Variant report

Variant	esv3490839
Chromosome Location	chr14:21565112-21567760
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	chr14:21567064-21567210	HepG2	liver:	n/a	n/a
2	BACH1	chr14:21566963-21567035	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr14:21566956-21567119	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr14:21566992-21567190	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr14:21566640-21566835	K562	blood:	n/a	chr14:21566787-21566796
6	CEBPB	chr14:21566797-21567029	Hela-S3	cervix:	n/a	n/a
7	CEBPD	chr14:21565859-21566462	HepG2	liver:	n/a	n/a
8	CEBPD	chr14:21566491-21567051	HepG2	liver:	n/a	n/a
9	CHD2	chr14:21566675-21567172	HepG2	liver:	n/a	chr14:21566788-21566798
10	CHD2	chr14:21565877-21566217	Hela-S3	cervix:	n/a	chr14:21566153-21566163
11	CHD2	chr14:21566761-21567020	H1-hESC	embryonic stem cell:	n/a	chr14:21566788-21566798
12	CHD2	chr14:21566647-21567112	Hela-S3	cervix:	n/a	chr14:21566660-21566670 chr14:21566788-21566798
13	CHD2	chr14:21566022-21566147	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr14:21565722-21566195	HepG2	liver:	n/a	chr14:21566153-21566163
15	CTCF	chr14:21566660-21566810	GM12865	blood:	n/a	chr14:21566782-21566791
16	CTCF	chr14:21566780-21566930	AG04449	skin:	n/a	chr14:21566782-21566791
17	CTCF	chr14:21566644-21566943	K562	blood:	n/a	chr14:21566782-21566791 chr14:21566658-21566671
18	CTCF	chr14:21566720-21566870	BJ	skin:	n/a	chr14:21566782-21566791
19	CTCF	chr14:21566700-21566850	GM12866	blood:	n/a	chr14:21566782-21566791
20	CTCF	chr14:21566771-21566828	GM12878	blood:	n/a	chr14:21566782-21566791
21	CTCF	chr14:21566700-21566850	GM12875	blood:	n/a	chr14:21566782-21566791
22	CTCF	chr14:21566740-21566890	Caco-2	colon:	n/a	chr14:21566782-21566791
23	CTCF	chr14:21566820-21566970	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr14:21566820-21566970	AG09309	skin:	n/a	n/a
25	CTCF	chr14:21566700-21566850	SK-N-SH_RA	brain:	n/a	chr14:21566782-21566791
26	CTCF	chr14:21566740-21566890	BJ	skin:	n/a	chr14:21566782-21566791
27	CTCF	chr14:21565460-21565610	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr14:21566646-21566921	HepG2	liver:	n/a	chr14:21566782-21566791 chr14:21566658-21566671
29	CTCF	chr14:21566680-21566830	SAEC	small airway:	n/a	chr14:21566782-21566791
30	CTCF	chr14:21566740-21566890	AG04450	lung:	n/a	chr14:21566782-21566791
31	CTCF	chr14:21566720-21566870	Caco-2	colon:	n/a	chr14:21566782-21566791
32	CTCF	chr14:21566740-21566890	GM12872	blood:	n/a	chr14:21566782-21566791
33	CTCF	chr14:21566700-21566850	HepG2	liver:	n/a	chr14:21566782-21566791
34	CTCF	chr14:21566780-21566930	GM12868	blood:	n/a	chr14:21566782-21566791
35	CTCF	chr14:21566740-21566890	GM12866	blood:	n/a	chr14:21566782-21566791
36	CTCF	chr14:21566740-21566890	HepG2	liver:	n/a	chr14:21566782-21566791
37	CTCF	chr14:21566900-21567050	GM12875	blood:	n/a	n/a
38	CTCF	chr14:21566776-21566831	IMR90	lung:	n/a	chr14:21566782-21566791
39	CTCF	chr14:21566760-21566910	HMEC	breast:	n/a	chr14:21566782-21566791
40	CTCF	chr14:21566780-21566930	HAc	cerebellar:	n/a	chr14:21566782-21566791
41	CTCF	chr14:21566760-21566910	AG09319	gingival:	n/a	chr14:21566782-21566791
42	CTCF	chr14:21566760-21566910	HRPEpiC	eye:	n/a	chr14:21566782-21566791
43	CTCF	chr14:21566920-21567070	HRE	kidney:	n/a	n/a
44	CTCF	chr14:21566760-21566910	HCPEpiC	choroid plexus:	n/a	chr14:21566782-21566791
45	CTCF	chr14:21566660-21566810	HUVEC	blood vessel:	n/a	chr14:21566782-21566791
46	CTCF	chr14:21566680-21566830	Hela-S3	cervix:	n/a	chr14:21566782-21566791
47	CTCF	chr14:21566780-21566930	RPTEC	kidney:	n/a	chr14:21566782-21566791
48	CTCF	chr14:21566832-21566843	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:21566743-21566768	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr14:21566800-21566950	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21567333-21567383	HEK293	kidney:	embryo
2	chr14:21566084-21566134	AoSMC	blood vessel:	n/a
3	chr14:21567520-21567570	PrEC	prostate:	n/a
4	chr14:21567520-21567570	NB4	blood:	n/a
5	chr14:21567020-21567070	GM12891	blood:	n/a
6	chr14:21567520-21567570	AG04450	lung:	fetal
7	chr14:21565335-21565385	PANC-1	pancreas:	n/a
8	chr14:21567020-21567070	HRCEpiC	kidney:	n/a
9	chr14:21567520-21567570	HAEpiC	amniotic membrane:	n/a
10	chr14:21566452-21566502	HUVEC	blood vessel:	n/a
11	chr14:21566698-21566748	GM12892	blood:	n/a
12	chr14:21566452-21566502	U87	brain:	n/a
13	chr14:21566452-21566502	HEEpiC	esophagus:	n/a
14	chr14:21567646-21567696	HEEpiC	esophagus:	n/a
15	chr14:21567520-21567570	ECC-1	luminal epithelium:	n/a
16	chr14:21566452-21566502	HNPCEpiC	eye:	n/a
17	chr14:21567333-21567383	HepG2	liver:	n/a
18	chr14:21566452-21566502	ProgFib	skin:	n/a
19	chr14:21565335-21565385	LNCaP	prostate:	n/a
20	chr14:21567020-21567070	HUVEC	blood vessel:	n/a
21	chr14:21567164-21567214	BJ	skin:	n/a
22	chr14:21566863-21566913	NHBE	bronchial:	n/a
23	chr14:21566698-21566748	K562	blood:	n/a
24	chr14:21567333-21567383	HCF	heart:	n/a
25	chr14:21567333-21567383	GM06990	blood:	n/a
26	chr14:21567520-21567570	BE2_C	brain:	n/a
27	chr14:21567164-21567214	HEK293	kidney:	embryo
28	chr14:21566863-21566913	GM12878	blood:	n/a
29	chr14:21567164-21567214	HL-60	blood:	n/a
30	chr14:21567646-21567696	Jurkat	blood:	n/a
31	chr14:21567646-21567696	HL-60	blood:	n/a
32	chr14:21565335-21565385	GM19239	blood:	n/a
33	chr14:21567020-21567070	HEEpiC	esophagus:	n/a
34	chr14:21567333-21567383	AG09309	skin:	n/a
35	chr14:21566863-21566913	PANC-1	pancreas:	n/a
36	chr14:21567646-21567696	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:21567646-21567696	HAEpiC	amniotic membrane:	n/a
38	chr14:21566863-21566913	Caco-2	colon:	n/a
39	chr14:21566452-21566502	AG09319	gingival:	n/a
40	chr14:21567520-21567570	GM12892	blood:	n/a
41	chr14:21566698-21566748	LNCaP	prostate:	n/a
42	chr14:21566084-21566134	BJ	skin:	n/a
43	chr14:21566698-21566748	BJ	skin:	n/a
44	chr14:21566698-21566748	AG10803	skin:	n/a
45	chr14:21565335-21565385	SK-N-SH_RA	brain:	n/a
46	chr14:21567333-21567383	NB4	blood:	n/a
47	chr14:21565335-21565385	NHDF-neo	bronchial:	n/a
48	chr14:21567520-21567570	HCPEpiC	choroid plexus:	n/a
49	chr14:21567520-21567570	Hela-S3	cervix:	n/a
50	chr14:21567333-21567383	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21534879..21542621-chr14:21563384..21568050,9	MCF-7	breast:
2	chr14:21563448..21565255-chr14:21566010..21568675,2	K562	blood:
3	chr14:21566818..21567426-chr5:145582956..145583681,2	Hela-S3	cervix:
4	chr14:21488163..21490230-chr14:21563775..21566660,2	K562	blood:
5	chr14:21529965..21532217-chr14:21564746..21566795,2	MCF-7	breast:
6	chr14:21520181..21522093-chr14:21562731..21565529,2	MCF-7	breast:
7	chr14:21559218..21562308-chr14:21563084..21566776,3	K562	blood:
8	chr14:21493156..21496539-chr14:21563277..21566869,4	K562	blood:
9	chr14:21535130..21541812-chr14:21564802..21576767,22	MCF-7	breast:
10	chr14:21560808..21562943-chr14:21563849..21565971,2	K562	blood:
11	chr14:21538435..21540879-chr14:21565246..21568452,4	K562	blood:
12	chr14:21493465..21495146-chr14:21564517..21566869,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDRG2-4	chr14:21566970-21567070	NONHSAT035653

Variant related genes	Relation type
TMEM253	TF binding region
ZNF219	TF binding region
TMEM253	CpG island
ZNF219	CpG island
ENSG00000165804	chromatin interactions
ENSG00000091009	chromatin interactions
ENSG00000232070	chromatin interactions
ENSG00000165795	chromatin interactions
ENSG00000165801	chromatin interactions

Extended variants
information (count: 53 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:53 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2319625	chr14:21565146-21565147	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2319626	chr14:21565149-21565150	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs145462239	chr14:21565173-21565174	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs2319627	chr14:21565189-21565190	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs139529198	chr14:21565210-21565211	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs181812225	chr14:21565245-21565246	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs145168638	chr14:21565461-21565462	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs563513831	chr14:21565525-21565526	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs529196610	chr14:21565535-21565536	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs549323818	chr14:21565545-21565546	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs147924751	chr14:21565547-21565548	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs186358365	chr14:21565569-21565570	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs551772750	chr14:21565707-21565708	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs369793244	chr14:21565732-21565733	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs537593788	chr14:21565795-21565796	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs550759574	chr14:21565834-21565835	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs567549041	chr14:21565971-21565972	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs536533535	chr14:21565989-21565990	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs2771315	chr14:21566003-21566004	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs573505502	chr14:21566030-21566031	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs10132732	chr14:21566277-21566278	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs534278641	chr14:21566642-21566643	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs557745933	chr14:21566806-21566807	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs543586855	chr14:21566926-21566927	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs563448693	chr14:21567006-21567007	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs191453915	chr14:21567072-21567073	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs542857911	chr14:21567075-21567076	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs559356509	chr14:21567111-21567112	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs551555110	chr14:21567132-21567133	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs528390137	chr14:21567165-21567166	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs551445571	chr14:21567195-21567196	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs565327875	chr14:21567233-21567234	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs141801608	chr14:21567236-21567237	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs564627691	chr14:21567282-21567283	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs12889457	chr14:21567333-21567334	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143814256	chr14:21567336-21567337	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs376840256	chr14:21567407-21567408	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs35669186	chr14:21567410-21567411	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs530123687	chr14:21567420-21567421	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs536421752	chr14:21567465-21567466	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs546796546	chr14:21567484-21567485	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs1952512	chr14:21567489-21567490	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs117522219	chr14:21567587-21567588	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs559591755	chr14:21567631-21567632	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs557462213	chr14:21567646-21567647	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs61978231	chr14:21567652-21567653	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs533236748	chr14:21567665-21567666	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs370143579	chr14:21567676-21567677	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs78148191	chr14:21567695-21567696	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs550234222	chr14:21567700-21567701	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21545200-21565600	Weak transcription	Psoas Muscle	Psoas
2	chr14:21555800-21565600	Weak transcription	HSMMtube	muscle
3	chr14:21555800-21566200	Weak transcription	HSMM	muscle
4	chr14:21556200-21565400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr14:21556400-21565200	Weak transcription	Primary T cells from cord blood	blood
6	chr14:21556400-21565600	Weak transcription	Primary B cells from cord blood	blood
7	chr14:21556600-21565200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr14:21556600-21565400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr14:21556800-21565200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr14:21558400-21565400	Weak transcription	Stomach Mucosa	stomach
11	chr14:21558800-21566600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr14:21559800-21566600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:21560200-21565400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr14:21560200-21565400	Weak transcription	Aorta	Aorta
15	chr14:21560400-21565400	Enhancers	Fetal Heart	heart
16	chr14:21560600-21565600	Enhancers	Brain Hippocampus Middle	brain
17	chr14:21560800-21565800	Weak transcription	Small Intestine	intestine
18	chr14:21561000-21565800	Weak transcription	Ovary	ovary
19	chr14:21561200-21565200	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr14:21561200-21565200	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr14:21561200-21565400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr14:21561200-21565400	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr14:21561200-21565400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr14:21561200-21565400	Weak transcription	Colonic Mucosa	Colon
25	chr14:21561200-21565400	Weak transcription	Dnd41	blood
26	chr14:21561200-21565600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr14:21561200-21565600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr14:21561400-21565200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr14:21561600-21565200	Weak transcription	Lung	lung
30	chr14:21561600-21565400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr14:21561600-21566600	Weak transcription	Gastric	stomach
32	chr14:21561600-21566800	Weak transcription	Spleen	Spleen
33	chr14:21561800-21565200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr14:21561800-21565200	Enhancers	Fetal Thymus	thymus
35	chr14:21562000-21566000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr14:21562200-21566800	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr14:21562400-21565200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr14:21562400-21565200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr14:21562400-21565200	Weak transcription	Pancreas	Pancrea
40	chr14:21562400-21565600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr14:21562600-21565200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr14:21562600-21565200	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr14:21562600-21565400	Weak transcription	NH-A	brain
44	chr14:21562600-21565600	Weak transcription	Brain Anterior Caudate	brain
45	chr14:21562600-21566800	Weak transcription	Liver	Liver
46	chr14:21562800-21565200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:21562800-21565200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr14:21562800-21565200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:21562800-21565200	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr14:21562800-21565200	Weak transcription	Fetal Muscle Trunk	muscle

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