Variant report

Variant	nsv972780
Chromosome Location	chr9:95008644-95049016
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:574)
CpG islands
(count:61)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr9:95017180-95017214	Hela-S3	cervix:	n/a	n/a
2	CCNT2	chr9:95017029-95017379	K562	blood:	n/a	n/a
3	CCNT2	chr9:95010027-95010227	K562	blood:	n/a	n/a
4	CCNT2	chr9:95029655-95029887	K562	blood:	n/a	n/a
5	CEBPB	chr9:95027457-95027780	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:95010301-95010616	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:95037907-95038205	Hela-S3	cervix:	n/a	chr9:95038064-95038075
8	CEBPB	chr9:95041877-95042119	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:95037893-95038269	A549	lung:	n/a	chr9:95038064-95038075
10	CEBPB	chr9:95020785-95021064	A549	lung:	n/a	n/a
11	CEBPB	chr9:95037958-95038210	K562	blood:	n/a	chr9:95038064-95038075
12	CEBPB	chr9:95037964-95038239	MCF-7	breast:	n/a	chr9:95038064-95038075
13	CEBPB	chr9:95027439-95027801	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:95037888-95038235	HepG2	liver:	n/a	chr9:95038064-95038075
15	CEBPB	chr9:95037920-95038231	IMR90	lung:	n/a	chr9:95038064-95038075
16	CEBPB	chr9:95020753-95020953	IMR90	lung:	n/a	n/a
17	CTCF	chr9:95037956-95038026	A549	lung:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
18	CTCF	chr9:95017160-95017310	A549	lung:	n/a	n/a
19	CTCF	chr9:95037920-95038070	NHEK	skin:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
20	CTCF	chr9:95037940-95038090	HBMEC	blood vessel:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
21	CTCF	chr9:95037980-95038130	HPAF	blood vessel:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
22	CTCF	chr9:95037880-95038030	HCFaa	heart:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
23	CTCF	chr9:95017320-95017470	GM12871	blood:	n/a	n/a
24	CTCF	chr9:95017340-95017490	HepG2	liver:	n/a	n/a
25	CTCF	chr9:95044067-95044117	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr9:95037920-95038070	HCT-116	colon:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
27	CTCF	chr9:95037920-95038070	HPAF	blood vessel:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
28	CTCF	chr9:95037960-95038110	SAEC	small airway:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
29	CTCF	chr9:95017340-95017490	GM12864	blood:	n/a	n/a
30	CTCF	chr9:95013280-95013430	GM12868	blood:	n/a	n/a
31	CTCF	chr9:95017337-95017390	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr9:95031289-95031399	HUVEC	blood vessel:	n/a	chr9:95031320-95031338
33	CTCF	chr9:95017388-95017394	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:95037880-95038030	HVMF	connective:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
35	CTCF	chr9:95017260-95017410	MCF-7	breast:	n/a	n/a
36	CTCF	chr9:95037920-95038070	HCPEpiC	choroid plexus:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
37	CTCF	chr9:95037999-95038008	NHEK	skin:	n/a	n/a
38	CTCF	chr9:95037960-95038110	HMEC	breast:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
39	CTCF	chr9:95037840-95037990	HL-60	blood:	n/a	n/a
40	CTCF	chr9:95017346-95017373	HepG2	liver:	n/a	n/a
41	CTCF	chr9:95017260-95017410	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr9:95037940-95038090	BJ	skin:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
43	CTCF	chr9:95017388-95017389	A549	lung:	n/a	n/a
44	CTCF	chr9:95037940-95038090	AG04449	skin:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
45	CTCF	chr9:95017260-95017410	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr9:95009620-95009770	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr9:95017280-95017430	HEK293	kidney:	n/a	n/a
48	CTCF	chr9:95037987-95038034	Fibrobl	skin:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
49	CTCF	chr9:95037920-95038070	HRE	kidney:	n/a	chr9:95038007-95038020 chr9:95038007-95038016
50	CTCF	chr9:95037940-95038090	SAEC	small airway:	n/a	chr9:95038007-95038020 chr9:95038007-95038016

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95021626-95021676	HEK293	kidney:	embryo
2	chr9:95021626-95021676	HCPEpiC	choroid plexus:	n/a
3	chr9:95021626-95021676	HAEpiC	amniotic membrane:	n/a
4	chr9:95021626-95021676	BJ	skin:	n/a
5	chr9:95021626-95021676	PANC-1	pancreas:	n/a
6	chr9:95021626-95021676	Caco-2	colon:	n/a
7	chr9:95021626-95021676	HL-60	blood:	n/a
8	chr9:95021626-95021676	T-47D	breast:	n/a
9	chr9:95021626-95021676	NB4	blood:	n/a
10	chr9:95021626-95021676	HMEC	breast:	n/a
11	chr9:95021626-95021676	HRCEpiC	kidney:	n/a
12	chr9:95021626-95021676	RPTEC	kidney:	n/a
13	chr9:95021626-95021676	AoSMC	blood vessel:	n/a
14	chr9:95021626-95021676	HepG2	liver:	n/a
15	chr9:95021626-95021676	GM12878	blood:	n/a
16	chr9:95021626-95021676	Jurkat	blood:	n/a
17	chr9:95021626-95021676	SK-N-MC	brain:	n/a
18	chr9:95021626-95021676	NHBE	bronchial:	n/a
19	chr9:95021626-95021676	HEEpiC	esophagus:	n/a
20	chr9:95021626-95021676	GM19239	blood:	n/a
21	chr9:95021626-95021676	GM06990	blood:	n/a
22	chr9:95021626-95021676	BE2_C	brain:	n/a
23	chr9:95021626-95021676	SK-N-SH_RA	brain:	n/a
24	chr9:95021626-95021676	AG09309	skin:	n/a
25	chr9:95021626-95021676	Hela-S3	cervix:	n/a
26	chr9:95021626-95021676	CMK	blood:	n/a
27	chr9:95021626-95021676	MCF-7	breast:	n/a
28	chr9:95021626-95021676	U87	brain:	n/a
29	chr9:95021626-95021676	HRPEpiC	eye:	n/a
30	chr9:95021626-95021676	HCF	heart:	n/a
31	chr9:95021626-95021676	PFSK-1	brain:	n/a
32	chr9:95021626-95021676	HCT-116	colon:	n/a
33	chr9:95021626-95021676	AG10803	skin:	n/a
34	chr9:95021626-95021676	MCF10A-Er-Src	breast:	n/a
35	chr9:95021626-95021676	NT2-D1	testis:	n/a
36	chr9:95021626-95021676	SKMC	muscle:	n/a
37	chr9:95021626-95021676	GM12892	blood:	n/a
38	chr9:95021626-95021676	LNCaP	prostate:	n/a
39	chr9:95021626-95021676	HIPEpiC	eye:	n/a
40	chr9:95021626-95021676	A549	lung:	n/a
41	chr9:95021626-95021676	HRE	kidney:	n/a
42	chr9:95021626-95021676	K562	blood:	n/a
43	chr9:95021626-95021676	ProgFib	skin:	n/a
44	chr9:95021626-95021676	AG04450	lung:	fetal
45	chr9:95021626-95021676	GM12891	blood:	n/a
46	chr9:95021626-95021676	H1-hESC	embryonic stem cell:	embryo
47	chr9:95021626-95021676	AG04449	skin:	fetal
48	chr9:95021626-95021676	PrEC	prostate:	n/a
49	chr9:95021626-95021676	AG09319	gingival:	n/a
50	chr9:95021626-95021676	ECC-1	luminal epithelium:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:95041855..95050591-chr9:95053528..95058799,10	MCF-7	breast:
2	chr9:95043031..95045621-chr9:95049059..95052537,3	MCF-7	breast:
3	chr9:94995085..94997450-chr9:95010156..95011938,2	K562	blood:
4	chr9:95015646..95017517-chr9:95025518..95027795,2	K562	blood:
5	chr9:95015004..95016544-chr9:95035822..95038255,2	MCF-7	breast:
6	chr9:95014006..95016847-chr9:95056028..95058859,3	K562	blood:
7	chr9:95007689..95009235-chr9:95012791..95014544,2	MCF-7	breast:
8	chr9:95015004..95016544-chr9:95035822..95038255,2	MCF-7	breast:
9	chr9:95024617..95027442-chr9:95030716..95033050,2	MCF-7	breast:
10	chr9:95031650..95034059-chr9:95066255..95068811,2	MCF-7	breast:
11	chr9:95007723..95009563-chr9:95039605..95041359,2	K562	blood:
12	chr9:95014052..95016554-chr9:95048045..95050815,3	K562	blood:
13	chr9:95031180..95034095-chr9:95036544..95038864,3	MCF-7	breast:
14	chr9:95017965..95021110-chr9:95023019..95027040,3	K562	blood:
15	chr9:95030257..95032627-chr9:95052424..95055321,2	MCF-7	breast:
16	chr9:95030040..95034061-chr9:95034516..95038123,4	MCF-7	breast:
17	chr9:95025809..95028763-chr9:95033711..95035364,2	MCF-7	breast:
18	chr9:95015317..95017895-chr9:95035421..95037158,2	K562	blood:
19	chr9:95010654..95012668-chr9:95080441..95082323,2	K562	blood:
20	chr9:95010625..95013356-chr9:95030582..95032463,3	K562	blood:
21	chr9:95017702..95020249-chr9:95048067..95050193,2	K562	blood:
22	chr9:95016044..95018877-chr9:95053693..95055992,2	MCF-7	breast:
23	chr9:95017965..95021110-chr9:95023019..95027040,3	K562	blood:
24	chr9:95013416..95016060-chr9:95050804..95054328,4	K562	blood:
25	chr9:95007723..95009563-chr9:95039605..95041359,2	K562	blood:
26	chr9:95020468..95022935-chr9:95048495..95050769,2	MCF-7	breast:
27	chr9:95018820..95020529-chr9:95042331..95043865,2	K562	blood:
28	chr9:95026992..95028632-chr9:95044045..95045593,2	MCF-7	breast:
29	chr9:95008635..95010246-chr9:95036891..95039178,2	K562	blood:
30	chr9:95030040..95034061-chr9:95034516..95038123,4	MCF-7	breast:
31	chr9:95008635..95010246-chr9:95036891..95039178,2	K562	blood:
32	chr9:95019906..95022765-chr9:95030244..95032331,2	K562	blood:
33	chr9:95012295..95015552-chr9:95048045..95050189,3	K562	blood:
34	chr9:95005805..95008585-chr9:95030951..95032624,2	MCF-7	breast:
35	chr9:95026365..95029765-chr9:95055659..95058477,3	MCF-7	breast:
36	chr9:95012752..95014483-chr9:95035831..95037613,2	K562	blood:
37	chr9:95010592..95014483-chr9:95035831..95038988,3	K562	blood:
38	chr9:95009835..95012585-chr9:95054447..95056967,2	MCF-7	breast:
39	chr9:95023776..95027446-chr9:95029561..95032473,5	K562	blood:
40	chr9:95035311..95039708-chr9:95055298..95058427,6	MCF-7	breast:
41	chr9:95019610..95022532-chr9:95024323..95027495,3	K562	blood:
42	chr9:95024617..95027442-chr9:95030716..95033050,2	MCF-7	breast:
43	chr9:95005657..95008042-chr9:95025879..95028616,2	K562	blood:
44	chr9:95012295..95015552-chr9:95048045..95050189,3	K562	blood:
45	chr9:95025809..95028763-chr9:95033711..95035364,2	MCF-7	breast:
46	chr9:95015317..95017895-chr9:95035421..95037158,2	K562	blood:
47	chr9:95005995..95010292-chr9:95015147..95019470,4	K562	blood:
48	chr9:94982687..94985411-chr9:95009602..95012209,2	K562	blood:
49	chr9:95018820..95020529-chr9:95042331..95043865,2	K562	blood:
50	chr9:95026992..95028632-chr9:95044045..95045593,2	MCF-7	breast:

No data

Variant related genes	Relation type
IARS	TF binding region
IARS	CpG island
ENSG00000196305	chromatin interactions
ENSG00000188312	chromatin interactions
ENSG00000239183	chromatin interactions
ENSG00000198000	chromatin interactions

Extended variants
information (count: 1557 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1557 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147628478	chr9:95008686-95008687	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs117139399	chr9:95008692-95008693	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374225241	chr9:95008711-95008712	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs189949672	chr9:95008749-95008750	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117882372	chr9:95008752-95008753	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534965557	chr9:95008800-95008801	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553631372	chr9:95008819-95008820	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574662600	chr9:95008821-95008822	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142282805	chr9:95008940-95008941	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs180839721	chr9:95008966-95008967	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566828938	chr9:95008985-95008986	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs575780365	chr9:95009001-95009002	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs145757091	chr9:95009008-95009009	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564685622	chr9:95009076-95009077	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs9409663	chr9:95009078-95009079	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs374702331	chr9:95009095-95009096	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138414306	chr9:95009129-95009130	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs148844565	chr9:95009174-95009175	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529902136	chr9:95009197-95009198	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185468749	chr9:95009198-95009199	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143516035	chr9:95009208-95009209	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs56374228	chr9:95009312-95009313	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs55894730	chr9:95009393-95009394	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188319188	chr9:95009430-95009431	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146124199	chr9:95009433-95009434	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs138995108	chr9:95009462-95009463	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs199733381	chr9:95009480-95009481	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs528461588	chr9:95009487-95009488	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181772533	chr9:95009493-95009494	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568444454	chr9:95009500-95009501	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs377405246	chr9:95009543-95009544	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574731177	chr9:95009544-95009545	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186487907	chr9:95009550-95009551	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142289796	chr9:95009628-95009629	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542590184	chr9:95009632-95009633	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs548248301	chr9:95009639-95009640	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs370120746	chr9:95009640-95009641	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs372931568	chr9:95009655-95009656	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs34561868	chr9:95009676-95009677	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs75415996	chr9:95009708-95009709	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs77245714	chr9:95009709-95009710	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145983857	chr9:95009731-95009732	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs190575779	chr9:95009739-95009740	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535050475	chr9:95009747-95009748	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369618278	chr9:95009749-95009750	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs138582820	chr9:95009771-95009772	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs141783555	chr9:95009778-95009779	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs2230404	chr9:95009786-95009787	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs148487313	chr9:95009826-95009827	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373999288	chr9:95009843-95009844	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Breast cancer	17133270	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
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94982800-95038400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:94982800-95045600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr9:94984000-95012400	Weak transcription	Stomach Mucosa	stomach
4	chr9:94990200-95054000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:94990400-95038200	Strong transcription	Primary T helper cells PMA-I stimulated	--
6	chr9:94991200-95038400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:94991200-95052400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr9:94991200-95053600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr9:94991400-95050400	Strong transcription	Dnd41	blood
10	chr9:94991400-95052400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:94991400-95053600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:94991400-95053800	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:94991400-95053800	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr9:94991800-95053800	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr9:94991800-95054000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:94994000-95053000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:94994200-95038000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:94994400-95038600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr9:94994600-95010800	Strong transcription	K562	blood
20	chr9:94994600-95051200	Strong transcription	Primary B cells from peripheral blood	blood
21	chr9:94995600-95038000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr9:94995600-95038600	Strong transcription	Primary T cells from cord blood	blood
23	chr9:94996000-95009800	Strong transcription	Fetal Intestine Small	intestine
24	chr9:94996000-95048600	Strong transcription	Fetal Stomach	stomach
25	chr9:94996200-95051400	Strong transcription	H1 Cell Line	embryonic stem cell
26	chr9:94996200-95051400	Strong transcription	Fetal Thymus	thymus
27	chr9:94996200-95052000	Strong transcription	Fetal Muscle Trunk	muscle
28	chr9:94996400-95051400	Strong transcription	Fetal Muscle Leg	muscle
29	chr9:94996400-95052000	Strong transcription	Duodenum Mucosa	Duodenum
30	chr9:94996600-95009800	Strong transcription	A549	lung
31	chr9:94996600-95011200	Strong transcription	GM12878-XiMat	blood
32	chr9:94996600-95035000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:94996600-95038400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr9:94996800-95014200	Strong transcription	Hela-S3	cervix
35	chr9:94996800-95037400	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr9:94996800-95038200	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr9:94996800-95042600	Strong transcription	Fetal Brain Female	brain
38	chr9:94997000-95042800	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr9:94998600-95011000	Strong transcription	Brain Inferior Temporal Lobe	brain
40	chr9:94998600-95042800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr9:94998600-95050600	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr9:94998600-95051200	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr9:94998600-95051600	Strong transcription	Adipose Nuclei	Adipose
44	chr9:94998800-95010600	Strong transcription	Ovary	ovary
45	chr9:94998800-95045000	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr9:94998800-95048000	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr9:94998800-95049600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:94998800-95050200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr9:94998800-95051400	Strong transcription	Fetal Intestine Large	intestine
50	chr9:94999000-95027400	Strong transcription	Fetal Lung	lung

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