Variant report

Variant	nsv1030287
Chromosome Location	chr9:15332709-15458001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1794)
CpG islands
(count:735)
Chromatin interactive
region (count:57)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1794 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15422587-15422682	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15357028-15357575	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15426284-15426484	K562	blood:	n/a	n/a
4	ARID3A	chr9:15422654-15422834	K562	blood:	n/a	n/a
5	ARID3A	chr9:15416889-15417137	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:15333319-15333669	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:15403228-15403452	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:15350374-15350711	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:15351035-15351548	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:15403256-15403512	K562	blood:	n/a	n/a
11	ARID3A	chr9:15423654-15424033	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:15423509-15423900	K562	blood:	n/a	n/a
13	ATF1	chr9:15386543-15386855	K562	blood:	n/a	n/a
14	ATF1	chr9:15416926-15417228	K562	blood:	n/a	n/a
15	ATF2	chr9:15426044-15426358	GM12878	blood:	n/a	n/a
16	ATF2	chr9:15416815-15417288	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:15416859-15417296	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr9:15422425-15422861	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr9:15425980-15426551	GM12878	blood:	n/a	n/a
20	ATF2	chr9:15422403-15423034	GM12878	blood:	n/a	n/a
21	ATF2	chr9:15422346-15422848	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr9:15422610-15422838	K562	blood:	n/a	n/a
23	ATF3	chr9:15416909-15417257	K562	blood:	n/a	n/a
24	BACH1	chr9:15370513-15370989	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr9:15424848-15425076	GM12878	blood:	n/a	chr9:15424968-15424977
26	BATF	chr9:15426020-15426415	GM12878	blood:	n/a	n/a
27	BATF	chr9:15426063-15426425	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:15422429-15422805	GM12878	blood:	n/a	chr9:15422614-15422627
29	BCL11A	chr9:15422513-15422747	GM12878	blood:	n/a	chr9:15422614-15422627
30	BCL3	chr9:15422174-15423029	A549	lung:	n/a	chr9:15422414-15422423 chr9:15422614-15422627
31	BCLAF1	chr9:15422376-15423136	GM12878	blood:	n/a	chr9:15422414-15422423 chr9:15422614-15422627
32	BCLAF1	chr9:15422287-15423154	GM12878	blood:	n/a	chr9:15422414-15422423 chr9:15422614-15422627
33	BCLAF1	chr9:15425904-15426489	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:15386531-15386879	K562	blood:	n/a	n/a
35	BHLHE40	chr9:15426347-15426389	K562	blood:	n/a	n/a
36	BHLHE40	chr9:15403322-15403478	K562	blood:	n/a	n/a
37	BHLHE40	chr9:15422162-15423396	K562	blood:	n/a	n/a
38	BHLHE40	chr9:15454046-15454311	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:15357545-15357594	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:15422278-15423305	GM12878	blood:	n/a	n/a
41	BHLHE40	chr9:15351043-15351484	HepG2	liver:	n/a	n/a
42	BRCA1	chr9:15422502-15422911	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr9:15422537-15422940	HepG2	liver:	n/a	n/a
44	BRCA1	chr9:15422481-15422931	GM12878	blood:	n/a	n/a
45	BRCA1	chr9:15422422-15423005	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr9:15422380-15422745	K562	blood:	n/a	n/a
47	CCNT2	chr9:15422421-15423210	K562	blood:	n/a	n/a
48	CEBPB	chr9:15386589-15386810	K562	blood:	n/a	n/a
49	CEBPB	chr9:15373052-15373063	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:15364953-15365251	A549	lung:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15425935-15425985	GM12891	blood:	n/a
2	chr9:15423618-15423668	ovcar-3	ovarian:	n/a
3	chr9:15422993-15423043	MCF-7	breast:	n/a
4	chr9:15425935-15425985	GM12891	blood:	n/a
5	chr9:15423618-15423668	ovcar-3	ovarian:	n/a
6	chr9:15422993-15423043	MCF-7	breast:	n/a
7	chr9:15423182-15423232	AG10803	skin:	n/a
8	chr9:15422943-15422993	PrEC	prostate:	n/a
9	chr9:15422589-15422639	SK-N-SH_RA	brain:	n/a
10	chr9:15420564-15420614	K562	blood:	n/a
11	chr9:15422589-15422639	AG04449	skin:	fetal
12	chr9:15425935-15425985	ECC-1	luminal epithelium:	n/a
13	chr9:15425935-15425985	SK-N-SH_RA	brain:	n/a
14	chr9:15422993-15423043	GM12891	blood:	n/a
15	chr9:15442613-15442663	NHDF-neo	bronchial:	n/a
16	chr9:15425935-15425985	K562	blood:	n/a
17	chr9:15422993-15423043	RPTEC	kidney:	n/a
18	chr9:15442613-15442663	HRCEpiC	kidney:	n/a
19	chr9:15401531-15401581	A549	lung:	n/a
20	chr9:15423182-15423232	NT2-D1	testis:	n/a
21	chr9:15425935-15425985	IMR90	lung:	fetal
22	chr9:15422943-15422993	MCF-7	breast:	n/a
23	chr9:15371248-15371298	H1-hESC	embryonic stem cell:	embryo
24	chr9:15422589-15422639	NT2-D1	testis:	n/a
25	chr9:15371248-15371298	NHBE	bronchial:	n/a
26	chr9:15401531-15401581	AG04450	lung:	fetal
27	chr9:15422943-15422993	HepG2	liver:	n/a
28	chr9:15401531-15401581	AG04449	skin:	fetal
29	chr9:15401531-15401581	MCF-7	breast:	n/a
30	chr9:15422943-15422993	SK-N-MC	brain:	n/a
31	chr9:15422993-15423043	HEK293	kidney:	embryo
32	chr9:15422589-15422639	BE2_C	brain:	n/a
33	chr9:15442613-15442663	SK-N-SH	brain:	n/a
34	chr9:15422769-15422819	BJ	skin:	n/a
35	chr9:15442613-15442663	MCF10A-Er-Src	breast:	n/a
36	chr9:15422589-15422639	Caco-2	colon:	n/a
37	chr9:15422769-15422819	HL-60	blood:	n/a
38	chr9:15401531-15401581	ovcar-3	ovarian:	n/a
39	chr9:15420564-15420614	PANC-1	pancreas:	n/a
40	chr9:15422589-15422639	SK-N-MC	brain:	n/a
41	chr9:15371248-15371298	HUVEC	blood vessel:	n/a
42	chr9:15425935-15425985	NH-A	brain:	n/a
43	chr9:15422993-15423043	GM19239	blood:	n/a
44	chr9:15442613-15442663	AG04449	skin:	fetal
45	chr9:15422943-15422993	BE2_C	brain:	n/a
46	chr9:15420564-15420614	NH-A	brain:	n/a
47	chr9:15420564-15420614	Caco-2	colon:	n/a
48	chr9:15423618-15423668	HepG2	liver:	n/a
49	chr9:15422376-15422426	IMR90	lung:	fetal
50	chr9:15423182-15423232	Caco-2	colon:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
2	chr9:15386697..15389614-chr9:15422790..15424352,2	K562	blood:
3	chr9:15332011..15334775-chr9:15347128..15349228,2	MCF-7	breast:
4	chr9:15422069..15423659-chr9:15430578..15433740,3	K562	blood:
5	chr9:15415166..15416789-chr9:15420978..15423004,2	MCF-7	breast:
6	chr9:15357011..15359248-chr9:15422187..15424051,2	MCF-7	breast:
7	chr9:15372087..15374863-chr9:15401359..15403431,2	MCF-7	breast:
8	chr9:15422138..15423750-chr9:15430824..15433204,2	K562	blood:
9	chr9:15422138..15423750-chr9:15430824..15433204,2	K562	blood:
10	chr9:15211338..15211919-chr9:15356761..15357369,2	MCF-7	breast:
11	chr11:71751691..71752198-chr9:15422276..15423243,2	HCT-116	colon:
12	chr9:15429263..15431513-chr9:15449169..15450709,2	K562	blood:
13	chr9:15452841..15455105-chr9:15460969..15462549,2	MCF-7	breast:
14	chr9:15393231..15396045-chr9:15401354..15402871,2	MCF-7	breast:
15	chr9:15414032..15416513-chr9:15421401..15423007,2	K562	blood:
16	chr9:15429263..15431513-chr9:15449169..15450709,2	K562	blood:
17	chr2:173940670..173941204-chr9:15422600..15423282,2	Hela-S3	cervix:
18	chr9:15305818..15308791-chr9:15400718..15402980,2	MCF-7	breast:
19	chr9:15420915..15423147-chr9:15426389..15428949,2	K562	blood:
20	chr1:11865371..11866248-chr9:15422460..15422973,2	Hela-S3	cervix:
21	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
22	chr9:15372087..15374863-chr9:15401359..15403431,2	MCF-7	breast:
23	chr9:15420090..15425077-chr9:15425243..15430966,9	MCF-7	breast:
24	chr9:15104624..15105430-chr9:15416660..15417504,2	MCF-7	breast:
25	chr9:15420595..15424773-chr9:15424796..15433036,11	MCF-7	breast:
26	chr9:15385459..15387196-chr9:15436159..15438276,2	K562	blood:
27	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
28	chr9:15421340..15424109-chr9:15510012..15511838,2	K562	blood:
29	chr9:15277443..15278337-chr9:15356714..15357650,2	MCF-7	breast:
30	chr9:15414997..15416790-chr9:15421464..15423490,2	MCF-7	breast:
31	chr9:15356402..15356902-chr9:134721602..134722134,2	NB4	blood:
32	chr1:205782053..205782858-chr9:15422168..15422987,2	HCT-116	colon:
33	chr9:15352501..15354066-chr9:15419261..15422025,2	MCF-7	breast:
34	chr2:217363452..217364033-chr9:15422219..15422852,2	HCT-116	colon:
35	chr9:15276373..15278004-chr9:15420785..15422574,2	MCF-7	breast:
36	chr1:159894793..159895333-chr9:15422180..15423023,2	Hela-S3	cervix:
37	chr9:15352501..15354066-chr9:15419261..15422025,2	MCF-7	breast:
38	chr17:56083086..56085615-chr9:15422777..15425325,2	MCF-7	breast:
39	chr9:15385459..15387196-chr9:15436159..15438276,2	K562	blood:
40	chr9:15399457..15401521-chr9:15510230..15512381,2	MCF-7	breast:
41	chr9:15418505..15420597-chr9:15421286..15424516,4	MCF-7	breast:
42	chr9:15305709..15307336-chr9:15348928..15350627,2	MCF-7	breast:
43	chr12:7052754..7053671-chr9:15422600..15423100,2	Hela-S3	cervix:
44	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
45	chr9:15450513..15453468-chr9:15464401..15466619,2	K562	blood:
46	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
47	chr9:15277764..15278338-chr9:15416698..15417388,2	MCF-7	breast:
48	chr9:15454833..15458437-chr9:15459733..15463748,4	K562	blood:
49	chr9:15211245..15212139-chr9:15416585..15417547,5	MCF-7	breast:
50	chr9:15277682..15279519-chr9:15415467..15418240,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-2	chr9:15348166-15348453	NONHSAT130262
2	lnc-C9orf93-5	chr9:15454152-15454489	predAs_ge08_PSIP1_1

No data

Variant related genes	Relation type
RN7SL157P	TF binding region
RNU6-319P	TF binding region
SNAPC3	TF binding region
RPL7P33	TF binding region
RN7SL157P	CpG island
RNU6-319P	CpG island
SNAPC3	CpG island
RPL7P33	CpG island
ENSG00000158710	chromatin interactions
ENSG00000011021	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000155158	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000133065	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000263817	chromatin interactions
ENSG00000164975	chromatin interactions
ENSG00000091436	chromatin interactions
ENSG00000197756	chromatin interactions
ENSG00000232485	chromatin interactions
ENSG00000251834	chromatin interactions
ENSG00000177000	chromatin interactions

Extended variants
information (count: 5375 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:5375 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180945063	chr9:15332725-15332726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs374021527	chr9:15332734-15332735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552844290	chr9:15332791-15332792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs114667501	chr9:15332818-15332819	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144021273	chr9:15332861-15332862	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532330053	chr9:15332909-15332910	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187718971	chr9:15332945-15332946	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566036535	chr9:15332962-15332963	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139666521	chr9:15332970-15332971	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs10124733	chr9:15333006-15333007	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs144526512	chr9:15333007-15333008	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537766486	chr9:15333025-15333026	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559247667	chr9:15333038-15333039	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549992979	chr9:15333053-15333054	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563428540	chr9:15333076-15333077	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192637513	chr9:15333121-15333122	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539649401	chr9:15333147-15333148	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553880516	chr9:15333159-15333160	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs572029988	chr9:15333339-15333340	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542672532	chr9:15333420-15333421	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554488234	chr9:15333435-15333436	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146646505	chr9:15333458-15333459	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543319515	chr9:15333522-15333523	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116352396	chr9:15333639-15333640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556203358	chr9:15333644-15333645	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372121247	chr9:15333701-15333702	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532415482	chr9:15333702-15333703	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs374618753	chr9:15333723-15333724	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376691203	chr9:15333762-15333763	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143257092	chr9:15333778-15333779	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2798748	chr9:15333788-15333789	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114009947	chr9:15333871-15333872	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77187993	chr9:15333952-15333953	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs57771103	chr9:15334008-15334009	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531087246	chr9:15334015-15334016	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2805010	chr9:15334020-15334021	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376442768	chr9:15334059-15334060	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201231706	chr9:15334186-15334187	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571159804	chr9:15334220-15334221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562155868	chr9:15334221-15334222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538667595	chr9:15334281-15334282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553502386	chr9:15334282-15334283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572242031	chr9:15334290-15334291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368837092	chr9:15334299-15334300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565642018	chr9:15334305-15334306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573222410	chr9:15334367-15334368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34754042	chr9:15334368-15334369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554609523	chr9:15334405-15334406	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532656669	chr9:15334440-15334441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533130817	chr9:15334447-15334448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:2155 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15328800-15332800	Weak transcription	A549	lung
2	chr9:15329400-15335000	Enhancers	Fetal Intestine Small	intestine
3	chr9:15330000-15346800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:15330800-15333400	Enhancers	Duodenum Mucosa	Duodenum
5	chr9:15331000-15332800	Enhancers	Liver	Liver
6	chr9:15331400-15335200	Enhancers	Fetal Intestine Large	intestine
7	chr9:15332000-15333200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:15332200-15333600	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr9:15332400-15335200	Enhancers	HepG2	liver
10	chr9:15332600-15333000	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr9:15332600-15333400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:15332600-15333600	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr9:15332600-15334400	Enhancers	Stomach Mucosa	stomach
14	chr9:15332800-15333000	Flanking Active TSS	Liver	Liver
15	chr9:15332800-15333000	Enhancers	A549	lung
16	chr9:15332800-15333800	Enhancers	Fetal Lung	lung
17	chr9:15333000-15333400	Enhancers	Liver	Liver
18	chr9:15333000-15333600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr9:15333000-15333800	Flanking Active TSS	A549	lung
20	chr9:15333200-15334000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:15333400-15334200	Flanking Active TSS	Liver	Liver
22	chr9:15333600-15334200	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr9:15334200-15334400	Enhancers	Liver	Liver
24	chr9:15335200-15337400	Weak transcription	HepG2	liver
25	chr9:15337400-15338600	Enhancers	HepG2	liver
26	chr9:15338600-15343600	Weak transcription	HepG2	liver
27	chr9:15343400-15344600	Enhancers	Fetal Intestine Small	intestine
28	chr9:15343600-15344600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:15343600-15344800	Enhancers	Fetal Intestine Large	intestine
30	chr9:15343600-15344800	Enhancers	HepG2	liver
31	chr9:15344200-15344400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr9:15344600-15346200	Weak transcription	Fetal Intestine Small	intestine
33	chr9:15344600-15346400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr9:15344800-15346000	Weak transcription	Fetal Intestine Large	intestine
35	chr9:15344800-15346600	Weak transcription	HepG2	liver
36	chr9:15346000-15347400	Enhancers	Fetal Intestine Large	intestine
37	chr9:15346200-15347600	Enhancers	Fetal Intestine Small	intestine
38	chr9:15346400-15347000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:15346600-15347400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr9:15346600-15348400	Enhancers	HepG2	liver
41	chr9:15346800-15347200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr9:15346800-15347200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr9:15346800-15347200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr9:15346800-15347400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr9:15346800-15347400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr9:15346800-15347400	Enhancers	Stomach Mucosa	stomach
47	chr9:15346800-15347600	Enhancers	Fetal Lung	lung
48	chr9:15347000-15347400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr9:15347000-15347600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:15347200-15347600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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