Variant report

Variant	nsv1035977
Chromosome Location	chr11:73581224-73617653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:1040)
Chromatin interactive
region (count:48)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:73587413-73588404	HepG2	liver:	n/a	n/a
2	ATF1	chr11:73587767-73588159	K562	blood:	n/a	n/a
3	ATF2	chr11:73587066-73588326	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:73587252-73588203	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:73587543-73588540	GM12878	blood:	n/a	n/a
6	ATF2	chr11:73587681-73588220	GM12878	blood:	n/a	n/a
7	BACH1	chr11:73588177-73588521	K562	blood:	n/a	n/a
8	BACH1	chr11:73613398-73613699	H1-hESC	embryonic stem cell:	n/a	chr11:73613545-73613559
9	BACH1	chr11:73613400-73613712	K562	blood:	n/a	chr11:73613545-73613559
10	BACH1	chr11:73587548-73588355	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr11:73587545-73588287	A549	lung:	n/a	chr11:73588018-73588027
12	BCL3	chr11:73587403-73588489	A549	lung:	n/a	chr11:73588018-73588027
13	BCLAF1	chr11:73587459-73588381	GM12878	blood:	n/a	chr11:73588018-73588027
14	BHLHE40	chr11:73587542-73588443	K562	blood:	n/a	chr11:73587728-73587744
15	BHLHE40	chr11:73591762-73591807	K562	blood:	n/a	n/a
16	BHLHE40	chr11:73587405-73588378	HepG2	liver:	n/a	chr11:73587728-73587744
17	BHLHE40	chr11:73587548-73588176	A549	lung:	n/a	chr11:73587728-73587744
18	BHLHE40	chr11:73587557-73588325	GM12878	blood:	n/a	chr11:73587728-73587744
19	BRCA1	chr11:73587250-73588306	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr11:73587435-73588007	HepG2	liver:	n/a	n/a
21	BRCA1	chr11:73587348-73588287	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr11:73587452-73588419	K562	blood:	n/a	n/a
23	CBX3	chr11:73591439-73591924	K562	blood:	n/a	n/a
24	CCNT2	chr11:73587609-73588220	K562	blood:	n/a	chr11:73587927-73587936
25	CEBPB	chr11:73587724-73588037	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:73616890-73617083	HepG2	liver:	n/a	chr11:73616971-73616982 chr11:73616922-73616933 chr11:73616971-73616984
27	CEBPB	chr11:73587700-73588004	K562	blood:	n/a	n/a
28	CEBPB	chr11:73605689-73606153	IMR90	lung:	n/a	n/a
29	CEBPB	chr11:73605817-73605992	A549	lung:	n/a	n/a
30	CEBPB	chr11:73587314-73588084	GM12878	blood:	n/a	n/a
31	CEBPB	chr11:73616917-73617114	K562	blood:	n/a	chr11:73616971-73616982 chr11:73616922-73616933 chr11:73617093-73617105 chr11:73616971-73616984
32	CEBPB	chr11:73587601-73588048	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:73586896-73586962	A549	lung:	n/a	n/a
34	CEBPB	chr11:73600188-73600480	IMR90	lung:	n/a	n/a
35	CEBPD	chr11:73587441-73588273	HepG2	liver:	n/a	n/a
36	CHD1	chr11:73586412-73588475	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr11:73587102-73588277	GM12878	blood:	n/a	n/a
38	CHD1	chr11:73586543-73586715	GM12878	blood:	n/a	n/a
39	CHD2	chr11:73586999-73588522	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr11:73583917-73583947	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr11:73587378-73588398	HepG2	liver:	n/a	n/a
42	CHD2	chr11:73587772-73588270	K562	blood:	n/a	n/a
43	CHD2	chr11:73587569-73588242	GM12878	blood:	n/a	n/a
44	CHD2	chr11:73587492-73588415	Hela-S3	cervix:	n/a	n/a
45	CREB1	chr11:73587406-73588358	HepG2	liver:	n/a	n/a
46	CREB1	chr11:73587489-73588350	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr11:73587535-73588441	HepG2	liver:	n/a	n/a
48	CREB1	chr11:73587519-73588324	A549	lung:	n/a	n/a
49	CREB1	chr11:73587355-73588436	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr11:73587700-73588126	A549	lung:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73587608-73587658	BE2_C	brain:	n/a
2	chr11:73588093-73588143	GM19239	blood:	n/a
3	chr11:73587864-73587914	HEEpiC	esophagus:	n/a
4	chr11:73587608-73587658	BE2_C	brain:	n/a
5	chr11:73588093-73588143	GM19239	blood:	n/a
6	chr11:73587864-73587914	HEEpiC	esophagus:	n/a
7	chr11:73587864-73587914	HepG2	liver:	n/a
8	chr11:73587722-73587772	PFSK-1	brain:	n/a
9	chr11:73581438-73581488	ECC-1	luminal epithelium:	n/a
10	chr11:73591256-73591306	Caco-2	colon:	n/a
11	chr11:73588074-73588124	HCM	heart:	n/a
12	chr11:73587722-73587772	IMR90	lung:	fetal
13	chr11:73588532-73588582	T-47D	breast:	n/a
14	chr11:73584244-73584294	HIPEpiC	eye:	n/a
15	chr11:73588532-73588582	HCPEpiC	choroid plexus:	n/a
16	chr11:73588430-73588480	IMR90	lung:	fetal
17	chr11:73587722-73587772	HRPEpiC	eye:	n/a
18	chr11:73586776-73586826	HRPEpiC	eye:	n/a
19	chr11:73588271-73588321	GM12892	blood:	n/a
20	chr11:73586776-73586826	H1-hESC	embryonic stem cell:	embryo
21	chr11:73587557-73587607	T-47D	breast:	n/a
22	chr11:73588271-73588321	HCT-116	colon:	n/a
23	chr11:73587608-73587658	Jurkat	blood:	n/a
24	chr11:73586776-73586826	GM12892	blood:	n/a
25	chr11:73587722-73587772	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:73588271-73588321	HRPEpiC	eye:	n/a
27	chr11:73587864-73587914	HCM	heart:	n/a
28	chr11:73591256-73591306	MCF-7	breast:	n/a
29	chr11:73588074-73588124	HNPCEpiC	eye:	n/a
30	chr11:73587952-73588002	HRE	kidney:	n/a
31	chr11:73588074-73588124	Jurkat	blood:	n/a
32	chr11:73586776-73586826	K562	blood:	n/a
33	chr11:73587864-73587914	ProgFib	skin:	n/a
34	chr11:73588532-73588582	NT2-D1	testis:	n/a
35	chr11:73588430-73588480	K562	blood:	n/a
36	chr11:73587557-73587607	HAEpiC	amniotic membrane:	n/a
37	chr11:73588430-73588480	BJ	skin:	n/a
38	chr11:73586776-73586826	NB4	blood:	n/a
39	chr11:73584244-73584294	SK-N-MC	brain:	n/a
40	chr11:73587915-73587965	PANC-1	pancreas:	n/a
41	chr11:73591256-73591306	SKMC	muscle:	n/a
42	chr11:73588532-73588582	HL-60	blood:	n/a
43	chr11:73587864-73587914	RPTEC	kidney:	n/a
44	chr11:73588430-73588480	ProgFib	skin:	n/a
45	chr11:73587952-73588002	GM12892	blood:	n/a
46	chr11:73591256-73591306	SK-N-MC	brain:	n/a
47	chr11:73587915-73587965	AG09309	skin:	n/a
48	chr11:73587608-73587658	HCM	heart:	n/a
49	chr11:73581438-73581488	Jurkat	blood:	n/a
50	chr11:73588074-73588124	Hepatocyte	liver:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:73585766..73589510-chr11:73599101..73602813,5	MCF-7	breast:
2	chr11:73585766..73589510-chr11:73599101..73602813,5	MCF-7	breast:
3	chr11:73497005..73500757-chr11:73586552..73589226,3	MCF-7	breast:
4	chr11:73587462..73590069-chr11:73692817..73694652,2	K562	blood:
5	chr11:73587269..73587939-chr19:49999399..50000301,2	Hela-S3	cervix:
6	chr11:73586190..73586861-chr5:179247491..179248383,2	MCF-7	breast:
7	chr11:73371085..73373574-chr11:73587519..73589689,2	MCF-7	breast:
8	chr11:73603516..73606235-chr11:73619849..73622149,2	K562	blood:
9	chr11:73567413..73569720-chr11:73578293..73583542,5	MCF-7	breast:
10	chr11:73587349..73588093-chr5:32174139..32174717,2	Hela-S3	cervix:
11	chr11:73617245..73618912-chr11:73620792..73622524,2	K562	blood:
12	chr11:73580836..73581458-chr6:73866841..73867761,2	MCF-7	breast:
13	chr11:73101451..73103302-chr11:73587436..73589979,2	MCF-7	breast:
14	chr11:73616949..73618962-chr11:73623554..73626249,2	K562	blood:
15	chr11:73592356..73594853-chr11:73596827..73598504,2	MCF-7	breast:
16	chr11:73496600..73498927-chr11:73587563..73589388,3	MCF-7	breast:
17	chr11:73497934..73501442-chr11:73586433..73589232,4	K562	blood:
18	chr11:73586614..73588298-chr11:73691679..73694031,2	MCF-7	breast:
19	chr11:73561146..73563311-chr11:73588199..73589761,2	K562	blood:
20	chr11:73596770..73599456-chr11:73604330..73606526,2	K562	blood:
21	chr1:45196591..45197186-chr11:73587825..73588807,2	Hela-S3	cervix:
22	chr11:73579249..73581313-chr11:73590994..73593823,2	K562	blood:
23	chr11:73569512..73571560-chr11:73581546..73584245,2	K562	blood:
24	chr11:73587101..73589496-chr11:73591176..73595056,3	MCF-7	breast:
25	chr11:73599833..73601446-chr11:73604982..73607037,2	K562	blood:
26	chr11:73490665..73492196-chr11:73612144..73614771,2	MCF-7	breast:
27	chr11:73587661..73589707-chr11:73590191..73593433,3	K562	blood:
28	chr11:73470519..73472838-chr11:73586575..73589489,2	MCF-7	breast:
29	chr11:73600327..73602691-chr11:73608708..73610968,2	MCF-7	breast:
30	chr11:73277014..73278822-chr11:73613258..73614797,2	K562	blood:
31	chr11:73576169..73580357-chr11:73581447..73584221,5	MCF-7	breast:
32	chr11:73586122..73588850-chr11:73605359..73608736,4	MCF-7	breast:
33	chr11:73581885..73584669-chr11:73588104..73591786,3	MCF-7	breast:
34	chr11:73497415..73503223-chr11:73585602..73589591,8	K562	blood:
35	chr11:73470293..73472350-chr11:73581492..73584395,2	MCF-7	breast:
36	chr11:73600327..73602691-chr11:73608708..73610968,2	MCF-7	breast:
37	chr11:73586195..73589455-chr11:73595184..73599458,5	K562	blood:
38	chr11:73561396..73563190-chr11:73586295..73588149,3	MCF-7	breast:
39	chr11:73586755..73589677-chr11:73602483..73604395,2	MCF-7	breast:
40	chr11:73587488..73590396-chr11:73595163..73597754,3	MCF-7	breast:
41	chr11:73572749..73574418-chr11:73579241..73582235,3	MCF-7	breast:
42	chr11:73616333..73618912-chr11:73619802..73622524,4	K562	blood:
43	chr11:73587992..73588608-chr12:51441696..51442224,2	Hela-S3	cervix:
44	chr11:73586922..73589181-chr11:73687473..73690308,2	K562	blood:
45	chr11:73586195..73589455-chr11:73595184..73599458,5	K562	blood:
46	chr11:73584965..73587189-chr11:73691735..73694698,2	K562	blood:
47	chr11:73579249..73581313-chr11:73590994..73593823,2	K562	blood:
48	chr11:73565085..73567966-chr11:73582133..73584937,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL48-2	chr11:73588019-73588113	NONHSAT022860
2	lnc-UCP2-2	chr11:73587524-73587611	NONHSAT022858
3	lnc-UCP2-2	chr11:73586804-73587164	NONHSAT022858
4	lnc-MRPL48-2	chr11:73589824-73591748	NONHSAT022860

No data

Variant related genes	Relation type
PAAF1	TF binding region
COA4	TF binding region
PAAF1	CpG island
COA4	CpG island
ENSG00000256034	chromatin interactions
ENSG00000142534	chromatin interactions
ENSG00000054967	chromatin interactions
ENSG00000161011	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000175575	chromatin interactions
ENSG00000175567	chromatin interactions
ENSG00000256681	chromatin interactions
ENSG00000175581	chromatin interactions
ENSG00000021300	chromatin interactions
ENSG00000272086	chromatin interactions
ENSG00000181924	chromatin interactions
ENSG00000175582	chromatin interactions
ENSG00000050426	chromatin interactions
ENSG00000113384	chromatin interactions

Extended variants
information (count: 1387 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1623476	chr11:73581224-73581225	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554265639	chr11:73581243-73581244	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192028511	chr11:73581277-73581278	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185001440	chr11:73581286-73581287	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548298060	chr11:73581294-73581295	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115454950	chr11:73581333-73581334	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533969962	chr11:73581353-73581354	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547411499	chr11:73581512-73581513	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs543616217	chr11:73581513-73581514	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs570739999	chr11:73581516-73581517	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11220	chr11:73581543-73581544	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs79212657	chr11:73581549-73581550	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541048228	chr11:73581624-73581625	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559735850	chr11:73581627-73581628	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs114306549	chr11:73581646-73581647	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368458058	chr11:73581667-73581668	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs10898949	chr11:73581672-73581673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs572585355	chr11:73581708-73581709	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs575176608	chr11:73581714-73581715	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs74509346	chr11:73581727-73581728	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375994165	chr11:73581747-73581748	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564492249	chr11:73581789-73581790	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs578196897	chr11:73581799-73581800	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544087196	chr11:73581887-73581888	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs12294934	chr11:73581908-73581909	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs531331125	chr11:73581941-73581942	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs147750112	chr11:73581957-73581958	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs200042973	chr11:73581974-73581975	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs371765004	chr11:73581987-73581988	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs570044774	chr11:73582029-73582030	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs142612204	chr11:73582100-73582101	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs190549595	chr11:73582108-73582109	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs547594565	chr11:73582109-73582110	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs570508593	chr11:73582156-73582157	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs539360247	chr11:73582184-73582185	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs549659382	chr11:73582185-73582186	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs367845418	chr11:73582214-73582215	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376514539	chr11:73582226-73582227	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs370071700	chr11:73582245-73582246	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs551673870	chr11:73582246-73582247	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs116617988	chr11:73582257-73582258	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs563174725	chr11:73582279-73582280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs535439549	chr11:73582319-73582320	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs146767537	chr11:73582357-73582358	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs575072989	chr11:73582371-73582372	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs148339605	chr11:73582411-73582412	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376731026	chr11:73582426-73582427	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534762310	chr11:73582432-73582433	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs181020467	chr11:73582444-73582445	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs12786008	chr11:73582448-73582449	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73499600-73583800	Weak transcription	Aorta	Aorta
2	chr11:73500400-73583800	Weak transcription	Colonic Mucosa	Colon
3	chr11:73518400-73584000	Weak transcription	Pancreas	Pancrea
4	chr11:73537400-73582600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr11:73539200-73583800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:73541800-73583600	Weak transcription	Esophagus	oesophagus
7	chr11:73548800-73582000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr11:73549800-73583600	Weak transcription	GM12878-XiMat	blood
9	chr11:73550400-73582400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:73564400-73586000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr11:73567600-73582200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:73571400-73586000	Weak transcription	Right Atrium	heart
13	chr11:73571600-73586200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr11:73573000-73586200	Weak transcription	Fetal Brain Male	brain
15	chr11:73573200-73584000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:73575400-73586000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr11:73575600-73582600	Weak transcription	Fetal Kidney	kidney
18	chr11:73575600-73583200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr11:73575600-73583800	Weak transcription	Spleen	Spleen
20	chr11:73575800-73581400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr11:73575800-73582200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr11:73575800-73583200	Weak transcription	Right Ventricle	heart
23	chr11:73575800-73583400	Weak transcription	Brain Angular Gyrus	brain
24	chr11:73575800-73583600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:73576000-73582400	Weak transcription	Adipose Nuclei	Adipose
26	chr11:73576000-73582400	Weak transcription	Brain Substantia Nigra	brain
27	chr11:73576000-73582600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:73576400-73581400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr11:73576400-73582400	Weak transcription	Brain Hippocampus Middle	brain
30	chr11:73576400-73582600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr11:73576400-73583000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr11:73576400-73586000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr11:73576600-73582000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr11:73576600-73583200	Weak transcription	Colon Smooth Muscle	Colon
35	chr11:73576600-73583200	Weak transcription	Left Ventricle	heart
36	chr11:73576600-73584000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr11:73577600-73582600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr11:73577800-73582400	Weak transcription	Lung	lung
39	chr11:73577800-73582800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:73578000-73582400	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr11:73578000-73582600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr11:73578000-73582600	Weak transcription	Hela-S3	cervix
43	chr11:73578000-73583600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr11:73578000-73583800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:73578000-73586400	Weak transcription	Fetal Heart	heart
46	chr11:73578200-73581400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr11:73578200-73581400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:73578200-73582000	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr11:73578200-73582200	Weak transcription	NH-A	brain
50	chr11:73578200-73582400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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