Variant report

Variant	esv3387789
Chromosome Location	chr10:43891371-43893919
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	chr10:43892798-43893411	K562	blood:	n/a	n/a
2	ARID3A	chr10:43892044-43892296	K562	blood:	n/a	chr10:43892110-43892118
3	ARID3A	chr10:43891438-43891819	K562	blood:	n/a	n/a
4	ARID3A	chr10:43891217-43892212	HepG2	liver:	n/a	chr10:43892110-43892118
5	ARID3A	chr10:43892495-43893285	HepG2	liver:	n/a	n/a
6	ATF2	chr10:43892624-43892978	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr10:43891867-43892324	GM12878	blood:	n/a	n/a
8	ATF2	chr10:43892485-43893095	GM12878	blood:	n/a	n/a
9	ATF3	chr10:43892571-43892839	GM12878	blood:	n/a	n/a
10	ATF3	chr10:43892493-43892834	HepG2	liver:	n/a	n/a
11	ATF3	chr10:43892451-43892948	K562	blood:	n/a	n/a
12	ATF3	chr10:43892603-43893090	A549	lung:	n/a	n/a
13	ATF3	chr10:43892491-43892912	GM12878	blood:	n/a	n/a
14	BACH1	chr10:43892173-43892220	K562	blood:	n/a	n/a
15	BACH1	chr10:43892568-43893314	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:43891056-43891449	K562	blood:	n/a	n/a
17	BACH1	chr10:43891708-43891916	K562	blood:	n/a	n/a
18	BATF	chr10:43892653-43892874	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:43892568-43892914	GM12878	blood:	n/a	chr10:43892835-43892844 chr10:43892579-43892592
20	BCL3	chr10:43892382-43892873	GM12878	blood:	n/a	chr10:43892835-43892844 chr10:43892557-43892566 chr10:43892579-43892592
21	BCL3	chr10:43891620-43893205	A549	lung:	n/a	chr10:43892923-43892932 chr10:43891819-43891828 chr10:43892274-43892287 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43893061-43893070 chr10:43892579-43892592
22	BCL3	chr10:43892530-43893390	K562	blood:	n/a	chr10:43892923-43892932 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43893061-43893070 chr10:43892579-43892592
23	BCL3	chr10:43892534-43893052	A549	lung:	n/a	chr10:43892923-43892932 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43892579-43892592
24	BCL3	chr10:43891996-43893049	GM12878	blood:	n/a	chr10:43892923-43892932 chr10:43892274-43892287 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43892579-43892592
25	BCLAF1	chr10:43892353-43893309	K562	blood:	n/a	chr10:43892923-43892932 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43893061-43893070 chr10:43892579-43892592
26	BCLAF1	chr10:43891709-43892305	GM12878	blood:	n/a	chr10:43891819-43891828 chr10:43892274-43892287
27	BCLAF1	chr10:43892384-43893114	GM12878	blood:	n/a	chr10:43892923-43892932 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43893061-43893070 chr10:43892579-43892592
28	BCLAF1	chr10:43891883-43892305	K562	blood:	n/a	chr10:43892274-43892287
29	BCLAF1	chr10:43892488-43893055	GM12878	blood:	n/a	chr10:43892923-43892932 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43892579-43892592
30	BCLAF1	chr10:43891834-43892276	GM12878	blood:	n/a	n/a
31	BCLAF1	chr10:43892516-43893671	K562	blood:	n/a	chr10:43892923-43892932 chr10:43892835-43892844 chr10:43892557-43892566 chr10:43893061-43893070 chr10:43892579-43892592
32	BHLHE40	chr10:43892454-43892991	HepG2	liver:	n/a	chr10:43892797-43892813
33	BHLHE40	chr10:43891162-43893030	HepG2	liver:	n/a	chr10:43892797-43892813
34	BHLHE40	chr10:43892631-43893015	A549	lung:	n/a	chr10:43892797-43892813
35	BHLHE40	chr10:43891188-43893121	K562	blood:	n/a	chr10:43892797-43892813
36	BHLHE40	chr10:43891147-43893259	GM12878	blood:	n/a	chr10:43892797-43892813
37	BRCA1	chr10:43891893-43891909	GM12878	blood:	n/a	n/a
38	BRCA1	chr10:43892448-43892979	HepG2	liver:	n/a	n/a
39	CBX3	chr10:43891281-43892380	K562	blood:	n/a	n/a
40	CBX3	chr10:43892500-43893159	K562	blood:	n/a	n/a
41	CBX3	chr10:43892603-43893093	K562	blood:	n/a	n/a
42	CBX3	chr10:43891200-43891783	K562	blood:	n/a	n/a
43	CCNT2	chr10:43890754-43893084	K562	blood:	n/a	chr10:43892423-43892432 chr10:43891402-43891411
44	CEBPB	chr10:43892702-43892829	HepG2	liver:	n/a	n/a
45	CEBPB	chr10:43892730-43892824	K562	blood:	n/a	n/a
46	CEBPB	chr10:43892566-43892696	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPD	chr10:43891664-43893022	HepG2	liver:	n/a	n/a
48	CEBPD	chr10:43891926-43893105	K562	blood:	n/a	n/a
49	CEBPD	chr10:43892129-43892509	HepG2	liver:	n/a	n/a
50	CEBPD	chr10:43891058-43893163	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43892910-43892960	Hepatocyte	liver:	n/a
2	chr10:43892790-43892840	GM12892	blood:	n/a
3	chr10:43892910-43892960	Hepatocyte	liver:	n/a
4	chr10:43892790-43892840	GM12892	blood:	n/a
5	chr10:43892819-43892869	HCT-116	colon:	n/a
6	chr10:43892910-43892960	U87	brain:	n/a
7	chr10:43892914-43892964	HRCEpiC	kidney:	n/a
8	chr10:43891547-43891597	SK-N-SH	brain:	n/a
9	chr10:43892914-43892964	Jurkat	blood:	n/a
10	chr10:43892908-43892958	GM12878	blood:	n/a
11	chr10:43893015-43893065	NHBE	bronchial:	n/a
12	chr10:43891547-43891597	HCM	heart:	n/a
13	chr10:43892819-43892869	HCM	heart:	n/a
14	chr10:43893015-43893065	HCF	heart:	n/a
15	chr10:43892908-43892958	HEEpiC	esophagus:	n/a
16	chr10:43892819-43892869	HPAEpiC	pulmonary alveolar:	n/a
17	chr10:43891459-43891509	SK-N-MC	brain:	n/a
18	chr10:43893015-43893065	IMR90	lung:	fetal
19	chr10:43892956-43893006	NB4	blood:	n/a
20	chr10:43892075-43892125	SAEC	small airway:	n/a
21	chr10:43892908-43892958	GM12892	blood:	n/a
22	chr10:43892908-43892958	NHBE	bronchial:	n/a
23	chr10:43891547-43891597	MCF10A-Er-Src	breast:	n/a
24	chr10:43892956-43893006	HRE	kidney:	n/a
25	chr10:43892914-43892964	BE2_C	brain:	n/a
26	chr10:43892790-43892840	SK-N-SH	brain:	n/a
27	chr10:43892819-43892869	Caco-2	colon:	n/a
28	chr10:43891547-43891597	SK-N-MC	brain:	n/a
29	chr10:43892908-43892958	T-47D	breast:	n/a
30	chr10:43892914-43892964	HAEpiC	amniotic membrane:	n/a
31	chr10:43893015-43893065	HMEC	breast:	n/a
32	chr10:43892946-43892996	HRPEpiC	eye:	n/a
33	chr10:43892908-43892958	MCF-7	breast:	n/a
34	chr10:43891459-43891509	A549	lung:	n/a
35	chr10:43892908-43892958	SAEC	small airway:	n/a
36	chr10:43891459-43891509	GM12878	blood:	n/a
37	chr10:43893015-43893065	SK-N-SH	brain:	n/a
38	chr10:43891547-43891597	HMEC	breast:	n/a
39	chr10:43892819-43892869	PANC-1	pancreas:	n/a
40	chr10:43891547-43891597	U87	brain:	n/a
41	chr10:43892914-43892964	BJ	skin:	n/a
42	chr10:43892956-43893006	Caco-2	colon:	n/a
43	chr10:43892819-43892869	HCF	heart:	n/a
44	chr10:43892956-43893006	AG10803	skin:	n/a
45	chr10:43892075-43892125	ProgFib	skin:	n/a
46	chr10:43892908-43892958	MCF10A-Er-Src	breast:	n/a
47	chr10:43892956-43893006	HAEpiC	amniotic membrane:	n/a
48	chr10:43892075-43892125	NT2-D1	testis:	n/a
49	chr10:43891459-43891509	Caco-2	colon:	n/a
50	chr10:43892790-43892840	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43696369..43700743-chr10:43891529..43894634,3	K562	blood:
2	chr10:43846613..43849361-chr10:43890166..43892037,2	MCF-7	breast:
3	chr10:43697420..43700683-chr10:43890424..43894292,4	K562	blood:
4	chr10:43891265..43892240-chr10:43903154..43903688,2	MCF-7	breast:
5	chr10:43891174..43892847-chr10:44101479..44103589,2	K562	blood:
6	chr10:43631919..43634384-chr10:43890115..43892168,2	K562	blood:
7	chr10:43887055..43906178-chr10:43946385..43955803,85	K562	blood:
8	chr10:43889891..43893674-chr10:43930869..43934431,5	MCF-7	breast:
9	chr1:152940729..152943667-chr10:43889848..43892528,2	MCF-7	breast:
10	chr10:43892832..43893757-chr10:43901832..43902783,2	MCF-7	breast:
11	chr10:43868968..43875759-chr10:43890269..43893335,11	MCF-7	breast:
12	chr10:43868700..43874062-chr10:43890607..43893448,6	MCF-7	breast:
13	chr10:43845449..43848194-chr10:43889287..43891526,2	K562	blood:

Variant related genes	Relation type
HNRNPF	TF binding region
HNRNPF	CpG island
ENSG00000150201	chromatin interactions
ENSG00000232004	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000243660	chromatin interactions
ENSG00000184148	chromatin interactions
ENSG00000198298	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000252532	chromatin interactions
ENSG00000198915	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563172418	chr10:43891377-43891378	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs76889847	chr10:43891378-43891379	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs555301833	chr10:43891385-43891386	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs575128016	chr10:43891485-43891486	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs192541698	chr10:43891507-43891508	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs376734311	chr10:43891527-43891528	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs72785266	chr10:43891533-43891534	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184922675	chr10:43891547-43891548	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs547271341	chr10:43891553-43891554	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs11817723	chr10:43891554-43891555	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs539205201	chr10:43891565-43891566	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs569062048	chr10:43891566-43891567	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs142127152	chr10:43891600-43891601	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs112532114	chr10:43891601-43891602	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs557565061	chr10:43891607-43891608	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs569384208	chr10:43891627-43891628	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs537140014	chr10:43891633-43891634	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs555217348	chr10:43891682-43891683	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs573534387	chr10:43891731-43891732	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs188934660	chr10:43891742-43891743	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs577532409	chr10:43891771-43891772	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs552820335	chr10:43891802-43891803	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs369793700	chr10:43891887-43891888	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs11548184	chr10:43891993-43891994	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372698599	chr10:43892012-43892013	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs76192158	chr10:43892096-43892097	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs530665446	chr10:43892127-43892128	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs543063217	chr10:43892140-43892141	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs370514624	chr10:43892178-43892179	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs561238783	chr10:43892182-43892183	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs534686425	chr10:43892211-43892212	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs528449187	chr10:43892222-43892223	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs547036522	chr10:43892251-43892252	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs571694401	chr10:43892297-43892298	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs532837578	chr10:43892310-43892311	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs370667436	chr10:43892341-43892342	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs376188239	chr10:43892388-43892389	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs551334907	chr10:43892393-43892394	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs569430600	chr10:43892473-43892474	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs111823384	chr10:43892477-43892478	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs554394310	chr10:43892481-43892482	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs375524790	chr10:43892513-43892514	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs536448974	chr10:43892514-43892515	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs181668101	chr10:43892531-43892532	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs11238535	chr10:43892535-43892536	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs565327848	chr10:43892577-43892578	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs534440909	chr10:43892579-43892580	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs373963172	chr10:43892594-43892595	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs186365280	chr10:43892599-43892600	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs368070314	chr10:43892643-43892644	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43888000-43891400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:43889000-43891400	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
3	chr10:43889000-43892000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
4	chr10:43889000-43892200	Transcr. at gene 5' and 3'	Dnd41	blood
5	chr10:43889200-43891400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:43889200-43891600	Genic enhancers	Primary B cells from peripheral blood	blood
7	chr10:43889800-43891400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
8	chr10:43889800-43891600	Weak transcription	Aorta	Aorta
9	chr10:43890000-43892000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr10:43890200-43891400	Enhancers	Primary hematopoietic stem cells	blood
11	chr10:43890200-43891400	Flanking Active TSS	Fetal Brain Female	brain
12	chr10:43890200-43891600	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:43890200-43891600	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
14	chr10:43890200-43891800	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
15	chr10:43890200-43891800	Flanking Active TSS	HUVEC	blood vessel
16	chr10:43890200-43892000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:43890200-43892000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
18	chr10:43890400-43891400	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr10:43890400-43891400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr10:43890400-43891600	Transcr. at gene 5' and 3'	A549	lung
21	chr10:43890400-43891800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr10:43890400-43891800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
23	chr10:43890400-43892000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr10:43890400-43892000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
25	chr10:43890400-43892200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
26	chr10:43890400-43893600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr10:43890600-43891400	Flanking Active TSS	Fetal Heart	heart
28	chr10:43890600-43891400	Transcr. at gene 5' and 3'	NHLF	lung
29	chr10:43890600-43891600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr10:43890600-43891600	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr10:43890600-43891600	Flanking Active TSS	HMEC	breast
32	chr10:43890600-43891800	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr10:43890600-43891800	Transcr. at gene 5' and 3'	K562	blood
34	chr10:43890600-43891800	Transcr. at gene 5' and 3'	Osteobl	bone
35	chr10:43890600-43892000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr10:43890600-43892000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
37	chr10:43890600-43892200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr10:43890600-43893000	Active TSS	Fetal Kidney	kidney
39	chr10:43890600-43893200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr10:43890600-43893200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr10:43890800-43891400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
42	chr10:43890800-43891400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr10:43890800-43891400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr10:43890800-43891400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr10:43890800-43891400	Flanking Active TSS	Colonic Mucosa	Colon
46	chr10:43890800-43891400	Transcr. at gene 5' and 3'	Thymus	Thymus
47	chr10:43890800-43891600	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
48	chr10:43890800-43891600	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr10:43890800-43891600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr10:43890800-43891600	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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