Variant report

Variant	esv3455479
Chromosome Location	chr21:45609616-45620726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45612981-45613248	K562	blood:	n/a	n/a
2	ARID3A	chr21:45613588-45613839	K562	blood:	n/a	n/a
3	ATF1	chr21:45613617-45613918	K562	blood:	n/a	n/a
4	ATF1	chr21:45616087-45617176	K562	blood:	n/a	n/a
5	ATF2	chr21:45615997-45616558	GM12878	blood:	n/a	n/a
6	ATF2	chr21:45615953-45616749	GM12878	blood:	n/a	n/a
7	ATF3	chr21:45616046-45616449	K562	blood:	n/a	n/a
8	ATF3	chr21:45616127-45616350	K562	blood:	n/a	n/a
9	BACH1	chr21:45613623-45613858	K562	blood:	n/a	n/a
10	BATF	chr21:45616096-45616518	GM12878	blood:	n/a	n/a
11	BATF	chr21:45616055-45616561	GM12878	blood:	n/a	n/a
12	BCL11A	chr21:45616126-45616490	GM12878	blood:	n/a	chr21:45616371-45616379
13	BCL11A	chr21:45616016-45616587	GM12878	blood:	n/a	chr21:45616371-45616379
14	BCLAF1	chr21:45615961-45616691	GM12878	blood:	n/a	chr21:45616371-45616379
15	BCLAF1	chr21:45615984-45616680	GM12878	blood:	n/a	chr21:45616371-45616379
16	BHLHE40	chr21:45614247-45614287	GM12878	blood:	n/a	n/a
17	BHLHE40	chr21:45616058-45616612	GM12878	blood:	n/a	n/a
18	BHLHE40	chr21:45616045-45616724	K562	blood:	n/a	n/a
19	BHLHE40	chr21:45613168-45613262	K562	blood:	n/a	n/a
20	BHLHE40	chr21:45615820-45615848	GM12878	blood:	n/a	n/a
21	BHLHE40	chr21:45613574-45613923	K562	blood:	n/a	n/a
22	BHLHE40	chr21:45617016-45617223	K562	blood:	n/a	n/a
23	BRCA1	chr21:45616217-45616417	GM12878	blood:	n/a	n/a
24	CBX3	chr21:45616117-45616479	K562	blood:	n/a	n/a
25	CCNT2	chr21:45616071-45616733	K562	blood:	n/a	chr21:45616560-45616580
26	CCNT2	chr21:45613627-45613908	K562	blood:	n/a	n/a
27	CEBPB	chr21:45614408-45614567	K562	blood:	n/a	n/a
28	CEBPB	chr21:45613067-45613249	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr21:45613160-45613204	K562	blood:	n/a	n/a
30	CEBPB	chr21:45614126-45614641	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr21:45616133-45616394	HepG2	liver:	n/a	chr21:45616256-45616267
32	CEBPB	chr21:45616078-45616543	K562	blood:	n/a	chr21:45616256-45616267
33	CEBPB	chr21:45616101-45616427	K562	blood:	n/a	chr21:45616256-45616267
34	CEBPB	chr21:45615941-45616614	GM12878	blood:	n/a	chr21:45616256-45616267
35	CEBPB	chr21:45613053-45613333	IMR90	lung:	n/a	n/a
36	CEBPB	chr21:45614140-45614636	K562	blood:	n/a	n/a
37	CEBPB	chr21:45614294-45614671	IMR90	lung:	n/a	n/a
38	CEBPB	chr21:45614152-45614631	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr21:45614342-45614644	A549	lung:	n/a	n/a
40	CEBPB	chr21:45614329-45614654	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr21:45616139-45616412	K562	blood:	n/a	chr21:45616256-45616267
42	CEBPB	chr21:45616191-45616330	IMR90	lung:	n/a	chr21:45616256-45616267
43	CEBPB	chr21:45619441-45619519	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr21:45616038-45616797	MCF-7	breast:	n/a	chr21:45616256-45616267
45	CEBPB	chr21:45614322-45614666	HepG2	liver:	n/a	n/a
46	CHD1	chr21:45615978-45616722	GM12878	blood:	n/a	chr21:45616323-45616333
47	CHD2	chr21:45613089-45613310	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr21:45619426-45619622	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr21:45615929-45616813	GM12878	blood:	n/a	chr21:45616323-45616333
50	CHD2	chr21:45614101-45614203	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45619449-45619499	HNPCEpiC	eye:	n/a
2	chr21:45619449-45619499	A549	lung:	n/a
3	chr21:45619449-45619499	GM12891	blood:	n/a
4	chr21:45619449-45619499	ovcar-3	ovarian:	n/a
5	chr21:45619449-45619499	Caco-2	colon:	n/a
6	chr21:45619449-45619499	HCM	heart:	n/a
7	chr21:45619449-45619499	ECC-1	luminal epithelium:	n/a
8	chr21:45619449-45619499	AoSMC	blood vessel:	n/a
9	chr21:45619449-45619499	LNCaP	prostate:	n/a
10	chr21:45619449-45619499	NHDF-neo	bronchial:	n/a
11	chr21:45619449-45619499	SK-N-MC	brain:	n/a
12	chr21:45619449-45619499	CMK	blood:	n/a
13	chr21:45619449-45619499	HRPEpiC	eye:	n/a
14	chr21:45619449-45619499	K562	blood:	n/a
15	chr21:45619449-45619499	HPAEpiC	pulmonary alveolar:	n/a
16	chr21:45619449-45619499	GM06990	blood:	n/a
17	chr21:45619449-45619499	PANC-1	pancreas:	n/a
18	chr21:45619449-45619499	ProgFib	skin:	n/a
19	chr21:45619449-45619499	SKMC	muscle:	n/a
20	chr21:45619449-45619499	NB4	blood:	n/a
21	chr21:45619449-45619499	IMR90	lung:	fetal
22	chr21:45619449-45619499	BJ	skin:	n/a
23	chr21:45619449-45619499	PrEC	prostate:	n/a
24	chr21:45619449-45619499	HCPEpiC	choroid plexus:	n/a
25	chr21:45619449-45619499	GM12878	blood:	n/a
26	chr21:45619449-45619499	AG04450	lung:	fetal
27	chr21:45619449-45619499	MCF-7	breast:	n/a
28	chr21:45619449-45619499	AG09309	skin:	n/a
29	chr21:45619449-45619499	AG04449	skin:	fetal
30	chr21:45619449-45619499	HRCEpiC	kidney:	n/a
31	chr21:45619449-45619499	HCF	heart:	n/a
32	chr21:45619449-45619499	SK-N-SH	brain:	n/a
33	chr21:45619449-45619499	AG09319	gingival:	n/a
34	chr21:45619449-45619499	GM19239	blood:	n/a
35	chr21:45619449-45619499	HEEpiC	esophagus:	n/a
36	chr21:45619449-45619499	GM12892	blood:	n/a
37	chr21:45619449-45619499	HUVEC	blood vessel:	n/a
38	chr21:45619449-45619499	NHBE	bronchial:	n/a
39	chr21:45619449-45619499	HRE	kidney:	n/a
40	chr21:45619449-45619499	MCF10A-Er-Src	breast:	n/a
41	chr21:45619449-45619499	U87	brain:	n/a
42	chr21:45619449-45619499	HEK293	kidney:	embryo
43	chr21:45619449-45619499	NT2-D1	testis:	n/a
44	chr21:45619449-45619499	NH-A	brain:	n/a
45	chr21:45619449-45619499	HIPEpiC	eye:	n/a
46	chr21:45619449-45619499	SK-N-SH_RA	brain:	n/a
47	chr21:45619449-45619499	Hela-S3	cervix:	n/a
48	chr21:45619449-45619499	Hepatocyte	liver:	n/a
49	chr21:45619449-45619499	PFSK-1	brain:	n/a
50	chr21:45619449-45619499	HL-60	blood:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45586838..45589344-chr21:45614842..45616536,2	MCF-7	breast:
2	chr21:45574056..45576001-chr21:45612468..45614888,2	MCF-7	breast:
3	chr21:45609994..45611618-chr21:45719686..45721405,2	MCF-7	breast:
4	chr21:45613209..45613813-chr21:45623826..45624382,2	NB4	blood:
5	chr21:45610065..45610976-chr21:45717590..45718626,4	MCF-7	breast:
6	chr21:45595676..45596715-chr21:45615636..45617128,25	MCF-7	breast:
7	chr21:45616221..45617876-chr21:45625272..45628231,2	K562	blood:
8	chr21:45612993..45620081-chr21:45620303..45625017,17	MCF-7	breast:
9	chr21:45607137..45608941-chr21:45615370..45617109,2	K562	blood:
10	chr21:45611519..45615384-chr21:45659181..45663993,7	MCF-7	breast:
11	chr21:45567927..45569479-chr21:45614833..45617390,2	K562	blood:
12	chr21:45615955..45617029-chr21:45660387..45661089,4	MCF-7	breast:
13	chr21:45609075..45610927-chr21:45615037..45616803,2	K562	blood:
14	chr21:45553470..45554986-chr21:45608150..45609834,2	MCF-7	breast:
15	chr21:45595676..45596652-chr21:45615636..45617063,9	MCF-7	breast:
16	chr21:45595680..45596514-chr21:45615830..45617060,14	MCF-7	breast:
17	chr21:45620341..45625358-chr21:45718389..45721509,5	MCF-7	breast:
18	chr21:45615189..45618434-chr21:45625221..45628569,5	MCF-7	breast:
19	chr21:45605212..45608621-chr21:45608817..45614047,5	K562	blood:
20	chr21:45612553..45615742-chr21:45666296..45670643,3	MCF-7	breast:
21	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
22	chr21:45593299..45595142-chr21:45615478..45617030,2	MCF-7	breast:
23	chr21:45607258..45609812-chr21:45714744..45717743,2	MCF-7	breast:
24	chr21:45610680..45613679-chr21:45657014..45661776,5	MCF-7	breast:
25	chr21:45570114..45570951-chr21:45616167..45617027,2	MCF-7	breast:
26	chr21:45615502..45617869-chr21:45667459..45670293,2	K562	blood:
27	chr21:45609075..45610927-chr21:45615037..45616803,2	K562	blood:
28	chr21:43796149..43796708-chr21:45616447..45617057,2	MCF-7	breast:
29	chr21:45604879..45610592-chr21:45658595..45664052,16	MCF-7	breast:
30	chr21:45614676..45619255-chr21:45657692..45665676,14	MCF-7	breast:
31	chr21:45565749..45567363-chr21:45612252..45614777,2	MCF-7	breast:
32	chr21:45574118..45574672-chr21:45616064..45616668,2	MCF-7	breast:
33	chr21:45589478..45591671-chr21:45607631..45610004,2	MCF-7	breast:
34	chr21:45557116..45559735-chr21:45615528..45618206,3	MCF-7	breast:
35	chr21:45610778..45612309-chr21:45667999..45669878,2	MCF-7	breast:
36	chr21:45610715..45617377-chr21:45717031..45721978,7	MCF-7	breast:
37	chr21:45565762..45568425-chr21:45616246..45618901,2	MCF-7	breast:
38	chr21:45568616..45570755-chr21:45615083..45617675,2	K562	blood:
39	chr21:45615955..45617029-chr21:45660335..45661089,5	MCF-7	breast:
40	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
41	chr21:45566742..45569322-chr21:45613127..45615094,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICOSLG-3	chr21:45613874-45613944	XLOC_014113
2	lnc-ICOSLG-3	chr21:45614149-45614187	XLOC_014113
3	lnc-ICOSLG-3	chr21:45610322-45610610	XLOC_014113
4	lnc-ICOSLG-2	chr21:45619132-45620582	XLOC_014114
5	lnc-ICOSLG-2	chr21:45620693-45621216	XLOC_014114

No data

Variant related genes	Relation type
ENSG00000232124	TF binding region
ENSG00000232124	CpG island
ENSG00000267913	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000232124	chromatin interactions
ENSG00000232698	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000232010	chromatin interactions

Extended variants
information (count: 491 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574914570	chr21:45609617-45609618	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191938685	chr21:45609680-45609681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552211573	chr21:45609687-45609688	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs570416563	chr21:45609749-45609750	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537837413	chr21:45609763-45609764	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148544783	chr21:45609863-45609864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367829484	chr21:45609868-45609869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549891423	chr21:45609892-45609893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568048633	chr21:45609893-45609894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141426683	chr21:45609902-45609903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs554047903	chr21:45609917-45609918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572711063	chr21:45609952-45609953	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs62228185	chr21:45609958-45609959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs150832171	chr21:45609980-45609981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376724017	chr21:45609993-45609994	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139605549	chr21:45610018-45610019	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543401448	chr21:45610085-45610086	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374850062	chr21:45610099-45610100	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs743475	chr21:45610100-45610101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542023456	chr21:45610146-45610147	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560049394	chr21:45610147-45610148	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs527587746	chr21:45610219-45610220	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs187379999	chr21:45610220-45610221	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs140132192	chr21:45610307-45610308	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs743476	chr21:45610369-45610370	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs549492171	chr21:45610393-45610394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs568171767	chr21:45610439-45610440	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs535165469	chr21:45610470-45610471	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs547976304	chr21:45610489-45610490	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs565886943	chr21:45610495-45610496	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs79845786	chr21:45610504-45610505	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs743477	chr21:45610518-45610519	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs558070472	chr21:45610528-45610529	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs149841653	chr21:45610571-45610572	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs113459440	chr21:45610581-45610582	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs193155480	chr21:45610620-45610621	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374785510	chr21:45610643-45610644	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185437781	chr21:45610653-45610654	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148592402	chr21:45610665-45610666	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34550147	chr21:45610701-45610702	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549795026	chr21:45610742-45610743	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376482346	chr21:45610815-45610816	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs762417	chr21:45610821-45610822	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs370486458	chr21:45610841-45610842	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546007505	chr21:45610862-45610863	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs535264002	chr21:45610865-45610866	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374808975	chr21:45610873-45610874	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs762418	chr21:45610893-45610894	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs372524033	chr21:45610913-45610914	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs762419	chr21:45610914-45610915	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

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
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
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45602800-45612200	Weak transcription	Right Atrium	heart
2	chr21:45605200-45610800	Weak transcription	Right Ventricle	heart
3	chr21:45605400-45610800	Weak transcription	Pancreas	Pancrea
4	chr21:45605400-45610800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr21:45605400-45612200	Weak transcription	Left Ventricle	heart
6	chr21:45605400-45613800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr21:45605600-45610600	Weak transcription	Brain Substantia Nigra	brain
8	chr21:45605800-45611400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr21:45606000-45610600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr21:45606000-45610800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr21:45606000-45613800	Weak transcription	Stomach Mucosa	stomach
12	chr21:45606200-45610800	Weak transcription	Spleen	Spleen
13	chr21:45606400-45610800	Weak transcription	Primary B cells from peripheral blood	blood
14	chr21:45606600-45610600	Weak transcription	Fetal Muscle Leg	muscle
15	chr21:45606800-45610800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr21:45607200-45609800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr21:45608600-45610400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr21:45608600-45610400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr21:45608600-45611000	Weak transcription	Gastric	stomach
20	chr21:45608600-45612000	Weak transcription	Esophagus	oesophagus
21	chr21:45608600-45612400	Weak transcription	Ovary	ovary
22	chr21:45608800-45610800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr21:45609800-45610200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr21:45609800-45610600	Enhancers	Fetal Muscle Trunk	muscle
25	chr21:45610200-45610400	Flanking Active TSS	NHDF-Ad	bronchial
26	chr21:45610200-45610600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr21:45610200-45610800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr21:45610200-45611000	Enhancers	Fetal Stomach	stomach
29	chr21:45610200-45611000	Enhancers	HepG2	liver
30	chr21:45610200-45614800	Enhancers	NHLF	lung
31	chr21:45610400-45610800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr21:45610400-45611800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr21:45610400-45615000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr21:45610400-45615400	Enhancers	NHDF-Ad	bronchial
35	chr21:45610400-45616000	Weak transcription	Thymus	Thymus
36	chr21:45610600-45610800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr21:45610600-45611200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
38	chr21:45610600-45611400	ZNF genes & repeats	Brain Substantia Nigra	brain
39	chr21:45610600-45612200	ZNF genes & repeats	Fetal Muscle Leg	muscle
40	chr21:45610800-45611000	Enhancers	Primary B cells from peripheral blood	blood
41	chr21:45610800-45611000	Enhancers	Right Ventricle	heart
42	chr21:45610800-45611000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr21:45610800-45611000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
44	chr21:45610800-45611200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr21:45610800-45611200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:45610800-45611200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr21:45610800-45611200	Bivalent Enhancer	Adipose Nuclei	Adipose
48	chr21:45610800-45611200	ZNF genes & repeats	Pancreas	Pancrea
49	chr21:45610800-45611200	Bivalent Enhancer	Rectal Smooth Muscle	rectum
50	chr21:45610800-45611200	Enhancers	Spleen	Spleen

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