Variant report

Variant	nsv897684
Chromosome Location	chr11:64047360-64060976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:836)
CpG islands
(count:2934)
Chromatin interactive
region (count:59)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:836 , 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	chr11:64052589-64052600	K562	blood:	n/a	n/a
2	ATF1	chr11:64052060-64052579	K562	blood:	n/a	n/a
3	ATF3	chr11:64053001-64053333	K562	blood:	n/a	n/a
4	ATF3	chr11:64052936-64053375	A549	lung:	n/a	n/a
5	BACH1	chr11:64059313-64059703	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:64052442-64052589	K562	blood:	n/a	n/a
7	BACH1	chr11:64052335-64053372	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:64053049-64053072	K562	blood:	n/a	n/a
9	BCL3	chr11:64052105-64052918	A549	lung:	n/a	n/a
10	BCL3	chr11:64052066-64053444	A549	lung:	n/a	chr11:64053299-64053308 chr11:64053008-64053021 chr11:64053257-64053270 chr11:64053183-64053196 chr11:64053315-64053324
11	BHLHE40	chr11:64053013-64053329	K562	blood:	n/a	chr11:64053178-64053194 chr11:64053289-64053305
12	BHLHE40	chr11:64059512-64059782	GM12878	blood:	n/a	chr11:64059701-64059717
13	BHLHE40	chr11:64052600-64052748	K562	blood:	n/a	n/a
14	BHLHE40	chr11:64052018-64052275	K562	blood:	n/a	n/a
15	BHLHE40	chr11:64052008-64053373	GM12878	blood:	n/a	chr11:64053178-64053194 chr11:64053003-64053019 chr11:64053289-64053305
16	BRCA1	chr11:64051776-64051910	GM12878	blood:	n/a	n/a
17	BRCA1	chr11:64052030-64052889	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr11:64053165-64053376	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:64052131-64052394	HepG2	liver:	n/a	n/a
20	CBX3	chr11:64052124-64052658	K562	blood:	n/a	n/a
21	CCNT2	chr11:64051905-64053471	K562	blood:	n/a	chr11:64053307-64053316 chr11:64052717-64052737
22	CEBPB	chr11:64052093-64052242	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:64051554-64051561	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:64052142-64052355	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:64052166-64052200	K562	blood:	n/a	n/a
26	CEBPB	chr11:64052986-64053320	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr11:64051949-64052488	HepG2	liver:	n/a	n/a
28	CEBPD	chr11:64052714-64053448	HepG2	liver:	n/a	n/a
29	CEBPD	chr11:64052499-64052870	K562	blood:	n/a	n/a
30	CHD1	chr11:64051966-64052749	GM12878	blood:	n/a	n/a
31	CHD2	chr11:64052047-64052756	K562	blood:	n/a	n/a
32	CHD2	chr11:64051921-64053646	Hela-S3	cervix:	n/a	chr11:64053197-64053207 chr11:64052773-64052783
33	CHD2	chr11:64052041-64052686	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr11:64053896-64054160	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr11:64052750-64053309	HepG2	liver:	n/a	chr11:64053197-64053207 chr11:64052773-64052783
36	CHD2	chr11:64052176-64052300	HepG2	liver:	n/a	n/a
37	CHD2	chr11:64051999-64053381	GM12878	blood:	n/a	chr11:64053197-64053207 chr11:64052773-64052783
38	CHD2	chr11:64052995-64053381	K562	blood:	n/a	chr11:64053197-64053207
39	CREB1	chr11:64051622-64052504	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr11:64051663-64053452	GM12878	blood:	n/a	n/a
41	CREB1	chr11:64052534-64053519	A549	lung:	n/a	n/a
42	CREB1	chr11:64051922-64052473	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr11:64051752-64052576	HepG2	liver:	n/a	n/a
44	CREB1	chr11:64051978-64052486	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr11:64051991-64052390	A549	lung:	n/a	n/a
46	CREB1	chr11:64051739-64053552	HepG2	liver:	n/a	n/a
47	CREB1	chr11:64051650-64052423	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr11:64051789-64052438	A549	lung:	n/a	n/a
49	CTBP2	chr11:64058361-64059911	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:64053940-64054090	HFF-Myc	foreskin:	n/a	n/a

(count:2934 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64051762-64051812	SK-N-SH	brain:	n/a
2	chr11:64053481-64053531	Jurkat	blood:	n/a
3	chr11:64059594-64059644	LNCaP	prostate:	n/a
4	chr11:64059057-64059107	NHBE	bronchial:	n/a
5	chr11:64055310-64055360	GM12892	blood:	n/a
6	chr11:64051814-64051864	K562	blood:	n/a
7	chr11:64051762-64051812	SK-N-SH	brain:	n/a
8	chr11:64053481-64053531	Jurkat	blood:	n/a
9	chr11:64059594-64059644	LNCaP	prostate:	n/a
10	chr11:64059057-64059107	NHBE	bronchial:	n/a
11	chr11:64055310-64055360	GM12892	blood:	n/a
12	chr11:64051814-64051864	K562	blood:	n/a
13	chr11:64059594-64059644	GM12878	blood:	n/a
14	chr11:64056910-64056960	GM06990	blood:	n/a
15	chr11:64058878-64058928	PANC-1	pancreas:	n/a
16	chr11:64051762-64051812	HEK293	kidney:	embryo
17	chr11:64053129-64053179	AG04450	lung:	fetal
18	chr11:64059054-64059104	HepG2	liver:	n/a
19	chr11:64053742-64053792	Hela-S3	cervix:	n/a
20	chr11:64053472-64053522	AG10803	skin:	n/a
21	chr11:64052260-64052310	NHBE	bronchial:	n/a
22	chr11:64058937-64058987	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:64051738-64051788	GM19239	blood:	n/a
24	chr11:64059479-64059529	A549	lung:	n/a
25	chr11:64051814-64051864	HCF	heart:	n/a
26	chr11:64051344-64051394	NH-A	brain:	n/a
27	chr11:64051738-64051788	SK-N-SH_RA	brain:	n/a
28	chr11:64059054-64059104	MCF10A-Er-Src	breast:	n/a
29	chr11:64053134-64053184	SK-N-SH	brain:	n/a
30	chr11:64051738-64051788	HRCEpiC	kidney:	n/a
31	chr11:64051738-64051788	HEK293	kidney:	embryo
32	chr11:64052165-64052215	AG10803	skin:	n/a
33	chr11:64051344-64051394	SK-N-SH_RA	brain:	n/a
34	chr11:64060409-64060459	A549	lung:	n/a
35	chr11:64058878-64058928	RPTEC	kidney:	n/a
36	chr11:64051344-64051394	AG09319	gingival:	n/a
37	chr11:64051725-64051775	BJ	skin:	n/a
38	chr11:64059479-64059529	CMK	blood:	n/a
39	chr11:64051753-64051803	SK-N-SH_RA	brain:	n/a
40	chr11:64052547-64052597	GM19239	blood:	n/a
41	chr11:64054159-64054209	AG09309	skin:	n/a
42	chr11:64057807-64057857	HAEpiC	amniotic membrane:	n/a
43	chr11:64058937-64058987	SK-N-SH_RA	brain:	n/a
44	chr11:64059937-64059987	HMEC	breast:	n/a
45	chr11:64055383-64055433	AoSMC	blood vessel:	n/a
46	chr11:64059594-64059644	SK-N-SH	brain:	n/a
47	chr11:64057771-64057821	MCF10A-Er-Src	breast:	n/a
48	chr11:64054159-64054209	SK-N-MC	brain:	n/a
49	chr11:64058937-64058987	NT2-D1	testis:	n/a
50	chr11:64058704-64058754	HCT-116	colon:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:64028752..64030892-chr11:64051770..64053907,2	MCF-7	breast:
2	chr11:63992951..63995163-chr11:64045482..64048307,2	MCF-7	breast:
3	chr11:63933268..63934996-chr11:64053626..64055323,2	MCF-7	breast:
4	chr11:63993205..63994873-chr11:64060700..64063524,2	MCF-7	breast:
5	chr11:64046688..64048904-chr11:64060394..64063372,2	MCF-7	breast:
6	chr11:64012924..64015359-chr11:64050536..64054535,6	MCF-7	breast:
7	chr11:64043284..64045946-chr11:64047398..64048977,2	MCF-7	breast:
8	chr11:64053151..64055063-chr11:64124109..64127002,2	K562	blood:
9	chr11:64052097..64054985-chr11:64084500..64086300,2	MCF-7	breast:
10	chr11:64052742..64053246-chr18:48556218..48556768,2	Hela-S3	cervix:
11	chr11:64037441..64038100-chr11:64052228..64053171,3	Hela-S3	cervix:
12	chr11:64000315..64002426-chr11:64053899..64055582,2	MCF-7	breast:
13	chr11:64012590..64014829-chr11:64057902..64059525,2	MCF-7	breast:
14	chr11:64052935..64055141-chr11:64085438..64088024,2	MCF-7	breast:
15	chr11:64049158..64050813-chr11:64051261..64054037,2	K562	blood:
16	chr11:64006794..64010904-chr11:64055205..64058214,4	MCF-7	breast:
17	chr11:64058435..64061008-chr11:64080225..64081908,2	K562	blood:
18	chr11:64013373..64015770-chr11:64059905..64062431,2	MCF-7	breast:
19	chr11:64033188..64045448-chr11:64059274..64075790,38	MCF-7	breast:
20	chr11:64017311..64024506-chr11:64050135..64055747,10	MCF-7	breast:
21	chr11:64050061..64052819-chr11:64080707..64082589,2	MCF-7	breast:
22	chr11:63977636..63979457-chr11:64056171..64057684,2	MCF-7	breast:
23	chr11:64053943..64056232-chr11:64083212..64085123,2	MCF-7	breast:
24	chr11:64032072..64048684-chr11:64048768..64055711,68	MCF-7	breast:
25	chr11:63994757..64000133-chr11:64050787..64054663,5	MCF-7	breast:
26	chr11:63949228..63955854-chr11:64049902..64053814,7	MCF-7	breast:
27	chr11:64037071..64037978-chr11:64052887..64053521,2	MCF-7	breast:
28	chr11:64051216..64053733-chr11:64084911..64087115,3	K562	blood:
29	chr11:64052517..64054991-chr11:64119891..64124085,3	K562	blood:
30	chr11:64053599..64055406-chr11:64121641..64123731,2	K562	blood:
31	chr11:64013225..64015116-chr11:64056938..64059333,2	MCF-7	breast:
32	chr11:64017360..64020043-chr11:64060077..64062122,2	MCF-7	breast:
33	chr11:64028329..64041732-chr11:64049023..64058851,39	MCF-7	breast:
34	chr11:64052231..64052896-chr6:7389691..7390274,2	Hela-S3	cervix:
35	chr11:64013049..64014994-chr11:64052537..64054255,3	MCF-7	breast:
36	chr11:64051216..64053700-chr11:64085412..64087115,2	K562	blood:
37	chr11:64041759..64043917-chr11:64044859..64047497,2	MCF-7	breast:
38	chr11:63994977..63999244-chr11:64052371..64054935,4	MCF-7	breast:
39	chr11:64011811..64014800-chr11:64054845..64057591,2	MCF-7	breast:
40	chr11:64016812..64021458-chr11:64049548..64056058,8	MCF-7	breast:
41	chr11:63952254..63954139-chr11:64052656..64054498,2	MCF-7	breast:
42	chr11:64032072..64048684-chr11:64048768..64055711,68	MCF-7	breast:
43	chr11:63932716..63934743-chr11:64051710..64053463,2	K562	blood:
44	chr11:64050229..64053074-chr11:64081177..64083173,2	MCF-7	breast:
45	chr11:64051486..64055490-chr11:64121214..64124233,3	MCF-7	breast:
46	chr11:64003822..64006272-chr11:64058913..64060452,2	MCF-7	breast:
47	chr11:64008214..64010501-chr11:64051864..64054015,3	MCF-7	breast:
48	chr11:63973628..63976272-chr11:64056827..64059574,2	MCF-7	breast:
49	chr11:63992108..63994970-chr11:64050201..64053443,5	MCF-7	breast:
50	chr11:64042595..64046939-chr11:64049156..64053929,8	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNK4-1	chr11:64058774-64059038	NONHSAT021980

No data

Variant related genes	Relation type
ENSG00000257069	TF binding region
ENSG00000207024	TF binding region
GPR137	TF binding region
BAD	TF binding region
KCNK4	TF binding region
ENSG00000257069	CpG island
ENSG00000207024	CpG island
GPR137	CpG island
BAD	CpG island
KCNK4	CpG island
ENSG00000173264	chromatin interactions
ENSG00000002330	chromatin interactions
ENSG00000110011	chromatin interactions
ENSG00000168071	chromatin interactions
ENSG00000133315	chromatin interactions
ENSG00000173486	chromatin interactions
ENSG00000149761	chromatin interactions
ENSG00000143418	chromatin interactions
ENSG00000173113	chromatin interactions
ENSG00000164304	chromatin interactions
ENSG00000162302	chromatin interactions
ENSG00000149782	chromatin interactions
ENSG00000256940	chromatin interactions
ENSG00000173153	chromatin interactions
ENSG00000257086	chromatin interactions
ENSG00000126432	chromatin interactions
ENSG00000149781	chromatin interactions
ENSG00000149743	chromatin interactions
ENSG00000236935	chromatin interactions
ENSG00000124784	chromatin interactions
ENSG00000168439	chromatin interactions
ENSG00000173457	chromatin interactions
ENSG00000141646	chromatin interactions
ENSG00000256116	chromatin interactions
ENSG00000173511	chromatin interactions

Extended variants
information (count: 544 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12184422	chr11:64047360-64047361	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112595668	chr11:64047398-64047399	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs553435079	chr11:64047437-64047438	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs573462945	chr11:64047483-64047484	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs373362544	chr11:64047512-64047513	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs373907756	chr11:64047516-64047517	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs542602201	chr11:64047525-64047526	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs555358689	chr11:64047527-64047528	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs11231742	chr11:64047556-64047557	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs573415459	chr11:64047572-64047573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs369730302	chr11:64047586-64047587	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs529314639	chr11:64047593-64047594	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs12271952	chr11:64047600-64047601	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184271158	chr11:64047605-64047606	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs376033066	chr11:64047617-64047618	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs560221362	chr11:64047631-64047632	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs529202127	chr11:64047648-64047649	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs188234250	chr11:64047653-64047654	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs376564586	chr11:64047660-64047661	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs180935436	chr11:64047676-64047677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs376974854	chr11:64047685-64047686	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs34298731	chr11:64047687-64047688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs371212872	chr11:64047717-64047718	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs544462311	chr11:64047740-64047741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs551135775	chr11:64047770-64047771	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs375471485	chr11:64047771-64047772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs144682603	chr11:64047804-64047805	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs398115461	chr11:64047831-64047832	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs201454553	chr11:64047832-64047833	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs199680403	chr11:64047833-64047834	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs186357628	chr11:64047846-64047847	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs540065124	chr11:64047847-64047848	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs368436941	chr11:64047858-64047859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs561062863	chr11:64047886-64047887	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs529877338	chr11:64047924-64047925	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs566917714	chr11:64047966-64047967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs1213140	chr11:64048025-64048026	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574905256	chr11:64048091-64048092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs377636994	chr11:64048096-64048097	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs537441930	chr11:64048105-64048106	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs557479854	chr11:64048115-64048116	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs577299407	chr11:64048158-64048159	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs539913626	chr11:64048218-64048219	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs566222890	chr11:64048259-64048260	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs560314691	chr11:64048284-64048285	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs573705641	chr11:64048285-64048286	Weak transcription Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs532040844	chr11:64048297-64048298	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs181635142	chr11:64048341-64048342	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs551860263	chr11:64048352-64048353	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs530972863	chr11:64048402-64048403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1350 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64039600-64049000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr11:64039600-64050400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr11:64039600-64050800	Weak transcription	Psoas Muscle	Psoas
4	chr11:64039600-64051000	Weak transcription	Fetal Kidney	kidney
5	chr11:64039600-64051000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:64039600-64051400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:64039600-64051400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:64039600-64051600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:64039800-64049000	Weak transcription	Colon Smooth Muscle	Colon
10	chr11:64039800-64050000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:64039800-64050800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr11:64039800-64051000	Weak transcription	Primary B cells from cord blood	blood
13	chr11:64039800-64051000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr11:64039800-64051000	Weak transcription	HSMM	muscle
15	chr11:64039800-64051000	Weak transcription	HUVEC	blood vessel
16	chr11:64039800-64051400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:64040000-64049000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:64040000-64050600	Strong transcription	Fetal Stomach	stomach
19	chr11:64040000-64050800	Weak transcription	Fetal Brain Male	brain
20	chr11:64040000-64051200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr11:64040200-64047400	Strong transcription	Fetal Muscle Leg	muscle
22	chr11:64040200-64047600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr11:64040200-64051400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:64040400-64050600	Weak transcription	GM12878-XiMat	blood
25	chr11:64040400-64051000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr11:64041400-64051000	Weak transcription	HepG2	liver
27	chr11:64042200-64050800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:64042400-64050600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:64042600-64047400	Strong transcription	Brain Anterior Caudate	brain
30	chr11:64042600-64047400	Strong transcription	Fetal Thymus	thymus
31	chr11:64042600-64050800	Strong transcription	Fetal Muscle Trunk	muscle
32	chr11:64043000-64047400	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr11:64043400-64051200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr11:64043400-64051400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:64043600-64051000	Weak transcription	K562	blood
36	chr11:64044000-64047400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr11:64044600-64050800	Weak transcription	Small Intestine	intestine
38	chr11:64044600-64051000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr11:64044800-64048600	Weak transcription	Right Atrium	heart
40	chr11:64044800-64051000	Weak transcription	NH-A	brain
41	chr11:64045000-64047800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:64045000-64050600	Weak transcription	Colonic Mucosa	Colon
43	chr11:64045000-64050800	Weak transcription	HMEC	breast
44	chr11:64045000-64051400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr11:64045200-64049600	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr11:64045200-64049600	Weak transcription	Stomach Mucosa	stomach
47	chr11:64045200-64050600	Weak transcription	NHDF-Ad	bronchial
48	chr11:64045200-64050800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:64045400-64050800	Weak transcription	Hela-S3	cervix
50	chr11:64045600-64051400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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