Variant report

Variant	esv3326861
Chromosome Location	chr9:79008157-79010705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:777)
CpG islands
(count:307)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:79009886-79010178	K562	blood:	n/a	n/a
2	ARID3A	chr9:79009242-79009417	K562	blood:	n/a	n/a
3	ARID3A	chr9:79010416-79010569	K562	blood:	n/a	n/a
4	ARID3A	chr9:79009069-79010337	HepG2	liver:	n/a	n/a
5	ATF1	chr9:79009279-79010167	K562	blood:	n/a	n/a
6	ATF2	chr9:79008503-79008878	GM12878	blood:	n/a	n/a
7	ATF2	chr9:79009116-79009631	GM12878	blood:	n/a	n/a
8	ATF2	chr9:79008405-79009087	GM12878	blood:	n/a	n/a
9	ATF3	chr9:79008877-79009039	K562	blood:	n/a	chr9:79008962-79008982
10	ATF3	chr9:79008826-79009138	HepG2	liver:	n/a	chr9:79008962-79008982
11	ATF3	chr9:79009084-79009589	A549	lung:	n/a	n/a
12	ATF3	chr9:79008773-79009216	H1-hESC	embryonic stem cell:	n/a	chr9:79008962-79008982
13	BACH1	chr9:79009163-79009323	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:79008729-79008898	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr9:79008469-79008981	GM12878	blood:	n/a	n/a
16	BATF	chr9:79008528-79008873	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:79008512-79009000	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:79008599-79008848	GM12878	blood:	n/a	n/a
19	BCL3	chr9:79008550-79008960	GM12878	blood:	n/a	n/a
20	BCL3	chr9:79008512-79009691	A549	lung:	n/a	n/a
21	BCLAF1	chr9:79009131-79009501	K562	blood:	n/a	n/a
22	BCLAF1	chr9:79008490-79009847	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:79008680-79010191	K562	blood:	n/a	chr9:79008940-79008956
24	BHLHE40	chr9:79008678-79009596	HepG2	liver:	n/a	chr9:79008940-79008956
25	BHLHE40	chr9:79008570-79009868	GM12878	blood:	n/a	chr9:79008940-79008956
26	BRCA1	chr9:79009244-79010187	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr9:79009225-79009411	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr9:79009048-79009481	K562	blood:	n/a	n/a
29	CCNT2	chr9:79008912-79009661	K562	blood:	n/a	n/a
30	CCNT2	chr9:79009900-79010133	K562	blood:	n/a	n/a
31	CEBPB	chr9:79009311-79009581	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr9:79009814-79010160	K562	blood:	n/a	n/a
33	CEBPB	chr9:79009124-79010212	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:79009808-79010135	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:79009925-79010089	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:79008468-79010201	Hela-S3	cervix:	n/a	chr9:79008596-79008609 chr9:79008598-79008609 chr9:79008593-79008610
37	CEBPB	chr9:79009830-79010201	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:79008389-79008906	GM12878	blood:	n/a	chr9:79008596-79008609 chr9:79008598-79008609 chr9:79008593-79008610
39	CEBPB	chr9:79009832-79010192	K562	blood:	n/a	n/a
40	CEBPD	chr9:79009044-79009407	HepG2	liver:	n/a	n/a
41	CEBPD	chr9:79009773-79010200	HepG2	liver:	n/a	n/a
42	CEBPD	chr9:79009095-79009398	HepG2	liver:	n/a	n/a
43	CHD1	chr9:79008877-79009257	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr9:79009557-79009782	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr9:79008916-79009489	GM12878	blood:	n/a	n/a
46	CHD1	chr9:79010428-79010523	GM12878	blood:	n/a	n/a
47	CHD2	chr9:79008996-79009989	K562	blood:	n/a	n/a
48	CHD2	chr9:79008694-79009584	HepG2	liver:	n/a	n/a
49	CHD2	chr9:79009847-79010150	HepG2	liver:	n/a	n/a
50	CHD2	chr9:79008579-79009953	GM12878	blood:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:79009726-79009776	SAEC	small airway:	n/a
2	chr9:79008793-79008843	HMEC	breast:	n/a
3	chr9:79009726-79009776	SAEC	small airway:	n/a
4	chr9:79008793-79008843	HMEC	breast:	n/a
5	chr9:79009433-79009483	HIPEpiC	eye:	n/a
6	chr9:79008793-79008843	NHDF-neo	bronchial:	n/a
7	chr9:79009566-79009616	LNCaP	prostate:	n/a
8	chr9:79008793-79008843	MCF10A-Er-Src	breast:	n/a
9	chr9:79009726-79009776	U87	brain:	n/a
10	chr9:79009566-79009616	PANC-1	pancreas:	n/a
11	chr9:79009726-79009776	BE2_C	brain:	n/a
12	chr9:79009738-79009788	NHDF-neo	bronchial:	n/a
13	chr9:79009433-79009483	SK-N-SH	brain:	n/a
14	chr9:79009738-79009788	NHBE	bronchial:	n/a
15	chr9:79009726-79009776	SK-N-SH_RA	brain:	n/a
16	chr9:79009738-79009788	U87	brain:	n/a
17	chr9:79009738-79009788	K562	blood:	n/a
18	chr9:79009738-79009788	GM12892	blood:	n/a
19	chr9:79009726-79009776	Hepatocyte	liver:	n/a
20	chr9:79009566-79009616	T-47D	breast:	n/a
21	chr9:79009433-79009483	HRCEpiC	kidney:	n/a
22	chr9:79008793-79008843	Caco-2	colon:	n/a
23	chr9:79009726-79009776	Jurkat	blood:	n/a
24	chr9:79009566-79009616	HL-60	blood:	n/a
25	chr9:79009726-79009776	Caco-2	colon:	n/a
26	chr9:79009726-79009776	IMR90	lung:	fetal
27	chr9:79009566-79009616	Hela-S3	cervix:	n/a
28	chr9:79009566-79009616	BE2_C	brain:	n/a
29	chr9:79009566-79009616	MCF10A-Er-Src	breast:	n/a
30	chr9:79008793-79008843	SAEC	small airway:	n/a
31	chr9:79009566-79009616	GM06990	blood:	n/a
32	chr9:79009566-79009616	BJ	skin:	n/a
33	chr9:79009566-79009616	NT2-D1	testis:	n/a
34	chr9:79009726-79009776	HCT-116	colon:	n/a
35	chr9:79008793-79008843	BJ	skin:	n/a
36	chr9:79009726-79009776	HCM	heart:	n/a
37	chr9:79009433-79009483	HRPEpiC	eye:	n/a
38	chr9:79009566-79009616	H1-hESC	embryonic stem cell:	embryo
39	chr9:79009738-79009788	IMR90	lung:	fetal
40	chr9:79008793-79008843	AG09309	skin:	n/a
41	chr9:79009726-79009776	HPAEpiC	pulmonary alveolar:	n/a
42	chr9:79009726-79009776	NHBE	bronchial:	n/a
43	chr9:79009738-79009788	ProgFib	skin:	n/a
44	chr9:79008793-79008843	SK-N-SH	brain:	n/a
45	chr9:79009566-79009616	Jurkat	blood:	n/a
46	chr9:79009566-79009616	HEK293	kidney:	embryo
47	chr9:79008793-79008843	HNPCEpiC	eye:	n/a
48	chr9:79009726-79009776	ProgFib	skin:	n/a
49	chr9:79009726-79009776	PrEC	prostate:	n/a
50	chr9:79009433-79009483	HAEpiC	amniotic membrane:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:2328555..2329211-chr9:79008711..79009422,2	Hela-S3	cervix:
2	chr9:78993024..78994920-chr9:79009980..79012177,2	MCF-7	breast:
3	chr11:2950199..2950844-chr9:79009261..79009909,2	HCT-116	colon:
4	chr7:92219030..92219725-chr9:79009125..79009872,2	HCT-116	colon:
5	chr9:79009527..79011124-chr9:79074048..79076040,2	MCF-7	breast:
6	chr9:79007886..79011336-chr9:79013243..79018063,7	MCF-7	breast:
7	chr9:79007540..79010172-chr9:79074126..79075718,2	MCF-7	breast:
8	chr15:75315805..75316441-chr9:79009750..79010363,2	Hela-S3	cervix:
9	chr9:79009596..79011512-chr9:79033569..79035078,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPSAP9	TF binding region
RFK	TF binding region
RPSAP9	CpG island
RFK	CpG island
ENSG00000233814	chromatin interactions
ENSG00000234545	chromatin interactions
ENSG00000130332	chromatin interactions
ENSG00000005206	chromatin interactions
ENSG00000138621	chromatin interactions
ENSG00000181649	chromatin interactions
ENSG00000234618	chromatin interactions
ENSG00000187210	chromatin interactions

Extended variants
information (count: 95 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567149837	chr9:79008191-79008192	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs2501922	chr9:79008243-79008244	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs560684072	chr9:79008280-79008281	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2490581	chr9:79008284-79008285	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35432738	chr9:79008305-79008306	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs568790342	chr9:79008309-79008310	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189433163	chr9:79008335-79008336	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544294683	chr9:79008357-79008358	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7022515	chr9:79008451-79008452	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs551321602	chr9:79008457-79008458	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140034228	chr9:79008477-79008478	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533836054	chr9:79008485-79008486	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs553581908	chr9:79008501-79008502	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs536039425	chr9:79008518-79008519	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs368958613	chr9:79008636-79008637	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs62567919	chr9:79008644-79008645	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7045064	chr9:79008674-79008675	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs142200055	chr9:79008693-79008694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs558087953	chr9:79008722-79008723	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs151223786	chr9:79008750-79008751	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs540664429	chr9:79008800-79008801	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs560368648	chr9:79008845-79008846	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs529375790	chr9:79008876-79008877	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs542385496	chr9:79008878-79008879	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs562357582	chr9:79008912-79008913	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs531460894	chr9:79008938-79008939	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs551388311	chr9:79008942-79008943	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs41288757	chr9:79008947-79008948	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs527278919	chr9:79008973-79008974	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs547401852	chr9:79008975-79008976	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs147845416	chr9:79009015-79009016	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs368029943	chr9:79009033-79009034	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs188086740	chr9:79009034-79009035	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs141491972	chr9:79009046-79009047	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs149930087	chr9:79009049-79009050	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs558211577	chr9:79009051-79009052	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs148289048	chr9:79009069-79009070	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs555959241	chr9:79009076-79009077	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs371365472	chr9:79009100-79009101	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs2490582	chr9:79009106-79009107	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs3739729	chr9:79009139-79009140	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373469309	chr9:79009180-79009181	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs11548954	chr9:79009204-79009205	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs11548952	chr9:79009236-79009237	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11548956	chr9:79009251-79009252	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs7026641	chr9:79009256-79009257	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs370875961	chr9:79009289-79009290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs142046364	chr9:79009290-79009291	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs3739730	chr9:79009347-79009348	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs542721406	chr9:79009354-79009355	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:78986600-79008400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:78988200-79008400	Weak transcription	Brain Substantia Nigra	brain
3	chr9:78988200-79008400	Weak transcription	Fetal Heart	heart
4	chr9:78988600-79008200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr9:78988800-79008400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr9:78990200-79008400	Weak transcription	Right Ventricle	heart
7	chr9:78990400-79008200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:78990400-79008400	Weak transcription	Fetal Kidney	kidney
9	chr9:78990600-79008400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr9:78990600-79008400	Weak transcription	Fetal Lung	lung
11	chr9:78990600-79008400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:78990800-79008400	Weak transcription	NHLF	lung
13	chr9:78992200-79008600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:78995200-79008400	Weak transcription	Stomach Mucosa	stomach
15	chr9:78995200-79008600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:78996000-79008400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr9:78997600-79008400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr9:78997800-79008400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr9:78998400-79008400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr9:78998800-79008600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr9:78999200-79008400	Weak transcription	NH-A	brain
22	chr9:78999400-79008600	Weak transcription	Spleen	Spleen
23	chr9:79000200-79008400	Weak transcription	Pancreas	Pancrea
24	chr9:79000400-79008400	Weak transcription	Thymus	Thymus
25	chr9:79002000-79008400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr9:79003000-79008200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:79003000-79008400	Weak transcription	Aorta	Aorta
28	chr9:79003000-79008400	Weak transcription	Left Ventricle	heart
29	chr9:79003000-79008600	Weak transcription	Esophagus	oesophagus
30	chr9:79003400-79008400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr9:79003400-79008400	Weak transcription	Placenta	Placenta
32	chr9:79003600-79008200	Weak transcription	HSMMtube	muscle
33	chr9:79003600-79008400	Weak transcription	Brain Germinal Matrix	brain
34	chr9:79003600-79008400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr9:79003800-79008400	Weak transcription	Osteobl	bone
36	chr9:79004000-79008200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr9:79004200-79008200	Weak transcription	Colon Smooth Muscle	Colon
38	chr9:79004200-79008400	Weak transcription	Primary T cells from cord blood	blood
39	chr9:79004200-79008400	Weak transcription	Fetal Thymus	thymus
40	chr9:79004200-79008400	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr9:79004400-79008400	Weak transcription	Primary B cells from cord blood	blood
42	chr9:79004400-79008400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr9:79004400-79008400	Weak transcription	Psoas Muscle	Psoas
44	chr9:79004600-79008400	Weak transcription	Fetal Stomach	stomach
45	chr9:79006000-79008400	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr9:79007000-79008400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr9:79007200-79008200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr9:79007200-79008400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr9:79007200-79008400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr9:79007200-79008400	Enhancers	Brain Hippocampus Middle	brain

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