Variant report

Variant	nsv1066811
Chromosome Location	chr21:48050388-48096945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1072)
CpG islands
(count:2198)
Chromatin interactive
region (count:108)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr21:48054800-48055606	GM12878	blood:	n/a	n/a
2	ATF3	chr21:48055257-48055907	A549	lung:	n/a	chr21:48055268-48055277
3	ATF3	chr21:48055226-48055739	K562	blood:	n/a	chr21:48055237-48055245 chr21:48055268-48055277
4	ATF3	chr21:48055269-48055747	A549	lung:	n/a	n/a
5	ATF3	chr21:48081183-48081378	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr21:48055269-48055855	K562	blood:	n/a	n/a
7	ATF3	chr21:48054937-48055231	K562	blood:	n/a	n/a
8	BATF	chr21:48058299-48058586	GM12878	blood:	n/a	n/a
9	BATF	chr21:48058236-48058618	GM12878	blood:	n/a	n/a
10	BCL11A	chr21:48058286-48058514	GM12878	blood:	n/a	n/a
11	BCL11A	chr21:48058312-48058550	GM12878	blood:	n/a	n/a
12	BCL3	chr21:48084505-48084827	GM12878	blood:	n/a	n/a
13	BCL3	chr21:48084540-48084760	GM12878	blood:	n/a	n/a
14	BCLAF1	chr21:48054738-48055175	GM12878	blood:	n/a	n/a
15	BCLAF1	chr21:48081154-48081530	GM12878	blood:	n/a	n/a
16	CBX3	chr21:48075124-48075496	K562	blood:	n/a	n/a
17	CBX3	chr21:48054356-48056106	K562	blood:	n/a	n/a
18	CEBPB	chr21:48058257-48058541	K562	blood:	n/a	n/a
19	CEBPB	chr21:48064981-48065204	K562	blood:	n/a	n/a
20	CEBPD	chr21:48055110-48055815	HepG2	liver:	n/a	n/a
21	CEBPD	chr21:48054859-48055913	K562	blood:	n/a	n/a
22	CEBPD	chr21:48087649-48087923	HepG2	liver:	n/a	n/a
23	CREB1	chr21:48054821-48056265	HepG2	liver:	n/a	n/a
24	CREB1	chr21:48054978-48055140	A549	lung:	n/a	n/a
25	CREB1	chr21:48081058-48081481	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr21:48054800-48055327	ECC-1	luminal epithelium:	n/a	n/a
27	CREB1	chr21:48054804-48055837	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr21:48054940-48056118	A549	lung:	n/a	n/a
29	CREB1	chr21:48054844-48055240	ECC-1	luminal epithelium:	n/a	n/a
30	CREB1	chr21:48054848-48056254	K562	blood:	n/a	n/a
31	CREB1	chr21:48054788-48056180	GM12878	blood:	n/a	n/a
32	CREB1	chr21:48054806-48056067	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr21:48059760-48059910	HMF	breast:	n/a	n/a
34	CTCF	chr21:48055006-48055179	GM19240	blood:	n/a	chr21:48055091-48055107
35	CTCF	chr21:48081200-48081350	BE2_C	brain:	n/a	n/a
36	CTCF	chr21:48081144-48081421	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr21:48081180-48081330	GM12867	blood:	n/a	n/a
38	CTCF	chr21:48059540-48059690	Caco-2	colon:	n/a	n/a
39	CTCF	chr21:48059760-48059910	HPF	lung:	n/a	n/a
40	CTCF	chr21:48081180-48081330	GM06990	blood:	n/a	n/a
41	CTCF	chr21:48054940-48055090	NHLF	lung:	n/a	n/a
42	CTCF	chr21:48054960-48055110	MCF-7	breast:	n/a	chr21:48055091-48055107
43	CTCF	chr21:48054980-48055130	HUVEC	blood vessel:	n/a	chr21:48055091-48055107
44	CTCF	chr21:48081200-48081350	GM12872	blood:	n/a	n/a
45	CTCF	chr21:48081163-48081432	MCF-7	breast:	n/a	n/a
46	CTCF	chr21:48081160-48081310	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr21:48059860-48060010	HCM	heart:	n/a	n/a
48	CTCF	chr21:48059800-48059950	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr21:48055000-48055150	AoAF	blood vessel:	n/a	chr21:48055091-48055107
50	CTCF	chr21:48055000-48055150	RPTEC	kidney:	n/a	chr21:48055091-48055107

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:48054563-48054613	GM12891	blood:	n/a
2	chr21:48090128-48090178	NHBE	bronchial:	n/a
3	chr21:48054563-48054613	GM12891	blood:	n/a
4	chr21:48090128-48090178	NHBE	bronchial:	n/a
5	chr21:48090128-48090178	GM06990	blood:	n/a
6	chr21:48085517-48085567	HAEpiC	amniotic membrane:	n/a
7	chr21:48090508-48090558	PFSK-1	brain:	n/a
8	chr21:48082402-48082452	Hela-S3	cervix:	n/a
9	chr21:48055224-48055274	PFSK-1	brain:	n/a
10	chr21:48087978-48088028	NB4	blood:	n/a
11	chr21:48055366-48055416	HCM	heart:	n/a
12	chr21:48084674-48084724	HCT-116	colon:	n/a
13	chr21:48078809-48078859	MCF-7	breast:	n/a
14	chr21:48079700-48079750	HL-60	blood:	n/a
15	chr21:48087589-48087639	ProgFib	skin:	n/a
16	chr21:48079700-48079750	HCF	heart:	n/a
17	chr21:48054897-48054947	AoSMC	blood vessel:	n/a
18	chr21:48081242-48081292	NT2-D1	testis:	n/a
19	chr21:48055224-48055274	GM19239	blood:	n/a
20	chr21:48055893-48055943	HMEC	breast:	n/a
21	chr21:48055893-48055943	HRCEpiC	kidney:	n/a
22	chr21:48088046-48088096	AG10803	skin:	n/a
23	chr21:48068452-48068502	HMEC	breast:	n/a
24	chr21:48091011-48091061	ovcar-3	ovarian:	n/a
25	chr21:48055338-48055388	HepG2	liver:	n/a
26	chr21:48068585-48068635	GM19239	blood:	n/a
27	chr21:48055893-48055943	NHBE	bronchial:	n/a
28	chr21:48084674-48084724	ProgFib	skin:	n/a
29	chr21:48085517-48085567	HRPEpiC	eye:	n/a
30	chr21:48068452-48068502	Hepatocyte	liver:	n/a
31	chr21:48082402-48082452	H1-hESC	embryonic stem cell:	embryo
32	chr21:48088046-48088096	ProgFib	skin:	n/a
33	chr21:48068638-48068688	NHBE	bronchial:	n/a
34	chr21:48068748-48068798	SK-N-MC	brain:	n/a
35	chr21:48068638-48068688	HEK293	kidney:	embryo
36	chr21:48054563-48054613	AG10803	skin:	n/a
37	chr21:48052757-48052807	BE2_C	brain:	n/a
38	chr21:48079700-48079750	HUVEC	blood vessel:	n/a
39	chr21:48055631-48055681	HIPEpiC	eye:	n/a
40	chr21:48055893-48055943	Hela-S3	cervix:	n/a
41	chr21:48068638-48068688	GM12891	blood:	n/a
42	chr21:48081066-48081116	HCF	heart:	n/a
43	chr21:48090128-48090178	HEK293	kidney:	embryo
44	chr21:48087978-48088028	PANC-1	pancreas:	n/a
45	chr21:48091011-48091061	HepG2	liver:	n/a
46	chr21:48081242-48081292	H1-hESC	embryonic stem cell:	embryo
47	chr21:48087452-48087502	GM19239	blood:	n/a
48	chr21:48087978-48088028	HMEC	breast:	n/a
49	chr21:48055893-48055943	NT2-D1	testis:	n/a
50	chr21:48052757-48052807	HIPEpiC	eye:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr21:48025522..48028149-chr21:48060514..48063166,2	MCF-7	breast:
2	chr21:48082813..48085393-chr21:48090322..48091989,3	MCF-7	breast:
3	chr21:48053543..48058001-chr21:48077675..48082884,7	K562	blood:
4	chr21:47945113..47947005-chr21:48054397..48057093,2	MCF-7	breast:
5	chr21:48055128..48057107-chr21:48067363..48069357,2	MCF-7	breast:
6	chr21:48085636..48087391-chr21:48088276..48090254,2	K562	blood:
7	chr21:48069135..48075784-chr21:48076835..48082817,8	MCF-7	breast:
8	chr21:48055000..48055796-chr9:132251161..132252102,2	Hela-S3	cervix:
9	chr21:48059291..48062346-chr21:48062349..48064586,4	MCF-7	breast:
10	chr21:48062111..48065887-chr21:48068207..48070347,4	K562	blood:
11	chr17:80250394..80251099-chr21:48055154..48055814,2	Hela-S3	cervix:
12	chr21:47741705..47745829-chr21:48053977..48057908,5	MCF-7	breast:
13	chr21:48044131..48047004-chr21:48048003..48050751,2	MCF-7	breast:
14	chr21:48076560..48080046-chr21:48082031..48085407,3	MCF-7	breast:
15	chr21:48054376..48056073-chr21:48072079..48074243,2	K562	blood:
16	chr21:47877118..47880921-chr21:48053345..48058142,9	K562	blood:
17	chr21:48055126..48055735-chr3:196359119..196359988,2	NB4	blood:
18	chr21:48061876..48063858-chr21:48067311..48068866,2	K562	blood:
19	chr12:52444987..52445506-chr21:48055114..48055948,2	Hela-S3	cervix:
20	chr14:75745044..75745708-chr21:48055135..48055722,2	Hela-S3	cervix:
21	chr21:48054236..48058001-chr21:48079083..48082780,4	K562	blood:
22	chr21:48082813..48085393-chr21:48090322..48091989,3	MCF-7	breast:
23	chr21:47979855..47982153-chr21:48055162..48056734,2	MCF-7	breast:
24	chr21:48055854..48056356-chr6:27860488..27861098,2	Hela-S3	cervix:
25	chr10:2781607..2783125-chr21:48064505..48066265,2	MCF-7	breast:
26	chr21:48081260..48084193-chr21:48084438..48088004,4	MCF-7	breast:
27	chr13:48877615..48878228-chr21:48055384..48056111,2	Hela-S3	cervix:
28	chr21:48092221..48094129-chr21:48096913..48098673,2	MCF-7	breast:
29	chr21:48054963..48055735-chr3:50329204..50329933,2	NB4	blood:
30	chr21:48066242..48069643-chr21:48070010..48074183,7	K562	blood:
31	chr21:48044480..48047952-chr21:48055875..48058667,3	MCF-7	breast:
32	chr21:48070689..48072483-chr21:48074893..48076580,2	K562	blood:
33	chr21:48054835..48055519-chr5:158523349..158524349,3	MCF-7	breast:
34	chr21:48055080..48055596-chr4:39046312..39046846,2	Hela-S3	cervix:
35	chr21:48005218..48007630-chr21:48055834..48057649,2	K562	blood:
36	chr21:48057607..48061852-chr21:48061868..48066803,5	K562	blood:
37	chr17:75136430..75137196-chr21:48055351..48055948,2	Hela-S3	cervix:
38	chr21:48093992..48095617-chr21:48097456..48100225,2	K562	blood:
39	chr21:47705393..47707000-chr21:48055095..48056977,2	K562	blood:
40	chr1:36396247..36397104-chr21:48055435..48056034,2	HCT-116	colon:
41	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
42	chr21:48086187..48087903-chr21:48090596..48092720,2	K562	blood:
43	chr21:48066242..48069643-chr21:48070010..48074183,7	K562	blood:
44	chr21:48066275..48067897-chr21:48072092..48074993,2	MCF-7	breast:
45	chr21:48053992..48056792-chr21:48084785..48087274,2	MCF-7	breast:
46	chr15:62352142..62352842-chr21:48087098..48087861,2	NB4	blood:
47	chr21:47972251..47974231-chr21:48053496..48055796,2	K562	blood:
48	chr21:48061876..48063858-chr21:48067311..48068866,2	K562	blood:
49	chr21:48079857..48085039-chr21:48086180..48089656,6	K562	blood:
50	chr21:47742343..47745058-chr21:48054003..48056846,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIP2A-5	chr21:48084207-48084862	NONHSAT083074
2	lnc-S100B-1	chr21:48073470-48073934	NONHSAT083076
3	lnc-DIP2A-5	chr21:48055527-48055675	NONHSAT083074

No data

Variant related genes	Relation type
PRMT2	TF binding region
DSTNP1	TF binding region
PRMT2	CpG island
DSTNP1	CpG island
ENSG00000233224	chromatin interactions
ENSG00000214706	chromatin interactions
ENSG00000196352	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000263583	chromatin interactions
ENSG00000139687	chromatin interactions
ENSG00000118873	chromatin interactions
ENSG00000231473	chromatin interactions
ENSG00000160307	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000202239	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000126070	chromatin interactions
ENSG00000204054	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000265692	chromatin interactions
ENSG00000272283	chromatin interactions
ENSG00000160310	chromatin interactions
ENSG00000259251	chromatin interactions
ENSG00000129003	chromatin interactions
ENSG00000164330	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000232065	chromatin interactions
ENSG00000261771	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000256061	chromatin interactions
ENSG00000129657	chromatin interactions
ENSG00000105699	chromatin interactions
ENSG00000247077	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000230982	chromatin interactions
ENSG00000109046	chromatin interactions
ENSG00000109790	chromatin interactions
ENSG00000170345	chromatin interactions

Extended variants
information (count: 2001 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:2001 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839367	chr21:48050388-48050389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553196584	chr21:48050390-48050391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548561124	chr21:48050424-48050425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534283831	chr21:48050446-48050447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375427655	chr21:48050448-48050449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185265504	chr21:48050461-48050462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573089094	chr21:48050462-48050463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs57023094	chr21:48050537-48050538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570608152	chr21:48050563-48050564	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556828430	chr21:48050590-48050591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs578208638	chr21:48050591-48050592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190421187	chr21:48050647-48050648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181175687	chr21:48050657-48050658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553351993	chr21:48050719-48050720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs79711905	chr21:48050727-48050728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186908513	chr21:48050750-48050751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538978720	chr21:48050799-48050800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191933689	chr21:48050877-48050878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145324003	chr21:48050879-48050880	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544443526	chr21:48050905-48050906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs34574083	chr21:48050910-48050911	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563081242	chr21:48050935-48050936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573671897	chr21:48050963-48050964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs76758659	chr21:48050978-48050979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530370407	chr21:48050997-48050998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542590171	chr21:48051049-48051050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560487388	chr21:48051055-48051056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527715935	chr21:48051074-48051075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552617700	chr21:48051175-48051176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs570827308	chr21:48051176-48051177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs141461307	chr21:48051186-48051187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183322343	chr21:48051188-48051189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145171285	chr21:48051195-48051196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535354964	chr21:48051286-48051287	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139001334	chr21:48051308-48051309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189070310	chr21:48051337-48051338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539036968	chr21:48051338-48051339	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557751829	chr21:48051361-48051362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576013457	chr21:48051425-48051426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543506224	chr21:48051465-48051466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370025005	chr21:48051477-48051478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144204296	chr21:48051535-48051536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201246931	chr21:48051537-48051538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199765838	chr21:48051538-48051539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573732101	chr21:48051600-48051601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368278209	chr21:48051603-48051604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs190735885	chr21:48051647-48051648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs140804598	chr21:48051728-48051729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs7278083	chr21:48051777-48051778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs528008454	chr21:48051868-48051869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:2492 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:48025800-48054800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr21:48042600-48054800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr21:48042800-48050600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr21:48046200-48050800	Enhancers	Primary T cells from cord blood	blood
5	chr21:48046800-48054800	Weak transcription	Right Atrium	heart
6	chr21:48047800-48053200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr21:48047800-48053800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr21:48048000-48052200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr21:48048000-48052600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr21:48048200-48052200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr21:48049000-48052200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr21:48049000-48052400	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr21:48049000-48052400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr21:48049000-48052400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr21:48049000-48053400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr21:48049000-48053800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr21:48049000-48053800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr21:48049000-48054200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr21:48049200-48051400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr21:48049800-48053000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr21:48050600-48052000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr21:48050800-48052000	Weak transcription	Primary T cells from cord blood	blood
23	chr21:48051400-48051800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr21:48051800-48054400	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr21:48052000-48052800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr21:48052000-48053000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr21:48052000-48053400	Enhancers	Primary T cells from cord blood	blood
28	chr21:48052000-48053800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr21:48052200-48052400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr21:48052200-48052400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr21:48052200-48053800	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr21:48052200-48054200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr21:48052200-48054800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr21:48052200-48054800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr21:48052400-48052800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr21:48052400-48053400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr21:48052400-48053400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr21:48052400-48053800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr21:48052400-48053800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr21:48052400-48054600	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr21:48052400-48054800	Enhancers	Fetal Thymus	thymus
42	chr21:48052600-48054800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr21:48052600-48054800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr21:48052800-48053200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr21:48052800-48053800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr21:48053000-48053400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr21:48053000-48054800	Enhancers	Primary T cells fromperipheralblood	blood
48	chr21:48053200-48054200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr21:48053200-48054800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr21:48053400-48053600	Enhancers	H1 Cell Line	embryonic stem cell

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