Variant report

Variant	nsv525502
Chromosome Location	chr7:7938596-7996590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:246)
Chromatin interactive
region (count:59)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:7972195-7972521	K562	blood:	n/a	n/a
2	ATF2	chr7:7983912-7985171	GM12878	blood:	n/a	n/a
3	ATF2	chr7:7958625-7959819	GM12878	blood:	n/a	n/a
4	ATF2	chr7:7984294-7985089	GM12878	blood:	n/a	n/a
5	ATF2	chr7:7958697-7959462	GM12878	blood:	n/a	n/a
6	ATF2	chr7:7959982-7960638	GM12878	blood:	n/a	n/a
7	ATF2	chr7:7960070-7960623	GM12878	blood:	n/a	n/a
8	ATF3	chr7:7972162-7972477	K562	blood:	n/a	n/a
9	BATF	chr7:7959077-7959459	GM12878	blood:	n/a	n/a
10	BATF	chr7:7960171-7960572	GM12878	blood:	n/a	n/a
11	BATF	chr7:7960131-7960582	GM12878	blood:	n/a	n/a
12	BATF	chr7:7984555-7984966	GM12878	blood:	n/a	n/a
13	BATF	chr7:7959098-7959450	GM12878	blood:	n/a	n/a
14	BATF	chr7:7958720-7959043	GM12878	blood:	n/a	n/a
15	BATF	chr7:7984167-7985001	GM12878	blood:	n/a	chr7:7984516-7984524
16	BCL11A	chr7:7984554-7984958	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:7984414-7985016	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:7958762-7959113	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:7960180-7960428	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:7959156-7959459	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:7960150-7960494	GM12878	blood:	n/a	n/a
22	BCL3	chr7:7960150-7960591	GM12878	blood:	n/a	n/a
23	BCL3	chr7:7984528-7984983	GM12878	blood:	n/a	n/a
24	BCL3	chr7:7984595-7984957	GM12878	blood:	n/a	n/a
25	BCLAF1	chr7:7960024-7960613	GM12878	blood:	n/a	n/a
26	BCLAF1	chr7:7958610-7959527	GM12878	blood:	n/a	n/a
27	BCLAF1	chr7:7984172-7984955	GM12878	blood:	n/a	chr7:7984248-7984255
28	BCLAF1	chr7:7984134-7985147	GM12878	blood:	n/a	chr7:7984248-7984255
29	BHLHE40	chr7:7984476-7985207	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:7958749-7959392	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:7960099-7960686	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:7950678-7951759	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr7:7952755-7953845	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:7952970-7953850	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:7986594-7986691	K562	blood:	n/a	chr7:7986610-7986621
36	CEBPB	chr7:7950791-7951591	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:7972263-7972521	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:7953116-7953416	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:7946979-7947288	Hela-S3	cervix:	n/a	chr7:7947128-7947139
40	CEBPB	chr7:7946960-7947282	HepG2	liver:	n/a	chr7:7947128-7947139
41	CEBPB	chr7:7951010-7951401	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:7961525-7961725	A549	lung:	n/a	n/a
43	CEBPB	chr7:7958504-7958634	A549	lung:	n/a	n/a
44	CEBPB	chr7:7962316-7962726	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:7984112-7985174	GM12878	blood:	n/a	n/a
46	CEBPB	chr7:7984571-7984987	GM12878	blood:	n/a	n/a
47	CEBPB	chr7:7986198-7986777	Hela-S3	cervix:	n/a	chr7:7986610-7986621
48	CEBPB	chr7:7986467-7986754	A549	lung:	n/a	chr7:7986610-7986621
49	CEBPB	chr7:7986475-7986789	IMR90	lung:	n/a	chr7:7986610-7986621
50	CEBPB	chr7:7958547-7958660	H1-hESC	embryonic stem cell:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7974904-7974954	BJ	skin:	n/a
2	chr7:7974904-7974954	HRPEpiC	eye:	n/a
3	chr7:7974904-7974954	BJ	skin:	n/a
4	chr7:7974904-7974954	HRPEpiC	eye:	n/a
5	chr7:7962810-7962860	HCT-116	colon:	n/a
6	chr7:7962810-7962860	HMEC	breast:	n/a
7	chr7:7974904-7974954	HCT-116	colon:	n/a
8	chr7:7995879-7995929	GM12892	blood:	n/a
9	chr7:7959339-7959389	ECC-1	luminal epithelium:	n/a
10	chr7:7974904-7974954	MCF-7	breast:	n/a
11	chr7:7962810-7962860	PANC-1	pancreas:	n/a
12	chr7:7974904-7974954	HEK293	kidney:	embryo
13	chr7:7959339-7959389	AG09319	gingival:	n/a
14	chr7:7995879-7995929	HRE	kidney:	n/a
15	chr7:7959339-7959389	AG04450	lung:	fetal
16	chr7:7974904-7974954	SAEC	small airway:	n/a
17	chr7:7962810-7962860	NT2-D1	testis:	n/a
18	chr7:7974904-7974954	NHBE	bronchial:	n/a
19	chr7:7959339-7959389	Caco-2	colon:	n/a
20	chr7:7962810-7962860	Jurkat	blood:	n/a
21	chr7:7995879-7995929	MCF10A-Er-Src	breast:	n/a
22	chr7:7962810-7962860	K562	blood:	n/a
23	chr7:7974904-7974954	NH-A	brain:	n/a
24	chr7:7995879-7995929	A549	lung:	n/a
25	chr7:7962810-7962860	HUVEC	blood vessel:	n/a
26	chr7:7974904-7974954	GM06990	blood:	n/a
27	chr7:7995879-7995929	ProgFib	skin:	n/a
28	chr7:7959339-7959389	HRE	kidney:	n/a
29	chr7:7959339-7959389	SKMC	muscle:	n/a
30	chr7:7995879-7995929	AG04450	lung:	fetal
31	chr7:7995879-7995929	K562	blood:	n/a
32	chr7:7995879-7995929	SK-N-SH	brain:	n/a
33	chr7:7959339-7959389	AG10803	skin:	n/a
34	chr7:7974904-7974954	HCPEpiC	choroid plexus:	n/a
35	chr7:7974904-7974954	GM12891	blood:	n/a
36	chr7:7959339-7959389	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:7974904-7974954	AG04450	lung:	fetal
38	chr7:7962810-7962860	Caco-2	colon:	n/a
39	chr7:7962810-7962860	NHDF-neo	bronchial:	n/a
40	chr7:7962810-7962860	AG09319	gingival:	n/a
41	chr7:7959339-7959389	HCPEpiC	choroid plexus:	n/a
42	chr7:7962810-7962860	MCF10A-Er-Src	breast:	n/a
43	chr7:7974904-7974954	HMEC	breast:	n/a
44	chr7:7995879-7995929	Hepatocyte	liver:	n/a
45	chr7:7974904-7974954	NB4	blood:	n/a
46	chr7:7974904-7974954	HUVEC	blood vessel:	n/a
47	chr7:7995879-7995929	LNCaP	prostate:	n/a
48	chr7:7974904-7974954	AG10803	skin:	n/a
49	chr7:7974904-7974954	LNCaP	prostate:	n/a
50	chr7:7995879-7995929	HCPEpiC	choroid plexus:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:7935711..7938261-chr7:7941744..7943349,2	K562	blood:
2	chr7:7971057..7974554-chr7:8007122..8010569,3	MCF-7	breast:
3	chr7:7958223..7960322-chr7:7962105..7964489,3	MCF-7	breast:
4	chr7:7956835..7959922-chr7:8007692..8010316,3	MCF-7	breast:
5	chr7:7967883..7969895-chr7:8007215..8009286,2	MCF-7	breast:
6	chr7:7951218..7952780-chr7:7955913..7958820,2	K562	blood:
7	chr1:65350348..65350931-chr7:7966977..7967736,2	MCF-7	breast:
8	chr7:7987002..7988972-chr7:8001307..8003918,2	K562	blood:
9	chr7:7985394..7987246-chr7:8007323..8009239,2	K562	blood:
10	chr7:7952035..7955913-chr7:7956512..7960009,4	MCF-7	breast:
11	chr7:7972587..7974133-chr7:8008432..8010040,2	MCF-7	breast:
12	chr7:7996397..7998249-chr7:8301058..8303680,2	MCF-7	breast:
13	chr7:7993781..7999497-chr7:8006665..8011144,9	MCF-7	breast:
14	chr7:7988942..7990791-chr7:8008442..8011147,2	K562	blood:
15	chr7:7947056..7948865-chr7:7950686..7953467,2	MCF-7	breast:
16	chr7:7920545..7923153-chr7:7947615..7949685,2	MCF-7	breast:
17	chr1:151028007..151030723-chr7:7959783..7961888,2	MCF-7	breast:
18	chr7:7949577..7953346-chr7:7959266..7963720,5	MCF-7	breast:
19	chr7:7950749..7951554-chr7:8008162..8008847,3	MCF-7	breast:
20	chr7:7953946..7955659-chr7:7959073..7960806,2	K562	blood:
21	chr7:7947370..7958537-chr7:8006160..8010935,22	MCF-7	breast:
22	chr7:7991342..7993380-chr7:8007489..8009789,2	MCF-7	breast:
23	chr7:7969976..7971625-chr7:7983223..7985791,2	MCF-7	breast:
24	chr7:7935831..7938842-chr7:8008024..8010603,3	MCF-7	breast:
25	chr7:7992434..7993007-chr8:144434639..144435482,2	MCF-7	breast:
26	chr7:7936554..7939221-chr7:8008179..8010269,3	MCF-7	breast:
27	chr7:7982231..7984516-chr7:7984634..7987020,2	MCF-7	breast:
28	chr7:7982231..7984516-chr7:7984634..7987020,2	MCF-7	breast:
29	chr7:7951069..7953394-chr7:7953998..7956483,2	K562	blood:
30	chr7:7980530..7982916-chr7:8007052..8009790,2	MCF-7	breast:
31	chr7:7973639..7976442-chr7:7979056..7980885,2	K562	blood:
32	chr7:7930260..7932176-chr7:7966125..7967661,2	K562	blood:
33	chr7:7944145..7947023-chr7:7968614..7970373,2	K562	blood:
34	chr7:7985182..7986874-chr7:7992150..7994347,2	K562	blood:
35	chr7:7951059..7955946-chr7:8007279..8010658,10	MCF-7	breast:
36	chr18:3245457..3248097-chr7:7961361..7963995,2	MCF-7	breast:
37	chr6:36077762..36078586-chr7:7965279..7966158,2	MCF-7	breast:
38	chr7:7951218..7952780-chr7:7955913..7958820,2	K562	blood:
39	chr7:7941789..7943515-chr7:8007285..8009574,2	MCF-7	breast:
40	chr7:7951069..7953394-chr7:7953998..7956483,2	K562	blood:
41	chr7:7960248..7962002-chr7:8129033..8131831,2	MCF-7	breast:
42	chr7:7973639..7976442-chr7:7979056..7980885,2	K562	blood:
43	chr7:7958467..7959967-chr7:8328195..8331123,2	K562	blood:
44	chr7:7949350..7952293-chr7:7956418..7958594,2	MCF-7	breast:
45	chr6:31239462..31239977-chr7:7984426..7984946,2	MCF-7	breast:
46	chr7:7948433..7950272-chr7:7951772..7953401,2	MCF-7	breast:
47	chr7:7947056..7948865-chr7:7950686..7953467,2	MCF-7	breast:
48	chr7:7961731..7965503-chr7:8006784..8010279,5	MCF-7	breast:
49	chr7:7985182..7986874-chr7:7992150..7994347,2	K562	blood:
50	chr7:7951350..7953467-chr7:8011566..8014289,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLCCI1-6	chr7:7938942-7939427	NONHSAT119135
2	lnc-ICA1-5	chr7:7956205-7956400	l_3361_chr7:7951501-7956400_thyroid
3	lnc-ICA1-1	chr7:7989470-7990137	NR_110018
4	lnc-GLCCI1-3	chr7:7977843-7978060	expReg_chr7_767_+
5	lnc-GLCCI1-6	chr7:7989470-7989923	NONHSAT119135
6	lnc-GLCCI1-6	chr7:7995277-7995362	NONHSAT119135
7	lnc-ICA1-5	chr7:7956100-7956171	l_3361_chr7:7951501-7956400_thyroid
8	lnc-ICA1-2	chr7:7989484-7990137	ENSG00000234141.1
9	lnc-GLCCI1-6	chr7:7983250-7983854	NONHSAT119135
10	lnc-GLCCI1-6	chr7:7968360-7968895	NONHSAT119135
11	lnc-ICA1-5	chr7:7951815-7952442	l_3361_chr7:7951501-7956400_thyroid
12	lnc-GLCCI1-6	chr7:7939478-7939517	NONHSAT119135
13	lnc-GLCCI1-6	chr7:7982071-7982499	NONHSAT119135
14	lnc-GLCCI1-5	chr7:7976601-7976991	expReg_chr7_762_+
15	lnc-GLCCI1-4	chr7:7977005-7977723	expReg_chr7_764_+
16	lnc-GLCCI1-6	chr7:7959367-7960001	NONHSAT119135
17	lnc-ICA1-5	chr7:7956009-7956662	NONHSAT119137
18	lnc-ICA1-2	chr7:7990303-7990340	ENSG00000234141.1
19	lnc-ICA1-5	chr7:7956828-7956865	NONHSAT119137
20	lnc-ICA1-5	chr7:7951502-7951811	l_3361_chr7:7951501-7956400_thyroid
21	lnc-ICA1-1	chr7:7990303-7990340	NR_110018
22	lnc-ICA1-1	chr7:7995492-7995647	NR_110018

No data

Variant related genes	Relation type
ENSG00000214998	TF binding region
RNU6-534P	TF binding region
ENSG00000234141	TF binding region
ENSG00000214998	CpG island
RNU6-534P	CpG island
ENSG00000234141	CpG island
ENSG00000101608	chromatin interactions
ENSG00000201747	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000229970	chromatin interactions
ENSG00000233108	chromatin interactions
ENSG00000003147	chromatin interactions
ENSG00000244239	chromatin interactions
ENSG00000213190	chromatin interactions
ENSG00000214998	chromatin interactions
ENSG00000272688	chromatin interactions
ENSG00000204525	chromatin interactions

Extended variants
information (count: 2252 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2252 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10486201	chr7:7938596-7938597	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	disease
2	rs142806851	chr7:7938597-7938598	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs556794893	chr7:7938612-7938613	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs374317601	chr7:7938667-7938668	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189649849	chr7:7938704-7938705	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567058306	chr7:7938780-7938781	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs533613197	chr7:7938791-7938792	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552241870	chr7:7938814-7938815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570502427	chr7:7938831-7938832	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs537428581	chr7:7938832-7938833	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555777056	chr7:7938861-7938862	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574353603	chr7:7938871-7938872	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs377020709	chr7:7938878-7938879	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs182294276	chr7:7938886-7938887	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs539396819	chr7:7938908-7938909	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs577168529	chr7:7938924-7938925	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs545718789	chr7:7938978-7938979	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs56364053	chr7:7938987-7938988	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577442043	chr7:7938988-7938989	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs188252175	chr7:7938989-7938990	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs147394174	chr7:7939023-7939024	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs556178430	chr7:7939057-7939058	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs10235557	chr7:7939156-7939157	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs542025863	chr7:7939190-7939191	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs35211091	chr7:7939204-7939205	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs548909134	chr7:7939220-7939221	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs560664454	chr7:7939227-7939228	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs527885343	chr7:7939245-7939246	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs552527275	chr7:7939247-7939248	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs556468485	chr7:7939287-7939288	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs570513778	chr7:7939301-7939302	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs559872977	chr7:7939324-7939325	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs10238652	chr7:7939329-7939330	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs555518537	chr7:7939406-7939407	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs139809921	chr7:7939433-7939434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371504257	chr7:7939475-7939476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535322703	chr7:7939488-7939489	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs73231792	chr7:7939513-7939514	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374026583	chr7:7939518-7939519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149536074	chr7:7939590-7939591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545923834	chr7:7939606-7939607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564063342	chr7:7939613-7939614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34989993	chr7:7939688-7939689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183309249	chr7:7939744-7939745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556557210	chr7:7939746-7939747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367999670	chr7:7939749-7939750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371491647	chr7:7939762-7939763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560820193	chr7:7939769-7939770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188196066	chr7:7939770-7939771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11763763	chr7:7939795-7939796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7897200-7942400	Weak transcription	Aorta	Aorta
2	chr7:7909600-7942400	Weak transcription	Left Ventricle	heart
3	chr7:7913200-7942400	Weak transcription	Primary T cells from cord blood	blood
4	chr7:7915800-7943000	Weak transcription	Gastric	stomach
5	chr7:7928600-7942400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:7930200-7951000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:7934600-7939000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:7935000-7942400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:7935000-7951600	Weak transcription	Pancreas	Pancrea
10	chr7:7935400-7952600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:7935600-7949000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:7936600-7938800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:7936600-7939000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:7936800-7938800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:7936800-7938800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:7937000-7938600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:7937200-7938600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:7937200-7938800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr7:7937400-7939800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:7937800-7938600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr7:7937800-7942400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:7937800-7942400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr7:7938000-7938600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr7:7938000-7938600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:7938000-7941600	Weak transcription	Fetal Heart	heart
26	chr7:7938600-7938800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:7938600-7938800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr7:7938600-7938800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:7938600-7939000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr7:7938600-7939000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:7938800-7939000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:7938800-7950600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr7:7939000-7942400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr7:7939000-7942600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr7:7939800-7942400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:7941600-7943000	Enhancers	Fetal Heart	heart
37	chr7:7942200-7942800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:7942400-7942600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:7942400-7942600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:7942400-7942600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:7942400-7942800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:7942400-7942800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:7942400-7942800	Enhancers	Primary T cells from cord blood	blood
44	chr7:7942400-7942800	Enhancers	Placenta Amnion	Placenta Amnion
45	chr7:7942400-7942800	Enhancers	Right Ventricle	heart
46	chr7:7942400-7943000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr7:7942400-7943000	Strong transcription	Aorta	Aorta
48	chr7:7942400-7943000	Enhancers	Left Ventricle	heart
49	chr7:7942400-7943000	Enhancers	Right Atrium	heart
50	chr7:7942400-7943000	Enhancers	Thymus	Thymus

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