Variant report

Variant	nsv599564
Chromosome Location	chr5:118465249-118621672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1620)
CpG islands
(count:1160)
Chromatin interactive
region (count:144)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118554812-118555173	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:118503944-118504095	K562	blood:	n/a	n/a
3	ARID3A	chr5:118505094-118505244	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:118606863-118607063	K562	blood:	n/a	n/a
5	ARID3A	chr5:118565756-118565843	K562	blood:	n/a	n/a
6	ARID3A	chr5:118591724-118592031	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:118516050-118516311	K562	blood:	n/a	n/a
8	ATF1	chr5:118494181-118494265	K562	blood:	n/a	n/a
9	ATF1	chr5:118515900-118516243	K562	blood:	n/a	n/a
10	ATF1	chr5:118621241-118621642	K562	blood:	n/a	n/a
11	ATF1	chr5:118603713-118604086	K562	blood:	n/a	n/a
12	ATF1	chr5:118604556-118605166	K562	blood:	n/a	n/a
13	ATF2	chr5:118556197-118556741	GM12878	blood:	n/a	n/a
14	ATF2	chr5:118556225-118556630	GM12878	blood:	n/a	n/a
15	ATF2	chr5:118610850-118611870	GM12878	blood:	n/a	n/a
16	ATF2	chr5:118603565-118604586	GM12878	blood:	n/a	n/a
17	ATF3	chr5:118604459-118604753	K562	blood:	n/a	n/a
18	ATF3	chr5:118523560-118523863	GM12878	blood:	n/a	chr5:118523740-118523749
19	BACH1	chr5:118604432-118604859	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr5:118610851-118611193	GM12878	blood:	n/a	chr5:118611044-118611057
21	BCLAF1	chr5:118603696-118605414	GM12878	blood:	n/a	chr5:118604659-118604672 chr5:118604655-118604668 chr5:118604239-118604252
22	BCLAF1	chr5:118610788-118611895	GM12878	blood:	n/a	chr5:118611300-118611309
23	BCLAF1	chr5:118603942-118604715	GM12878	blood:	n/a	chr5:118604659-118604672 chr5:118604655-118604668 chr5:118604239-118604252
24	BHLHE40	chr5:118609077-118609241	K562	blood:	n/a	n/a
25	BHLHE40	chr5:118591568-118591967	HepG2	liver:	n/a	n/a
26	BHLHE40	chr5:118611510-118611750	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:118603661-118604624	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:118614004-118614140	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:118603717-118605368	K562	blood:	n/a	n/a
30	BHLHE40	chr5:118603723-118604934	HepG2	liver:	n/a	n/a
31	BHLHE40	chr5:118604935-118605354	GM12878	blood:	n/a	n/a
32	BRCA1	chr5:118604267-118604673	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr5:118604032-118604440	GM12878	blood:	n/a	n/a
34	BRCA1	chr5:118603773-118604195	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr5:118609985-118610634	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr5:118604429-118604629	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr5:118604416-118604566	HepG2	liver:	n/a	n/a
38	CBX3	chr5:118471412-118471779	K562	blood:	n/a	n/a
39	CBX3	chr5:118591281-118592096	K562	blood:	n/a	n/a
40	CBX3	chr5:118609841-118610673	HCT-116	colon:	n/a	n/a
41	CBX3	chr5:118603518-118605307	K562	blood:	n/a	n/a
42	CBX3	chr5:118593138-118593677	K562	blood:	n/a	n/a
43	CBX3	chr5:118591346-118591586	K562	blood:	n/a	n/a
44	CBX3	chr5:118472387-118472685	K562	blood:	n/a	n/a
45	CBX3	chr5:118593081-118593712	K562	blood:	n/a	n/a
46	CBX3	chr5:118472322-118472731	K562	blood:	n/a	n/a
47	CCNT2	chr5:118604019-118605526	K562	blood:	n/a	chr5:118604994-118605014
48	CEBPB	chr5:118617064-118617330	A549	lung:	n/a	chr5:118617194-118617203
49	CEBPB	chr5:118606749-118607035	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:118610891-118611208	Hela-S3	cervix:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118604943-118604993	AG09319	gingival:	n/a
2	chr5:118604943-118604993	AG09319	gingival:	n/a
3	chr5:118604540-118604590	GM06990	blood:	n/a
4	chr5:118609965-118610015	HL-60	blood:	n/a
5	chr5:118603804-118603854	HL-60	blood:	n/a
6	chr5:118609258-118609308	Caco-2	colon:	n/a
7	chr5:118608672-118608722	HRPEpiC	eye:	n/a
8	chr5:118609258-118609308	PANC-1	pancreas:	n/a
9	chr5:118603742-118603792	NB4	blood:	n/a
10	chr5:118604943-118604993	NT2-D1	testis:	n/a
11	chr5:118609467-118609517	U87	brain:	n/a
12	chr5:118604262-118604312	MCF-7	breast:	n/a
13	chr5:118604943-118604993	HL-60	blood:	n/a
14	chr5:118603908-118603958	AoSMC	blood vessel:	n/a
15	chr5:118604807-118604857	GM19239	blood:	n/a
16	chr5:118609258-118609308	SK-N-SH	brain:	n/a
17	chr5:118609965-118610015	MCF-7	breast:	n/a
18	chr5:118608672-118608722	GM12892	blood:	n/a
19	chr5:118502651-118502701	HIPEpiC	eye:	n/a
20	chr5:118603880-118603930	A549	lung:	n/a
21	chr5:118604262-118604312	SK-N-MC	brain:	n/a
22	chr5:118603938-118603988	HEK293	kidney:	embryo
23	chr5:118603742-118603792	GM19239	blood:	n/a
24	chr5:118603880-118603930	HepG2	liver:	n/a
25	chr5:118604262-118604312	ovcar-3	ovarian:	n/a
26	chr5:118604807-118604857	SK-N-SH_RA	brain:	n/a
27	chr5:118604943-118604993	IMR90	lung:	fetal
28	chr5:118604807-118604857	PANC-1	pancreas:	n/a
29	chr5:118609965-118610015	A549	lung:	n/a
30	chr5:118502651-118502701	LNCaP	prostate:	n/a
31	chr5:118604807-118604857	AG10803	skin:	n/a
32	chr5:118604262-118604312	HEK293	kidney:	embryo
33	chr5:118603908-118603958	HCPEpiC	choroid plexus:	n/a
34	chr5:118609467-118609517	Hepatocyte	liver:	n/a
35	chr5:118502651-118502701	AG09319	gingival:	n/a
36	chr5:118603804-118603854	U87	brain:	n/a
37	chr5:118580164-118580214	RPTEC	kidney:	n/a
38	chr5:118609965-118610015	T-47D	breast:	n/a
39	chr5:118604262-118604312	NT2-D1	testis:	n/a
40	chr5:118603880-118603930	H1-hESC	embryonic stem cell:	embryo
41	chr5:118584299-118584349	CMK	blood:	n/a
42	chr5:118609258-118609308	LNCaP	prostate:	n/a
43	chr5:118603880-118603930	HCF	heart:	n/a
44	chr5:118603880-118603930	BE2_C	brain:	n/a
45	chr5:118580164-118580214	GM12891	blood:	n/a
46	chr5:118584299-118584349	SK-N-SH	brain:	n/a
47	chr5:118608672-118608722	H1-hESC	embryonic stem cell:	embryo
48	chr5:118603804-118603854	HCF	heart:	n/a
49	chr5:118604943-118604993	GM12891	blood:	n/a
50	chr5:118604807-118604857	BE2_C	brain:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:118549863..118550376-chr7:16168238..16169156,2	MCF-7	breast:
2	chr5:118583032..118585646-chr5:118590465..118591965,2	K562	blood:
3	chr5:118574799..118576857-chr5:118580303..118583195,3	K562	blood:
4	chr5:118465720..118469192-chr5:118469871..118473875,5	K562	blood:
5	chr5:118478650..118480412-chr5:118485694..118488311,3	K562	blood:
6	chr5:118596062..118599581-chr5:118601071..118605353,5	MCF-7	breast:
7	chr5:118494371..118496864-chr5:118503410..118506409,2	K562	blood:
8	chr5:118573504..118576319-chr5:118580787..118583650,2	K562	blood:
9	chr5:118494371..118496864-chr5:118503410..118506409,2	K562	blood:
10	chr5:118582682..118585597-chr5:118588093..118590395,3	MCF-7	breast:
11	chr3:48342633..48343492-chr5:118604190..118604719,2	HCT-116	colon:
12	chr5:118478650..118480412-chr5:118485694..118488311,3	K562	blood:
13	chr1:33282573..33283573-chr5:118604777..118605431,2	Hela-S3	cervix:
14	chr5:118581217..118584329-chr5:118602907..118604848,3	K562	blood:
15	chr5:118597056..118599082-chr5:118600428..118603358,2	K562	blood:
16	chr5:118586532..118588054-chr5:118602135..118604215,2	K562	blood:
17	chr5:118478650..118480412-chr5:118485694..118488246,2	K562	blood:
18	chr5:118612244..118613864-chr5:118618736..118620267,2	K562	blood:
19	chr5:118323897..118324678-chr5:118591546..118592389,2	MCF-7	breast:
20	chr5:118559801..118561992-chr5:118562252..118565088,2	K562	blood:
21	chr5:118565495..118568249-chr5:118569908..118571816,2	K562	blood:
22	chr5:118570748..118572621-chr5:118572841..118575732,2	MCF-7	breast:
23	chr5:118607071..118610754-chr5:118620607..118623123,4	K562	blood:
24	chr13:111367305..111368155-chr5:118604250..118604937,2	NB4	blood:
25	chr2:105654308..105655008-chr5:118603902..118604609,2	HCT-116	colon:
26	chr5:118405445..118408256-chr5:118508657..118510829,2	MCF-7	breast:
27	chr5:118604153..118605024-chrX:49028222..49028829,2	Hela-S3	cervix:
28	chr5:118567020..118569794-chr5:118587970..118590169,2	K562	blood:
29	chr5:118608930..118611747-chr5:118623733..118626239,2	MCF-7	breast:
30	chr5:118506899..118509414-chr5:118511277..118513937,2	MCF-7	breast:
31	chr5:118565495..118568249-chr5:118569908..118571816,2	K562	blood:
32	chr5:118609066..118610745-chr5:118637168..118638991,2	K562	blood:
33	chr5:118551365..118552971-chr5:118559798..118561455,2	K562	blood:
34	chr5:118553070..118555553-chr5:118571329..118573313,2	K562	blood:
35	chr11:64878891..64879742-chr5:118606808..118607308,2	NB4	blood:
36	chr5:118593519..118596091-chr5:118597746..118599406,2	K562	blood:
37	chr5:118463365..118465744-chr5:118468945..118471414,3	K562	blood:
38	chr5:118599452..118601690-chr5:118601827..118605890,4	K562	blood:
39	chr5:118579079..118581230-chr5:118604088..118605942,2	MCF-7	breast:
40	chr5:118603726..118606822-chr5:118616119..118619037,3	MCF-7	breast:
41	chr5:118323277..118326022-chr5:118603985..118605806,3	MCF-7	breast:
42	chr5:118510458..118512160-chr5:118512976..118516180,3	K562	blood:
43	chr5:118604371..118606578-chr5:118640818..118642432,2	K562	blood:
44	chr5:118406323..118408758-chr5:118602921..118606339,4	MCF-7	breast:
45	chr5:118606735..118608940-chr5:118610555..118612827,2	MCF-7	breast:
46	chr5:118323865..118326797-chr5:118601908..118603876,2	K562	blood:
47	chr5:118620088..118622247-chr5:118651505..118654456,2	K562	blood:
48	chr5:118406002..118408491-chr5:118610029..118612989,2	MCF-7	breast:
49	chr5:118549930..118551447-chr5:118556250..118558321,2	K562	blood:
50	chr5:118564790..118566564-chr5:118567290..118569739,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-8	chr5:118468346-118468577	NONHSAT103423

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5706	chr5:118490341-118490362	MIMAT0022500

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	DMXL1	hsa-miR-9-5p	chr5:118584038-118584059
2	DMXL1	hsa-miR-92a-3p	chr5:118584515-118584522
3	DMXL1	hsa-miR-92a-3p	chr5:118584501-118584522

Variant related genes	Relation type
ENSG00000248885	TF binding region
RNU6-701P	TF binding region
TNFAIP8	TF binding region
DMXL1	TF binding region
ENSG00000266587	TF binding region
LAMTOR3P2	TF binding region
MIR5706	TF binding region
ENSG00000248885	CpG island
RNU6-701P	CpG island
TNFAIP8	CpG island
DMXL1	CpG island
ENSG00000266587	CpG island
LAMTOR3P2	CpG island
MIR5706	CpG island
ENSG00000135972	chromatin interactions
ENSG00000116497	chromatin interactions
ENSG00000224509	chromatin interactions
ENSG00000102007	chromatin interactions
ENSG00000172869	chromatin interactions
ENSG00000248885	chromatin interactions
ENSG00000145779	chromatin interactions
ENSG00000169570	chromatin interactions
ENSG00000266587	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000254501	chromatin interactions
ENSG00000243333	chromatin interactions
ENSG00000095319	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000172113	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000173653	chromatin interactions
ENSG00000249494	chromatin interactions
ENSG00000134684	chromatin interactions
ENSG00000175283	chromatin interactions
ENSG00000248979	chromatin interactions

Extended variants
information (count: 6456 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6456 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7735538	chr5:118465249-118465250	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs562249068	chr5:118465254-118465255	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531271550	chr5:118465264-118465265	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs545021700	chr5:118465276-118465277	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs190908820	chr5:118465280-118465281	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs143361151	chr5:118465287-118465288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547704944	chr5:118465293-118465294	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561124105	chr5:118465298-118465299	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182791047	chr5:118465315-118465316	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs199815327	chr5:118465339-118465340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs113808923	chr5:118465349-118465350	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569350939	chr5:118465357-118465358	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537937042	chr5:118465370-118465371	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs191625864	chr5:118465424-118465425	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs571550398	chr5:118465427-118465428	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs146247852	chr5:118465452-118465453	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs183393352	chr5:118465489-118465490	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs139383947	chr5:118465494-118465495	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs144152686	chr5:118465523-118465524	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs556321921	chr5:118465564-118465565	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs187575707	chr5:118465575-118465576	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs544771895	chr5:118465577-118465578	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs192792005	chr5:118465586-118465587	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs10037191	chr5:118465617-118465618	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs144873227	chr5:118465679-118465680	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs184380342	chr5:118465689-118465690	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs560593944	chr5:118465690-118465691	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs76118228	chr5:118465707-118465708	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs116398336	chr5:118465726-118465727	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200049576	chr5:118465797-118465798	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373578414	chr5:118465805-118465806	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs531881513	chr5:118465812-118465813	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs551577500	chr5:118465852-118465853	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs149031386	chr5:118465862-118465863	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142074644	chr5:118465903-118465904	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189276744	chr5:118465915-118465916	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112571398	chr5:118465958-118465959	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs151164529	chr5:118465971-118465972	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556762312	chr5:118465990-118465991	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74940465	chr5:118465994-118465995	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140167068	chr5:118466030-118466031	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs192583368	chr5:118466036-118466037	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs558371917	chr5:118466039-118466040	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs56776489	chr5:118466052-118466053	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs541043359	chr5:118466102-118466103	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560852547	chr5:118466119-118466120	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568684203	chr5:118466124-118466125	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543738724	chr5:118466130-118466131	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563541149	chr5:118466162-118466163	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532218276	chr5:118466167-118466168	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:3920 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118409000-118471200	Weak transcription	Gastric	stomach
2	chr5:118412200-118522800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr5:118414400-118472200	Weak transcription	Pancreas	Pancrea
4	chr5:118415400-118471600	Weak transcription	Right Ventricle	heart
5	chr5:118430200-118471400	Weak transcription	Colonic Mucosa	Colon
6	chr5:118430800-118472200	Weak transcription	Esophagus	oesophagus
7	chr5:118431000-118472200	Weak transcription	Small Intestine	intestine
8	chr5:118433000-118466800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr5:118433000-118468600	Weak transcription	Fetal Heart	heart
10	chr5:118434200-118471000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:118438600-118484400	Weak transcription	NHLF	lung
12	chr5:118442200-118472200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr5:118443200-118472200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:118444000-118472000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:118444800-118471200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:118445600-118467200	Weak transcription	A549	lung
17	chr5:118447400-118485400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr5:118448800-118471600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr5:118450400-118496800	Weak transcription	Stomach Mucosa	stomach
20	chr5:118451200-118533400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr5:118452600-118468800	Weak transcription	NHDF-Ad	bronchial
22	chr5:118452800-118472400	Weak transcription	Hela-S3	cervix
23	chr5:118453000-118472400	Weak transcription	Psoas Muscle	Psoas
24	chr5:118453600-118471200	Weak transcription	Aorta	Aorta
25	chr5:118453800-118522800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr5:118454200-118468800	Weak transcription	Osteobl	bone
27	chr5:118455000-118465400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr5:118456200-118468600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr5:118456800-118469200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr5:118456800-118483200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr5:118456800-118484600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr5:118457000-118468600	Weak transcription	Ovary	ovary
33	chr5:118457000-118468600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr5:118457000-118468600	Weak transcription	Thymus	Thymus
35	chr5:118457000-118471200	Weak transcription	Lung	lung
36	chr5:118457000-118472200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr5:118457000-118472200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:118458800-118470600	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr5:118459000-118465800	Strong transcription	Liver	Liver
40	chr5:118459200-118465800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr5:118459200-118468600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr5:118459400-118471000	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr5:118459600-118468400	Weak transcription	Brain Germinal Matrix	brain
44	chr5:118459600-118471200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr5:118459600-118471200	Weak transcription	Spleen	Spleen
46	chr5:118460200-118465600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr5:118460200-118468800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr5:118460200-118469200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr5:118460800-118471000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr5:118461000-118465800	Strong transcription	Fetal Thymus	thymus

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