Variant report

Variant	esv3410012
Chromosome Location	chr15:43027685-43030233
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	chr15:43029205-43029320	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43030048-43030327	HepG2	liver:	n/a	n/a
3	ATF3	chr15:43029026-43029443	K562	blood:	n/a	n/a
4	BACH1	chr15:43029146-43029218	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr15:43029194-43029684	K562	blood:	n/a	chr15:43029327-43029343
6	BHLHE40	chr15:43029125-43029621	GM12878	blood:	n/a	chr15:43029327-43029343
7	BRCA1	chr15:43029093-43029475	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr15:43029043-43029634	K562	blood:	n/a	n/a
9	CBX3	chr15:43029963-43030363	K562	blood:	n/a	n/a
10	CCNT2	chr15:43028482-43029698	K562	blood:	n/a	n/a
11	CEBPB	chr15:43030134-43030327	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:43029236-43029574	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr15:43029131-43029486	HepG2	liver:	n/a	n/a
14	CHD1	chr15:43028787-43029166	GM12878	blood:	n/a	n/a
15	CHD2	chr15:43029474-43029674	GM12878	blood:	n/a	n/a
16	CHD2	chr15:43028887-43029640	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr15:43029116-43029266	K562	blood:	n/a	n/a
18	CHD2	chr15:43029167-43029173	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:43029402-43029581	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr15:43029865-43030006	K562	blood:	n/a	n/a
21	CHD2	chr15:43028738-43028847	HepG2	liver:	n/a	n/a
22	CHD2	chr15:43029073-43029293	HepG2	liver:	n/a	n/a
23	CHD2	chr15:43029512-43029626	HepG2	liver:	n/a	n/a
24	CREB1	chr15:43029120-43029386	A549	lung:	n/a	n/a
25	CREB1	chr15:43028993-43029648	K562	blood:	n/a	n/a
26	CTCF	chr15:43029060-43029210	Hela-S3	cervix:	n/a	chr15:43029185-43029195
27	CTCF	chr15:43030200-43030350	HVMF	connective:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
28	CTCF	chr15:43030180-43030330	HMF	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
29	CTCF	chr15:43029154-43029196	K562	blood:	n/a	chr15:43029185-43029195
30	CTCF	chr15:43030160-43030310	Hela-S3	cervix:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
31	CTCF	chr15:43030115-43030349	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
32	CTCF	chr15:43030146-43030335	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
33	CTCF	chr15:43030160-43030310	HPAF	blood vessel:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
34	CTCF	chr15:43030080-43030230	BJ	skin:	n/a	n/a
35	CTCF	chr15:43028965-43029666	H1-hESC	embryonic stem cell:	n/a	chr15:43029185-43029195
36	CTCF	chr15:43029140-43029290	GM12872	blood:	n/a	chr15:43029185-43029195
37	CTCF	chr15:43030047-43030484	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
38	CTCF	chr15:43030029-43030446	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
39	CTCF	chr15:43029264-43029273	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr15:43030157-43030313	GM12892	blood:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
41	CTCF	chr15:43029160-43029310	GM12865	blood:	n/a	chr15:43029185-43029195
42	CTCF	chr15:43029200-43029350	GM12869	blood:	n/a	n/a
43	CTCF	chr15:43030061-43030345	K562	blood:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
44	CTCF	chr15:43030140-43030290	GM12872	blood:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
45	CTCF	chr15:43030160-43030310	HepG2	liver:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
46	CTCF	chr15:43029229-43029262	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr15:43030120-43030270	AG10803	skin:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
48	CTCF	chr15:43029217-43029227	GM12892	blood:	n/a	n/a
49	CTCF	chr15:43029129-43029422	GM12878	blood:	n/a	chr15:43029185-43029195
50	CTCF	chr15:43029080-43029230	SK-N-SH_RA	brain:	n/a	chr15:43029185-43029195

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43027820-43027870	HMEC	breast:	n/a
2	chr15:43029438-43029488	AG04449	skin:	fetal
3	chr15:43027820-43027870	HMEC	breast:	n/a
4	chr15:43029438-43029488	AG04449	skin:	fetal
5	chr15:43029799-43029849	HUVEC	blood vessel:	n/a
6	chr15:43029643-43029693	HIPEpiC	eye:	n/a
7	chr15:43028932-43028982	GM12878	blood:	n/a
8	chr15:43027820-43027870	Caco-2	colon:	n/a
9	chr15:43029438-43029488	LNCaP	prostate:	n/a
10	chr15:43029643-43029693	HRCEpiC	kidney:	n/a
11	chr15:43029799-43029849	ovcar-3	ovarian:	n/a
12	chr15:43029799-43029849	HAEpiC	amniotic membrane:	n/a
13	chr15:43029643-43029693	NB4	blood:	n/a
14	chr15:43029432-43029482	HepG2	liver:	n/a
15	chr15:43028916-43028966	SK-N-MC	brain:	n/a
16	chr15:43029643-43029693	HepG2	liver:	n/a
17	chr15:43029438-43029488	NT2-D1	testis:	n/a
18	chr15:43029643-43029693	HCM	heart:	n/a
19	chr15:43029432-43029482	Hela-S3	cervix:	n/a
20	chr15:43029558-43029608	HCPEpiC	choroid plexus:	n/a
21	chr15:43029558-43029608	SK-N-MC	brain:	n/a
22	chr15:43029242-43029292	BJ	skin:	n/a
23	chr15:43029202-43029252	Hepatocyte	liver:	n/a
24	chr15:43029242-43029292	HCF	heart:	n/a
25	chr15:43029438-43029488	BE2_C	brain:	n/a
26	chr15:43029799-43029849	A549	lung:	n/a
27	chr15:43029643-43029693	AoSMC	blood vessel:	n/a
28	chr15:43029643-43029693	HEEpiC	esophagus:	n/a
29	chr15:43028916-43028966	A549	lung:	n/a
30	chr15:43028932-43028982	GM06990	blood:	n/a
31	chr15:43028932-43028982	Jurkat	blood:	n/a
32	chr15:43028916-43028966	U87	brain:	n/a
33	chr15:43028463-43028513	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:43028916-43028966	AG04449	skin:	fetal
35	chr15:43029558-43029608	ovcar-3	ovarian:	n/a
36	chr15:43029799-43029849	NH-A	brain:	n/a
37	chr15:43028932-43028982	NT2-D1	testis:	n/a
38	chr15:43029558-43029608	GM12891	blood:	n/a
39	chr15:43028463-43028513	ECC-1	luminal epithelium:	n/a
40	chr15:43029438-43029488	GM12891	blood:	n/a
41	chr15:43028932-43028982	Hela-S3	cervix:	n/a
42	chr15:43028463-43028513	NHDF-neo	bronchial:	n/a
43	chr15:43029438-43029488	SAEC	small airway:	n/a
44	chr15:43029799-43029849	NHDF-neo	bronchial:	n/a
45	chr15:43029432-43029482	SAEC	small airway:	n/a
46	chr15:43029432-43029482	GM12892	blood:	n/a
47	chr15:43029558-43029608	SAEC	small airway:	n/a
48	chr15:43028916-43028966	HCPEpiC	choroid plexus:	n/a
49	chr15:43029202-43029252	NH-A	brain:	n/a
50	chr15:43029643-43029693	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:43014319..43018768-chr15:43027782..43030873,5	MCF-7	breast:
2	chr15:43028764..43029357-chr7:100183650..100184158,2	Hela-S3	cervix:
3	chr15:43019448..43022159-chr15:43025632..43028520,2	MCF-7	breast:
4	chr15:43029097..43029683-chr8:22102019..22102704,2	HCT-116	colon:
5	chr15:43029256..43031403-chr15:43210732..43214178,4	K562	blood:

Variant related genes	Relation type
ENSG00000246283	TF binding region
CDAN1	TF binding region
ENSG00000246283	CpG island
CDAN1	CpG island
ENSG00000106336	chromatin interactions
ENSG00000208037	chromatin interactions
ENSG00000140326	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000168495	chromatin interactions
ENSG00000128881	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368963454	chr15:43027687-43027688	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs373152749	chr15:43027690-43027691	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs376917557	chr15:43027694-43027695	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs369938325	chr15:43027698-43027699	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs550223257	chr15:43027709-43027710	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs373790041	chr15:43027719-43027720	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs61745955	chr15:43027745-43027746	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs202161681	chr15:43027748-43027749	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs146087685	chr15:43027798-43027799	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs371090455	chr15:43027807-43027808	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375828457	chr15:43027813-43027814	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs552779240	chr15:43027824-43027825	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs76599133	chr15:43027835-43027836	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs531376075	chr15:43027845-43027846	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs191624595	chr15:43027847-43027848	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs151004903	chr15:43027848-43027849	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs374597821	chr15:43027875-43027876	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs368595516	chr15:43027889-43027890	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs558575598	chr15:43027894-43027895	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs549900345	chr15:43027897-43027898	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs370916890	chr15:43027900-43027901	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs375152608	chr15:43027907-43027908	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577928192	chr15:43027909-43027910	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs368067759	chr15:43027910-43027911	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs543877806	chr15:43027926-43027927	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs140100277	chr15:43027927-43027928	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574213547	chr15:43027968-43027969	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376744765	chr15:43028026-43028027	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs370729097	chr15:43028044-43028045	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs543228844	chr15:43028059-43028060	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs199787046	chr15:43028085-43028086	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184207000	chr15:43028089-43028090	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372653695	chr15:43028099-43028100	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139936073	chr15:43028115-43028116	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs571317942	chr15:43028141-43028142	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143391538	chr15:43028207-43028208	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112317805	chr15:43028222-43028223	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200994232	chr15:43028241-43028242	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374111927	chr15:43028244-43028245	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs146716516	chr15:43028252-43028253	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530521066	chr15:43028278-43028279	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375923006	chr15:43028287-43028288	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs370228678	chr15:43028294-43028295	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560630349	chr15:43028338-43028339	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs529704255	chr15:43028340-43028341	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188826309	chr15:43028369-43028370	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs546310338	chr15:43028412-43028413	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566611704	chr15:43028429-43028430	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538462509	chr15:43028431-43028432	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552437769	chr15:43028433-43028434	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43008200-43027800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr15:43008800-43027800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:43009000-43027800	Strong transcription	Fetal Intestine Large	intestine
4	chr15:43009200-43027800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr15:43009600-43027800	Strong transcription	Left Ventricle	heart
6	chr15:43010200-43027800	Strong transcription	Gastric	stomach
7	chr15:43010400-43027800	Strong transcription	Placenta	Placenta
8	chr15:43011600-43028000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:43011800-43027800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr15:43014000-43027800	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr15:43014200-43027800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:43014600-43027800	Strong transcription	Fetal Thymus	thymus
13	chr15:43014800-43027800	Strong transcription	NHEK	skin
14	chr15:43015000-43027800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr15:43015000-43027800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr15:43015000-43027800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr15:43016200-43028000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr15:43018400-43028200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr15:43019600-43027800	Strong transcription	Muscle Satellite Cultured Cells	--
20	chr15:43020200-43028000	Weak transcription	Right Atrium	heart
21	chr15:43021200-43027800	Strong transcription	Brain Cingulate Gyrus	brain
22	chr15:43022800-43027800	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr15:43023000-43027800	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr15:43023000-43028000	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr15:43023400-43028000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr15:43023600-43027800	Strong transcription	Primary hematopoietic stem cells	blood
27	chr15:43023600-43027800	Weak transcription	A549	lung
28	chr15:43023600-43028400	Weak transcription	Small Intestine	intestine
29	chr15:43023800-43028000	Weak transcription	Psoas Muscle	Psoas
30	chr15:43024600-43028000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr15:43024800-43028200	Weak transcription	NH-A	brain
32	chr15:43025000-43028000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr15:43026200-43028000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr15:43026200-43028000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr15:43026400-43028000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:43026400-43028200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr15:43026600-43028000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr15:43026600-43028000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:43026600-43028000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:43026600-43028000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr15:43026600-43028000	Weak transcription	Aorta	Aorta
42	chr15:43026600-43028000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
43	chr15:43026600-43028000	Enhancers	GM12878-XiMat	blood
44	chr15:43026600-43028000	Genic enhancers	HepG2	liver
45	chr15:43026800-43027800	Weak transcription	Stomach Mucosa	stomach
46	chr15:43026800-43028000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr15:43026800-43028000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr15:43026800-43028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:43026800-43028000	Weak transcription	Brain Substantia Nigra	brain
50	chr15:43026800-43028000	Genic enhancers	Fetal Stomach	stomach

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