Variant report

Variant	nsv915897
Chromosome Location	chr3:75471836-75793433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6992)
CpG islands
(count:4457)
Chromatin interactive
region (count:15)
LncRNA
region (count:43)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:6992 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
2	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
3	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
4	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
5	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
7	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
9	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
11	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
12	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
14	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
15	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
16	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
17	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
18	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
19	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
20	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
21	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
22	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
23	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
24	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
25	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
26	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
27	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
28	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
29	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
30	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
31	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
32	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
33	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
34	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
35	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
36	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
37	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
38	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
39	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
40	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
41	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
42	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
43	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
44	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
45	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
46	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
47	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
48	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
49	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
50	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a

(count:4457 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75671115-75671165	HIPEpiC	eye:	n/a
2	chr3:75705922-75705972	HCF	heart:	n/a
3	chr3:75629433-75629483	U87	brain:	n/a
4	chr3:75629039-75629089	NHBE	bronchial:	n/a
5	chr3:75671115-75671165	HIPEpiC	eye:	n/a
6	chr3:75705922-75705972	HCF	heart:	n/a
7	chr3:75629433-75629483	U87	brain:	n/a
8	chr3:75629039-75629089	NHBE	bronchial:	n/a
9	chr3:75555994-75556044	AG09309	skin:	n/a
10	chr3:75484440-75484490	IMR90	lung:	fetal
11	chr3:75705922-75705972	AoSMC	blood vessel:	n/a
12	chr3:75664059-75664109	A549	lung:	n/a
13	chr3:75704824-75704874	K562	blood:	n/a
14	chr3:75704824-75704874	CMK	blood:	n/a
15	chr3:75482182-75482232	HRCEpiC	kidney:	n/a
16	chr3:75717248-75717298	HEK293	kidney:	embryo
17	chr3:75487529-75487579	GM12892	blood:	n/a
18	chr3:75704824-75704874	GM12892	blood:	n/a
19	chr3:75719158-75719208	BJ	skin:	n/a
20	chr3:75707560-75707610	HEK293	kidney:	embryo
21	chr3:75671793-75671843	AG09319	gingival:	n/a
22	chr3:75705922-75705972	HEEpiC	esophagus:	n/a
23	chr3:75668627-75668677	HCT-116	colon:	n/a
24	chr3:75719149-75719199	HepG2	liver:	n/a
25	chr3:75556027-75556077	HAEpiC	amniotic membrane:	n/a
26	chr3:75553723-75553773	SAEC	small airway:	n/a
27	chr3:75712695-75712745	HRCEpiC	kidney:	n/a
28	chr3:75671115-75671165	SAEC	small airway:	n/a
29	chr3:75555938-75555988	LNCaP	prostate:	n/a
30	chr3:75715783-75715833	SK-N-SH_RA	brain:	n/a
31	chr3:75661799-75661849	HRE	kidney:	n/a
32	chr3:75661206-75661256	HUVEC	blood vessel:	n/a
33	chr3:75705108-75705158	HCT-116	colon:	n/a
34	chr3:75485110-75485160	RPTEC	kidney:	n/a
35	chr3:75659629-75659679	HIPEpiC	eye:	n/a
36	chr3:75628932-75628982	SK-N-SH_RA	brain:	n/a
37	chr3:75717453-75717503	Hela-S3	cervix:	n/a
38	chr3:75484209-75484259	HMEC	breast:	n/a
39	chr3:75704498-75704548	HCF	heart:	n/a
40	chr3:75701993-75702043	PrEC	prostate:	n/a
41	chr3:75707805-75707855	HCM	heart:	n/a
42	chr3:75679024-75679074	GM12878	blood:	n/a
43	chr3:75555994-75556044	HEEpiC	esophagus:	n/a
44	chr3:75482182-75482232	Caco-2	colon:	n/a
45	chr3:75668035-75668085	HepG2	liver:	n/a
46	chr3:75664059-75664109	HCPEpiC	choroid plexus:	n/a
47	chr3:75668627-75668677	HEEpiC	esophagus:	n/a
48	chr3:75667994-75668044	IMR90	lung:	fetal
49	chr3:75658735-75658785	GM12891	blood:	n/a
50	chr3:75666381-75666431	ovcar-3	ovarian:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
2	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
3	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
4	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:
5	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
6	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
7	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
8	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:
9	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
10	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
11	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
12	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
13	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
14	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
15	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
2	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
3	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
4	lnc-FRG2C-3	chr3:75505768-75506637	ENSG00000272690.1
5	lnc-FRG2C-3	chr3:75501683-75501794	NONHSAT090533
6	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
7	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
8	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
9	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
10	lnc-FRG2C-3	chr3:75496316-75496447	ENSG00000272690.1
11	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
12	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
13	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
14	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
15	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
16	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
17	lnc-FRG2C-3	chr3:75501348-75501809	ENSG00000272690.1
18	lnc-FRG2C-3	chr3:75492659-75492797	ENSG00000272690.1
19	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
20	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
21	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
22	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
23	lnc-FRG2C-3	chr3:75497520-75500553	NONHSAT090533
24	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
25	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
26	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
27	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
28	lnc-FRG2C-3	chr3:75492659-75492775	XLOC_002710
29	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
30	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
31	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
32	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
33	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710
34	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
35	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710
36	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
37	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
38	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
39	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
40	lnc-FRG2C-3	chr3:75501683-75501802	ENSG00000272690.1
41	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
42	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
43	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4273	chr3:75787441-75787458	MIMAT0016903
hsa-miR-1324	chr3:75679974-75679997	MIMAT0005956

No data

Variant related genes	Relation type
UNC93B3	TF binding region
FRG2C	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
MIR4273	TF binding region
LINC00960	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
RARRES2P1	TF binding region
ENSG00000272690	TF binding region
FAM86DP	TF binding region
ENSG00000221602	TF binding region
AGGF1P3	TF binding region
RN7SL92P	TF binding region
ENPP7P2	TF binding region
ENSG00000236138	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
FRG2C	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
MIR4273	CpG island
LINC00960	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
RARRES2P1	CpG island
ENSG00000272690	CpG island
FAM86DP	CpG island
ENSG00000221602	CpG island
AGGF1P3	CpG island
RN7SL92P	CpG island
ENPP7P2	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000168298	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000236829	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000232815	chromatin interactions
SFRS5	miRNA target sites
ITGB1	miRNA target sites

Extended variants
information (count: 19080 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:19080 , 50 per page) page: 1 2 3 4 5 6 7 ... 382

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559631590	chr3:75471848-75471849	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs3763577	chr3:75471854-75471855	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs541789282	chr3:75471886-75471887	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs3763578	chr3:75471889-75471890	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs530442308	chr3:75471893-75471894	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs552211105	chr3:75471902-75471903	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs144066863	chr3:75471908-75471909	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs528219310	chr3:75471934-75471935	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs547575942	chr3:75471942-75471943	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567903755	chr3:75471943-75471944	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs565967381	chr3:75471954-75471955	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs536929656	chr3:75471962-75471963	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs80339356	chr3:75472064-75472065	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370954383	chr3:75472092-75472093	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192061651	chr3:75472100-75472101	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537058525	chr3:75472123-75472124	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559044570	chr3:75472145-75472146	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201926500	chr3:75472184-75472185	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148633782	chr3:75472187-75472188	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200089461	chr3:75472196-75472197	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1140148	chr3:75472197-75472198	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11537690	chr3:75472209-75472210	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs553185627	chr3:75472210-75472211	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151154670	chr3:75472217-75472218	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574571744	chr3:75472227-75472228	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542074565	chr3:75472249-75472250	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563446058	chr3:75472259-75472260	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs62259122	chr3:75472260-75472261	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs111470838	chr3:75472261-75472262	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs143233800	chr3:75472267-75472268	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183982087	chr3:75472270-75472271	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539115861	chr3:75472272-75472273	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187727124	chr3:75472275-75472276	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111581298	chr3:75472289-75472290	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530246203	chr3:75472292-75472293	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189826284	chr3:75472346-75472347	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570254902	chr3:75472392-75472393	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537792847	chr3:75472409-75472410	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558980260	chr3:75472410-75472411	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570889759	chr3:75472433-75472434	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535097441	chr3:75472449-75472450	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146696229	chr3:75472450-75472451	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574536671	chr3:75472452-75472453	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563866900	chr3:75472467-75472468	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111651848	chr3:75472471-75472472	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557168309	chr3:75472500-75472501	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575440367	chr3:75472509-75472510	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111739829	chr3:75472554-75472555	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141114096	chr3:75472555-75472556	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572527299	chr3:75472581-75472582	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:3773 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75463200-75474600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:75464000-75476000	Weak transcription	Pancreas	Pancrea
3	chr3:75464200-75474800	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:75465400-75474000	Weak transcription	Fetal Intestine Large	intestine
5	chr3:75465400-75474800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:75465400-75476200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:75465600-75474600	Weak transcription	Right Ventricle	heart
8	chr3:75465600-75474600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr3:75465600-75474800	Weak transcription	Aorta	Aorta
10	chr3:75467000-75472000	Weak transcription	Lung	lung
11	chr3:75467000-75477000	Weak transcription	NH-A	brain
12	chr3:75467200-75472200	Weak transcription	Gastric	stomach
13	chr3:75467200-75474600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:75467600-75474600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:75467600-75484400	Weak transcription	Stomach Mucosa	stomach
16	chr3:75467800-75474600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr3:75467800-75474600	Weak transcription	Spleen	Spleen
18	chr3:75467800-75476400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:75467800-75480000	Weak transcription	A549	lung
20	chr3:75467800-75483600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr3:75468000-75474800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:75468400-75473200	Enhancers	Fetal Muscle Leg	muscle
23	chr3:75468800-75474800	Weak transcription	NHLF	lung
24	chr3:75469400-75483000	Weak transcription	NHEK	skin
25	chr3:75469600-75474800	Weak transcription	Ovary	ovary
26	chr3:75469600-75483600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:75470000-75477600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr3:75470000-75478200	Weak transcription	HMEC	breast
29	chr3:75470000-75482200	Weak transcription	Right Atrium	heart
30	chr3:75470200-75474600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr3:75470200-75474800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr3:75470200-75478600	Weak transcription	Fetal Lung	lung
33	chr3:75470200-75483400	Weak transcription	Rectal Smooth Muscle	rectum
34	chr3:75470200-75483600	Weak transcription	Brain Substantia Nigra	brain
35	chr3:75470400-75476400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr3:75470400-75478600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:75470400-75483400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr3:75470600-75474400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr3:75470600-75474600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr3:75470800-75473000	Weak transcription	Liver	Liver
41	chr3:75470800-75478200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr3:75470800-75482400	Weak transcription	Psoas Muscle	Psoas
43	chr3:75470800-75482600	Strong transcription	Fetal Stomach	stomach
44	chr3:75471400-75472000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:75471400-75472000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr3:75471400-75472000	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr3:75471400-75472600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr3:75471400-75472600	Strong transcription	Fetal Intestine Small	intestine
49	chr3:75471400-75472600	Enhancers	Osteobl	bone
50	chr3:75471400-75476400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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