SKMC	muscle:	n/a
44	chr12:12620523-12620573	T-47D	breast:	n/a
45	chr12:12618750-12618800	SK-N-SH_RA	brain:	n/a
46	chr12:12605470-12605520	HRPEpiC	eye:	n/a
47	chr12:12618591-12618641	SK-N-MC	brain:	n/a
48	chr12:12619103-12619153	SK-N-SH	brain:	n/a
49	chr12:12620523-12620573	HEEpiC	esophagus:	n/a
50	chr12:12618750-12618800	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:12598434..12601352-chr12:12712226..12715206,2	MCF-7	breast:
2	chr12:12603549..12606314-chr12:12607892..12609493,2	K562	blood:
3	chr12:12601179..12604143-chr12:12610929..12612812,2	MCF-7	breast:
4	chr12:12603843..12606415-chr12:12711459..12714793,4	MCF-7	breast:
5	chr12:12601431..12605552-chr12:12620970..12623954,4	MCF-7	breast:
6	chr12:12610566..12612701-chr12:12615346..12617410,2	K562	blood:
7	chr12:12604694..12606790-chr12:12616651..12618443,2	MCF-7	breast:
8	chr12:12612821..12616513-chr12:12617624..12619681,3	K562	blood:
9	chr12:12612821..12616513-chr12:12617624..12619681,3	K562	blood:
10	chr12:12624389..12628986-chr12:12712843..12715997,4	MCF-7	breast:
11	chr12:12609394..12612369-chr12:12615599..12621309,5	MCF-7	breast:
12	chr12:12584951..12586524-chr12:12601320..12603317,2	MCF-7	breast:
13	chr12:12594582..12598614-chr12:12600481..12604032,6	MCF-7	breast:
14	chr12:12601179..12604143-chr12:12610929..12612812,2	MCF-7	breast:
15	chr12:12609394..12612369-chr12:12615599..12621309,5	MCF-7	breast:
16	chr12:12610566..12612701-chr12:12615346..12617410,2	K562	blood:
17	chr12:12618969..12622557-chr12:12713241..12717041,4	MCF-7	breast:
18	chr12:12582548..12584902-chr12:12602163..12604980,2	MCF-7	breast:
19	chr12:12627271..12628158-chr12:12857310..12857811,2	K562	blood:
20	chr12:12601516..12605200-chr12:12712636..12717506,6	MCF-7	breast:
21	chr12:12601119..12602763-chr12:12605326..12608232,2	MCF-7	breast:
22	chr12:12602493..12604331-chr12:12739964..12742647,2	MCF-7	breast:
23	chr12:12620353..12622386-chr12:12763745..12766320,2	MCF-7	breast:
24	chr12:12602118..12604673-chr12:12687247..12689420,2	MCF-7	breast:
25	chr12:12617418..12619693-chr12:12712639..12714780,2	MCF-7	breast:
26	chr12:12621139..12623205-chr12:12630638..12633247,2	K562	blood:
27	chr12:12550464..12553838-chr12:12621141..12625480,5	MCF-7	breast:
28	chr12:12625312..12627407-chr12:12628734..12630245,2	MCF-7	breast:
29	chr12:12626427..12628119-chr12:12644483..12647018,2	K562	blood:
30	chr12:12601826..12603513-chr12:12715714..12717891,2	MCF-7	breast:
31	chr12:12509893..12512192-chr12:12607942..12610815,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DUSP16-1	chr12:12627157-12629731	NONHSAT026975
2	lnc-LOH12CR1-3	chr12:12626618-12628831	NONHSAT026972
3	lnc-DUSP16-3	chr12:12605037-12605415	NONHSAT026970

Variant related genes	Relation type
ENSG00000271370	TF binding region
ENSG00000271370	CpG island
ENSG00000111269	chromatin interactions
ENSG00000271370	chromatin interactions
ENSG00000111266	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000205791	chromatin interactions

Extended variants
information (count: 1265 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11054914	chr12:12600080-12600081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189927094	chr12:12600090-12600091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532422789	chr12:12600128-12600129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181080434	chr12:12600202-12600203	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563076294	chr12:12600225-12600226	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373657622	chr12:12600249-12600250	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs79171384	chr12:12600259-12600260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548848421	chr12:12600267-12600268	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567077332	chr12:12600289-12600290	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528143900	chr12:12600313-12600314	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186591518	chr12:12600365-12600366	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571185578	chr12:12600372-12600373	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141160430	chr12:12600412-12600413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561881588	chr12:12600415-12600416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538290241	chr12:12600514-12600515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs116808169	chr12:12600515-12600516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569103536	chr12:12600529-12600530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565461294	chr12:12600547-12600548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35764737	chr12:12600583-12600584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146956805	chr12:12600624-12600625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs137963998	chr12:12600625-12600626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs113763784	chr12:12600668-12600669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572705228	chr12:12600687-12600688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs140913699	chr12:12600690-12600691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7309503	chr12:12600701-12600702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs143535766	chr12:12600724-12600725	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537509912	chr12:12600761-12600762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544310159	chr12:12600773-12600774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534661469	chr12:12600789-12600790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147289942	chr12:12600810-12600811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575073492	chr12:12600819-12600820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111980848	chr12:12600825-12600826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542541847	chr12:12600842-12600843	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560638135	chr12:12600886-12600887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527900344	chr12:12600924-12600925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191340073	chr12:12601041-12601042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183659339	chr12:12601050-12601051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534431771	chr12:12601088-12601089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs112133663	chr12:12601098-12601099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs188485737	chr12:12601099-12601100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs60022096	chr12:12601157-12601158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568844847	chr12:12601203-12601204	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs536095801	chr12:12601214-12601215	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190759108	chr12:12601216-12601217	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs368138135	chr12:12601260-12601261	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs148357267	chr12:12601284-12601285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs566296764	chr12:12601310-12601311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs533775561	chr12:12601336-12601337	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368446359	chr12:12601353-12601354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558990811	chr12:12601395-12601396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	17690704	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
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
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	21088497	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12587400-12600200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:12587400-12600200	Weak transcription	Ovary	ovary
3	chr12:12589800-12607200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:12590400-12601800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:12590600-12614600	Weak transcription	Primary B cells from cord blood	blood
6	chr12:12592200-12600400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:12592200-12602200	Enhancers	Fetal Thymus	thymus
8	chr12:12594400-12600200	Weak transcription	Lung	lung
9	chr12:12594400-12618200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr12:12594800-12600400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr12:12595000-12602200	Weak transcription	Placenta	Placenta
12	chr12:12595200-12600200	Weak transcription	Fetal Intestine Large	intestine
13	chr12:12595200-12602800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:12595200-12609200	Weak transcription	GM12878-XiMat	blood
15	chr12:12595200-12618600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr12:12595800-12600200	Weak transcription	Fetal Intestine Small	intestine
17	chr12:12596000-12602200	Weak transcription	A549	lung
18	chr12:12596000-12620200	Weak transcription	HSMM	muscle
19	chr12:12596000-12629800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr12:12596200-12620600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:12596400-12600600	Weak transcription	Hela-S3	cervix
22	chr12:12596400-12603200	Weak transcription	Aorta	Aorta
23	chr12:12596600-12601000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr12:12596800-12602000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr12:12596800-12602400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr12:12596800-12603000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr12:12596800-12604600	Weak transcription	NHLF	lung
28	chr12:12596800-12618200	Weak transcription	Primary T cells from cord blood	blood
29	chr12:12596800-12618200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr12:12597000-12600200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr12:12597000-12600200	Weak transcription	Right Atrium	heart
32	chr12:12597000-12600400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr12:12597000-12601600	Weak transcription	Spleen	Spleen
34	chr12:12597000-12602400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr12:12597000-12602600	Weak transcription	Esophagus	oesophagus
36	chr12:12597000-12603000	Weak transcription	Psoas Muscle	Psoas
37	chr12:12597000-12617800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:12597200-12603000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr12:12597400-12600200	Weak transcription	Fetal Stomach	stomach
40	chr12:12597400-12601600	Weak transcription	Pancreas	Pancrea
41	chr12:12597400-12601800	Weak transcription	Liver	Liver
42	chr12:12597400-12618200	Weak transcription	Gastric	stomach
43	chr12:12597400-12629000	Weak transcription	Rectal Smooth Muscle	rectum
44	chr12:12597600-12600200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr12:12597600-12600200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr12:12597600-12600200	Weak transcription	Fetal Muscle Leg	muscle
47	chr12:12597600-12600200	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr12:12597600-12600400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr12:12597600-12602000	Weak transcription	Stomach Smooth Muscle	stomach
50	chr12:12598000-12602200	Enhancers	HepG2	liver

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