Variant report

Variant	nsv1040484
Chromosome Location	chr11:32951066-33093204
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2532)
CpG islands
(count:2381)
Chromatin interactive
region (count:117)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2532 , 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	chr11:33040791-33040796	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33040233-33040432	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:33060598-33061311	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:33037131-33037894	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:33056563-33056800	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:33039311-33039873	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:33087228-33087452	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:32975953-32975956	K562	blood:	n/a	n/a
9	ARID3A	chr11:33082889-33083186	HepG2	liver:	n/a	n/a
10	ATF1	chr11:33061781-33062183	K562	blood:	n/a	n/a
11	ATF1	chr11:33046458-33046503	K562	blood:	n/a	n/a
12	ATF2	chr11:33084755-33085573	GM12878	blood:	n/a	n/a
13	ATF2	chr11:33060527-33061459	GM12878	blood:	n/a	n/a
14	ATF2	chr11:33033025-33033631	GM12878	blood:	n/a	n/a
15	ATF2	chr11:33087103-33087525	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr11:33060524-33061142	GM12878	blood:	n/a	n/a
17	ATF2	chr11:33084702-33085604	GM12878	blood:	n/a	n/a
18	ATF2	chr11:33060718-33061305	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr11:33061740-33062561	GM12878	blood:	n/a	n/a
20	ATF3	chr11:33060822-33061247	A549	lung:	n/a	n/a
21	ATF3	chr11:33037205-33037643	K562	blood:	n/a	chr11:33037392-33037401
22	ATF3	chr11:33065778-33066364	A549	lung:	n/a	n/a
23	ATF3	chr11:33037237-33037556	H1-hESC	embryonic stem cell:	n/a	chr11:33037392-33037401
24	ATF3	chr11:33082752-33083351	A549	lung:	n/a	n/a
25	ATF3	chr11:33087178-33087489	K562	blood:	n/a	n/a
26	ATF3	chr11:33037116-33037523	H1-hESC	embryonic stem cell:	n/a	chr11:33037392-33037401
27	ATF3	chr11:33037243-33037511	HepG2	liver:	n/a	chr11:33037392-33037401
28	ATF3	chr11:33082676-33083347	A549	lung:	n/a	n/a
29	BACH1	chr11:33037926-33038067	K562	blood:	n/a	n/a
30	BACH1	chr11:33087142-33087581	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr11:33037095-33037637	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr11:33060708-33061471	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr11:33033447-33033795	GM12878	blood:	n/a	n/a
34	BATF	chr11:33082711-33082946	GM12878	blood:	n/a	n/a
35	BATF	chr11:33033109-33033283	GM12878	blood:	n/a	n/a
36	BATF	chr11:33082959-33083281	GM12878	blood:	n/a	chr11:33083122-33083133
37	BATF	chr11:33032861-33033393	GM12878	blood:	n/a	n/a
38	BATF	chr11:33084779-33085352	GM12878	blood:	n/a	chr11:33085032-33085043
39	BATF	chr11:33084835-33085294	GM12878	blood:	n/a	chr11:33085032-33085043
40	BATF	chr11:33033446-33033786	GM12878	blood:	n/a	n/a
41	BATF	chr11:33082732-33083178	GM12878	blood:	n/a	chr11:33083122-33083133
42	BCL11A	chr11:33033092-33033386	GM12878	blood:	n/a	chr11:33033228-33033237
43	BCL11A	chr11:33084835-33085303	GM12878	blood:	n/a	chr11:33085192-33085201
44	BCL11A	chr11:33084854-33085108	GM12878	blood:	n/a	n/a
45	BCL3	chr11:33082729-33083335	A549	lung:	n/a	n/a
46	BCL3	chr11:33084858-33085479	GM12878	blood:	n/a	chr11:33085192-33085201
47	BCL3	chr11:33060421-33061205	A549	lung:	n/a	chr11:33060578-33060587 chr11:33060991-33061004 chr11:33061189-33061202
48	BCL3	chr11:33082670-33083366	A549	lung:	n/a	n/a
49	BCL3	chr11:33065480-33066476	A549	lung:	n/a	n/a
50	BCLAF1	chr11:33084829-33085455	GM12878	blood:	n/a	chr11:33085192-33085201

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33037542-33037592	HRE	kidney:	n/a
2	chr11:33061007-33061057	NB4	blood:	n/a
3	chr11:33037542-33037592	HRE	kidney:	n/a
4	chr11:33061007-33061057	NB4	blood:	n/a
5	chr11:33060817-33060867	HCF	heart:	n/a
6	chr11:33084877-33084927	MCF10A-Er-Src	breast:	n/a
7	chr11:33023005-33023055	CMK	blood:	n/a
8	chr11:33061845-33061895	U87	brain:	n/a
9	chr11:33083021-33083071	HRE	kidney:	n/a
10	chr11:33036664-33036714	HAEpiC	amniotic membrane:	n/a
11	chr11:33038313-33038363	CMK	blood:	n/a
12	chr11:33060702-33060752	K562	blood:	n/a
13	chr11:33037916-33037966	NB4	blood:	n/a
14	chr11:33060711-33060761	SKMC	muscle:	n/a
15	chr11:33058248-33058298	GM19239	blood:	n/a
16	chr11:33037542-33037592	CMK	blood:	n/a
17	chr11:33037792-33037842	NH-A	brain:	n/a
18	chr11:33061388-33061438	K562	blood:	n/a
19	chr11:33058248-33058298	SAEC	small airway:	n/a
20	chr11:33037792-33037842	BE2_C	brain:	n/a
21	chr11:33065566-33065616	Caco-2	colon:	n/a
22	chr11:33061716-33061766	ovcar-3	ovarian:	n/a
23	chr11:33037792-33037842	HRE	kidney:	n/a
24	chr11:33033607-33033657	GM19239	blood:	n/a
25	chr11:33060817-33060867	ProgFib	skin:	n/a
26	chr11:32951061-32951111	HRE	kidney:	n/a
27	chr11:32951061-32951111	SK-N-MC	brain:	n/a
28	chr11:33061907-33061957	ProgFib	skin:	n/a
29	chr11:33060767-33060817	AG04450	lung:	fetal
30	chr11:32951061-32951111	GM12878	blood:	n/a
31	chr11:33081126-33081176	ProgFib	skin:	n/a
32	chr11:33060800-33060850	ProgFib	skin:	n/a
33	chr11:33037626-33037676	HEK293	kidney:	embryo
34	chr11:33083021-33083071	HCPEpiC	choroid plexus:	n/a
35	chr11:33084877-33084927	HIPEpiC	eye:	n/a
36	chr11:33060817-33060867	H1-hESC	embryonic stem cell:	embryo
37	chr11:33087476-33087526	GM06990	blood:	n/a
38	chr11:33049259-33049309	RPTEC	kidney:	n/a
39	chr11:33060762-33060812	SK-N-SH_RA	brain:	n/a
40	chr11:33065566-33065616	NT2-D1	testis:	n/a
41	chr11:33049259-33049309	SK-N-MC	brain:	n/a
42	chr11:33084877-33084927	HNPCEpiC	eye:	n/a
43	chr11:33040743-33040793	BJ	skin:	n/a
44	chr11:33023005-33023055	AG04449	skin:	fetal
45	chr11:33060762-33060812	HRCEpiC	kidney:	n/a
46	chr11:33061388-33061438	HRCEpiC	kidney:	n/a
47	chr11:33037916-33037966	GM12878	blood:	n/a
48	chr11:33060817-33060867	GM12878	blood:	n/a
49	chr11:33037530-33037580	SKMC	muscle:	n/a
50	chr11:33037624-33037674	PFSK-1	brain:	n/a

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:33035752..33039107-chr11:33059295..33062622,5	K562	blood:
2	chr11:32981687..32982746-chr11:33086877..33087798,8	MCF-7	breast:
3	chr11:33047529..33049150-chr11:33058361..33061018,2	MCF-7	breast:
4	chr11:32915892..32917470-chr11:32980726..32982282,2	K562	blood:
5	chr11:33061309..33062300-chr17:73775483..73776000,2	Hela-S3	cervix:
6	chr11:32912801..32916780-chr11:33060030..33062962,4	MCF-7	breast:
7	chr11:33086202..33088002-chr11:33090924..33093139,2	K562	blood:
8	chr11:33035752..33039107-chr11:33059295..33062622,5	K562	blood:
9	chr11:33066866..33070509-chr11:33072993..33075884,4	K562	blood:
10	chr11:33041861..33044073-chr11:33051404..33053946,2	K562	blood:
11	chr11:33063482..33065628-chr11:33072339..33074325,2	K562	blood:
12	chr11:32982327..32984023-chr11:33390393..33392493,2	K562	blood:
13	chr11:33060258..33062554-chr11:33087783..33089763,2	K562	blood:
14	chr11:32949447..32951560-chr11:32996072..32998442,2	K562	blood:
15	chr11:33060104..33063412-chr11:33064220..33068420,5	K562	blood:
16	chr11:32913485..32915612-chr11:33052114..33054886,2	K562	blood:
17	chr11:32996304..32999169-chr11:33001880..33003438,2	MCF-7	breast:
18	chr1:249132356..249133012-chr11:33061402..33062060,2	Hela-S3	cervix:
19	chr11:32914058..32916371-chr11:32975765..32977557,2	MCF-7	breast:
20	chr11:33040311..33043058-chr11:33088314..33090844,2	K562	blood:
21	chr11:33038166..33041060-chr11:33046643..33049387,2	MCF-7	breast:
22	chr11:33050169..33051693-chr11:33062523..33065107,2	MCF-7	breast:
23	chr11:33033569..33035626-chr11:33052548..33054662,2	K562	blood:
24	chr11:33075700..33077900-chr11:33079839..33081933,2	MCF-7	breast:
25	chr11:32949447..32951560-chr11:32996072..32998442,2	K562	blood:
26	chr11:33033569..33035626-chr11:33052548..33054662,2	K562	blood:
27	chr11:33035321..33039472-chr11:33059106..33064085,11	K562	blood:
28	chr11:33028329..33030227-chr11:33059191..33062094,2	MCF-7	breast:
29	chr11:33068761..33070509-chr11:33073480..33075884,2	K562	blood:
30	chr11:33004824..33006532-chr11:33024941..33027529,2	K562	blood:
31	chr11:32942975..32945695-chr11:32951329..32953837,2	K562	blood:
32	chr11:33004103..33008077-chr11:33008139..33011033,3	MCF-7	breast:
33	chr11:33043473..33045913-chr11:33047452..33049632,3	K562	blood:
34	chr11:33059371..33062523-chr11:33080463..33084324,4	MCF-7	breast:
35	chr11:32913653..32915700-chr11:33084774..33087612,2	K562	blood:
36	chr11:33035440..33037281-chr11:33038611..33040663,2	K562	blood:
37	chr11:32988347..32990488-chr11:32993525..32996077,2	K562	blood:
38	chr11:33036057..33037952-chr11:33070370..33072360,2	K562	blood:
39	chr11:32970671..32972775-chr11:32979842..32982658,2	K562	blood:
40	chr11:32970671..32972775-chr11:32979842..32982658,2	K562	blood:
41	chr11:33049034..33053308-chr11:33058288..33062133,5	K562	blood:
42	chr11:33032509..33034576-chr11:33039239..33041376,2	MCF-7	breast:
43	chr11:32982069..32982796-chr11:33086887..33087818,6	K562	blood:
44	chr11:33059557..33062519-chr11:33089882..33091963,2	MCF-7	breast:
45	chr11:32914351..32916676-chr11:33059902..33062238,2	K562	blood:
46	chr11:32988347..32990488-chr11:32993525..32996077,2	K562	blood:
47	chr11:32850121..32852277-chr11:33088797..33091531,2	MCF-7	breast:
48	chr11:33066540..33068366-chr11:33072316..33075265,3	K562	blood:
49	chr11:33043183..33045594-chr11:33046266..33049632,4	K562	blood:
50	chr11:32950716..32952924-chr11:32954824..32956515,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSTF3-1	chr11:33025345-33025436	NONHSAT018681
2	lnc-CSTF3-1	chr11:33036823-33036899	NONHSAT018681
3	lnc-CSTF3-1	chr11:32978271-32978312	NONHSAT018681
4	lnc-CSTF3-1	chr11:32977870-32978000	NONHSAT018681

No data

Variant related genes	Relation type
TCP11L1	TF binding region
DEPDC7	TF binding region
QSER1	TF binding region
ENSG00000200615	TF binding region
TCP11L1	CpG island
DEPDC7	CpG island
QSER1	CpG island
ENSG00000200615	CpG island
ENSG00000067225	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000086200	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000163348	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000119314	chromatin interactions
ENSG00000200615	chromatin interactions
ENSG00000171161	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000086189	chromatin interactions
ENSG00000121690	chromatin interactions
ENSG00000231770	chromatin interactions
ENSG00000271380	chromatin interactions

Extended variants
information (count: 4958 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4958 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530297459	chr11:32951069-32951070	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs548973582	chr11:32951080-32951081	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs151308288	chr11:32951081-32951082	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs537986610	chr11:32951082-32951083	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs372494527	chr11:32951112-32951113	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs551491791	chr11:32951115-32951116	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs571495518	chr11:32951143-32951144	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533998879	chr11:32951152-32951153	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs553650471	chr11:32951189-32951190	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs573887056	chr11:32951209-32951210	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs536108416	chr11:32951277-32951278	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs191401827	chr11:32951460-32951461	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs150493160	chr11:32951468-32951469	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs538000693	chr11:32951489-32951490	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs545136039	chr11:32951530-32951531	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs565018504	chr11:32951589-32951590	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs184592015	chr11:32951592-32951593	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs541243919	chr11:32951612-32951613	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs557415908	chr11:32951652-32951653	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs555860716	chr11:32951655-32951656	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs189378162	chr11:32951669-32951670	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs12800879	chr11:32951670-32951671	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs146410049	chr11:32951685-32951686	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs576385323	chr11:32951698-32951699	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs7358504	chr11:32951722-32951723	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs562545882	chr11:32951742-32951743	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs531310765	chr11:32951787-32951788	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs112916324	chr11:32951806-32951807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs7358507	chr11:32951836-32951837	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571379329	chr11:32951847-32951848	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs376539244	chr11:32951859-32951860	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs191905219	chr11:32951865-32951866	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs184335290	chr11:32951890-32951891	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs567343817	chr11:32951950-32951951	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs7358531	chr11:32951981-32951982	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371399079	chr11:32952099-32952100	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs556166214	chr11:32952153-32952154	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs569746384	chr11:32952176-32952177	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs538672664	chr11:32952184-32952185	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs12288319	chr11:32952188-32952189	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576315575	chr11:32952205-32952206	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs572218433	chr11:32952230-32952231	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs140802556	chr11:32952256-32952257	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs370907155	chr11:32952257-32952258	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs555193106	chr11:32952320-32952321	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs574925136	chr11:32952328-32952329	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs544130506	chr11:32952333-32952334	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs111288333	chr11:32952349-32952350	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs201354635	chr11:32952352-32952353	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371362945	chr11:32952383-32952384	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3929 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32916000-32953200	Weak transcription	Pancreas	Pancrea
2	chr11:32916200-32953200	Weak transcription	Right Ventricle	heart
3	chr11:32916400-32952800	Weak transcription	Fetal Intestine Small	intestine
4	chr11:32916400-32953200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr11:32916400-32953400	Weak transcription	NHLF	lung
6	chr11:32916400-32953600	Weak transcription	NHDF-Ad	bronchial
7	chr11:32917000-32952800	Weak transcription	Primary B cells from cord blood	blood
8	chr11:32917400-32953000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr11:32917600-32952800	Weak transcription	Fetal Stomach	stomach
10	chr11:32918000-32953200	Weak transcription	Fetal Brain Female	brain
11	chr11:32918600-32953600	Weak transcription	Fetal Brain Male	brain
12	chr11:32919600-32953000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:32921200-32952800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr11:32921200-32953200	Weak transcription	Primary T cells from cord blood	blood
15	chr11:32922600-32951200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:32922800-32952800	Weak transcription	Fetal Muscle Leg	muscle
17	chr11:32924000-32952800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:32924000-32952800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr11:32924000-32953200	Weak transcription	Left Ventricle	heart
20	chr11:32924400-32951200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr11:32926400-32952800	Weak transcription	Ovary	ovary
22	chr11:32927200-32953200	Weak transcription	Fetal Heart	heart
23	chr11:32927400-32951200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:32927400-32953400	Weak transcription	Fetal Kidney	kidney
25	chr11:32928200-32952800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:32930600-32951200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr11:32933400-32953200	Weak transcription	K562	blood
28	chr11:32935400-32953400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:32936600-32952800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr11:32936600-32952800	Weak transcription	HepG2	liver
31	chr11:32936800-32953000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr11:32937400-32953400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr11:32938200-32953200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr11:32938400-32951200	Weak transcription	A549	lung
35	chr11:32940000-32952800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr11:32940200-32953200	Weak transcription	NH-A	brain
37	chr11:32940200-32953400	Weak transcription	Psoas Muscle	Psoas
38	chr11:32940400-32953200	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:32941000-32953200	Weak transcription	Fetal Lung	lung
40	chr11:32941200-32952800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr11:32941200-32953400	Weak transcription	Colon Smooth Muscle	Colon
42	chr11:32941400-32952200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:32941400-32952600	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr11:32941400-32952800	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr11:32941400-32952800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:32941400-32953000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr11:32941400-32953200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:32941400-32953200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr11:32941400-32953400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr11:32941800-32952800	Weak transcription	Fetal Intestine Large	intestine

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