Variant report

Variant	nsv876736
Chromosome Location	chr3:45900621-46027410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2539)
CpG islands
(count:1466)
Chromatin interactive
region (count:133)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:2539 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:45980346-45980598	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:45900370-45900900	K562	blood:	n/a	n/a
3	ARID3A	chr3:46022962-46023285	K562	blood:	n/a	n/a
4	ATF1	chr3:45900618-45900948	K562	blood:	n/a	n/a
5	ATF1	chr3:46022873-46023180	K562	blood:	n/a	n/a
6	ATF1	chr3:45922572-45922995	K562	blood:	n/a	n/a
7	ATF2	chr3:45956866-45958008	GM12878	blood:	n/a	n/a
8	ATF2	chr3:45902059-45903360	GM12878	blood:	n/a	n/a
9	ATF2	chr3:45919446-45920259	GM12878	blood:	n/a	n/a
10	ATF2	chr3:45905943-45907539	GM12878	blood:	n/a	n/a
11	ATF2	chr3:45901909-45903366	GM12878	blood:	n/a	n/a
12	ATF2	chr3:45909676-45910221	GM12878	blood:	n/a	n/a
13	ATF2	chr3:45919519-45920097	GM12878	blood:	n/a	n/a
14	ATF2	chr3:45922157-45923463	GM12878	blood:	n/a	n/a
15	ATF2	chr3:45980281-45980708	GM12878	blood:	n/a	n/a
16	ATF2	chr3:45913861-45914528	GM12878	blood:	n/a	n/a
17	ATF2	chr3:45956156-45956800	GM12878	blood:	n/a	n/a
18	ATF2	chr3:45909665-45910140	GM12878	blood:	n/a	n/a
19	ATF2	chr3:45925962-45926765	GM12878	blood:	n/a	n/a
20	ATF2	chr3:45946371-45946856	GM12878	blood:	n/a	n/a
21	ATF2	chr3:46005445-46006026	GM12878	blood:	n/a	n/a
22	ATF2	chr3:46003437-46003906	GM12878	blood:	n/a	n/a
23	ATF2	chr3:45928591-45929079	GM12878	blood:	n/a	n/a
24	ATF2	chr3:45956959-45957917	GM12878	blood:	n/a	n/a
25	ATF2	chr3:45930639-45931249	GM12878	blood:	n/a	n/a
26	ATF2	chr3:45926058-45926927	GM12878	blood:	n/a	n/a
27	ATF2	chr3:45911509-45911982	GM12878	blood:	n/a	n/a
28	ATF2	chr3:45906058-45907427	GM12878	blood:	n/a	n/a
29	ATF2	chr3:45946048-45946983	GM12878	blood:	n/a	n/a
30	ATF2	chr3:45922026-45923542	GM12878	blood:	n/a	n/a
31	BATF	chr3:45906146-45906690	GM12878	blood:	n/a	n/a
32	BATF	chr3:45902487-45903266	GM12878	blood:	n/a	n/a
33	BATF	chr3:46014073-46014305	GM12878	blood:	n/a	n/a
34	BATF	chr3:45946442-45946814	GM12878	blood:	n/a	n/a
35	BATF	chr3:45926206-45926753	GM12878	blood:	n/a	n/a
36	BATF	chr3:46003490-46003863	GM12878	blood:	n/a	n/a
37	BATF	chr3:46005598-46005941	GM12878	blood:	n/a	chr3:46005739-46005750
38	BATF	chr3:45926309-45926719	GM12878	blood:	n/a	n/a
39	BATF	chr3:45957111-45957763	GM12878	blood:	n/a	n/a
40	BATF	chr3:45907111-45907376	GM12878	blood:	n/a	n/a
41	BATF	chr3:45906172-45907409	GM12878	blood:	n/a	n/a
42	BATF	chr3:45956977-45957806	GM12878	blood:	n/a	n/a
43	BATF	chr3:46003494-46003821	GM12878	blood:	n/a	n/a
44	BATF	chr3:45914023-45914427	GM12878	blood:	n/a	n/a
45	BATF	chr3:46005516-46006009	GM12878	blood:	n/a	chr3:46005739-46005750
46	BATF	chr3:45919646-45920019	GM12878	blood:	n/a	n/a
47	BATF	chr3:45902623-45903078	GM12878	blood:	n/a	n/a
48	BATF	chr3:45922240-45923470	GM12878	blood:	n/a	chr3:45923099-45923108
49	BATF	chr3:45970563-45970835	GM12878	blood:	n/a	n/a
50	BCL11A	chr3:45946415-45946869	GM12878	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:45927601-45927651	Caco-2	colon:	n/a
2	chr3:45927914-45927964	K562	blood:	n/a
3	chr3:45927601-45927651	Caco-2	colon:	n/a
4	chr3:45927914-45927964	K562	blood:	n/a
5	chr3:45981161-45981211	NHDF-neo	bronchial:	n/a
6	chr3:46000900-46000950	HL-60	blood:	n/a
7	chr3:45928007-45928057	Hela-S3	cervix:	n/a
8	chr3:45989744-45989794	ProgFib	skin:	n/a
9	chr3:45985168-45985218	AG09319	gingival:	n/a
10	chr3:45928007-45928057	Jurkat	blood:	n/a
11	chr3:45927601-45927651	Hepatocyte	liver:	n/a
12	chr3:45984838-45984888	HNPCEpiC	eye:	n/a
13	chr3:45928137-45928187	MCF-7	breast:	n/a
14	chr3:45969823-45969873	PANC-1	pancreas:	n/a
15	chr3:45957664-45957714	GM06990	blood:	n/a
16	chr3:45969823-45969873	AoSMC	blood vessel:	n/a
17	chr3:45927630-45927680	SK-N-SH_RA	brain:	n/a
18	chr3:45928137-45928187	GM12892	blood:	n/a
19	chr3:45983792-45983842	GM19239	blood:	n/a
20	chr3:45928137-45928187	AG09309	skin:	n/a
21	chr3:46000900-46000950	HCM	heart:	n/a
22	chr3:45927601-45927651	ovcar-3	ovarian:	n/a
23	chr3:45985168-45985218	ProgFib	skin:	n/a
24	chr3:45969823-45969873	HRCEpiC	kidney:	n/a
25	chr3:45984942-45984992	ovcar-3	ovarian:	n/a
26	chr3:45984838-45984888	PANC-1	pancreas:	n/a
27	chr3:45932141-45932191	T-47D	breast:	n/a
28	chr3:45928137-45928187	GM12878	blood:	n/a
29	chr3:45984942-45984992	GM12892	blood:	n/a
30	chr3:45927601-45927651	AoSMC	blood vessel:	n/a
31	chr3:45984743-45984793	GM12878	blood:	n/a
32	chr3:45942460-45942510	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:45989744-45989794	HNPCEpiC	eye:	n/a
34	chr3:45927589-45927639	PrEC	prostate:	n/a
35	chr3:45942460-45942510	ovcar-3	ovarian:	n/a
36	chr3:45969823-45969873	ECC-1	luminal epithelium:	n/a
37	chr3:45927601-45927651	CMK	blood:	n/a
38	chr3:45928007-45928057	HEK293	kidney:	embryo
39	chr3:45984942-45984992	H1-hESC	embryonic stem cell:	embryo
40	chr3:45961867-45961917	SAEC	small airway:	n/a
41	chr3:45984942-45984992	MCF-7	breast:	n/a
42	chr3:45957664-45957714	T-47D	breast:	n/a
43	chr3:45942460-45942510	HCPEpiC	choroid plexus:	n/a
44	chr3:45984838-45984888	K562	blood:	n/a
45	chr3:45928007-45928057	T-47D	breast:	n/a
46	chr3:45927589-45927639	GM12892	blood:	n/a
47	chr3:45932141-45932191	H1-hESC	embryonic stem cell:	embryo
48	chr3:46000900-46000950	HIPEpiC	eye:	n/a
49	chr3:45961867-45961917	HIPEpiC	eye:	n/a
50	chr3:45932141-45932191	AG09309	skin:	n/a

(count:133 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:46022722..46024858-chr3:46024939..46027896,2	K562	blood:
2	chr3:45926033..45927764-chr3:45930886..45932816,3	K562	blood:
3	chr3:46011530..46014566-chr3:46015264..46018457,3	K562	blood:
4	chr3:46009297..46011383-chr3:46015916..46019063,3	K562	blood:
5	chr3:45979978..45982491-chr3:46035904..46038054,2	MCF-7	breast:
6	chr3:45932573..45935155-chr3:45936845..45938513,2	MCF-7	breast:
7	chr3:46017706..46019852-chr3:46035209..46037613,2	K562	blood:
8	chr3:45893387..45895518-chr3:45899980..45902424,2	K562	blood:
9	chr3:45924572..45927755-chr3:45930051..45931656,3	K562	blood:
10	chr3:46011776..46015982-chr3:46034359..46039002,5	K562	blood:
11	chr3:45944264..45946380-chr3:45950311..45953306,2	MCF-7	breast:
12	chr3:45958439..45960531-chr3:46002605..46005170,2	K562	blood:
13	chr3:45920568..45923381-chr3:45930767..45933246,2	K562	blood:
14	chr3:45952412..45954426-chr3:45964464..45966839,2	K562	blood:
15	chr3:45908212..45911820-chr3:45911912..45916177,5	K562	blood:
16	chr3:45936711..45939307-chr3:45956614..45959025,2	MCF-7	breast:
17	chr3:45901181..45903986-chr3:45910875..45912786,2	K562	blood:
18	chr3:45999781..46002304-chr3:46004371..46006277,3	K562	blood:
19	chr3:45997101..45998721-chr3:46017987..46020675,2	K562	blood:
20	chr3:46014022..46017742-chr3:46018515..46020350,3	MCF-7	breast:
21	chr3:45926033..45927764-chr3:45930886..45932816,3	K562	blood:
22	chr3:45948473..45949050-chr3:46120491..46121161,2	K562	blood:
23	chr3:46008363..46011066-chr3:46026720..46029201,2	MCF-7	breast:
24	chr3:45980561..45981539-chr3:46118125..46119072,2	MCF-7	breast:
25	chr3:45970362..45970959-chr3:46120109..46120778,2	MCF-7	breast:
26	chr3:45973841..45976554-chr3:45977102..45979618,2	MCF-7	breast:
27	chr3:46015505..46018391-chr3:46024106..46026296,2	K562	blood:
28	chr3:45978904..45980774-chr3:45983050..45984937,2	MCF-7	breast:
29	chr3:45992901..45995659-chr3:45998923..46000689,2	K562	blood:
30	chr3:45931810..45934147-chr3:45942830..45944362,2	K562	blood:
31	chr3:46013767..46016030-chr3:46019815..46022441,2	K562	blood:
32	chr3:45979997..45980877-chr3:46419945..46420540,2	K562	blood:
33	chr3:45947295..45949529-chr3:45954537..45956111,2	K562	blood:
34	chr14:95015548..95016451-chr3:45948367..45948914,2	MCF-7	breast:
35	chr3:46023503..46025098-chr3:46030445..46033156,2	K562	blood:
36	chr3:45976449..45979237-chr3:45991973..45993587,2	K562	blood:
37	chr3:45882084..45884480-chr3:45897163..45900621,3	K562	blood:
38	chr3:45952412..45954426-chr3:45964464..45966839,2	K562	blood:
39	chr3:45980001..45980840-chr3:46121974..46122633,2	K562	blood:
40	chr3:46026501..46029475-chr3:46032165..46035137,4	MCF-7	breast:
41	chr3:46024602..46026106-chr3:46028613..46030507,2	MCF-7	breast:
42	chr3:46002701..46006681-chr3:46007479..46011297,4	K562	blood:
43	chr3:46019979..46023374-chr3:46034093..46037294,5	K562	blood:
44	chr3:45970697..45972556-chr3:46017144..46019977,2	K562	blood:
45	chr3:46019490..46020101-chr3:46029374..46029909,2	MCF-7	breast:
46	chr3:45965432..45966076-chr3:46120033..46120908,2	K562	blood:
47	chr3:45997101..45998721-chr3:46017987..46020675,2	K562	blood:
48	chr3:45978672..45979831-chr3:46120014..46120974,3	MCF-7	breast:
49	chr3:46000938..46003324-chr3:46007900..46010295,2	K562	blood:
50	chr3:46009297..46011383-chr3:46015916..46019063,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LZTFL1-2	chr3:45964090-45964518	predAs_ge08_CXCR6_2
2	lnc-CXCR6-1	chr3:45936399-45936446	NONHSAT089422
3	lnc-CXCR6-1	chr3:45942303-45942367	NONHSAT089422
4	lnc-FYCO1-3	chr3:45925132-45925605	NONHSAT089420
5	lnc-CXCR6-1	chr3:45936398-45936600	NONHSAT089421
6	lnc-SLC6A20-4	chr3:45956913-45957204	NONHSAT089419
7	lnc-SLC6A20-4	chr3:45954612-45954669	NONHSAT089419
8	lnc-CXCR6-1	chr3:45928002-45928147	NONHSAT089421
9	lnc-FYCO1-4	chr3:45918858-45919327	predAs_ge08_CCR9_3
10	lnc-FYCO1-1	chr3:46026073-46026514	NONHSAT089425
11	lnc-CXCR6-1	chr3:45928054-45928147	NONHSAT089422
12	lnc-LZTFL1-1	chr3:45963121-45963934	predAs_ge08_CXCR6_1

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FYCO1	hsa-miR-373-3p	chr3:45959891-45959910
2	FYCO1	hsa-miR-130b-3p	chr3:45959639-45959633
3	CCR9	hsa-miR-335-5p	chr3:45943575-45943599
4	CCR9	hsa-miR-155-5p	chr3:45944578-45944597
5	FYCO1	hsa-miR-93-5p	chr3:45959631-45959652
6	CCR9	hsa-miR-146a-5p	chr3:45943730-45943750
7	FYCO1	hsa-miR-130b-3p	chr3:45959633-45959654
8	FYCO1	hsa-miR-93-5p	chr3:45959637-45959630
9	FYCO1	hsa-miR-373-3p	chr3:45959792-45959814
10	CCR9	hsa-miR-335-5p	chr3:45943840-45943862
11	FYCO1	hsa-miR-373-3p	chr3:45959798-45959792
12	FYCO1	hsa-miR-93-5p	chr3:45959890-45959912
13	FYCO1	hsa-miR-93-5p	chr3:45959797-45959791
14	FYCO1	hsa-miR-93-5p	chr3:45959791-45959812

Variant related genes	Relation type
ENSG00000236930	TF binding region
CCR9	TF binding region
CXCR6	TF binding region
ENSG00000201635	TF binding region
FYCO1	TF binding region
LZTFL1	TF binding region
ENSG00000236930	CpG island
CCR9	CpG island
CXCR6	CpG island
ENSG00000201635	CpG island
FYCO1	CpG island
LZTFL1	CpG island
ENSG00000163820	chromatin interactions
ENSG00000236930	chromatin interactions
ENSG00000169564	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000173585	chromatin interactions
ENSG00000163818	chromatin interactions
ENSG00000201635	chromatin interactions

Extended variants
information (count: 4722 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4722 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7614952	chr3:45900621-45900622	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76374459	chr3:45900634-45900635	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78392262	chr3:45900655-45900656	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553609190	chr3:45900685-45900686	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371069920	chr3:45900793-45900794	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs137999827	chr3:45900832-45900833	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs372274199	chr3:45900901-45900902	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs149455146	chr3:45900902-45900903	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs116729937	chr3:45900910-45900911	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs75251577	chr3:45900915-45900916	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs144629920	chr3:45900929-45900930	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs116920238	chr3:45900960-45900961	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs112534379	chr3:45900964-45900965	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs547121216	chr3:45900967-45900968	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs73064425	chr3:45901089-45901090	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539062553	chr3:45901132-45901133	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529904846	chr3:45901220-45901221	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548467346	chr3:45901285-45901286	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569723386	chr3:45901287-45901288	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181452336	chr3:45901290-45901291	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199859008	chr3:45901318-45901319	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115372223	chr3:45901375-45901376	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77340888	chr3:45901530-45901531	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535014839	chr3:45901572-45901573	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554079132	chr3:45901573-45901574	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553134107	chr3:45901575-45901576	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138727962	chr3:45901597-45901598	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535730241	chr3:45901607-45901608	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557658584	chr3:45901690-45901691	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs55966195	chr3:45901722-45901723	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141862212	chr3:45901808-45901809	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558224208	chr3:45901832-45901833	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576567615	chr3:45901870-45901871	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551365052	chr3:45901885-45901886	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186137098	chr3:45901900-45901901	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34516627	chr3:45901956-45901957	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11291259	chr3:45901957-45901958	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78642937	chr3:45901967-45901968	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201923247	chr3:45901968-45901969	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201546651	chr3:45901969-45901970	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559038951	chr3:45901981-45901982	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529713005	chr3:45901993-45901994	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191048768	chr3:45902020-45902021	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563609742	chr3:45902029-45902030	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552686348	chr3:45902066-45902067	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574391526	chr3:45902107-45902108	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530703090	chr3:45902120-45902121	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146233235	chr3:45902176-45902177	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148040223	chr3:45902205-45902206	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs528538047	chr3:45902217-45902218	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3549 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:45890000-45907400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:45891800-45905200	Weak transcription	Psoas Muscle	Psoas
3	chr3:45894600-45906200	Genic enhancers	Dnd41	blood
4	chr3:45894800-45900800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr3:45895600-45902200	Weak transcription	Primary T cells from cord blood	blood
6	chr3:45896600-45902600	Weak transcription	Thymus	Thymus
7	chr3:45898200-45902400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr3:45898400-45902200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr3:45899200-45902800	Enhancers	Liver	Liver
10	chr3:45900200-45901000	Enhancers	Primary B cells from cord blood	blood
11	chr3:45900200-45901000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr3:45900200-45901000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr3:45900400-45900800	Enhancers	Duodenum Mucosa	Duodenum
14	chr3:45900400-45901000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr3:45900400-45901000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:45900400-45901000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:45900400-45901000	Enhancers	Fetal Thymus	thymus
18	chr3:45900400-45901200	Enhancers	Primary hematopoietic stem cells	blood
19	chr3:45900400-45901400	Enhancers	Primary B cells from peripheral blood	blood
20	chr3:45900400-45902200	Enhancers	GM12878-XiMat	blood
21	chr3:45900600-45900800	Enhancers	K562	blood
22	chr3:45900600-45901600	Weak transcription	Fetal Intestine Small	intestine
23	chr3:45900600-45902200	Weak transcription	Stomach Mucosa	stomach
24	chr3:45900800-45901000	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr3:45900800-45901000	Flanking Active TSS	K562	blood
26	chr3:45900800-45902200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr3:45901000-45901200	Enhancers	K562	blood
28	chr3:45901000-45902000	Weak transcription	Fetal Thymus	thymus
29	chr3:45901200-45901600	Weak transcription	K562	blood
30	chr3:45901400-45902400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr3:45901600-45902200	Enhancers	K562	blood
32	chr3:45901600-45904200	Enhancers	Fetal Intestine Large	intestine
33	chr3:45901600-45904200	Enhancers	Fetal Intestine Small	intestine
34	chr3:45902000-45903800	Enhancers	Fetal Thymus	thymus
35	chr3:45902200-45902400	Enhancers	Gastric	stomach
36	chr3:45902200-45902800	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr3:45902200-45902800	Enhancers	Stomach Mucosa	stomach
38	chr3:45902200-45903200	Bivalent Enhancer	K562	blood
39	chr3:45902200-45903400	Enhancers	Primary T cells from cord blood	blood
40	chr3:45902200-45903600	Enhancers	Duodenum Mucosa	Duodenum
41	chr3:45902200-45903600	Flanking Active TSS	GM12878-XiMat	blood
42	chr3:45902400-45902800	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr3:45902400-45902800	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr3:45902400-45903200	Enhancers	Primary B cells from peripheral blood	blood
45	chr3:45902400-45903200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr3:45902400-45903600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr3:45902600-45903200	Enhancers	Thymus	Thymus
48	chr3:45902600-45910200	Weak transcription	Gastric	stomach
49	chr3:45902800-45903200	Flanking Active TSS	Liver	Liver
50	chr3:45902800-45903600	Weak transcription	Primary T helper cells fromperipheralblood	blood

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