Variant report

Variant	nsv1055772
Chromosome Location	chr21:45353436-45373304
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:881)
CpG islands
(count:366)
Chromatin interactive
region (count:98)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:881 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45357354-45357424	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:45357065-45357134	K562	blood:	n/a	n/a
3	ARID3A	chr21:45358945-45359370	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:45358856-45359345	K562	blood:	n/a	n/a
5	ATF2	chr21:45357627-45358193	GM12878	blood:	n/a	n/a
6	ATF2	chr21:45358407-45359355	GM12878	blood:	n/a	n/a
7	ATF2	chr21:45358396-45359339	GM12878	blood:	n/a	n/a
8	ATF3	chr21:45358851-45359181	HepG2	liver:	n/a	n/a
9	ATF3	chr21:45358820-45359346	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr21:45358498-45359301	GM12878	blood:	n/a	n/a
11	ATF3	chr21:45358564-45359291	K562	blood:	n/a	n/a
12	ATF3	chr21:45358895-45359334	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr21:45358999-45359218	GM12878	blood:	n/a	n/a
14	BACH1	chr21:45358805-45359222	K562	blood:	n/a	n/a
15	BACH1	chr21:45358712-45359296	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr21:45358597-45359241	GM12878	blood:	n/a	n/a
17	BCL11A	chr21:45358500-45358940	GM12878	blood:	n/a	n/a
18	BCL11A	chr21:45358578-45359106	GM12878	blood:	n/a	n/a
19	BCL3	chr21:45365039-45365367	GM12878	blood:	n/a	n/a
20	BCL3	chr21:45358534-45359093	GM12878	blood:	n/a	n/a
21	BCL3	chr21:45364964-45365329	GM12878	blood:	n/a	n/a
22	BCL3	chr21:45358431-45359295	GM12878	blood:	n/a	n/a
23	BCLAF1	chr21:45358386-45359381	GM12878	blood:	n/a	n/a
24	BCLAF1	chr21:45358437-45359319	GM12878	blood:	n/a	n/a
25	BHLHE40	chr21:45358435-45359327	GM12878	blood:	n/a	chr21:45358926-45358942
26	BHLHE40	chr21:45357726-45358069	GM12878	blood:	n/a	n/a
27	BHLHE40	chr21:45358493-45359279	K562	blood:	n/a	chr21:45358926-45358942
28	BHLHE40	chr21:45358634-45359363	HepG2	liver:	n/a	chr21:45358926-45358942
29	BRCA1	chr21:45358603-45358626	GM12878	blood:	n/a	n/a
30	BRCA1	chr21:45358994-45359246	HepG2	liver:	n/a	n/a
31	BRCA1	chr21:45359040-45359247	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr21:45358839-45359300	GM12878	blood:	n/a	n/a
33	BRCA1	chr21:45358962-45359266	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr21:45357090-45357584	K562	blood:	n/a	n/a
35	CBX3	chr21:45357200-45357525	K562	blood:	n/a	n/a
36	CBX3	chr21:45358419-45359334	K562	blood:	n/a	n/a
37	CCNT2	chr21:45358654-45359310	K562	blood:	n/a	chr21:45359186-45359195
38	CEBPB	chr21:45361715-45361816	A549	lung:	n/a	n/a
39	CEBPB	chr21:45368416-45368546	K562	blood:	n/a	n/a
40	CEBPB	chr21:45361677-45361833	IMR90	lung:	n/a	n/a
41	CEBPB	chr21:45358935-45359236	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr21:45357329-45357586	HepG2	liver:	n/a	chr21:45357500-45357511
43	CEBPB	chr21:45357356-45357682	HepG2	liver:	n/a	chr21:45357500-45357511
44	CEBPB	chr21:45357453-45357612	IMR90	lung:	n/a	chr21:45357500-45357511
45	CEBPB	chr21:45361745-45361784	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr21:45361613-45361926	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr21:45361357-45361470	HepG2	liver:	n/a	n/a
48	CEBPB	chr21:45359001-45359219	GM12878	blood:	n/a	n/a
49	CEBPB	chr21:45357314-45357684	K562	blood:	n/a	chr21:45357500-45357511
50	CEBPB	chr21:45358885-45359215	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45364410-45364460	HL-60	blood:	n/a
2	chr21:45361964-45362014	K562	blood:	n/a
3	chr21:45361964-45362014	HCPEpiC	choroid plexus:	n/a
4	chr21:45360804-45360854	PrEC	prostate:	n/a
5	chr21:45361964-45362014	HRPEpiC	eye:	n/a
6	chr21:45363474-45363524	AG09319	gingival:	n/a
7	chr21:45360804-45360854	RPTEC	kidney:	n/a
8	chr21:45364410-45364460	AG04449	skin:	fetal
9	chr21:45364410-45364460	HPAEpiC	pulmonary alveolar:	n/a
10	chr21:45361964-45362014	HUVEC	blood vessel:	n/a
11	chr21:45367182-45367232	HMEC	breast:	n/a
12	chr21:45364410-45364460	HCF	heart:	n/a
13	chr21:45367182-45367232	HepG2	liver:	n/a
14	chr21:45363474-45363524	T-47D	breast:	n/a
15	chr21:45360804-45360854	HMEC	breast:	n/a
16	chr21:45361964-45362014	RPTEC	kidney:	n/a
17	chr21:45367182-45367232	CMK	blood:	n/a
18	chr21:45364410-45364460	GM19239	blood:	n/a
19	chr21:45363474-45363524	ProgFib	skin:	n/a
20	chr21:45363775-45363825	GM19239	blood:	n/a
21	chr21:45361964-45362014	LNCaP	prostate:	n/a
22	chr21:45363775-45363825	NH-A	brain:	n/a
23	chr21:45363775-45363825	AG09309	skin:	n/a
24	chr21:45363474-45363524	HUVEC	blood vessel:	n/a
25	chr21:45367182-45367232	BE2_C	brain:	n/a
26	chr21:45367182-45367232	SK-N-SH	brain:	n/a
27	chr21:45363775-45363825	HMEC	breast:	n/a
28	chr21:45364410-45364460	MCF-7	breast:	n/a
29	chr21:45360804-45360854	NB4	blood:	n/a
30	chr21:45367182-45367232	Caco-2	colon:	n/a
31	chr21:45364410-45364460	GM06990	blood:	n/a
32	chr21:45367182-45367232	GM06990	blood:	n/a
33	chr21:45367182-45367232	HEK293	kidney:	embryo
34	chr21:45367182-45367232	PrEC	prostate:	n/a
35	chr21:45364410-45364460	AoSMC	blood vessel:	n/a
36	chr21:45363775-45363825	NHBE	bronchial:	n/a
37	chr21:45367182-45367232	ECC-1	luminal epithelium:	n/a
38	chr21:45367182-45367232	HUVEC	blood vessel:	n/a
39	chr21:45367182-45367232	A549	lung:	n/a
40	chr21:45363775-45363825	HUVEC	blood vessel:	n/a
41	chr21:45364410-45364460	AG09309	skin:	n/a
42	chr21:45361964-45362014	GM12892	blood:	n/a
43	chr21:45364410-45364460	CMK	blood:	n/a
44	chr21:45363474-45363524	GM12892	blood:	n/a
45	chr21:45364410-45364460	A549	lung:	n/a
46	chr21:45364410-45364460	SAEC	small airway:	n/a
47	chr21:45363474-45363524	AG04449	skin:	fetal
48	chr21:45363775-45363825	SAEC	small airway:	n/a
49	chr21:45367182-45367232	GM12892	blood:	n/a
50	chr21:45363775-45363825	BJ	skin:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:45236177..45236793-chr21:45358789..45359315,2	MCF-7	breast:
2	chr21:45362716..45365648-chr21:45369841..45372206,2	MCF-7	breast:
3	chr20:52815882..52816401-chr21:45359058..45359696,2	MCF-7	breast:
4	chr21:45303695..45304459-chr21:45359035..45359612,2	MCF-7	breast:
5	chr21:45357462..45359128-chr21:45444905..45447348,2	K562	blood:
6	chr21:45223833..45232004-chr21:45356708..45361221,12	K562	blood:
7	chr21:45358391..45361361-chr21:45366953..45369647,2	MCF-7	breast:
8	chr21:45279077..45280867-chr21:45358882..45361761,2	K562	blood:
9	chr21:45335675..45337724-chr21:45358357..45360411,2	K562	blood:
10	chr21:45261344..45263558-chr21:45354374..45356683,2	K562	blood:
11	chr21:45233511..45236046-chr21:45357246..45359137,3	K562	blood:
12	chr21:45349952..45352425-chr21:45363835..45365722,2	K562	blood:
13	chr21:45137547..45139437-chr21:45356749..45358555,2	K562	blood:
14	chr21:45230951..45231574-chr21:45358755..45359268,2	MCF-7	breast:
15	chr21:45358600..45359641-chr21:45394697..45395938,6	MCF-7	breast:
16	chr21:45330659..45332526-chr21:45353655..45356430,2	K562	blood:
17	chr21:45358568..45359567-chr21:45394821..45396082,11	MCF-7	breast:
18	chr21:45335260..45337221-chr21:45351705..45354017,2	K562	blood:
19	chr21:45233392..45235627-chr21:45355114..45357134,2	K562	blood:
20	chr21:45371946..45375677-chr21:45376772..45380405,4	K562	blood:
21	chr21:45368958..45371465-chr21:45372849..45375980,3	K562	blood:
22	chr21:45361403..45363347-chr21:45436825..45439305,2	K562	blood:
23	chr21:45249286..45250425-chr21:45358859..45359776,4	MCF-7	breast:
24	chr21:45358695..45359504-chr21:45376371..45377288,2	MCF-7	breast:
25	chr21:45368958..45371465-chr21:45372849..45375980,3	K562	blood:
26	chr21:45367943..45370581-chr21:45429600..45432583,3	K562	blood:
27	chr21:45281403..45288287-chr21:45354667..45363125,18	K562	blood:
28	chr21:45340582..45343200-chr21:45355048..45357219,2	MCF-7	breast:
29	chr21:45348204..45349934-chr21:45358596..45359626,8	MCF-7	breast:
30	chr21:45323009..45324981-chr21:45353834..45356371,2	K562	blood:
31	chr21:45285861..45287868-chr21:45358752..45361142,2	K562	blood:
32	chr21:45340527..45345737-chr21:45352879..45360873,10	K562	blood:
33	chr21:45210542..45212642-chr21:45354588..45357125,2	K562	blood:
34	chr21:45366021..45369525-chr21:45388691..45391384,4	K562	blood:
35	chr21:45358902..45359545-chr21:45487441..45487957,2	MCF-7	breast:
36	chr21:45230367..45231197-chr21:45361732..45362367,2	K562	blood:
37	chr21:45355633..45358053-chr21:45363187..45364790,2	K562	blood:
38	chr21:45299527..45301699-chr21:45352590..45355103,2	K562	blood:
39	chr21:45365752..45369442-chr21:45370702..45375252,7	MCF-7	breast:
40	chr21:45208821..45209846-chr21:45358654..45359522,7	K562	blood:
41	chr21:45301296..45303412-chr21:45359569..45361087,2	MCF-7	breast:
42	chr21:45350751..45352749-chr21:45352921..45355084,2	K562	blood:
43	chr21:45370723..45373935-chr21:45374637..45377762,3	K562	blood:
44	chr21:45232218..45234898-chr21:45363794..45365365,2	MCF-7	breast:
45	chr21:45209147..45210147-chr21:45359011..45359569,2	MCF-7	breast:
46	chr21:45354193..45356078-chr21:45363330..45365754,2	MCF-7	breast:
47	chr21:45366033..45367987-chr21:45430998..45433821,2	MCF-7	breast:
48	chr21:45195046..45197218-chr21:45357463..45360101,2	K562	blood:
49	chr21:45365116..45368184-chr21:45371047..45373438,4	K562	blood:
50	chr21:45352880..45356983-chr21:45357815..45359696,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRAPPC10-3	chr21:45368035-45368223	NONHSAT082465
2	lnc-TRAPPC10-3	chr21:45366891-45366939	NONHSAT082465

No data

Variant related genes	Relation type
AGPAT3	TF binding region
AGPAT3	CpG island
ENSG00000160209	chromatin interactions
ENSG00000215458	chromatin interactions
ENSG00000160216	chromatin interactions
ENSG00000235374	chromatin interactions
ENSG00000160218	chromatin interactions
ENSG00000160214	chromatin interactions
ENSG00000159208	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000160213	chromatin interactions

Extended variants
information (count: 926 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532863412	chr21:45353439-45353440	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs533129001	chr21:45353461-45353462	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376253803	chr21:45353514-45353515	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551616227	chr21:45353550-45353551	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562886888	chr21:45353606-45353607	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368835246	chr21:45353623-45353624	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530067221	chr21:45353646-45353647	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs115999771	chr21:45353680-45353681	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77242501	chr21:45353708-45353709	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534466697	chr21:45353709-45353710	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568233486	chr21:45353728-45353729	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571421512	chr21:45353732-45353733	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376309818	chr21:45353789-45353790	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538938266	chr21:45353802-45353803	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537173842	chr21:45353809-45353810	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557007026	chr21:45353869-45353870	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572496121	chr21:45353877-45353878	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575154935	chr21:45353880-45353881	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs140375941	chr21:45353914-45353915	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554664104	chr21:45353915-45353916	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149962182	chr21:45353916-45353917	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145118641	chr21:45353924-45353925	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565492396	chr21:45353966-45353967	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192584686	chr21:45354021-45354022	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544870479	chr21:45354050-45354051	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563088571	chr21:45354114-45354115	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546099094	chr21:45354115-45354116	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550934239	chr21:45354155-45354156	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375214394	chr21:45354161-45354162	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116266386	chr21:45354172-45354173	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs3788082	chr21:45354189-45354190	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs149136824	chr21:45354211-45354212	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145022000	chr21:45354212-45354213	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538484481	chr21:45354218-45354219	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111337978	chr21:45354219-45354220	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576177806	chr21:45354239-45354240	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569097630	chr21:45354288-45354289	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536207669	chr21:45354290-45354291	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554626805	chr21:45354328-45354329	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572941848	chr21:45354346-45354347	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183604016	chr21:45354362-45354363	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558399651	chr21:45354374-45354375	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs570794834	chr21:45354397-45354398	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372572775	chr21:45354424-45354425	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544522884	chr21:45354439-45354440	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2838440	chr21:45354442-45354443	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs574792991	chr21:45354462-45354463	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541791564	chr21:45354503-45354504	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560127613	chr21:45354539-45354540	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527712274	chr21:45354554-45354555	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	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
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	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 cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	19805367	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	17426248	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45337600-45358600	Weak transcription	Osteobl	bone
2	chr21:45338800-45358600	Weak transcription	Hela-S3	cervix
3	chr21:45340800-45358800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr21:45341400-45358600	Weak transcription	A549	lung
5	chr21:45342200-45357000	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr21:45342200-45358800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr21:45342400-45356400	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr21:45342600-45354600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr21:45343000-45357600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr21:45343000-45372400	Weak transcription	Small Intestine	intestine
11	chr21:45343400-45355200	Weak transcription	Brain Germinal Matrix	brain
12	chr21:45343400-45355600	Weak transcription	Brain Angular Gyrus	brain
13	chr21:45343600-45358000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr21:45343800-45356000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr21:45343800-45356200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr21:45343800-45357600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr21:45343800-45358600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr21:45343800-45358600	Weak transcription	HSMM	muscle
19	chr21:45343800-45358800	Weak transcription	Ovary	ovary
20	chr21:45343800-45379800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr21:45344000-45357200	Strong transcription	Fetal Stomach	stomach
22	chr21:45344400-45358400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr21:45345200-45358600	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr21:45345400-45358600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr21:45345600-45353800	Weak transcription	Colonic Mucosa	Colon
26	chr21:45345800-45354800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr21:45346400-45355400	Weak transcription	Fetal Lung	lung
28	chr21:45347600-45354600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr21:45348400-45354000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr21:45348400-45356000	Weak transcription	Right Atrium	heart
31	chr21:45348400-45363800	Weak transcription	Aorta	Aorta
32	chr21:45348800-45355200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr21:45348800-45356600	Weak transcription	Colon Smooth Muscle	Colon
34	chr21:45348800-45358600	Weak transcription	NHEK	skin
35	chr21:45349000-45354400	Weak transcription	K562	blood
36	chr21:45349200-45355200	Weak transcription	Brain Hippocampus Middle	brain
37	chr21:45349200-45355400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr21:45349400-45355600	Strong transcription	Fetal Intestine Large	intestine
39	chr21:45349400-45357000	Strong transcription	Fetal Intestine Small	intestine
40	chr21:45349400-45359200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr21:45349800-45354200	Weak transcription	Placenta	Placenta
42	chr21:45349800-45355200	Weak transcription	Stomach Mucosa	stomach
43	chr21:45349800-45357600	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr21:45350000-45353800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr21:45350000-45354800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr21:45350000-45357600	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr21:45350000-45358400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr21:45350200-45353600	Weak transcription	Esophagus	oesophagus
49	chr21:45350200-45354800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr21:45350200-45355000	Weak transcription	Brain Substantia Nigra	brain

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