Variant report

Variant	nsv1051180
Chromosome Location	chr9:92869383-93141038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1748)
CpG islands
(count:185)
Chromatin interactive
region (count:65)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:92931825-92932207	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:92904198-92904310	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:92904934-92905202	HepG2	liver:	n/a	n/a
4	ATF2	chr9:92951642-92951847	GM12878	blood:	n/a	n/a
5	ATF2	chr9:93049726-93050109	GM12878	blood:	n/a	n/a
6	BACH1	chr9:93088508-93088797	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:93088544-93088830	K562	blood:	n/a	n/a
8	BACH1	chr9:92989234-92989338	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:92999499-92999649	GM12878	blood:	n/a	n/a
10	BATF	chr9:92989064-92989394	GM12878	blood:	n/a	n/a
11	BATF	chr9:93049762-93050054	GM12878	blood:	n/a	n/a
12	BATF	chr9:93038508-93038817	GM12878	blood:	n/a	n/a
13	BATF	chr9:93049789-93050096	GM12878	blood:	n/a	n/a
14	BATF	chr9:92989140-92989405	GM12878	blood:	n/a	n/a
15	BATF	chr9:92965282-92965468	GM12878	blood:	n/a	n/a
16	BATF	chr9:93038458-93038777	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:92951613-92951890	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:92951650-92951969	GM12878	blood:	n/a	n/a
19	BCL3	chr9:92988991-92989508	A549	lung:	n/a	n/a
20	BCL3	chr9:92874436-92874653	GM12878	blood:	n/a	n/a
21	BCL3	chr9:92989044-92989494	A549	lung:	n/a	n/a
22	BCL3	chr9:93063601-93063866	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:93049743-93050128	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:92989171-92989351	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:92951617-92952004	GM12878	blood:	n/a	n/a
26	BRCA1	chr9:92904079-92904353	H1-hESC	embryonic stem cell:	n/a	n/a
27	CCNT2	chr9:93013376-93013527	K562	blood:	n/a	n/a
28	CEBPB	chr9:93011423-93011691	A549	lung:	n/a	chr9:93011567-93011578 chr9:93011531-93011542
29	CEBPB	chr9:93000337-93000525	K562	blood:	n/a	n/a
30	CEBPB	chr9:93050622-93050837	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:92887393-92887787	HCT-116	colon:	n/a	n/a
32	CEBPB	chr9:92887341-92887659	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:93069270-93069439	A549	lung:	n/a	chr9:93069351-93069362
34	CEBPB	chr9:92962033-92962255	HepG2	liver:	n/a	chr9:92962129-92962140
35	CEBPB	chr9:93050591-93050923	MCF-7	breast:	n/a	n/a
36	CEBPB	chr9:93069304-93069454	HepG2	liver:	n/a	chr9:93069351-93069362
37	CEBPB	chr9:92904138-92904343	A549	lung:	n/a	n/a
38	CEBPB	chr9:93094378-93094918	A549	lung:	n/a	n/a
39	CEBPB	chr9:92887261-92887722	HCT-116	colon:	n/a	n/a
40	CEBPB	chr9:93011425-93011709	Hela-S3	cervix:	n/a	chr9:93011567-93011578 chr9:93011531-93011542
41	CEBPB	chr9:92980940-92981132	A549	lung:	n/a	n/a
42	CEBPB	chr9:92904090-92904500	HCT-116	colon:	n/a	n/a
43	CEBPB	chr9:92873827-92873940	HepG2	liver:	n/a	chr9:92873895-92873912 chr9:92873897-92873908 chr9:92873896-92873909
44	CEBPB	chr9:92887362-92887646	K562	blood:	n/a	n/a
45	CEBPB	chr9:93016581-93016902	IMR90	lung:	n/a	chr9:93016688-93016699
46	CEBPB	chr9:92960993-92961257	A549	lung:	n/a	chr9:92961075-92961086 chr9:92961211-92961224 chr9:92961211-92961222 chr9:92961077-92961088 chr9:92961075-92961088
47	CEBPB	chr9:93016538-93016930	H1-hESC	embryonic stem cell:	n/a	chr9:93016688-93016699
48	CEBPB	chr9:93094451-93094892	A549	lung:	n/a	n/a
49	CEBPB	chr9:93016582-93017011	A549	lung:	n/a	chr9:93016688-93016699
50	CEBPB	chr9:93000303-93000594	K562	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:92982316-92982366	HUVEC	blood vessel:	n/a
2	chr9:92983726-92983776	HIPEpiC	eye:	n/a
3	chr9:92982316-92982366	HUVEC	blood vessel:	n/a
4	chr9:92983726-92983776	HIPEpiC	eye:	n/a
5	chr9:92983726-92983776	HCM	heart:	n/a
6	chr9:92983726-92983776	HMEC	breast:	n/a
7	chr9:92982316-92982366	HRCEpiC	kidney:	n/a
8	chr9:92982316-92982366	PANC-1	pancreas:	n/a
9	chr9:92983726-92983776	NH-A	brain:	n/a
10	chr9:92983726-92983776	SK-N-SH_RA	brain:	n/a
11	chr9:92983726-92983776	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:92983726-92983776	AG04449	skin:	fetal
13	chr9:92983726-92983776	ECC-1	luminal epithelium:	n/a
14	chr9:92982316-92982366	HCM	heart:	n/a
15	chr9:92981825-92981875	GM12878	blood:	n/a
16	chr9:92981825-92981875	HCT-116	colon:	n/a
17	chr9:92981825-92981875	GM06990	blood:	n/a
18	chr9:92983726-92983776	PrEC	prostate:	n/a
19	chr9:92981825-92981875	SK-N-SH	brain:	n/a
20	chr9:92982316-92982366	GM19239	blood:	n/a
21	chr9:92982316-92982366	SK-N-MC	brain:	n/a
22	chr9:92983726-92983776	NT2-D1	testis:	n/a
23	chr9:92982316-92982366	ovcar-3	ovarian:	n/a
24	chr9:92982316-92982366	AG04450	lung:	fetal
25	chr9:92982316-92982366	AG10803	skin:	n/a
26	chr9:92982316-92982366	MCF-7	breast:	n/a
27	chr9:92981825-92981875	HAEpiC	amniotic membrane:	n/a
28	chr9:92981825-92981875	PrEC	prostate:	n/a
29	chr9:92983726-92983776	SKMC	muscle:	n/a
30	chr9:92981825-92981875	Hepatocyte	liver:	n/a
31	chr9:92983726-92983776	H1-hESC	embryonic stem cell:	embryo
32	chr9:92983726-92983776	ovcar-3	ovarian:	n/a
33	chr9:92981825-92981875	HEEpiC	esophagus:	n/a
34	chr9:92982316-92982366	NH-A	brain:	n/a
35	chr9:92983726-92983776	SK-N-MC	brain:	n/a
36	chr9:92981825-92981875	Caco-2	colon:	n/a
37	chr9:92982316-92982366	PFSK-1	brain:	n/a
38	chr9:92981825-92981875	Hela-S3	cervix:	n/a
39	chr9:92982316-92982366	GM12892	blood:	n/a
40	chr9:92982316-92982366	HRPEpiC	eye:	n/a
41	chr9:92981825-92981875	HRPEpiC	eye:	n/a
42	chr9:92982316-92982366	BJ	skin:	n/a
43	chr9:92981825-92981875	HRE	kidney:	n/a
44	chr9:92983726-92983776	HEK293	kidney:	embryo
45	chr9:92983726-92983776	GM12892	blood:	n/a
46	chr9:92982316-92982366	SK-N-SH	brain:	n/a
47	chr9:92982316-92982366	Jurkat	blood:	n/a
48	chr9:92983726-92983776	HepG2	liver:	n/a
49	chr9:92982316-92982366	K562	blood:	n/a
50	chr9:92981825-92981875	Jurkat	blood:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:3000005..3000535-chr9:93027281..93027801,2	MCF-7	breast:
2	chr9:92904585..92905563-chr9:92981517..92982470,9	MCF-7	breast:
3	chr9:92918798..92921681-chr9:92947393..92950211,2	MCF-7	breast:
4	chr9:93080690..93081223-chr9:93404884..93405881,2	MCF-7	breast:
5	chr8:105501678..105502178-chr9:92935952..92936785,2	MCF-7	breast:
6	chr9:92903793..92904418-chr9:92981541..92982063,2	MCF-7	breast:
7	chr9:92921559..92924018-chr9:92927054..92929355,2	MCF-7	breast:
8	chr1:45195117..45197029-chr9:93118640..93120158,2	K562	blood:
9	chr9:92887879..92890112-chr9:92900517..92902714,2	MCF-7	breast:
10	chr9:93011546..93013972-chr9:93052355..93054328,2	MCF-7	breast:
11	chr9:92921559..92924018-chr9:92927054..92929355,2	MCF-7	breast:
12	chr9:93011546..93013972-chr9:93052355..93054328,2	MCF-7	breast:
13	chr9:92905785..92906382-chr9:92981694..92982360,2	MCF-7	breast:
14	chr9:93005901..93009302-chr9:93010303..93013281,3	MCF-7	breast:
15	chr9:92906459..92907062-chr9:92981976..92982746,2	MCF-7	breast:
16	chr9:92218691..92220524-chr9:92868412..92870856,2	MCF-7	breast:
17	chr9:92218934..92221525-chr9:92879229..92881109,2	MCF-7	breast:
18	chr9:93005901..93009302-chr9:93010303..93013281,3	MCF-7	breast:
19	chr9:93101009..93103302-chr9:93104269..93106230,2	MCF-7	breast:
20	chr9:92889944..92891846-chr9:92907899..92909483,2	MCF-7	breast:
21	chr9:92904585..92905563-chr9:92981517..92982470,9	MCF-7	breast:
22	chr9:92936090..92938700-chr9:92964176..92966160,2	MCF-7	breast:
23	chr9:92872786..92875588-chr9:92878982..92882592,3	MCF-7	breast:
24	chr9:92904573..92905325-chr9:92981766..92982487,4	MCF-7	breast:
25	chr9:92867095..92868871-chr9:92870698..92872494,2	K562	blood:
26	chr9:93011380..93015382-chr9:93016799..93018434,3	MCF-7	breast:
27	chr9:93011459..93013580-chr9:93031679..93033930,2	MCF-7	breast:
28	chr9:93103277..93106203-chr9:93118468..93120864,2	MCF-7	breast:
29	chr9:92218340..92221221-chr9:92903297..92904947,2	MCF-7	breast:
30	chr9:93011380..93015382-chr9:93016799..93018434,3	MCF-7	breast:
31	chr9:92931518..92933376-chr9:92938266..92940376,2	MCF-7	breast:
32	chr9:93051393..93052284-chr9:93404958..93405482,2	MCF-7	breast:
33	chr9:92903793..92904418-chr9:92981541..92982063,2	MCF-7	breast:
34	chr9:92919520..92922138-chr9:92936094..92937963,2	MCF-7	breast:
35	chr9:93102527..93105084-chr9:93106529..93108300,2	K562	blood:
36	chr9:93011459..93013580-chr9:93031679..93033930,2	MCF-7	breast:
37	chr9:93067169..93069123-chr9:93074585..93076643,2	MCF-7	breast:
38	chr9:92906459..92907062-chr9:92981976..92982746,2	MCF-7	breast:
39	chr9:92889944..92891846-chr9:92907899..92909483,2	MCF-7	breast:
40	chr9:93101009..93103302-chr9:93104269..93106230,2	MCF-7	breast:
41	chr9:93140741..93143322-chr9:93148992..93151722,2	K562	blood:
42	chr9:93080535..93081683-chr9:93405150..93405933,3	MCF-7	breast:
43	chr1:45185888..45187495-chr9:93118658..93120159,2	K562	blood:
44	chr9:93080247..93081211-chr9:93633166..93633778,2	MCF-7	breast:
45	chr9:93080522..93081160-chr9:93309889..93310591,3	MCF-7	breast:
46	chr9:92904050..92904947-chr9:93535978..93536876,3	MCF-7	breast:
47	chr9:92989065..92989678-chr9:93404924..93405630,3	MCF-7	breast:
48	chr9:93067169..93069123-chr9:93074585..93076643,2	MCF-7	breast:
49	chr9:93102527..93105084-chr9:93106529..93108300,2	K562	blood:
50	chr9:92208153..92210576-chr9:92868061..92870070,3	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIRAS2-11	chr9:92921241-92921663	NONHSAT132995
2	lnc-SYK-9	chr9:93087618-93087758	NONHSAT133000
3	lnc-DIRAS2-13	chr9:92907060-92907485	NONHSAT132993
4	lnc-DIRAS2-12	chr9:92920310-92920928	NONHSAT132994
5	lnc-DIRAS2-13	chr9:92907195-92907485	l_3807_chr9:92907194-92908622_whiteBloodCell
6	lnc-DIRAS2-11	chr9:92965108-92965190	NONHSAT132995
7	lnc-DIRAS2-2	chr9:93063178-93063935	NR_109795
8	lnc-SYK-11	chr9:92964974-92967679	NONHSAT132996
9	lnc-DIRAS2-13	chr9:92908568-92908622	l_3807_chr9:92907194-92908622_whiteBloodCell
10	lnc-DIRAS2-10	chr9:93034039-93034046	NONHSAT132997
11	lnc-DIRAS2-14	chr9:92875629-92877235	ucscGeneNc_uc004ard_1
12	lnc-SYK-11	chr9:92961872-92961910	NONHSAT132996
13	lnc-DIRAS2-13	chr9:92909226-92909407	NONHSAT132993
14	lnc-DIRAS2-10	chr9:93028093-93029379	NONHSAT132997
15	lnc-DIRAS2-13	chr9:92908568-92908774	NONHSAT132993
16	lnc-DIRAS2-14	chr9:92871560-92871730	ucscGeneNc_uc004ard_1
17	lnc-SYK-9	chr9:93093837-93093904	NONHSAT133000

No data

Variant related genes	Relation type
OR7E116P	TF binding region
OR7E31P	TF binding region
OR7E116P	CpG island
OR7E31P	CpG island
ENSG00000062716	chromatin interactions
ENSG00000124588	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000165023	chromatin interactions
ENSG00000130222	chromatin interactions

Extended variants
information (count: 7939 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7939 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192512880	chr9:92869394-92869395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559463215	chr9:92869402-92869403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371336266	chr9:92869417-92869418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149931578	chr9:92869418-92869419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555660599	chr9:92869419-92869420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572269074	chr9:92869433-92869434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540891368	chr9:92869463-92869464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142452097	chr9:92869469-92869470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112358533	chr9:92869543-92869544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144705704	chr9:92869544-92869545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183540656	chr9:92869547-92869548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187468465	chr9:92869548-92869549	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs374891255	chr9:92869578-92869579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs76214238	chr9:92869589-92869590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192280501	chr9:92869603-92869604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75097403	chr9:92869626-92869627	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528001022	chr9:92869693-92869694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184791272	chr9:92869737-92869738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189650344	chr9:92869738-92869739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572973127	chr9:92869742-92869743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534347368	chr9:92869764-92869765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs58892304	chr9:92869765-92869766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs78991605	chr9:92869772-92869773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535913132	chr9:92869793-92869794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs77440276	chr9:92869800-92869801	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs571867032	chr9:92869849-92869850	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78574918	chr9:92869855-92869856	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557622697	chr9:92869857-92869858	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113146773	chr9:92869894-92869895	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532052001	chr9:92869946-92869947	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543031122	chr9:92869992-92869993	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs141541422	chr9:92870001-92870002	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192566493	chr9:92870037-92870038	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542668529	chr9:92870057-92870058	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs73484375	chr9:92870060-92870061	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369937665	chr9:92870062-92870063	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs75801915	chr9:92870076-92870077	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs527883960	chr9:92870090-92870091	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1854444	chr9:92870113-92870114	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184353804	chr9:92870120-92870121	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532891286	chr9:92870141-92870142	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533391645	chr9:92870159-92870160	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552921733	chr9:92870197-92870198	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs549926084	chr9:92870209-92870210	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568163600	chr9:92870210-92870211	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs529820931	chr9:92870214-92870215	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188326320	chr9:92870292-92870293	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs1329047	chr9:92870296-92870297	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565582194	chr9:92870310-92870311	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534496213	chr9:92870323-92870324	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Glioma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	17133270	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD

Chromatin state (count:848 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92858600-92870200	Weak transcription	Right Atrium	heart
2	chr9:92860800-92870200	Weak transcription	Right Ventricle	heart
3	chr9:92861800-92870200	Weak transcription	Pancreas	Pancrea
4	chr9:92862800-92869400	Weak transcription	Brain Germinal Matrix	brain
5	chr9:92864600-92870200	Weak transcription	Fetal Stomach	stomach
6	chr9:92864800-92869400	Weak transcription	Fetal Lung	lung
7	chr9:92864800-92870400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr9:92866600-92869400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr9:92866600-92869400	Weak transcription	Small Intestine	intestine
10	chr9:92866600-92871800	Enhancers	Fetal Muscle Leg	muscle
11	chr9:92867200-92869800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr9:92867800-92869400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr9:92867800-92869400	Weak transcription	Lung	lung
14	chr9:92867800-92870200	Weak transcription	Psoas Muscle	Psoas
15	chr9:92868000-92871200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr9:92868800-92869600	Enhancers	Fetal Muscle Trunk	muscle
17	chr9:92868800-92872000	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr9:92869000-92869600	Enhancers	Primary B cells from cord blood	blood
19	chr9:92869000-92869800	Enhancers	Liver	Liver
20	chr9:92869000-92870400	Enhancers	HSMMtube	muscle
21	chr9:92869000-92870800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr9:92869000-92870800	Enhancers	Colon Smooth Muscle	Colon
23	chr9:92869000-92871200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:92869000-92872200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:92869200-92869600	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr9:92869200-92869800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr9:92869200-92869800	Enhancers	NHEK	skin
28	chr9:92869200-92870000	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr9:92869200-92870200	Enhancers	Stomach Mucosa	stomach
30	chr9:92869200-92870800	Enhancers	HSMM	muscle
31	chr9:92869200-92871200	Enhancers	Rectal Smooth Muscle	rectum
32	chr9:92869400-92869600	Enhancers	Primary T cells from cord blood	blood
33	chr9:92869400-92869600	Enhancers	Primary hematopoietic stem cells	blood
34	chr9:92869400-92869600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr9:92869400-92869600	Enhancers	Small Intestine	intestine
36	chr9:92869400-92869800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr9:92869400-92870000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr9:92869400-92870600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr9:92869400-92870800	Enhancers	Lung	lung
40	chr9:92869400-92871000	Enhancers	Adipose Nuclei	Adipose
41	chr9:92869400-92871000	Enhancers	Fetal Lung	lung
42	chr9:92869400-92871200	Enhancers	Brain Germinal Matrix	brain
43	chr9:92869400-92871200	Enhancers	Left Ventricle	heart
44	chr9:92869400-92871600	Enhancers	Ovary	ovary
45	chr9:92869600-92870000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr9:92869600-92870000	Weak transcription	Small Intestine	intestine
47	chr9:92869600-92870600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr9:92869600-92871200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr9:92869600-92871400	Weak transcription	Fetal Muscle Trunk	muscle
50	chr9:92869800-92870800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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