Variant report

Variant	nsv824985
Chromosome Location	chr9:96337735-96340349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:364)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:96339995-96340072	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:96339631-96339675	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:96338618-96338801	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr9:96338048-96338301	K562	blood:	n/a	n/a
5	BHLHE40	chr9:96338010-96338256	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:96339920-96339967	GM12878	blood:	n/a	n/a
7	BRCA1	chr9:96338141-96338210	HepG2	liver:	n/a	n/a
8	CCNT2	chr9:96338204-96339839	K562	blood:	n/a	chr9:96339670-96339679
9	CEBPB	chr9:96339886-96340346	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr9:96339728-96340272	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:96339810-96339859	HepG2	liver:	n/a	n/a
12	CHD1	chr9:96339479-96339955	GM12878	blood:	n/a	chr9:96339542-96339552
13	CHD1	chr9:96338055-96338452	GM12878	blood:	n/a	n/a
14	CHD2	chr9:96337690-96338284	GM12878	blood:	n/a	chr9:96337908-96337918
15	CHD2	chr9:96337926-96338362	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr9:96338668-96338754	GM12878	blood:	n/a	n/a
17	CHD2	chr9:96339138-96339190	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr9:96338428-96339320	HepG2	liver:	n/a	n/a
19	CREB1	chr9:96338486-96338940	A549	lung:	n/a	n/a
20	CTBP2	chr9:96337422-96338326	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr9:96337940-96338090	GM12873	blood:	n/a	n/a
22	CTCF	chr9:96339061-96339174	Lung_OC	lung:	n/a	n/a
23	E2F4	chr9:96338068-96338188	GM12878	blood:	n/a	n/a
24	E2F6	chr9:96339492-96339682	K562	blood:	n/a	chr9:96339536-96339545
25	E2F6	chr9:96338968-96339123	K562	blood:	n/a	n/a
26	E2F6	chr9:96338530-96338852	K562	blood:	n/a	chr9:96338780-96338795
27	E2F6	chr9:96339230-96339449	K562	blood:	n/a	chr9:96339432-96339444
28	E2F6	chr9:96338128-96339226	K562	blood:	n/a	chr9:96338780-96338795
29	EBF1	chr9:96338034-96338237	GM12878	blood:	n/a	n/a
30	EGR1	chr9:96338088-96339176	K562	blood:	n/a	chr9:96338381-96338391 chr9:96338156-96338165 chr9:96338697-96338707
31	EGR1	chr9:96338526-96339059	GM12878	blood:	n/a	chr9:96338697-96338707
32	EGR1	chr9:96338790-96339019	GM12878	blood:	n/a	n/a
33	EGR1	chr9:96338327-96339180	K562	blood:	n/a	chr9:96338381-96338391 chr9:96338697-96338707
34	EGR1	chr9:96338554-96339101	ECC-1	luminal epithelium:	n/a	chr9:96338697-96338707
35	ELF1	chr9:96337983-96338391	K562	blood:	n/a	chr9:96338152-96338165 chr9:96338153-96338164
36	ELF1	chr9:96337620-96338744	GM12878	blood:	n/a	chr9:96338152-96338165 chr9:96338153-96338164
37	ELK1	chr9:96338075-96338256	Hela-S3	cervix:	n/a	n/a
38	EP300	chr9:96338079-96338345	GM12878	blood:	n/a	chr9:96338155-96338164
39	EP300	chr9:96338248-96338363	K562	blood:	n/a	n/a
40	EP300	chr9:96339870-96340284	T-47D	breast:	n/a	n/a
41	EP300	chr9:96338117-96338441	GM12878	blood:	n/a	chr9:96338155-96338164
42	ETS1	chr9:96338682-96338915	K562	blood:	n/a	n/a
43	FOXA1	chr9:96339921-96340301	T-47D	breast:	n/a	n/a
44	GATA1	chr9:96338113-96338627	PBDE	blood:	n/a	n/a
45	GATA3	chr9:96339735-96340501	MCF-7	breast:	n/a	n/a
46	GATA3	chr9:96339904-96340266	T-47D	breast:	n/a	n/a
47	GATA3	chr9:96339673-96340548	MCF-7	breast:	n/a	n/a
48	GATA3	chr9:96339890-96340244	T-47D	breast:	n/a	n/a
49	GTF2B	chr9:96338179-96338431	K562	blood:	n/a	n/a
50	GTF2F1	chr9:96339936-96340175	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96337982-96338032	NT2-D1	testis:	n/a
2	chr9:96337982-96338032	GM12892	blood:	n/a
3	chr9:96337982-96338032	K562	blood:	n/a
4	chr9:96339159-96339209	MCF10A-Er-Src	breast:	n/a
5	chr9:96339159-96339209	LNCaP	prostate:	n/a
6	chr9:96337982-96338032	NB4	blood:	n/a
7	chr9:96339738-96339788	ECC-1	luminal epithelium:	n/a
8	chr9:96337982-96338032	HRPEpiC	eye:	n/a
9	chr9:96339738-96339788	A549	lung:	n/a
10	chr9:96337982-96338032	SK-N-SH	brain:	n/a
11	chr9:96338308-96338358	SAEC	small airway:	n/a
12	chr9:96339159-96339209	HUVEC	blood vessel:	n/a
13	chr9:96338308-96338358	Jurkat	blood:	n/a
14	chr9:96337982-96338032	Hela-S3	cervix:	n/a
15	chr9:96338308-96338358	HRPEpiC	eye:	n/a
16	chr9:96338308-96338358	GM12892	blood:	n/a
17	chr9:96338308-96338358	AG09319	gingival:	n/a
18	chr9:96337982-96338032	ECC-1	luminal epithelium:	n/a
19	chr9:96338308-96338358	AG04449	skin:	fetal
20	chr9:96339159-96339209	RPTEC	kidney:	n/a
21	chr9:96337982-96338032	NHDF-neo	bronchial:	n/a
22	chr9:96337982-96338032	HAEpiC	amniotic membrane:	n/a
23	chr9:96339159-96339209	ECC-1	luminal epithelium:	n/a
24	chr9:96339738-96339788	HL-60	blood:	n/a
25	chr9:96337982-96338032	NHBE	bronchial:	n/a
26	chr9:96338308-96338358	H1-hESC	embryonic stem cell:	embryo
27	chr9:96339738-96339788	PANC-1	pancreas:	n/a
28	chr9:96337982-96338032	A549	lung:	n/a
29	chr9:96339159-96339209	HCM	heart:	n/a
30	chr9:96339738-96339788	NB4	blood:	n/a
31	chr9:96337982-96338032	HCT-116	colon:	n/a
32	chr9:96338308-96338358	K562	blood:	n/a
33	chr9:96339738-96339788	HAEpiC	amniotic membrane:	n/a
34	chr9:96339159-96339209	AoSMC	blood vessel:	n/a
35	chr9:96339738-96339788	HCF	heart:	n/a
36	chr9:96338308-96338358	NB4	blood:	n/a
37	chr9:96339159-96339209	HepG2	liver:	n/a
38	chr9:96338308-96338358	RPTEC	kidney:	n/a
39	chr9:96338308-96338358	HRE	kidney:	n/a
40	chr9:96339159-96339209	HMEC	breast:	n/a
41	chr9:96339159-96339209	HPAEpiC	pulmonary alveolar:	n/a
42	chr9:96339159-96339209	CMK	blood:	n/a
43	chr9:96339159-96339209	NH-A	brain:	n/a
44	chr9:96339159-96339209	Caco-2	colon:	n/a
45	chr9:96339738-96339788	IMR90	lung:	fetal
46	chr9:96338308-96338358	Hepatocyte	liver:	n/a
47	chr9:96339738-96339788	AG10803	skin:	n/a
48	chr9:96337982-96338032	ovcar-3	ovarian:	n/a
49	chr9:96338308-96338358	NHBE	bronchial:	n/a
50	chr9:96339738-96339788	SK-N-MC	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43121431..43122251-chr9:96338410..96338951,2	Hela-S3	cervix:
2	chr9:96289339..96291734-chr9:96339194..96341014,2	MCF-7	breast:
3	chr9:96328414..96329044-chr9:96339964..96340763,2	MCF-7	breast:
4	chr8:101964530..101966057-chr9:96338377..96341052,2	MCF-7	breast:
5	chr9:95818234..95820974-chr9:96339140..96341685,2	MCF-7	breast:
6	chr9:96213158..96214882-chr9:96338001..96341678,3	K562	blood:
7	chr9:96211528..96214948-chr9:96337573..96343441,10	MCF-7	breast:
8	chr15:64672393..64674955-chr9:96338463..96341441,2	MCF-7	breast:
9	chr9:96337024..96339848-chr9:96617971..96619932,2	MCF-7	breast:
10	chr9:96298295..96300963-chr9:96339660..96341258,2	MCF-7	breast:
11	chr9:96214499..96217099-chr9:96338317..96340265,2	K562	blood:
12	chr9:96207292..96208805-chr9:96339241..96341688,2	MCF-7	breast:
13	chr9:95894803..95898160-chr9:96337820..96340366,3	MCF-7	breast:
14	chr9:96337657..96339290-chr9:96927321..96930180,2	K562	blood:
15	chr14:52455551..52457081-chr9:96338294..96340039,2	MCF-7	breast:
16	chr8:144819610..144821971-chr9:96337841..96340310,2	MCF-7	breast:
17	chr9:96211672..96218862-chr9:96335264..96341672,16	MCF-7	breast:
18	chr9:95895154..95898000-chr9:96338001..96340609,3	MCF-7	breast:
19	chr9:96323290..96325963-chr9:96339113..96341830,2	MCF-7	breast:
20	chr9:95856094..95858375-chr9:96337008..96340445,3	MCF-7	breast:

No data

Variant related genes	Relation type
PHF2	TF binding region
PHF2	CpG island
ENSG00000223446	chromatin interactions
ENSG00000203499	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000087302	chromatin interactions
ENSG00000166803	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000131669	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000231990	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000048828	chromatin interactions

Extended variants
information (count: 63 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:63 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555964147	chr9:96337764-96337765	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs141555748	chr9:96337765-96337766	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs544936658	chr9:96337780-96337781	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs370527608	chr9:96337817-96337818	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs563044625	chr9:96337873-96337874	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs577876853	chr9:96337952-96337953	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs567886772	chr9:96337968-96337969	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs545016766	chr9:96337983-96337984	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs560087069	chr9:96338057-96338058	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs527807732	chr9:96338064-96338065	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs951447	chr9:96338098-96338099	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs373669743	chr9:96338165-96338166	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs190442602	chr9:96338222-96338223	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs561957026	chr9:96338273-96338274	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs201381559	chr9:96338331-96338332	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs567007822	chr9:96338346-96338347	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs529071693	chr9:96338363-96338364	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs10821161	chr9:96338382-96338383	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs13291198	chr9:96338395-96338396	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs569075240	chr9:96338422-96338423	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs539719496	chr9:96338450-96338451	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs551426594	chr9:96338455-96338456	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs373079508	chr9:96338463-96338464	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs376304495	chr9:96338496-96338497	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs555168144	chr9:96338508-96338509	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs567307775	chr9:96338528-96338529	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs538064700	chr9:96338529-96338530	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs556682996	chr9:96338615-96338616	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs577938714	chr9:96338674-96338675	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs181251873	chr9:96338847-96338848	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs373859680	chr9:96339045-96339046	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs553782112	chr9:96339070-96339071	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs376714355	chr9:96339178-96339179	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs572096342	chr9:96339211-96339212	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs543152850	chr9:96339266-96339267	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs185358843	chr9:96339293-96339294	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs561226606	chr9:96339397-96339398	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs149596611	chr9:96339425-96339426	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs544101366	chr9:96339464-96339465	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs112087911	chr9:96339517-96339518	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs562653054	chr9:96339531-96339532	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs148039142	chr9:96339551-96339552	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs369432723	chr9:96339760-96339761	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs551693560	chr9:96339824-96339825	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs370431189	chr9:96339924-96339925	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs112367648	chr9:96339973-96339974	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs75508131	chr9:96339994-96339995	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs142508043	chr9:96340030-96340031	Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs548922530	chr9:96340043-96340044	Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs79332603	chr9:96340064-96340065	Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96336600-96337800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr9:96336600-96337800	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr9:96336600-96337800	Enhancers	Spleen	Spleen
4	chr9:96336800-96337800	Enhancers	Primary B cells from peripheral blood	blood
5	chr9:96336800-96337800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr9:96336800-96338000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr9:96337000-96337800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
8	chr9:96337000-96338200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr9:96337000-96338400	Enhancers	Fetal Heart	heart
10	chr9:96337200-96337800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:96337200-96337800	Flanking Active TSS	Colon Smooth Muscle	Colon
12	chr9:96337200-96337800	Flanking Active TSS	NHDF-Ad	bronchial
13	chr9:96337200-96337800	Flanking Active TSS	Osteobl	bone
14	chr9:96337200-96338000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:96337200-96338000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:96337200-96338000	Enhancers	Fetal Brain Male	brain
17	chr9:96337200-96338000	Flanking Active TSS	Rectal Smooth Muscle	rectum
18	chr9:96337200-96338000	Flanking Active TSS	HepG2	liver
19	chr9:96337200-96338200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr9:96337200-96338200	Flanking Active TSS	Placenta	Placenta
21	chr9:96337200-96338200	Flanking Active TSS	Dnd41	blood
22	chr9:96337200-96338400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr9:96337200-96338400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr9:96337200-96338400	Flanking Active TSS	Stomach Smooth Muscle	stomach
25	chr9:96337400-96337800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr9:96337400-96337800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr9:96337400-96337800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr9:96337400-96337800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:96337400-96337800	Enhancers	Primary B cells from cord blood	blood
30	chr9:96337400-96337800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr9:96337400-96337800	Enhancers	Liver	Liver
32	chr9:96337400-96337800	Flanking Active TSS	Brain Cingulate Gyrus	brain
33	chr9:96337400-96337800	Flanking Active TSS	Brain Germinal Matrix	brain
34	chr9:96337400-96337800	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr9:96337400-96337800	Flanking Active TSS	HSMM	muscle
36	chr9:96337400-96337800	Enhancers	K562	blood
37	chr9:96337400-96338000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
38	chr9:96337400-96338000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:96337400-96338000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr9:96337400-96338000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:96337400-96338000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr9:96337400-96338000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr9:96337400-96338000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr9:96337400-96338000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:96337400-96338000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
46	chr9:96337400-96338000	Flanking Active TSS	Brain Substantia Nigra	brain
47	chr9:96337400-96338000	Flanking Active TSS	Colonic Mucosa	Colon
48	chr9:96337400-96338000	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr9:96337400-96338000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr9:96337400-96338000	Flanking Active TSS	Fetal Intestine Large	intestine

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